WO2005069855A2 - Modulators of angiogenesis - Google Patents

Modulators of angiogenesis Download PDF

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WO2005069855A2
WO2005069855A2 PCT/US2005/001194 US2005001194W WO2005069855A2 WO 2005069855 A2 WO2005069855 A2 WO 2005069855A2 US 2005001194 W US2005001194 W US 2005001194W WO 2005069855 A2 WO2005069855 A2 WO 2005069855A2
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protein
angiogenesis
compound
ofthe
polypeptide
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PCT/US2005/001194
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French (fr)
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WO2005069855A3 (en
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Weiduan Xu
Sacha J. Holland
James Lorens
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Rigel Pharmaceuticals, Inc.
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Priority to EP05705695A priority Critical patent/EP1721158A4/en
Publication of WO2005069855A2 publication Critical patent/WO2005069855A2/en
Publication of WO2005069855A3 publication Critical patent/WO2005069855A3/en

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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/566—Immunoassay; Biospecific binding assay; Materials therefor using specific carrier or receptor proteins as ligand binding reagents where possible specific carrier or receptor proteins are classified with their target compounds
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/26—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
    • C12Q1/32—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase involving dehydrogenase
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/34—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving hydrolase
    • C12Q1/37—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving hydrolase involving peptidase or proteinase
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/48—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving transferase
    • C12Q1/485—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving transferase involving kinase
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
    • G01N2333/475—Assays involving growth factors
    • G01N2333/515—Angiogenesic factors; Angiogenin

Definitions

  • the present invention relates to regulation of angiogenesis.
  • the invention further relates to methods for identifying and using agents, including small organic molecules, antibodies, peptides, cyclic peptides, nucleic acids, antisense nucleic acids, RNAi, and ribozymes, that modulate angiogenesis; as well as to the use of expression profiles and compositions in diagnosis and therapy of angiogenesis and cancer.
  • Angiogenesis is typically limited in a normal adult to the placenta, ovary, endometrium and sites of wound healing.
  • angiogenesis or its absence, plays an important role in the maintenance of a variety of pathological states. Some of these states are characterized by neovascularization, e.g., cancer and tumorigenesis, e.g., endometriosis, diabetic retinopathy, glaucoma, glomerulonephritis, and age related macular degeneration.
  • Others e.g., stroke, infertility, heart disease, e.g., restenosis, ulcers, and scleroderma, are diseases of angiogenic insufficiency. Therefore, there is a need to identify nucleic acids encoding proteins involved in the regulation of angiogenesis, to identify, e.g., modulators of angiogenesis, as well as new therapeutic and diagnostic applications.
  • Novel targets for anti-angiogenic therapy have been identified using a functional genetic screen based on vascular endothelial growth factor receptor 2 (VEGFR2) ligand binding triggered receptor internalization. Inhibition or activation of these targets (by small molecule inhibitors; protein, antibody and peptide therapeutics; RNAi; antisense; gene therapy etc.) have therapeutic value in modulating angiogenesis, e.g., breast, lung, colon, ovarian, liver, thyroid, stomach, bladder, and prostate cancer, basal cell carcinoma, melanoma, lymphomas, leukemias, e.g., myeloid leukemia (CML and AML), endometriosis, diabetic retinopathy, glaucoma, glomerulonephritis, age related macular degeneration, as well as, e.g., stroke, infertility, heart disease, e.g., restenosis, ulcers, and scleroderma.
  • VEGFR2 vascular endothelial
  • the present invention therefore provides nucleic acids encoding proteins involved in modulation of (VEGFR2) ligand binding triggered receptor internalization and modulation of angiogenesis.
  • the invention therefore provides methods of screening for compounds, e.g., small organic molecules, antibodies, nucleic acids, peptides, cyclic peptides, nucleic acids, antisense molecules, RNAi, and ribozymes, that are capable of modulating angiogenesis, e.g., either activating or inhibiting angiogenesis.
  • Therapeutic and diagnostic methods and reagents are also provided.
  • the present invention provides a method for identifying a compound that modulates angiogenesis, the method comprising the steps of: (i) contacting the compound with an angiogenesis modulating polypeptide or fragment thereof, the polypeptide encoded by a nucleic acid that hybridizes under stringent conditions to a reference nucleic acid encoding the polypeptide, the polypeptide selected from the group consisting of ubiquitin hydrolase (USP37), calcium/calmodulin-dependent protein kinase ⁇ (CAMKK2), methionine adenosyltransferase II ⁇ (Mat2A), carnitine palmitoyltransferase II (CPT-2), DDX5 RNA helicase, acetyl-coenzyme A acyltransferase (ACAA1), glucosamine-6-phosphate isomerase (GNPI), 24- dehydrocholesterol reductase (DHCR24), selenoprotein T (
  • the functional effect is determined in vitro. In another embodiment, the functional effect is a physical effect. In another embodiment, the functional effect is determined by measuring ligand binding to the polypeptide. In another embodiment, the functional effect is a chemical effect. [0010] In one embodiment, the polypeptide is expressed in a eukaryotic host cell. In another embodiment, the functional effect is a physical effect. In another embodiment, the functional effect is determined by measuring ligand binding to the polypeptide. In another embodiment, the functional effect is a chemical or phenotypic effect. In another embodiment, the polypeptide is expressed in a eukaryotic host cell, e.g., an endothelial cell. In another embodiment, the functional effect is determined by measuring VEGF-R2 surface expression, ov/33 expression, haptotaxis, or tumor growth in vivo.
  • modulation is inhibition of angiogenesis.
  • the polypeptide is recombinant.
  • the compound is an antibody, a peptide, an antisense molecule, a RNAi molecule, or a small organic molecule.
  • the present invention provides a method for identifying a compound that modulates angiogenesis, the method comprising the steps of (i) contacting the compound with an angiogenesis modulating polypeptide or fragment or inactive variant thereof, the polypeptide selected from the group consisting of ubiquitin hydrolase (USP37), calcium/calmodulin-dependent protein kinase ⁇ (CAMKK2), methionine adenosyltransferase II ⁇ (Mat2A), camitine palmitoyltransferase II (CPT-2), DDX5 RNA helicase, acetyl-coenzyme A acyltransferase (ACAAl), glucosamine-6-phosphate isomerase (GNPI), 24-dehydrocholesterol reductase (DHCR24
  • the subject is a human.
  • the compound is an antibody, an antisense molecule, a peptide, or an RNAi molecule, or a small organic molecule.
  • the compound inhibits angiogenesis.
  • Figure 1 shows a clone encoding USP-37 isolated in a VEGFR-2 upregulation assay.
  • Figure 2 shows USP37 RNA expression in cell lines.
  • FIG. 3 shows that USP-37 is overexpressed in colon carcinomas.
  • Figure 4 shows USP-37 RNAi data.
  • Figure 5 shows USP-37 RNAi data.
  • Figure 6 shows USP-37 RNAi data.
  • Figure 7 shows USP-37 RNAi data.
  • Figure 8 shows USP-37 RNAi data.
  • FIG. 9 summarizes USP-37 data.
  • Fgure 10 shows a clone encoding CaMKK2 isolated in a VEGFR-2 upregulation assay.
  • Figure 11 shows the mRNA expression profile of CaMKK2.
  • Figure 12 shows CaMKK2 RNAi data.
  • Figure 13 shows CaMKK2 RNAi data.
  • Figure 14 shows a CaMKK2 inhibitor STO-609.
  • Figure 15 shows that STO-609 downregulates VEGF2-R levels.
  • Figure 16 shows a summary of CaMKK2 data.
  • Figure 17 shows STO-609 data.
  • Figure 18 shows STO-609 data.
  • FIG. 19 shows STO-609 data.
  • Figure 20 summarizes STO-609 data.
  • VEGF receptor internalization screening strategy to identify proteins involved in regulating angiogenesis.
  • complex libraries of cDNAs were expressed in human primary endothelial cells (e.g., HUVECS, Clonetic CC-2519).
  • HUVEC cells that switch to a differentiated angiostatic state can be identified using a VEGFR2 internalization assay.
  • EGM-2 media Clonetics EGM-2 bullet kit CC-3162
  • EGM-2 media Cells are cultured in starvation medium (EGMS with 0.1%FCS plus 1% BSA in place of VEGF and FCS) at 37°C for 16 hours.
  • the starved HUVECs are stimulated with VEGF stimulation medium at 37°C for 1.5 hours, trypsinized, and stained with VEGFR2 antibody. Single cells exhibiting increased VEGF-R2 expression (i.e., blocked receptor internalization) were selected using FACS analysis.
  • the cDNAs are isolated and sequenced to identify proteins involved in angiogenesis.
  • the cDNAs can represent, e.g., full length transcripts, transcript fragments, 3' untranslated regions, or antisense molecules. In one embodiment, the cDNA acts as a dominant negative mutant.
  • a functional genetic screening strategy can also be used to identify proteins involved in regulating endothelial cell migration on specific matrix components, e.g. vitronectin.
  • a retroviral-based system can be used to stably express complex libraries of various types of genetic elements (e.g. cDNAs and GFP-fusions) in human primary endothelial cells (e.g. HUVECs). Starting with early passage primary endothelial cells representing an "angiogenic state" (i.e., proliferative, highly motile), single cells that have switched to a more differentiated "angiostatic state” (i.e., quiescent, reduced motility) can be identified.
  • angiostatic state i.e., quiescent, reduced motility
  • HUVEC cells can be established which allowed highly efficient migration of HUVEC cells along a haptotactic gradient of specific matrix proteins (e.g. vitronectin / fibronectin) in a Boyden chamber assay.
  • specific matrix proteins e.g. vitronectin / fibronectin
  • Large populations of HUVEC cells are infected with a GFP-fused cDNA library and selected for impaired haptotaxis.
  • Additional assays for proteins involved in angiogenesis include a HUVEC/smooth muscle cell co-culture assay for endothelial tube formation, and chemo-invasion assays.
  • human/mouse tumor xenograft assays mouse sponge angiogenesis and tumorigenesis assays (sponge with human ECs +/- human tumor cells in SCID mice), a collagen-antibody induced arthritis model for RA, and retinal neovascularization assays can be used to identify angiogenesis proteins in vivo and to assay for modulators of such proteins.
  • angiogenesis proteins identified using the VEGFR2 internalization assay described herein, e.g., methionine adenosyltransferase II ⁇ (Mat2A) (hit: fragment), camitine palmitoyltransferase II (CPT-2) (hit: fragment), DDX5 RNA helicase (hit: full- length), calcium calmodulin-dependent protein kinase ⁇ (CAMKK2) (hit: fragment), acetyl-coenzyme A acyltransferase (ACAAl) (hit: fragment), glucosamine-6-phosphate isomerase (GNPI) (hit: full-length), 24-dehydrocholesterol reductase (DHCR24) (hit: fragment), selenoprotein T (SELT) (hit: fragment), protein tyrosine phosphatase, receptor type, B (PTPRB) (hit: full-length), glucosidase ⁇ acid (GBA)
  • Modulators include small organic molecules, nucleic acids, peptides, cyclic peptides, antibodies, antisense molecules, RNAi molecules, and ribozymes.
  • the nucleic acids and proteins of the invention are also useful for diagnostic applications, using, e.g., nucleic acid probes, ohgonucleotides, and antibodies.
  • These polypeptides are also involved in tumorigenesis and cellular proliferation, and are useful for the development of therapeutic molecules to treat diseases associated with angiogenesis, tumorigenesis, and cellular proliferation.
  • the polypeptides described herein and the nucleic acids encoding them are useful for diagnostic assays for diseases associated with angiogenesis, tumorigenesis, and cellular proliferation.
  • the protein ubiquitin hydrolase (USP37) is involved in angiogenesis.
  • Ubiquitin hydrolase plays a role in the hydrolysis of esters formed between thiols and the C-terminal glycine residue ofthe polypeptide ubiquitin, and of AMP- ubiquitin.
  • In vitro hydrolase assays with ubiquitin hydrolase can be used to assay for ubiquitin hydrolase modulators and thus for modulators of angiogenesis.
  • the accession number for USP73 polypeptide is NP_065986 and the accession number for the nucleic acid is NM_020935. See also AB046814 and BAB13420.
  • USP-37 is part of a novel family of ubiquitin hydrolases, most cvlosedly related to USP 26 and 29. conserveed catalytic residues include the Cys bos (GNTCYmN) and the His box (HIGSTSSSDH).
  • the protein CAMKK2 is involved in angiogenesis.
  • CAMKK2 belongs to the Serine/Threonine protein kinase family, and to the
  • CAMKK2 plays a role in the calcium/calmodulin-dependent (CaM) kinase cascade by phosphorylating the downstream kinases CaMKl and CaMK4. Seven transcript variants encoding six distinct isoforms have been identified for CAMKK2. Additional splice variants have been described but their full-length nature has not been determined. The identified isoforms exhibit a distinct ability to undergo autophosphorylation and to phosphorylate the downstream kinases. In vitro serme/threonine kinase assays with CAMKK2 can be used to assay for CAMKK2 modulators and thus for modulators of angiogenesis.
  • CAMKK2 nucleic acids are as follows: NM_006549 (variant 1), NM_ 153499 (variant 2), NM_172216 (variant 3), NM 53500 (variant 4), and NM_172226 (variant 7).
  • Mat2A is involved in angiogenesis.
  • Mat2A is an enzyme that catalyzes the formation of S-adenosylmethionine from methionine and ATP.
  • ⁇ , ⁇ , and ⁇ there are three distinct forms of a Mat2A designated as ⁇ , ⁇ , and ⁇ . ⁇ and ⁇ are expressed only in adult liver, while ⁇ is widely distributed in extrahepatic tissues.
  • Mat2A is expressed in, e.g., invasive adenocarcinoma, bronchioalveolar carcinoma, CD34+, T negative chronic myelogenous leukemia, invasive carcinoma, early stage papillary serous carcinoma, serous adenocarcinoma, oligodendroglioma, metastatic melanoma, and normal gingival.
  • In vitro enzyme assays with Mat2A can be used to assay for Mat2A modulators and thus for modulators of angiogenesis.
  • the accession number for Mar2A polypeptide is NP005902 and the accession number for the nucleic acid is NM_005911.
  • the protein CPT-2 is involved in angiogenesis.
  • CPT2 is a nuclear protein which is transported to the mitochondrial inner membrane. CPT2 together with camitine palmitoyltransferase I oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty- acid (LCFA) oxidation disorders. Defects in CPT2 are the cause of camitine palmitoyltransferase II deficiency (CPT-II deficiency), an autosomal recessive disorder characterized by recurrent myoglobinuria, episodes of muscle pain, stiffness, and rhabdomyolysis.
  • CPT-II deficiency camitine palmitoyltransferase II deficiency
  • CPT-II deficiency an autosomal recessive disorder characterized by recurrent myoglobinuria, episodes of muscle pain, stiffness, and rhabdomyolysis.
  • CPT2 is a component ofthe fatty acid ⁇ - oxidation cycle. CPT2 is expressed in pituitary adenomas, posterior rhombomeres, lens, mammary gland, and human placenta.
  • accession number for CPT-2 polypeptide is NP_000089 and the accession number for CPT-2 nucleic acid is NM_000098.
  • DDX5 is involved in angiogenesis.
  • DDX5 RNA helicase is a DEAD box protein, characterized by the conserved motif Asp-Glu- Ala-Asp (DEAD).
  • DEAD box proteins are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division.
  • DDX5 encodes a DEAD box protein, which is a RNA-dependent ATPase, and also a proliferation-associated nuclear antigen, highly specifically reacting with the simian virus 40 tumor antigen.
  • DDX5 consists of 13 exons, and alternatively splicing transcripts containing several intron sequences have been detected, but no isoforms encoded by these transcripts are identified.
  • DDX5 also has an RNA-dependent ATPase activity, the rate of ATP hydrolysis is highly stimulated by single-stranded RNA.
  • DDX5 is expressed in bulk germ cell seminoma, follicular adenoma, bulk alveolar tumor, juvenile granulosa tumor, normal gingival, anterior rhombomeres, thymus, pituitary, and liver.
  • In vitro helicase assays with DDX5 can be used to assay for DDX5 modulators and thus for modulators of angiogenesis.
  • the accession number for DDX5 nucleic acid is NM_004396 and the accession number for the polypeptide is NP_004387.
  • the protein ACAAl is involved in angiogenesis.
  • ACAAl is a thiolase operative in the /3-oxidation system ofthe peroxisomes. Deficiency of ACAAl leads to pseudo-Zellweger syndrome.
  • In vitro thiolase assays with ACAAl can be used to assay for ACAAl modulators and thus for modulators of angiogenesis.
  • the accession number for the nucleic acid is NM_001607 and the accession number for the polypeptide is NP_001598.
  • the protein GNPI is involved in angiogenesis.
  • GNPI converts glucosamine-6-phosphate to fructose-6-phosphate.
  • GNPI is expressed in invasive ductal carcinoma, meningioma, melanoma, melanotic melanoma, moderately- differentiated adenocarcinoma, adult brain, hypernephroma, pheochromocytoma, and lung tumors.
  • the accession number for the nucleic acid is NM_005471 and the accession number for the protein is NP__005462.
  • the protein DHCR24 is involved in angiogenesis.
  • DHCR24 catalyzes the reduction of the ⁇ -24 double bond of sterol intermediates during . cholesterol biosynthesis.
  • DHCR24 protects cells from oxidative stress by reducing caspase 3 activity during apoptosis induced by oxidative stress.
  • DHCR24 also protects against amyloid-beta peptide-induced apoptosis.
  • DHCR24 is highly expressed in brain and adrenal gland, with moderate expression in liver, lung, spleen, prostate and spinal cord, low expression in heart, uterus and prostate.
  • the accession number for the nucleic acid is NM_014762 and the accession number for the polypeptide is NP_055577.
  • the protein SELT is involved in angiogenesis.
  • SELT plays a role in selenocysteine incorporation and is associated with endothelial cells, probably through heparin-binding properties.
  • SELT prevents the damage of vascular endothelium caused by reactive oxygen species.
  • SELT is expressed in melanotic melanoma, acute myelogenous leukemia, embryonal carcinoma, hypemephroma, and chronic myelogenous leukemia.
  • the accession number for the nucleic acid is BC026350 and the accession number for the protein is AAH26350.
  • the protein PTPRB is involved in angiogenesis.
  • PTPRB is a signaling molecule that regulates a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation.
  • PTPRB is specifically expressed in vascular Ecs throughout mouse development.
  • PTPRB binds to VE-cadherin in COS cells, dephosphorylates VEGFR2 phosphorylated VE-cadherin, co- immunoprecipitates with Tiell and dephosphorylates Tiell.
  • the accession number for the nucleic acid is NM_002837 and the accession number for the protein is NP_002828.
  • the protein GB A is involved in angiogenesis.
  • GBA is a j8-glucocerebrosidase (glucosylceramidase, jS-D-glucosyl-N-acylsphingosine glucohydrolase) that degrades sphingolipid glucocerebrosides. Defects in GBA are the cause of gaucher disease (gd), the most prevalent lysosomal storage disease. In vitro ⁇ - glucocerebrosidase assays with GBA can be used to assay for GBA modulators and thus for modulators of angiogenesis.
  • the accession number for the nucleic acid is NM_000157 and the accession number for the polypeptide is NP_000148.
  • the protein UAP1 is involved in angiogenesis.
  • UAP1 is expressed in skin, carcinoma cell, normal gingival, colonic mucosa, normal endometrium, and Ewing's sarcoma.
  • the accession number for the nucleic acid is NM_003115 and the accession number for the polypeptide is NP_003106.
  • the protein MRPL30 is involved in angiogenesis. MRPL30 catalyzes the transfer ofthe lipoyl group from lipoyl-AMP to the specific lysine residue ofthe lipoate-dependent enzymes.
  • the accession number for the nucleic acid is NM_145212 and the accession number for the polypeptide is NP_660213.
  • the protein CCT3 is involved in angiogenesis. CCT3 is a molecular chaperone that assists protein folding upon ATP hydrolysis. CCT3 is known to play a role, in vitro, in the folding of actin and tubulin. CCT3 plays a role in the assembly ofthe Von Hippel-Lindau ubiquitylation complex.
  • the accession number for the nucleic acid is AL833197 and the accession number for the polypeptide is NP_005989.
  • the protein HSPA8 is involved in angiogenesis.
  • HSPA8 belongs to the heat shock protein 70 family.
  • HSPA8 binds to nascent polypeptides to facilitate correct folding.
  • HSPA8 also functions as an ATPase in the disassembly of clathrin-coated vesicles during transport of membrane components through the cell.
  • the accession number for the nucleic acid is NM_006597 and the accession number for the polypeptide is NP_006588.
  • the protein SLC16A1 is involved in angiogenesis.
  • SLC16A1 is a proton-linked monocarboxylate transporter.
  • SLC16A1 catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate.
  • Defects in SLC16A1 are the cause of symptomatic deficiency in lactate transport (SDLT), characterized by a subnormal erythrocyte lactate transport and signs of muscle injury during exercise and heat exposure.
  • SDLT lactate transport
  • the accession number for the nucleic acid is NM_003051 and the accession number for the polypeptide is NP_003042.
  • the protein SH2 of Abl is involved in angiogenesis.
  • SH2 of Abl is a SH2 domain protein, similar to the tyrosine-protein kinase Abl. Arm and Abl proteins function cooperatively at adherens junctions in both the ens and epidermis.
  • In vitro tyrosine kinase assays with SH2 of Abl can be used to assay for SH2 of Abl modulators and thus for modulators of angiogenesis.
  • the accession number for the nucleic acid is AK074067 and the accession number for the protein is BAB84893.
  • disorder associated with angiogenesis or “disease associated with angiogenesis” herein is meant a disease state which is marked by either an excess or a deficit of vessel development.
  • Angiogenesis disorders associated with increased angiogenesis include, but are not limited to, breast, lung, colon, ovarian, liver, stomach, bladder, thyroid, and prostate cancer, basal cell carcinoma, melanoma, lymphomas, leukemias, e.g., myeloid leukemia (AML, CML), endometriosis, diabetic retinopathy, glaucoma, glomeralonephritis, rheumatoid arthritis, and age related macular degeneration.
  • AML myeloid leukemia
  • CML myeloid leukemia
  • endometriosis diabetic retinopathy
  • glaucoma glomeralonephritis
  • rheumatoid arthritis and age related macular degeneration.
  • Pathological states for which it may be desirable to increase angiogenesis include stroke, infertility, heart disease, e.g., restenosis, ulcers, and scleroderma.
  • An increase in angiogenesis may also be desirable in transplantation or for artificial or in vitro growth of organs.
  • disorder associated with cellular proliferation or tumorigenesis or “disease associated with cellular proliferation or tumorigenesis” herein is meant a disease state which is marked by either an excess or a deficit of cellular proliferation or apoptosis.
  • disorders associated with increased cellular proliferation include, but are not limited to, cancer and non-cancerous pathological proliferation.
  • angiogenesis polypeptide or a nucleic acid encoding an “angiogenesis polypeptide” refer to nucleic acid and polypeptide polymorphic variants, alleles, mutants, and interspecies homologs that: (1) have an amino acid sequence that has greater than about 60% amino acid sequence identity, 65%, 70%, 75%, 80%, 85%, 90%, preferably 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% or greater amino acid sequence identity, preferably over a region of over a region of at least about 25, 50, 100, 200, 500, 1000, or more amino acids, to a polypeptide encoded by a referenced nucleic acid or an amino acid sequence described herein; (2) specifically bind to antibodies, e.g., polyclonal antibodies, raised against an immunogen comprising a referenced amino acid sequence, immunogenic fragments thereof, and conservatively modified variants thereof;
  • nucleic acid sequence that has greater than about 95%, preferably greater than about 96%, 97%, 98%, 99%, or higher nucleotide sequence identity, preferably over a region of at least about 25, 50, 100, 200, 500, 1000, or more nucleotides, to a reference nucleic acid sequence.
  • a polynucleotide or polypeptide sequence is typically from a mammal including, but not limited to, primate, e.g., human; rodent, e.g., rat, mouse, hamster; cow, pig, horse, sheep, or any mammal.
  • the nucleic acids and proteins ofthe invention include both naturally occurring or recombinant molecules.
  • the phrase "functional effects" in the context of assays for testing compounds that modulate activity of an angiogenesis protein includes the determination of a parameter that is indirectly or directly under the influence of an angiogenesis polypeptide, e.g., a chemical or phenotypic effect such as loss-of angiogenesis phenotype represented by a change in expression of a cell surface marker ov 33 integrin, changes in cellular migration, e.g., haptotaxis, changes in endothelial tube formation, changes in VEGF receptor internalization, and changes in tumor growth; or enzymatic activity; or, e.g., a physical effect such as ligand binding or inhibition of ligand binding.
  • a parameter that is indirectly or directly under the influence of an angiogenesis polypeptide e.g., a chemical or phenotypic effect such as loss-of angiogenesis phenotype represented by a change in expression of a cell surface marker ov 33 integrin, changes in cellular migration, e.
  • a functional effect therefore includes ligand binding activity, the ability of cells to proliferate, expression in cells undergoing angiogenesis, and other characteristics of angiogenic cells.
  • “Functional effects” include in vitro, in vivo, and ex vivo activities. ⁇
  • determining the functional effect is meant assaying for a compound that increases or decreases a parameter that is indirectly or directly under the influence of an angiogenesis protein, e.g., measuring physical and chemical or phenotypic effects.
  • Such functional effects can be measured by any means known to those skilled in the art, e.g., changes in spectroscopic characteristics (e.g., fluorescence, absorbance, refractive index); hydrodynamic (e.g., shape), chromatographic; or solubility properties for the protein; ligand binding assays, e.g., binding to antibodies; measuring inducible markers or transcriptional activation ofthe angiogenesis protein; measuring changes in enzymatic activity; the ability to increase or decrease cellular proliferation, apoptosis, cell cycle arrest, measuring changes in cell surface markers, e.g., ovjS3 integrin.
  • Determination of the functional effect of a compound on angiogenesis can also be performed using assays known to those of skill in the art such as endothelial cell tube formation assays; haptotaxis assays; the eze CAM assay; the mouse comeal assay; VEGF receptor assays, co-culture tube formation assays, and assays that assess vascularization of an implanted tumor.
  • Tumorigenesis can be measured using in vivo mouse models such as a xenograft model.
  • the functional effects can be evaluated by many means known to those skilled in the art, e.g., microscopy for quantitative or qualitative measures of alterations in morphological features, e.g., tube or blood vessel formation, measurement of changes in RNA or protein levels for angiogenesis-associated sequences, measurement of RNA stability, identification of downstream or reporter gene expression (CAT, luciferase, ⁇ - gal, GFP and the like), e.g., via chemiluminescence, fluorescence, colorimetric reactions, antibody binding, inducible markers, etc.
  • microscopy for quantitative or qualitative measures of alterations in morphological features, e.g., tube or blood vessel formation, measurement of changes in RNA or protein levels for angiogenesis-associated sequences, measurement of RNA stability, identification of downstream or reporter gene expression (CAT, luciferase, ⁇ - gal, GFP and the like), e.g., via chemiluminescence, fluorescence, colorimetric reactions, antibody binding, inducible markers, etc.
  • Inhibitors are used to refer to activating, inhibitory, or modulating molecules identified using in vitro and in vivo assays of angiogenesis polynucleotide and polypeptide sequences.
  • Inhibitors are compounds that, e.g., bind to, partially or totally block activity, decrease, prevent, delay activation, inactivate, desensitize, or down regulate the activity or expression of angiogenesis proteins, e.g., antagonists.
  • Activators are compounds that increase, open, activate, facilitate, enhance activation, sensitize, agonize, or up regulate angiogenesis protein activity, agonists.
  • Inhibitors, activators, or modulators also include genetically modified versions of angiogenesis proteins, e.g., versions with altered activity, as well as naturally occurring and synthetic ligands, antagonists, agonists, antibodies, peptides, cyclic peptides, nucleic acids, antisense molecules, ribozymes, RNAi molecules, small organic molecules and the like.
  • Such assays for inhibitors and activators include, e.g., expressing angiogenesis protein in vitro, in cells, or cell extracts, applying putative modulator compounds, and then determining the functional effects on activity, as described above.
  • Samples or assays comprising angiogenesis proteins that are treated with a potential activator, inhibitor, or modulator are compared to control samples without the inhibitor, activator, or modulator to examine the extent of inhibition.
  • Control samples (untreated with inhibitors) are assigned a relative protein activity value of 100%.
  • Inhibition of an angiogenesis protein is achieved when the activity value relative to the control is about 80%, preferably 50%, more preferably 25-0%.
  • Activation of an angiogenesis protein is achieved when the activity value relative to the control (untreated with activators) is 110%, more preferably 150%, more preferably 200-500% (i.e., two to five fold higher relative to the control), more preferably 1000-3000% higher.
  • test compound or “drug candidate” or “modulator” or grammatical equivalents as used herein describes any molecule, either naturally occurring or synthetic, e.g., protein, oligopeptide (e.g., from about 5 to about 25 amino acids in length, preferably from about 10 to 20 or 12 to 18 amino acids in length, preferably 12, 15, or 18 amino acids in length), small organic molecule, polysaccharide, peptide, circular peptide, lipid, fatty acid, siRNA, polynucleotide, oligonucleotide, etc., to be tested for the capacity to directly or indirectly modulate angiogenesis.
  • protein oligopeptide (e.g., from about 5 to about 25 amino acids in length, preferably from about 10 to 20 or 12 to 18 amino acids in length, preferably 12, 15, or 18 amino acids in length)
  • small organic molecule polysaccharide, peptide, circular peptide, lipid, fatty acid, siRNA, polynucleotide, oligonucle
  • the test compound can be in the form of a library of test compounds, such as a combinatorial or randomized library that provides a sufficient range of diversity.
  • Test compounds are optionally linked to a fusion partner, e.g., targeting compounds, rescue compounds, dimerization compounds, stabilizing compounds, addressable compounds, and other functional moieties.
  • a fusion partner e.g., targeting compounds, rescue compounds, dimerization compounds, stabilizing compounds, addressable compounds, and other functional moieties.
  • new chemical entities with useful properties are generated by identifying a test compound (called a "lead compound") with some desirable property or activity, e.g., inhibiting activity, creating variants ofthe lead compound, and evaluating the property and activity of those variant compounds.
  • HTS high throughput screening
  • a "small organic molecule” refers to an organic molecule, either naturally occurring or synthetic, that has a molecular weight of more than about 50 daltons and less than about 2500 daltons, preferably less than about 2000 daltons, preferably between about 100 to about 1000 daltons, more preferably between about 200 to about 500 daltons.
  • RNAi molecule or an “siRNA” refers to a nucleic acid that forms a double stranded RNA, which double stranded RNA has the ability to reduce or inhibit expression of a gene or target gene when the siRNA expressed in the same cell as the gene or target gene.
  • siRNA thus refers to the double stranded RNA formed by the complementary strands.
  • an siRNA refers to a nucleic acid that has substantial or complete identity to a target gene and forms a double stranded siRNA.
  • the sequence ofthe siRNA can correspond to the full length target gene, or a subsequence thereof.
  • the siRNA is at least about 15-50 nucleotides in length (e.g., each complementary sequence ofthe double stranded siRNA is 15-50 nucleotides in length, and the double stranded siRNA is about 15-50 base pairs in length, preferable about preferably about 20-30 base nucleotides, preferably about 20-25 nucleotides in length, e.g., 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleotides in length.
  • Bio sample include sections of tissues such as biopsy and autopsy samples, and frozen sections taken for histologic purposes. Such samples include blood, sputum, tissue, cultured cells, e.g., primary cultures, explants, and transformed cells, stool, urine, etc.
  • a biological sample is typically obtained from a eukaryotic organism, most preferably a mammal such as a primate, e.g., chimpanzee or human; cow; dog; cat; a rodent, e.g., guinea pig, rat, mouse; rabbit; or a bird; reptile; or fish.
  • nucleic acids or polypeptide sequences refer to two or more sequences or subsequences that are the same or have a specified percentage of amino acid residues or nucleotides that are the same (i.e., about 70% identity, preferably 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or higher identity over a specified region (e.g., SEQ ID NO:l or 2), when compared and aligned for maximum correspondence over a comparison window or designated region) as measured using a BLAST or BLAST 2.0 sequence comparison algorithms with default parameters described below, or by manual alignment and visual inspection (see, e.g., NCBI web site or the like).
  • a specified region e.g., SEQ ID NO:l or 2
  • sequences are then said to be "substantially identical.”
  • This definition also refers to, or may be applied to, the compliment of a test sequence.
  • the definition also includes sequences that have deletions and/or additions, as well as those that have substitutions.
  • the preferred algorithms can account for gaps and the like.
  • identity exists over a region that is at least about 25 amino acids or nucleotides in length, or more preferably over a region that is 50-100 amino acids or nucleotides in length.
  • sequence comparison typically one sequence acts as a reference sequence, to which test sequences are compared.
  • test and reference sequences are entered into a computer, subsequence coordinates are designated, if necessary, and sequence algorithm program parameters are designated. Preferably, default program parameters can be used, or alternative parameters can be designated.
  • sequence comparison algorithm then calculates the percent sequence identities for the test sequences relative to the reference sequence, based on the program parameters.
  • a “comparison window”, as used herein, includes reference to a segment of any one ofthe number of contiguous positions selected from the group consisting of from 20 to 600, usually about 50 to about 200, more usually about 100 to about 150 in which a sequence may be compared to a reference sequence ofthe same number of contiguous positions after the two sequences are optimally aligned.
  • Methods of alignment of sequences for comparison are well-known in the art.
  • Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman & Wunsch, J Mol. Biol.
  • a preferred example of algorithm that is suitable for determining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al, Nuc. Acids Res. 25:3389-3402 (1977) and Altschul et al, J. Mol. Biol. 215:403-410 (1990), respectively.
  • BLAST and BLAST 2.0 are used, with the parameters described herein, to determine percent sequence identity for the nucleic acids and proteins ofthe invention.
  • Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information.
  • This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length W in the query sequence, which either match or satisfy some positive-valued threshold score T when aligned with a word ofthe same length in a database sequence.
  • T is referred to as the neighborhood word score threshold (Altschul et ah, supra).
  • a scoring matrix is used to calculate the cumulative score. Extension ofthe word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached.
  • the BLAST algorithm parameters W, T, and X determine the sensitivity and speed ofthe alignment.
  • Nucleic acid refers to deoxyribonucleotides or ribonucleotides and polymers thereof in single- or double-stranded form.
  • the term encompasses nucleic acids containing known nucleotide analogs or modified backbone residues or linkages, which are synthetic, naturally occurring, and non-naturally occurring, which have similar binding properties as the reference nucleic acid, and which are metabolized in a manner similar to the reference nucleotides. Examples of such analogs include, without limitation, phosphorothioates, phosphoramidates, methyl phosphonates, chiral-methyl phosphonates, 2-O-methyl ribonucleotides, peptide-nucleic acids (PNAs).
  • PNAs peptide-nucleic acids
  • nucleic acid sequence also implicitly encompasses conservatively modified variants thereof (e.g., degenerate codon substitutions) and complementary sequences, as well as the sequence explicitly indicated.
  • degenerate codon substitutions may be achieved by generating sequences in which the third position of one or more selected (or all) codons is substituted with mixed- base and/or deoxyinosine residues (Batzer et al., Nucleic Acid Res. 19:5081 (1991); Ohtsuka et al, J. Biol. Chem. 260:2605-2608 (1985); Rossolini et ah, Mol. Cell. Probes 8:91-98 (1994)).
  • nucleic acid is used interchangeably with gene, cDNA, mRNA, oligonucleotide, and polynucleotide.
  • a particular nucleic acid sequence also implicitly encompasses "splice variants.”
  • a particular protein encoded by a nucleic acid implicitly encompasses any protein encoded by a splice variant of that nucleic acid.
  • "Splice variants,” as the name suggests, are products of alternative splicing of a gene. After transcription, an initial nucleic acid transcript may be spliced such that different (alternate) nucleic acid splice products encode different polypeptides.
  • Mechanisms for the production of splice variants vary, but include alternate splicing of exons. Alternate polypeptides derived from the same nucleic acid by read-through transcription are also encompassed by this definition. Any products of a splicing reaction, including recombinant forms ofthe splice products, are included in this definition.
  • polypeptide peptide
  • protein protein
  • amino acid polymers in which one or more amino acid residue is an artificial chemical mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers and non-naturally occurring amino acid polymer.
  • amino acid refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function in a manner similar to the naturally occurring amino acids.
  • Naturally occurring amino acids are those encoded by the genetic code, as well as those amino acids that are later modified, e.g., hydroxyproline, ⁇ -carboxyglutamate, and O-phosphoserine.
  • Amino acid analogs refers to compounds that have the same basic chemical structure as a naturally occurring amino acid, i.e., an carbon that is bound to a hydrogen, a carboxyl group, an amino group, and an R group, e.g., homoserine, norleucine, methionine sulfoxide, methionine methyl sulfonium. Such analogs have modified R groups (e.g., norleucine) or modified peptide backbones, but retain the same basic chemical structure as a naturally occurring amino acid.
  • Amino acid mimetics refers to chemical compounds that have a structure that is different from the general chemical structure of an amino acid, but that functions in a manner similar to a naturally occurring amino acid.
  • Amino acids may be referred to herein by either their commonly known three letter symbols or by the one-letter symbols recommended by the IUPAC-IUB Biochemical Nomenclature Commission. Nucleotides, likewise, may be referred to by their commonly accepted single-letter codes.
  • "Conservatively modified variants" applies to both amino acid and nucleic acid sequences. With respect to particular nucleic acid sequences, conservatively modified variants refers to those nucleic acids which encode identical or essentially identical amino acid sequences, or where the nucleic acid does not encode an amino acid sequence, to essentially identical sequences. Because ofthe degeneracy ofthe genetic code, a large number of functionally identical nucleic acids encode any given protein.
  • the codons GCA, GCC, GCG and GCU all encode the amino acid alanine.
  • the codon can be altered to any ofthe corresponding codons described without altering the encoded polypeptide.
  • Such nucleic acid variations are "silent variations," which are one species of conservatively modified variations. Every nucleic acid sequence herein which encodes a polypeptide also describes every possible silent variation ofthe nucleic acid.
  • each codon in a nucleic acid except AUG, which is ordinarily the only codon for metMonine, and TGG, which is ordinarily the only codon for tryptophan) can be modified to yield a functionally identical molecule.
  • each silent variation of a nucleic acid which encodes a polypeptide is implicit in each described sequence with respect to the expression product, but not with respect to actual probe sequences.
  • amino acid sequences one of skill will recognize that individual substitutions, deletions or additions to a nucleic acid, peptide, polypeptide, or protein sequence which alters, adds or deletes a single amino acid or a small percentage of amino acids in the encoded sequence is a "conservatively modified variant" where the alteration results in the substitution of an amino acid with a chemically similar amino acid. Conservative substitution tables providing functionally similar amino acids are well known in the art. Such conservatively modified variants are in addition to and do not exclude polymorphic variants, interspecies homologs, and alleles ofthe invention.
  • the following eight groups each contain amino acids that are conservative substitutions for one another: 1) Alanine (A), Glycine (G); 2) Aspartic acid (D), Glutamic acid (E); 3) Asparagine (N), Glutamine (Q); 4) Arginine (R), Lysine (K); 5) Isoleucine (I), Leucine (L), Methionine (M), Valine (V); 6) Phenylalanine (F), Tyrosine (Y), Tryptophan (W); 7) Serine (S), Threonine (T); and 8) Cysteine (C), Methionine (M) (see, e.g., Creighton, Proteins (1984)).
  • Macromolecular structures such as polypeptide structures can be described in terms of various levels of organization. For a general discussion of this organization, see, e.g., Alberts et al., Molecular Biology ofthe Cell (3 rd ed., 1994) and Cantor and Schimmel, Biophysical Chemistry Part I: The Conformation of Biological Macromolecules (1980).
  • 'Trimary structure refers to the amino acid sequence of a particular peptide.
  • “Secondary structure” refers to locally ordered, three dimensional structures within a polypeptide. These structures are commonly known as domains, e.g., transmembrane domains, pore domains, and cytoplasmic tail domains.
  • Domains are portions of a polypeptide that form a compact unit ofthe polypeptide and are typically 15 to 350 amino acids long. Exemplary domains include domains with enzymatic activity, e.g., ligand binding domains, etc. Typical domains are made up of sections of lesser organization such as stretches of /3-sheet and ⁇ -helices. "Tertiary structure” refers to the complete three dimensional structure of a polypeptide monomer. "Quaternary structure” refers to the three dimensional structure formed by the noncovalent association of independent tertiary units. Anisotropic terms are also known as energy terms.
  • a “label” or a “detectable moiety” is a composition detectable by spectroscopic, photochemical, biochemical, immunochemical, chemical, or other physical means.
  • useful labels include 32 P, fluorescent dyes, electron-dense reagents, enzymes (e.g., as commonly used in an ELISA), biotin, digoxigenin, or haptens and proteins which can be made detectable, e.g., by incorporating a radiolabel into the peptide or used to detect antibodies specifically reactive with the peptide.
  • recombinant when used with reference, e.g., to a cell, or nucleic acid, protein, or vector, indicates that the cell, nucleic acid, protein or vector, has been modified by the introduction of a heterologous nucleic acid or protein or the alteration of a native nucleic acid or protein, or that the cell is derived from a cell so modified.
  • recombinant cells express genes that are not found within the native (non- recombinant) form ofthe cell or express native genes that are otherwise abnormally expressed, under expressed or not expressed at all. ;
  • heterologous when used with reference to portions of a nucleic acid indicates that the nucleic acid comprises two or more subsequences that are not found in the same relationship to each other in nature.
  • the nucleic acid is typically recombinantly produced, having two or more sequences from unrelated genes arranged to make a new functional nucleic acid, e.g., a promoter from one source and a coding region from another source.
  • a heterologous protein indicates that the protein ( comprises two or more subsequences that are not found in the same relationship to each other in nature (e.g., a fusion protein).
  • stringent hybridization conditions refers to conditions under which a probe will hybridize to its target subsequence, typically in a complex mixture of nucleic acids, but to no other sequences. Stringent conditions are sequence-dependent and will be different in different circumstances. Longer sequences hybridize specifically at higher temperatures. An extensive guide to the hybridization of nucleic acids is found in Tijssen, Techniques in Biochemistry and Molecular Biology—Hybridization with Nucleic Probes, "Overview of principles of hybridization and the strategy of nucleic acid assays” (1993). Generally, stringent conditions are selected to be about 5-10°C lower than the thermal melting point (T m ) for the specific sequence at a defined ionic strength pH.
  • T m thermal melting point
  • the T m is the temperature (under defined ionic strength, pH, and nucleic concentration) at which 50% ofthe probes complementary to the target hybridize to the target sequence at equilibrium (as the target sequences are present in excess, at T m , 50% ofthe probes are occupied at equilibrium).
  • Stringent conditions may also be achieved with the addition of destabilizing agents such as formamide.
  • a positive signal is at least two times background, preferably 10 times background hybridization.
  • Exemplary stringent hybridization conditions can be as following: 50% formamide, 5x SSC, and 1% SDS, incubating at 42°C, or, 5x SSC, 1% SDS, incubating at 65°C, with wash in 0.2x SSC, and 0.1% SDS at 65°C.
  • nucleic acids that do not hybridize to each other under stringent conditions are still substantially identical if the polypeptides which they encode are substantially identical. This occurs, for example, when a copy of a nucleic acid is created using the maximum codon degeneracy permitted by the genetic code. In such cases, the nucleic acids typically hybridize under moderately stringent hybridization conditions.
  • Exemplary "moderately stringent hybridization conditions” include a hybridization in a buffer of 40% formamide, 1 M NaCI, 1% SDS at 37°C, and a wash in IX SSC at 45°C. A positive hybridization is at least twice background.
  • Those of ordinary skill will readily recognize that alternative hybridization and wash conditions can be utilized to provide conditions of similar stringency. Additional guidelines for determining hybridization parameters are provided in numerous reference, e.g., and Current Protocols in Molecular Biology, ed. Ausubel, et al.
  • a temperature of about 36°C is typical for low stringency amplification, although annealing temperatures may vary between about 32°C and 48°C depending on primer length.
  • a temperature of about 62°C is typical, although high stringency annealing temperatures can range from about 50°C to about 65°C, depending on the primer length and specificity.
  • Typical cycle conditions for both high and low stringency amplifications include a denaturation phase of 90°C - 95°C for 30 sec - 2 min., an annealing phase lasting 30 sec. - 2 min., and an extension phase of about 72°C for 1 - 2 min. Protocols and guidelines for low and high stringency amplification reactions are provided, e.g., in Innis et al (1990) PCR Protocols, A Guide to Methods and Applications, Academic Press, Inc. N.Y.).
  • Antibody refers to a polypeptide comprising a framework region from an immunoglobulin gene or fragments thereof that specifically binds and recognizes an antigen.
  • the recognized immunoglobulin genes include the kappa, lambda, alpha, gamma, delta, epsilon, and mu constant region genes, as well as the myriad immunoglobulin variable region genes.
  • Light chains are classified as either kappa or lambda.
  • Heavy chains are classified as gamma, mu, alpha, delta, or epsilon, which in turn define the immunoglobulin classes, IgG, IgM, IgA, IgD and IgE, respectively.
  • the antigen-binding region of an antibody will be most critical in specificity and affinity of binding.
  • An exemplary immunoglobulin (antibody) structural unit comprises a tetramer.
  • Each tetramer is composed of two identical pairs of polypeptide chains, each pair having one "light” (about 25 kD) and one "heavy" chain (about 50-70 kD).
  • the N-terminus of each chain defines a variable region of about 100 to 110 or more amino acids primarily responsible for antigen recognition.
  • the terms variable light chain (V L ) and variable heavy chain (V H ) refer to these light and heavy chains respectively.
  • Antibodies exist, e.g., as intact immunoglobulins or as a number of well- characterized fragments produced by digestion with various peptidases.
  • pepsin digests an antibody below the disulfide linkages in the hinge region to produce F(ab)' 2j a dimer of Fab which itself is a light chain joined to V H -C H 1 by a disulfide bond.
  • the F(ab)' 2 may be reduced under mild conditions to break the disulfide linkage in the hinge region, thereby converting the F(ab)' 2 dimer into an Fab' monomer.
  • the Fab' monomer is essentially Fab with part ofthe hinge region (see Fundamental Immunology (Paul ed., 3d ed. 1993).
  • antibody fragments are defined in terms ofthe digestion of an intact antibody, one of skill will appreciate that such fragments may be synthesized de novo either chemically or by using recombinant DNA methodology.
  • antibody also includes antibody fragments either produced by the modification of whole antibodies, or those synthesized de novo using recombinant DNA methodologies (e.g., single chain Fv) or those identified using phage display libraries (see, e.g., McCafferty et al, Nature 348:552-554 (1990))
  • antibodies e.g., recombinant, monoclonal, or polyclonal antibodies
  • many technique known in the art can be used (see, e.g. , Kohler & Milstein, Nature 256:495-497 (1975); Kozbor et al, Immunology Today 4: 72 (1983); Cole et al, pp. 77-96 in Monoclonal Antibodies and Cancer Therapy, Alan R. Liss, Inc. (1985); Coligan, Current Protocols in Immunology (1991); Harlow & Lane, Antibodies, A Laboratory Manual (1988); and Goding, Monoclonal Antibodies: Principles and Practice (2d ed. 1986)).
  • the genes encoding the heavy and hght chains of an antibody of interest can be cloned from a cell, e.g., the genes encoding a monoclonal antibody can be cloned from a hybridoma and used to produce a recombinant monoclonal antibody.
  • Gene libraries encoding heavy and light chains of monoclonal antibodies can also be made from hybridoma or plasma cells. Random combinations ofthe heavy and light chain gene products generate a large pool of antibodies with different antigenic specificity (see, e.g., Kuby, Immunology (3 rd ed. 1997)).
  • Techniques for the production of single chain antibodies or recombinant antibodies U.S. Patent 4,946,778, U.S. Patent No.
  • transgenic mice or other organisms such as other mammals, may be used to express humanized or human antibodies (see, e.g., U.S. Patent Nos. 5,545,807; 5,545,806; 5,569,825; 5,625,126; 5,633,425; 5,661,016, Marks etal, Bio/Technology 10:779-783 (1992); Lonberg et al, Nature 368:856-859 (1994); Morrison, Nature 368:812-13 (1994); Fishwild et al, Nature Biotechnology 14:845-51 (1996); Neuberger, Nature Biotechnology 14:826 (1996); and Lonberg & Huszar, Intern.
  • phage display technology can be used to identify antibodies and heteromeric Fab fragments that specifically bind to selected antigens (see, e.g., McCafferty et al, Nature 348:552-554 (1990); Marks et al, Biotechnology 10:779-783 (1992)).
  • Antibodies can also be made bispecific, i.e., able to recognize two different antigens (see, e.g., WO 93/08829, Traunecker et al, EMBOJ. 10:3655-3659 (1991); and Suresh et al, Methods in Enzymology 121:210 (1986)).
  • Antibodies can also be heteroconjugates, e.g., two covalently joined antibodies, or immunotoxins (see, e.g., U.S. Patent No. 4,676,980 , WO 91/00360; WO 92/200373; and EP 03089).
  • a humanized antibody has one or more amino acid residues introduced into it from a source which is non-human. These non-human amino acid residues are often referred to as import residues, which are typically taken from an import variable domain. Humanization can be essentially performed following the method of Winter and co-workers (see, e.g., Jones et al, Nature 321:522-525 (1986); Riechmann et al., Nature 332:323-327 (1988); Verhoeyen et al, Science 239:1534-1536 (1988) and Presta, Curr. Op. Struct.
  • humanized antibodies are chimeric antibodies (U.S. Patent No. 4,816,567), wherein substantially less than an intact human variable domain has been substituted by the corresponding sequence from a non-human species.
  • humanized antibodies are typically human antibodies in which some CDR residues and possibly some FR residues are substituted by residues from analogous sites in rodent antibodies.
  • a "chimeric antibody” is an antibody molecule in which (a) the constant region, or a portion thereof, is altered, replaced or exchanged so that the antigen binding site (variable region) is linked to a constant region of a different or altered class, effector function and/or species, or an entirely different molecule which confers new properties to the chimeric antibody, e.g., an enzyme, toxin, hormone, growth factor, drug, etc.; or (b) the variable region, or a portion thereof, is altered, replaced or exchanged with a variable region having a different or altered antigen specificity.
  • the antibody is conjugated to an "effector" moiety.
  • the effector moiety can be any number of molecules, including labeling moieties such as radioactive labels or fluorescent labels, or can be a therapeutic moiety.
  • the antibody modulates the activity ofthe protein.
  • the specified antibodies bind to a particular protein at least two times the background and more typically more than 10 to 100 times background.
  • an antibody that is selected for its specificity for a particular protein.
  • polyclonal antibodies, polymorphic variants, alleles, orthologs, and conservatively modified variants, or splice variants, or portions thereof can be selected to obtain only those polyclonal antibodies that are specifically immunoreactive with angiogenesis proteins and not with other proteins. This selection may be achieved by subtracting out antibodies that cross-react with other molecules.
  • a variety of immunoassay formats may be used to select antibodies specifically immunoreactive with a particular protein.
  • solid-phase ELISA immunoassays are routinely used to select antibodies specifically immunoreactive with a protein (see, e.g., Harlow & Lane, Antibodies, A Laboratory Manual (1988) for a description of immunoassay formats and conditions that can be used to determine specific immunoreacti vity) .
  • Assays for proteins that modulate angiogenesis are routinely used to select antibodies specifically immunoreactive with a protein (see, e.g., Harlow & Lane, Antibodies, A Laboratory Manual (1988) for a description of immunoassay formats and conditions that can be used to determine specific immunoreacti vity).
  • High throughput functional genomics assays can be used to identify modulators of angiogenesis. Such assays can monitor changes in cell surface marker expression, ⁇ v/33 integrin production, proliferation, and differentiation using either cell lines or primary cells. Typically, early passage or primary endothelial cells are contacted with a cDNA or a random peptide library (encoded by nucleic acids).
  • the cDNA library can comprise sense, antisense, full length, and truncated cDNAs.
  • the peptide library is encoded by nucleic acids.
  • the effect ofthe cDNA or peptide library on the endothelial cells is then monitored, using an assay such as cell surface marker expression (e.g., ov/33 integrin) or a phenotypic assay for angiogenesis such as migration towards an ECM (extracellular matrix) component (see, e.g., Klemke et al, J. Cell Biol.
  • an assay such as cell surface marker expression (e.g., ov/33 integrin) or a phenotypic assay for angiogenesis such as migration towards an ECM (extracellular matrix) component (see, e.g., Klemke et al, J. Cell Biol.
  • endothelial cell tube formation assays as well as other bioassays such as the chick CAM assay, the mouse corneal assay, haptotaxis assays, VEGF-R assays, co-culture tube formation assays, and assays measuring the effect of administering potential modulators on implanted tumors.
  • bioassays such as the chick CAM assay, the mouse corneal assay, haptotaxis assays, VEGF-R assays, co-culture tube formation assays, and assays measuring the effect of administering potential modulators on implanted tumors.
  • the effect ofthe cDNA or peptide can be validated and distinguished from somatic mutations, using, e.g., regulatable expression ofthe nucleic acid such as expression from a tetracycline promoter.
  • cDNAs and nucleic acids encoding peptides can be rescued using techniques known to those of skill in the art, e.g., using a sequence tags.
  • In vivo assays for tumor growth, such as mouse xenograft models, can also be used.
  • Proteins interacting with the peptide or with the protein encoded by the cDNA can be isolated using a yeast two-hybrid system, mammalian two hybrid system, or phage display screen, etc. Targets so identified can be further used as bait in these assays to identify additional members ofthe angiogenesis pathway, which members are also targets for drug development (see, e.g., Fields et al, Nature 340:245 (1989); Vasavada et al, Proc. Nat'lAcad. Sci. USA 88:10686 (1991); Fearon t ⁇ /., Proc. Natl Acad. Sci. USA 89:7958 (1992); Dang et al, Mol. Cell Biol.
  • Suitable endothelial cell lines include human umbilical vein cells (see, e.g., Jaffe et al, J. Clin. Invest. 52:2745-2754 (1973)); human adult dermal capillary-derived cells (see, e.g., Davison et al, In Vitro 19:937-945 (1983)); human adipose capillary derived cells (see, e.g., Kem et al, J. Clin Invest. 71:1822-1829 (1983); bovine aorta (see, e.g., Booyse et al, Thromb. Diathes. Ahemorrh.
  • rat brain capillary derived cells see, e.g., Bowman et al, In Vitro 17:353-362 (1981)).
  • Suitable angiogenesis cell surface markers include alphavbeta3 integrin (see, e.g., Elicerir & Cheresh, Cancer J. Sci. Am. 6 Supp. 3:S245-249 (2000), Maeshima et al, J Biol. Chem. (June 8, 2001)).
  • Cell surface markers such as ⁇ v/33 can be assayed using fluorescently labeled antibodies and FACS. Cell proliferation can be measured using 3 H-thymidine or dye inclusion. Angiogenesis phenotype is measured by loss of phenotype observation.
  • cDNA libraries are made from any suitable source, preferably from endothelial cells. Libraries encoding random peptides are made according to techniques well known to those of skill in the art (see, e.g., U.S. Patent No. 6,153,380, 6,114,111, and 6,180,343). Any suitable vector can be used for the cDNA and peptide libraries, mcluding, e.g., retroviral vectors.
  • target proteins that modulate angiogenesis are identified using a high throughput cell based assay (using a microtiter plate format) and FACS screening for av ⁇ 3 cell surface expression.
  • cDNA libraries are made which include, e.g., sense, antisense, full length, and truncated cDNAs. The cDNAs are cloned into a retroviral vector. Endothelial cells are infected with the library, cultured for a short effector phase and then the cells with reduced ctv ⁇ 3 surface levels are enriched by antibody staining and magnetic cell sorting. The enriched cell population is then sorted into microtiter plates using fluorescent antibodies and FACS.
  • Resultant cell colonies are analyzed by immunofluorescence for reduced ⁇ v/33 surface levels. Selected colonies are infected with wild type MMLV virus to rescue the proviral vector. The infectious supernatant is used to infect endothelial cells, which are subsequently analyzed for ⁇ vj83 levels by FACS. The cDNA is isolated and sequenced to determined if it represents a wild type or mutated cDNA, e.g., whether the cDNA represents a negative transdominant mutant. Optionally, a marker such as GFP can be used to select for retrovirally infected cells. Isolation of nucleic acids [0104] This invention relies on routine techniques in the field of recombinant genetics.
  • Nucleic acids, polymorphic variants, orthologs, and alleles can be isolated using nucleic acid probes and ohgonucleotides under stringent hybridization conditions, by screening libraries.
  • expression libraries can be used to clone angiogenesis proteins, polymorphic variants, orthologs, and alleles by detecting expressed homologs immunologically with antisera or purified antibodies made against human angiogenesis proteins or portions thereof.
  • RNA e.g., endothelial cells
  • the mRNA is then made into cDNA using reverse transcriptase, ligated into a recombinant vector, and transfected into a recombinant host for propagation, screening and cloning.
  • Methods for making and screening cDNA libraries are well known (see, e.g., Gubler & Hoffman, Gene 25:263-269 (1983); Sambrook et al, supra; Ausubel et al, supra).
  • the DNA is extracted from the tissue and either mechanically sheared or enzymatically digested to yield fragments of about 12-20 kb. The fragments are then separated by gradient centrifugation from undesired sizes and are constructed in bacteriophage lambda vectors. These vectors and phage are packaged in vitro. Recombinant phage are analyzed by plaque hybridization as described in Benton & Davis, Science 196:180-182 (1977). Colony hybridization is carried out as generally described in Grunstein et al, Proc. Natl. Acad. Sci. USA., 72:3961-3965 (1975).
  • An alternative method of isolating nucleic acids and orthologs, alleles, mutants, polymorphic variants, and conservatively modified variants combines the use of synthetic oligonucleotide primers and amplification of an RNA or DNA template (see U.S. Patents 4,683,195 and 4,683,202; PCR Protocols: A Guide to Methods and Applications (Innis et al, eds, 1990)).
  • Methods such as polymerase chain reaction (PCR) and ligase chain reaction (LCR) can be used to amplify nucleic acid sequences directly from mRNA, from cDNA, from genomic libraries or cDNA libraries.
  • Degenerate ohgonucleotides can be designed to amplify homologs using the sequences provided herein. Restriction endonuclease sites can be incorporated into the primers. Polymerase chain reaction or other in vitro amplification methods may also be useful, for example, to clone nucleic acid sequences that code for proteins to be expressed, to make nucleic acids to use as probes for detecting the presence of angiogenesis protein encoding mRNA in physiological samples, for nucleic acid sequencing, or for other purposes. Genes amplified by the PCR reaction can be purified from agarose gels and cloned into an appropriate vector.
  • Gene expression can also be analyzed by techniques known in the art, e.g., reverse transcription and amplification of mRNA, isolation of total RNA or poly A +
  • RNA RNA, northern blotting, dot blotting, in situ hybridization, RNase protection, high density polynucleotide array technology, e.g., and the like.
  • Nucleic acids can be used with high density oligonucleotide array technology (e.g., GeneChipTM) to identify angiogenesis protein, orthologs, alleles, conservatively modified variants, and polymorphic variants in this invention.
  • GeneChipTM high density oligonucleotide array technology
  • the homologs being identified are linked to a known disease state, they can be used with GeneChipTM as a diagnostic tool in detecting the disease in a biological sample, see, e.g., Gunthand et al, AIDS Res. Hum. Retroviruses 14: 869-876 (1998); Kozal et al, Nat. Med. 2:753-759 (1996); Matson et al, Anal Biochem.
  • the gene is typically cloned into intermediate vectors before transformation into prokaryotic or eukaryotic cells for replication and/or expression.
  • These intermediate vectors are typically prokaryote vectors, e.g., plasmids, or shuttle vectors.
  • a cloned gene such as those cDNAs encoding an angiogenesis protein
  • Suitable bacterial promoters are well known in the art and described, e.g., in Sambrook et al, and Ausubel et al, supra.
  • Bacterial expression systems for expressing the protein are available in, e.g., E.
  • kits for such expression systems are commercially available.
  • Eukaryotic expression systems for mammalian cells, yeast, and insect cells are well known in the art and are also commercially available.
  • Selection of the promoter used to direct expression of a heterologous nucleic acid depends on the particular application.
  • the promoter is preferably positioned about the same distance from the heterologous transcription start site as it is from the transcription start site in its natural setting. As is known in the art, however, some variation in this distance can be accommodated without loss of promoter function.
  • the expression vector typically contains a transcription unit or expression cassette that contains all the additional elements required for the expression ofthe nucleic acid in host cells.
  • a typical expression cassette thus contains a promoter operably linked to the nucleic acid sequence and signals required for efficient polyadenylation ofthe transcript, ribosome binding sites, and translation termination. Additional elements ofthe cassette may include enhancers and, if genomic DNA is used as the structural gene, introns with functional splice donor and acceptor sites.
  • the expression cassette should also contain a transcription termination region downstream ofthe structural gene to provide for efficient termination.
  • the termination region may be obtained from the same gene as the promoter sequence or may be obtained from different genes.
  • the particular expression vector used to transport the genetic information into the cell is not particularly critical. Any ofthe conventional vectors used for expression in eukaryotic or prokaryotic cells may be used. Standard bacterial expression vectors include plasmids such as pBR322 based plasmids, pSKF, pET23D, and fusion expression systems such as MBP, GST, and LacZ. Epitope tags can also be added to recombinant proteins to provide convenient methods of isolation, e.g., c-myc.
  • Expression vectors containing regulatory elements from eukaryotic viruses are typically used in eukaryotic expression vectors, e.g., S V40 vectors, papilloma virus vectors, retroviral vectors, and vectors derived from Epstein-Barr virus.
  • exemplary eukaryotic vectors include pMSG, pAV009/A + , pMTO10/A + , pMAMneo-5, baculovirus pDSVE, and any other vector allowing expression of proteins under the direction ofthe CMV promoter, S V40 early promoter, S V40 later promoter, metallothionein promoter, murine mammary tumor virus promoter, Rous sarcoma virus promoter, polyhedrin promoter, or other promoters shown effective for expression in eukaryotic cells.
  • Expression of proteins from eukaryotic vectors can be also be regulated using inducible promoters.
  • inducible promoters With inducible promoters, expression levels are tied to the concentration of inducing agents, such as tetracycline or ecdysone, by the incorporation of response elements for these agents into the promoter. Generally, high level expression is obtained from inducible promoters only in the presence ofthe inducing agent; basal expression levels are minimal. Inducible expression vectors are often chosen if expression ofthe protein of interest is detrimental to eukaryotic cells. [0119] In one embodiment, the vectors ofthe invention have a regulatable promoter, e.g., tet-regulated systems and the RU-486 system (see, e.g., Gossen & Bujard, Proc. Nat'lAcad. Sci.
  • a regulatable promoter e.g., tet-regulated systems and the RU-486 system
  • high yield expression systems not involving gene amplification are also suitable, such as using a baculovirus vector in insect cells, with a protein encoding sequence under the direction ofthe polyhedrin promoter or other strong baculovirus promoters.
  • the elements that are typically included in expression vectors also include a replicon that functions in E. coli, a gene encoding antibiotic resistance to permit selection of bacteria that harbor recombinant plasmids, and unique restriction sites in nonessential regions ofthe plasmid to allow insertion of eukaryotic sequences.
  • the particular antibiotic resistance gene chosen is not critical, any ofthe many resistance genes known in the art are suitable.
  • the prokaryotic sequences are preferably chosen such that they do not interfere with the replication ofthe DNA in eukaryotic cells, if necessary.
  • Standard transfection methods are used to produce bacterial, mammalian, yeast or insect cell lines that express large quantities of protein, which are then purified using standard techniques (.see, e.g., Colley et al, J. Biol. Chem. 264:17619-17622 (1989); Guide to Protein Purification, in Methods in Enzymology, vol. 182 (Deutscher, ed., 1990)). Transformation of eukaryotic and prokaryotic cells are performed according to standard techniques (see, e.g., Morrison, J. Bad. 132:349-351 (1977); Clark-Curtiss & Curtiss, Methods in Enzymology 101:347-362 (Wu et al., eds, 1983).
  • Any of the well-known procedures for introducing foreign nucleotide sequences into host cells may be used. These include the use of calcium phosphate transfection, polybrene, protoplast fusion, electroporation, biolistics, liposomes, microinjection, plasma vectors, viral vectors and any ofthe other well known methods for introducing cloned genomic DNA, cDNA, synthetic DNA or other foreign genetic material into a host cell (see, e.g., Sambrook et al, supra). It is only necessary that the particular genetic engineering procedure used be capable of successfully introducing at least one gene into the host cell capable of expressing the protein of choice.
  • the transfected cells are cultured under conditions favoring expression ofthe protein of choice, which is recovered from the culture using standard techniques identified below.
  • Naturally occurring protein can be purified, e.g., from human tissue.
  • Recombinant protein can be purified from any suitable expression system.
  • the protein may be purified to substantial purity by standard techniques, including selective precipitation with such substances as ammonium sulfate; column chromatography, irnmunopiirification methods, and others (see, e.g., Scopes, Protein Purification: Principles and Practice (1982); U.S. Patent No. 4,673,641; Ausubel et al, supra; and Sambrook et al, supra).
  • proteins having established molecular adhesion properties can be reversible fused to the protein.
  • angiogenesis protein can be selectively adsorbed to a purification column and then freed from the column in a relatively pure form. The fused protein is then removed by enzymatic activity. Finally, protein could be purified using immunoaffinity columns.
  • Recombinant proteins are expressed by transformed bacteria in large amounts, typically after promoter induction; but expression can be constitutive. Promoter induction with IPTG is one example of an inducible promoter system. Bacteria are grown according to standard procedures in the art. Fresh or frozen bacteria cells are used for isolation of protein. [0129] Proteins expressed in bacteria may form insoluble aggregates ("inclusion bodies"). Several protocols are suitable for purification of protein inclusion bodies.
  • purification of inclusion bodies typically involves the extraction, separation and/or purification of inclusion bodies by disruption of bacterial cells, e.g., by incubation in a buffer of 50 mM TRIS/HCL pH 7.5, 50 mM NaCI, 5 mM MgCl 2 , 1 mM DTT, 0.1 mM ATP, and 1 mM PMSF.
  • the cell suspension can be lysed using 2-3 passages through a French Press, homogenized using a Polytron (Brinkman Instruments) or sonicated on ice. Alternate methods of lysing bacteria are apparent to those of skill in the art (see, e.g., Sambrook et al, supra; Ausubel et al, supra).
  • the inclusion bodies are solubilized, and the lysed cell suspension is typically centrifuged to remove unwanted insoluble matter. Proteins that formed the inclusion bodies may be renatured by dilution or dialysis with a compatible buffer. Suitable solvents include, but are not limited to urea (from about 4 M to about 8 M), formamide (at least about 80%, volume/volume basis), and guanidine hydrochloride (from about 4 M to about 8 M).
  • Some solvents which are capable of solubilizing aggregate-forming proteins are inappropriate for use in this procedure due to the possibility of irreversible denaturation ofthe proteins, accompanied by a lack of immunogenicity and/or activity.
  • SDS sodium dodecyl sulfate
  • 70% formic acid are inappropriate for use in this procedure due to the possibility of irreversible denaturation ofthe proteins, accompanied by a lack of immunogenicity and/or activity.
  • guanidine hydrochloride and similar agents are denaturants, this denaturation is not irreversible and renaturation may occur upon removal (by dialysis, for example) or dilution ofthe denaturant, allowing re-formation of immunologically and/or biologically active protein.
  • Other suitable buffers are known to those skilled in the art. Human proteins are separated from other bacterial proteins by standard separation techniques, e.g., with Ni-NTA agarose resin.
  • the periplasmic fraction ofthe bacteria can be isolated by cold osmotic shock in addition to other methods known to skill in the art.
  • the bacterial cells are centrifuged to form a pellet. The pellet is resuspended in a buffer containing 20% sucrose.
  • the bacteria are centrifuged and the pellet is resuspended in ice-cold 5 mM MgSO 4 and kept in an ice bath for approximately 10 minutes.
  • the cell suspension is centrifuged and the supernatant decanted and saved.
  • the recombinant proteins present in the supernatant can be separated from the host proteins by standard separation techniques well known to those of skill in the art.
  • an initial salt fractionation can separate many ofthe unwanted host cell proteins (or proteins derived from the cell culture media) from the recombinant protein of interest.
  • the preferred salt is ammonium sulfate.
  • Ammonium sulfate precipitates proteins by effectively reducing the amount of water in the protein mixture. Proteins then precipitate on the basis of their solubility. The more hydrophobic a protein is, the more likely it is to precipitate at lower ammonium sulfate concentrations.
  • a typical protocol includes adding saturated ammonium sulfate to a protein solution so that the resultant ammonium sulfate concentration is between 20-30%. This concentration will precipitate the most hydrophobic of proteins.
  • the precipitate is then discarded (unless the protein of interest is hydrophobic) and ammonium sulfate is added to the supernatant to a concentration known to precipitate the protein of interest.
  • the precipitate is then solubilized in buffer and the excess salt removed if necessary, either through dialysis or diafiltration.
  • Other methods that rely on solubility of proteins, such as cold ethanol precipitation, are well known to those of skill in the art and can be used to fractionate complex protein mixtures.
  • Size differential filtration [0133] The molecular weight of the protein can be used to isolate it from proteins of greater and lesser size using ultrafiltration through membranes of different pore size (for example, Amicon or Millipore membranes).
  • the protein mixture is ultrafiltered through a membrane with a pore size that has a lower molecular weight cutoff than the molecular weight ofthe protein of interest.
  • the retentate ofthe ultrafiltration is then ultrafiltered against a membrane with a molecular cut off greater than the molecular weight ofthe protein of interest.
  • the recombinant protein will pass through the membrane into the filtrate.
  • the filtrate can then be chromatographed as described below.
  • the protein can also be separated from other proteins on the basis of its size, net surface charge, hydrophobicity, and affinity for ligands.
  • antibodies raised against proteins can be conjugated to column matrices and the proteins immunopurif ⁇ ed. All of these methods are well known in the art. It will be apparent to one of skill that chromatographic techniques can be performed at any scale and using equipment from many different manufacturers (e.g., Pharmacia Biotech).
  • Assays for modulators of angiogenesis proteins A. Assays [0135] Modulation of an angiogenesis protein, and corresponding modulation of angiogenesis, can be assessed using a variety of in vitro and in vivo assays, including high throughput ligand binding and cell based assays, as described herein. Such assays can be used to test for inhibitors and activators ofthe angiogenesis protein, and, consequently, inhibitors and activators of angiogenesis. Such modulators ofthe angiogenesis protein are useful for treating angiogenesis disorders. Modulators ofthe angiogenesis protein are tested using either recombinant or naturally occumng protein, preferably human protein.
  • Measurement of an angiogenic or loss-of-angiogenesis phenotype on the protein or cell expressing the protein can be performed using a variety of assays, in vitro, in vivo, and ex vivo.
  • recombinant or naturally occurring protein can be used in vitro, in a ligand binding or enzymatic function assay.
  • Protein present in a cellular extract can also be used in in vitro assays.
  • Cell- and animal-based in vivo assays can also be used to assay for angiogenesis modulators.
  • any suitable physical, chemical, or phenotypic change that affects activity or binding can be used to assess the influence of a test compound on the polypeptide of this invention.
  • the functional effects are determined using intact cells or animals, one can also measure a variety of effects such as, in the case of angiogenesis associated with tumors, tumor growth, neovascularization, endothelial tube formation, cell surface markers such as ⁇ v/33, hormone release, transcriptional changes to both known and uncharacterized genetic markers (e.g., northern blots), changes in cell metabolism such as cell growth or pH changes, and changes in intracellular second messengers such as cGMP.
  • measurement of ov/33 integrin cell surface expression and FACS sorting is used to identify modulators of angiogenesis.
  • Assays to identify compounds with angiogenesis modulating activity, e.g., anti- angiogenic activity, can be performed in vitro, e.g., binding assays.
  • Purified recombinant or naturally occurring protein can be used in the in vitro methods ofthe invention.
  • the recombinant or naturally occurring protein can be part of a cellular lysate.
  • the assay can be either solid state or soluble.
  • the protein is bound to a solid support, either covalently or non-covalently.
  • the in vitro assays ofthe invention are ligand binding or ligand affinity assays, either non-competitive or competitive.
  • Other in vitro assays include measuring changes in spectroscopic (e.g., fluorescence, absorbance, refractive index), hydrodynamic (e.g., shape), chromatographic, or solubility properties for the protein.
  • a high throughput binding assay is performed in which the protein or chimera comprising a fragment thereof is contacted with a potential modulator and incubated for a suitable amount of time.
  • the potential modulator is bound to a solid support, and the protein is added.
  • the protein is bound to a solid support.
  • modulators can be used, as described below, including small organic molecules, peptides, and antibodies.
  • assays can be used to identify angiogenesis-modulator binding, including labeled protein- protein binding assays, electrophoretic mobility shifts, immunoassays, and the like.
  • the binding ofthe candidate modulator is determined through the use of competitive binding assays, where interference with binding of a known ligand is measured in the presence of a potential modulator. Often, either the potential modulator or the known ligand is labeled.
  • Cell-based in vivo assays [0139]
  • the protein is expressed in a cell, and functional, e.g., physical and chemical or phenotypic, changes are assayed to identify angiogenesis modulators, preferably anti-angiogenesis compounds.
  • Cells expressing angiogenesis proteins can also be used in binding assays or enzymatic assays. Any suitable functional effect can be measured, as described herein.
  • hgand binding, cell surface marker expression, cellular proliferation, VEGF-R assays, co-culture assays for tube formation, and cell migration assays are all suitable assays to identify potential modulators using a cell based system.
  • Suitable cells for such cell based assays include both primary endothelial cells and cell lines, as described herein.
  • the protein can be naturally occurring or recombinant.
  • loss-of angiogenesis phenotype is measured by contacting endothelial cells comprising an angiogenesis target with a potential modulator.
  • Modulation of angiogenesis is identified by screening for cell surface marker expression, e.g., ⁇ v / 33 integrin expression levels, using fluorescent antibodies and FACS sorting.
  • cellular proliferation can be measured using 3 H- thymidine incorporation or dye inclusion.
  • cellular polypeptide levels are determined by measuring the level of protein or mRNA.
  • the level of protein or proteins are measured using immunoassays such as western blotting, ELISA and the like with an antibody that selectively binds to the polypeptide or a fragment thereof.
  • immunoassays such as western blotting, ELISA and the like with an antibody that selectively binds to the polypeptide or a fragment thereof.
  • amplification e.g., using PCR, LCR, or hybridization assays, e.g., northern hybridization, RNAse protection, dot blotting, are prefe ⁇ ed.
  • protein expression can be measured using a reporter gene system.
  • a reporter gene system can be devised using an angiogenesis protein promoter operably linked to a reporter gene such as chlorarnphenicol acetyltransferase, firefly luciferase, bacterial luciferase, ⁇ -galactosidase and alkaline phosphatase.
  • the protein of interest can be used as an indirect reporter via attachment to a second reporter such as red or green fluorescent protein (see, e.g., Mistili & Spector, Nature Biotechnology 15:961-964 (1997)).
  • the reporter construct is typically transfected into a cell. After treatment with a potential modulator, the amount of reporter gene transcription, translation, or activity is measured according to standard techniques known to those of skill in the art.
  • a variety of phenotypic angiogenesis assays are known to those of skill in the art. Various models have been employed to evaluate angiogenesis (e.g., Croix et al., Science 289:1197-1202 (2000) and Kahn et al, Amer. J. Pathol 156:1887-1900).
  • Assessment of angiogenesis in the presence of a potential modulator can be performed using cell-culture-based assays, e.g., endothelial cell tube formation assays and haptotaxis assays, as well as other animal based bioassays such as the chick CAM assay, the mouse comeal assay, and assays measuring the effect of administering potential modulators on implanted tumors.
  • cell-culture-based assays e.g., endothelial cell tube formation assays and haptotaxis assays
  • other animal based bioassays such as the chick CAM assay, the mouse comeal assay, and assays measuring the effect of administering potential modulators on implanted tumors.
  • any suitable functional effect can be measured, as described herein.
  • cellular morphology e.g., cell volume, nuclear volume, cell perimeter, and nuclear perimeter
  • ligand binding e.g., kinase activity, apoptosis
  • cell surface marker expression e.g., cell surface marker expression
  • GFP positivity and dye dilution assays e.g., cell tracker assays with dyes that bind to cell membranes
  • DNA synthesis assays e.g., 3 H-thymidine and fluorescent DNA-binding dyes such as BrdU or Hoescht dye with FACS analysis
  • Go/Gi cell cycle arrest are all suitable assays to identify potential modulators using a cell based system.
  • Suitable cells for such cell based assays include both primary cancer or tumor cells and cell lines, as described herein, e.g., A549 (lung), MCF7 (breast, p53 wild-type), H1299 (lung, p53 null), Hela (cervical), PC3 (prostate, p53 mutant), MDA-MB-231 (breast, p53 wild-type). Cancer cell lines can be p53 mutant, p53 null, or express wild type p53.
  • Animal models [0146] A number of animal based assays for angiogenesis phenotypes are known to those of skill in the art and can be used to assay for modulators of angiogenesis.
  • the chick CAM assay is described by O'Reilly, et al. Cell 79: 315-328 (1994). Briefly, 3 day old chicken embryos with intact yolks are separated from the egg and placed in a petri dish. After 3 days of incubation, a methylcellulose disc containing the protein to be tested is applied to the CAM of individual embryos. After about 48 hours of incubation, the embryos and CAMs are observed to determine whether endothelial growth has been inhibited. [0147] The mouse comeal assay involves implanting a growth factor-containing pellet, along with another pellet containing the suspected endothelial growth inhibitor, in the cornea of a mouse and observing the pattern of capillaries that are elaborated in the cornea.
  • Angiogenesis can also be measured by determining the extent of neovascularization of a tumor.
  • carcinoma cells can be subcutaneously inoculated into athymic or nude mice or SOD mice and tumor growth then monitored. Immunoassays using endothelial cell-specific antibodies are typically used to stain for vascularization of tumor and the number of vessels in the tumor.
  • animal models of angiogenesis find use in screening for modulators of angiogenesis.
  • transgenic animal technology including gene knockout technology, for example as a result of homologous recombination with an appropriate gene targeting vector, or gene overexpression, will result in the absence or increased expression ofthe protein.
  • the same technology can also be applied to make knock-out cells.
  • tissue-specific expression or knockout ofthe protein may be necessary.
  • Transgenic animals generated by such methods find use as animal models of angiogenesis and are additionally useful in screening for modulators of angiogenesis.
  • Knock-out cells and transgenic mice can be made by insertion of a marker gene or other heterologous gene into the endogenous gene site in the mouse genome via homologous recombination. Such mice can also be made by substituting the endogenous gene with a mutated version ofthe gene, or by mutating the endogenous gene, e.g., by exposure to carcinogens.
  • a DNA construct is introduced into the nuclei of embryonic stem cells. Cells containing the newly engineered genetic lesion are injected into a host mouse embryo, which is re-implanted into a recipient female. Some of these embryos develop into chimeric mice that possess germ cells partially derived from the mutant cell line.
  • Chimeric targeted mice can be derived according to Hogan et al, Manipulating the Mouse Embryo: A Laboratory Manual, Cold Spring Harbor Laboratory (1988) and Teratocarcinomas and Embryonic Stem Cells: A Practical Approach, Robertson, ed., IRL Press, Washington, D.C., (1987).
  • the compounds tested as modulators ofthe angiogenesis protein can be any small organic molecule, or a biological entity, such as a protein, e.g., an antibody or peptide, a sugar, a nucleic acid, e.g., an antisense oligonucleotide, RNAi molecule, or a ribozyme, or a lipid.
  • modulators can be genetically altered versions of an angiogenesis protein.
  • test compounds will be small organic molecules, peptides, lipids, and lipid analogs.
  • any chemical compound can be used as a potential modulator or ligand in the assays ofthe invention, although most often compounds can be dissolved in aqueous or organic (especially DMSO-based) solutions are used.
  • the assays are designed to screen large chemical libraries by automating the assay steps and providing compounds from any convenient source to assays, which are typically run in parallel (e.g., in microtiter formats on microtiter plates in robotic assays). It will be appreciated that there are many suppliers of chemical compounds, including Sigma (St. Louis, MO), Aldrich (St. Louis, MO), Sigma- Aldrich (St. Louis, MO), Fluka Chemika-Biochemica Analytika (Buchs Switzerland) and the like.
  • high throughput screening methods involve providing a combinatorial small organic molecule or peptide library containing a large number of potential therapeutic compounds (potential modulator or ligand compounds). Such "combinatorial chemical libraries” or “ligand libraries” are then screened in one or more assays, as described herein, to identify those library members (particular chemical species or subclasses) that display a desired characteristic activity. The compounds thus identified can serve as conventional "lead compounds" or can themselves be used as potential or actual therapeutics.
  • a combinatorial chemical library is a collection of diverse chemical compounds generated by either chemical synthesis or biological synthesis, by combining a number of chemical "building blocks” such as reagents.
  • a linear combinatorial chemical library such as a polypeptide library is formed by combining a set of chemical building blocks (amino acids) in every possible way for a given compound length (i.e., the number of amino acids in a polypeptide compound). Millions of chemical compounds can be synthesized through such combinatorial mixing of chemical building blocks.
  • combinatorial chemical libraries include, but are not limited to, peptide libraries (see, e.g., U.S. Patent 5,010,175, Furka, Int. J. Pept. Prot. Res. 37:487-493 (1991) and Houghton et al, Nature 354:84-88 (1991)).
  • Other chemistries for generating chemical diversity libraries can also be used.
  • Such chemistries include, but are not limited to: peptoids (e.g., PCT Publication No. WO 91/19735), encoded peptides (e.g., PCT Publication No.
  • WO 93/20242 random bio-oligomers (e.g., PCT Publication No. WO 92/00091), benzodiazepines (e.g., U.S. Pat. No. 5,288,514), diversomers such as hydantoins, benzodiazepines and dipeptides (Hobbs et al, Proc. Nat. Acad. Sci. USA 90:6909-6913 (1993)), vinylogous polypeptides (Hagihara et al, J. Amer. Chem. Soc.
  • nucleic acid libraries see Ausubel, Berger and Sambrook, all supra
  • peptide nucleic acid libraries see, e.g., U.S. Patent 5,539,083
  • antibody libraries see, e.g., Vaughn et al, Nature Biotechnology, 14(3):309-314 (1996) and PCT/US96/10287)
  • carbohydrate libraries see, e.g., Liang et al, Science, 274:1520-1522 (1996) and U.S. Patent 5,593,853
  • small organic molecule libraries see, e.g., benzodiazepines, Baum C&EN, Jan 18, page 33 (1993); isoprenoids, U.S. Patent
  • the invention provides soluble assays using an angiogenesis protein, or a cell or tissue expressing an angiogenesis protein, either naturally occurring or recombinant.
  • the invention provides solid phase based in vitro assays in a high throughput format, where the angiogenesis protein is attached to a solid phase substrate. Any one ofthe assays described herein can be adapted for high throughput screening, e.g., ligand binding, cellular proliferation, cell surface marker flux, e.g., ⁇ v/33 integrin, etc.
  • the cell-based system using ⁇ v/33 integrin modulation and FACS assays is used in a high throughput format for identifying modulators of angiogenesis proteins, and therefore modulators of T cell angiogenesis.
  • each well of a microtiter plate can be used to run a separate assay against a selected potential modulator, or, if concentration or incubation time effects are to be observed, every 5-10 wells can test a single modulator.
  • a single standard microtiter plate can assay about 100 (e.g., 96) modulators.
  • 1536 well plates are used, then a single plate can easily assay from about 100- about 1500 different compounds. It is possible to assay many plates per day; assay screens for up to about 6,000, 20,000, 50,000, or more than 100,000 different compounds are possible using the integrated systems ofthe invention.
  • the protein of interest or a fragment thereof e.g., an extracellular domain, or a cell comprising the protein of interest or a fragment thereof as part of a fusion protein can be bound to the solid state component, directly or indirectly, via covalent or non covalent linkage e.g., via a tag.
  • the tag can be any of a variety of components. In general, a molecule which binds the tag (a tag binder) is fixed to a solid support, and the tagged molecule of interest is attached to the solid support by interaction of the tag and the tag binder. [0161] A number of tags and tag binders can be used, based upon known molecular interactions well described in the literature.
  • a tag has a natural binder, for example, biotin, protein A, or protein G
  • tag binders avidin, streptavidin, neutravidin, the Fc region of an immunoglobulin, etc.
  • Antibodies to molecules with natural binders such as biotin are also widely available and appropriate tag binders; .see, SIGMA Immunochemicals 1998 catalogue SIGMA, St. Louis MO).
  • any haptenic or antigenic compound can be used in combination with an appropriate antibody to form a tag/tag binder pair. Thousands of specific antibodies are commercially available and many additional antibodies are described in the literature.
  • the tag is a first antibody and the tag binder is a second antibody wliich recognizes the first antibody.
  • receptor-ligand interactions are also appropriate as tag and tag-binder pairs.
  • agonists and antagonists of cell membrane receptors e.g., cell receptor- ligand interactions such as transferrin, c-kit, viral receptor ligands, cytokine receptors, chemokine receptors, interleukin receptors, immunoglobulin receptors and antibodies, the cadherein family, the integrin family, the selectin family, and the like; see, e.g., Pigott & Power, The Adhesion Molecule Facts Book I (1993).
  • toxins and venoms can all interact with various cell receptors.
  • hormones e.g., opiates, steroids, etc.
  • intracellular receptors e.g. which mediate the effects of various small ligands, including steroids, thyroid hormone, retinoids and vitamin D; peptides
  • lectins e.g. which mediate the effects of various small ligands, including steroids, thyroid hormone, retinoids and vitamin D; peptides
  • drugs lectins
  • sugars e.g., nucleic acids (both linear and cyclic polymer configurations), oligosaccharides, proteins, phospholipids and antibodies
  • nucleic acids both linear and cyclic polymer configurations
  • oligosaccharides oligosaccharides
  • proteins e.g.,
  • Synthetic polymers such as polyurethanes, polyesters, polycarbonates, polyureas, polyamides, polyethyleneimines, polyarylene sulfides, polysiloxanes, polyimides, and polyacetates can also form an appropriate tag or tag binder. Many other tag/tag binder pairs are also useful in assay systems described herein, as would be apparent to one of skill upon review of this disclosure.
  • Common linkers such as peptides, polyethers, and the like can also serve as tags, and include polypeptide sequences, such as poly gly sequences of between about 5 and 200 amino acids.
  • Such flexible linkers are known to persons of skill in the art. For example, poly(ethelyne glycol) linkers are available from Shearwater Polymers, Inc. Huntsville, Alabama. These linkers optionally have amide linkages, sulfhydryl linkages, or heterofunctional linkages.
  • Tag binders are fixed to solid substrates using any of a variety of methods currently available.
  • Solid substrates are commonly derivatized or functionalized by exposing all or a portion ofthe substrate to a chemical reagent which fixes a chemical group to the surface which is reactive with a portion ofthe tag binder.
  • groups which are suitable for attachment to a longer chain portion would include amines, hydroxyl, thiol, and carboxyl groups.
  • Aminoalkylsilanes and hydroxyalkylsilanes can be used to functionalize a variety of surfaces, such as glass surfaces. The construction of such solid phase biopolymer arrays is well described in the literature. See, e.g., Merrifield, J Am. Chem. Soc.
  • Non-chemical approaches for fixing tag binders to substrates include other common methods, such as heat, cross-linking by UV radiation, and the like.
  • immunoassays In addition to the detection of gene and gene expression using nucleic acid hybridization technology, one can also use immunoassays to detect proteins ofthe invention. Such assays are useful for screening for modulators of angiogenesis, as well as for therapeutic and diagnostic applications. Immunoassays can be used to qualitatively or quantitatively analyze angiogenesis protein. A general overview ofthe applicable technology can be found in Harlow & Lane, Antibodies: A Laboratory Manual (1988). A.
  • Such techniques include antibody preparation by selection of antibodies from libraries of recombinant antibodies in phage or similar vectors, as well as preparation of polyclonal and monoclonal antibodies by immunizing rabbits or mice (see, e.g., Huse et al, Science 246:1275-1281 (1989); Ward et al, Nature 341:544-546 (1989)).
  • a number of immunogens comprising portions of an angiogenesis protein may be used to produce antibodies specifically reactive with protein.
  • recombinant protein or an antigenic fragment thereof can be isolated as described herein.
  • Recombinant protein can be expressed in eukaryotic or prokaryotic cells as described above, and purified as generally described above.
  • Recombinant protein is the preferred immunogen for the production of monoclonal or polyclonal antibodies.
  • a synthetic peptide derived from the sequences disclosed herein and conjugated to a carrier protein can be used an immunogen.
  • Naturally occurring protein may also be used either in pure or impure form.
  • the product is then injected into an animal capable of producing antibodies. Either monoclonal or polyclonal antibodies may be generated, for subsequent use in immunoassays to measure the protein.
  • mice e.g., BALB/C mice
  • rabbits is immunized with the protein using a standard adjuvant, such as Freund's adjuvant, and a standard immunization protocol.
  • the animal's immune response to the immunogen preparation is monitored by taking test bleeds and determining the titer of reactivity to the beta subunits.
  • blood is collected from the animal and antisera are prepared. Further fractionation ofthe antisera to enrich for antibodies reactive to the protein can be done if desired (see, Harlow & Lane, supra).
  • Monoclonal antibodies may be obtained by various techniques familiar to those skilled in the art. Briefly, spleen cells from an animal immunized with a desired antigen are immortalized, commonly by fusion with a myeloma cell (see, Kohler & Milstein, Eur. J. Immunol. 6:511-519 (1976)). Alternative methods of immortalization include transformation with Epstein Barr Virus, oncogenes, or retroviruses, or other methods well known in the art. Colonies arising from single immortalized cells are screened for production of antibodies ofthe desired specificity and affinity for the antigen, and yield ofthe monoclonal antibodies produced by such cells may be enhanced by various techniques, including injection into the peritoneal cavity of a vertebrate host. Alternatively, one may isolate DNA sequences which encode a monoclonal antibody or a binding fragment thereof by screening a DNA library from human B cells according to the general protocol outlined by Huse, et al, Science 246:1275-1281 (1989).
  • Monoclonal antibodies and polyclonal sera are collected and titered against the immunogen protein in an immunoassay, for example, a solid phase immunoassay with the immunogen immobilized on a solid support.
  • an immunoassay for example, a solid phase immunoassay with the immunogen immobilized on a solid support.
  • polyclonal antisera with a titer of 10 4 or greater are selected and tested for their cross reactivity against non- angiogenesis proteins, using a competitive binding immunoassay.
  • Specific polyclonal antisera and monoclonal antibodies will usually bind with a K of at least about 0.1 mM, more usually at least about 1 ⁇ M, preferably at least about 0.1 ⁇ M or better, and most preferably, 0.01 ⁇ M or better.
  • Antibodies specific only for a particular ortholog such as a human ortholog, can also be made, by subtracting out other cross-reacting orthologs from a species such as a non-human mammal. In this manner, antibodies that bind only to a desired protein may be obtained.
  • the protein can be detected by a variety of immunoassay methods.
  • the antibody can be used therapeutically as modulators.
  • the immunoassays ofthe present invention can be performed in any of several configurations, which are reviewed extensively in Enzyme Immunoassay (Maggio, ed., 1980); and Harlow & Lane, supra. B. Immunological binding assays
  • Protein can be detected and/or quantified using any of a number of well recognized immunological binding assays (see, e.g., U.S. Patents 4,366,241; 4,376,110; 4,517,288; and 4,837,168).
  • immunological binding assays see also Methods in Cell Biology: Antibodies in Cell Biology, volume 37 (Asai, ed. 1993); Basic and Clinical Immunology (Stites & Terr, eds., 7th ed. 1991).
  • Immunological binding assays typically use an antibody that specifically binds to a protein or antigen of choice (in this case the protein or antigenic subsequence thereof).
  • the antibody may be produced by any of a number of means well known to those of skill in the art and as described above.
  • Immunoassays also often use a labeling agent to specifically bind to and label the complex formed by the antibody and antigen.
  • the labeling agent may itself be one of the moieties comprising the antibody/antigen complex.
  • the labeling agent may be a labeled protein or a labeled antibody.
  • the labeling agent may be a third moiety, such a secondary antibody, that specifically binds to the antibody/protein complex (a secondary antibody is typically specific to antibodies ofthe species from which the first antibody is derived).
  • Other proteins capable of specifically binding immunoglobuhn constant regions, such as protein A or protein G may also be used as the label agent.
  • the labeling agent can be modified with a detectable moiety, such as biotin, to which another molecule can specifically bind, such as streptavidin.
  • detectable moieties are well known to those skilled in the art.
  • incubation and/or washing steps may be required after each combination of reagents. Incubation steps can vary from about 5 seconds to several hours, optionally from about 5 minutes to about 24 hours. However, the incubation time will depend upon the assay format, antigen, volume of solution, concentrations, and the like. Usually, the assays will be carried out at ambient temperature, although they can be conducted over a range of temperatures, such as 10°C to 40°C.
  • Non-competitive assay formats Immunoassays for detecting protein in samples may be either competitive or noncompetitive.
  • Noncompetitive immunoassays are assays in which the amount of antigen is directly measured.
  • the antibodies can be bound directly to a solid substrate on which they are immobilized. These immobilized antibodies then capture protein present in the test sample. Proteins thus immobilized are then bound by a labeling agent, such as a second antibody bearing a label.
  • the second antibody may lack a label, but it may, in turn, be bound by a labeled third antibody specific to antibodies ofthe species from which the second antibody is derived.
  • the second or third antibody is typically modified with a detectable moiety, such as biotin, to which another molecule specifically binds, e.g., streptavidin, to provide a detectable moiety.
  • Competitive assay formats such as biotin, to which another molecule specifically binds, e.g., streptavidin, to provide a detectable
  • the amount of protein present in the sample is measured indirectly by measuring the amount of a known, added (exogenous) protein displaced (competed away) from an antibody by the unknown protein present in a sample.
  • a known amount of protein is added to a sample and the sample is then contacted with an antibody that specifically binds to protein.
  • the amount of exogenous protein bound to the antibody is inversely proportional to the concentration of protein present in the sample.
  • the antibody is immobilized on a solid substrate.
  • the amount of protein bound to the antibody may be determined either by measuring the amount of protein present in protein antibody complex, or alternatively by measuring the amount of remaining uncomplexed protein.
  • the amount of protein may be detected by providing a labeled molecule.
  • a hapten inhibition assay is another prefe ⁇ ed competitive assay.
  • the known protein is immobilized on a solid substrate.
  • a known amount of antibody is added to the sample, and the sample is then contacted with the immobilized protein.
  • the amount of antibody bound to the known immobihzed protein is inversely proportional to the amount of protein present in the sample.
  • the amount of immobilized antibody may be detected by detecting either the immobilized fraction of antibody or the fraction ofthe antibody that remains in solution. Detection may be direct where the antibody is labeled or indirect by the subsequent addition of a labeled moiety that specifically binds to the antibody as described above.
  • Immunoassays in the competitive binding format can also be used for crossreactivity determinations.
  • a protein can be immobilized to a solid support. Proteins are added to the assay that compete for binding ofthe antisera to the immobilized antigen. The ability ofthe added proteins to compete for binding ofthe antisera to the immobilized protein is compared to the ability ofthe protein to compete with itself. The percent crossreactivity for the above proteins is calculated, using standard calculations. Those antisera with less than 10% crossreactivity with each ofthe added proteins listed above are selected and pooled. The cross-reacting antibodies are optionally removed from the pooled antisera by immunoabsorption with the added considered proteins, e.g., distantly related homologs.
  • the immunoabsorbed and pooled antisera are then used in a competitive binding immunoassay as described above to compare a second protein, thought to be perhaps an allele or polymorphic variant of a protein, to the immunogen protein.
  • the two proteins are each assayed at a wide range of concentrations and the amount of each protein required to inhibit 50% ofthe binding ofthe antisera to the immobilized protein is determined. If the amount ofthe second protein required to inhibit 50% of binding is less than 10 times the amount ofthe protein that is required to inhibit 50% of binding, then the second protein is said to specifically bind to the polyclonal antibodies generated to the immunogen.
  • Western blot (immunoblot) analysis is used to detect and quantify the presence of protein in the sample.
  • the technique generally comprises separating sample proteins by gel electrophoresis on the basis of molecular weight, transferring the separated proteins to a suitable solid support, (such as a nitrocellulose filter, a nylon filter, or derivatized nylon filter), and incubating the sample with the antibodies that specifically bind the protein.
  • the antibodies specifically bind to the protein on the solid support.
  • These antibodies may be directly labeled or alternatively may be subsequently detected using labeled antibodies (e.g., labeled sheep anti-mouse antibodies) that specifically bind to the antibodies.
  • LOA liposome immunoassays
  • the particular label or detectable group used in the assay is not a critical aspect ofthe invention, as long as it does not significantly interfere with the specific binding of the antibody used in the assay.
  • the detectable group can be any material having a detectable physical or chemical property.
  • Such detectable labels have been well- developed in the field of immunoassays and, in general, most any label useful in such methods can be applied to the present invention.
  • a label is any composition detectable by spectroscopic, photochemical, biochemical, immunochemical, electrical, optical or chemical means.
  • Useful labels in the present invention include, magnetic beads (e.g., DYNABEADSTM), fluorescent dyes (e.g., fluorescein isothiocyanate, Texas red, rhodamine, and the like), radiolabels (e.g., H, I, S, C, or P), enzymes (e.g., horse radish peroxidase, alkaline phosphatase and others commonly used in an ELISA), and colorimetric labels such as colloidal gold or colored glass or plastic beads (e.g., polystyrene, polypropylene, latex, etc.).
  • magnetic beads e.g., DYNABEADSTM
  • fluorescent dyes e.g., fluorescein isothiocyanate, Texas red, rhodamine, and the like
  • radiolabels e.g., H, I, S, C, or P
  • enzymes e.g., horse radish peroxidase, alkaline
  • the label may be coupled directly or indirectly to the desired component of the assay according to methods well known in the art. As indicated above, a wide variety of labels may be used, with the choice of label depending on sensitivity required, ease of conjugation with the compound, stability requirements, available instrumentation, and disposal provisions.
  • Non-radioactive labels are often attached by indirect means.
  • a ligand molecule e.g., biotin
  • the ligand then binds to another molecules (e.g., streptavidin) molecule, which is either inherently detectable or covalently bound to a signal system, such as a detectable enzyme, a fluorescent compound, or a chemiluminescent compound.
  • a signal system such as a detectable enzyme, a fluorescent compound, or a chemiluminescent compound.
  • the ligands and their targets can be used in any suitable combination with antibodies that recognize the protein, or secondary antibodies.
  • the molecules can also be conjugated directly to signal generating compounds, e.g., by conjugation with an enzyme or fluorophore.
  • Enzymes of interest as labels will primarily be hydrolases, particularly phosphatases, esterases and glycosidases, or oxidotases, particularly peroxidases.
  • Fluorescent compounds include fluorescein and its derivatives, rhodamine and its derivatives, dansyl, umbelliferone, etc.
  • Chemiluminescent compounds include luciferin, and 2,3-dihydrophthalazinediones, e.g., luminol.
  • Means of detecting labels are well known to those of skill in the art.
  • means for detection include a scintillation counter or photographic film as in autoradiography.
  • the label is a fluorescent label, it may be detected by exciting the fluorochrome with the appropriate wavelength of light and detecting the resulting fluorescence. The fluorescence may be detected visually, by means of photographic film, by the use of electronic detectors such as charge coupled devices (CCDs) or photomultipliers and the like.
  • CCDs charge coupled devices
  • enzymatic labels may be detected by providing the appropriate substrates for the enzyme and detecting the resulting reaction product.
  • simple colorimetric labels may be detected simply by observing the color associated with the label. Thus, in various dipstick assays, conjugated gold often appears pink, while various conjugated beads appear the color ofthe bead.
  • agglutination assays can be used to detect the presence ofthe target antibodies.
  • antigen-coated particles are agglutinated by samples comprising the target antibodies.
  • none ofthe components need be labeled and the presence of the target antibody is detected by simple visual inspection.
  • the present invention provides the nucleic acids of angiogenesis associated protein for the transfection of cells in vitro and in vivo. These nucleic acids can be inserted into any of a number of well-known vectors for the transfection of target cells and organisms as described below.
  • the nucleic acids are transfected into cells, ex vivo or in vivo, through the interaction ofthe vector and the target cell.
  • the nucleic acid under 10 the control of a promoter, then expresses a protein of the present invention, thereby mitigating the effects of absent, partial inactivation, or abnormal expression ofthe angiogenesis gene, particularly as it relates to angiogenesis.
  • the compositions are administered to a patient in an amount sufficient to elicit a therapeutic response in the- ' patient. An amount adequate to accomplish this is defined as "therapeutically effective
  • the nucleic acids ofthe invention can also be used to make transgenic animals, such as transgenic mice, either by knock-out or overexpression. Such animals are useful, 30 e.g., for testing modulators of angiogenesis.
  • Pharmaceutical compositions and administration Pharmaceutically acceptable carriers are determined in part by the particular composition being administered (e.g., nucleic acid, protein, modulatory compounds or transduced cell), as well as by the particular method used to administer the composition. Accordingly, there are a wide variety of suitable formulations of pharmaceutical compositions ofthe present invention (see, e.g., Remington 's Pharmaceutical Sciences, 17 th ed., 1989). Administration can be in any convenient manner, e.g., by injection, oral administration, inhalation, transdermal application, or rectal administration.
  • Formulations suitable for oral administration can consist of (a) liquid solutions, such as an effective amount ofthe packaged nucleic acid suspended in diluents, such as water, saline or PEG 400; (b) capsules, sachets or tablets, each containing a predetermined amount ofthe active ingredient, as liquids, solids, granules or gelatin; (c) suspensions in an appropriate liquid; and (d) suitable emulsions.
  • liquid solutions such as an effective amount ofthe packaged nucleic acid suspended in diluents, such as water, saline or PEG 400
  • capsules, sachets or tablets each containing a predetermined amount ofthe active ingredient, as liquids, solids, granules or gelatin
  • suspensions in an appropriate liquid such as water, saline or PEG 400
  • Tablet forms can include one or more of lactose, sucrose, mannitol, sorbitol, calcium phosphates, com starch, potato starch, microcrystalline cellulose, gelatin, colloidal silicon dioxide, talc, magnesium stearate, stearic acid, and other excipients, colorants, fillers, binders, diluents, buffering agents, moistening agents, preservatives, flavoring agents, dyes, disintegrating agents, and pharmaceutically compatible carriers.
  • Lozenge forms can comprise the active ingredient in a flavor, e.g., sucrose, as well as pastilles comprising the active ingredient in an inert base, such as gelatin and glycerin or sucrose and acacia emulsions, gels, and the like containing, in addition to the active ingredient, carriers known in the art.
  • a flavor e.g., sucrose
  • an inert base such as gelatin and glycerin or sucrose and acacia emulsions, gels, and the like containing, in addition to the active ingredient, carriers known in the art.
  • Aerosol formulations i.e., they can be "nebulized" to be administered via inhalation. Aerosol formulations can be placed into pressurized acceptable propellants, such as dichlorodifluoromethane, propane, nitrogen, and the like.
  • Formulations suitable for parenteral administration include aqueous and non-aqueous, isotonic sterile injection solutions, which can contain antioxidants, buffers, bacteriostats, and solutes that render the formulation isotonic with the blood ofthe intended recipient, and aqueous and non- aqueous sterile suspensions that can include suspending agents, solubilizers, thickening agents, stabilizers, and preservatives.
  • compositions can be administered, for example, by intravenous infusion, orally, topically, intraperitoneally, intravesically or intrathecally.
  • Parenteral adnrinistration and intravenous administration are the preferred methods of administration.
  • the formulations of commends can be presented in unit-dose or multi-dose sealed containers, such as ampules and vials.
  • Injection solutions and suspensions can be prepared from sterile powders, granules, and tablets ofthe kind previously described.
  • Cells transduced by nucleic acids for ex vivo therapy can also be administered intravenously or parenterally as described above.
  • the dose administered to a patient should be sufficient to effect a beneficial therapeutic response in the patient over time.
  • the dose will be determined by the efficacy ofthe particular vector employed and the condition of the patient, as well as the body weight or surface area ofthe patient to be treated.
  • the size ofthe dose also will be determined by the existence, nature, and extent of any adverse side-effects that accompany the administration of a particular vector, or transduced cell type in a particular patient.
  • the physician evaluates circulating plasma levels ofthe vector, vector toxicities, progression ofthe disease, and the production of anti- vector antibodies.
  • the dose equivalent of a naked nucleic acid from a vector is from about 1 ⁇ g to 100 ⁇ g for a typical 70 kilogram patient, and doses of vectors which include a retroviral particle are calculated to yield an equivalent amount of therapeutic nucleic acid.
  • compounds and transduced cells ofthe present invention can be administered at a rate determined by the LD-50 ofthe inhibitor, vector, or transduced cell type, and the side-effects ofthe inhibitor, vector or cell type at various concentrations, as applied to the mass and overall health ofthe patient. Administration can be accomplished via single or divided doses.
  • Example 1 Identification of genes involved in modulation of angiogenesis in vitro
  • a retroviral system complex libraries of cDNAs have been expressed in human primary endothelial cells (e.g., HUVECS, Cloneitc CC-2519).
  • HUVEC cells that switch to a differentiated angiostatic state can be identified using a VEGFR2 internalization assay.
  • EGM-2 media Clonetics EGM-2 bullet kit CC-3162
  • HUVECs Co-culture of HUVECs on smooth muscle cells was used to confirm that genes identified via VEGR2 internalization are genes that encode angiogenesis proteins.
  • Smooth muscle cells (Clonetics Pulmonary Artery SMCs CC-2581) are plated at 40,000 cells per well of a collagen coated 24 well tissue culture plate and grown to confluency. HUVECs are plated onto the smooth muscle cells at 22,000 cells per well.
  • the phenotype of vascular bed formation is determined as follows: photographs are taken and formation of tubular morphology ofthe HUVECs is determined empirically.
  • the co- culture assay is typically used to confirm an anti-angiogenic phenotype.
  • NM_000098 Homo sapiens camitine palmitoyltransferase II (CPT2) , nuclear gene encoding mitochondrial protein, mRNA gi
  • CPT-2 A 606760.9
  • NM_006549 Homo sapiens calcium/calmodulin-dependent protein kinase kinase 2, beta (CAMKK2) , transcript variant 1, mRNA gi I 27437014 I ref
  • [27437014] 1 gagcctgggg aggtcgaggg tgcagcgag ⁇ ⁇ gtgat ⁇ gtg ⁇ ta ⁇ tgcact ccagcctggg 61 caacacagag agaccctgtc tcaaaacaaa ⁇ aaa ⁇ aaaaaa caaacaaaagaa aaaaaatgg gagtgggccg ggcggtga ⁇ t ⁇ a ⁇ acctg taatcc ⁇ agc 181 actttcggag gccaaggcgg gtggatcacgg
  • ACAAl NM_001607 Homo sapiens acetyl-Coenzyme A acyltransferase 1 (peroxisomal 3- oxoacyl-Coenzyme A thiolase) (ACAAl) , nuclear gene encoding mitochondrial protein, mRNA gi
  • GNPI NM_005471 Homo sapiens glucosamine-6-phosphate deaminase 1 (GNPDAl) , mRNA gi I 315428511 ref
  • NM_014762 Homo sapiens 24-dehydrocholesterol reductase (DHCR24) , mRNA gi 113375617 I ref
  • BC026350 Homo sapiens selenoprotein T, mRNA ( ⁇ DNA clone MGC:26803 IMAGE : 4796883) , complete eds gi
  • NM_002837 Homo sapiens protein tyrosine phosphatase, re ⁇ eptor type, B (PTPRB) , mRNA gi 118491009 I ref
  • NM_003115 Homo sapiens UDP-N-a ⁇ teylglu ⁇ osamine pyrophosphorylase 1 (UAPl) , mRNA gi I 34147515 I ref
  • NM_145212.l Homo sapiens mitochondrial ribosomal protein L30 (MRPL30) , nuclear gene encoding mitochondrial protein, transcript variant 1, mRNA
  • NM_016503 Homo sapiens mito ⁇ hondrial ribosomal protein L30 (MRPL30) , nu ⁇ lear gene encoding mitochondrial protein, transcript variant 2, mRNA gi I 217356011 ref
  • NM_005998 Homo sapiens chaperonin containing TCPl, subunit 3 (gamma) (CCT3) , mRNA gi I 315422911 ref
  • [31542291] 1 gtctggttct ctctctccag aaggtt ⁇ tg ⁇ cggttcccc agctctgggt acc ⁇ ggctct 61 g ⁇ atcgcgtc gccatgatgg gccatcgt ⁇ agtgctcgtg ⁇ t ⁇ agccaga acacaaagcg 121 tgaatc ⁇ gga agaaaagtt ⁇ aatctggaa cat ⁇ aatgct gccaagacta ttgcagatat 181 catccgaaca tgtttgggac ccaagtccat gatg
  • HSPA8 NM_006597 Homo sapiens heat sho ⁇ k 70kDa protein 8 (HSPA8) , trans ⁇ ript variant 1, mRNA gi I 24234684 I ref
  • SEQ ID NO: 20 SH2 of Abl AK074067.l

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Abstract

The present invention relates to regulation of angiogenesis. The invention further relates to methods for identifying and using agents, including small organic molecules, antibodies, peptides, cyclic peptides, nucleic acids, antisense nucleic acids, RNAi, and ribozymes, that modulate angiogenesis; as well as to the use of expression profiles and compositions in diagnosis and therapy of angiogenesis and cancer.

Description

MODULATORS OF ANGIOGENESIS
CROSS-REFERENCES TO RELATED APPLICATIONS [0001] The present application claims the benefit of USSN 60/536,310, filed January 13, 2004, herein incorporated by reference in its entirety.
STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED RESEARCH AND DEVELOPMENT [0002] Not applicable.
FIELD OF THE INVENTION [0003] The present invention relates to regulation of angiogenesis. The invention further relates to methods for identifying and using agents, including small organic molecules, antibodies, peptides, cyclic peptides, nucleic acids, antisense nucleic acids, RNAi, and ribozymes, that modulate angiogenesis; as well as to the use of expression profiles and compositions in diagnosis and therapy of angiogenesis and cancer.
BACKGROUND OF THE INVENTION [0004] The migration of activated endothelial cells through a vitronectin-rich provisional matrix is critical to the foπnation of new blood vessels during angiogenesis and is dependent on adhesion receptors containing alphav integrins (such as alphavbeta3 which binds to vitronectin). Pgptide and antibody inhibitors of alphavbeta3 integrin inhibit tumor growth in vivo.
[0005] Angiogenesis is typically limited in a normal adult to the placenta, ovary, endometrium and sites of wound healing. However, angiogenesis, or its absence, plays an important role in the maintenance of a variety of pathological states. Some of these states are characterized by neovascularization, e.g., cancer and tumorigenesis, e.g., endometriosis, diabetic retinopathy, glaucoma, glomerulonephritis, and age related macular degeneration. Others, e.g., stroke, infertility, heart disease, e.g., restenosis, ulcers, and scleroderma, are diseases of angiogenic insufficiency. Therefore, there is a need to identify nucleic acids encoding proteins involved in the regulation of angiogenesis, to identify, e.g., modulators of angiogenesis, as well as new therapeutic and diagnostic applications.
SUMMARY OF THE INVENTION [0006] Novel targets for anti-angiogenic therapy have been identified using a functional genetic screen based on vascular endothelial growth factor receptor 2 (VEGFR2) ligand binding triggered receptor internalization. Inhibition or activation of these targets (by small molecule inhibitors; protein, antibody and peptide therapeutics; RNAi; antisense; gene therapy etc.) have therapeutic value in modulating angiogenesis,, e.g., breast, lung, colon, ovarian, liver, thyroid, stomach, bladder, and prostate cancer, basal cell carcinoma, melanoma, lymphomas, leukemias, e.g., myeloid leukemia (CML and AML), endometriosis, diabetic retinopathy, glaucoma, glomerulonephritis, age related macular degeneration, as well as, e.g., stroke, infertility, heart disease, e.g., restenosis, ulcers, and scleroderma. [0007] The present invention therefore provides nucleic acids encoding proteins involved in modulation of (VEGFR2) ligand binding triggered receptor internalization and modulation of angiogenesis. The invention therefore provides methods of screening for compounds, e.g., small organic molecules, antibodies, nucleic acids, peptides, cyclic peptides, nucleic acids, antisense molecules, RNAi, and ribozymes, that are capable of modulating angiogenesis, e.g., either activating or inhibiting angiogenesis. Therapeutic and diagnostic methods and reagents are also provided.
[0008] In one aspect, the present invention provides a method for identifying a compound that modulates angiogenesis, the method comprising the steps of: (i) contacting the compound with an angiogenesis modulating polypeptide or fragment thereof, the polypeptide encoded by a nucleic acid that hybridizes under stringent conditions to a reference nucleic acid encoding the polypeptide, the polypeptide selected from the group consisting of ubiquitin hydrolase (USP37), calcium/calmodulin-dependent protein kinase β (CAMKK2), methionine adenosyltransferase II α (Mat2A), carnitine palmitoyltransferase II (CPT-2), DDX5 RNA helicase, acetyl-coenzyme A acyltransferase (ACAA1), glucosamine-6-phosphate isomerase (GNPI), 24- dehydrocholesterol reductase (DHCR24), selenoprotein T (SELT), protein tyrosine phosphatase, receptor type, B (PTPRB), glucosidase β acid (GBA), UDP-N- acteylglucosamine pyrophosphorylase 1 (UAP1), mitochondrial ribosomal protein L30 (MRPL30), chaperonin containing TCP1, subunit 3 γ (CCT3), HSPA8, solute carrier family 16 (monocarboxylic acid transporters), and member 1 (SLC16A1), SH2 of Abl; and (ii) determining the functional effect ofthe compound upon the polypeptide. [0009] In one embodiment, the functional effect is determined in vitro. In another embodiment, the functional effect is a physical effect. In another embodiment, the functional effect is determined by measuring ligand binding to the polypeptide. In another embodiment, the functional effect is a chemical effect. [0010] In one embodiment, the polypeptide is expressed in a eukaryotic host cell. In another embodiment, the functional effect is a physical effect. In another embodiment, the functional effect is determined by measuring ligand binding to the polypeptide. In another embodiment, the functional effect is a chemical or phenotypic effect. In another embodiment, the polypeptide is expressed in a eukaryotic host cell, e.g., an endothelial cell. In another embodiment, the functional effect is determined by measuring VEGF-R2 surface expression, ov/33 expression, haptotaxis, or tumor growth in vivo.
[0011] In one embodiment, modulation is inhibition of angiogenesis.
[0012] In one embodiment, the polypeptide is recombinant.
[0013] In one embodiment, the compound is an antibody, a peptide, an antisense molecule, a RNAi molecule, or a small organic molecule. [0014] In another aspect, the present invention provides a method for identifying a compound that modulates angiogenesis, the method comprising the steps of (i) contacting the compound with an angiogenesis modulating polypeptide or fragment or inactive variant thereof, the polypeptide selected from the group consisting of ubiquitin hydrolase (USP37), calcium/calmodulin-dependent protein kinase β (CAMKK2), methionine adenosyltransferase II α (Mat2A), camitine palmitoyltransferase II (CPT-2), DDX5 RNA helicase, acetyl-coenzyme A acyltransferase (ACAAl), glucosamine-6-phosphate isomerase (GNPI), 24-dehydrocholesterol reductase (DHCR24), selenoprotein T (SELT), protein tyrosine phosphatase, receptor type, B (PTPRB), glucosidase β acid (GBA), UDP- N-acteylglucosamine pyrophosphorylase 1 (UAP1), mitochondrial ribosomal protein L30 (MRPL30), chaperonin containing TCP1, subunit 3 γ (CCT3), HSPA8, solute carrier family 16 (monocarboxylic acid transporters), and member 1 (SLC16A1), SH2 of Abl; (ii) determining the physical effect ofthe compound upon the polypeptide or fragment thereof or inactive variant thereof; and (iii) determining the chemical or phenotypic effect ofthe compound upon a cell comprising the polypeptide or fragment thereof or inactive variant thereof, thereby identifying a compound that modulates or angiogenesis. [0015] In another aspect, the present invention provides a method of modulating angiogenesis in a subject, the method comprising the step of administering to the subject a therapeutically effective amount of a compound identified using the methods described herein.
[0016] In one embodiment, the subject is a human. [0017] In one embodiment, the compound is an antibody, an antisense molecule, a peptide, or an RNAi molecule, or a small organic molecule.
[0018] In one embodiment, the compound inhibits angiogenesis.
BRIEF DESCRIPTION OF THE DRAWINGS [0019] Figure 1 shows a clone encoding USP-37 isolated in a VEGFR-2 upregulation assay.
[0020] Figure 2 shows USP37 RNA expression in cell lines.
[0021] Figure 3 shows that USP-37 is overexpressed in colon carcinomas.
[0022] Figure 4 shows USP-37 RNAi data.
[0023] Figure 5 shows USP-37 RNAi data.
[0024] Figure 6 shows USP-37 RNAi data.
[0025] Figure 7 shows USP-37 RNAi data.
[0026] Figure 8 shows USP-37 RNAi data.
[0027] Figure 9 summarizes USP-37 data. [0028] Fgure 10 shows a clone encoding CaMKK2 isolated in a VEGFR-2 upregulation assay.
[0029] Figure 11 shows the mRNA expression profile of CaMKK2. [0030] Figure 12 shows CaMKK2 RNAi data.
[0031] Figure 13 shows CaMKK2 RNAi data.
[0032] Figure 14 shows a CaMKK2 inhibitor STO-609.
[0033] Figure 15 shows that STO-609 downregulates VEGF2-R levels.
[0034] Figure 16 shows a summary of CaMKK2 data.
[0035] Figure 17 shows STO-609 data.
[0036] Figure 18 shows STO-609 data.
[0037] Figure 19 shows STO-609 data. [0038] Figure 20 summarizes STO-609 data.
DETAILED DESCRIPTION OF THE INVENTION I. Introduction
[0039] We have used a VEGF receptor internalization screening strategy to identify proteins involved in regulating angiogenesis. Using a retroviral system, complex libraries of cDNAs were expressed in human primary endothelial cells (e.g., HUVECS, Clonetic CC-2519). HUVEC cells that switch to a differentiated angiostatic state can be identified using a VEGFR2 internalization assay. After infection with a retroviral cDNA library, cells are seeded in EGM-2 media (Clonetics EGM-2 bullet kit CC-3162) and grown to log phase. Cells are are cultured in starvation medium (EGMS with 0.1%FCS plus 1% BSA in place of VEGF and FCS) at 37°C for 16 hours. The starved HUVECs are stimulated with VEGF stimulation medium at 37°C for 1.5 hours, trypsinized, and stained with VEGFR2 antibody. Single cells exhibiting increased VEGF-R2 expression (i.e., blocked receptor internalization) were selected using FACS analysis. The cDNAs are isolated and sequenced to identify proteins involved in angiogenesis. The cDNAs can represent, e.g., full length transcripts, transcript fragments, 3' untranslated regions, or antisense molecules. In one embodiment, the cDNA acts as a dominant negative mutant.
[0040] A functional genetic screening strategy can also be used to identify proteins involved in regulating endothelial cell migration on specific matrix components, e.g. vitronectin. A retroviral-based system can be used to stably express complex libraries of various types of genetic elements (e.g. cDNAs and GFP-fusions) in human primary endothelial cells (e.g. HUVECs). Starting with early passage primary endothelial cells representing an "angiogenic state" (i.e., proliferative, highly motile), single cells that have switched to a more differentiated "angiostatic state" (i.e., quiescent, reduced motility) can be identified. To focus on the migration step ofthe angiogenic cycle, conditions can be established which allowed highly efficient migration of HUVEC cells along a haptotactic gradient of specific matrix proteins (e.g. vitronectin / fibronectin) in a Boyden chamber assay. Large populations of HUVEC cells are infected with a GFP-fused cDNA library and selected for impaired haptotaxis. Additional assays for proteins involved in angiogenesis include a HUVEC/smooth muscle cell co-culture assay for endothelial tube formation, and chemo-invasion assays. Finally, human/mouse tumor xenograft assays, mouse sponge angiogenesis and tumorigenesis assays (sponge with human ECs +/- human tumor cells in SCID mice), a collagen-antibody induced arthritis model for RA, and retinal neovascularization assays can be used to identify angiogenesis proteins in vivo and to assay for modulators of such proteins.
[0041] The angiogenesis proteins identified using the VEGFR2 internalization assay described herein, e.g., methionine adenosyltransferase II α (Mat2A) (hit: fragment), camitine palmitoyltransferase II (CPT-2) (hit: fragment), DDX5 RNA helicase (hit: full- length), calcium calmodulin-dependent protein kinase β (CAMKK2) (hit: fragment), acetyl-coenzyme A acyltransferase (ACAAl) (hit: fragment), glucosamine-6-phosphate isomerase (GNPI) (hit: full-length), 24-dehydrocholesterol reductase (DHCR24) (hit: fragment), selenoprotein T (SELT) (hit: fragment), protein tyrosine phosphatase, receptor type, B (PTPRB) (hit: full-length), glucosidase β acid (GBA) (hit: antisense), UDP-N- acteylglucosamine pyrophosphorylase 1 (UAP1) (hit: full-length), mitochondrial ribosomal protein L30 (MRPL30) (hit: fragment), chaperonin containing TCPl, subunit 3 γ (CCT3) (hit: fragment), HSPA8 (hit: full-length), solute carrier family 16 (monocarboxylic acid transporters), member 1 (SLC16A1) (hit: fragment), SH2 of Abl (hit: fragment), and ubiquitin hydrolase (USP37) (hit: 3' UTR), therefore represent targets for the development of angiogenic drugs, preferably anti-angiogenic drugs, e.g., anti- angiogenic drugs for treatment of neovascularization, e.g., cancer, diabetic retinopathy, endometriosis, glomerulonephritis, restenosis, glaucoma, rheumatoid arthritis, and age related macular degeneration, or angiogenic drugs for treatment of angiogenic insufficiency, e.g., stroke, infertility, heart disease, ulcers, and scleroderma. Modulators include small organic molecules, nucleic acids, peptides, cyclic peptides, antibodies, antisense molecules, RNAi molecules, and ribozymes. The nucleic acids and proteins of the invention are also useful for diagnostic applications, using, e.g., nucleic acid probes, ohgonucleotides, and antibodies. These polypeptides are also involved in tumorigenesis and cellular proliferation, and are useful for the development of therapeutic molecules to treat diseases associated with angiogenesis, tumorigenesis, and cellular proliferation. Furthermore, the polypeptides described herein and the nucleic acids encoding them are useful for diagnostic assays for diseases associated with angiogenesis, tumorigenesis, and cellular proliferation. [0042] In another embodiment, the protein ubiquitin hydrolase (USP37) is involved in angiogenesis. Ubiquitin hydrolase plays a role in the hydrolysis of esters formed between thiols and the C-terminal glycine residue ofthe polypeptide ubiquitin, and of AMP- ubiquitin. In vitro hydrolase assays with ubiquitin hydrolase can be used to assay for ubiquitin hydrolase modulators and thus for modulators of angiogenesis. The accession number for USP73 polypeptide is NP_065986 and the accession number for the nucleic acid is NM_020935. See also AB046814 and BAB13420. USP-37 is part of a novel family of ubiquitin hydrolases, most cvlosedly related to USP 26 and 29. Conserved catalytic residues include the Cys bos (GNTCYmN) and the His box (HIGSTSSSDH).
[0043] In another embodiment, the protein CAMKK2 is involved in angiogenesis. CAMKK2 belongs to the Serine/Threonine protein kinase family, and to the
Ca(2+)/calmodulin-dependent protein kinase subfamily. CAMKK2 plays a role in the calcium/calmodulin-dependent (CaM) kinase cascade by phosphorylating the downstream kinases CaMKl and CaMK4. Seven transcript variants encoding six distinct isoforms have been identified for CAMKK2. Additional splice variants have been described but their full-length nature has not been determined. The identified isoforms exhibit a distinct ability to undergo autophosphorylation and to phosphorylate the downstream kinases. In vitro serme/threonine kinase assays with CAMKK2 can be used to assay for CAMKK2 modulators and thus for modulators of angiogenesis. Accession numbers for CAMKK2 nucleic acids are as follows: NM_006549 (variant 1), NM_ 153499 (variant 2), NM_172216 (variant 3), NM 53500 (variant 4), and NM_172226 (variant 7).
Accession numbers for CAMKK2 polypeptides are as follows: NP_ )06540 (variant 1), NP_757380 (variant 2), NP_757365 (variant 3), NP_705720 (variant 4), and P_757380 (variant 7). [0044] In another embodiment, the protein Mat2A is involved in angiogenesis. Mat2A is an enzyme that catalyzes the formation of S-adenosylmethionine from methionine and ATP. hi mammalian tissues, there are three distinct forms of a Mat2A designated as α, β, and γ. α and β are expressed only in adult liver, while γ is widely distributed in extrahepatic tissues. Mat2A is expressed in, e.g., invasive adenocarcinoma, bronchioalveolar carcinoma, CD34+, T negative chronic myelogenous leukemia, invasive carcinoma, early stage papillary serous carcinoma, serous adenocarcinoma, oligodendroglioma, metastatic melanoma, and normal gingival. In vitro enzyme assays with Mat2A can be used to assay for Mat2A modulators and thus for modulators of angiogenesis. The accession number for Mar2A polypeptide is NP005902 and the accession number for the nucleic acid is NM_005911. [0045] In another embodiment, the protein CPT-2 is involved in angiogenesis. CPT2 is a nuclear protein which is transported to the mitochondrial inner membrane. CPT2 together with camitine palmitoyltransferase I oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty- acid (LCFA) oxidation disorders. Defects in CPT2 are the cause of camitine palmitoyltransferase II deficiency (CPT-II deficiency), an autosomal recessive disorder characterized by recurrent myoglobinuria, episodes of muscle pain, stiffness, and rhabdomyolysis. these symptoms are triggered by prolonged exercise, fasting or viral infection and patients are usually young adults, in addition to this classical, late-onset, muscular type, a hepatic or hepatocardiomuscular form has been reported in infants, clinical pictures in these children or neonates include hypoketotic hypoglycemia, liver dysfunction, cardiomyopathy and sudden death. CPT2 is a component ofthe fatty acid β- oxidation cycle. CPT2 is expressed in pituitary adenomas, posterior rhombomeres, lens, mammary gland, and human placenta. The accession number for CPT-2 polypeptide is NP_000089 and the accession number for CPT-2 nucleic acid is NM_000098.
[0046] In another embodiment, the protein DDX5 is involved in angiogenesis. DDX5 RNA helicase is a DEAD box protein, characterized by the conserved motif Asp-Glu- Ala-Asp (DEAD). DEAD box proteins are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. DDX5 encodes a DEAD box protein, which is a RNA-dependent ATPase, and also a proliferation-associated nuclear antigen, highly specifically reacting with the simian virus 40 tumor antigen. DDX5 consists of 13 exons, and alternatively splicing transcripts containing several intron sequences have been detected, but no isoforms encoded by these transcripts are identified. DDX5 also has an RNA-dependent ATPase activity, the rate of ATP hydrolysis is highly stimulated by single-stranded RNA. DDX5 is expressed in bulk germ cell seminoma, follicular adenoma, bulk alveolar tumor, juvenile granulosa tumor, normal gingival, anterior rhombomeres, thymus, pituitary, and liver. In vitro helicase assays with DDX5 can be used to assay for DDX5 modulators and thus for modulators of angiogenesis. The accession number for DDX5 nucleic acid is NM_004396 and the accession number for the polypeptide is NP_004387.
[0047] In another embodiment, the protein ACAAl is involved in angiogenesis. ACAAl is a thiolase operative in the /3-oxidation system ofthe peroxisomes. Deficiency of ACAAl leads to pseudo-Zellweger syndrome. In vitro thiolase assays with ACAAl can be used to assay for ACAAl modulators and thus for modulators of angiogenesis. The accession number for the nucleic acid is NM_001607 and the accession number for the polypeptide is NP_001598.
[0048] In another embodiment, the protein GNPI is involved in angiogenesis. GNPI converts glucosamine-6-phosphate to fructose-6-phosphate. GNPI is expressed in invasive ductal carcinoma, meningioma, melanoma, melanotic melanoma, moderately- differentiated adenocarcinoma, adult brain, hypernephroma, pheochromocytoma, and lung tumors. The accession number for the nucleic acid is NM_005471 and the accession number for the protein is NP__005462.
[0049] In another embodiment, the protein DHCR24 is involved in angiogenesis. DHCR24 catalyzes the reduction of the δ-24 double bond of sterol intermediates during . cholesterol biosynthesis. DHCR24 protects cells from oxidative stress by reducing caspase 3 activity during apoptosis induced by oxidative stress. DHCR24 also protects against amyloid-beta peptide-induced apoptosis. DHCR24 is highly expressed in brain and adrenal gland, with moderate expression in liver, lung, spleen, prostate and spinal cord, low expression in heart, uterus and prostate. The accession number for the nucleic acid is NM_014762 and the accession number for the polypeptide is NP_055577. [0050] In another embodiment, the protein SELT is involved in angiogenesis. SELT plays a role in selenocysteine incorporation and is associated with endothelial cells, probably through heparin-binding properties. SELT prevents the damage of vascular endothelium caused by reactive oxygen species. SELT is expressed in melanotic melanoma, acute myelogenous leukemia, embryonal carcinoma, hypemephroma, and chronic myelogenous leukemia. The accession number for the nucleic acid is BC026350 and the accession number for the protein is AAH26350.
[0051] In another embodiment, the protein PTPRB is involved in angiogenesis. PTPRB is a signaling molecule that regulates a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. PTPRB is specifically expressed in vascular Ecs throughout mouse development. PTPRB binds to VE-cadherin in COS cells, dephosphorylates VEGFR2 phosphorylated VE-cadherin, co- immunoprecipitates with Tiell and dephosphorylates Tiell. The accession number for the nucleic acid is NM_002837 and the accession number for the protein is NP_002828.
[0052] In another embodiment, the protein GB A is involved in angiogenesis. GBA is a j8-glucocerebrosidase (glucosylceramidase, jS-D-glucosyl-N-acylsphingosine glucohydrolase) that degrades sphingolipid glucocerebrosides. Defects in GBA are the cause of gaucher disease (gd), the most prevalent lysosomal storage disease. In vitro β- glucocerebrosidase assays with GBA can be used to assay for GBA modulators and thus for modulators of angiogenesis. The accession number for the nucleic acid is NM_000157 and the accession number for the polypeptide is NP_000148.
[0053] In another embodiment, the protein UAP1 is involved in angiogenesis. UAP1 is expressed in skin, carcinoma cell, normal gingival, colonic mucosa, normal endometrium, and Ewing's sarcoma. The accession number for the nucleic acid is NM_003115 and the accession number for the polypeptide is NP_003106.
[0054] hi another embodiment, the protein MRPL30 is involved in angiogenesis. MRPL30 catalyzes the transfer ofthe lipoyl group from lipoyl-AMP to the specific lysine residue ofthe lipoate-dependent enzymes. The accession number for the nucleic acid is NM_145212 and the accession number for the polypeptide is NP_660213. [0055] In another embodiment, the protein CCT3 is involved in angiogenesis. CCT3 is a molecular chaperone that assists protein folding upon ATP hydrolysis. CCT3 is known to play a role, in vitro, in the folding of actin and tubulin. CCT3 plays a role in the assembly ofthe Von Hippel-Lindau ubiquitylation complex. The accession number for the nucleic acid is AL833197 and the accession number for the polypeptide is NP_005989.
[0056] In another embodiment, the protein HSPA8 is involved in angiogenesis. HSPA8 belongs to the heat shock protein 70 family. HSPA8 binds to nascent polypeptides to facilitate correct folding. HSPA8 also functions as an ATPase in the disassembly of clathrin-coated vesicles during transport of membrane components through the cell. The accession number for the nucleic acid is NM_006597 and the accession number for the polypeptide is NP_006588. [0057] In another embodiment, the protein SLC16A1 is involved in angiogenesis. SLC16A1 is a proton-linked monocarboxylate transporter. SLC16A1 catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate. Defects in SLC16A1 are the cause of symptomatic deficiency in lactate transport (SDLT), characterized by a subnormal erythrocyte lactate transport and signs of muscle injury during exercise and heat exposure. The accession number for the nucleic acid is NM_003051 and the accession number for the polypeptide is NP_003042.
[0058] In another embodiment, the protein SH2 of Abl is involved in angiogenesis. SH2 of Abl is a SH2 domain protein, similar to the tyrosine-protein kinase Abl. Arm and Abl proteins function cooperatively at adherens junctions in both the ens and epidermis. In vitro tyrosine kinase assays with SH2 of Abl can be used to assay for SH2 of Abl modulators and thus for modulators of angiogenesis. The accession number for the nucleic acid is AK074067 and the accession number for the protein is BAB84893.
II. Definitions
[0059] By "disorder associated with angiogenesis" or "disease associated with angiogenesis" herein is meant a disease state which is marked by either an excess or a deficit of vessel development. Angiogenesis disorders associated with increased angiogenesis include, but are not limited to, breast, lung, colon, ovarian, liver, stomach, bladder, thyroid, and prostate cancer, basal cell carcinoma, melanoma, lymphomas, leukemias, e.g., myeloid leukemia (AML, CML), endometriosis, diabetic retinopathy, glaucoma, glomeralonephritis, rheumatoid arthritis, and age related macular degeneration. Pathological states for which it may be desirable to increase angiogenesis include stroke, infertility, heart disease, e.g., restenosis, ulcers, and scleroderma. An increase in angiogenesis may also be desirable in transplantation or for artificial or in vitro growth of organs.
[0060] By "disorder associated with cellular proliferation or tumorigenesis" or "disease associated with cellular proliferation or tumorigenesis" herein is meant a disease state which is marked by either an excess or a deficit of cellular proliferation or apoptosis. Such disorders associated with increased cellular proliferation include, but are not limited to, cancer and non-cancerous pathological proliferation. [0061] The term "angiogenesis polypeptide" or a nucleic acid encoding an "angiogenesis polypeptide" refer to nucleic acid and polypeptide polymorphic variants, alleles, mutants, and interspecies homologs that: (1) have an amino acid sequence that has greater than about 60% amino acid sequence identity, 65%, 70%, 75%, 80%, 85%, 90%, preferably 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% or greater amino acid sequence identity, preferably over a region of over a region of at least about 25, 50, 100, 200, 500, 1000, or more amino acids, to a polypeptide encoded by a referenced nucleic acid or an amino acid sequence described herein; (2) specifically bind to antibodies, e.g., polyclonal antibodies, raised against an immunogen comprising a referenced amino acid sequence, immunogenic fragments thereof, and conservatively modified variants thereof;
(3) specifically hybridize under stringent hybridization conditions to a nucleic acid encoding a referenced amino acid sequence, and conservatively modified variants thereof;
(4) have a nucleic acid sequence that has greater than about 95%, preferably greater than about 96%, 97%, 98%, 99%, or higher nucleotide sequence identity, preferably over a region of at least about 25, 50, 100, 200, 500, 1000, or more nucleotides, to a reference nucleic acid sequence. A polynucleotide or polypeptide sequence is typically from a mammal including, but not limited to, primate, e.g., human; rodent, e.g., rat, mouse, hamster; cow, pig, horse, sheep, or any mammal. The nucleic acids and proteins ofthe invention include both naturally occurring or recombinant molecules. [0062] The phrase "functional effects" in the context of assays for testing compounds that modulate activity of an angiogenesis protein includes the determination of a parameter that is indirectly or directly under the influence of an angiogenesis polypeptide, e.g., a chemical or phenotypic effect such as loss-of angiogenesis phenotype represented by a change in expression of a cell surface marker ov 33 integrin, changes in cellular migration, e.g., haptotaxis, changes in endothelial tube formation, changes in VEGF receptor internalization, and changes in tumor growth; or enzymatic activity; or, e.g., a physical effect such as ligand binding or inhibition of ligand binding. A functional effect therefore includes ligand binding activity, the ability of cells to proliferate, expression in cells undergoing angiogenesis, and other characteristics of angiogenic cells. "Functional effects" include in vitro, in vivo, and ex vivo activities. \
[0063] By "determining the functional effect" is meant assaying for a compound that increases or decreases a parameter that is indirectly or directly under the influence of an angiogenesis protein, e.g., measuring physical and chemical or phenotypic effects. Such functional effects can be measured by any means known to those skilled in the art, e.g., changes in spectroscopic characteristics (e.g., fluorescence, absorbance, refractive index); hydrodynamic (e.g., shape), chromatographic; or solubility properties for the protein; ligand binding assays, e.g., binding to antibodies; measuring inducible markers or transcriptional activation ofthe angiogenesis protein; measuring changes in enzymatic activity; the ability to increase or decrease cellular proliferation, apoptosis, cell cycle arrest, measuring changes in cell surface markers, e.g., ovjS3 integrin. Determination of the functional effect of a compound on angiogenesis can also be performed using assays known to those of skill in the art such as endothelial cell tube formation assays; haptotaxis assays; the chide CAM assay; the mouse comeal assay; VEGF receptor assays, co-culture tube formation assays, and assays that assess vascularization of an implanted tumor. Tumorigenesis can be measured using in vivo mouse models such as a xenograft model. The functional effects can be evaluated by many means known to those skilled in the art, e.g., microscopy for quantitative or qualitative measures of alterations in morphological features, e.g., tube or blood vessel formation, measurement of changes in RNA or protein levels for angiogenesis-associated sequences, measurement of RNA stability, identification of downstream or reporter gene expression (CAT, luciferase, β- gal, GFP and the like), e.g., via chemiluminescence, fluorescence, colorimetric reactions, antibody binding, inducible markers, etc.
[0064] "Inhibitors," "activators," and "modulators" of angiogenesis polynucleotide and polypeptide sequences are used to refer to activating, inhibitory, or modulating molecules identified using in vitro and in vivo assays of angiogenesis polynucleotide and polypeptide sequences. Inhibitors are compounds that, e.g., bind to, partially or totally block activity, decrease, prevent, delay activation, inactivate, desensitize, or down regulate the activity or expression of angiogenesis proteins, e.g., antagonists. "Activators" are compounds that increase, open, activate, facilitate, enhance activation, sensitize, agonize, or up regulate angiogenesis protein activity, agonists. Inhibitors, activators, or modulators also include genetically modified versions of angiogenesis proteins, e.g., versions with altered activity, as well as naturally occurring and synthetic ligands, antagonists, agonists, antibodies, peptides, cyclic peptides, nucleic acids, antisense molecules, ribozymes, RNAi molecules, small organic molecules and the like. Such assays for inhibitors and activators include, e.g., expressing angiogenesis protein in vitro, in cells, or cell extracts, applying putative modulator compounds, and then determining the functional effects on activity, as described above. [0065] Samples or assays comprising angiogenesis proteins that are treated with a potential activator, inhibitor, or modulator are compared to control samples without the inhibitor, activator, or modulator to examine the extent of inhibition. Control samples (untreated with inhibitors) are assigned a relative protein activity value of 100%. Inhibition of an angiogenesis protein is achieved when the activity value relative to the control is about 80%, preferably 50%, more preferably 25-0%. Activation of an angiogenesis protein is achieved when the activity value relative to the control (untreated with activators) is 110%, more preferably 150%, more preferably 200-500% (i.e., two to five fold higher relative to the control), more preferably 1000-3000% higher.
[0066] The term "test compound" or "drug candidate" or "modulator" or grammatical equivalents as used herein describes any molecule, either naturally occurring or synthetic, e.g., protein, oligopeptide (e.g., from about 5 to about 25 amino acids in length, preferably from about 10 to 20 or 12 to 18 amino acids in length, preferably 12, 15, or 18 amino acids in length), small organic molecule, polysaccharide, peptide, circular peptide, lipid, fatty acid, siRNA, polynucleotide, oligonucleotide, etc., to be tested for the capacity to directly or indirectly modulate angiogenesis. The test compound can be in the form of a library of test compounds, such as a combinatorial or randomized library that provides a sufficient range of diversity. Test compounds are optionally linked to a fusion partner, e.g., targeting compounds, rescue compounds, dimerization compounds, stabilizing compounds, addressable compounds, and other functional moieties. Conventionally, new chemical entities with useful properties are generated by identifying a test compound (called a "lead compound") with some desirable property or activity, e.g., inhibiting activity, creating variants ofthe lead compound, and evaluating the property and activity of those variant compounds. Often, high throughput screening (HTS) methods are employed for such an analysis. [0067] A "small organic molecule" refers to an organic molecule, either naturally occurring or synthetic, that has a molecular weight of more than about 50 daltons and less than about 2500 daltons, preferably less than about 2000 daltons, preferably between about 100 to about 1000 daltons, more preferably between about 200 to about 500 daltons. [0068] "RNAi molecule" or an "siRNA" refers to a nucleic acid that forms a double stranded RNA, which double stranded RNA has the ability to reduce or inhibit expression of a gene or target gene when the siRNA expressed in the same cell as the gene or target gene. "siRNA" thus refers to the double stranded RNA formed by the complementary strands. The complementary portions ofthe siRNA that hybridize to form the double stranded molecule typically have substantial or complete identity. In one embodiment, an siRNA refers to a nucleic acid that has substantial or complete identity to a target gene and forms a double stranded siRNA. The sequence ofthe siRNA can correspond to the full length target gene, or a subsequence thereof. Typically, the siRNA is at least about 15-50 nucleotides in length (e.g., each complementary sequence ofthe double stranded siRNA is 15-50 nucleotides in length, and the double stranded siRNA is about 15-50 base pairs in length, preferable about preferably about 20-30 base nucleotides, preferably about 20-25 nucleotides in length, e.g., 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleotides in length.
[0069] "Biological sample" include sections of tissues such as biopsy and autopsy samples, and frozen sections taken for histologic purposes. Such samples include blood, sputum, tissue, cultured cells, e.g., primary cultures, explants, and transformed cells, stool, urine, etc. A biological sample is typically obtained from a eukaryotic organism, most preferably a mammal such as a primate, e.g., chimpanzee or human; cow; dog; cat; a rodent, e.g., guinea pig, rat, mouse; rabbit; or a bird; reptile; or fish.
[0070] The terms "identical" or percent "identity," in the context of two or more nucleic acids or polypeptide sequences, refer to two or more sequences or subsequences that are the same or have a specified percentage of amino acid residues or nucleotides that are the same (i.e., about 70% identity, preferably 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or higher identity over a specified region (e.g., SEQ ID NO:l or 2), when compared and aligned for maximum correspondence over a comparison window or designated region) as measured using a BLAST or BLAST 2.0 sequence comparison algorithms with default parameters described below, or by manual alignment and visual inspection (see, e.g., NCBI web site or the like). Such sequences are then said to be "substantially identical." This definition also refers to, or may be applied to, the compliment of a test sequence. The definition also includes sequences that have deletions and/or additions, as well as those that have substitutions. As described below, the preferred algorithms can account for gaps and the like. Preferably, identity exists over a region that is at least about 25 amino acids or nucleotides in length, or more preferably over a region that is 50-100 amino acids or nucleotides in length. [0071] For sequence comparison, typically one sequence acts as a reference sequence, to which test sequences are compared. When using a sequence comparison algorithm, test and reference sequences are entered into a computer, subsequence coordinates are designated, if necessary, and sequence algorithm program parameters are designated. Preferably, default program parameters can be used, or alternative parameters can be designated. The sequence comparison algorithm then calculates the percent sequence identities for the test sequences relative to the reference sequence, based on the program parameters.
[0072] A "comparison window", as used herein, includes reference to a segment of any one ofthe number of contiguous positions selected from the group consisting of from 20 to 600, usually about 50 to about 200, more usually about 100 to about 150 in which a sequence may be compared to a reference sequence ofthe same number of contiguous positions after the two sequences are optimally aligned. Methods of alignment of sequences for comparison are well-known in the art. Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman & Wunsch, J Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat 7. Acad. Sci. USA 85:2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, WI), or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology (Ausubel et al., eds. 1995 supplement)).
[0073] A preferred example of algorithm that is suitable for determining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al, Nuc. Acids Res. 25:3389-3402 (1977) and Altschul et al, J. Mol. Biol. 215:403-410 (1990), respectively. BLAST and BLAST 2.0 are used, with the parameters described herein, to determine percent sequence identity for the nucleic acids and proteins ofthe invention. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information. This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length W in the query sequence, which either match or satisfy some positive-valued threshold score T when aligned with a word ofthe same length in a database sequence. T is referred to as the neighborhood word score threshold (Altschul et ah, supra). These initial neighborhood word hits act as seeds for initiating searches to find longer HSPs containing them. The word hits are extended in both directions along each sequence for as far as the cumulative alignment score can be increased. Cumulative scores are calculated using, for nucleotide sequences, the parameters M (reward score for a pair of matching residues; always > 0) and N (penalty score for mismatching residues; always < 0). For amino acid sequences, a scoring matrix is used to calculate the cumulative score. Extension ofthe word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T, and X determine the sensitivity and speed ofthe alignment. The BLASTN program (for nucleotide sequences) uses as defaults a wordlength (W) of 11, an expectation (E) of 10, M=5, N=-4 and a comparison of both strands. For amino acid sequences, the BLASTP program uses as defaults a wordlength of 3, and expectation (E) of 10, and the BLOSUM62 scoring matrix (see Henikoff & Henikoff, Proc. Natl. Acad. Sci. USA 89:10915 (1989)) alignments (B) of 50, expectation (E) of 10, M=5, N=-4, and a comparison of both strands.
[0074] "Nucleic acid" refers to deoxyribonucleotides or ribonucleotides and polymers thereof in single- or double-stranded form. The term encompasses nucleic acids containing known nucleotide analogs or modified backbone residues or linkages, which are synthetic, naturally occurring, and non-naturally occurring, which have similar binding properties as the reference nucleic acid, and which are metabolized in a manner similar to the reference nucleotides. Examples of such analogs include, without limitation, phosphorothioates, phosphoramidates, methyl phosphonates, chiral-methyl phosphonates, 2-O-methyl ribonucleotides, peptide-nucleic acids (PNAs). [0075] Unless otherwise indicated, a particular nucleic acid sequence also implicitly encompasses conservatively modified variants thereof (e.g., degenerate codon substitutions) and complementary sequences, as well as the sequence explicitly indicated. Specifically, degenerate codon substitutions may be achieved by generating sequences in which the third position of one or more selected (or all) codons is substituted with mixed- base and/or deoxyinosine residues (Batzer et al., Nucleic Acid Res. 19:5081 (1991); Ohtsuka et al, J. Biol. Chem. 260:2605-2608 (1985); Rossolini et ah, Mol. Cell. Probes 8:91-98 (1994)). The term nucleic acid is used interchangeably with gene, cDNA, mRNA, oligonucleotide, and polynucleotide.
[0076] A particular nucleic acid sequence also implicitly encompasses "splice variants." Similarly, a particular protein encoded by a nucleic acid implicitly encompasses any protein encoded by a splice variant of that nucleic acid. "Splice variants," as the name suggests, are products of alternative splicing of a gene. After transcription, an initial nucleic acid transcript may be spliced such that different (alternate) nucleic acid splice products encode different polypeptides. Mechanisms for the production of splice variants vary, but include alternate splicing of exons. Alternate polypeptides derived from the same nucleic acid by read-through transcription are also encompassed by this definition. Any products of a splicing reaction, including recombinant forms ofthe splice products, are included in this definition.
[0077] The terms "polypeptide," "peptide" and "protein" are used interchangeably herein to refer to a polymer of amino acid residues. The terms apply to amino acid polymers in which one or more amino acid residue is an artificial chemical mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers and non-naturally occurring amino acid polymer.
[0078] The term "amino acid" refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function in a manner similar to the naturally occurring amino acids. Naturally occurring amino acids are those encoded by the genetic code, as well as those amino acids that are later modified, e.g., hydroxyproline, γ-carboxyglutamate, and O-phosphoserine. Amino acid analogs refers to compounds that have the same basic chemical structure as a naturally occurring amino acid, i.e., an carbon that is bound to a hydrogen, a carboxyl group, an amino group, and an R group, e.g., homoserine, norleucine, methionine sulfoxide, methionine methyl sulfonium. Such analogs have modified R groups (e.g., norleucine) or modified peptide backbones, but retain the same basic chemical structure as a naturally occurring amino acid. Amino acid mimetics refers to chemical compounds that have a structure that is different from the general chemical structure of an amino acid, but that functions in a manner similar to a naturally occurring amino acid. [0079] Amino acids may be referred to herein by either their commonly known three letter symbols or by the one-letter symbols recommended by the IUPAC-IUB Biochemical Nomenclature Commission. Nucleotides, likewise, may be referred to by their commonly accepted single-letter codes. [0080] "Conservatively modified variants" applies to both amino acid and nucleic acid sequences. With respect to particular nucleic acid sequences, conservatively modified variants refers to those nucleic acids which encode identical or essentially identical amino acid sequences, or where the nucleic acid does not encode an amino acid sequence, to essentially identical sequences. Because ofthe degeneracy ofthe genetic code, a large number of functionally identical nucleic acids encode any given protein. For instance, the codons GCA, GCC, GCG and GCU all encode the amino acid alanine. Thus, at every position where an alanine is specified by a codon, the codon can be altered to any ofthe corresponding codons described without altering the encoded polypeptide. Such nucleic acid variations are "silent variations," which are one species of conservatively modified variations. Every nucleic acid sequence herein which encodes a polypeptide also describes every possible silent variation ofthe nucleic acid. One of skill will recognize that each codon in a nucleic acid (except AUG, which is ordinarily the only codon for metMonine, and TGG, which is ordinarily the only codon for tryptophan) can be modified to yield a functionally identical molecule. Accordingly, each silent variation of a nucleic acid which encodes a polypeptide is implicit in each described sequence with respect to the expression product, but not with respect to actual probe sequences. [0081] As to amino acid sequences, one of skill will recognize that individual substitutions, deletions or additions to a nucleic acid, peptide, polypeptide, or protein sequence which alters, adds or deletes a single amino acid or a small percentage of amino acids in the encoded sequence is a "conservatively modified variant" where the alteration results in the substitution of an amino acid with a chemically similar amino acid. Conservative substitution tables providing functionally similar amino acids are well known in the art. Such conservatively modified variants are in addition to and do not exclude polymorphic variants, interspecies homologs, and alleles ofthe invention.
[0082] The following eight groups each contain amino acids that are conservative substitutions for one another: 1) Alanine (A), Glycine (G); 2) Aspartic acid (D), Glutamic acid (E); 3) Asparagine (N), Glutamine (Q); 4) Arginine (R), Lysine (K); 5) Isoleucine (I), Leucine (L), Methionine (M), Valine (V); 6) Phenylalanine (F), Tyrosine (Y), Tryptophan (W); 7) Serine (S), Threonine (T); and 8) Cysteine (C), Methionine (M) (see, e.g., Creighton, Proteins (1984)).
[0083] Macromolecular structures such as polypeptide structures can be described in terms of various levels of organization. For a general discussion of this organization, see, e.g., Alberts et al., Molecular Biology ofthe Cell (3rd ed., 1994) and Cantor and Schimmel, Biophysical Chemistry Part I: The Conformation of Biological Macromolecules (1980). 'Trimary structure" refers to the amino acid sequence of a particular peptide. "Secondary structure" refers to locally ordered, three dimensional structures within a polypeptide. These structures are commonly known as domains, e.g., transmembrane domains, pore domains, and cytoplasmic tail domains. Domains are portions of a polypeptide that form a compact unit ofthe polypeptide and are typically 15 to 350 amino acids long. Exemplary domains include domains with enzymatic activity, e.g., ligand binding domains, etc. Typical domains are made up of sections of lesser organization such as stretches of /3-sheet and α-helices. "Tertiary structure" refers to the complete three dimensional structure of a polypeptide monomer. "Quaternary structure" refers to the three dimensional structure formed by the noncovalent association of independent tertiary units. Anisotropic terms are also known as energy terms.
[0084] A "label" or a "detectable moiety" is a composition detectable by spectroscopic, photochemical, biochemical, immunochemical, chemical, or other physical means. For example, useful labels include 32P, fluorescent dyes, electron-dense reagents, enzymes (e.g., as commonly used in an ELISA), biotin, digoxigenin, or haptens and proteins which can be made detectable, e.g., by incorporating a radiolabel into the peptide or used to detect antibodies specifically reactive with the peptide.
[0085] The term "recombinant" when used with reference, e.g., to a cell, or nucleic acid, protein, or vector, indicates that the cell, nucleic acid, protein or vector, has been modified by the introduction of a heterologous nucleic acid or protein or the alteration of a native nucleic acid or protein, or that the cell is derived from a cell so modified. Thus, for example, recombinant cells express genes that are not found within the native (non- recombinant) form ofthe cell or express native genes that are otherwise abnormally expressed, under expressed or not expressed at all. ;
[0086] The term "heterologous" when used with reference to portions of a nucleic acid indicates that the nucleic acid comprises two or more subsequences that are not found in the same relationship to each other in nature. For instance, the nucleic acid is typically recombinantly produced, having two or more sequences from unrelated genes arranged to make a new functional nucleic acid, e.g., a promoter from one source and a coding region from another source. Similarly, a heterologous protein indicates that the protein ( comprises two or more subsequences that are not found in the same relationship to each other in nature (e.g., a fusion protein).
[0087] The phrase "stringent hybridization conditions" refers to conditions under which a probe will hybridize to its target subsequence, typically in a complex mixture of nucleic acids, but to no other sequences. Stringent conditions are sequence-dependent and will be different in different circumstances. Longer sequences hybridize specifically at higher temperatures. An extensive guide to the hybridization of nucleic acids is found in Tijssen, Techniques in Biochemistry and Molecular Biology—Hybridization with Nucleic Probes, "Overview of principles of hybridization and the strategy of nucleic acid assays" (1993). Generally, stringent conditions are selected to be about 5-10°C lower than the thermal melting point (Tm) for the specific sequence at a defined ionic strength pH. The Tm is the temperature (under defined ionic strength, pH, and nucleic concentration) at which 50% ofthe probes complementary to the target hybridize to the target sequence at equilibrium (as the target sequences are present in excess, at Tm, 50% ofthe probes are occupied at equilibrium). Stringent conditions may also be achieved with the addition of destabilizing agents such as formamide. For selective or specific hybridization, a positive signal is at least two times background, preferably 10 times background hybridization. Exemplary stringent hybridization conditions can be as following: 50% formamide, 5x SSC, and 1% SDS, incubating at 42°C, or, 5x SSC, 1% SDS, incubating at 65°C, with wash in 0.2x SSC, and 0.1% SDS at 65°C. [0088] Nucleic acids that do not hybridize to each other under stringent conditions are still substantially identical if the polypeptides which they encode are substantially identical. This occurs, for example, when a copy of a nucleic acid is created using the maximum codon degeneracy permitted by the genetic code. In such cases, the nucleic acids typically hybridize under moderately stringent hybridization conditions. Exemplary "moderately stringent hybridization conditions" include a hybridization in a buffer of 40% formamide, 1 M NaCI, 1% SDS at 37°C, and a wash in IX SSC at 45°C. A positive hybridization is at least twice background. Those of ordinary skill will readily recognize that alternative hybridization and wash conditions can be utilized to provide conditions of similar stringency. Additional guidelines for determining hybridization parameters are provided in numerous reference, e.g., and Current Protocols in Molecular Biology, ed. Ausubel, et al.
[0089] For PCR, a temperature of about 36°C is typical for low stringency amplification, although annealing temperatures may vary between about 32°C and 48°C depending on primer length. For high stringency PCR amplification, a temperature of about 62°C is typical, although high stringency annealing temperatures can range from about 50°C to about 65°C, depending on the primer length and specificity. Typical cycle conditions for both high and low stringency amplifications include a denaturation phase of 90°C - 95°C for 30 sec - 2 min., an annealing phase lasting 30 sec. - 2 min., and an extension phase of about 72°C for 1 - 2 min. Protocols and guidelines for low and high stringency amplification reactions are provided, e.g., in Innis et al (1990) PCR Protocols, A Guide to Methods and Applications, Academic Press, Inc. N.Y.).
[0090] "Antibody" refers to a polypeptide comprising a framework region from an immunoglobulin gene or fragments thereof that specifically binds and recognizes an antigen. The recognized immunoglobulin genes include the kappa, lambda, alpha, gamma, delta, epsilon, and mu constant region genes, as well as the myriad immunoglobulin variable region genes. Light chains are classified as either kappa or lambda. Heavy chains are classified as gamma, mu, alpha, delta, or epsilon, which in turn define the immunoglobulin classes, IgG, IgM, IgA, IgD and IgE, respectively. Typically, the antigen-binding region of an antibody will be most critical in specificity and affinity of binding.
[0091] An exemplary immunoglobulin (antibody) structural unit comprises a tetramer. Each tetramer is composed of two identical pairs of polypeptide chains, each pair having one "light" (about 25 kD) and one "heavy" chain (about 50-70 kD). The N-terminus of each chain defines a variable region of about 100 to 110 or more amino acids primarily responsible for antigen recognition. The terms variable light chain (VL) and variable heavy chain (VH) refer to these light and heavy chains respectively. [0092] Antibodies exist, e.g., as intact immunoglobulins or as a number of well- characterized fragments produced by digestion with various peptidases. Thus, for example, pepsin digests an antibody below the disulfide linkages in the hinge region to produce F(ab)'2j a dimer of Fab which itself is a light chain joined to VH-CH1 by a disulfide bond. The F(ab)'2 may be reduced under mild conditions to break the disulfide linkage in the hinge region, thereby converting the F(ab)'2 dimer into an Fab' monomer. The Fab' monomer is essentially Fab with part ofthe hinge region (see Fundamental Immunology (Paul ed., 3d ed. 1993). While various antibody fragments are defined in terms ofthe digestion of an intact antibody, one of skill will appreciate that such fragments may be synthesized de novo either chemically or by using recombinant DNA methodology. Thus, the term antibody, as used herein, also includes antibody fragments either produced by the modification of whole antibodies, or those synthesized de novo using recombinant DNA methodologies (e.g., single chain Fv) or those identified using phage display libraries (see, e.g., McCafferty et al, Nature 348:552-554 (1990))
[0093] For preparation of antibodies, e.g., recombinant, monoclonal, or polyclonal antibodies, many technique known in the art can be used (see, e.g. , Kohler & Milstein, Nature 256:495-497 (1975); Kozbor et al, Immunology Today 4: 72 (1983); Cole et al, pp. 77-96 in Monoclonal Antibodies and Cancer Therapy, Alan R. Liss, Inc. (1985); Coligan, Current Protocols in Immunology (1991); Harlow & Lane, Antibodies, A Laboratory Manual (1988); and Goding, Monoclonal Antibodies: Principles and Practice (2d ed. 1986)). The genes encoding the heavy and hght chains of an antibody of interest can be cloned from a cell, e.g., the genes encoding a monoclonal antibody can be cloned from a hybridoma and used to produce a recombinant monoclonal antibody. Gene libraries encoding heavy and light chains of monoclonal antibodies can also be made from hybridoma or plasma cells. Random combinations ofthe heavy and light chain gene products generate a large pool of antibodies with different antigenic specificity (see, e.g., Kuby, Immunology (3rd ed. 1997)). Techniques for the production of single chain antibodies or recombinant antibodies (U.S. Patent 4,946,778, U.S. Patent No. 4,816,567) can be adapted to produce antibodies to polypeptides of this invention. Also, transgenic mice, or other organisms such as other mammals, may be used to express humanized or human antibodies (see, e.g., U.S. Patent Nos. 5,545,807; 5,545,806; 5,569,825; 5,625,126; 5,633,425; 5,661,016, Marks etal, Bio/Technology 10:779-783 (1992); Lonberg et al, Nature 368:856-859 (1994); Morrison, Nature 368:812-13 (1994); Fishwild et al, Nature Biotechnology 14:845-51 (1996); Neuberger, Nature Biotechnology 14:826 (1996); and Lonberg & Huszar, Intern. Rev. Immunol 13:65-93 (1995)). Alternatively, phage display technology can be used to identify antibodies and heteromeric Fab fragments that specifically bind to selected antigens (see, e.g., McCafferty et al, Nature 348:552-554 (1990); Marks et al, Biotechnology 10:779-783 (1992)). Antibodies can also be made bispecific, i.e., able to recognize two different antigens (see, e.g., WO 93/08829, Traunecker et al, EMBOJ. 10:3655-3659 (1991); and Suresh et al, Methods in Enzymology 121:210 (1986)). Antibodies can also be heteroconjugates, e.g., two covalently joined antibodies, or immunotoxins (see, e.g., U.S. Patent No. 4,676,980 , WO 91/00360; WO 92/200373; and EP 03089).
[0094] Methods for humanizing or primatizing non-human antibodies are well known in the art. Generally, a humanized antibody has one or more amino acid residues introduced into it from a source which is non-human. These non-human amino acid residues are often referred to as import residues, which are typically taken from an import variable domain. Humanization can be essentially performed following the method of Winter and co-workers (see, e.g., Jones et al, Nature 321:522-525 (1986); Riechmann et al., Nature 332:323-327 (1988); Verhoeyen et al, Science 239:1534-1536 (1988) and Presta, Curr. Op. Struct. Biol 2:593-596 (1992)), by substituting rodent CDRs or CDR sequences for the corresponding sequences of a human antibody. Accordingly, such humanized antibodies are chimeric antibodies (U.S. Patent No. 4,816,567), wherein substantially less than an intact human variable domain has been substituted by the corresponding sequence from a non-human species. In practice, humanized antibodies are typically human antibodies in which some CDR residues and possibly some FR residues are substituted by residues from analogous sites in rodent antibodies.
[0095] A "chimeric antibody" is an antibody molecule in which (a) the constant region, or a portion thereof, is altered, replaced or exchanged so that the antigen binding site (variable region) is linked to a constant region of a different or altered class, effector function and/or species, or an entirely different molecule which confers new properties to the chimeric antibody, e.g., an enzyme, toxin, hormone, growth factor, drug, etc.; or (b) the variable region, or a portion thereof, is altered, replaced or exchanged with a variable region having a different or altered antigen specificity. [0096] In one embodiment, the antibody is conjugated to an "effector" moiety. The effector moiety can be any number of molecules, including labeling moieties such as radioactive labels or fluorescent labels, or can be a therapeutic moiety. In one aspect the antibody modulates the activity ofthe protein. [0097] The phrase "specifically (or selectively) binds" to an antibody or "specifically (or selectively) immunoreactive with," when referring to a protein or peptide, refers to a binding reaction that is determinative ofthe presence ofthe protein, often in a heterogeneous population of proteins and other biologies. Thus, under designated immunoassay conditions, the specified antibodies bind to a particular protein at least two times the background and more typically more than 10 to 100 times background. Specific binding to an antibody under such conditions requires an antibody that is selected for its specificity for a particular protein. For example, polyclonal antibodies, polymorphic variants, alleles, orthologs, and conservatively modified variants, or splice variants, or portions thereof, can be selected to obtain only those polyclonal antibodies that are specifically immunoreactive with angiogenesis proteins and not with other proteins. This selection may be achieved by subtracting out antibodies that cross-react with other molecules. A variety of immunoassay formats may be used to select antibodies specifically immunoreactive with a particular protein. For example, solid-phase ELISA immunoassays are routinely used to select antibodies specifically immunoreactive with a protein (see, e.g., Harlow & Lane, Antibodies, A Laboratory Manual (1988) for a description of immunoassay formats and conditions that can be used to determine specific immunoreacti vity) . III. Assays for proteins that modulate angiogenesis
[0098] High throughput functional genomics assays can be used to identify modulators of angiogenesis. Such assays can monitor changes in cell surface marker expression, αv/33 integrin production, proliferation, and differentiation using either cell lines or primary cells. Typically, early passage or primary endothelial cells are contacted with a cDNA or a random peptide library (encoded by nucleic acids). The cDNA library can comprise sense, antisense, full length, and truncated cDNAs. The peptide library is encoded by nucleic acids. The effect ofthe cDNA or peptide library on the endothelial cells is then monitored, using an assay such as cell surface marker expression (e.g., ov/33 integrin) or a phenotypic assay for angiogenesis such as migration towards an ECM (extracellular matrix) component (see, e.g., Klemke et al, J. Cell Biol. 4:961-972 (1998)) or endothelial cell tube formation assays, as well as other bioassays such as the chick CAM assay, the mouse corneal assay, haptotaxis assays, VEGF-R assays, co-culture tube formation assays, and assays measuring the effect of administering potential modulators on implanted tumors. The effect ofthe cDNA or peptide can be validated and distinguished from somatic mutations, using, e.g., regulatable expression ofthe nucleic acid such as expression from a tetracycline promoter. cDNAs and nucleic acids encoding peptides can be rescued using techniques known to those of skill in the art, e.g., using a sequence tags. In vivo assays for tumor growth, such as mouse xenograft models, can also be used.
[0099] Proteins interacting with the peptide or with the protein encoded by the cDNA can be isolated using a yeast two-hybrid system, mammalian two hybrid system, or phage display screen, etc. Targets so identified can be further used as bait in these assays to identify additional members ofthe angiogenesis pathway, which members are also targets for drug development (see, e.g., Fields et al, Nature 340:245 (1989); Vasavada et al, Proc. Nat'lAcad. Sci. USA 88:10686 (1991); Fearon t α/., Proc. Natl Acad. Sci. USA 89:7958 (1992); Dang et al, Mol. Cell Biol. 11:954 (1991); Chien et al, Proc. Nat 'I Acad. Sci. USA 9578 (1991); and U.S. Patent Nos. 5,283,173, 5,667,973, 5,468,614, 5,525,490, and 5,637,463).
[0100] Suitable endothelial cell lines include human umbilical vein cells (see, e.g., Jaffe et al, J. Clin. Invest. 52:2745-2754 (1973)); human adult dermal capillary-derived cells (see, e.g., Davison et al, In Vitro 19:937-945 (1983)); human adipose capillary derived cells (see, e.g., Kem et al, J. Clin Invest. 71:1822-1829 (1983); bovine aorta (see, e.g., Booyse et al, Thromb. Diathes. Ahemorrh. 34:825-839 (1975); and rat brain capillary derived cells (see, e.g., Bowman et al, In Vitro 17:353-362 (1981)). For culture of endothelial cell lines, explants, and primary cells, see Freshney et al, Culture of Animal Cells (3rd ed. 1994). Suitable angiogenesis cell surface markers include alphavbeta3 integrin (see, e.g., Elicerir & Cheresh, Cancer J. Sci. Am. 6 Supp. 3:S245-249 (2000), Maeshima et al, J Biol. Chem. (June 8, 2001)). [0101] Cell surface markers such as αv/33 can be assayed using fluorescently labeled antibodies and FACS. Cell proliferation can be measured using 3H-thymidine or dye inclusion. Angiogenesis phenotype is measured by loss of phenotype observation.
[0102] cDNA libraries are made from any suitable source, preferably from endothelial cells. Libraries encoding random peptides are made according to techniques well known to those of skill in the art (see, e.g., U.S. Patent No. 6,153,380, 6,114,111, and 6,180,343). Any suitable vector can be used for the cDNA and peptide libraries, mcluding, e.g., retroviral vectors.
[0103] In a preferred embodiment, target proteins that modulate angiogenesis are identified using a high throughput cell based assay (using a microtiter plate format) and FACS screening for avβ3 cell surface expression. cDNA libraries are made which include, e.g., sense, antisense, full length, and truncated cDNAs. The cDNAs are cloned into a retroviral vector. Endothelial cells are infected with the library, cultured for a short effector phase and then the cells with reduced ctvβ3 surface levels are enriched by antibody staining and magnetic cell sorting. The enriched cell population is then sorted into microtiter plates using fluorescent antibodies and FACS. Resultant cell colonies are analyzed by immunofluorescence for reduced αv/33 surface levels. Selected colonies are infected with wild type MMLV virus to rescue the proviral vector. The infectious supernatant is used to infect endothelial cells, which are subsequently analyzed for αvj83 levels by FACS. The cDNA is isolated and sequenced to determined if it represents a wild type or mutated cDNA, e.g., whether the cDNA represents a negative transdominant mutant. Optionally, a marker such as GFP can be used to select for retrovirally infected cells. Isolation of nucleic acids [0104] This invention relies on routine techniques in the field of recombinant genetics. Basic texts disclosing the general methods of use in this invention include Sambrook et al., Molecular Cloning, A Laboratory Manual (2nd ed. 1989); Kriegler, Gene Transfer and Expression: A Laboratory Manual (1990); and Current Protocols in Molecular Biology (Ausubel et al, eds., 1994)).
[0105] Nucleic acids, polymorphic variants, orthologs, and alleles can be isolated using nucleic acid probes and ohgonucleotides under stringent hybridization conditions, by screening libraries. Alternatively, expression libraries can be used to clone angiogenesis proteins, polymorphic variants, orthologs, and alleles by detecting expressed homologs immunologically with antisera or purified antibodies made against human angiogenesis proteins or portions thereof.
[0106] To make a cDNA library, one should choose a source that is rich in the desired RNA, e.g., endothelial cells. The mRNA is then made into cDNA using reverse transcriptase, ligated into a recombinant vector, and transfected into a recombinant host for propagation, screening and cloning. Methods for making and screening cDNA libraries are well known (see, e.g., Gubler & Hoffman, Gene 25:263-269 (1983); Sambrook et al, supra; Ausubel et al, supra).
[0107] For a genomic library, the DNA is extracted from the tissue and either mechanically sheared or enzymatically digested to yield fragments of about 12-20 kb. The fragments are then separated by gradient centrifugation from undesired sizes and are constructed in bacteriophage lambda vectors. These vectors and phage are packaged in vitro. Recombinant phage are analyzed by plaque hybridization as described in Benton & Davis, Science 196:180-182 (1977). Colony hybridization is carried out as generally described in Grunstein et al, Proc. Natl. Acad. Sci. USA., 72:3961-3965 (1975).
[0108] An alternative method of isolating nucleic acids and orthologs, alleles, mutants, polymorphic variants, and conservatively modified variants combines the use of synthetic oligonucleotide primers and amplification of an RNA or DNA template (see U.S. Patents 4,683,195 and 4,683,202; PCR Protocols: A Guide to Methods and Applications (Innis et al, eds, 1990)). Methods such as polymerase chain reaction (PCR) and ligase chain reaction (LCR) can be used to amplify nucleic acid sequences directly from mRNA, from cDNA, from genomic libraries or cDNA libraries. Degenerate ohgonucleotides can be designed to amplify homologs using the sequences provided herein. Restriction endonuclease sites can be incorporated into the primers. Polymerase chain reaction or other in vitro amplification methods may also be useful, for example, to clone nucleic acid sequences that code for proteins to be expressed, to make nucleic acids to use as probes for detecting the presence of angiogenesis protein encoding mRNA in physiological samples, for nucleic acid sequencing, or for other purposes. Genes amplified by the PCR reaction can be purified from agarose gels and cloned into an appropriate vector.
[0109] Gene expression can also be analyzed by techniques known in the art, e.g., reverse transcription and amplification of mRNA, isolation of total RNA or poly A+
RNA, northern blotting, dot blotting, in situ hybridization, RNase protection, high density polynucleotide array technology, e.g., and the like.
[0110] Nucleic acids can be used with high density oligonucleotide array technology (e.g., GeneChip™) to identify angiogenesis protein, orthologs, alleles, conservatively modified variants, and polymorphic variants in this invention. In the case where the homologs being identified are linked to a known disease state, they can be used with GeneChip™ as a diagnostic tool in detecting the disease in a biological sample, see, e.g., Gunthand et al, AIDS Res. Hum. Retroviruses 14: 869-876 (1998); Kozal et al, Nat. Med. 2:753-759 (1996); Matson et al, Anal Biochem. 224:110-106 (1995); Lockhart et al, Nat. Biotechnol. 14:1675-1680 (1996); Gingeras et al, Genome Res. 8:435-448 (1998); Hacia et al, Nucleic Acids Res. 26:3865-3866 (1998).
[0111] The gene is typically cloned into intermediate vectors before transformation into prokaryotic or eukaryotic cells for replication and/or expression. These intermediate vectors are typically prokaryote vectors, e.g., plasmids, or shuttle vectors.
Expression in prokaryotes and eukaryotes
[0112] To obtain high level expression of a cloned gene, such as those cDNAs encoding an angiogenesis protein, one typically subclones the desired nucleic acid into an expression vector that contains a strong promoter to direct transcription, a transcription/translation terminator, and if for a nucleic acid encoding a protein, a ribosome binding site for translational initiation. Suitable bacterial promoters are well known in the art and described, e.g., in Sambrook et al, and Ausubel et al, supra. Bacterial expression systems for expressing the protein are available in, e.g., E. coli, Bacillus sp., and Salmonella (Palva et al, Gene 22:229-235 (1983); Mosbach et al, Nature 302:543-545 (1983). Kits for such expression systems are commercially available. Eukaryotic expression systems for mammalian cells, yeast, and insect cells are well known in the art and are also commercially available. [0113] Selection of the promoter used to direct expression of a heterologous nucleic acid depends on the particular application. The promoter is preferably positioned about the same distance from the heterologous transcription start site as it is from the transcription start site in its natural setting. As is known in the art, however, some variation in this distance can be accommodated without loss of promoter function. [0114] In addition to the promoter, the expression vector typically contains a transcription unit or expression cassette that contains all the additional elements required for the expression ofthe nucleic acid in host cells. A typical expression cassette thus contains a promoter operably linked to the nucleic acid sequence and signals required for efficient polyadenylation ofthe transcript, ribosome binding sites, and translation termination. Additional elements ofthe cassette may include enhancers and, if genomic DNA is used as the structural gene, introns with functional splice donor and acceptor sites.
[0115] In addition to a promoter sequence, the expression cassette should also contain a transcription termination region downstream ofthe structural gene to provide for efficient termination. The termination region may be obtained from the same gene as the promoter sequence or may be obtained from different genes.
[0116] The particular expression vector used to transport the genetic information into the cell is not particularly critical. Any ofthe conventional vectors used for expression in eukaryotic or prokaryotic cells may be used. Standard bacterial expression vectors include plasmids such as pBR322 based plasmids, pSKF, pET23D, and fusion expression systems such as MBP, GST, and LacZ. Epitope tags can also be added to recombinant proteins to provide convenient methods of isolation, e.g., c-myc.
[0117] Expression vectors containing regulatory elements from eukaryotic viruses are typically used in eukaryotic expression vectors, e.g., S V40 vectors, papilloma virus vectors, retroviral vectors, and vectors derived from Epstein-Barr virus. Other exemplary eukaryotic vectors include pMSG, pAV009/A+, pMTO10/A+, pMAMneo-5, baculovirus pDSVE, and any other vector allowing expression of proteins under the direction ofthe CMV promoter, S V40 early promoter, S V40 later promoter, metallothionein promoter, murine mammary tumor virus promoter, Rous sarcoma virus promoter, polyhedrin promoter, or other promoters shown effective for expression in eukaryotic cells. [0118] Expression of proteins from eukaryotic vectors can be also be regulated using inducible promoters. With inducible promoters, expression levels are tied to the concentration of inducing agents, such as tetracycline or ecdysone, by the incorporation of response elements for these agents into the promoter. Generally, high level expression is obtained from inducible promoters only in the presence ofthe inducing agent; basal expression levels are minimal. Inducible expression vectors are often chosen if expression ofthe protein of interest is detrimental to eukaryotic cells. [0119] In one embodiment, the vectors ofthe invention have a regulatable promoter, e.g., tet-regulated systems and the RU-486 system (see, e.g., Gossen & Bujard, Proc. Nat'lAcad. Sci. USA 89:5547 (1992); Oligino et al, Gene Ther. 5:491-496 (1998); Wang et al, Gene Ther. 4:432-441 (1997); Neering et al, Blood 88:1147-1155 (1996); and Rendahl et al, Nat. Biotechnol. 16:757-761 (1998)). These impart small molecule control on the expression ofthe candidate target nucleic acids. This beneficial feature can be used to determine that a desired phenotype is caused by a transfected cDNA rather than a somatic mutation. [0120] Some expression systems have markers that provide gene amplification such as thymidine kinase and dihydrofolate reductase. Alternatively, high yield expression systems not involving gene amplification are also suitable, such as using a baculovirus vector in insect cells, with a protein encoding sequence under the direction ofthe polyhedrin promoter or other strong baculovirus promoters. [0121] The elements that are typically included in expression vectors also include a replicon that functions in E. coli, a gene encoding antibiotic resistance to permit selection of bacteria that harbor recombinant plasmids, and unique restriction sites in nonessential regions ofthe plasmid to allow insertion of eukaryotic sequences. The particular antibiotic resistance gene chosen is not critical, any ofthe many resistance genes known in the art are suitable. The prokaryotic sequences are preferably chosen such that they do not interfere with the replication ofthe DNA in eukaryotic cells, if necessary. [0122] Standard transfection methods are used to produce bacterial, mammalian, yeast or insect cell lines that express large quantities of protein, which are then purified using standard techniques (.see, e.g., Colley et al, J. Biol. Chem. 264:17619-17622 (1989); Guide to Protein Purification, in Methods in Enzymology, vol. 182 (Deutscher, ed., 1990)). Transformation of eukaryotic and prokaryotic cells are performed according to standard techniques (see, e.g., Morrison, J. Bad. 132:349-351 (1977); Clark-Curtiss & Curtiss, Methods in Enzymology 101:347-362 (Wu et al., eds, 1983).
[0123] Any of the well-known procedures for introducing foreign nucleotide sequences into host cells may be used. These include the use of calcium phosphate transfection, polybrene, protoplast fusion, electroporation, biolistics, liposomes, microinjection, plasma vectors, viral vectors and any ofthe other well known methods for introducing cloned genomic DNA, cDNA, synthetic DNA or other foreign genetic material into a host cell (see, e.g., Sambrook et al, supra). It is only necessary that the particular genetic engineering procedure used be capable of successfully introducing at least one gene into the host cell capable of expressing the protein of choice.
[0124] After the expression vector is introduced into the cells, the transfected cells are cultured under conditions favoring expression ofthe protein of choice, which is recovered from the culture using standard techniques identified below.
Purification of polypeptides
[0125] Either naturally occurring or recombinant protein can be purified for use in functional assays. Naturally occurring protein can be purified, e.g., from human tissue. Recombinant protein can be purified from any suitable expression system.
[0126] The protein may be purified to substantial purity by standard techniques, including selective precipitation with such substances as ammonium sulfate; column chromatography, irnmunopiirification methods, and others (see, e.g., Scopes, Protein Purification: Principles and Practice (1982); U.S. Patent No. 4,673,641; Ausubel et al, supra; and Sambrook et al, supra).
[0127] A number of procedures can be employed when recombinant protein is being purified. For example, proteins having established molecular adhesion properties can be reversible fused to the protein. With the appropriate ligand, angiogenesis protein can be selectively adsorbed to a purification column and then freed from the column in a relatively pure form. The fused protein is then removed by enzymatic activity. Finally, protein could be purified using immunoaffinity columns.
A. Purification of protein from recombinant bacteria [0128] Recombinant proteins are expressed by transformed bacteria in large amounts, typically after promoter induction; but expression can be constitutive. Promoter induction with IPTG is one example of an inducible promoter system. Bacteria are grown according to standard procedures in the art. Fresh or frozen bacteria cells are used for isolation of protein. [0129] Proteins expressed in bacteria may form insoluble aggregates ("inclusion bodies"). Several protocols are suitable for purification of protein inclusion bodies. For example, purification of inclusion bodies typically involves the extraction, separation and/or purification of inclusion bodies by disruption of bacterial cells, e.g., by incubation in a buffer of 50 mM TRIS/HCL pH 7.5, 50 mM NaCI, 5 mM MgCl2, 1 mM DTT, 0.1 mM ATP, and 1 mM PMSF. The cell suspension can be lysed using 2-3 passages through a French Press, homogenized using a Polytron (Brinkman Instruments) or sonicated on ice. Alternate methods of lysing bacteria are apparent to those of skill in the art (see, e.g., Sambrook et al, supra; Ausubel et al, supra).
[0130] If necessary, the inclusion bodies are solubilized, and the lysed cell suspension is typically centrifuged to remove unwanted insoluble matter. Proteins that formed the inclusion bodies may be renatured by dilution or dialysis with a compatible buffer. Suitable solvents include, but are not limited to urea (from about 4 M to about 8 M), formamide (at least about 80%, volume/volume basis), and guanidine hydrochloride (from about 4 M to about 8 M). Some solvents which are capable of solubilizing aggregate-forming proteins, for example SDS (sodium dodecyl sulfate), 70% formic acid, are inappropriate for use in this procedure due to the possibility of irreversible denaturation ofthe proteins, accompanied by a lack of immunogenicity and/or activity. Although guanidine hydrochloride and similar agents are denaturants, this denaturation is not irreversible and renaturation may occur upon removal (by dialysis, for example) or dilution ofthe denaturant, allowing re-formation of immunologically and/or biologically active protein. Other suitable buffers are known to those skilled in the art. Human proteins are separated from other bacterial proteins by standard separation techniques, e.g., with Ni-NTA agarose resin.
[0131] Alternatively, it is possible to purify protein from bacteria periplasm. After lysis ofthe bacteria, the periplasmic fraction ofthe bacteria can be isolated by cold osmotic shock in addition to other methods known to skill in the art. To isolate recombinant proteins from the periplasm, the bacterial cells are centrifuged to form a pellet. The pellet is resuspended in a buffer containing 20% sucrose. To lyse the cells, the bacteria are centrifuged and the pellet is resuspended in ice-cold 5 mM MgSO4 and kept in an ice bath for approximately 10 minutes. The cell suspension is centrifuged and the supernatant decanted and saved. The recombinant proteins present in the supernatant can be separated from the host proteins by standard separation techniques well known to those of skill in the art.
B. Standard protein separation techniques for purifying proteins Solubility fractionation
[0132] Often as an initial step, particularly if the protein mixture is complex, an initial salt fractionation can separate many ofthe unwanted host cell proteins (or proteins derived from the cell culture media) from the recombinant protein of interest. The preferred salt is ammonium sulfate. Ammonium sulfate precipitates proteins by effectively reducing the amount of water in the protein mixture. Proteins then precipitate on the basis of their solubility. The more hydrophobic a protein is, the more likely it is to precipitate at lower ammonium sulfate concentrations. A typical protocol includes adding saturated ammonium sulfate to a protein solution so that the resultant ammonium sulfate concentration is between 20-30%. This concentration will precipitate the most hydrophobic of proteins. The precipitate is then discarded (unless the protein of interest is hydrophobic) and ammonium sulfate is added to the supernatant to a concentration known to precipitate the protein of interest. The precipitate is then solubilized in buffer and the excess salt removed if necessary, either through dialysis or diafiltration. Other methods that rely on solubility of proteins, such as cold ethanol precipitation, are well known to those of skill in the art and can be used to fractionate complex protein mixtures. Size differential filtration [0133] The molecular weight of the protein can be used to isolate it from proteins of greater and lesser size using ultrafiltration through membranes of different pore size (for example, Amicon or Millipore membranes). As a first step, the protein mixture is ultrafiltered through a membrane with a pore size that has a lower molecular weight cutoff than the molecular weight ofthe protein of interest. The retentate ofthe ultrafiltration is then ultrafiltered against a membrane with a molecular cut off greater than the molecular weight ofthe protein of interest. The recombinant protein will pass through the membrane into the filtrate. The filtrate can then be chromatographed as described below.
Column chromatography [0134] The protein can also be separated from other proteins on the basis of its size, net surface charge, hydrophobicity, and affinity for ligands. In addition, antibodies raised against proteins can be conjugated to column matrices and the proteins immunopurifϊed. All of these methods are well known in the art. It will be apparent to one of skill that chromatographic techniques can be performed at any scale and using equipment from many different manufacturers (e.g., Pharmacia Biotech).
Assays for modulators of angiogenesis proteins A. Assays [0135] Modulation of an angiogenesis protein, and corresponding modulation of angiogenesis, can be assessed using a variety of in vitro and in vivo assays, including high throughput ligand binding and cell based assays, as described herein. Such assays can be used to test for inhibitors and activators ofthe angiogenesis protein, and, consequently, inhibitors and activators of angiogenesis. Such modulators ofthe angiogenesis protein are useful for treating angiogenesis disorders. Modulators ofthe angiogenesis protein are tested using either recombinant or naturally occumng protein, preferably human protein.
[0136] Measurement of an angiogenic or loss-of-angiogenesis phenotype on the protein or cell expressing the protein, either recombinant or naturally occurring, can be performed using a variety of assays, in vitro, in vivo, and ex vivo. For example, recombinant or naturally occurring protein can be used in vitro, in a ligand binding or enzymatic function assay. Protein present in a cellular extract can also be used in in vitro assays. Cell- and animal-based in vivo assays can also be used to assay for angiogenesis modulators. Any suitable physical, chemical, or phenotypic change that affects activity or binding can be used to assess the influence of a test compound on the polypeptide of this invention. When the functional effects are determined using intact cells or animals, one can also measure a variety of effects such as, in the case of angiogenesis associated with tumors, tumor growth, neovascularization, endothelial tube formation, cell surface markers such as αv/33, hormone release, transcriptional changes to both known and uncharacterized genetic markers (e.g., northern blots), changes in cell metabolism such as cell growth or pH changes, and changes in intracellular second messengers such as cGMP. In one embodiment, measurement of ov/33 integrin cell surface expression and FACS sorting is used to identify modulators of angiogenesis.
In vitro assays [0137] Assays to identify compounds with angiogenesis modulating activity, e.g., anti- angiogenic activity, can be performed in vitro, e.g., binding assays. Purified recombinant or naturally occurring protein can be used in the in vitro methods ofthe invention. In addition to purified protein, the recombinant or naturally occurring protein can be part of a cellular lysate. As described below, the assay can be either solid state or soluble. Preferably, the protein is bound to a solid support, either covalently or non-covalently. Often, the in vitro assays ofthe invention are ligand binding or ligand affinity assays, either non-competitive or competitive. Other in vitro assays include measuring changes in spectroscopic (e.g., fluorescence, absorbance, refractive index), hydrodynamic (e.g., shape), chromatographic, or solubility properties for the protein.
[0138] In one embodiment, a high throughput binding assay is performed in which the protein or chimera comprising a fragment thereof is contacted with a potential modulator and incubated for a suitable amount of time. In one embodiment, the potential modulator is bound to a solid support, and the protein is added. In another embodiment, the protein is bound to a solid support. A wide variety of modulators can be used, as described below, including small organic molecules, peptides, and antibodies. A wide variety of assays can be used to identify angiogenesis-modulator binding, including labeled protein- protein binding assays, electrophoretic mobility shifts, immunoassays, and the like. In some cases, the binding ofthe candidate modulator is determined through the use of competitive binding assays, where interference with binding of a known ligand is measured in the presence of a potential modulator. Often, either the potential modulator or the known ligand is labeled. Cell-based in vivo assays [0139] In another embodiment, the protein is expressed in a cell, and functional, e.g., physical and chemical or phenotypic, changes are assayed to identify angiogenesis modulators, preferably anti-angiogenesis compounds. Cells expressing angiogenesis proteins can also be used in binding assays or enzymatic assays. Any suitable functional effect can be measured, as described herein. For example, hgand binding, cell surface marker expression, cellular proliferation, VEGF-R assays, co-culture assays for tube formation, and cell migration assays are all suitable assays to identify potential modulators using a cell based system. Suitable cells for such cell based assays include both primary endothelial cells and cell lines, as described herein. The protein can be naturally occurring or recombinant.
[0140] As described above, in one embodiment, loss-of angiogenesis phenotype is measured by contacting endothelial cells comprising an angiogenesis target with a potential modulator. Modulation of angiogenesis is identified by screening for cell surface marker expression, e.g., αv/33 integrin expression levels, using fluorescent antibodies and FACS sorting.
[0141] In another embodiment, cellular proliferation can be measured using 3H- thymidine incorporation or dye inclusion.
[0142] In another embodiment, cellular polypeptide levels are determined by measuring the level of protein or mRNA. The level of protein or proteins are measured using immunoassays such as western blotting, ELISA and the like with an antibody that selectively binds to the polypeptide or a fragment thereof. For measurement of mRNA, amplification, e.g., using PCR, LCR, or hybridization assays, e.g., northern hybridization, RNAse protection, dot blotting, are prefeπed. The level of protein or mRNA is detected using directly or indirectly labeled detection agents, e.g., fluorescently or radioactively labeled nucleic acids, radioactively or enzymatically labeled antibodies, and the like, as described herein. [0143] Alternatively, protein expression can be measured using a reporter gene system. Such a system can be devised using an angiogenesis protein promoter operably linked to a reporter gene such as chlorarnphenicol acetyltransferase, firefly luciferase, bacterial luciferase, β-galactosidase and alkaline phosphatase. Furthermore, the protein of interest can be used as an indirect reporter via attachment to a second reporter such as red or green fluorescent protein (see, e.g., Mistili & Spector, Nature Biotechnology 15:961-964 (1997)). The reporter construct is typically transfected into a cell. After treatment with a potential modulator, the amount of reporter gene transcription, translation, or activity is measured according to standard techniques known to those of skill in the art. [0144] A variety of phenotypic angiogenesis assays are known to those of skill in the art. Various models have been employed to evaluate angiogenesis (e.g., Croix et al., Science 289:1197-1202 (2000) and Kahn et al, Amer. J. Pathol 156:1887-1900). Assessment of angiogenesis in the presence of a potential modulator can be performed using cell-culture-based assays, e.g., endothelial cell tube formation assays and haptotaxis assays, as well as other animal based bioassays such as the chick CAM assay, the mouse comeal assay, and assays measuring the effect of administering potential modulators on implanted tumors.
[0145] For determination of cellular proliferation, any suitable functional effect can be measured, as described herein. For example, cellular morphology (e.g., cell volume, nuclear volume, cell perimeter, and nuclear perimeter), ligand binding, kinase activity, apoptosis, cell surface marker expression, cellular proliferation, GFP positivity and dye dilution assays (e.g., cell tracker assays with dyes that bind to cell membranes), DNA synthesis assays (e.g., 3H-thymidine and fluorescent DNA-binding dyes such as BrdU or Hoescht dye with FACS analysis), Go/Gi cell cycle arrest, are all suitable assays to identify potential modulators using a cell based system. Suitable cells for such cell based assays include both primary cancer or tumor cells and cell lines, as described herein, e.g., A549 (lung), MCF7 (breast, p53 wild-type), H1299 (lung, p53 null), Hela (cervical), PC3 (prostate, p53 mutant), MDA-MB-231 (breast, p53 wild-type). Cancer cell lines can be p53 mutant, p53 null, or express wild type p53. Animal models [0146] A number of animal based assays for angiogenesis phenotypes are known to those of skill in the art and can be used to assay for modulators of angiogenesis. For example, the chick CAM assay is described by O'Reilly, et al. Cell 79: 315-328 (1994). Briefly, 3 day old chicken embryos with intact yolks are separated from the egg and placed in a petri dish. After 3 days of incubation, a methylcellulose disc containing the protein to be tested is applied to the CAM of individual embryos. After about 48 hours of incubation, the embryos and CAMs are observed to determine whether endothelial growth has been inhibited. [0147] The mouse comeal assay involves implanting a growth factor-containing pellet, along with another pellet containing the suspected endothelial growth inhibitor, in the cornea of a mouse and observing the pattern of capillaries that are elaborated in the cornea.
[0148] Angiogenesis can also be measured by determining the extent of neovascularization of a tumor. For example, carcinoma cells can be subcutaneously inoculated into athymic or nude mice or SOD mice and tumor growth then monitored. Immunoassays using endothelial cell-specific antibodies are typically used to stain for vascularization of tumor and the number of vessels in the tumor.
[0149] As described above, animal models of angiogenesis find use in screening for modulators of angiogenesis. Similarly, transgenic animal technology including gene knockout technology, for example as a result of homologous recombination with an appropriate gene targeting vector, or gene overexpression, will result in the absence or increased expression ofthe protein. The same technology can also be applied to make knock-out cells. When desired, tissue-specific expression or knockout ofthe protein may be necessary. Transgenic animals generated by such methods find use as animal models of angiogenesis and are additionally useful in screening for modulators of angiogenesis.
[0150] Knock-out cells and transgenic mice can be made by insertion of a marker gene or other heterologous gene into the endogenous gene site in the mouse genome via homologous recombination. Such mice can also be made by substituting the endogenous gene with a mutated version ofthe gene, or by mutating the endogenous gene, e.g., by exposure to carcinogens. [0151] A DNA construct is introduced into the nuclei of embryonic stem cells. Cells containing the newly engineered genetic lesion are injected into a host mouse embryo, which is re-implanted into a recipient female. Some of these embryos develop into chimeric mice that possess germ cells partially derived from the mutant cell line. Therefore, by breeding the chimeric mice it is possible to obtain a new line of mice containing the introduced genetic lesion (see, e.g., Capecchi et al, Science 244:1288 (1989)). Chimeric targeted mice can be derived according to Hogan et al, Manipulating the Mouse Embryo: A Laboratory Manual, Cold Spring Harbor Laboratory (1988) and Teratocarcinomas and Embryonic Stem Cells: A Practical Approach, Robertson, ed., IRL Press, Washington, D.C., (1987).
B. Modulators [0152] The compounds tested as modulators ofthe angiogenesis protein can be any small organic molecule, or a biological entity, such as a protein, e.g., an antibody or peptide, a sugar, a nucleic acid, e.g., an antisense oligonucleotide, RNAi molecule, or a ribozyme, or a lipid. Alternatively, modulators can be genetically altered versions of an angiogenesis protein. Typically, test compounds will be small organic molecules, peptides, lipids, and lipid analogs.
[0153] Essentially any chemical compound can be used as a potential modulator or ligand in the assays ofthe invention, although most often compounds can be dissolved in aqueous or organic (especially DMSO-based) solutions are used. The assays are designed to screen large chemical libraries by automating the assay steps and providing compounds from any convenient source to assays, which are typically run in parallel (e.g., in microtiter formats on microtiter plates in robotic assays). It will be appreciated that there are many suppliers of chemical compounds, including Sigma (St. Louis, MO), Aldrich (St. Louis, MO), Sigma- Aldrich (St. Louis, MO), Fluka Chemika-Biochemica Analytika (Buchs Switzerland) and the like.
[0154] hi one preferred embodiment, high throughput screening methods involve providing a combinatorial small organic molecule or peptide library containing a large number of potential therapeutic compounds (potential modulator or ligand compounds). Such "combinatorial chemical libraries" or "ligand libraries" are then screened in one or more assays, as described herein, to identify those library members (particular chemical species or subclasses) that display a desired characteristic activity. The compounds thus identified can serve as conventional "lead compounds" or can themselves be used as potential or actual therapeutics. [0155] A combinatorial chemical library is a collection of diverse chemical compounds generated by either chemical synthesis or biological synthesis, by combining a number of chemical "building blocks" such as reagents. For example, a linear combinatorial chemical library such as a polypeptide library is formed by combining a set of chemical building blocks (amino acids) in every possible way for a given compound length (i.e., the number of amino acids in a polypeptide compound). Millions of chemical compounds can be synthesized through such combinatorial mixing of chemical building blocks.
[0156] Preparation and screening of combinatorial chemical libraries is well known to those of skill in the art. Such combinatorial chemical libraries include, but are not limited to, peptide libraries (see, e.g., U.S. Patent 5,010,175, Furka, Int. J. Pept. Prot. Res. 37:487-493 (1991) and Houghton et al, Nature 354:84-88 (1991)). Other chemistries for generating chemical diversity libraries can also be used. Such chemistries include, but are not limited to: peptoids (e.g., PCT Publication No. WO 91/19735), encoded peptides (e.g., PCT Publication No. WO 93/20242), random bio-oligomers (e.g., PCT Publication No. WO 92/00091), benzodiazepines (e.g., U.S. Pat. No. 5,288,514), diversomers such as hydantoins, benzodiazepines and dipeptides (Hobbs et al, Proc. Nat. Acad. Sci. USA 90:6909-6913 (1993)), vinylogous polypeptides (Hagihara et al, J. Amer. Chem. Soc.
114:6568 (1992)), nonpeptidal peptidomimetics with glucose scaffolding (Hirschmann et al, J. Amer. Chem. Soc. 114:9217-9218 (1992)), analogous organic syntheses of small compound libraries (Chen et al, J. Amer. Chem. Soc. 116:2661 (1994)), oligocarbamates (Cho et al,' Science 261:1303 (1993)), and/or peptidyl phosphonates (Campbell et al, J. Org. Chem. 59:658 (1994)), nucleic acid libraries (see Ausubel, Berger and Sambrook, all supra), peptide nucleic acid libraries (see, e.g., U.S. Patent 5,539,083), antibody libraries (see, e.g., Vaughn et al, Nature Biotechnology, 14(3):309-314 (1996) and PCT/US96/10287), carbohydrate libraries (see, e.g., Liang et al, Science, 274:1520-1522 (1996) and U.S. Patent 5,593,853), small organic molecule libraries (see, e.g., benzodiazepines, Baum C&EN, Jan 18, page 33 (1993); isoprenoids, U.S. Patent
5,569,588; thiazolidinones and metathiazanones, U.S. Patent 5,549,974; pyrrolidines, U.S. Patents 5,525,735 and 5,519,134; morpholino compounds, U.S. Patent 5,506,337; benzodiazepines, 5,288,514, and the like). [0157] Devices for the preparation of combinatorial libraries are commercially available (see, e.g., 357 MPS, 390 MPS, Advanced Chem Tech, Louisville KY, Symphony, Rainin, Woburn, MA, 433 A Applied Biosystems, Foster City, CA, 9050 Plus, Millipore, Bedford, MA). In addition, numerous combinatorial libraries are themselves commercially available (see, e.g., ComGenex, Princeton, N.J., Asinex, Moscow, Ru, Tripos, Inc., St. Louis, MO, ChemStar, Ltd, Moscow, RU, 3D Pharmaceuticals, Exton, PA, Martek Biosciences, Columbia, MD, etc.).
C. Solid State and soluble high throughput assays [0158] In one embodiment the invention provides soluble assays using an angiogenesis protein, or a cell or tissue expressing an angiogenesis protein, either naturally occurring or recombinant. In another embodiment, the invention provides solid phase based in vitro assays in a high throughput format, where the angiogenesis protein is attached to a solid phase substrate. Any one ofthe assays described herein can be adapted for high throughput screening, e.g., ligand binding, cellular proliferation, cell surface marker flux, e.g., αv/33 integrin, etc. In one preferred embodiment, the cell-based system using αv/33 integrin modulation and FACS assays is used in a high throughput format for identifying modulators of angiogenesis proteins, and therefore modulators of T cell angiogenesis.
[0159] In the high throughput assays ofthe invention, either soluble or solid state, it is possible to screen up to several thousand different modulators or ligands in a single day. This methodology can be used for angiogenesis proteins in vitro, or for cell-based assays comprising an angiogenesis protein. In particular, each well of a microtiter plate can be used to run a separate assay against a selected potential modulator, or, if concentration or incubation time effects are to be observed, every 5-10 wells can test a single modulator. Thus, a single standard microtiter plate can assay about 100 (e.g., 96) modulators. If
1536 well plates are used, then a single plate can easily assay from about 100- about 1500 different compounds. It is possible to assay many plates per day; assay screens for up to about 6,000, 20,000, 50,000, or more than 100,000 different compounds are possible using the integrated systems ofthe invention.
[0160] For a solid state reaction, the protein of interest or a fragment thereof, e.g., an extracellular domain, or a cell comprising the protein of interest or a fragment thereof as part of a fusion protein can be bound to the solid state component, directly or indirectly, via covalent or non covalent linkage e.g., via a tag. The tag can be any of a variety of components. In general, a molecule which binds the tag (a tag binder) is fixed to a solid support, and the tagged molecule of interest is attached to the solid support by interaction of the tag and the tag binder. [0161] A number of tags and tag binders can be used, based upon known molecular interactions well described in the literature. For example, where a tag has a natural binder, for example, biotin, protein A, or protein G, it can be used in conjunction with appropriate tag binders (avidin, streptavidin, neutravidin, the Fc region of an immunoglobulin, etc.) Antibodies to molecules with natural binders such as biotin are also widely available and appropriate tag binders; .see, SIGMA Immunochemicals 1998 catalogue SIGMA, St. Louis MO). [0162] Similarly, any haptenic or antigenic compound can be used in combination with an appropriate antibody to form a tag/tag binder pair. Thousands of specific antibodies are commercially available and many additional antibodies are described in the literature. For example, in one common configuration, the tag is a first antibody and the tag binder is a second antibody wliich recognizes the first antibody. In addition to antibody-antigen interactions, receptor-ligand interactions are also appropriate as tag and tag-binder pairs. For example, agonists and antagonists of cell membrane receptors (e.g., cell receptor- ligand interactions such as transferrin, c-kit, viral receptor ligands, cytokine receptors, chemokine receptors, interleukin receptors, immunoglobulin receptors and antibodies, the cadherein family, the integrin family, the selectin family, and the like; see, e.g., Pigott & Power, The Adhesion Molecule Facts Book I (1993). Similarly, toxins and venoms, viral epitopes, hormones (e.g., opiates, steroids, etc.), intracellular receptors (e.g. which mediate the effects of various small ligands, including steroids, thyroid hormone, retinoids and vitamin D; peptides), drugs, lectins, sugars, nucleic acids (both linear and cyclic polymer configurations), oligosaccharides, proteins, phospholipids and antibodies can all interact with various cell receptors.
[0163] Synthetic polymers, such as polyurethanes, polyesters, polycarbonates, polyureas, polyamides, polyethyleneimines, polyarylene sulfides, polysiloxanes, polyimides, and polyacetates can also form an appropriate tag or tag binder. Many other tag/tag binder pairs are also useful in assay systems described herein, as would be apparent to one of skill upon review of this disclosure. [0164] Common linkers such as peptides, polyethers, and the like can also serve as tags, and include polypeptide sequences, such as poly gly sequences of between about 5 and 200 amino acids. Such flexible linkers are known to persons of skill in the art. For example, poly(ethelyne glycol) linkers are available from Shearwater Polymers, Inc. Huntsville, Alabama. These linkers optionally have amide linkages, sulfhydryl linkages, or heterofunctional linkages.
[0165] Tag binders are fixed to solid substrates using any of a variety of methods currently available. Solid substrates are commonly derivatized or functionalized by exposing all or a portion ofthe substrate to a chemical reagent which fixes a chemical group to the surface which is reactive with a portion ofthe tag binder. For example, groups which are suitable for attachment to a longer chain portion would include amines, hydroxyl, thiol, and carboxyl groups. Aminoalkylsilanes and hydroxyalkylsilanes can be used to functionalize a variety of surfaces, such as glass surfaces. The construction of such solid phase biopolymer arrays is well described in the literature. See, e.g., Merrifield, J Am. Chem. Soc. 85:2149-2154 (1963) (describing solid phase synthesis of, e.g., peptides); Geysen et al, J. Immun. Meth. 102:259-274 (1987) (describing synthesis of solid phase components on pins); Frank & Doring, Tetrahedron 44:60316040 (1988) (describing synthesis of various peptide sequences on cellulose disks); Fodor et al, Science, 251:767-777 (1991); Sheldon et al, Clinical Chemistry 39(4):718-719 (1993); and Kozal et al, Nature Medicine 2(7):753759 (1996) (all describing arrays of biopolymers fixed to solid substrates). Non-chemical approaches for fixing tag binders to substrates include other common methods, such as heat, cross-linking by UV radiation, and the like.
Antibodies to angiogenesis polypeptides
[0166] In addition to the detection of gene and gene expression using nucleic acid hybridization technology, one can also use immunoassays to detect proteins ofthe invention. Such assays are useful for screening for modulators of angiogenesis, as well as for therapeutic and diagnostic applications. Immunoassays can be used to qualitatively or quantitatively analyze angiogenesis protein. A general overview ofthe applicable technology can be found in Harlow & Lane, Antibodies: A Laboratory Manual (1988). A. Production of antibodies [0167] Methods of producing polyclonal and monoclonal antibodies that react specifically with the angiogenesis proteins are known to those of skill in the art (see, e.g., Coligan, Current Protocols in Immunology (1991); Harlow & Lane, supra; Goding, Monoclonal Antibodies: Principles and Practice (2d ed. 1 86); and Kohler & Milstein, Nature 256:495-497 (1975). Such techniques include antibody preparation by selection of antibodies from libraries of recombinant antibodies in phage or similar vectors, as well as preparation of polyclonal and monoclonal antibodies by immunizing rabbits or mice (see, e.g., Huse et al, Science 246:1275-1281 (1989); Ward et al, Nature 341:544-546 (1989)). [0168] A number of immunogens comprising portions of an angiogenesis protein may be used to produce antibodies specifically reactive with protein. For example, recombinant protein or an antigenic fragment thereof, can be isolated as described herein. Recombinant protein can be expressed in eukaryotic or prokaryotic cells as described above, and purified as generally described above. Recombinant protein is the preferred immunogen for the production of monoclonal or polyclonal antibodies. Alternatively, a synthetic peptide derived from the sequences disclosed herein and conjugated to a carrier protein can be used an immunogen. Naturally occurring protein may also be used either in pure or impure form. The product is then injected into an animal capable of producing antibodies. Either monoclonal or polyclonal antibodies may be generated, for subsequent use in immunoassays to measure the protein.
[0169] Methods of production of polyclonal antibodies are known to those of skill in the art. An inbred strain of mice (e.g., BALB/C mice) or rabbits is immunized with the protein using a standard adjuvant, such as Freund's adjuvant, and a standard immunization protocol. The animal's immune response to the immunogen preparation is monitored by taking test bleeds and determining the titer of reactivity to the beta subunits. When appropriately high titers of antibody to the immunogen are obtained, blood is collected from the animal and antisera are prepared. Further fractionation ofthe antisera to enrich for antibodies reactive to the protein can be done if desired (see, Harlow & Lane, supra).
[0170] Monoclonal antibodies may be obtained by various techniques familiar to those skilled in the art. Briefly, spleen cells from an animal immunized with a desired antigen are immortalized, commonly by fusion with a myeloma cell (see, Kohler & Milstein, Eur. J. Immunol. 6:511-519 (1976)). Alternative methods of immortalization include transformation with Epstein Barr Virus, oncogenes, or retroviruses, or other methods well known in the art. Colonies arising from single immortalized cells are screened for production of antibodies ofthe desired specificity and affinity for the antigen, and yield ofthe monoclonal antibodies produced by such cells may be enhanced by various techniques, including injection into the peritoneal cavity of a vertebrate host. Alternatively, one may isolate DNA sequences which encode a monoclonal antibody or a binding fragment thereof by screening a DNA library from human B cells according to the general protocol outlined by Huse, et al, Science 246:1275-1281 (1989).
[0171] Monoclonal antibodies and polyclonal sera are collected and titered against the immunogen protein in an immunoassay, for example, a solid phase immunoassay with the immunogen immobilized on a solid support. Typically, polyclonal antisera with a titer of 104 or greater are selected and tested for their cross reactivity against non- angiogenesis proteins, using a competitive binding immunoassay. Specific polyclonal antisera and monoclonal antibodies will usually bind with a K of at least about 0.1 mM, more usually at least about 1 μM, preferably at least about 0.1 μM or better, and most preferably, 0.01 μM or better. Antibodies specific only for a particular ortholog, such as a human ortholog, can also be made, by subtracting out other cross-reacting orthologs from a species such as a non-human mammal. In this manner, antibodies that bind only to a desired protein may be obtained.
[0172] Once the specific antibodies against the protein are available, the protein can be detected by a variety of immunoassay methods. In addition, the antibody can be used therapeutically as modulators. For a review of immunological and immunoassay procedures, see Basic and Clinical Immunology (Stites & Terr eds., 7th ed. 1991).
Moreover, the immunoassays ofthe present invention can be performed in any of several configurations, which are reviewed extensively in Enzyme Immunoassay (Maggio, ed., 1980); and Harlow & Lane, supra. B. Immunological binding assays
[0173] Protein can be detected and/or quantified using any of a number of well recognized immunological binding assays (see, e.g., U.S. Patents 4,366,241; 4,376,110; 4,517,288; and 4,837,168). For a review ofthe general immunoassays, see also Methods in Cell Biology: Antibodies in Cell Biology, volume 37 (Asai, ed. 1993); Basic and Clinical Immunology (Stites & Terr, eds., 7th ed. 1991). Immunological binding assays (or immunoassays) typically use an antibody that specifically binds to a protein or antigen of choice (in this case the protein or antigenic subsequence thereof). The antibody may be produced by any of a number of means well known to those of skill in the art and as described above. [0174] Immunoassays also often use a labeling agent to specifically bind to and label the complex formed by the antibody and antigen. The labeling agent may itself be one of the moieties comprising the antibody/antigen complex. Thus, the labeling agent may be a labeled protein or a labeled antibody. Alternatively, the labeling agent may be a third moiety, such a secondary antibody, that specifically binds to the antibody/protein complex (a secondary antibody is typically specific to antibodies ofthe species from which the first antibody is derived). Other proteins capable of specifically binding immunoglobuhn constant regions, such as protein A or protein G may also be used as the label agent. These proteins exhibit a strong non-immunogenic reactivity with immunoglobulin constant regions from a variety of species (see, e.g., Kronval et al, J. Immunol. 111:1401-1406 (1973); Akerstrom et al., J. Immunol. 135:2589-2542 (1985)). The labeling agent can be modified with a detectable moiety, such as biotin, to which another molecule can specifically bind, such as streptavidin. A variety of detectable moieties are well known to those skilled in the art.
[0175] Throughout the assays, incubation and/or washing steps may be required after each combination of reagents. Incubation steps can vary from about 5 seconds to several hours, optionally from about 5 minutes to about 24 hours. However, the incubation time will depend upon the assay format, antigen, volume of solution, concentrations, and the like. Usually, the assays will be carried out at ambient temperature, although they can be conducted over a range of temperatures, such as 10°C to 40°C.
Non-competitive assay formats [0176] Immunoassays for detecting protein in samples may be either competitive or noncompetitive. Noncompetitive immunoassays are assays in which the amount of antigen is directly measured. In one prefeπed "sandwich" assay, for example, the antibodies can be bound directly to a solid substrate on which they are immobilized. These immobilized antibodies then capture protein present in the test sample. Proteins thus immobilized are then bound by a labeling agent, such as a second antibody bearing a label. Alternatively, the second antibody may lack a label, but it may, in turn, be bound by a labeled third antibody specific to antibodies ofthe species from which the second antibody is derived. The second or third antibody is typically modified with a detectable moiety, such as biotin, to which another molecule specifically binds, e.g., streptavidin, to provide a detectable moiety. Competitive assay formats
[0177] In competitive assays, the amount of protein present in the sample is measured indirectly by measuring the amount of a known, added (exogenous) protein displaced (competed away) from an antibody by the unknown protein present in a sample. In one competitive assay, a known amount of protein is added to a sample and the sample is then contacted with an antibody that specifically binds to protein. The amount of exogenous protein bound to the antibody is inversely proportional to the concentration of protein present in the sample. In a particularly preferred embodiment, the antibody is immobilized on a solid substrate. The amount of protein bound to the antibody may be determined either by measuring the amount of protein present in protein antibody complex, or alternatively by measuring the amount of remaining uncomplexed protein. The amount of protein may be detected by providing a labeled molecule.
[0178] A hapten inhibition assay is another prefeπed competitive assay. In this assay the known protein is immobilized on a solid substrate. A known amount of antibody is added to the sample, and the sample is then contacted with the immobilized protein. The amount of antibody bound to the known immobihzed protein is inversely proportional to the amount of protein present in the sample. Again, the amount of immobilized antibody may be detected by detecting either the immobilized fraction of antibody or the fraction ofthe antibody that remains in solution. Detection may be direct where the antibody is labeled or indirect by the subsequent addition of a labeled moiety that specifically binds to the antibody as described above. Cross-reactivity determinations [0179] Immunoassays in the competitive binding format can also be used for crossreactivity determinations. For example, a protein can be immobilized to a solid support. Proteins are added to the assay that compete for binding ofthe antisera to the immobilized antigen. The ability ofthe added proteins to compete for binding ofthe antisera to the immobilized protein is compared to the ability ofthe protein to compete with itself. The percent crossreactivity for the above proteins is calculated, using standard calculations. Those antisera with less than 10% crossreactivity with each ofthe added proteins listed above are selected and pooled. The cross-reacting antibodies are optionally removed from the pooled antisera by immunoabsorption with the added considered proteins, e.g., distantly related homologs.
[0180] The immunoabsorbed and pooled antisera are then used in a competitive binding immunoassay as described above to compare a second protein, thought to be perhaps an allele or polymorphic variant of a protein, to the immunogen protein. In order to make this comparison, the two proteins are each assayed at a wide range of concentrations and the amount of each protein required to inhibit 50% ofthe binding ofthe antisera to the immobilized protein is determined. If the amount ofthe second protein required to inhibit 50% of binding is less than 10 times the amount ofthe protein that is required to inhibit 50% of binding, then the second protein is said to specifically bind to the polyclonal antibodies generated to the immunogen.
Other assay formats [0181] Western blot (immunoblot) analysis is used to detect and quantify the presence of protein in the sample. The technique generally comprises separating sample proteins by gel electrophoresis on the basis of molecular weight, transferring the separated proteins to a suitable solid support, (such as a nitrocellulose filter, a nylon filter, or derivatized nylon filter), and incubating the sample with the antibodies that specifically bind the protein. The antibodies specifically bind to the protein on the solid support. These antibodies may be directly labeled or alternatively may be subsequently detected using labeled antibodies (e.g., labeled sheep anti-mouse antibodies) that specifically bind to the antibodies. [0182] Other assay formats include liposome immunoassays (LIA), which use liposomes designed to bind specific molecules (e.g., antibodies) and release encapsulated reagents or markers. The released chemicals are then detected according to standard techniques (see Monroe et al., Amer. Clin. Prod. Rev. 5:34-41 (1986)).
Reduction of non-specific binding [0183] One of skill in the art will appreciate that it is often desirable to minimize nonspecific binding in immunoassays. Particularly, where the assay involves an antigen or antibody immobilized on a solid substrate it is desirable to minimize the amount of non- specific binding to the substrate. Means of reducing such non-specific binding are well known to those of skill in the art. Typically, this technique involves coating the substrate with a proteinaceous composition. In particular, protein compositions such as bovine serum albumin (BSA), nonfat powdered milk, and gelatin are widely used with powdered milk being most preferred.
Labels
[0184] The particular label or detectable group used in the assay is not a critical aspect ofthe invention, as long as it does not significantly interfere with the specific binding of the antibody used in the assay. The detectable group can be any material having a detectable physical or chemical property. Such detectable labels have been well- developed in the field of immunoassays and, in general, most any label useful in such methods can be applied to the present invention. Thus, a label is any composition detectable by spectroscopic, photochemical, biochemical, immunochemical, electrical, optical or chemical means. Useful labels in the present invention include, magnetic beads (e.g., DYNABEADS™), fluorescent dyes (e.g., fluorescein isothiocyanate, Texas red, rhodamine, and the like), radiolabels (e.g., H, I, S, C, or P), enzymes (e.g., horse radish peroxidase, alkaline phosphatase and others commonly used in an ELISA), and colorimetric labels such as colloidal gold or colored glass or plastic beads (e.g., polystyrene, polypropylene, latex, etc.).
[0185] The label may be coupled directly or indirectly to the desired component of the assay according to methods well known in the art. As indicated above, a wide variety of labels may be used, with the choice of label depending on sensitivity required, ease of conjugation with the compound, stability requirements, available instrumentation, and disposal provisions.
[0186] Non-radioactive labels are often attached by indirect means. Generally, a ligand molecule (e.g., biotin) is covalently bound to the molecule. The ligand then binds to another molecules (e.g., streptavidin) molecule, which is either inherently detectable or covalently bound to a signal system, such as a detectable enzyme, a fluorescent compound, or a chemiluminescent compound. The ligands and their targets can be used in any suitable combination with antibodies that recognize the protein, or secondary antibodies. [0187] The molecules can also be conjugated directly to signal generating compounds, e.g., by conjugation with an enzyme or fluorophore. Enzymes of interest as labels will primarily be hydrolases, particularly phosphatases, esterases and glycosidases, or oxidotases, particularly peroxidases. Fluorescent compounds include fluorescein and its derivatives, rhodamine and its derivatives, dansyl, umbelliferone, etc. Chemiluminescent compounds include luciferin, and 2,3-dihydrophthalazinediones, e.g., luminol. For a review of various labeling or signal producing systems that may be used, see U.S. Patent No. 4,391,904.
[0188] Means of detecting labels are well known to those of skill in the art. Thus, for example, where the label is a radioactive label, means for detection include a scintillation counter or photographic film as in autoradiography. Where the label is a fluorescent label, it may be detected by exciting the fluorochrome with the appropriate wavelength of light and detecting the resulting fluorescence. The fluorescence may be detected visually, by means of photographic film, by the use of electronic detectors such as charge coupled devices (CCDs) or photomultipliers and the like. Similarly, enzymatic labels may be detected by providing the appropriate substrates for the enzyme and detecting the resulting reaction product. Finally simple colorimetric labels may be detected simply by observing the color associated with the label. Thus, in various dipstick assays, conjugated gold often appears pink, while various conjugated beads appear the color ofthe bead.
[0189] Some assay formats do not require the use of labeled components. For instance, agglutination assays can be used to detect the presence ofthe target antibodies. In this case, antigen-coated particles are agglutinated by samples comprising the target antibodies. In this format, none ofthe components need be labeled and the presence of the target antibody is detected by simple visual inspection.
Gene therapy 5 [0190] The present invention provides the nucleic acids of angiogenesis associated protein for the transfection of cells in vitro and in vivo. These nucleic acids can be inserted into any of a number of well-known vectors for the transfection of target cells and organisms as described below. The nucleic acids are transfected into cells, ex vivo or in vivo, through the interaction ofthe vector and the target cell. The nucleic acid, under 10 the control of a promoter, then expresses a protein of the present invention, thereby mitigating the effects of absent, partial inactivation, or abnormal expression ofthe angiogenesis gene, particularly as it relates to angiogenesis. The compositions are administered to a patient in an amount sufficient to elicit a therapeutic response in the- ' patient. An amount adequate to accomplish this is defined as "therapeutically effective
15 dose or amount." [0191] Such gene therapy procedures have been used to correct acquired and inherited genetic defects, cancer, and other diseases in a number of contexts. The ability to express artificial genes in humans facilitates the prevention and/or cure of many important human diseases, including many diseases which are not amenable to treatment by other therapies
20 (for a review of gene therapy procedures, see Anderson, Science 256:808-813 (1992); Nabel & Feigner, ΗBTECH 11:211-217 (1993); Mitani & Caskey, TIBTECH 11:162- 166 (1993); Mulligan, Science 926-932 (1993); Dillon, TIBTECH 11:167-175 (1993); Miller, Nature 357:455-460 (1992); Van Brunt, Biotechnology 6(10):1149-1154 (1998); Vigne, Restorative Neurology and Neuroscience 8:35-36 (1995); Kremer & Perricaudet,
25 British Medical Bulletin 51(l):31-44 (1995); Haddada et al, in Current Topics in Microbiology and Immunology (Doerfler & Bδhm eds., 1995); and Yu et al, Gene Therapy 1:13-26 (1994)).
[0192] The nucleic acids ofthe invention can also be used to make transgenic animals, such as transgenic mice, either by knock-out or overexpression. Such animals are useful, 30 e.g., for testing modulators of angiogenesis. Pharmaceutical compositions and administration [0193] Pharmaceutically acceptable carriers are determined in part by the particular composition being administered (e.g., nucleic acid, protein, modulatory compounds or transduced cell), as well as by the particular method used to administer the composition. Accordingly, there are a wide variety of suitable formulations of pharmaceutical compositions ofthe present invention (see, e.g., Remington 's Pharmaceutical Sciences, 17th ed., 1989). Administration can be in any convenient manner, e.g., by injection, oral administration, inhalation, transdermal application, or rectal administration.
[0194] Formulations suitable for oral administration can consist of (a) liquid solutions, such as an effective amount ofthe packaged nucleic acid suspended in diluents, such as water, saline or PEG 400; (b) capsules, sachets or tablets, each containing a predetermined amount ofthe active ingredient, as liquids, solids, granules or gelatin; (c) suspensions in an appropriate liquid; and (d) suitable emulsions. Tablet forms can include one or more of lactose, sucrose, mannitol, sorbitol, calcium phosphates, com starch, potato starch, microcrystalline cellulose, gelatin, colloidal silicon dioxide, talc, magnesium stearate, stearic acid, and other excipients, colorants, fillers, binders, diluents, buffering agents, moistening agents, preservatives, flavoring agents, dyes, disintegrating agents, and pharmaceutically compatible carriers. Lozenge forms can comprise the active ingredient in a flavor, e.g., sucrose, as well as pastilles comprising the active ingredient in an inert base, such as gelatin and glycerin or sucrose and acacia emulsions, gels, and the like containing, in addition to the active ingredient, carriers known in the art.
[0195] The compound of choice, alone or in combination with other suitable components, can be made into aerosol formulations (i.e., they can be "nebulized") to be administered via inhalation. Aerosol formulations can be placed into pressurized acceptable propellants, such as dichlorodifluoromethane, propane, nitrogen, and the like.
[0196] Formulations suitable for parenteral administration, such as, for example, by intraarticular (in the joints), intravenous, intramuscular, intradermal, intraperitoneal, and subcutaneous routes, include aqueous and non-aqueous, isotonic sterile injection solutions, which can contain antioxidants, buffers, bacteriostats, and solutes that render the formulation isotonic with the blood ofthe intended recipient, and aqueous and non- aqueous sterile suspensions that can include suspending agents, solubilizers, thickening agents, stabilizers, and preservatives. In the practice of this invention, compositions can be administered, for example, by intravenous infusion, orally, topically, intraperitoneally, intravesically or intrathecally. Parenteral adnrinistration and intravenous administration are the preferred methods of administration. The formulations of commends can be presented in unit-dose or multi-dose sealed containers, such as ampules and vials. [0197] Injection solutions and suspensions can be prepared from sterile powders, granules, and tablets ofthe kind previously described. Cells transduced by nucleic acids for ex vivo therapy can also be administered intravenously or parenterally as described above. [0198] The dose administered to a patient, in the context ofthe present invention should be sufficient to effect a beneficial therapeutic response in the patient over time. The dose will be determined by the efficacy ofthe particular vector employed and the condition of the patient, as well as the body weight or surface area ofthe patient to be treated. The size ofthe dose also will be determined by the existence, nature, and extent of any adverse side-effects that accompany the administration of a particular vector, or transduced cell type in a particular patient.
[0199] In determining the effective amount ofthe vector to be administered in the treatment or prophylaxis of conditions owing to diminished or abeπant expression ofthe angiogenesis protein, the physician evaluates circulating plasma levels ofthe vector, vector toxicities, progression ofthe disease, and the production of anti- vector antibodies. In general, the dose equivalent of a naked nucleic acid from a vector is from about 1 μg to 100 μg for a typical 70 kilogram patient, and doses of vectors which include a retroviral particle are calculated to yield an equivalent amount of therapeutic nucleic acid.
[0200] For administration, compounds and transduced cells ofthe present invention can be administered at a rate determined by the LD-50 ofthe inhibitor, vector, or transduced cell type, and the side-effects ofthe inhibitor, vector or cell type at various concentrations, as applied to the mass and overall health ofthe patient. Administration can be accomplished via single or divided doses.
EXAMPLES [0201] The following examples are offered to illustrate, but not to limit the claimed invention. Example 1: Identification of genes involved in modulation of angiogenesis in vitro [0202] Using a retroviral system, complex libraries of cDNAs have been expressed in human primary endothelial cells (e.g., HUVECS, Cloneitc CC-2519). HUVEC cells that switch to a differentiated angiostatic state can be identified using a VEGFR2 internalization assay. After infection with a retroviral cDNA library, cells are seeded in EGM-2 media (Clonetics EGM-2 bullet kit CC-3162) and grown to log phase. Cells are cultured in starvation medium (EGMS with 0.1%FCS plus 1% BSA in place of VEGF and FCS) at 37°C for 16 hours. The starved HUVECs are stimulated with VEGF stimulation medium at 37°C for 1.5 hours, trypsinized, and stained with VEGFR2 antibody. Single cells exhibiting increased VEGF-R2 expression (i.e., blocked or inhibited receptor internalization) were selected using FACS analysis.
[0203] Co-culture of HUVECs on smooth muscle cells was used to confirm that genes identified via VEGR2 internalization are genes that encode angiogenesis proteins. Smooth muscle cells (Clonetics Pulmonary Artery SMCs CC-2581) are plated at 40,000 cells per well of a collagen coated 24 well tissue culture plate and grown to confluency. HUVECs are plated onto the smooth muscle cells at 22,000 cells per well. The phenotype of vascular bed formation is determined as follows: photographs are taken and formation of tubular morphology ofthe HUVECs is determined empirically. The co- culture assay is typically used to confirm an anti-angiogenic phenotype.
[0204] It is understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and scope ofthe appended claims. All publications, patents, and patent applications cited herein are hereby incorporated by reference in their entirety for all purposes. INFORMAL SEQUENCE LISTING
SEQ ID Nθ:l
Mat2A
NM_005911.2| Homo sapiens methionine adenosyltransferase II, alpha (MAT2A) , mRNA
1 ggcacgaggc gcccgcctgc tacgagtaga acgctgtσcg cagcttgcgc atttcgcagc 61 cgctgccgcc tcgccgctgc tccttcgtaa ggccacttcc gcacaccgac accaacatga 121 acggacagct caacggcttσ cacgaggcgt tcatcgagga gggcacattc cttttcacct 181 cagagtcggt cggggaaggc cacccagata agatttgtga ccaaatcagt gatgctgtcc 241 ttgatgccca ccttcagcag gatcctgatg ccaaagtagc ttgtgaaact gttgctaaaa 301 ctggaatgat ccttcttgct ggggaaatta catccagagc tgctgttgac taccagaaag 361 tggttcgtga agctgttaaa cacattggat atgatgattc ttccaaaggt tttgactaca 421 agacttgtaa cgtgctggta gccttggagc aacagtcacc agatattgct caaggtgttc 481 atcttgacag aaatgaagaa gacattggtg ctggagacca gggcttaatg tttggctatg 541 ccactgatga aactgaggag tgtatgcctt taaccattgt cttggcacac aagctaaatg 601 ccaaactggc agaaσtacgc cgtaatggca ctttgccttg gttacgccct gattctaaaa 661 ctcaagttac tgtgcagtat atgcaggatc gaggtgctgt gcttcccatc agagtccaca 721 caattgttat atctgttcag catgatgaag aggtttgtct tgatgaaatg agggatgccc 781 taaaggagaa agtcatcaaa gcagttgtgc ctgcgaaata ccttgatgag gatacaatct 841 accacctaca gcσaagtggc agatttgtta ttggtgggcc tσagggtgat gctggtttga 901 ctggacgcaa aatcattgtg gacacttatg gcggttgggg tgctcatgga ggaggtgcct 961 tttcaggaaa ggattatacc aaggtcgacc gttcagctgc ttatgctgct cgttgggtgg 1021 caaaatccct tgttaaagga ggtctgtgcc ggagggttct tgttcaggtc tcttatgcta 1081 ttggagtttc tcatccatta tctatctcca ttttccatta tggtacctct cagaagagtg 1141 agagagagct attagagatt gtgaagaaga atttcgatct ccgccctggg gtcattgtca 1201 gggatctgga tctgaagaag ccaatttatc agaggactgc agcctatggc cactttggta 1261 gggacagctt cccatgggaa gtgcccaaaa agcttaaata ttgaaagtgt tagccttttt 1321 tccccagact tgttggcgta ggctacagag aagccttcaa gctctgaggg aaagggccct 1381 ccttcctaaa ttttσctgtc ctctttcagc tcctgaccag ttgcagtcac tctagtcaat 1441 gacatgaatt ttagcttttg tgggggactg taagttgggc ttgctattct gtccctaggt 1501 gttttgttca ccattataat gaatttagtg agcataggtg atccatgtaa ctgcctagaa 1561 acaacactgt agtaaataat gctttgaaat tgaacctttg tgccctatca cccaacgctc 1621 caaagtcata attgcattga ctttccccac cagatgctga aaatgtcctt gtgatgtgca 1681 cgtaaagtac ttgtagttcc acttatagcc tctgtctggc aatgccacag ccctgtcagc 1741 atgaatttgt aatgtcttga gctctattat gaatgtgaag ccttcccctt atcctccctg 1801 taacttgatc catttctaat tatgtagctc tttgtcaggg agtgttccct atccaatcaa 1861 tcttgcatgt aacgcaagtt cccagttgga gctccagcct gacatcaaaa aaggcagtta 1921 ccattaaacc atctccctgg tgcttatgct cttaattgcc acctctaaca gcaccaaatc 1981 aaaatctctc cactttcagc tgtcttttgg aggacgtacg taataaggtt ttaatttagt 2041 aaaccaatcc tatgcatggt ttcagcacta gccaaacctc accaactcct agttctagaa 2101 aaacaggcac ttggcagcct tgtgatgtca tacagagaag tcacagggca gtacctgagg 2161 gtctgtaggt tgcacacttt ggtaccagat aacttttttt tttctttata agaaagcctg 2221 agtactccac actgcacaat aactcctccc agggttttaa ctttgtttta ttttcaaaac 2281 caggtccaat gagctttctg aacagctggt gtagctacag agaaaccagc ttccttcaga 2341 gagcagtgct tttggcgggg aggaggaaat cccttcatac ttgaacgttt tctaattgct 2401 tatttattgt attctggggt atggcgtaag tacagagaag ccatcacctc agatggcagc 2461 ttttaaaaga tttttttttt ttctctcaac accatgattc ctttaacaac atgtttccag 2521 cattcccagg taggccaagg tgtcctacag aaaaaccttg ggttagacct acagggggtc 2581 tggctggtgt taacagaagg gagggcagag ctggtgcggc tggccatgga gaaagctgac 2641 ttggctggtg tggtacagag aagccagctt gtttacatgc ttattccatg actgcttgcc 2701 ctaagcagaa agtgcctttc aggatctatt tttggaggtt tattacgtat gtctggttct 2761 caattccaac agtttaatga agatctaaat aaaatgctag gttctacctt aaaaaaaaaa 2821 aaaaaaaa
SEQ ID NO: 2
CPT-2
NM_000098 Homo sapiens camitine palmitoyltransferase II (CPT2) , nuclear gene encoding mitochondrial protein, mRNA gi|4503022 | ref |NM_000098.11 [4503022]
1 ctcatatcta gaattttggg taggtacttt gaatcattac gatctatcta cttcttaggt 61 gaggaaatag aggtttaaaa tttagtccac agtctcgcaa ggatggagcc tggatcaaat 121 tttgggttat cagattccaa tcacgtttct tagcttttct tttttttttc caactccagt 181 ttctgtcttg ctccaaaaaa ggggaaggag cggctgcggc gctcggtttc ccgcctccta 241 gggaagggaa gggagacgag σaacgcggag gctggggccc ccttccgggc ggggcctact 301 agtgggcggg gcctgtcagt gagcggcccc tgcccggaag gagccagtcc ggggcggagc 361 cgatggcctt acaggggccg gaagtggcct gcgggcggag aagtgcctca ggagtcctga 421 cgcagtgtct tgggcgctaa cggcggcggc ggccttgtgt ttagactcca gaactcccca 481 cttgccgcgt tctcgccgcc gcaggctccc gggacgatgg tgccccgcct gctgctgcgc 541 gcctggcccc ggggccccgc ggttggtccg ggagccccca gtcggcccct cagcgccggc 601 tccgggcccg gccagtacct gcagcgcagc atcgtgccca ccatgcacta ccaggacagc 661 ctgcccaggc tgcctattcc caaacttgaa gacaccatta ggagatacct cagtgcacag 721 aagcctctct tgaatgatgg ccagttcagg aaaacagaac aattttgcaa gagttttgaa 781 aatgggattg gaaaagaact gcatgagcag ctggttgctc tggaσaaaca gaataaacat 841 acaagctaca tttcgggacc ctggtttgat atgtacctat ctgctcgaga ctccgttgtt 901 ctgaacttta atccatttat ggctttcaat cctgacccaa aatctgagta taatgaccag 961 ctcacccggg caaccaaσat gactgtttct gccatccggt ttctgaagac aσtccgggct 1021 ggccttctgg agccagaagt gttccacttg aaccctgcaa aaagtgacac tatcaccttc 1081 aagagactca tacgctttgt gccttcctct ctgtcctggt atggggccta cctggtcaat 1141 gcgtatcccc tggatatgtσ ccagtatttt cggcttttca actcaactcg tttacccaaa 1201 cccagtcggg atgaactctt cactgatgac aaggccagac acctcctggt cctaaggaaa 1261 ggaaattttt atatctttga tgtcctggat caagatggga acattgtgag cccctcggaa 1321 atccaggcac atctgaagta cattctctca gacagcagcc ccgcccccga gtttcccctg 1381 gcatacctga ccagtgagaa ccgagacatc tgggcagagc tcaggcagaa gctgatgagt 1441 agtggcaatg aggagagcct gaggaaagtg gactcggcag tgttctgtct ctgcctagat 1501 gacttcccca ttaaggacct tgtccacttg tcccacaata tgctgcatgg ggatggcaca 1561 aaccgctggt ttgataaatc ctttaacctc attatcgcca aggatggctc tactgccgtc 1621 cactttgagc actcttgggg tgatggtgtg gcagtgctca gattttttaa tgaagtattt 1681 aaagacagca ctcagacccc tgccgtcact ccacagagcc agccagctac caσtgactct 1741 actgtcacgg tgcagaaact caacttcgag ctgactgatg ccttaaagac tggcatcaca 1801 gctgctaagg aaaagtttga tgccaccatg aaaaccctca ctattgactg cgtccagttt 1861 cagagaggag gcaaagaatt cctgaagaag caaaagctga gccctgacgc agttgcccag 1921 ctggcattcc agatggcctt cctgcggcag tacgggcaga cagtggccac ctacgagtcc 1981 tgtagcactg ccgcattcaa gcacggccgc actgagacca tccgcccggc ctccgtctat 2041 acaaagaggt gctctgaggc ctttgtcagg gagccctcca ggcacagtgc tggtgagctt 2101 cagcagatga tggttgagtg ctccaagtac catggccagc tgaccaaaga agcagcaatg 2161 ggccagggct ttgaccgaca cttgtttgct ctgcggcatc tggcagcagc caaagggatc 2221 atcttgcctg agctctacct ggaccctgca tacgggcaga taaaccacaa tgtcctgtcc 2281 acgagcacac tgagcagccc agcagtgaac cttgggggct ttgcccctgt ggtctctgat 2341 ggctttggtg ttgggtatgc tgttcatgac aactggatag gctgcaatgt ctcttcctac 2401 ccaggccgca atgcccggga gtttctccaa tgtgtggaga aggccttaga agacatgttt 2461 gatgccttag aaggcaaatc catcaaaagt taacttctgg gcagatgaaa agctaccatc 2521 acttcctcat catgaaaact gggaggccgg gcatggtggc tcatgcctgt aatcccagca 2581 ttttgagagg ctgaggcggg tggatcactt gaggtcagga gtttgagacc aacctggcca 2641 acatggtgaa accttgtctc tactaaaaat acaagaatta gctgggtgtg gtggcatgtg 2701 cctatatccc agctactggg aggttgaagc agaattgctt gaacccagga ggtggaggtt 2761 gcagtgagct gagatcacac cactgcactc cggcctgggc gacagagcga gactgtctca 2821 aaaagacaaa aaagaaaaaa aactggggcc tgtgtagcca gtgggtgcta ttctgtgaaa 2881 ctaatcataa gctgcctagg cagccagcta caggcttgag ctttaaattc atggttttaa 2941 agctaaacgt aatttccact tgggactaga tcacaactga agataacaag agatttaagt 3001 tttaagggca tttaatcagg aggaaaggtt tggaaaacta actcaggtgt atttattgtt 3061 taagcagaaa taaagtttaa tttttgcttg
SEQ ID NO: 3
CPT-2 A 606760.9| Human DNA sequence from clone RP5-1024G6 on chromosome 1, complete sequence (CPT-2, camitine palmitoyltransferasell)
1 gctgtgtcgg aggaagtcag caagtggaga atagagaatc ccacccctcc tctggagcag 61 agaactccct gggcctggtg tttggagaac acgcctggga aaccccggtc tccagcatcg 121 agtctatgct cccctgcaag gcactttcaσ ccttttcctc accctttcag cattacctcc 181 tactccttcc gtcacccctc cagctccaat gacaccaaac cactgcaggg tcctggaacg 241 ctgcatcctg tctcaggctt ctgcaccttt gcctgtgcta tttccttggc ctagaatgtc 301 cttccttgtσ atgaaagtta caggttaaat ccccctcttc ttcgaagcct tccctgatta 361 ccctagatac aataccttct ctttttctca ctctaactca ggcccttcac agtcaccagc 421 tggggattca cctagctccc ttttaagtgg ctctgacaag gaaataagaa tctatgaaaa 481 taaaatcaaa tctctgtttg ttaccatgtc atttgaaatc acctcaatgg agaatcctca 1 541 aagttggagg gtatattggc aggggcaggg gggtgctagg gatagcctga ggagcaaggt 601 gttgtataat gggcagcaag tggcctcaga gatgcttctg gggaggcttg agctgcacag 661 actgagatgc tatggcaaag aagagacatg gtgttggcga aaataaatgc caagtcacag 721 gtgcagctgc ctcaccctgc agaagcaggc gtgcagttga gctgttcttc accaggccct 781 ctgcttgggt tatgctgtgg ggagagcagc aggggttgac ttatttgcta atgattaatg 841 attaatgatt cgccagggct acaggcgggg ccaacccagc ctgggaaggc ggggatagga 901 aggcttcσca gaggagacgt ggtttaggca gaggcctcaa taagccaggg aagggggtgc 961 tggtcaaggg agaggggaga cgacagtctg atttaggccg gaggcgtgac agcagggcct 1021 cccagggcta gcagtgcatc ggtgggctgc agtggccatc ggggctgggg ccttacacct 1081 tccaccatgt gtcaaaatga gtttaggtct ggccgggtga gctcccatct gagtctgtcg 1141 tgacgacagc tcggggtatg ttggctgctt tccagagaca taccagaggσ gccttaatct 1201 ccctgacacg tcttcccagc tcgctggaag ctgggccctt ccgggaaggt tttctgtggg 1261 caacaaatgc agctgatcca gctgggtgtg gattcctgcg agctttagtc accgaggggc 1321 tgtcctgacc tcgctgaggg ctagtccttt cccacatttg cctcagagga tgggagaaag 1381 tgactctgtg gtggcaactc agacacacgc cttccttttt cccttccagt cccccgtcta 1441 aatctgtcac ttaatggaaa tgaggcctgg gcgcccataa gcccctgagc cgctctgtgt 1501 tgagcaccga ctgtgtacca ggctctggct gggtactctg acaccttcac ctagaagggc 1561 cctgaccagg gggagccagg gacccctcca cattcactgg gtcagtcaag cctgggggct 1621 ctaagtctgt gcagtacaat tacatagcat ccattacact acttaaattg aaattaatca 1681 aaattaaata ggaccaggcc cagaggttca tgcctgtaat cccagcactt tgggaggctg 1741 aggtgggagg atggcttgag cccgggagtt tcagaccagc ctgggcaaca tggggagacc 1801 ctgcctatac aaataatttt aaaaattcac tgggcatggt cgtgtgtgcc tgtggtctca 1861 ggtacttcgc aggctgaagt gaaaggatca tttgaagcct gggaatttga agttgcagtg 1921 agccgtgatg gaactgcact ctatgctggg caacagtgta ggatcctgtc tcaaaaaaaa 1981 atttatatag tttagaattc agtccctccg ttgcactagc cacatttcaa gggctcaata 2041 gctgtatgtg gccagtagct accatgttgg acagcacagt tagagaacgt ttccatgatc 2101 acagaaagtt ctactgaact ctctacagtc accctgaacc aaattcaaag ctcagccttt 2161 ggcttggaag gtgtgcgact ttgccgaagt tagcgaacct ctcagagcct cttttctgtg 2221 cctataaaag cccatgcact ttccattgca tcatacttcc tctcatttgσ atataaaagt 2281 taggacaaag tataaagtta aaccctccag ccagtttaga ttaggtttcc aaattagtta 2341 ggatttttgt taataaatac taggaaacta aatcaagctg gctttggtta aaagggaatt 2401 tataagcagg gctgactgtg taatttgtga ggσccactgc aaaatgagca cgtggggctc 2461 ttctttccaa aagcaggaaa aaagtgcatc aaaggtacta aaatatatag ctttatttct 2521 tccacagttt ctσtctctca acttatcatg atgtttttta tttgtgattt tgtcattctt 2581 aagtaaataa aaataacaat tttaaattag tagcattaac tttatcattc acσttttttt 2641 tttttttttt tttttgagct ggagtcttac tctgtcaccc aggctggagt tctgtggctt 2701 gatctcagct cactgcaacc tctgcctcct gggttaaaga gaatctcctg cctcagactc 2761 ctgagtagct gggattacag gcgcacacca ccacgσccgg ctaatttttg tatttttagt 2821 agagatgggg tttcaccatg ttggtcaggc tggtctcgaa ctcctgacct caagtgatcc 2881 gcccaccttg gcctcccaaa gtgctgtgat tacaagcatg agccaccgtg tccggccctt 2941 catcttcaca ctcactgtgc aatgccagtt ttaaatgcaa atataagagc atttaactca 3001 catgcagaat caccaaagtt atacagtttg tatttagtag ctcatacatg cgtgtgtatt 3061 tcattttttg ccagatggtg gaaatgctgc acaaaactaa tccaactgtt tttatttcac 3121 ttctcaatgc atatccattc catctgtcct ctctaccttt gactcactga tgagtaagga 3181 agaactggaa agaaaaggaa ctctggtggt cctctcattc ccttgctgtt gatgttatca 3241 ctttcagtgt ttaagtagtt ggctaatgca ggtgagtaac actagtaaga aaggatatga 3301 taaaattcct tggtcgtttg catttttaga atgcaatttt ttgttcttcc tatgttcgaa 3361 acaagttctg gtttgaggaa agtgaggctt ctcgtgagtc ttggtgcctc tgcttactta 3421 gctgtggaca taacacactt acctgacacc tatttgagtc ttgctgaact cccatgcgtt 3481 gccagtttaσ cagaactσtg tgctcatggg acattacaca cgctgtatga ggatggagtg 3541 gcaactacca gtggcggcat gtatattgga cgtgtttttt ctgtttgtgt gtatactcta 3601 ttgtcccatc agactttgct tataagacac aagttcaaag ataaaattat taagaattta 3661 gtgacagtga caacagagca ttaaaccaag cacaggggcc cttctgagca tggggccctg 3721 tgctactgcg cagatcatag aaccaggaaa ccggtcccat ttataagacc aggtgagcat 3781 gggttttgca gaacccaagg acaagagcag aactgaactg caaagaccct ctgaaccagg 3841 tacttgattg ttaatggaat tatctctcac accagctctc ctttctacat gtctgatttg 3901 tccattcatt cttcattcaa catatatatg ttgagaggtg gcataaggta ttgattaaga 3961 gcacaaactc aggaaccaaa tgacttgtgt ttgaatctta gctccttcac ctactctttt 4021 tggaactgta ggcaagttac tctgtgttcc agttttagtt ttctcatatt gagtgtaggg 4081 ataataatat tctaccttat agggttgtta taaggagcaa atgaattaca tgtatgaagc 4141 ttaagacagt tgtctgatca tagtaagcac tatctatcta tctatctata tctatgttac 4201 tattattact atgtgccaga catattccgg acacttggaa tactgtaata aaccgaaata 4261 gacaacaatc cctgctttta tagagcctac atttggtgat gacatttatg ttacattatt 4321 ctttctctaa tgaacccatc tccactacta ctgtggtcca cagggaggaa gcatggccac 4381 cagcagctct gtttcactcc agtgccacag ttctcaggga aggttctgac tggcccagtt 4441 tagaccaatc tcctgcagcc agtaggggca gggagcaggg tcacattatt tacagttgct 4501 gcttctatgg taactctgta gatgtgtgta gtagcagtta gaaaagtgga tacatgaggc 4561 agacacagca aaatatctag tacattgtcc caggcactca gctcttggca tggcttgctt 4621 agtaaaacct tggttttσtg ttctttcttg tgtaaaatgc ctaacatctt atatccagtg 4681 aggctgctct agaacttagg gtcagtggct cgaggttcct tgttgcttgt cttcttctct 4741 gatgtctgcc tcggcccttt atggcagcag gcacctgggg cctσacccac agagtgcaca 4801 ggattcacca atgttgttga gttgttgatt catcaatgtt gttgaaaaaa tgttaatttt 4861 cttctctgtg atatagcatt ccatgatatg aatggaatat tatatataag atactgttta 4921 tgaacgtttg tggttttttt ttccagtttt tgaccatcat tttaacaacg ctgctagaaa 4981 cattcttgaa tactaatgta catgtacaag agtttctcta ggatatatac gtagcaatag 5041 aattgctagg tcacagatta tgcagatggt caacgttagt aggtaataac tgtttccaaa 5101 ttagttttac caactaatat gttcacccac aatgtctgta agttcccatt gttccgcatg 5161 gttactgaca tttgatattg attaattttt aactcttgcc aatctggtag gtgtgaaatg 5221 gtgttccata gtggtttaaa tttgcatttc cctgattagt gagactgaat atattgtcct 5281 atgtttgtga gtcatccatg cctcctcttt ggtgaaattg ctgttcattt gcctattttt 5341 aattgggttg tttgtctttt cacatacatt ataaatattc tttatataat ctggatatta 5401 actctttatt gtttatatgt gttttcctgt ttatgactta tctgtcttta gataaacaga 5461 agttctaact tttaatgtaa ctgaatctat cattcttttt tgttatgact tgtctctgtc 5521 ttattttaaa aacctcccac tccagtaaag ttattcttct gtgtaaattt ctaagagtag 5581 tttacttttc cttttctcat acaggtaatt aactaacctg gttaaagact gatgtaagag 5641 tctaatatcc cgttttcttt aagatctact aattgtccta gtatcacata ttgaaaaatc 5701 tatccttcca cctgaaacta aaatggctgc tctgaaataa aatcaagttc tgtatatgtc 5761 tgggtctgtt tctgggttcc cattggttgg tttgtctata tctttgtcaa taccactctt 5821 gtctggatca ctataagtta atgataattt ttgatacttt gcaaggcaag tcctatcttt 5881 gtcttcttca ggaatgtatt agttttcact gggcatggtg gttcacacct gtaatcccag 5941 cactttggga ggccgaggtg ggtggattgc ctggggtcag gaattcaaga ccagcctgac 6001 aaacatggtg aaaccccgtc tctactaaaa atacaaaaat tagcagggca tggtggcgca . 6061 tgcctgtaat cccagctact tggaaggctg aggctggaga atcacttgaa cctgggaggc 6121 ggaggttgca atgagccgag atggcgccac tgcactgcac tccagcctgg gcaacaagag 6181 caaaactctg cctcaaaaaa aaaaaaaaaa aaaggaatgt attagtcttc aataaaacgt 6241 tttaaaggaa aacttgtcaa gttccagaaa aaaattgaga tttttattgt aattgcatgg 6301 gaacttttaa atcaatttga gagaatgaac atctttatga tattaactct tccaatttgt 6361 gaacatatct ttcaatttat ttagatcttg tttctatagt tttattttgc tccataaaag 6421 tgttgaataa ctttttaaag atctattctc atatatctta tttttatgct actgtaaata 6481 gcgttctgtt ttattgcatt ttctgttttt tgctatagac ataaaattga ttattgcacc 6541 ttgatttttt tcttttcttt tctttttttt ttttgagaca gagtcttgct cttttactca 6601 ggctgaagtg'cagtggctct atcttggctc actgcaaact ccgcctcctg ggttcaaggg 6661 attcttctgc σtcagcctcc cgagtagctg ggactatagg catgcgccac catgccctgc 6721 taatttttgt attattagta gagatggggt ttcaccatat tggccaggct ggtcttgaac 6781 tcctgacctt gggatctgcc tgccttggcc tcccaaagtg ctgagattac aggcgtgagc 6841 aaccgcacct ggcctgcacc ttgattttgt attctgttga ctgactatat tctcttaatc 6901 tttggggttt tctatgtaga taagcatatc atcagcaaac aataatagct ttgcttcttc 6961 catttcaatc cttacaccat attttatata tgtatattat atatgtatat atgttatgta 7021 ttttttattt gttgcttgct tgcttgtttg tttgttcacc ttacagccct ggctgagccc 7081 tctagcacaa aactgaataa aaatcatgat gtgaggcact caggtcttgg tcttgatctt 7141 aagaggaatg ctttcaacat tttaccatta gtattgccat tgctataggg ggtttttgcc 7201 catgcccttt atcagattaa gaacgttctc ttttattcct agtttgttaa aaaggggttt 7261 tgctttttgg ttttttgatg ttgaatttta ttttatttat ttttattttt tgagacaggg 7321 tctcgctctg tcacccaggc tggagtacaa tggcatgatc atagctcaca gcaatctcca 7381 cctcctgagc tcaactatcc tcccacctca ccctcccaag tagctgggac tacaggcatg 7441 cgccaccaca cctggctaat ttttgtagag acgagtttca ctatgttgcc caggctgctc * 7501 tcacactcct ggcctcaagt gatccaccca cctcagcctc ctcacgtgct gggattatag 7561 gcatgagcta ccgtgccctg ccagatgtta aatttttgtc aaattatttt tctcttttaa 7621 tttattaatg tggtgaatta tattaaataa ctgtgaaaca ttgtaacaat cttgtataac 7681 agaaataaac acaacttggc catgatttct tcttcttatt gttatcatta tttttattta 7741 aacgtggttg ctttatattg cacttttaaa actcacaaaa agctttacaa tatctgcatt 7801 cctctactta atcatcaaag ctttatggta agacaatgaa aattttattt catcaattgg 7861 gcatactaaa aaacaatgaa aaattaacaa acaaatctcc ttaatcaaga acattccgta 7921 aaatacacac tctggcatgc gtctgaattc atccctccta aaattagact ttaaaaggct 7981 ttaaaaaaaa tctcaaacag atttcaatac tgactagcct accagaacaa agctgatagc 8041 aagctataaa cagctttcaa tgttgaatgt aatttggggg aagtggagaa gaagaaatta 8101 tctgctgaac ctacatttaa gtgcatctgt tagtaagact tctctaattt aatgaatttc 8161 aacaaagtga acaagttctt tgσctttggt agtttctcgg attttatttt taaacttgtg 8221 acatcttgac taaaggaatg gaatcctggg actagaatat ttaaggaaga ggacaacatt 8281 gaggcgggaa agaggaaaaa taagattagt actttcttag atagctaaaa tgggtaacaa 8341 ataatcccag ctactcagga agctgaggca gagaattgct tgaacccaag aggcagagtt 8401 tgcagtgagc cgaaatcacg ccattgcact ccagcctggg caacatagcg agattccatc 8461 ttaaaaaaaa aaaaaaaaaa aaaaagaata ccagagttga tatgtagggt ttagtttgac 8521 ttatgttttt aaaaaattag ataagtataa catctaaatg gcaaatagaa caattaaaga 8581 tggtctcatt taggaaatgt taaaaactaa ttatcctcaa ttatgtttta aatttgtgga 8641 atgacatagc agatattttg agcatcatta taggatccaa ttaaaattat gcatactgct 8701 attttσactt ttttttttcg agatgagatc ttgcttctgc tgcctaggct gaagtgcagt 8761 ggcacgatca tagctcattg caacatcaaa ttcctgggct gaagcgatcc tcccatctca 8821 gccttcagag tagctaggac tacaggcaca tgccaccatg cccagctaat tttttttttt 8881 ttttggtaga ggctgaatct cactatgttg cccaggctgg tctccaactc ctggccccaa 8941 gcaatcctca tgccttggct tcccacagtg ctgggattac aggtgtgagc cactctgcct 9001 ggcctattta cacttttttt ttttcttttt aacccaacta ctcaacgtgg catattttca 9061 cttttaatat aatttatata tacctgggga agctcttttt gatattatca gtagaggcca 9121 ctaaaaataa tgccagaatt ccagtgagaa gagagtagaa atggaaagaa aatgggagga 9181 taaagaaatt gggtagtaat aagaaacagg atttttaagg ttttctcact agttaactaa 9241 tgccacaaaa ttgcgtattt tggctcaatg tcagtgggct gctggaaggg accaggaaat 9301 gagtgcaata tcctaaccat cccaggtaga ttcttaacta acccatgatt tggatggctc 9361 acttgtgaag ggagtgcttt ggcctcctcg cttcctttct tccttttcct ttttttattt 9421 tttttttttg agactgagtc tagctcttgt ttccgagcaa tttttgagaa atctcaactt 9481 taaaatatcc ctcaagttgc cccctttcat tagtcttgta aataatattg tttaagactc 9541 acacattggt gagagtcagg aattattagg attattttaa tagcagacat tgagttcatt 9601 tacttggaaa gaaaaatttt attccgaggt gactttcaga gatttaagtg ctctatttta 9661 ccattgaatg agaatttttc tcaaagcaaa tattctctaa gatgctagag tattcagctt 9721 attgggatag taccctttaa cttattaaaa gttacaaagt ctaagaaaaa gcatgcaagt 9781 cttgagaatc actgctgtga attctaacag ggagggcctg aagcctggaa gcctggctga 9841 cagtcctgca gaccagagtg gggacttgtg gtgcctcttc cagtctgccc atggccgccc 9901 atagaccatt tggcatgtac ttcctcccct ctgaggtcca taaaagccct gggatcagcc 9961 agagaagggc agaggatgga gaggacagag agatgactgg cgactggatg atcagctgca 10021 gagaggagct gaaagctcct gctgaaagct gggaagccaa ccgggacctg ccttcagaga 10081 gcagccaccc tctccagggc ctcctgtctg ctgagagctg aacgctggat gagacaacct 10141 gcctacagag aggagctgcc cgctgagggt ctcctctgaa ctgtcctaac actcaacaaa 10201 gcttctcttc gtcttgctcg cccttcattg tctgagtacc ttattcttcc tggatgcagg 10261 acaagaactc gggcaaaggc accactgccc acagaagttt ctggccagaa aagtgacacc 10321 ccaaagatcc cgtaacacta tgagatgcaa agactacaaa tgtttaagtg gaatgatctc 10381 taacctgtaa attacactcc tgtaacaagc aaatgattac atactgtgga agactacaga 10441 acataagtac agaaagctgc tctccaaggc tgcattctca aagcttgaaa agttaattgg 10501 cccatcattt tggtacagta ggtagctagt caagcatgag cagggcagga gagggctccc 10561 tatacctcac cacaaatgtc aggcaaccat caggtgatgg tcaggtggtt gttaactgtc 10621 tgtttaaaat aataattggt tgcagctggt gccagggaaa ggccgtctcc cagtagatag 10681 aaacacctga aacaggtggt cagctgctta atctcaggag ttgggcaact gggctcaagc 10741 atgctcacta agaggcaaaa tggtgagttt aactgataca tgactttcca gggacattcg 10801 gctggtaagg gaagaatgcc tcaagtgagc atgcatacaa ctccagtgaa cacactgtgc 10861 acactcccct cccaagggct ggcaggtcac tgtgcacacg gacagcccaa gggaagaatc 10921 aggggagaag ggacgcaagg catgccaaca tgtacaaccc caagtcaaag gtgaaatggc 10981 acacttgatc actcaagttg cccaggtggc tctttcccaa gtgtacttta cttcctttca 11041 ttcctgccct aaagcttttt aataaacctt cactcctgct ctaaaacttg cctcagtctc 11101 tccctctgcc tcgtgcccct cggtcaaatt ctttcctctg aggacgσaag aattgaggtt 11161 gctacagacc tgtacagatt cgccgtcact aataatttta gaaagaaaaa aagatgaaca 11221 tggattagga gggtctacat gtgggaaaaa aattgcaact aagatatttt agagagccca 11281 cctctagtaa caaaagaaaa aataggcccg gcacggtggc tcacacctgt aatcccagca 11341 ctttgggagg ccgaggcagg tggatcctga ggcctcccca gaagcagatg ctgσcatgct 11401 ccctgtacag cctgcagaac tgtgagccaa ttaaacatct tttccttgta aattacccag 11461 tctcaggtat ttcttσatag cagtgagaga acagctaata cggtagσcat ctctgggggg 11521 acatcgagga ggctctcatt ctcctagaag tctttccaat tcatattatc ctcagaccat 11581 agttcatctc ttctgtaagc cacaactctg ggccaccagg aaacccagta catgtagttg 11641 tctgcttgcc accgctcaat tttttatttt tatgcattat gtataactat gtatgtttcg 11701 taacttccca acataggctt tcctaattat ctttttgttc cttttataaa caagctttat 11761 tgaggtatga tttacatact gtataattta cccaaagtgc acacttcaat cgtttttagt 11821 aggtttactg agttgtgcaa tcatcatgac agtcccattt tagaacactt ccacatcccc 11881 aagagcccct catgcccact tttagccaat ccccattccc atctccaaca ccaggcaatc 11941 actaatatgc tttccatctc catagatttg cctcttctgg acattttata aaaatgcagt 12001 catacaatct gggttctttt ttttctcatt ttactctgca tatgttctag gctcatccat 12061 gtttgcagca tggatcagta gttactccct cttaccattg aatggtaggt actacattgt 12121 atggatgtac cccatttttt tttctactca ctgattgatg gacatttgta ctcacatttt 12181 ggcttttatg aataatgctg ctatgaacct tcatgcaaaa gcttttctgt agacatgttt 12241 catttatctt gagtagctac ctatgagtcc cattgctagg ttgctggata catttatgtt 12301 taccttttta agaaactgcc aagctgtttt ccaaagtttc cgcaccattt taccttcctg 12361 ccaccaatgt atgaggattc tgatgtctcc acagtgttgc ccacaggtat tattgtctgt 12421 gttcttcatt acagctgtcc taatggccat gaagtggtat ctcattttgg ttttaatttg 12481 catattacta atgactaata atgttgagca tcttttcatg tgcttattaa tcatttatat 12541 atcttcttca gtgaagtgtt tactcaaatc tcttccctat tttaaaaatt aggggctggg 12601 cgtggtggct catgccttgt aatcccaaca ttttgggagg ccgaggtggg tggatcacga 12661 ggtcaggaga tcgagaccat σctggctaac atggtgaaac cccattttta ataaaaatac 12721 aaaaaattag ctgggcatgg aggcacgcag ctgtagtccc agctactcag gaggctgagg 12781 caggagaatc gcttgaaccc gggaggcaga ggttgcagtg agtcgggatc gcgccactgc 12841 actccagcct gggtgataga gcgagactcc atctcaaaaa aaaaaaaatt gggttgtctt 12901 cttcttactg cgttgtaaga gttccatata ttctggatat gaaagccttt ttgttgttgt 12961 ttgttttgtg tttttgtttt ttggagacag agtctcactc tgtcacgcag gctggaatgc 13021 cagtcatatg atcatagttc actgaggcct caaattagtt cctgggctca agcaatcctc 13081 ctgcctcagc cttccaagta actgggacta caggtgcatg ccacσatgct tggctaaaat 13141 ctttatcagt ggccaggcgc agtggttcac atctgtaatc ccacactttg gcaggccgag 13201 accagcggat cacctgaggt tagaagtttg agaccagcct ggccaacatg gtgaaacccc 13261 gtctgtactg aaaatgcaaa aattagccag gtgtggtggc aggcgcatct aatcccagct 13321 actcaggacg ctggggcagg agaatcactt gaacctggga ggcagaagct gcagtgagcg 13381 aagaccatgc cactgcactt cagcctgggc aacagagcaa gattccgtct caaaaaacta 13441 aactaaaata aaataaaaaa cctttatcag aattatgatt tgcaaatatt tactcccagc 13501 ctgtcgctta tctttctcat ttacttaata gtgactttga aagtataaaa gtgtgtaatt 13561 tttattaact ccaatttatt gatttttttc atttatgagt tatgctttta atgttgtatc 13621 tgagaactct gcttaactgg agatcacgaa gagtttctcc tatgctttct tctaaaagct 13681 ttatagtttt atcacttaag tttaggtcta caatccattt tgaattaatt tttgtgtgtt 13741 gtataagtta aggatccaaa ttcacctttg tggttgggtg tgatggctca cacctataat 13801 cctagcactt tgggagttga ggcaggaaga tggtttgaag tcaggagttt gagaccagcc 13861 tggccaacat agtaagaccc ccatctctac aaaaaaattt tcaaaattta gcctggtgtg 13921 gttgtgcatg ctggcagtcσ taactactca ggaggctgaa gcaggagagt tcaagagttc 13981 aaggtcatag tgagctatga tcatgcttgc attccagcgt gggtgacaga gtgaaacctc 14041 atctcaagca atcaatcaat cagctcatct tttttatgag gataaccaat tgttccagca 14101 ccattattgg aaaaccttgt gttatggttt ggatagttgt cccctccaaa tctcatgttt 14161 gaaatgtgat cctgagtgtt agaggtgggc ctagtgggag cagtctggat catggggatg 14221 ggccgctcat gaatggcttg gtgccatcct cgcagtagag tgagtttttg ctctgttagt 14281 tcactcaaga gctggttggt ttttgaaaga gtctggtgcc tcccttcttt ctcattcttt 14341 tgtgctcttt cttgccatgt gacacacctg ctccccctca ccttctgcct ggagtaacag 14401 ctgcctgagg cttcatcaga agctgggtgg atgctggagc catgctttta tagcctgcag 14461 atccatgagc caattaaacc ttttttcttt ataaattgcc tagtctaagg tattccttta 14521 tagcagcaca aaatggacta atacaccttg ttgatttctg ataaccctat tgtggtcaga 14581 aaatgagaat atatgatagt aatcctttga atagacgtgc tttatgatac tcagttttca 14641 taaatgctcc acatgtgctt ggaaagactg tgtattttgc agatgagtcc agtgttatat 14701 gcatatccat tagattaaac ttgagaatcc attcgttcaa atctcctgta tctgtgctca 14761 tttttttttt tttttggtct acttgatcta tcaattgatt gaaacatgtt aaaatctacc 14821 attctgaggc cgggcacagt ggctcacgcc tgtaatccca gcactttggg aggccgaggt 14881 gggcggatca cctgaggtta gaagtttgag accatcctgg ctaacacggt gaaaccccgt 14941 ctctactaaa aatacaaaaa caaaattagc cgagcatggt ggcaggcacc tgtaatccca 15001 gctactcggg aggctgaggc gggagaatgg cgtgaactcg ggaggtggtg cttgcagcga 15061 gccaagatcg cgccactgca ctccaacctg ggcgacagag cgagactccg tctccaaaaa 15121 aaaaaaagtg tttgattagg tcaccttctc catgattcct tcattagtaa gttgttccca 15181 ggagtaattt gtgaacactg tggggacttg gcctctgcct tctcagagct tagcgttgag 15241 cagcagatag aaaatgtacc atcaacctac ttacaaatct gcaaatgggc ctgccttcca 15301 gaatttcact tgtaaatcca tgtttagtta ttagaataat ttattctttt gggggattaa 15361 aaagttatac actcttctgt atattggatt cttggcccca ttgatggaaa aaacatttct 15421 tcctttatac ataattattt acagctactt atgatggggt tgtggctcag aaaatccatc 15481 atgaagtcaa agaatggtta agtcaagcca acctatgttg ggaaccacct gtatagtgat 15541 atatattaat atttatattg aaaaatcata ggagaaaaca tgtagctcaa aaaaaaatac 15601 tactttcttt gtgcctgaca cagagtggat actacataaa tatatgtata caaatattat 15661 agataaaact aactttcttt tggtatctgt taccttcttt aattttcaaa gttgatgcat 15721 aaggtggatt ataggaagaa aaggtggttg agggccacag gcagagaagc tggttccctc 15781 cctcaagtcc aagaggagag ctcaggccag agattggaga tgaggccaaa gaggtctgct 15841 ggaccctgaa ccagaatgag aacatctgaa tgacttctga gcagggcagg ggcccaggca 15901 tcgtggctgc cagtcacatg gggtgtggga agcctggcct gggccaaagg tccagggcca 15961 cagagtattg tcctatgaag gcaagaaggc ccctagccct aggcccctcc ctgttcccac 16021 agtggggttg tgtacatgct cactcggatt ccacagggca ggggtcacat agctgaggcc 16081 acaaagccag tatggggaga gcctggtgct cccccagcca cctgactatt tccattccct 16141 gtggctggtc cacagggaac catggcatcc tggttgcagg tacccaccca gagaggagtg 16201 gaggggaaag gaaaaagggg tgccttttcc ttgagggaag gggcctggtc atttgcttct 16261 gataggccct gatcagccct gtaataaatt ttgaatgagt tactaaattc tgattttcaa 16321 gaactaaatt ttaggtagaa aacaatatta aaaattaaaa gtcaaaccaa aatttaaaaa 16381 actacttaag tgaccaggca cggtggctca tgcctgtaat cctggcactt tgggaggcca 16441 aggtgggtgg atcacgaggt caggagtttg agaccagcct gaccaatatg gtgaaacccc 16501 gtctctacta aaaatacaaa aattagctgg gtgtggtggc gtgctactgt aatctcagct 16561 acttgggagg ctcaggtagg agaattgσtt gaacctgaga gacagaggtt gcagtgagcc 16621 aagatcatgc cactgcactc cagcctgggc aacagagtga gactccgtct caaaaaacaa 16681 aacaaaaact acttaagcat aagtcaaaaa acaagagaca aactgggaaa aattatttgc 16741 agctcatatc accaaggatt aattcσctta atatataaaa agcttctaga aataaagaaa 16801 tacaagatta ttaattgatg tggttttgct gtgtccccac gcaaatctca tcttgaattg 16861 tattatagtt cccataatcc ccatgtattg tgggaggtaa tttaatcatg ggggtggtca 16921 acgtcatgct attctcatga cagtgagtga gtt'ctcatga gatctgatgg ttttataagg 16981 ggσttttccc ccttttgctc ggcacttctc cttgttacca ccttgtgaag aaggacatgt 17041 ttgcttσctc ttctgccacg attgtaagtt tcctgaggct tccccagcca tgctgaacta 17101 tgagtcaatt aaacctcttt cctttataaa ttacccagtc tcaggtatgt ctttattagc 17161 agcatgagaa tgaactaata cctcaatctc acagaaaaaa gagcagaaga cacaaaaagg 17221 tagtttaσgg tcaaagaaat acagatggct ttaaacatat gcaaaggtgg gcaacttcat 17281 tcaataaata tagattaaaa ctacactagg tggctgggca aggtgtctca cacctgtaat 17341 cccagcactt tgggatgcca aagtgctagg attgctttaa cccagcagtt caagaccagc 17401 ctgggtaaca tagagagact tcatctccac aaaaaaataa aaaattaact gggcacggtg 17461 atttgtgctc gtagtcccag ctactcggga gactaaggtg aaaggatctc ttgagcctgg 17521 aaagtcgagt ctgcagtgag cagtgatcat accactgcac tccagccttg gtgacaaagc 17581 gagaccctgt ctcaaaaaca aaacaaaaca aagtacacta ggctacaact tttcacctca 17641 cagactggca aaatcccaac acattctgtt ggtaagtttg tggtgaagca aaatgctctc 17701 attcattgta gatgggaatc cttaaggagc agcaatttga caacatctat gacatttcca 17761 agtttattta ccctttgatc ctgcatctca catctaggaa ttcatcctct gatatgcaca 17821 agcacgaaat gacacatgtg caaggttagc aactgccata atagcaaata gtaacagcaa 17881 aagatggaaa taacctacga tcattcagtg ggaattggtt agtctgtgat acatccacac 17941 gatgacttca tagggatgta tagaaaataa taaactttgt acctaaatgg aaagatctct 18001 agcatacatt aagtaataaa actatggtgc agattagtaa ttgtgtaaga aaagagaaaa 18061 caagaataaa cacctgtgtt accagtattt atgaaagaga cattggaaag acacattaga 18121 aactaagagg aatgtgtgtt tattaacaga gagcagcggt tctcaaactt cagcgtggat 18181 tagcatcaca gggagggttt gttaaaatgc aaaccactgg ctcccgctcc tacagcttct 18241 gattcagtgg gtgcggagtg gagccacaaa acctgcattt cttttctttt tctccttttg 18301 cttttttttc ttttttcttt ctttctttat tttattttat tttatttttt gagacaggat 18361 cttgctgtgt catcttgctg tgtcacctag gctggagtgc agtggcgcaa tcctagccca 18421 atgcaggctc atactcctgg gctcaagaaa tccttccgct ttggcctccc aaagctctgg 18481 gattgcgggc gtgaaccacc gtgccctgcc taaaaatgtg catttctaac aagttcccag 18541 gggtgctgac gctgccagtc agggaaccaa gtttgggcca gaaaatggaa tggagttaga 18601 ggctggagca ggtcttctca gggtacatct tttctatttt gattttttaa aaacttgcaa 18661 atctattacc tactcaaaaa taagcttaat tcaaaaaacg tttaaaatgt tcaataaaag 18721 aagctgctcc tcagtcactc cctactttct tagcttgttt tgtttttctt tacaacaatt 18781 aatattgtac ctaaaattat gctatttttt tttttacttt ctctcccaac tagaataggg 18841 taaggacatt gtcttctatt tccctctatt tccaacaσta atattgtgcc tgccacgtag 18901 taggtactca agaaatagct gtttggccag gtgtggtggc tcacgcctgt aatctttggg 18961 aggctgaggt gggtgaatca cttgaggtca tgaattcgag accagcctgg ccaacacgta 19021 tttttctcta ctaaaaatac aaaaattagc ttggcatggt ggtgtatgcc tgtagtccca 19081 gctactcagg agactgaggc agaggaatct cttgaacccg ggaggcagag gttgcagtga 19141 gccgagaacg cgccactgca ctccagtttc agtgacagag caagactcca tctccgaaga 19201 aagaaagaaa gagagaaaga gagaaagaaa gagagagaga gaaggaaaga aagaaagaaa 19261 agaaagagag aaagaaaaag aaagaaagga gggagggagg gagggaagga aggaaggaag 19321 gaagggctgt tgaatgaata aagggaatga atgaattctc ttagtcttca gtagatcagt 19381 gatcttggta agtcactgga gagcttttaa aacataccca tatccccatc aaatccccag 19441 ttctgagtga attgtttggg ggtggggccc cgcattgagt tgagggtgat gggagcccct 19501 ggtctaaacc acagctatgt agagacttat ggtttggatt gtgcatataa agtgagtata 19561 ttagtatata gaccctgctg catttttgta cattgctttg ggggctggtt ctgaggctct 19621 ttttgatctg gagaccctaa catcctttcc ctctcttttc tctttcagtt gcctacagat 19681 ctggaagcct tgctgaaaag acaccttaat ggcctagcag ctcttttagg caaggagcaa 19741 ttcagatgtt gaatgatgga acacaaaaac ccacagcaga catggtggct gatgcttgta 19801 atcccagcac tttgσaaggt tgaggtaggg ggattgcttg agctcagaag tttaagacca 19861 gcctaggtaa cacagtgaga ccccatccct acaaaaaatc aaaaaattag ctgggcatgg 19921 tggtgcacat ctgtagtccc agcttcctgg aaggctgagg caggaggatc tcttgagccc 19981 aggaggtcaa gcctgtggtg agttgtaatt gtgccactgc actccaacct gggtgaσaga 20041 gcaagacctt gtctcaaaaa aataaaataa attggtgttg cggttaatgg tcttcatgta 20101 ggtttttccc gctgtggagc agggcaggac aatgagtctg gatgctggct cccctgcatt 20161 ttagttctgc agtgaagttg tggggcctga gggctcagga cactgtgctg caatcatgct 20221 gcatagtcag agtgaaaaaa gactgggtta gggagtcaca gagtcacagc atccagcccc 20281 attggccatt cagcaattct gtgaccttcc atctctggtc agtttcctca tctgtaaaat 20341 ggggatgcta atgcctgtct cttagggcca ctgggagaat gaaatgttag ttatttttcg 20401 gcttttcagt tgagttattg catcagctac gttcgtagtt tacccccttg gtttattaag 20461 taatagttgt aaaagtttat aacaggtcac gaattggcgg cacctttgta ttgattggca 20521 ctcaaagtga cttacaaaaa cttggcttaa ttgccaacat ttaaaaacta gggatcttac 20581 ataaaaatct ggatttgtgg cttcattgga aacatctgca tgaccacaaσ tgctggagct 20641 gagagtcagc tgcttgttcc tgatcccaaa ccccatgact cctggacacc ttctgcctcc 20701 taccccttat ctccctggat tccctgagtg gcttgctgct ggaggctgtg agtacctagt 20761 ttataacccc agttgataaa gtgctttcac ctgcttcatc tcattagact tttacctatg 20821 agggaggtgt tagtattgtt ccctttacag gagaagaaac taaagctgag atgttacagg 20881 acctactctg ggttagtaat aacagcaacc gcaataaata gtaatttgta ctggctgttt 20941 accatgtgcc aggcattatt ctaagcactt tacatgttta atttaattct ctcaatctta 21001 tcagatattg tcattattcc tattttatga ataaggaaat tgaggtagtg acaggtcaag 21061 tagatttccc aaagtcacac agccagaaag ctcaaaataa actgaagact tctgggtcct 21121 aatccacact tgttccagag tcctgcagtg caggctttcc ttcctttctc tctttctctt 21181 ctttaaaatg ggtgagtcta tggggcccag cttctggtaa gagtttgtaa gtgttgtttg 21241 gtgggagggg tgggctcgtg ttttgtagga tttgttccct gctgcctcσt cagcacctgc 21301 aacaatgcct ggcatgtggc aagagcacaa gaaagagtga aagccaatgg caacagggca 21361 acatcggcag ctttcagggc tccagtgtct ctaatgattg gcacacgggc gaagacctac 21421 tacgtggcat gcagtgggtg ggctcccagc tcttgagcag ctcaagtcca ggtaagaatc 21481 actgacaaat gaaattcaaa tatggggtgt gtgtggacat gagtcgcttg ccaaaaagtt 21541 acctttcccc ttaaaaataa tcaatgaccc acttgtgata tttgcattaa aggctaaaca 21601 ttgaataagg gaagtcaagg ctgcagtgag ctgtgattgt accactgcac tctggcctgg 21661 gtgacagagc aagaccctgt ctcaaaaagg acaaaaaaag aaagaaagaa aaagtccgcc 21721 aaacaaaaac cactcggatt tatgattcac ctcctttttg ctttaggaaa acaaattatt 21781 ggccataatt ctcaaaatgg agttggaaac tgagctgcta gcactggatg acctctatca 21841 agaaactagc tacatctcag gaacaagata gtttctgttc agttcagcca acccgagctc 21901 ctgcctgggc tgggcgttgg gctgggcacc gaggctgcac agctgctgag ctctggccct 21961 gcctccagga gctcagtctg tgggatatgt actgcacaga gacagctcgg gactctagac 22021 atagctcgga gggtaaggga agtcttcccg ggggaggtgt cagctgggct gagtttcgat 22081 gaactaatgt tgtccaggtg aataagggag agaatggata gaaaaagcgc aaggcagtag 22141 tgagactcat gagagatctg gaaacttcac agcttctgtg gttctccatg gacttgctgt 22201 tgtctgagtg tccacatgag tgaaggtgga agaatgggtg tgggctctct gtccaggcag 22261 gtggggtccc atcagggata atcagtatσt gcccagtaat gaagattgtt ttgacacatg 22321 caggtggtgc tgcactcttc cttccaacca ctgcccatta ggggacaggc cgagtcagtt 22381 tgtgcctatc ttgccctatc tccttcaatg aagaaagtga atgctgcaag taatacatgt 22441 tcattgtcaa aaactaagaa aaatgtaaat accccatagg ccaggtgcgg tggctcacac 22501 ctgtaatccc agcactgtgg aaggcaaagg caggtggact gcctgaggtc aggaatttga 22561 gaccaggctg gccaacacag caaaacccca tttctactaa aaatacaaaa aattagctgg 22621 gcgtggtggt gcatgcctgt aatcccagct actcaggagg ctgaggcagg agaatcactt 22681 gaacccggga ggtggaggtt gtggtgagct gagattgcac cattgcactc cagcctgggc 22741 aacaagaaca aaactccatc tcagaaaaaa aaaaagaaaa ttccccgtaa tccaaccctg 22801 agaaataact ttttagttta tattcccaaa tatttttcta tgtctaaatt ttttgttttg 22861 cagaaacata catattggtt tttttctttt ctgttgtggt aaaatataca ttacagaaaa 22921 ttagcaaaat catggaacca acccaagtgt ctaccagtgg ttgactggat aaagaaaata 22981 tagtacacat acaccgtgga atactatgca gcatgaaaag aatgaaatca tgtcctttgt 23041 agcaacatgg atggaactgg aggccattat cctaagtgaa ggggtggcct gcccctccac 23101 acctgtgggt atttctagtc aggtgggata agagacttag aaaagaaaga agacacagag 23161 acaaagtaca gagaaacaac agtgggccca agggaσcggc gctcagcata ccaaggacct 23221 gcaccggcac cggtctctga gttccctcag tttttattga ttattatctt cattatttca 23281 gtaaaaagga atgtagtagg agggcagggt gataataagg agaaagtcag caacaaacac 23341 gtgagcaata gaatctatgt catcattaag ttcaagggaa ggtactatga ttggacgtgc 23401 acgtaggcca gatttatgtt tctctccacc σaaacatctc agtggagtaa agaataacaa 23461 ggcagcattg ctgcaaacat gtctcgcctc ccaccatagg gcggtttttc tctcatgtca 23521 gaattgaaca aatgtacaat cgggttttat accaagacat tcagttccca ggggcaggca 23581 ggagacagtg gccttcctct atctcaactg caagaggctt tcctctttta ttaattcatc 23641 tcagcacaga ccctttacgg gtgtcgggct gggggacagt caggtctttc tcatcccatg 23701 aggccatatt tcagactatc acatggggag aaaccttgga caatacccca ctttcaaggg 23761 cagaggtccc tgcggctttc cgcagtgcac tgttcccctg gtttattgag actagagaac 23821 ggcgatgaσt tttaccaagc atattgcttg taaacatttt gttaacaagg cacatcctgc 23881 acagccctag atcccttaaa ccttgatttσ atacaacacg tgtttttgtg agσtccaggt 23941 tggggcaaag tggctggggc aaagctacaa attaacatct cagcaaagca attgtttaaa 24001 atacaggtct ttttcaaaat ggagtctctt atgtctttcc tttctacata gacacagtaa 24061 cagtctgatc tctctttctt ttccctacac ctaactgaca agcagaaagt caaatattcc 24121 atgttctcag ttatacatgg gagataacaa tgggtacaca tggacataca ggtggagaaa 24181 acagacagca ggaactacaa agtgggggtg ggctgacaaa ttccctattg tgtgcaatgt 24241 tcaatatttt ggcaaagctc aatatggtgg ggattgggat tctagtgtac ccatcactaa 24301 taaaaatcaa aataaaaaat caaatcacac tacacacatg caaatatgtg acatgatgga 24361 tattttaatt aggttgattt aattattctg taatgtatac atatatcaaa aaattccatt 24421 gtaccctgta aatatataca atcattgcca atttaaaaaa ttcattgtgg gccaggcgtg 24481 gtggctcaca cctgtaatcc cagcagtttg gggggccgca gcagttgaat cacctgaggt 24541 caggagttcg aaaccagcct ggccaacatg gtgaaacccc gtctctacta aaaaatacaa 24601 aaattagtgg ggtgttgtgg tgcatgcctg taattccagc tactcaggag gctaaggcag 24661 gagaatcact tgaacccggg aggcggaggt tgcagtgagc cgagatcatg ccattcattg 24721 cactccagcc tgggcaagag agcgagactt cgtctcaaag aaaaaaaata cattgtgaaa 24781 ttaaaaaaaa atactttctc ataaaattta caatttacaa ttttatccat ttttaagcat 24841 gcagttctgt ggcactgagt gcattcaaat tgttatgcaa cgatcaccat catccatctc 24901 cagaacttta tttttatttt tttatttttg tattttcttt tgagacaaag tctcactttg 24961 ttgcccaggc tggagtgcaa tggcacaatc ttggcccact gcaacctcca cctccctggt 25021 tcaagcgatt gtcctgcctc agcctcccaa gcagctggga ttacaggtgt gcaccaccac 25081 ggctggttaa tttttgtatt tttagtagag atggggtttc accatgttgg ccaggctggt 25141 ttcgaactcc tgacctcaag tgatccacct acctcagcct cccaaagtgc tgggattaca 25201 ggtgtgagcc accgtgcccg gcccagaact ttaaaaatat tctccaatgg aaactctgca 25261 tctattaaac aataactccc cattttccct cctcccagcc cctggcaacc atcattctac 25321 tttctctgaa tgccaccact ctacgtactt catataagta gaatcataaa atatttgtcc 25381 ttatgtggct gacatatttc acttagcaca atgtcctcaa cgttcgccca tgcggtagca 25441 tatatcagga tttccttcct tttaggctgc agagaattat gatcgcgcca ctgcacccca 25501 gcttgggtga cagagtgaga acctgtctct taattaaaaa aaaaaaaaaa aagagtccag 25561 gcatggtggt tcacttctgt taattctacc acttcggaag gccaaggtag gaggatccct 25621 tgagtccaag agtttgagac cagcctgggc aacatgctga aaccccatct ctacaaagcc 25681 cacaaaaatt agctgggtgt ggtggcacac ttgtggtctc agctatttag gagactgagg 25741 tgggagaata acttgagcct gggaggctga ggctgcagtg agccaagatc acaccactgc 25801 actctatcct gggtgacaga ataagacctt gtctaaaaaa acaaaagaat ttccttcctt 25861 tttaagtctg aataatattc cactgtatgt atagatcaca ttttgcttac ccattcacct 25921 gtcaatggac atttggattg tgtctatgtt ctagctattg tatatactgc tttttaactt 25981 aatctattat gaacatcttt tcagatgaat aattaaattt tcccaatgcc ttttttagtg 26041 gctgctttat agtacattac ctgactgttc cacaatgtag ttgactattc cttgagggtt 26101 ggaaatttag tttgtttctg attttttgct ctaatataca cggctggaat aaatccccta 26161 cgaacaacat ctttgcatgc ctggctgatt atgactttca gacaaaagaa tgtgcacagg 26221 tttcggcctc cggcacccat tgctgggccc ttgttacaag cagcctgtgc atctgaggag 26281 gcctaagcct gagctgccgc acacatcccc atccctgaag accagagagc accatgatgc 26341 caggggtccc tgcgcctcct ggaagtgaag aatgttgctg cagctccaag ctcgtagggt 26401 aagtctgtgg gaataaatcc aggaggacct tcagggagat tccaatgaac tcctggttat 26461 tctgattctt tggaaaatga aattttctgg ttaattgaac ttcttgactg gctgaatcca 26521 gtctaaatgc cttcaaatag acccctacct ggcacaccat catgcttccσ ttttgttttg 26581 tcagtttgtt tgttttaaat aaggagtttc tctctgtcat ccatgctata gtgtagtggc 26641 atgatcctag ctcactgtgg cctccaactc ctggactcaa gtgatcatct ttcctcagcc 26701 tcccaaatag ctgggactgc aggcttgtgc caccacaccc agctgattta aaaaaaaatt 26761 tgtagagatg gggtcttctt ctgttgcctg ggcttgactg gatcgcctgg cctcaagtga 26821 tcσtcccacc tcagcctccc aaagcactcc cagcaccacg cctggtccat aatgcatctt 26881 aaaaatgcag atgacatgtt ataattttgc agatattgtt gtgaaatgtc ttgagtgccc 26941 agaacagggc gagccacaca aaagatgcag aagtcgaaca atgctggtgg tggggctaca 27001 tgcaacctgg gagctgctgt tgaactaagt gcccagcagg agcttgtctt cttattattt 27061 actgatcata aaattgagta cagactgctc tcatcctcct tctgtggggt tccttgattc 27121 tcttggttgt ttagactgtg gataaaaggg cttttggtag ttgctgggga gaaaggtcag 27181 cagcagcagt gatgagaaag cagcatgccc acaggtggaa gcctcggaag gggttcctga 27241 gaggctgctc cgcctgtgag gtgcgggaag cacagggtcc tccagctcag ttaaccatgc 27301 atagtggcag gcactgctcc taaaacacag agtagtcaat cttcctagaa aatgcaaaat 27361 gctcttctga ctccactttt tttttttaag tattcaaaac atccttttca agccctgttt 27421 agctcttttt atagctgtgt ttggacagac tgaacagatg aaatttactt aacacttcca 27481 gtgtgggtct ttggttgatc actacagagc ctatgttttg aataaaattt tgaatttgca 27541 catcagcaag aattctgcca tgagaattta ttttaacata aaagccaaga ctgttctcct 27601 tgcctccatc cctcggcttt tcctcccctc ctccctcttt cccttgctcc atccacaatg 27661 gaattctcac cattttccca gaacaccatg cccttttttg tctgtgtctt tgcacgctct 27721 tcccattgcc tggagtgccc tctaggtcca tctagtgacc caaataagac tttaagccta 27781 aacacaaatg tcccctcttt tctgacgtcc tcatggacac acccctggta taaaatcact 27841 tcctcctctg tgcaccgaat ggtgtctcac σcatccgtga cagcacttac cacaccgtgc 27901 atctgctcac ctgctcacca tctgtctccc cagaaagact gccagσtcct caagggcagg 27961 gaccatgtct ccttcactca gcacctttgg ctcaagaaca ctaagatatt tggacccttg 28021 aagtctcagt ttcctcatct gtaaattagg aaaaacacaa catcactgaa ggagataggg 28081 gaggactaaa ggagctgtgc tgtgcttggt acacaggaaa tattcagtaa aaattcacca 28141 ttttcaggga ttcgttattt tagaagttta ccaaaatgct ccctctcctc tccccctgct 28201 tcctctcccc tcccctccct ctcctctccc ctctcctccc ctcccctccc tctcccctcc 28261 cctccctctc ctctcctccc ctccctctcc tcctctcccc tccctctcct cctctcccct 28321 ccctctcctc ctctcccctc cctctcctcc tctcccctcc ctctcctctc ctcctgcttc 28381 ctctcccctc ccctccctgt cctctcccct ctcctcccct cccctccctt cccctctcct ' 28441 ctcctctcct cctctctcat atacacacac tcacacacac tatcactcac acacactcac 28501 acacactcta acacacactc acctacaagc acgcacgcac gcgcacgcgc*gcgcgcgcac 28561 acacacacac acacacacac acacttgaga tggctgacct ggaggccacc gtttgcccca 28621 ggggtagatg ccagaaatgg gccagcttga aacagatggc aaatactcag ctctgaagga 28681 caagctgcct ggtctaggcc taσaggtata agaaagaaga tatttcaagg aggaaatgaa 28741 aaggcagaac aagttccccg tcccctgtca tcatgctcgg ctctgagσtg gagacaggtg 28801 ggaggttttg gagaaggagt aagagctcca gatgtgagtg tgaagggacc tctaccctgc 28861 ctggctagat agcttcagga tcgccttcca cattccctct tcaccctctc cactcggctc 28921 tctgccccgg gaagttgagc tataaacaca tcaatgggcc tctctgacca gtgcctctgg 28981 ttggattcag atcatgggga acagtaacag gacaaagaag gcaggaggaa agtgagggtg 29041 ggtatttatt ccggggcttc cttctgccaa ggtcctatgg ctctggtcat ggcggctgcg 29101 ggtggtaaca gcacctacgt tactagctag ctcagggata ctgcactgga catgggtttc 29161 cccgcaccct gcccacacct tcataaataa tctctgtatt taattctctt caaaacacac 29221 catttgaaca ataccgtcgg ctccctgccc ctgcccttcc atccctggcc aaggagacac 29281 aggttaatgt tcccctggaa cttgagggga cccaggagtg gagaggattt gctccctgca 29341 tactctcagg agttttcgtg agttgctgcc ttacagatgt gtctgactct gggaatgtga 29401 ggagaacgat aaatggggtg gcatggctca tgtgggcaaa aσagggctgg agatggtgtg 29461 ttagtccgtt ttcacactgc tatgaagaaa tacctgagac tggtaattta taaaggaaaa 29521 aggtggggtt tttttttttt tttttttttt ttggaggcag agtctcgctc tatcccccag 29581 gctggagtgc agtggcacga tctcggctcc acctcccagg ttcaagcaat tctcctgcct 29641 aagcctcctg agtagctggg attacaggtg catgccacca tgcccggcta atttttgtat 29701 ttttagtagt gacagggttt caccatgttg gtcaggctgg tcttgaattc ctgttctcgc 29761 gtgatcggcc tgcctcagcc tcccaaagtg ctgggattac aggcgtgagc cacagcgccc 29821 agccaggaaa aagctttaat tgactcagtt ctgcattgct gggaaggcct caggaaactt 29881 aacaatcatg gcagaaggca aaggagaagc aggcaccttc ttcacaggg,t ggcaggaaga 29941 agtgccaagc aaggggggaa agccccttat aaaaccatta gatctcgtga gaaatcactc 30001 actatcacaa gaacagcatg ggagtaacca cccccacatc aggaattttc cctatagtga 30061 ctctgttggg gtatagagat atcagagaga gagagagaga aagcacgctt gcagatcagc 30121 tgcagatgaa ctgactgtcc gtgtgaggga catggctgaa ttcttagagt gctgtctgtg 30181 atggttaatt ttatatgtca gcttggctgg gccatggtgc ctagatcttt ggttaaacat 30241 tctaacattt ttctggatgt ttctgtcaaa gtgttttttg gaagacatta acatttaaat 30301 gggtggattc tgagtcaacc agattgcctt ccatgacgtg ggcgagtgtc atctaataag 30361 ctgaagaaca aagactgacc tcccctaagc aagaagaatg atgccagcag gctgactgtg 30421 ggctcgatct gcagctcttc cctgggtctσ σagσtgσtgg σctgtcctgc agactttgga 30481 cttgcacctc cacaatcaca tgagccaatt ccttaaaata gacctttctt tttctaggta 30541 taggtacaca tcctgttggc tctgttcccc tgccaagatg ggagccaatc aattccagca 30601 gaatgtgtgg ggcctcattc gaatgaatgt ttgtgccctc ttggcagaca tggcgaatta 30661 ttcaagagca ggaagccagt tcaggatgga gcaaagtgtt atccttgact tcttcctcca 30721 gcttccgtcc ccatcaatct gtgtagtggc caacccttcc cacttcccac atttactctc 30781 tctcttactg ctactcctta atccgagcca tccatggaaa tccccagcca atagcatggg 30841 acagttgacg gtctaactct cagcattcat ccctctcgtt cccagσattt gct'ctatgσa 30901 tcaggcatgc aaacccttcc ccactacttg tagagcccat gctcctttat acctcttgta 30961 tttcattcac caaaaatctc taataagggc tgactgtgta caaccctgtg ctaagggcgg 31021 aacacgcagt cccaggtttc aaagagctca gaatctaagg gaaagagagg cttggaaacg 31081 gattaagtgc aaccacgtcc tggccacaga ggggaggaaa gaagccctgg tgaaggctct 31141 ttgcagaggg agggaacgtc tttattttat gcatgttctt ccctttgcta ccttgtgcct 31201 cttcaccagg aaacatctca tcctgcagct gaataccgtc tccctactca gtggtatcta 31261 ctgccacctσ catgctctgt ccagagctag ttσattgttc ccttcccagt gctccttcat 31321 attttctatt tactactttc ttcctttatt acatcaagta atactaccaa atactgctcc 31381 tctagcattt gccctgtgct gcgcatgtgc tcgccctgca accacctttg gggcaggtac 31441 tatcgtatca tatcgtatca tcattggctc agggtataag tatcttgctt agtaactcat 31501 ggctcgtgaa attagtcatt tcataatctc aagttgctga gcacttgtct ggcgcagagt 31561 agagagcaaa tatttgtcta atggaagtgt gtttgtgaaa atgctgggct gtgtaaacta 31621 aacagaacgg aataaaatca gctagagggg tttgccaggg aagacttcaa aagcagaggg 31681 catttgtttc tctcttgcca ccactaatgt ttctcagtgt ctggggcgag agccaggaga 31741 gagaagccag gtagtcccat cgttggaaaa ggccacagcg ccttgctgcc acccactgac 31801 agcagcatgg agctctgcag ttccaggact gcctgtgcag ggggccatcc ctggtaccat 31861 gcccctctcc cttctgtgtg ccagctgggc tgtctccctt tcctggccag ggctgtccct 31921 gctgaatgcc aaacatctgc agacagggtt tgcaaacagc tggctcaaag ttctgagctt 31981 ttgtgatctc atccaagtgc ctggctatgg ggaacaggct tattttcctg ggctaccagc 32041 actggagtgg tggaaattac attagacttg gattcagagg cctgcatttg attctgagcc 32101 ctgccacttt acagctaaat aaatgatact gaacctctgt ttccttcgct gtaaaatgga 32161 aatgatgatc attcctacct catagggttg ttaggggagt aagacaatag acatggggca 32221 tgcttgtaac tgtgttctgc tgaaacatgt gagagagtgt caataattaa aagaagcaag 32281 agttcctcaa gtcacagtca tgccaagatg tctagacaat ccctttagtt tatctcagtt 32341 cattattgag atgcgaggtc tacatagcag ggaaattaat tgttgcactg aatggaccag 32401 atttagttat tcactgaggt gggctgacac cttgggacta gcacagcatc tggaggcgga 32461 aactctggaa atgaatcccc aagtgctgtt tgtgtaatct aagcatcatt tcttcagttc 32521 taaaattggg gccataatct ccacattgta catgcccttg gacccagcaa tcttgctctt 32581 ggattatatc ccagaaggcg tatacggtga tgtgtagaag gatattcgtc gtggtggtgt 32641 ttgtggtagc agacaggaga gatattggag gttttcacca ccagggaatg gataagtcaa 32701 ccacagtgga tgcgcctgtg gaattccgga cagcaggcag aagcaatgga ctagatgtac 32761 acagagcagc atggagaatt cttcaaaaca gtgttgggta ggctgggcat ggtggctcac 32821 gcctgtaatc ccagcacttt gagaggccaa ggcgggtgga tcatgaggtc aggagatcaa 32881 gaccatcctg gctaacatgg tgaaaacccg tctctactaa aaaaaataca aaaaaaaaaa 32941 aaaaaattag ccagacgtgg ttgcggacgc ctgtagtccc tgctacttgg gaggctgagg 33001 caggagaatg gcatgaacct gggaggcgga gcttgcagtg agccaagatc acaccactcc 33061 actccagcct gggcaacaga gcaagactcc atctcgaaag aaaaaaaaaa gtcacctaat 33121 tagaacaaag acactcctat cacccagtaa attccaagag attaggagtt ttgtgtcaga 33181 aactggggtc aaagaσaaaa tattagaaca aaagatgtac ctagcactct cattgcagat 33241 tacaagtgtt ttaggagctc tgtgtcagga accatggatg aggaacaaaa aaaattctta 33301 ttataaatca taatattggg ggtatagagt aaaacaagaa aagagaagag cattgcaaag 33361 atσagtgata atagtagagt gttaacctag atgtataacc aactcagttt cctgσagcag 33421 aaaatgtttt aaatgtctat cctgaggtgt tgtaagaatt agacataata ttcataaagg ) 33481 ttcctgacac agtgcttggc ccatgagaga tgctgcagaa atggaagctc cttttatcat 33541 tctctcattg atcaaataat gtaccaagtg cccactttgt gcaggacgct gtgcaaggat 33601 ccatgggaga gacaaagact gggtgtctct caggaacttg agcatagcag atgggacaga 33661 atggcaatgg gaggggagaa ccctcatctg aagctgcaga gaagacacta tcagacctcc 33721 tcagcttcca aattgaggct gaaagaagtg acttgctcaa ggtcacacag ccagttaggg 33781 gctgagctaa gggcaactgt ctaggtctcc agggcctttt cagagcatca cccaagccag 33841 tgtggctggt ggggtgactc agattcttga cttcaccgca caaaagaatt tgagggtggg 33901 tccaaagtaa gagtaggcaa agaagtttat tgcagagtga aagtacactc tcagaggcag 33961 agtgggctgc tcagaggcag agacagcccc cagtgtccca agggaattcc ctttatgaga 34021 gctgtacaga catatgcatg aactactggt gaggtgaagt gcaaaggctg acctatggtt 34081 ggtgtatgca ctcagcatct acatgctttc acatgcattg catgttatca ctagcgtaga 34141 aaatcaccca gaggtgtgtt tattaaaatg aggaaaaatc actaagttaa accttgagcc 34201 tagctgctca tatgagaccc aggagaagtc cttagtccac cccσaσaagc caggaatttg 34261 tagctaatag cttcttgggg ttttagtgct gattggctac agattgggga agctgcatca 34321 catcatgaac aatgggtttt tgttctcttt ctcaggtggt actaggtatc aggaacttgt 34381 agccatctgg cggtctgccg gtagcctgta ggactgctta caggtaggtg ctgatgcaca 34441 aggggggcct gctttgaaag gagcccatgg ggcttcacac caggggacaa gtcagtgtgg 34501 cctcctcacc ttccttatcc tgcctcacca atacatctga atccaagaga gtggaaggct 34561 ggtacctcct gtctcacctt ctgctctgac aatcctccct cacactcctc ttcggtttac 34621 ccactcaccc atgtgcatgt gtgcaatgga gaaataaatt aggagattgt tttaaaaatg 34681 caatttggta gctaaaatct ttctgaatag ggggtccatg ggaaaaaagt gaaaaggttc 34741 tgaaccctgg cagaggtgaa gctctaagga gcaaatctcc ttggggtggt taattttaca 34801 tgtcaacttg actgggtcat ggggtgtcca gatagttggc ttacttctgg gtgcatctgt 34861 gagggtgctt ctggatgatg ttggtgtttg aattggtggc tgagtaaagc agacagccct 34921 ctcσagggtg ggtggcacca tccaatctgt caggggcctg aatagaaσaa acaggcagag 34981 gaaggctgag tttgtcctct gcctggatgc ctgagttgca acatttgtct tctcctgctc 35041 tcagactggg accataggct cccctggtcc ttaggccttc agacttggac tgaacgacac 35101 cactgacttt cccaggtctc cagcttgcag atggcaggaa gaggttcttc ccagcctcca 35161 cagtcatgta agccaattcc ttacaataaa tgtcttcata tctacacatc ctattgctta 35221 tgtttctctg gagaagcctg actaatacat tcctgttctc ccttttccag gcctgcccag 35281 ctgctttagt gattccgggt cagagtcttg caatcagaag caactcccac cctcagccct 35341 caaaatgggc catctcaaat cttactagcc aatggcactc caaggagagg gaggagcagt 35401 gtccctgtaa gctccttcca gcctttatca tcctttgact tgtccctaaa atatcctatt 35461 ccccaaagat ggcaagagcg cctcccgaga aggaggagca agggcatctc catggagccc 35521 cgctctσtga gctctgactg agggtggggg aaggagagaa ctctgggtct ggctcacggg 35581 gtgccatgtg tcaggcagca ggtccttgtg aagtctccag agatgtgagg agttggtcgt 35641 aacagcccag ggaaggagag gtagacgtgg caaacgggag agacaggtcc ccaaaggctt 35701 tgccgacttc ttgccagcct tgatccacca gagctataat ggcctttcct actatttcag 35761 aaaaacccaa aactttcccc acagagttca aaatgggatt ggcaaggagc tgaataccat 35821 attggttttc tgagatgagc acagtcagca cactagctcc gagtcagaaa gggcaagaga 35881 ggagggcgag acaattctct aagtgatggg aaccttccct gtctgggagt ttggctcagc 35941 tgtgagctgg gttaatgtgg ctgcagaagg gaagcatggt tcatgtccag ccagcaggga 36001 σactgtccca gagctgcgct cagccctcat agactggctc catttacctc tcacgcagca 36061 ccccatgagc tgagggcggt tctgtggcca tgttacacat aaggaaatag gatgcagagc 36121 tgatgacttg cccaagatca cactactggg gagtggtgga attagaattt gaacccagat 36181 tgcctagccc attagcctaa ccactaatca aagσagcagc tcaaσtgtag ccgagtcatt 36241 aggaatσtcc cagcttatgg ctgagaaagc aagaaaaatg aatctttacc atgcagggcc 36301 ggagtcaaag tgcacgtcat tcagtgcacg tttcttctga agaatatttc ttatggaaat 36361 gcattctgcg gggtcacaat ggctcatgcc tgtaatccca gcactttggg aggctgaggt 36421 gggcggatcg cttgagccca gaagtttgag accagcctgg gcaaattaag gagaccttgt 36481 ctctacaaaa aattaaaaaa ttagcccagc atggtggcat gtgcctgtgg acctaggtac 36541 gcaggaggct gaggtgggag ggtcacttga gcctgggaag tcgaggctgc agtgagccgt 36601 gatcgcacσa cagcactcca gcctgggtaa cagagtcaga ccccgtcccc tcccctgaca 36661 aaaaaaagag ataaatatat tctagggaaa catcaatcta taaccataat tcctatattc 36721 tcagtatcat ctcttatttt ttggggggct gcctgctcat tgaacagcag agcatggcat 36781 ggggtttcat cacatcσaaσ ataσaacctc ccttccaacσ taactgattt tccacagtgt 36841 ttctcagcac tgtcatagaa ctaccgctta tggaatgtat gaatgacatt attacaagat 36901 atttaaagag atttaaaagt ataaaacctg aataaaagcc accacaatca cttggtgtgt 36961 gcaaacaaca ccccggttca gacatcactg acaggacgtg tcagggattt caccttaccg 37021 gσtaaagtgg cgccaccgtg tggcaagaat gtaaacgcta tttgcaatgg acttggatag 37081 gcagcttcga aattacgtga gccttagttc tttttattta attggtgaga gttgcattat 37141 tccaaagttg taggcatcaa gtcagacttt attagtatcg cgtgtcacac gatttctaat 37201 tcctatcatt taaattgggc cgatagggac ccctccatgc cgtgtggtga gtgctgggat 37261 ttgggcatgt gctgggcatc tggacatgac agggcctaga ggaggaggta aagtgtaggg 37321 aggctcccag aggaggtgac ctgtgagtca gattttgaga gttttccaaa ggaacgcacg 37381 gaagtggaca gcagagaaaa gggaggacga tattccaggc acagagagca gagtagagaa 37441 tgccataaca tcacagaagg acatgaggta ttggtgaaag gttgggtgtt tagctgttgt 37501 tttgattggt agttaggctc atggactagg gagtaagaca gtctgggttc aaattctatt 37561 ccatcacttc ccagtagtgt gatcttgggc aagtcatcag ctctgcatct tatttcctta 37621 agtcttgaga ggggagtgga ggtggagctg gggctagaga ggagggtcag ggccgggtgg 37681 aaaatgccat acggtgccat gagaaggagc ctttctcσtg caggagtgga ggtcactgaa 37741 ggacaggcag gtctgtgttt agacagatta ccagtagcag ggtggatgtt ggactagaag 37801 agagaagaaa ccacaaacag gggaactagt tagcagactg ttgaagaagt ctcccatccc 37861 ttcatgaatt ctacaaatac tgaatgccca cactgtgcca gcgactgttc tgggcattag 37921 agatctataa gacaacaaaa taaagactgt tgccctctgg gagcctacac cttactaggg 37981 ggagacaggc aacaaacaca taaataatat gatatatagt gtttcagata atatgaaaag 38041 caatgggaaa aaaataaagc agggaaggag gatagagaac gtgggcaggg ttgcaatttt 38101 agataagggg atcagcgaag gccctggtga gaaaaggatt aaaaggccta aagggagtga 38161 gggaggaaag cattccaggt cccagggaaa gccttccagg cagagagaac agcaaaggca 38221 gagcctgagg tcagagcgtt cctggtgaga tcttgggaaa gcaaggaggc cagtgtggct 38281 ggagcagaat caaggcaggc agggtggggg ccaggggcaa catcagagac aggggaggag 38341 gcaaactgtg tagggtgggg ttggcaaagc ttatctgtaa agggccggac agtaaacata 38401 atatttcaga ctttgtgcac cacgtggtct ctcttgcaac tgctgaactc tgcccttgta 38461 gtgtgaaaac agccacagac caaatgtaaa agaataaaca tggctgtttc aacaaaactt 38521 tacttacaaa aatgggtgat gggtcagaat ggcctgcaca ccatagtctg tcaaccctga 38581 tgtaggacat tagagacact gaaggtctta gttttacttg aataagatgg agagctatca 38641 cagggttttg agtaaagaag gagcacaatg taactgatgt tgcatttgga tcattctggc 38701 tgctgtgtga gaatagactg catgggggtc cggggtggaa gtagggagac caactctatt 38761 atttattctc tgagtgacct tgggcaagtc acacagcctc cctggccttc agtttcctct 38821 tttgtaaact ggggtaatag tgtaatgata cctagcttat ggagcggttg tgaagggtaa 38881 atgaatcaac atatgcaaag cacaagggaa gtgcctggca cacagtaagc actatatatg 38941 gtagccattt ttattaatgc agtcatttag acaagataca gtgatggcat gaaccaggtt 39001 atgctggtag aagtaataaa aagtgatctg attctggaca tattttgaag gtagagcaaa 39061 cagaattttc agatgatttg tatacagggt ggagagaaag agagaaatta aggaagattt 39121 taactttttt gtctgagtaa ctgaaaaatg gagttgttct ttacctagaa gagaaaagcc 39181 gtgggaagaa tgagttttca ggggatcatg aagaattcaa tgttagacag taggatctgt 39241 aagcctcatt cagaggagag cccattgaaa gttaaggaga tgagaaagaa ccaacaaaga 39301 taatggaaat gaggcagaca gcgaggtagg cagaaaacca gaaggacttg gcatcctgga 39361 gttcaaggga ggaaggcact ggaaggaggg aggtgtgcat caaattttga taggtcaggt 39421 aagctgagga taagaatcac tgggtttagc aatgtagaag actggagcag ttttggtgga 39481 gtggtgggtg cgcaagcctg agggagcagg tttaacagag aatggaaact gagtgtttgc 39541 agacagcaag tagaaacagσ tgttggggaa aattggctga aaggggaaga tggaaaatga 39601 ggccataact ggggcaagcc atgaggtcca gacagagatg acaagcgata atggagcaat 39661 agatatcaag ggccttggaa gatgggatga gacgagtcca aaggcatttc tgatgaagag 39721 gacctggaga ctgtcgaggt gtgtggagtg agggagaagt ctaggctggc tcccgggttc 39781 ctggcgtgca taactgaggg ggttgttggg agcagcattc cttctctgtg ctttggtagc 39841 atcttgggca tgctgctatt gccgcataca ttgcactgtc atataattgt ttatgagtct 39901 gcctgctatt tgaagactgt gccatgttcc atatttatct ctgtgcaact ggtgtagagt 39961 gagtgcttgg aagcgaagca gcagctccgg gaaggccgca gtttcagtgg tctggtcttg 40021 acaagacagc gatttatttc ttccatgccc catgatagag catatttctσ ctgttctgtc 40081 tacatctctg tagggtccag ccctacatgg cctgtgggtt tttctcttcg tgtgcggaga 40141 tgagagatcg tagaaataaa gacacaaggc agagatagaa gaaaagacag ctgggcccag 40201 gggaccacta ccaccaaggc gcggagatcg gtagtggccc ctaatgcctg gttgtgctgt 40261 tatttattgt atacaaggca agagggcagg gtaaggagtg tgagtcgtct ccaatgatag 40321 gtaaggtcgc gcgagtcacg tggccacagg acaaataggg agcctttccc tatttggtag 40381 tcgaggaaga gagagagagg acagcttacg tcattatttc ttctatgtat ttcttggaga 40441 gatcaaagac tttaatactt tcactatttc tgctactgct atctagaagg tggagccaag 40501 tgtacagggc agaacatgaa agtggaccag gagcgtgacc gctgaagcac agcatcagaa 40561 ggagacgttt aggcctctgg atggctgtgg gtgggcctga ttaatgtcag gccttccaca 40621 agaggtggtg gagcagagtc ttctctaact ccccccgggg aagggagact tcctttcccg 40681 gtctgctaag taacgggtgc cttcccaggc actggcgcta ccgctagacc aaggagccct 40741 ctagtggccc tgtctgggca taacagaggg ctcacacttg tcttctggtc acttctcacc 40801 atgtσccttc agctcctatc tctgtatggc ctggtttttc ctaggttata attgtagaac 40861 aaagattatt ataatattgg aataaagagt aatgctataa actaatgatt aataatattc 40921 atatataatc atatctataa tctatttcta gtataactat tcttattgta tatattttct 40981 ttattacact ggaacagctt gtgcccttgg tctcttgcct cggcacctgg gtagcttgcc 41041 gcccacacat ctccactgcc cttcctttcc agagattcca atggattctt acctaagatg 41101 ccataactca accatagtta atagggaagt atggttggca ttccatcagg atcccagagc 41161 tgagtatgac aactagggct acaacccaac tgtttcctgt tgagtttctg gagccctgtt 41221 aggtgtggtt gtctggaatc tgagctgttg catccctatc cccatatgac tgaccctgaσ 41281 atcttttaga agttgattca gtggtgccct aacattggtg tggcccactg atcctccatg 41341 cccagaatct tccccatgga tgattccatc ttctgctttt taacacaagc cagcaatcca 41401 agctctagga agacaaactt tacactgatg aaatgactσa atacctcttg gtgctgagga 41461 agggctattt ttatatttcc aatgctttat ggactgttgt gaggcctcag aaatccaggc 41521 tcctctgaag tacatcctct taggcaacag ccccacccac agtcccctgt cctacctgac 41581 aataaaaaac tgagatgcat gggcgaggct gagggagaag ctggtgagca acggcaacac 41641 aaggcagtga agagagggga cttgggaacg tggcagtgaa aaaagtcagc ctgtgtctca 41701 gtgatgtgtg tgtgagggac ccaaacactc aacccagatc acattctatg ggaaaggtga 41761 ggattaaatg aaatgacata gatacagcga agagcacagg gtgggcagtt agtaattttt 41821 agctgccttt tcttttacta tttgaaatgt gcattataaa ttacaaagtg acagatgcta 41881 gttgctagga tgaggcaggt accagtccaa tggactagac aagtgtttct caaactctaa 41941 tgtacctaag aaatagctgg ggatcttgtt gatctgtgga ttctgtttca gcgggtctag 42001 gatgatgtct gagatcctac aggtctaaca agctcccagg tgattccaat tcattgaact 42061 ctttgaatag caaaggtcta gaacagcggt cttacccagg ctacacattc aaatgatcta 42121 gtgagattta taaagtatgg gctttctgct cttgcactcc atctactgaa tcagaatttc 42181 cagtggtgga gcttagacat ttacagtttt aataggcaag ccagatgact ctagtgttca 42241 gccaggactg aagaccactg gcctaaggcc ctgtattctt tσtaattctg ttctccagct 42301 aattctgatt cattcaatca gtgatatttg ttgagσttct attctctgcc aggcagtgaa 42361 tttggcaagg agaacaaaca aaaaaaccag caatgacagt gcatatgcta aatgctgggc 42421 agaggatgcc ttgcatggga gcccaggaca gtgggtgtgg tgatttagcc atcttgattg 42481 gtcacaggca aggaaggctt ctctgtggga ggtgagggta ggactgagtt taaagaagga 42541 atagaaccaa gttagaacaa taggaaaagc cgtaaaataa cataacatgc tggaaaagac 42601 ttgagttcac tcaagggaag ggtaagtaac taggctggag aagacattag gaagaagatc 42661 atgaaggggt gctaagttag gagtttgact ttcatcctga atgctaggat tttaagaaga 42721 ctgaatgttg gaaaatagca aacaσaaaaσ aaacattcag cctcaacatt ataattttga 42781 tgttactatt attattatta ccggtttgtg tttaagagat attatactga caataggatg 42841 gagaattggc tacaggagac ctaggctaga aacagggaaa gtggtcacaa actattatag 42901 taacccagtc aaggaatgag acagatatga aggaggtaga tttggcagga cttgaaagac 42961 atggttcttg caataattta aacattccca tgtgcacata gcagtttgca aattcctttc 43021 atataacaaa cttgagaagg agttagcata agcattagtc caattttact aataaaggaa 43081 actgagactc agaaatgaac tgacttattt acggtcacat gacaagtgtg tgagcaattc 43141 tggtttatct gactcaacat σaggcattcc ttttgctgtg ttgggccgcc tcctataagg 43201 tagacatcct atatgaacac tgggaagggt ggggtaacσc ctcctggttg gcatgtgggg 43261 tgtactggtg tggccttaaa gggaccctga ggccgggcgt ggtggctcat ccctataatc 43321 ccagcacttt gggagtctga agtagatgta ttgcctgagc tcaggagttt gagaccagcc 43381 tgggcaatat ggcaaaaccc cgtctctacc aaaaatacaa aaaattagct gggtgtggtg 43441 gcacgcacct gtgatccaag ctatggaggc tgaggtggga ggattgcttg agcctgggag 43501 gtggaggttg cagtgtgctg agattgggcc actgcactcc agcctgcatg acagagtgag 43561 aacccttctc aaacaaataa atacatacat ttaaaataaa taaagggacc ctgagttcaa 43621 caactctgtt accattaact cgacattccc agatatggaa ataggggcca gagtctcaac 43681 actggaattt tcagacagtt ttgagaagaa tccatcaagg gctcccagct tttcccaaca 43741 aaatcttaga gctgacaggt tatgaaagca aagtagcaat ggaagtacag atattggagc 43801 agttggcagg ggtaggggaa gttatcctga tccatctttg cctttgtctc tgtttcaaag 43861 ccatgtccct ttctccactc attcccctca tttccctctt ctccatcaat taatttccac 43921 ctctctctaa tctctgcctt ccccctggct gctcctctca ggcttcaagt ttgctccaaa 43981 ctcactcatc cttaaaggac cacctcatct tagtcctgcc atattctcaa gctactgccc 44041 tgcagagσta ataaacaact ccacccacgc ttcacagagg aacgggaagg tttaatctga 44101 tttttacgtc tgtcgtctga ctactgtctc tgattatctc aagttcaaag ttggccttct 44161 gattactgtg actctctttg agaactgata atggσttaca aatggattcc tttaccacac 44221 ttttgttcgt ctgatgtttc atggactgtc tctgtgtaaa cttagttatt taatgtctca 44281 tactttgggg gatagtgcat cagtgaggaa tctgtttggc tattaacttt gttttaaaca 44341 tataacatag acagagatga tacacatσaa atgatttgtc tcacaggcaa aaaggcaggg 44401 gaaggtactt gtaggctaga gcagcagcσc ctttacacaa tcgtcagcgt tctaggcccc 44461 tctgtctttt cacactgtca cctttggcat gttggtttgc ggcccaaagg ctgcaagatg 44521 gcagtgcatc tccaagcatc ctccaggtag gcagaagcaa gaagggcaaa gtggggaaaa 44581 ccgggccttg ccagccaact ctgccactct ctattgagaa gacaaaagct ttcctggagt 44641 ccacacccag tagaattctg tgtccatctc atttcacaca gccgcctaca gctggaaggt 44701 agctaaggag gagtgttttg gatgggctgg gtcagtcaac aagcagcatc gttcacatat 44761 cctcatatat atggggaaga ctttgcttat ggtttagctg tgtgcaaaac aagttacagt 44821 gactggtgtt tcagatgtca ggacctgtat taggtgtagc ataaattctg tcaagtgaag 44881 actaccatct cccttttaca gataaggaag ctgaagagca gagaggtgga ataacttatt 44941 gaagctcata caacctgaag aaaagtattt ttctgttaaa acaaacatac attatgacat 45001 aaaaccaaaa aatcctcacc aattttagag ataaaaatta gtgactgcac agacattcca 45061 tatggcaggg gtcaccaacc σctgggctgc agacccctgt cagtggσgtg ttaggatctg 45121 ggtcgcaσag caggaggtga gccatgagcc agcattacct cctgagctcc gcctgctggt 45181 gcgagctcct tatgagaatc taactaatgc σtgatgacct gaggcaaaac agtttcatcc 45241 caaaaccacc cccacccccc aacccccgtc catggaaaaa ttgtccctgg tgccaaaaag 45301 gtctgggacc actgccatat ggactatgcc cttgactctc ccaaaggaac atttccccat 45361 tcctcactcg ctggggtacσ tσgctgggaa agtatgagaa gccccagcgg ccaccgtcac 45421 gtggggataa caagatatac acaaaaaagt gagcttccgc cacgggaatt caggcctgat 45481 gcagtctgtg atgtgaggat gtctcaggca ctgccatgca gatgagtggg aaatgaaggg 45541 gactgatggg aagtgccctg aggtgacagg agggagcagt tσccgaggga gccacaatgg 45601 tcagggaggg cttgggggat tggcagatag aagtgggcct tgaaaggaaa ataagagttg 45661 tacaagcaag aaggagatag aaacggtatt ccaggtgatg agaaaagtat gcccaaattt 45721 tggaagccag agagtgggat actccaggga gagtgaaaag acagcctggc tagaggaaat 45781 gggtcctgaa ggagagaaat gagagatcac tctggaaagg aagtctgggg ctggttcctg 45841 aggaaagtcc cctgagatcc aacatcttσt tctgttcttt ctacccacag gtcaggaatt 45901 acacagatat tgtttgctct gcagacctga gctgcctctt aagggtgctg attacacagc 45961 σttcttcatc tcagσσtatg tccagatgga tcacagaatc ctcaccacaa gggagctggc 46021 cagcctgacσ tggaaggtgg gggctttcct gccattggtg cctattgctt tgggcttgca 46081 tactcagtac aggttgacac ctaactctaa tgccacctgc tatgccaaca ggaccatcca 46141 gaaactcaac caaggcacca cagactgctg gggaaaggtt σttgσtgttt taaataaσat 46201 gtccaggccg ggcacaatgg ctcacgccag taatcccagc actttgggag gccgaggaag 46261 gcggatcacc cgagctcaag agttcaagac cagcctggcc aacatggtaa atcctgtσtc 46321 tactaaaaat acaaaaaaaa aaaaaaaaat tagctgggtt ggtggcacac acctgtagtc 46381 ccagctactc gggaggctga ggcatgagaa tcacttgaac ctgggtggca gaggttgcag 46441 tgagccgaga tcacaccact gcactσcagc ctgggtgaca gaccaagact ccgtcttaat 46501 aaaaaataaa taaataaata acaagtccat catcagttag gccctgaσca aatgggctag 46561 gggacatgag gacagatggg gacggggaaa aaaaggagca gataccttag σtcaggtcct 46621 catccccagc tgggttccct tctcctccaa ggaatccttt ccaggagtgg agaaagaggc 46681 atctcagtca gaσagccagg gtccctggag gccagacttt ttcatcccct ttcacatgtg 46741 aagaggctga ataatcatct tatccccctg tattagctca ttctcacatt gctataaaga 46801 actacctgag actgggtaat ttataaagaa aagagataga gccaggcatg gtggctcatg 46861 cctgtaatca aagcactttg ggaggatgag gtgggcagat cacctgaggt caggagttσg 46921 agaccagcct ggccaacatg gtgaaaccca gtctctacta aaaatacaag aattagccag 46981 atgtggtggc ctgcgσσtgσ aatccσagct actcagaagg σttaggcagg agaatcactt 47041 gaacctggga ggσagaggtt gσagtgagcc aagatcccac cactgcaσtσ σagcctgggc 47101 aagacagtga gaccatatca aaaaaaaaaa aaaaaaaaag aaaaaaaaga aaaagaaaaa 47161 gaaaaagaaa aaaagaaaga agaaaagaaa agaaaggaaa ggaaaaaaga aaagaaaaga 47221 ggtttaattg actcatggtt ccacaggctg tacaggaagc atggctgggg aggcctcagg 47281 aaacttacaa tcacggcaga agatgaaggg gaagcaggσa tgtσttacat ggctggagga 47341 ggaaggagag agagtgaagg aggaggtgct acacacttta aacaaccaga tctcatgaga 47401 actcactcac tatcaagaga acagcaaggg ggaaatctgc ccccatgatc caaaccgtgt 47461 cacctgcctg tattatctct gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt 47521 gtgtgtgtgt gtgtgtgatg gggtctcact ctgtcaccca ggctagagga gcatgatcat 47581 agctcactca ctgcagcctc aaatttgagg gatcctcctg ggctcaagct atcctcctgc 47641 cttagcctcc caagtagcta ggactgtgcσ tagctaaaat accaaactct tgatttcagc 47701 tccttttgtc atcatttgtc catttcttct acaatcttaa atttttttga ctggggtttc 47761 tatgttgctg aatttggtga cattttcact aacccagaac acacacacac acacacacac 47821 acacacacac acacacagcc ccattaaagt tctttccttc aatgaaattg gcaaaggggc 47881 ataaagaaaa ctggaaccta aggacccagt gaggaagσaa agttccactt tσcactggaa 47941 actggtcttt tacaataatc ccattgcacc taggagctgg accaggctgt tattttagag 48001 tttaaaagtt gtcσtcσctt cttctaσσtg gctactggct tggggcttta ggtgggtgag 48061 gσctaσσtcc acaagaaaaa tccaσagtga aaatggtgac agttggaggg tgctggagtt 48121 gagcttagcc ttcctcactt cagaagagct aaatgcatac aggagtgcaa cagaagtcag 48181 gaatctattg ccagaggggc cagagagggg caagggcctt cctgctctag ggcccttccc 48241 cagaagatgt tagctatggg tcaagtctct acctcctccc caacccccat tσtσcattgc 48301 atccttggaa ccaggagccc agaaacctgc cagcccagat gaccaggacc atgtttgaga 48361 tgcataaatt tggtcctctg gatccttcaa aagtacactg tatttgtcac tccccgtaga 48421 ccctcatgca ataagttctt catgctctgt acatcgattc tttttctcca gcagttctga 48481 gcaatgcttc aaaaacgaaa catcagattc cttgtaaagt taaaaggaac agattttttt 48541 cccacatacc atgaatttct cattgattgg tttagttaca atatctaatg tgtccacagg 48601 tatgttttaa aagttccttt atggggcaga gagagcattt ttttaatact ctggtttcac 48661 ttttttgcat ttaaatactt tctcacatac tσaatattta taaaagggtt agagttcatt 48721 ttaacaaatσ ccattaaata ggcagggctt ttcaaggtct tgcctatgaa tttcctcatt 48781 tcaagcactg tttagtccag gtaagctcca atagaacctg agaacttggg actgccaggc 48841 caactctagg tactagttσc tgacatttct ttgaatattt gggtggtcac atttgttttc 48901 tttggtcata cttacccaac tggacctctt ttttgttgaa atgtgaactc tactgctagc 48961 cagttaaagt tcattgtttt tcagaacttt gattttgaag atgaatatga ctttaaσctg 49021 gccatcatgt actgcttttt catagttaat tcaaaacaga gcagaactct ggggattagt 49081 tcaatagaaa caatgtattc ttcaggatct ttctctaagt agaggaactt tcttgaccct 49141 tacacagcaa tatatggact ttttggacta ccagctcatg gttattctta atgtgatcca 49201 gaccccaggg ccatccccag gaaaaggaag caaagcacct ccccacagta ggcctgtgct 49261 agacacagtg gacacacagt ggaaacaagg tccctgccca aagacctcaa aatttattgt 49321 gagagatgaa ttggtaatta aatagctgat tattttaaaa gccctaatac agttgtgttt 49381 catgtacata actgtaaatg aatgtaaaaa gtgctgtaaa atcacagtgg gagggattca 49441 ttcttgcagt gaggaagaag gatgaggatt gaggaagact tcaaagaggt gagttttgaa 49501 atagggtttg aaggacaagt aagagtttac taggcagaga tgcatggaaa gaacattcca 49561 ggcagcagag acagctaaaa taaataaata aataagtcgc agagtaagga aaaggatggg 49621 aatgagaagt ggttcagtgt tactacagca tagagcaagc ttgtccaacc cacagctcag 49681 gatggctttg aatgaggcca acacaaatta gtaaacttta ttaaaatatg agatattttt 49741 acaattttgt tttgtttttg cttattagct atcattagta ttagtgtatt ttatgtgtgg 49801 cccaagacaa ttcttcttcc agtgtggctc agggaagtca aaagattgga cacccσtggσ 49861 atagagtatt ttggggtgac atgatgggag ctggagaagt aggtaggggt cagaattcag 49921 aaggccttgg aσacσagcct aaaggcttag agttgctccc attggccatg cactcaccaa 49981 aggtgttcac gtccctcttt tggctgttag attggatggg ctcaatcttt tggccctctg 50041 tctctagaat agagccgctg cttttctact gggcccacta tttcttcctg gtcctctgat 50101 ccσcttagca ctaσacagat ctcgatattt gcctcgggta tcaaggctct gaaaatgatc 50161 aggatttaga ggagatggct cattttcaga aagagtttta tattctccct ctggccttat 50221 acactacagg caaatggcac cgatgttttg gagttgggcc agttgggcct tttctσccct 50281 caagagagga ggattcgata ttcagtgttt ctgaatttca tgcttagttc ttaagccatt 50341 tcccatttgc cctaagaaat aagagctggc agcaagctgc gctgtttttt tctaaacggg 50401 aaatgggtta agcatttgtg atcaccactg aatgagtgcc agagctggtt agtgatcttc 50461 ctgttcaatc cgaggtcacc taactagata acaaagagct gaaactaaaa gtccggtctc 50521 ctgaσtccca atccagtact ctttctggtg tgctccagct tctggctσtg cttagccaat 50581 tatggaacag acagaatgta cttggctgcc cσaaaσggct aaagggcagt tctgttccca 50641 aaatggaatt ctgttgtgcc tcaagctagg cagcataatt gtgtgtcttt tggtaaσtσc 50701 ctgtcttctt ctgtaaaatg ggagtagagc ctacttaatc ctgcagσtac ttctaagatc 50761 agggattggg gcgtggtggg ctgttctgca gctgttttgt gatggatgag ggatgataga 50821 tctatgttca agtagcggaa tcttagagtc aggagttgga aggaatcttg gaggtggtct 50881 gtggtgacag gaagcctctt ccaatagact gaacacggaa gacttcctag agccggagga 50941 caagggtttc tttcctctta gcagtgagct tcttgttttt ggaaatgctc aagccaagaa 51001 tggatgttca ggcagagggg attccgctcg gaaggggctt tctgcactga agtggtggcc 51061 agcgggaaac tccaggtttc caactcctgc acaaatcctt tctaatatcc atccactcag 51121 gtgagctggc agggcagtag ctgtgcaggg ttcagggtca ttatatgtca atgaccttca 51181 gcacggatta ctaacaaσag taacatccgt taccgtttac tgctttccta ttaagcacca 51241 tgcactgtgc ataacatgtt atctttatct catatctaga attttgggag gtactttgaa 51301 tcattacgat ctatctaσtt σttaggtgag gaaatagagg tttaaaattt agtccacagt 51361 ctcgcaagga tggagσctgg atcaaatttt gggttatcag attcσaatσa cgtttcttag 51421 cttttctttt ttttttccaa ctccagtttc tgtcttgctc caaaaaaggg gaaggagcgg 51481 ctgcggcgct cggtttcccg cctcctaggg aagggaaggg agaσgagσag cgcggaggct 51541 ggggccccct tccgggcggg gcctaσtagt gggcggggcc tgtcagtgag cggccσctgc 51601 ccggaaggag ccagtσcggg gcggagccga tggccttaca ggggccggaa gtggσσtgcg 51661 ggcggagaag tgcctcagga gtcctgacgc agtgtcttgg gσgctaaσgg cggcggcggσ 51721 σttgtgttta gactccagaa ctccccactt gccgcgttct cgccgccgca ggctcσcggg 51781 acgatggtgc cccgcctgct gctgcgcgcc tggccccggg gccccgcggt tggtccggga 51841 gcccσcagtc ggcccctcag cgccggctcc gggcccggcc agtacctgca gcgcagcatc 51901 gtgcccacσa tgcactacca ggacagcctg cccaggtgag cctggcctcσ gggtccccgc 51961 cgcccgccgc cgtcσcagga tcggccccaa cctgactgca gtcactcatg actcctctag 52021 tgaacccgtt tccgccccca agcccctacc atggaggctg ccacagcccc taatctggaa 52081 gtcttgggac ttttcacaat ctcctagcac aggaacctca gaaccctcaa attctcttcc 52141 agaacccctc gatgctatct cagattctcc atcttgaacg cttctcagat tccctctcct 52201 ttaacctaac ttccagccag ctatcctgag tcctcttctc cctgaaaaat gccagacctg 52261 catatttcca gcgccgctgt aatccctcga ctatggtgtc tcctgaagta ctttaatgaσ 52321 tgcctcacat tcctacccgg aatatgggta ggctgattcc taatacatca tggttaccat 52381 tccttaactt ctcccagcac cgccttcacc cctgtcactc aggaccctca gccccacctc 52441 ccatttctcc agtactctgt tctttcaccc cccatgagcc cccacaagca cagccctgaa 52501 gtgttcacσc ttgtcctcaa ctgaccctcc cccatgtttt taaatcttta atctcctaaa 52561 tccagtgttc acccggaaac ctttcactct ctccaagccc tcctcaacag gttcctcccc 52621 tcaaaatatc cttcctcacc cacagtaccc cttgtaagtg cagctcaccc tcacagaatt 52681 ctagacacca ccctσagtac cccatccaca ctccatcata ctcagatcca gggtccaccc 52741 aaatttctct tctcctcσtc accactggct accctgcctt cgaaacactt cacccagaat 52801 cgacttcccc tctgaaaaga gccctagtaa atcctcttcc ccttcσctcc cccagtactt 52861 tcttaaatcc agcttccagt tcttccagσc ttcgaactcσ gctttσgtσt gagttgccag 52921 atctccttct tcaatattag aaattttctt caccσtctaa accaaaccta aactaacttc 52981 taacttactg agtgagtaac tcagttcctg gagccaagtt caaaatttgt ctcaaagaσc 53041 cttctcacct tatttctcac caaactgccc tcagggattc cccacactcc aagagctaga 53101 ggccaggctt cttccccatg tgtggaacat tgtgtcacag gcctcacccg agctgσtggg 53161 ttgtttttct ctgcatctgg gaccacttaa cccaacgtca tcactacata ccctcaccct 53221 ctcaggagga tcgagtgatt cttgtgaaat tacattttgt gcaaacatct aagacatgaa 53281 aatgagatta tctacacgtg gcaggaggga ggaagaaaaa ggggσtttgt gcctgtggca 53341 taagcctggt acatgcttcc accctgtcaa cctgtgtgta tgagctgagc cagtatatgg 53401 gtgaaaggtg aggactgaca gaacctgtct tcacttgcca agttcagagt cagatggtca 53461 ctgactttca ggcaggcctg ggccccaccc aggtttaaga tcagagggat tttctgcact 53521 ttagaattgg aaagctggaa agaatattca agattattta ttccaacccc atccatagca 53581 cagtctgtag gaatctggag gtaccaattc aaactccagt tcaaatagta ccactagtσa 53641 cctacgcata accttaagca accaacctcc cccagacctc cattacctta tttgtaaatt 53701 gggagttaga tgagagatga gattccttct gtcgctcaga ttctagactg gtaaaatgta 53761 taatctttca cactcactca ttgatgtcac acttggtgaa aagσcctgac tttgaggtct 53821 ggtagaatgt agttgcagat tσtggatctg caagtcttta gctataattt ggggcaattc 53881 tgttcacttc attgagccac agttttattt tggttttttt gagacagtct cgctctgttg 53941 cccaggctgg agtgcagtgg ccctatctcg gctcactgca acttctgcct cσcgggttca 54001 aaggatcctc ccgcctcagc ctcccaagta gctgggatta caagcatgtg ccaccacacc 54061 cagctaattt ttgtattttt agtagagatg gagtttcacc atgttggcca ggctggtctc 54121 aatctcctga cctcaagtga tctgctcttg gcctcccatc tgggaccaca ggcatgcacc 54181 atcatgcctg gctgattttt tgtatctttt atagagacag ggtttcgcca tgttgcccag 54241 gctggtcttg aactcctgga ctcgagcaat ctgcctgcct cggcctccca aagtgctggg 54301 attacaggtg tgaaccaccg tgcccagctt cactccagaa atttttaagt aggacttttt 54361 taaatcaaat tgccattgtc tctaatctag aattttgttt aaaaggaaga aggtaaactt 54421 tσatgaatat tcctactgta ataaaactaa atαttaaaca tatgtaggca actggaatta 54481 tgaggtagct gagatagtat ttggaatttt tctgagtaag tcagtgaatg taaggggatc 54541 tgtggtgtta aagtgttgta aatgggtact tagtgcagtc taagtσσata atggcagtaa 54601 ataattgatt tatttttgtc atattatgga taaacatgca ttacaaataa actgatgaac 54661 cacagtatat cttatattag gcttttaaac tgctttatgt atcatgtttc agttttccta 54721 aatgactgat acatttcagt attttgcata tcagtgttaa ttttgagttg gtagaggcag 54781 cctaacaaac tctgattgtt ttgctattag gggatatttc cttcaataaa accaatgaat 54841 tgaaagagaa aatacacctc actttactgt ccatgtgttt tcatttcaca ataagccagt 54901 aacttcatca ccatagccat ctttgggaat cactagtaga cagaatgata agtaggcaaa 54961 ttgctgttcc tgttatttaa gcacagggac tatttggttc ttcctaatgg cgttcctggt 55021 atctgggcat ggctcactgg tcgattccta ccttttagtg actgtagccc ccatatatgg 55081 σtggcccttg gacagatctg tgtttcactc ttatataatt atttgttgta aaatgcagaa 55141 gaaaatttaa aaaatagaac cttttcattt tatcctaggg gagaaaaatg cagttgttca 55201 aactaagggt agaattaaat cagggccaat acagtgttag cacaggtgtt atcattgtga 55261 ccagaaaaca ggaattcttg gggcagcttc tgcttcccca ttttgaatct attattgtta 55321 tttaaaataa ttatatttgt attttactta aagatttagt tgttatttta cttaaaagta 55381 gagttaccat tgatatactt ggcattagta aacccattga ttctgatttg tcagtcgctt 55441 ctgattattg gttttggggg aggaaattaa tgatctagta atcagttcat tagcttgtaa 55501 agctaattaa σσtcttccat atactgtcag ccttacactg accctgcttt ctccccaggc 55561 tgcctattcc caaacttgaa gacaccatta ggagatacct cagtgcacag aagcctctct 55621 tgaatgatgg ccagttcagg taaacactga gaaccttggg tgagcatagt tggggtggtt 55681 caagacaggc tggcaagtag tggtggacca agcttcaggg aatgtctgtg acgtggctgg 55741 gtctccagga acccagaacc tagttgtaca tctgcaagtt caggaaatag attttcattc 55801 atgaaggaσt gaccaagccc cgagagttcσ tσtaaacagg ctσaacagga gatagtttat 55861 aagccagaat gccaaatgtg tactttccct tagcaggtgt acσtgggagg σtσgctggtσ 55921 ctggtcattt atagagagca tgtacccttg gaagggaggt ccattgagga gaccataσgg 55981 cagaccagaa gtctgcatcg tgagcatgtt tattgagttg gatagcatgc ctccaaaatt 56041 tatgσccttt ttcatgaaat ttagtatatg atcttatttg gaattagggt tgtggcagat 56101 gtaattagtt aagatgaggt cctactggag tattgtgggt ccttaattaa atatgactgg 56161 tgtccttgta agaagacaca gagacagcgg tgtgaggaca caggcagaga ttgtgtcctc 56221 tgcctgtgtc aacaagccaa ggcatgccag ggattgctgg caacaccaga atctaagaga 56281 aagccatgca aσagattctt σcccagtctt cagagaagat atagtcctac tgacacctgg 56341 attttgtcct taaagcttcc agaactgtga gagaataaat ttctgttgtt ttcagccacc 56401 cagtttgtgg tgttttgtta tagcagtcct aggaagcaaa tacagcatgg aattggaaaa 56461 taatatcaaa tattgtcaaa aagtggattg cattaagσtc ttatagccta gtgtagtact 56521 ctttttccat aatggaaatt tttctgtaca ggtaactggc attgttgttg gaatcacaga 56581 actcttcact ggacagtgat ggagaagcag atgaattatc cataatctag gcctctgttt 56641 tcaaatattt gttattagtσ atttaaagtt tctcttgata tggtaatagc taccagttat 56701 tgagtattat gttttaggat attctaaatc cttagcttta taaatatttt taatcttgta 56761 aagtggtatt attatccatt ttacacatca agaaaccgag actcagatca agtaacttat 56821 ccaagatcac acagtttgaa aagcaacaga gctaggattc agacttaact tctgttgact 56881 ccagagcttg tgtccttttc tccatgccaa actgσctcct aggatatgga ttattttgtg 56941 agatgttgat tgattttcct aatcattcat tttaagaagg tagtctagat tatcaatttt 57001 agattgattc ctgttctggt tagaggtact ttctgatctc attccaggtt ttagggctat 57061 gctgttgggg acccaaaact ctattatgag ttcctcgcca tgaaσσtaaa aatcatgtat 57121 tccσtaσcat ggtttgattt tgtcttttct tgaatgtttt aggaaaacag aacaattttg 57181 caagagtttt gaaaatggga ttggaaaaga actgcatgag cagctggttg ctctggacaa 57241 acagaataaa catacaagct acatttcggg taggtaggct gggctgtggg tatgatttct 57301 cσcagagccc tcσataatga aaagtaaggc atattctctc ctgttttggt ctcagagata 57361 tttttggtga gaccagcaaa tgaagtaacg tctσatσctc ccttcctgag gtaaattaag 57421 gctgagtgtg ttcctcctct actgaggtgt tgacttgagc ccatgctcaa gaatgatggc 57481 αagσcttctc tgtagatggg attgaggcag aacctaatca atggtcctgt ctgaaaagga 57541 tgσaggatta agtcctatgt cctatatσat tσtgggtσct tcactgtcag acagaactgt 57601 cctctccagc ctσttctctc accaσσcacc ctgacataσt tcctgσtaaa σtσσtcattg 57661 ctccctgaac ccttagtctt tcattctttt gtgcσtttat σσatgctgtt cccaσtaσca 57721 tttttttgcc tggcaaattc ttcttttaag atccaaggag gatggttttc tgtgaaacct 57781 tctcagtcct ttttcctttc σattcagagt tggttgcttσ σacctctgtt cctacagσac 57841 ttσttttaat ttagtttata tatttacσaa ggttataσat gσatatagtt taaagaatca 57901 gaσagttσta taaggcttgt taggaaaaac agcaacttcc tσatcatctt atttcccact 57961 tctcact tc agctcctaaa tcttttgtta tatacσccσg tatσtctaaa ttagatactt 58021 accttactgc atcttgattt ttttgσttta gtcattagct attgaσatct cactgtagaa 58081 gattagaatt cagcagtact ttacatccca ccaσatatgt gggatgtgta taσaσatact 58141 tcctatcαcc ttattttcac agcataggga tttgtaattt tgggtaactc agtatctagt 58201 tttatgctat tatgatcata gaaacactat tgtcagctga ctcatgtagc atattgggat 58261 tgtttttcct ttccagtaca aaσtttttgt tttctctgaa gttaataatt gttσcatctt 58321 ttctcttgtt tagttttcta tgtgcttact aatttacccσ σagaσtcttσ σcaagctgtc 58381 tgaatctcct ctcaatacat gaaagcagat tggacattct atcccttttg gtcttcttga 58441 cgaaacttct tccagaactt gcgacatgct gtagtctgga tttgtgaacσ tcttggccta 58501 ctgtgaagσt gctctcctgt gctctttcac catcagctgg ggcatctgtc atctctctct 58561 catgttggga ctcgtgtttc ttgtctttca tattttctta tttcttggct ttttcttttt 58621 cttttttttt ttttttaaat cagagcacat attσcctgta σtatctggaa acagaatatg 58681 ggaagcaaaa attttaaaat ggcσcttata cttcattgat aatttgtttg gctgggtttg 58741 aaattatttt cccacagaat tttggaggct ttgctccatt gtcttttagc atccagtgtt 58801 gctgttggta aatctaatgt tattctgaga cttaatcttt tgactacttσ ttctctctgc 58861 ctttggaagσ tttttagaat tttctctttg tσcccagtgt tttgaaattt caggtaatgt 58921 gttttagtat gtgttgggcσ aσtctgtgag tcctttgaat ctggaatctc atccttσagg 58981 tctgggatat ttccttgttt tatttctttg gctttcttcσ tctccatttt ttttctctgt 59041 tttttctttg tggaactcta ttattattca ggtgtagaat ttctgggtct catcctctaa 59101 ttttσttttσ tσtcacattt ttcatctctt actctttttg ttacattttσ ttgggagaσt 59161 taσttaattt taatctctca ' acctgttttt aaaactcctg ctttcctatt ttttacttσσ 59221 acaagctctt ttttcttctt atggtgttct ttttaaaaat agtttatctc tgataatttt 59281 tttttaagat ctσttσtctc ttcatagtct gttgσσtcca agttgctttt cttctgtttg 59341 ctttgσσctt ttctttcttc agatgcttca taatcctgtg ttgtcttcga tatgagtgag 59401 atattaaaaa gctcttggaa gctatgtgga tgggggtgag gcttg'tcagt tacaggcttt 59461 gctσtaatgt gattgatatg gtttggctct atgtccσcac ccaaatctca tσttgaattg 59521 taatσσccac gtgttgaagg agggacctgg agggaggtga ttggatcatg ggggcagttt 59581 tccccatgct' gttctcatga tagttagtgg tttctcacga gctσtgatag ttaaaaagtg 59641 ttcagcagtt σσcccaσttg ttcgctttct ctcctgctgc caσataagat gtgcσttgσt 59701 tσσσcttcac σttgcgctgt gattgtaagt ttcctgaggc σtcccσagσσ aσaaggaact 59761 gtcagtcaat tagaσσtσtt ttctttataa attacccagt σtσaggtggt tctttatagc 59821 agtgtgaaaa tggactaata tagaaaactg gtaccaggag gggggcattg ctacaaagat 59881 acctgaaaat gtggaaacaa ctttggaact ggttaatagg cagaggttgg aacagtttgg 59941 aggggtcaga agaagaσagg aagatgtcag aσagtttgga aσttcttaga gagttgaatg 60001 gttttgacca aaatgctgat agagatatgg acaatgaagt ccaggctgag gtggtctcag 60061 atggagatga ggaacttatt gggaactgga gcaaaggtca ctctactgtg ctttagcaga 60121 gagactggtg gcattttgtc cctgtcctag agatctgcag aactttgaaσ ttgagagggg 60181 tgatttaggg tgtctgacag aagaaacttc taagcaacaa agσattcaag atggcttttt 60241 ctgaaagcat atggtcatat gcattcacag agagatgatg tgaaagtggg acttatgttt 60301 aaaagggaag cagagcataa aagtttggac aatttgcagc ctgaccatgσ agtagaaaag 60361 aaaaacccat tttctgggga gaaattcaag ccacaagctg σagaaatttg σataagtaat 60421 gagaagccaa atgttaatag' ccaagaσaat ggggagaatg tcttgagggc atttcagaga 60481 tσtttacagt agcccctccσ agcataggcc cagaggccta agagggaaaa atggtttcct 60541 gggcσctgct gttctgtgca gcctcgggac atggtgccct gtgtcσσagg σactccagct 60601 cσagccatgg σtaaaagggg σcaaggcaca gctctggcca ttgcttσaga gggtgσaagc 60661 cσcaagcatt ggaggαttcc ccatggtgtt gggcatgcag gtgtgcagaa aaσaagagtt 60721 gaggtttgaa aacctcgtcc ggccgggtgc ggtggctcac gcσtgtaatα ccagcacttt 60781 gggaggccaa ggcgggtgga tcaσaaggtσ aggagatσga gaσσatσctg gctaaσatgg 60841 tgaaaσcctg tctgtattaa aaatacaaaa aaaattagcc gggtgtggtg gcgtgcacct 60901 gtgtσccagc tgctggggag gctgaggcag gagaatagcg tgaacσcagg aggcagagct 60961 tgcagtgagc caagatagca σσactgcact ccagtσtggg tgaσagagσa agactccatt 61021 tcaaaaaaaa aaaaaaaaaa aaagagacaa cσtcctccta catttcagag gctatatgga 61081 aacacσtgga tgtccaggσa gaagtσtgσt gσaggggtga agccσtcatg gagatσctct 61141 actagggcaa tgcagatggg aaatatgggg ttagagcσcc cacaσagagt tcccaatggg 61201 gagσctagtg gaactgtgag aagagggcca ctgcccttca gaccσσagaa tggtagatσσ 61261 aσσgacagtt tgcacσatgt gσctggaaaa gccacaggca ttcaatgcca gσctgtaaaa 61321 gcaaσcatgg ggctgtactσ tgcagagcca caggggcagg gctaccaaag gccttgggag 61381 ccσacttctt acatcagcat gccctggatg tgagacatgg agtcaaagat tattttggag 61441 ctttaagatt taatggσtgσ cctgctggat ttcaggσttg σgtggggcct gtagcccctc 61501 tgttttggσσ aatttσtccc ttttggaatg ggagcattta cccaatgctt gtaacaσcag 61561 tgtatcttga aaataactaa ttggtttttg attttacaga σtσataggca gaaggaactt 61621 gσctttactc agatgagaσt ttggcttgta attttgagtt aatgctggaa tgagttaaga 61681 ctctggggσa σtgttgggaa gacatggttg tgttttgaaa tgttagaagt acatgaaatt 61741 tgggagaggσ σagggσagaa tgatgtggtt tggctctgtg tctcσaacca aatctgatct 61801 tgaattgtaa taatcccσaa gtgtσaaggg agggacctag tgggaggtga ttggatcatg 61861 gggtagtttσ σccσatgσtt ttcttgtgat agtgagttct catgagatct gatggtttaa 61921 aagtgtttgg cagttcctac tccttgcttg ttσtσtσtcc tgσtgctgtg taagatgtgc 61981 cttgcttccc σtttgσcttc caccatgatt gtaagtttcc taaggccttc ccagσσatgc 62041 ggaactaagt cagttaagct tctcttσttt ataaattatσ σagtσtσagg tagttcttta 62101 tagcagtgtg aaaacagact aatacagtga tcσagctaaa σtgσttcσσt gggttgσσσσ 62161 taatggtagt gtagttgggt tagcttcσct agggaggctt ttccagtaaa ctgccaaaag 62221 gttgctagtg ttgtagaagg cagggtaagt aagggaagaa ggtttgagat σtσaaαtgtg 62281 attσaggtσt σσσagtttta ttttatttat ttattttttg agaσagagtσ tσattttgtσ 62341 aσccaggctg gagtgcagtg gtgσgatctc agσtcactgc aacctcagcc tcctgggttc 62401 aagtgattct cctgcctcag ccttctgagt agctgggact acaggcacgt gcσaσgacac 62461 σtggctaatt ttttgtattt ttagcggaga σggtgtttca ccatgttagc caggatggtc 62521 ttgatctcct gaσσtcatga tacacccaσc tcgccσtccc aaattgctgg gattaσcagc 62581 ataagσσaσt gσacccagcc cccagtttta ttatctccag agagtaaaac ttaagtcttc 62641 tacaggagtg aggagggaat ctcaggttgt ggtagtggtg atataattga atagtccttc 62701 aaccagatgt atσtaggttg ccaattactg agσσσtσtgg gggttσtgσt gtgσaaatσa 62761 tatgatttσt tggctttctσ tσctgccaat ttaggattgg σtttcttgag tctgctttag 62821 tcattaσcag ttgcataagt gctttcσagc ttccagtatt tgttttctcg tctcσσattσ 62881 tσttggαctg actggtttat gtctctttga aattσttttg ctaaaggggg gtcagaggσa 62941 tgaatttatg tσttctttca tcaaatatat cttatσσacc agtaσttttα tctcaσσatt 63001 ttagtgcatt gcgttatgtt ttaattattt gσctcσttca σσagagtttt tσagaatσaa 63061 agaccatgtc σtattσσtct ctaaatcccσ tggaccaagg cctggcacag caσtgattct 63121 caagggatgg aatgagtgga tggaσσaaσa aatgagtaaσ agagaaatσt gcatctatta 63181 atσcttttcc σagtgctata catatgaaca ttatttgcct gaatgatagt cσttatttat 63241 agagtttatt catgtttact aatσccagca ggaactttcc ctgacatatt ttctgataaa 63301 atattgσttσ tggaattttt acaggtaaaa catctatagg aaσtσagagg gctagtctga 63361 gtgatccatg caσtgatatt tataatagct tttttagtac tttctaaaca gggagtgtac 63421 aaatgtacac tgtacataga aggacaatga agacgttccc σσcttatcgg ggagcaatca 63481 agtatgattg ttgcccσtga aaggagatga agσaagagaa acctaaagag atggggtggg 63541 aattaaσtat tσtgttσcag catgaatgca agtggagtgt taσσatattt tattccttta 63601 aaσσaagaaa ggaaaσagaa gaggaagaaa aagcaattaa taaacattag gaaaatgcaa 63661 accaaatctg caatgσtata σtaσtttaca cctacσagaa tatσtccacg ccacaagaca 63721 tgtaacaagt gctgctgagg atgtggaaaa attggaaccσ tcacagacag ctcgtgggaa 63781 tggtgcagcc actttggaaa acatcctggc agttcctcaa aggttaaaσa gagacttacσ 63841 atgtgatagt agttccactc ctagctatgt cσataσaaaa aσatgtataa gaatgttσat 63901 aaσaacataa ttcttaatag ctaggtgcag tggctσacac σtgtaatccc agcactttaa 63961 gaggσtgagg tgagaggatt acttgaggcc aggagcttga aaσcagcctg agcaacataa 64021 taagaσccca tctctacσaa aaataaaaaa attagσσagg σtggtggtgt gσatctgtag 64081 tcctagctac ttgggaggσt gaggtgggag gatcgσttga gσccagggtt caaggctgca 64141 gtgagccatg atcataccac tgcaatccag cctggatgat agaaatcctg tgtctcttaa 64201 aaaaaaaaaa ggcaatgtaa ttcataataa agagtggaaa cagttσaaat gtccattacc 64261 tgatgagtgg ataaacaaaa tatagtatat cσatataatg gaaσattgtt αagcgσtaag 64321 aagaaatgaa gaacttaaat gctacaacat ggatgaacct taaaaaσatt attaggaggc 64381 cgaggcgggt ggatcacctg aggtcaggag tttgagacca gcctgcccaa catggtgaaa 64441 σcctgtσtσt actaaaaatc caaaaattat ctgggcatgg tggaggacgc ctgtaatσσσ 64501 agσtactcag gaggctgagg caggagaatc gcttcaatcc gggaggσgga ggttgσagtg 64561 agccgagatt gcagσactgt tctccagcσt gggσgaσagg agcgagcctc cgtcccaaaa 64621 aaacaaaaσa aaaaσattat tgtaagtgat agaagσtaaa tgcaaaacac σatatattgt 64681 atgaσcccat ttgtatgtσt tgaattattg cagagcaaaa acattcaggg aattσttσtc 64741 tctggaggtt gatgσcattt cctttgtσta tgcttgaatt ttttttcttc ttcaaatttt 64801 atttttaggg acagσattaa cattttatgt tatttttttc tttttatttt ttaggaσcct 64861 ggtttgatat gtacσtatct gctσgagaσt ccgttgttσt gaaσtttaat σcatttatgg 64921 ctttσaatσσ tgaσccaaaa tctgagtata atgacσagct cacccgggca accaacatga 64981 ctgtttctgc catccggttt ctgaagacac tccgggctgg σσttσtggag σcagaagtgt 65041 tccacttgaa ccctgcaaaa agtgacaσta tσaccttcaa gagactcata cgσtttgtgc 65101 cttcctctσt gtσctggtat ggggcctacc tggtcaatgc gtatσσcσtg gatatgtαcc 65161 agtattttcg gcttttσaaσ tcaactcgtt tacccaaaσc cagtcgggat gaactcttca 65221 σtgatgaσaa ggσcagacaσ ctcctggtcc taaggaaagg aaatttttat atctttgatg 65281 tcctggatca agatgggaac attgtgagσc cσtσggaaat ccaggcacat ctgaagtaσa 65341 ttσtσtσaga σagcagccσσ gccccσgagt ttcccσtggσ atacctgaσc agtgagaacc 65401 gagacatσtg ggσagagctσ aggσagaagσ tgatgagtag tggσaatgag gagagcctga 65461 ggaaagtgga σtσggcagtg ttctgtctct gσctagatga cttccσcatt aaggaccttg 65521 tccacttgtc ccacaatatg ctgcatgggg atggcacaaa cσgσtggttt gataaatσct 65581 ttaacctcat tatcgccaag gatggctcta ctgccgtσσa σtttgagσaσ tcttggggtg 65641 atggtgtggc agtgctcaga ttttttaatg aagtatttaa agacagcact cagacccctg 65701 σcgtcactσc acagagccag ccagctacca ctgactctac tgtσacggtg cagaaactca 65761 acttcgagσt gaσtgatgcc ttaaagactg gcatcacagc tgctaaggaa aagtttgatg 65821 ccaccatgaa aaccctcaσt attgaσtgcg tccagtttca gagaggaggc aaagaattcc 65881 tgaagaagca aaagσtgagσ cctgacgcag ttgcccagσt ggσattccag atggccttcc 65941 tgcggcagta cgggcagaca gtggccacct acgagtcctg tagcactgσc gcattcaagc 66001 acggccgcac tgagaσcatc cgcccggcct ccgtσtataσ aaagaggtgσ tctgaggcσt 66061 ttgtσaggga gccctσσagg cacagtgσtg gtgagσttca gcagatgatg gttgagtgct 66121 ccaagtacca tggcσagctg accaaagaag σagcaatggg tgaggcaggg gtggggagσa 66181 tgσccttggg tσttgtσctc agtgcttggg taagcaagcc taaatσattc tactσcaaat 66241 ctgatttcta cσσgttσact aggtttaatc catcgσcaaσ tσccσaaatt tttcttttct 66301 accctagcag tctgaacagσ cacactagcc actagggatc agaatgttct tgσctσctaa 66361 gcaggggtgg ggaaatgcat gtgtctttgt cctσatttaa g'gtσaσtttσ agσtgtgaσg 66421 σattaattσt tttttctttc tttttttttt ttttttttgg agaσaagagt ttσcctccgt 66481 σcaggctgga gtgcaatggc gtgatctcgg ctcactgcaa cσtαcacccσ σaggttσaag 66541 tgattσtcct gcctctgcct cccaagtagc tgggataata ggcaσσcgcσ actacacctg 66601 gctagttttt gcatttttag taaagaaggg gttttgccat tttggcσagg ctggtcttga 66661 actcctgaσσ tσaggtgatσ catσcctctc agcctσccaa agttσtagga atacaggcgt 66721 gagσcaccgc acctggcctt tttttttttg gagacacggt ctcattctgt σacccaggσt 66781 ggagtacagt ggtgcaatca tggctcaσtg caacσtσaac ttcσttggσt σaaacaatcc 66841 tcctgcctca gcctcccaaa tagσtgggaσ tataggcatg caσcacσatg σσcagctgat 66901 attttaattt tttttttttt ttgagatgga ctcttgctct gttgcσσagg σtggagtgσa 66961 gtggcacaat σtσagσtσaσ tgcaacctct gcctcσtggg ttσaagσgat tctcctgσct 67021 cagcσtcctg agtagttggg actacaggct tatgσcacca tgcccagσta atttttatat 67081 tttσaataga gaσggggttt σactatgttg gcσaggttgg tαtcaaactσ ctgacctcat 67141 gatσtaσσcg cσtσaσσctc σσaaagtgσt gggattatag gcgtaagcca ccatgccggg 67201 σσtaattttt aaaatttttt gtagagatga ggtσccactg tattgcσσaa ggtggtσtσa 67261 aaσtσctggg ctcaagcaat cctcctgσct tggcctccca aagcactagg attataggca 67321 tgσaccactg cacccaaσσt ttttctatta ctgattggtt atcagactca cttttgaaaa 67381 tttaggattt ctaaacttac ggcccσacta gcttσaσctc agttgtaatg tgtctgctct 67441 σtgtaaacag gttatctcag aagctcttσt σaattgtcat cσgtσattaσ σtttttttga 67501 taaaattcaa gacσtggaaa ggacctggag ggtcatagtt gtcctttcat gttgctatga 67561 agtgctggaa gtgaaaggga cctccaagaσ attσtaatct tctcttcctc σattttatag 67621 ggagaaaacc aagσcactgg ccccgttaca cagcaagtta gtagtaagac tgagattcga 67681 accσtggtca aacagacttt ccattttgtt ccactgactc aatcttctct tttacacttg 67741 aatcagactt ttagttttat tgtagttttt gagtccatag ctgtαttσσt gtactgtσtt 67801 gaσtctttga ctaaactgat ttcaσatctt taaaattatg ctttcσtttt aggctσattt 67861 ttagσtσagc tgttgacagc tatttttaaa tgtaaσatga cataatatat ttcctaaata 67921 atttaaaata atctagcttg agctgctctg aaggttagtc agttggtggt gtgcatagag 67981 gtagagcctt cccccactσt caaggatgct gtgaggggta ttcctaccat gtggtgagtt 68041 gggaggtttt cctgaggtσσ ttttσσatcc tgagactσtg gttttσcatt ttgtttσtσa 68101 σaggccaggg ctttgaccga cacttgtttg σtσtgσggσa tσtggcagca gσcaaaggga 68161 tcatcttgcc tgagctctaσ ctggacσctg cataσgggσa gataaacσaσ aatgtσσtgt 68221 σcacgagσac actgagσagc cσagσagtga aσcttggggg σtttgσccct gtggtctctg 68281 atggctttgg tgttgggtat gctgttcatg aσaaσtggat aggσtgcaat gtctσttσσt 68341 aσσcaggccg caatgcccgg gagtttσtσc aatgtgtgga gaaggcctta gaagacatgt 68401 ttgatgcctt agaaggσaaa tσcatcaaaa gttaacttct gggcagatga aaagctacca 68461 tσacttcctc atσatgaaaa ctgggaggσc gggcatggtg gctcatgσσt gtaatσccag 68521 cattttgaga ggctgaggcg ggtggatcac ttgaggtcag gagtttgaga ccaacctggc 68581 caacatggtg aaaccttgtc tctactaaaa atacaaaaat tagctgggtg tggtggcatg 68641 tgcctataat ccσagctact tgggaggttg aagcagaatt gσttgaaccσ aggaggtgga 68701 ggttgσagtg agσtgagatσ acaccactgc aσtccggcct gggσgacaga gσgagaσtgt 68761 ctcaaaaaaa caaaaaagaa aaaaaaactg gggcctgtgt agσσagtggg tgctattctg 68821 tgaaaσtaat cataagctgσ σtaggσagcc agσtaσaggc ttgagcttta aattσatggt 68881 tttaaagσta aaσgtaattt ccacttggga ctagatcaca actgaagata aσaagagatt 68941 taagttttaa gggσatttaa tσaggaggaa aggtttggaa aactaactca ggtgtattta 69001 ttgtttaagc agaaataaag tttaattttt gcttgaagat ggttcttaat ttcttttaac 69061 ctaattcσta atσctcacaa agatctttcc aaσagσaagt tcagtaagtt caggtaacag 69121 tacgtcacca ttggσttctg gctcattgag tgatggtggg atcgσggttt catctctgta 69181 aacttgccct tgaσtgggga gataαcatct ccttaaaaat actσttcatt ttcctaagga 69241 gtgaactgct gctgcacgaa ttσttatttg tggagggagt agσtgσctσc ttacttcacc 69301 ttσatgσacc agtgcagcgt gaacaggggσ tttattgatg gggσttggga agctgtaata 69361 aagtccagσa tgσagattgt gaaggtttcg tatagccacc aggagacaag ggtcaaagga 69421 acgagcctσt gtgggctctg ctgcttagag tactttgtcc tttσtcagtt cttaagggca 69481 actgggaagg aagagggatc agcacttcac aaactggtgg gtgacσtcat agattcσcac 69541 agactσctgg gccttttcat catagtcagt ccagtcctgg gaaacaaaat ggcattgtta 69601 gcctcacaac gσagaatgσa gccatgtgga gagσagaaaa ctgggactta aaaggccσag 69661 ctσaggσtct gactcaaata atcatgaaσa tgtatgaσσσ tgaaσagagσ cagatagctc 69721 aggcctgaat tctagσtctt tcagttgtat gactgtgggσ aaatcactta acttctctga 69781 gtσccttctc σgagtσctgt cttctattta aaaaaaacaa aaacaaaaaa aggacaatgg 69841 agttσatatt gaatgttgaa agaatcaaat gaggtaacaσ atttaaaagc actcagcagσ 69901 cgggcgtggt ggctσatgcc tgtaatσσσa gσaσtttggg aggσσaaggc aggtggatca 69961 tttσaggtσa ggggtσσgag aσcatcctgg cσaaσaaggt gaaacccggt σtctactaaa 70021 aatacaaaaa atagccagga atggtggcag gcgcσtgtaa tσccagctac ttgggaggct 70081 gaggtaggag gatcacttga gσccaggagg cagaggttgc agtgagctga cattgcacca 70141 ctgcactcca gcctgggcga cagagtgaga ttgtctσaaa aaatacataa aataaaataa 70201 aagcactcag catagtgagt gcctggcaca tgtaagagct σagtagatgσ tagσtgσtgt 70261 tattaggtgc tgagcaaatg aaatgaagtt tttgtccttσ σttcaaggσt tgagσacaag 70321 gcttttσtat σtgαagggta gtaatatgtc cagtaataca gactatttct tgttσttσat 70381 ggtagttagg tgσagtaaag σσaσσaσaaa cactgaatta gggaatactg aatgaatact 70441 ccccggggaa atacagggtt aggttcctat gagcctctgg tcacattttc atcaaccaat 70501 σaataatcta gctttatgtg tttctgttta aagataactt atttaatata tattgttgat 70561 tcatgaaσtc aσagσcagαa gσactatagc tσatgcctga ataaagctta tctaacacgt 70621 attctσtσtg taaggggcat catagctttσ tσatacgtag gaacattaga aagσacttta 70681 gcactatacσ tgtggcσatt tσaaσagcaa aatcactaac aaaaagcaca aaaatacaga 70741 gttggctttc cattgatgag σcttgtccac caaaaaaata attccσacca ggtgσcctaσ 70801 agtaσctccc aaagσcσσσa agtσtσatac cttctcctgσ agattaatgt σactgaaggc 70861 tgtccctgac tccacacctt cagcagcaaa cccagcctgc agggcacaag aaggtaccag 70921 ttagtcttgg caaaagaagg cattgggcta taagtaaggg cσggσσaggσ tgctggctct 70981 tσtσacactt ctgggatgga ggacagagat gcagtatgag tacctgtctt ggaataactg 71041 ctgagσttσσ aggacccggc agctgcatca gaactagagt ggtggtttct ctgaattaca 71101 gcσttggaσc agaaggcagc aggggcagcg taatccσttσ cactagccct ggtttgctga 71161 aggctcctgg gcatgtcatt tcσcaggttg gaccttagtt attgataaaa cggggatgaa 71221 gtatttgctc ttσtgσctac ctcaσagatt tgttgtgagg tgaaaσatgc acaaataaag 71281 ggggatgagc acσagctcaa gtcagataga tctgggttga aactatagct ccactgctta 71341 ctgtgtgaσσ ctgagcaagt tgσaaaatct cttcagttcσ ttσctcatσt gaagaaσagg 71401 atgaataaat tσatagggtt accataagaa ttaaatgtgg taacatgtaa aaatgatggc 71461 atgggtgccc aagσataσag cagccaσtta agggacaatt attactaccg ctagaaagga 71521 gaatgtctag tσσatggtat σtgtaggtag σacagttσtg gctgtcactt cataσatccc 71581 ctcccσaaag aσaaagattc cccagaaaga tacacacaσa σσtgσggctg gaaatcaact 71641 ggttσaaggσ cccggcactc aaaσtσcact attgtcttga agttctcatt gtcttcagcc 71701 tagaaaggaa gtgtgttgag gaggcaggcc caaatgagct σtσaggatga σσccatggcc 71761 cctctccttσ ctgccaaatg ggcacttact gσσσσtggag gσσtagtatg agacccagga 71821 agaactcatc cccttσttag aggaagαctg ccttgggcac σtgσtcccta' tgaagctttσ 71881 tgtagacagc agacatggag gctgcagaag agcgtggatg ctggggtcaa cctgσctgga 71941 tgtaaggtaa gctσtgccta tcttcccctc tgggcccaag attcctaaac tgtcaaatag 72001 agccgaggaa aσσtσtaσaa ttttactgtc agattttgaa atgcatataa agtgcccagc 72061 acagtgσtσa ataaatagta aataaaatta tσaaσaσcaa aaatatgaac aagaatgtta 72121 agctccaaag tctctagatc atccaaacag acccagtaca cttaaccata gσcttttgct 72181 gaccatctgσ catgσagtaa gggcagaggg ctgtcttata gcctttgaaa tggttatgta 72241 tgtggagggg gσacctcttg gggggcaggt ggccaggaaa ttcatgcσta σσtgacctat 72301 gggcttaggg accacaagtg ccatgcσcta cattσagtct catσctgtca ttcactgtaa 72361 agtaatttσσ tgσacactga ccaσatσtct ggcactggta aggcacttct ctgttagggc 72421 cctagttcga ttcttgtttt ttgtattttc cactagatta ttatgtacgt gaaggcgagt 72481 cσtcatttaa tttctσttta acttcaggaσ aaagccaaga atttggcaca aσtcaagata 72541 ctttaaataa ataσcaaata aggaataggt gaatacatat aactggσttt σtttaaacaa 72601 acagatσcaa agcacacσct ccctcacctt tgggσtaact tgttaacact gatgatataa 72661 aggatgggat gcaσcaaacg aσtaccσσac cσatggtttc agagaaagct tgctagtccc 72721 ctaaaatgaa gacaaggcaa gtgctσtcag tgatgcaaac tgaacagcta ggttgtgtca 72781 gaggtcccct gagctctcac agcccagccσ tσataagaag gσactgcaag aggcaatata 72841 cσaagσactc agtgtaσagt ggataaatga ctgagtcaaa gaagaaσtaa gttcatgagt 72901 gaatgtccta tggσaggtca ctctgatgca ggcatgactc tagaacccag acctaσtaaσ 72961 tccagttagg atttaagσcc accatcσctg ccaσtacagc agcaaaσtta σattgtaagg 73021 cttgatggtg ctgσttaaaa tctctgaaat agaaaagaga acacaaagtt gaσttgagtc 73081 cataccctcg cσσσagccag gtgcccaσat gtggccσtga aaaagatσaσ gσtgtaσagg 73141 tgtσggσatc ttaggcctga ctccacασtc aggtaacatg agtctacttt cagcctggtg 73201 ccaggaagct gtgggccacc ctggσagaac tcagtacgσa σagσctgacc taccgatgga 73261 attttctσtt gcacaσagct tgcacttctg gaccatggaa gcactgccac ggσcccσctt 73321 cagtgσσaca ctgtcctggc aaaaagcaaa cagaactttc agtcacatat gaattagatg 73381 tacagtcctg aggagatσga gσσcaccatt tattgtσcac ttaaagagaσ σaagaσccag 73441 aaagggtaac ttactaggaσ aagaσtσσtg ggaaggσttc ctgaggaaaa taaaaaaagg 73501 gcttcccctt gattttgaac tctgcctcat acctcaaaga tgcctattga atccagtgct 73561 gatσacactg acacσtaσcc tcccaaacca caaaaagcag ggagcaaaga actggagaga 73621 tgaaggccag tttccccaaa tσσctgccca gaagtgtatg tgtgtttgtg agtgtttatg 73681 ttgggggttg ggcggggaaσ agttaσσatc agccggatgt actgccaσtt gtσcgaaatσ 73741 tσaσσaσagt tgccaσattt catctttggg gaaaaagaat gttagtaaag cagctggctc 73801 tgctgcaαag acaccaagga aagggtaaga acagtgggag gtgggσaggc tcatgatcta 73861 σσttcttgat ggcaatctσa cttcatccσt aacacσtgcc ccaacaagga caaaaσtaga 73921 aσtatσtσtg ggcaaaggat aggtaaggct gtttασtatg ccggcgtgcσ caccctcctc 73981 tatgaagtgc tcagtgtggc σggggattσa aggcacctgt ggtgcagaaa tggtttcagc 74041 ggaggtgagg ggggggaata tggagagatt tgttagaaga tacaaaatta cagctatatg 74101 ggaggaataa gttctagtgt tσtatagσac tgtaggatga ctatagσtga caataatata 74161 tagtttcaaa tagσtaggat attaaatgσt σccaacacaa agaaatgata cacgtttgag 74221 gtgaatatgc taaσtacctt gatctgatσa caatacatta catttatσgg aacatcacta 74281 tatacσccat aaatatgtaσ aattctgtgt caattaagaa aaaaaaagag aaatggcctc 74341 agcaggcccc cgaccσactc tgσttggtta gctttatgtt σccacaggcσ ctgtatgtca74401 ctggtataag cacttatcaσ tctattgtta σtctattttt ctgtctcctt cactσgattc 74461 cgcttcttca agσσaaagaa σagattσtσc caagtaagcc σtggtattca ggcttcaaaa 74521 tσctgggaaa caaaagtagt ccggaggcag cttccσgaaa aaσagggctt ttgagaggta 74581 cagaaggatg σtgggatttt tgacσaggag taaaacagag cagaagctσt gggatσtgga 74641 agagtgaaga gcctcgaact gctggggaag gggaggσσtc tgtagaccat gccactaggg 74701 tacσagσttt accagtgtgg gagggσtaag gaagggtgga ttaσgcacaa aattaaacta 74761 tttσacaata aagaaaacca aatcaataaa cgaaaggcga actattcacc ttattaaata 74821 atcacaagcg tccσttcaag tagcatttcg tttagtgtcc atttacagaσ σaσgaaatat 74881 ttaaσaσagg gaagaaσtaσ aaaatgaagc tttccaagaσ tgccaattag agataaacca 74941 atacacttta atagaaagca aaσgtaaaat tctaactagg aaaaccccga acacttaatg 75001 tgcctggtta aatattttct catactgccg gagagaaggc tσσggttcag cactgagatc 75061 aggacgggcc tcctctcccc gggccσcgcc ccggccgcaσ cttcaggtac σaσσggaagt 75121 σσtσgcccac gggccggagg ttggtgatgt tctσcagcgt ggctttgagt tgcagcgσga 75181 ttttσtgagg gggagggcca gagcgactgc gtcagccgtg σσtgcgcagc σccaσgcctg 75241 σσcgaccctσ σcgcattccσ agcσgtgggt gσσaσaggga gaσaσtcctt ctgcctcctg 75301 ctccttσagσ gσgcacccac tσgcttcatc tcσtcctggc gcgagctgtt gcctcccaga 75361 ccctcgcσac ctcccctccg tgtccσcgcg gcgggcggcc tcccσtcacσ ccσatggtag 75421 ccctctcσgc cσggtgσtgg σtgσggccct tgcσgttgct ttσcggcgcg tcgtaaaagg 75481 cgggtgσσgt σtgσgcaccc tcagtagggc ggggσcgggg ccgggccgcg gggσagggac 75541 ttctgcgcgc cgσtgctcgc σtggcccact gggcttttcg catσtgggga tσtggggσσa 75601 gtggaggtca gcσaggtccg cgagcaacct gtgctcaggc σagσggaagσ σtgaσtσσag 75661 gattcggtgg tgcσacagac agttactgaa cgccaatttt gtgσctgctt taagcgaaca 75721 ggacagttcσ tgaσcctcag ttσtttσcag gctσttσact actctgcctg ccctggaaσt 75781 tσtσagatσa σgtcagctcc ctctgcccag gggaaaagct acaaaaggaa gagttcσaag 75841 actgcσaaat aaagataaaσ caatacgctt taaaaagtag aatgtattgg tttatcagat 75901 ttggggatga tgcctttctt caaactgccc tttσσtgttt cacccaagag acctggtttc 75961 taggcccttc tσσagagttt gccctgtgtσ cacatσcttc tcactgtggt ccttgcgaσt 76021 ggaσattσcc cttσagσtgg ctcttttttg ggagσσσaσc tggcttatσc ttctctcata 76081 acgtttattg aactttattt tacctggcct cctgtσσagg σtaσatctga gaccatgcag 76141 gagσtgtgga gattaaσggt aaaaggaaσa gσaσattσaa gaσtσttσta ggaggtgggg 76201 σaagatagcc aaatagaacc ctcσagtgat cctcσtσctc ctσttccctg gcaggaacaσ 76261 caaactgaaσ aaσtatccac acaagaaagc accttcatga gaaccaaaac tcaggtagca 76321 atcaσagtag σtggttgtaa cgtcacatca agatataagg caatggctgg gtgcggtggc 76381 tcacacσtgt aatcccagtg ctttgggagg ctgaggcggg cagaccacct gaggtcagga 76441 gtttgagacc tagctggcca acatagtgaa aσσσtgtctc tactaaaaat acaaaaatσa 76501 gσσgagtatg gσagtgcaca cctgtagtcc cagctactcc ggaggctaag gcaggagaat 76561 tgtttgaacc σgggaggtgg aggttgtagt gagctgagat catgccattg caσtσtagcc 76621 tgggtgacag agtgagactc tatctσataa aagaagaaaa aaaaaggaac aaggcaatga 76681 agagggtagg aaagacagtc ttgaattgct acσaσcaccc ctcσσtcatc ctctggcagc 76741 acctggctgσ σtggcataga gagagaatct gtgtgcttat gggactttgσ attggaaσtg 76801 agttttgccc tgtcacagtg gaaagcaaσt cagggσagaa ttσagctagt gcσcacagag 76861 gaagcactta gagaaaccct agccagaggg gaatcatcca tccαagtggt caggttctgg 76921 cgagcσccaσ σaccactggc taaagtgσtt cagggtcσta aataaattσg aaaggσagtc 76981 taggccacaa agactgcaat tcσtgggcaa gtcσtggtgc tgtgctgagc tcagagcccg 77041 tggacttggg gtgcacacag cctagtgaga tacσagttgg ggagccaaag gagtgtttat 77101 gtcaσσagtc cσσcaacccc aggσagσaσa gctcacggct ccaggagaga ctσσtttσcc 77161 ttagaggaaa ggagagggga aagtaaagag gactttgtct tacagcttgg ataccatcσc 77221 agccacagta gaataaaaca ccaαgσagag tσσσgaagcc cccttgcσag gctctatctc 77281 σcagatattt ctagagctac catgggccag aagggaaccc gctgctttga aggaaaggac 77341 cσagtcctgg σaggattcat cacctgctga ctaaagagct gttgggcσtt gaataaaσat 77401 ttgtaatagc caαagtactg ggtgaggccc agtactgtgc tgccttcagg tgtgaccσag 77461 tgσcttccca gtaatggttg ccacagggag agaσtccttσ tgσttaagga aaagagagga 77521 aagagttaaa aaggagttgg tσttgσaaσt tgggtaσσag σtσagσcaca gtaaaataaa 77581 gcaccaagta ggtttctaaa gcccggaσtc catgccctag σtσctggaca gσatttctaa 77641 acccaccctg ggccagaagg gaacctgcσa ccccaaaggg taagacacaa gcctggctgg 77701 attcaccacc tgctgactaa agagcctttg ggctttgaat aaaσatcagc aataaccagg 77761 σaatagtcac catgggcσtt gggcaagaσc cactactgtg σtggσttσag gtttgaσaca 77821 gcaσagttσc agcagtggtg gσcacagggg tgσttgtgtσ actcctctσc caactccagg 77881 cagσtσagσa tggagagaga gactcσattt atttgggaga aagtaaggga agataaαaag 77941 agactctgσσ tggtaatcca gggaattctc tcggatctta cccaagaσσa tσaaggcagt 78001 acctctgagt ctacaagagt cacagcatcg ctgggtttgg ggtgcσccσt aatgcagtta 78061 cagctgcagt gaccaaatat ttacatσaσa acactσattt σcctttgagt aσttggaaaa 78121 gσcttctgaa gaaggatgag tacaaataag cccaaaσtgt gaaaattatg ataaatacct 78181 aattattcaa tgctctgcat tgaccaacag tcacaaacat caataσσatc caagaaaaca 78241 tgacctaatσ aaatgaacta aataaggcac cagtgaσcaa tcσαagagtg aσagagatat 78301 gtgaσctttc agagaattσa σtgtσaσtga gaaagctcag tgaaattcaa gatagcacag 78361 agaaggaact cagaatcctg ccagataaaσ ttaacaaaga gatggaaaaa ggaactσaga 78421 atcctgccag ataaatttga caaagagatg gaaataattt taaaaattaa atagaaattσ 78481 tggagctgat aaattcaact gataσaσσaa agaatgσacc agggtσtσta aacatgagaa 78541 ctgatσaagσ agaagaaaga attagtgagc ttgaaggcag gctgtttgaa aatacaσaga 78601 agaattgaaa gaaaaaataa σaaaaaagga tgaagtatgσ σtaσaatatσ tagacaatgg 78661 ccacaaatgg gcaaatσtaa gagttattgg ccttaaagag aaggtagaga gaaattagga 78721 tagaaagttt attcaaagga agaataacgg aactttccaa acctagagaa atatataaat 78781 attσaagtac aagaaagtta tagaatacca agcagattta acσσaaataa gactacctca 78841 tgtcatttaa taatσagact cccaaagatc aaagataaag aaaggatcct aaaagcagca 78901 agaaaaaaga aacaaataac acacaaagaa gσtσσaatgg gtctggcagc aggcttctct 78961 gtggaaagct taσaggσσag gagagtggσa tgaσatttaa agtaσtgaag aaaaaaaaca 79021 tttatcσtag aatagtatat σcagcaaaaa tgtcσtttaa acatgaagga aaaataaaga 79081 tttσσtagac aaacaaaagc tgagggattt tgtcaacaσa σcagaccttt ccttcaagaa 79141 atgctaaaga gtgtttttσa gtσtgaaaga aaaggatgtt aagσaatgag aaatσgtctg 79201 acggcacaaa aσtcattggg aatggtaact aσaσagacaa atgcaaaaga ttttaaσaσt 79261 aattgtgtgt aaaσtactca tatattgagt agcaagacta aaagatgaac ctatcaaaaa 79321 taataacttt tcaaaacata gacagtataa gatataaata ggggcσaggσ aσggtggσtt 79381 atgσccataa tσccagσaσt ttgggaggcc gaggcaggtg gatσgσttga gctcaggagt 79441 tcaggggcaa catggtgaaa σcacatctσt aσtaaaaata caaaaaatta gccaggcatg 79501 gtggσatatg σctatggtcc cagσttttcg ggagcctgag atgggaggat cgcttgagcc 79561 tgggaggcgg aggttgcaat cagccaagat cacaccacta aactccagcc tgggtgacag 79621 ggcaagaccc tgtctσaaaa aaaaaaaaaa aaaaaaatat atatatatat atagatagat 79681 agaσagacag acagaσagaσ agaσagacag ataggctggg caσagtggσt σacacctgta 79741 attctagcac tttgggaggσ tgaggtagga cgacggcttc agcacaggag tttgagacca 79801 gccaaaccct gtttttttσt tttgtttttt tttttttttt ttgagatgga gtttσattct 79861 tgttgcσcag gctggagtgc aatggcatga tσtσggσtca ccgcaacctσ tgcctcσσag 79921 attcaagtga ttctcctgtc tcagcσtσtc gagtagctga gattaσaggσ atgcacσaσσ 79981 atgccaggct aattttgtat ttttagtaga gatggggttt ctσσatgttg gtσaggσtgg 80041 tctcaaactc ctgacctcag gtgatσcgcc tgcctcggcc tcασaaagtg ctgggattac 80101 aggcgtgagc caccatgσcc ggtctσtttt tattttttat tttttgagat ggagttttgc 80161 ttttgtcgcc caggcttgag tgcagtggσg aaatσtcggc tcacggcaaσ ctccaactσα 80221 tgggttσgag σgattσtcct gcctccgcct ctcgagtagt tgggattaca ggcgtgcgcσ 80281 aσσaσagtσg aσtaattttt tatttttagt aσagatgagg tttcaccagg ttggccagga 80341 tggtctcgaa ctcctgaσct caggtgatcc acccacctca gactcccaaa gtactgggat 80401 taσagggtga gσcattgcac ccggσcaaga atactttact aaagtttttt ttgcctcaga 80461 aaaσaaaaga σtcttttatc acctgaggtc ccgtσacttc tttaaagttt agagtgaσtt 80521 tttttgatgt ctactttact accaacttgc ttcattgccc σaagtactct tataggggga 80581 ggtgcactgg agtσaggaac cctgacatct cagtgσtgtt σttaaσttgc cσcatagtσt 80641 ttgaaggagt agagtgtggt ggaaaaagaa tgggtccagg agtσaggaca cttgggacct 80701 tgtcccaagc tggσctgttt ttagtagggt gagtttaggc taatcacttc σcttcaaatg 80761 aggcttagta aggcctggtt cctttcagca ggtgcaatct gttσaaccag tactgtgctt 80821 aaagaagcca tgσaatttag aagaaagaaa aagttgtcta caggtσtaσσ tgctgaacaa 80881 attcccacac tatacaactt ggtcttggtc ctgaatggct gttggtattσ tgattttaaa 80941 atggattaat ggaaaacttt tctgagacca aacattttat cctgttatca tgtaagaaaσ 81001 caaagtattt tcccctacac tgaaatacct actaaaacct aaaatatttg tatctataaa 81061 aggtgatttt aaaaactcca accaccatac tatttcatac ctaaaccatc aaaccagtgt 81121 taaatttcct taatggtatt aattttactt tttttttttt tttgaσatgg ggtctσgσtg 81181 ttgcσcaggc tgaagtgcag tggtacaaac tctgctcgσt gσagcctctg σtccagggtc 81241 caagcgattt tcctgσctca gcttcctgag tagctgggat tacaggctta tgccacσaσg 81301 cccagσtaat ttttgtattt σtagtagaca ggttttcacσ atgttagcca ggcaggtctt 81361 ggtgacccgc ctgcctσggt σtcccaaagt gttgggatta caggtgtgag cσaccacatc 81421 tggcccaatt ttacattttt ttgaatσatt atccaaatag ggtccaaaσa ttgtgttatg 81481 tgtctcttaa gtctccttta taagctccca ttctatctgt ttcccttgta atttattgaa 81541 gaaaccaggt catttgcctt ggaatttσσt ctcaatatgg ctgattgaag tσccaσtgta 81601 tttttaaaaα atgtttctgt attctcttat ttσctataaa atcataggta tatctagaga 81661 gttgattaga tttgattttt gggcaatact tcacatagaa tgttagtgtt ctacaaagta 81721 attgagaaga gttcaσatgt tαaggtσttt ataaaataat aaaaattgga ttttatcaca 81781 tatttattaa agaσaatσat ttatagttca taaaaaaata ctgσσσtgat atacacaaaa 81841 ttttσtaσtc cσacccaccc cσcatgtcca caccaatatt σagtctagat tggtttaatc 81901 ttgaagtgta atcσaataag actgaagacσ aaacacttσa ggtcctggac aagataataa 81961 aatactcgta agccttσtgg atσcctaaaa tacaaaagga aaaaagttta ggcattaaaa 82021 ctttgaccca tcaagtgtcc ctaaaaagga aaagactata tattaaaacg gtatattatg 82081 aggtaattta aatatgctga gtttttaata tagggaaatg cttaσattaa gtgaaaaaat 82141 ataattaaaa taaσaattat taatσtσaaσ tgtatttttt atgcttctta aaaagtatat 82201 attgtattaa tgcatagaat aaatgσatta aagactaaaa agaaatactg caagatagta 82261 ataatggttg tσtgattgat aaacttgtgg atgattttcc cσtttσtaσt tttctacatt 82321 tcctgtattt tσtacaatga gσatgtatta ctttcagagt tagaaaaσtt tttttgtttt 82381 gttttgtttt gttttttgag acagagtttt gctcttgttg ccσaggσtgg agtgcaatgg 82441 catgatcttg gσtσactgta acctσcgcct cσcaggttca agagattctc ctgcctcagc 82501 ctcccgagta gctaggatta caggcatgσa σcacgcctgg ctaatttttt gtatttttag 82561 tagagatggg gtttctccat gttggttagg ctggtcttga aσtccσgaσc tcaggtgatσ 82621 σgσctgcσtσ ggσσtσccaa agtgctggga ttacaggtgt gagccaccaσ aσcσggcccg 82681 agttaggaaa acttttttaa aaagtagtag taσtaagcag gaccaagagg ttgaagatta 82741 σtgtggcatc aσtggctaag aagagtgtcc aaaggaagac aattacgσσα aacatttgcc 82801 aaaagtgagc cgtacctaat cctgaaccσt σaaaaσgtaa gagcσaaaga agttgσcaaa 82861 ttctaaggat tctttgtagc acataggttc atgcctcaaσ ttgataatct gccccactga 82921 caaσatgaat tttaaaatσt tgatσccttt tcaccaaacc aatgcttttg taaaaaacaa 82981 taaatttaag gσtgggcgcg gtggctcaσg σctgtaattc cagσaσtttg ggaggσcgag 83041 gcaggcggat catgaggtca ggagttcaag accagcctgg ccaaσatggt gaaaccctgt 83101 ctctaσtaaa aatacaaaaa aattagccgg gtgtggtggσ aggtgcctgt agtccσagct 83161 actcaggagg ctgaggcagg agaatcactt gaactcagga ggσagaggtt gcagtgagct 83221 gagattgcgσ cactgcactc σagtσcgggt gacagtggga gactcσatσt σaaaataata 83281 ataataataa atttataata aaataaaaσt tagatσctaa aaaatgtcaa gtttcactga 83341 agtcagattt taagatgtgc cagtσtσaaσ agtcacactg agaaagctat tcagaσtσgg 83401 tgaσtσtaσa gtttatσatg agσaσttttt tggcatattc cattttttct tσtggctgct 83461 cctatgcatt aatctatatg tgtgtgtcaa caagaagctc gcagtagcaa tggctgaatg 83521 aaacaccaaa agtaatagga gcaagtcctc aaaaataatt tggggttσct cσctaacaag 83581 aaggacaaag ctgcccacct gcattttgca tttgccσcag ctσttσcσat aatggtccσa 83641 atttggttaa ggtttcttat caatctgctc caaaacagac aσaactggat ataaggatca 83701 tgcacactta cttggattga ttgacatcaa taagggaacc aatttttgat gttgtaaaag 83761 aaatgtgttc atαtσcaatg acgatttcaa gctcctagaa aσattttaga aaatcgaagt 83821 caagtagaat tggattattc atσaagcaca cagaaggatt aatcatttgc caaatcaαac 83881 aaacttgact acagatggcc acaaaaacaa gggcagttca ctctgagcac taaactgtgc 83941 tgggcactag aaacaagaga taaatacagσ tσatatttag aagaagttgt acccttaagg 84001 ccctacσatt tσtσagattt ggaaaaatct atgtaggttt tttttttttt tttcctgaga 84061 cagagtctσa ctctgttgcσ σaggctggag tgcaσtggσa tgatσtcggc tcactgcaac 84121 ctσcgcctcc σaggttcaag cgattctcσt gσctcagctt cctgagtggc tgggactaσa 84181 ggtgcccgcσ accacgcccg gctaattttt tttgtatttt tagtagagac ggggtttcac 84241 cgtgttagcc aggatggatt tttttgtatt tttaatagag acagggtttc gccatgttgg 84301 ccaggctggt ctcgaactcσ tgacctσagg tgatccgσct gcctσagcσt σtcaagtgct 84361 gggattatag gtataagcca ctgcgcccag cctatgtagt attttgtatg agttttcatt 84421 gtcaacaatg tggagtaaca tgaatacaσc tatgttttaa aaataccaaa caattggact 84481 gggtgtggtg actcatacct gtaatcσσag σagtttggga ggccaatgca ggagaatcac 84541 ttgagσσcag gagtttaaga cctgtctggg caaσttggct aaacctcatσ tgtaσaaaaa 84601 ataσgaaaaσ tagσtgggtg tggtggtgtg σatσσgtggt σccagctaσt agagaggctg 84661 aggtgggagg attcσttσac ccσaggaggt σaaggctgca gtgagccatg atctcatcaσ 84721 tgtactccag cttgggcaac agagtgagaσ σctgtctσσa acaacaacaa acaaaaacaa 84781 aaaccaaaga atctaatcta tctaggcaac ttσσagacct taggtttgat σcccactttg 84841 tcactcσσta catgtatgat gttggatctc aatttccaaa cagtgacatg agtaccataa 84901 ccttσaaaaa gtatσtatgt gtagcctact gggtgctggc tattgttσtc agtgσtttgg 84961 aσagataagt aaaaccaagc aaaccaaaga tctctgccct gtggaattca tattcttgtg 85021 aggcctattt actttttctt ctttttgatt catatatcct ttttgttata attcaatcag 85081 aaaatcgaaa aaactgagat gtttσcaata ctσagattta taaattattg ccataσttgt 85141 gtcagatttt ttttaaaaaa gaagtaaaat attacaaagt ttatgtcσat σtσccattσt 85201 gttctccctc ctgtatcccg atttgttcσa σtσttgtttc agatttggta gtatgttttt 85261 acttatttct ttttagatac aggatσtσac tctgtcactg aagctgaagt atagtagtag 85321 gatcatagct cactgtaacc σtgagctcct gggσtσatgc tatactgcaσ σtttagcttc 85381 tcgaatagct aggactacag gtatgcgcca σcaσgcccag ttaattttta gggttttttt 85441 ttttttcttt gtagaaaaaa aggtσtσaσt gtgσtσaggc tggtcttgag ctσσtggσct 85501 caagtcatcc tcccaccttg gσσtcccaat taagaacaaa agtgctggga atgcaggσat 85561 gagtσaσtgσ acctggcσta gaσgtggtag tgtgctttaa aatttttaca aaatggtctt 85621 attataσata σtttttaσat ttttcattcσ acattgtttt cgagatttat σaatgt.tgag 85681 ttacacagat σtagσtcatt agttttaaat gcttgtggta ttccatttcc ctactgaaat 85741 aaacttaagt tttaaatttt tattcctata aaσaatgtag caagaatatt cttctataca 85801 tctccttgta catgtgaata tgtctccata taattcctag tattttaaat gctgccagat 85861 gσcacaaaat tactσcctaa σgσggttata σtaattttat tctcactctt ttσtcatatc 85921 attttttaaa ttcggcagat ttttttctgt ttttattcta atgggtctga aatggtatσt 85981 cactgttgtc ctttσatttt aσaaatgaag σcgtaaatct tttcatatta gσcacttgtt 86041 tgatcttgta agttatσtat tσataaσσtt tgσacattct gccacgggac agtcttttta 86101 ttaatttgta attctttata tattctggat ggagaactct tgccagtttt atgttttgca 86161 gataacttct tccagtctat ggcttatctt tcaactttat cttgσcatct tttgtcaaac 86221 ctaagttgta aagaagtcaa atttaccaat cttacccctt aaggagtttt aaaaactσct 86281 tctctaccσa gaaataataσ aagtσtatat tσtgtttaaa atttttgatt tσtatggcct 86341 aattttaaaa atattccata aatacattgt cagσtgtcct ggtacaattt gttaaataat 86401 tcgttσtttt cccattaatg tgaaagtcca cctσtgtagc acacttttct aagtttccat 86461 atattcatag gttggtttσt gggσtσtσta ttσtgttσca ttggtttagc tgtcaattcc 86521 cgaggcaata tcatactaca aatgacσaca gctttgtaag aaatttσcag tattattttg 86581 gctaσtcttg cctctgattt tccatgaatt taatgctcat tctatttgat tctaaaggga 86641 aaaaaatcct actgcgattt ttatttgaat taagagtgaa tttataaatt actttgttga 86701 aaaσtgaσat σtttatgata ctgaatcttg σσatccacaa aaaσgataσa tatttttgtσ 86761 σttσtataaa gσcctttσaa gttttgtaca tcttgttaaa tgσattσcca agttctttat 86821 aactcttctt gcaattatta atggaattga ttttaattac agtatccaat ggcttattgc 86881 tggtacaaag gaatatgccc ttccctcttt aσagaattgt tgtgatggta gaacgagtta 86941 atagaaataa aaattttata agtggtaaag caaaatacat atatatgata ttactgagct 87001 cccttgaaca taaattaaag ttaactttag taagtactga gggtggattt ttaaaaaaaa 87061 ctcttcaagg gttggtccat cattttgaga ttattaggaa tgagtttata tgggttttca 87121 tattaattta aσaaatacat tattattgag σttttactat acatgggtac tattttagtσ 87181 aσtagagata cagcagtgga aaaσactgaa aagcaagtaa gacaatttta gacaatagca 87241 agtgctacaa agacaacaca tattgtgata aaactgaaag σaaaaagaaa aaaaaacaca 87301 aaaagacaaσ acaacagatc tttttcttaa tgatgggaag cgaσttctta gattggatgg 87361 acaggσaaga catcactgag gaagtgaσtt ttgaagacct σaataataga gaσagtσttg 87421 tataaagtta aaggaagaat attttaggσg gaatgtggca agtgcaaagg ccctgaagta 87481 agaaσcaσσt aggtatgtσt gaggaacaga aatgaagcta gtaaggtttg aaσaσcatga 87541 cagattggaa gcccggtaaa agataaggtg ggagtttgaa ttttaagtac agtgggaagc 87601 cattggagtt taaatcagtg gaatacataa gcaaatttac gtttttaaag atσagaσcag 87661 taggatgcgg cggcttacgc ctgtaaccaσ agcactttgg gagggtaagg caggcggatc 87721 aσσtgaggtσ aggagtttga gaσtagσσtg gccaacatgg tgaaacgcca tσtctactac 87781 aaatacaaaa attagσtggg σatggtggag gacgcσtgta atcccagcta ttcgggaggc 87841 tgaggcagga gaatcgcttg aacccaggag gcagaggtta σagtgagctg agattatgcc 87901 actgcactcc agcctgggcg acagagcgag actccaaσtc aaaaaaaaaa taataaataa 87961 atcaσactgg ctttcaggat ggaaaaatgg atggtatgga acaagaggaa aaacaaggaa 88021 atctattaga agtctggatt aggatggtag ca'gtσaagag tgaaaataσc ttttctgtta 88081 attcagttca atatgacagt ggcttttatt ttttagttac caaaatggtg ctcagaatga 88141 atatatacat taatgtatat aaatatacat gaatttaaat acatacactg aattatttgt 88201 atgattttcc tttcattaga ttgttgaaat aattatgttc tatttctctt tgtatctcca 88261 caatgσtttg tσcatagtag ttagtaagtg agataggcaa σaaaagcttt aagtggagga 88321 gggagtgtgg ggggtσttat ttgtaagatt tctgcaσtac aggataatca ataaaacaσa 88381 cctgccggcc σactcggtca ggaggaggσc acaatgcatc atcctαtttg gtaatttσac 88441 tgtcgtcaat tattctcttc agttσctcca tσacgctttt atgtacataa gσctgaacgc 88501 aagttaaaaa acaaaatgta tgttgtatcc ttaagcagtg ctttgactca gatagtgatg 88561 gaagataaaa ataactgttc ctgcagactt atttctggca tctccttaag tgggaagaca 88621 ttσatgσtca acσtcggcat gatgcaggtg agggacacgg tcagaagtat cσagtaactg 88681 caσctcagtσ ccσtatctag ctgttaαtaσ αtcctggtac atcctgttca σatggccσtt 88741 σtgcctgccc acatacccaa ctcacaacga aacccaaaac aggtctgtga gtgcccσctg 88801 ccatggtttg aatgtttttg tctcσtccaa aaaaatcata σtgaaattaa tσcccaaagc 88861 aaσagtgtta agagataggg cctttaggag gtgatcaggc σttgagggca gaggccccag 88921 ggatagatta gtgctttagg agagagctta agggaactag ctggcccctt tcttgttctt 88981 tσaccatatg aggaσacagc attσattσct tctggaggat gcaaaaacaa ggσacagttg 89041 tggaagcaga gactgggccc tcactagaca ctgaacttgc cagcgccttg atcttggact 89101 ttccagcctc caaaattgtg agaaatatat ttttaσtgct taσaaattaσ ccagtctcag 89161 gcattttgtt gcagcaaaaa agagactgcg aσaσσcacat gccctggtta ttcttttttt 89221 tttttttttt tgaaacggag cσttgσtσtg tσgσσcaggc tggagtgσag tggtgσgatσ 89281 tσggσtσatt gcgaactctg σctcctgggt tcatgccatt ctcctgcctσ agσσtσctaa 89341 gtagctggga ctacaggcaα σcgccacσat gσσtggctaa tttttttgta ttttcagtac 89401 agacagggct tcaccgtatt agccaggatg gtαtσgatσt cctgaσσtσg tgatσσgccσ 89461 gcctcggcct cccaaagtgσ tgggattaca ggtgtgagtc accgσgcccg gccagttatt 89521 cttaactagg taataσaσtc ctgaggagca aaatgtattt taaaagatat gcctgtgtaa 89581 aaaaatagtg aggatattga catgtgtgaa taagcataaa atσaatagct aaaataacaa 89641 tatgaaaata tatgctaaga cattttcaaa ggtggcaaag tggttaaaag gaaagagtag 89701 ctttgatgaa gccttaatga tgtagtagaa atcacagaac ggagaataca aactttactg 89761 gggcaggatt gggaattcct gctgtatctc ttactagcag gggtaaσtσa gaaσaagαct 89821 cataattaat acctgggσσt ttattttctt atttgtaagg gggctataat accctccccσ 89881 atσacatggg cttaσaatca gggttaaata agatgccacg cctgacatct aacatgcatt 89941 caatgatgtc aactgσtttσ ccatgσtσcc tttcccaσtσ agatgtaaat taaatagctc 90001 ttcattgtgt accatgtaca cagggaatat agagcaσttt aaatagaaσa tatttaattt 90061 tatgaσagσa cttgggagtg ggaggtagct tttattattc ctgtttttac aggtgaagaa 90121 acagagattt atσaagttca gccaggaact tgcσcaaggt cacatggggt agtaagcagc 90181 agactcaggg ttσaaacσaa ggtatgtcaa aggttacσag taattgattσ cacaatgtaa 90241 aataaaaaaa tcccaactaa aagatgattt gggaaataat cσagaagctg tctacagaσa 90301 tgtgtσtσtc tccctgttct ttatctttca atactactag aaacaataaa aacaatgcaa 90361 gacaaaaagc tgaaatgtag caaatgaagg actctcagaa ggcagaaggc tcatacctσt 90421 tttctgatca tgacatcatt cttgtaattg σtgttgttgg σatatσttaa cttcσσtgtg 90481 ggggσaaaaa aσaatttσaa σgtataataa aaacatatga ataaagcatc aataσcatgc 90541 caaggcatca gσagttgσcc aaaatgtatσ taacttgcta aaagtgtcta acagatttat 90601 tatttactct taaggtattt caacaatact agtcttttσa gttσttσaσt tcaggcttaa 90661 aσagccaaat atacagctga aactcaacta ctgcaaaaag cagctcaggt ggggtataaa 90721 cacaggcagg ctcttttσtg actttgtcaa atcacatttt tgcaggtgaa tgtcctgaaa 90781 acaggσσtag taactgataa cttaccgaca cataggacσt σσtgaggctσ aaatgagctg 90841 tgaaaacatt ttgaaaactg taggatgcag tttacatata ttatσatgtg actgtgccat 90901 actctatttc tgtgatggag aagctgσtgσ ttttatcact gagcacattt ggtacacaag 90961 accctttgcσ σatgtgtgσa tσtgacagat taatggtggg gatgaggaga agacagaagg 91021 aaatagaaga catgtagact agaagacata catgtgagat gagcccagtg aatttattcσ 91081 aaσagσctct gtgctgtσtσ tctgcctcaa gtttcttcac attcagttca ctgtccatac 91141 agtggacaag gtgatgtggt aacagatcta tcagattagg ttactctaat aσtttgataa 91201 agtσaatggσ tttccactgσ cttcctggta aaatσcaaac tcctcaaσat ggcataσagσ 91261 taagσtaagc ccσtgcctgc ttttccagcσ tcattσσtgc caatattctt ctctcacaca 91321 gctgaagtca aactacttgg tttctgcctg aaacatccca agcacttttt ggttttcagc 91381 ttσtttgσat gσtgtctaaa atgccttσtt gactcttctt cgtctcσtaa σcaattcσtc 91441 acatcccctc σtcccatcat tttatgtagg aagcctσctc tgaccctcag gcttggttag 91501 gtgcaccσtt σtctgctgcg agcctcctct gtttcttttt accacaacac ctaatgtgct 91561 gttttatcac tgcttacaaa tctatctccc tσacagtcga ggcctgtcag attσatcttt 91621 gtgccccact tagtggatgt σttctgtcat ctttgattgc tctttccttσ acσacagtgc 91681 ctσtgccaaσ aaaatcctat caacgatcaa agtccagttg gttσtgσctc caacagtttc 91741 ctaaatcttt ctctccattt ctactatctc tgtagtccca accagtatct tttttttttt 91801 ttttttttga gacagagtct tgctctgtca σccaggctgg ggtacagtgg caσtatctca 91861 gcttgctgca acctccgcσc caggttcaag agattctcσt gtαtcagcσt cccgagcagc 91921 tgggattaca ggcgtctgcc accacacccg gσtaattttt gtatttttag tagaggcggg 91981 gtttcaσσat gttggccagg ctggtcttga actσctgacc tcaagtgatc cgcatacctc 92041 ggcctccσaa agggσtgaga ttacaggctt gagccaccgc gccσggccσc caacatcttt 92101 cgtgtcttga caactgcaac agtctσctaa tcaatagccσ tgtttccact cttgσccatt 92161 ccgcaσccaa taaccagaat gσtttttcaa gaagagatσa catttcttσt σtgσttaaaa 92221 ccttccaagc ccggccgggc gσggtggσtc acacctgtaa tcccagcact ttgggacgcc 92281 gaggcgggσg tatcacctga ggtcaggagt tcgagaccag cctggσcaac atggtgaaac 92341 tccgtctcta ctaaaaatac aaaattagcc gggcgtggtg gtgggcgσct ataattccag 92401 ctactcggga ggctgaggca ggagaatcaσ ttgaacccgg gaggcggagg ttgσaataag 92461 ccgagatcgc gccattgcaσ tccagαctgg gcaaaaagag cgaaagccgt ctcaaaaaaa 92521 aaaaaaaaaa aaaggccttσ σaagtccaaa ctttttaccg tggtctataa agaσctaaga 92581 ggtgccgσtc ctacctacct atσcgacatc atctcctgct atσtccσagσ tcaccactct 92641 tcaaccaσac tgaσcacctg agacacgcσt agctcattσc cgcσctgcag σcttgacatc 92701 tggtattccc tttgtgtaga atggtcttcc ttatgagctt cacaaggctg agcσcttctt 92761 gttaattagg actcggctgc aatataσcct ttaσagagag ctctctaatg gccaacctat 92821 ctaaaagσag σccatccagσ aattattcta ccatgttatt ttttgaσσaσ tσaσtgσtat 92881 ctggaatcat ctttttgttt atgatctctc tcccggcagt aaaacacaag ttccacgaga 92941 ggggaagttt gtctaccttσ gσtgccgtat tcccaaagag tggaaσagag αctggcacac 93001 agtgggcgtt σagtσaacgt ttgctgaatg gatagaaaga ccccgtggag cagacacagt 93061 ggcgttcctt taagatctgc actgcacagg tctcagtccc tσcctσctct agttσcσcac 93121 agatttσσga σcctσggcct σσσcactcgc cggσccccag gσctggtccc σgctcccggσ 93181 gggσggσagg σtgcttttac σgtσcggtcg aaaσtσaaac tσcaggaact cgtggccgaa 93241 cttgcσσttg tgσcccacgt agtaacgcag ataaaagtca ctctccatgg ctcccaaaag 93301 acaacσgagσ ctgaacttcc aagagcaagc cgcactgσcg cσgtctgcgc ccgacactga 93361 cgtttgcggσ ggσgcgcgga agtgacgtca ggtcσcgtcg tcgctgcgtg gaggggttcc 93421 ttctcgctaa cctcttcgcc cggaagtggc aacaagactg caacatcccc tcacgcσtag 93481 tctgtaaaga actttgttta accσggaggc ggggccagcc agctccgccc ctccagctgg 93541 acgcgggagσ gaggttgagg ttcatacccσ tgggttctct σσaggσctga ggcggagagc 93601 cagccgcctg cctacctctg ggctttgaaσ cccgggtctg gtgaσttcgc ttaaagacct 93661 cgggσcgaag gcσcgccagg ctcaacctσg gttσaσagga σcccσgactt gtgtgagtcg 93721 tacaccgctc tttaσcgtct ctggaσσtag gtcatctcgg cagtaaaatg gggtgaaatg 93781 acccgacctc cccggaggat gccgcgσacg atgtgtgcct σaagttggσt tcσaσtgaσc 93841 tgaactgtta agaaagccct cctcagtgaσ gccttσcctg aatccaσagt ggagattgcc 93901 gttttcσtgg aactaattca cccacactta σccatttcat ccctttcσaσ σttttatttc 93961 tacctttctg cccσaσtgat ctctagaata ggtgctggga gacgttagag tatttgatct 94021 cccactcccc agtcatccσa cttaccgagσ agtaattctc tgcctggctg σaσattgcaa 94081 tcacttggga agcctctaaa aatactgatg ccagggctct acccσaagσσ agttaaaatc 94141 tccagcgctg gacctgggσa ttggtacttt ttgtaaagct ttcaggtgag tσagagttga 94201 ggaccactga ccaaagaggt cctttctttt cagggtaaag ttgtcctσtg tgaagccttt 94261 σtggσtσtgg aaaaaattta cagttgagta ggcσσagggc aatσaagatc ataattatgt 94321 aataggaacc tgctttcaσt catctaagtt ccaggσttag aaagaatgaa tggttctaga 94381 gacagtgccg agatgacatc attcttgggt cctggcggct agaactgtat aσgattσtgt 94441 aagttgggac agcagtctct gattcctatt cccagtcttt tctttttgag acggagtttc 94501 gctcttgttg cσcaggctgg agtgcaatgg agtgatctσa gttcaccgca aσctcgccta 94561 cctaattttt aaaσtttttg tagaggcaaa gtctccαtat gttgσccacg ctggtctσaa 94621 aσtσctgggt tcaagtgatt ctcctgcctt agcctccσaa gtagσtggga ttacaggcat 94681 gσgccaσσat gtcσagctaa tttttgtaat tttctgtttt tagtagagac ggggtttcac 94741 catgttggcc aggctggtσt σgaactcccg acctσaggcg atσσgtσtgc ctcggcσtcc 94801 caaagtgctg ggattacagg catgagccac cgcgcccggc cctcagtctt aacacggagt 94861 ccttttσtcc ctgcaaaagc attagcagca gagtgtagag taggtgtggt gggggaaaaa 94921 tcaσtggaca caggttaaaa taatccσtgt gtaacaatga ctcattgtaa ccaaaggtga 94981 aσcgactcaa ctttttagac ttcagtttcc ttctctttaa aatgagσata ataatgtaca 95041 cctagcagaa ctgttgtaag aaacaatgtc tcggaaacta aattgctgta aaacσataag 95101 aσatttttat tacaaaacac tggatatggg tggtaaσaag ggaattgtat aaaσgagaag 95161 ggggctagac acagtggσtc atacctgtag tcccagcact ttgggaggct gaggσaggag 95221 gatcacttga gcccaggagt ttgagaccag cctgggcaac ataggagact gtctctacaa 95281 aaaatttaaa aaataggtag gtgtggtggt gcacacctgt agtcσtagct acttgggagg 95341 ctgaggtagg aggataattt gagcσtggga ggtcgaggct gtagggaacc atgatσacac 95401 cattacactc cagcctgggt gacaaagcaa gaσcctgtct caaaaaaaaa aaaaaagaga 95461 aaaaaagaaa agggaccagg tatσaagcac ctaataaatg tcagσcσcta gggtcaatgg 95521 gattacctgt gcttgttctt tgaatcatca caaσaatσtt gaggtggtaa ttagagttaa 95581 gtatgtagag ggattaagca attgctacaa ggttattttc caggagtaaa attataaaaa 95641 tσataagtga atσtggggat σttσagatgt ggσaaataaσ aaaagtgttg agaaatttaa 95701 aggaσaσaca actccagtσa ggσtgtgaag taatσcaggt ttctggatat gagacatggt 95761 gtaactgaaa gagcatggtc tgtgtgtctg cagtgσσtgσ attσagσatσ atttatttga 95821 gσatccaσtg agtgtcatgt gcagagagga tacaatgttg agcaagacag ttgttcaσag 95881 agcttgσaga ggaggcagtt aaggagcata caagcaatta caatgtaagg ataagattac 95941 caataaagga agcacagagg actatggaag cacatgaggt gactcctaat ccagtgσagg 96001 gtσcttaggg aaatgttcct gaaggaaatg ttccagacgg aggcσcagaa ctgtgtgatt 96061 agaatataga gtagtgagtg atgaagctgg agaσagggσa gaagσcaaat catgaagggt 96121 tttataagcc atattaaaag agtttgggca aacccaagaa tattggattt ttgtgccagσ 96181 aaagcagttg aagagcttta agσaggaaag tggaaagaag tggtggtgat acatctatgg 96241 tactttagaa agacactttg gctgcagtct tgtaggttag attggaaaat gaaaagacta 96301 gaagtatgac attcagataa gtagtttaag taatctatta gctgggσagg gtggcgtgca 96361 cctgtagccc σagctactcg ggaggctgag acaggagaat tgcttgagσc caggaggcgg 96421 aggttgσaat gagαtatgat cctaσσaσtg tactcσagσc tgggtaacag agtacgaccc 96481 tgtctσttaa aaaaaaaaaa aaaaaaaagt aatggagata gaaaagtgga tggatttgag 96541 atggaatacc ataatttaag gggtaggσaa aggatactaa gatgtggcca gagagatagg 96601 agaaaaaaca tgaaatgtta tcatggaagc caaaataaga atatgccaag aaaagagtgg 96661 ctaacagtgt taactaσtgc ttccaggtca aggaagagca agactgaaaa tgtttaccag 96721 atttataatσ gaggaggtcc tggatgacct tggcaaaagc aacσσcaatg gcatgggaat 96781 gaatggtaag gσagaagtat tgggatgσaa gtaggcaaaa attgttatcg aagtacagag 96841 gtgagttatσ taacctagtc ttagagaaaa gggaaggσtt σctggaggag gcattaccta 96901 agtggagtaσ tcaaggacaa ataggagtta gtcatgtgga ggσagagaag gaaaatttag 96961 gcagagaatg ctacatgtaσ aattgctσtt tgggggcact aaaaataaσσ ttgtgacttt 97021 gggcagttac tttgcccatt ttctcatcta taaaatggga gtggatagta ttgatagtat 97081 ttatctcacc gaattgttga σaaagattgg gataatttat atagaataσt ggtacacatt 97141 agggactcag taatagttca ctccccctca ttaaagtatt acaatgaaac aaaacttaaa 97201 agattttttt taaatgaatt taatctctct ctagaaacag tgσaσtgatt ttacaaatgt 97261 ccacatttgg ttttcagttt accaagatga tgccagtata gctagtgaga tgcagcaσσc 97321 catcctcagσ σσσσtcgcσt ctggaagaga caccagactg caaagggσaσ cgcgtacaga 97381 agctaacgga acttgaatga caagacaaaa agagcagaat cagttagtgt gacacaacat 97441 tctaacatgc σtgattσtta catcaaatat ggtaaσtttg gggttggtag ggggagacaa 97501 acaaggagaa tσcacttggg aacaatttga tgaagtttgσ aaatcagσaσ tttaccccσa 97561 aattaaσaaσ agcttgtatg gaaaaaaaaa tgctctttta aaagtatatg gtttggacag 97621 gtatatttgt tttσtcttgt agtttttgta aaaaagtatc aaaaccttgg σtttaaatat 97681 atatatatat atatatatac acacaσacac acgtggcttt ttaaaaatta cttttttata 97741 gσacaaagtg tttgtaaatg cagagggttt ctgσtaattc ttgactgtgσ aσatggtgσa 97801 tagcctgaat gaacagagct tcctgatttt tttttaaσtg aaaaattgaa gcagtaattc 97861 tttaaccttc taaattctcc ataσcctaaa aatacagtgt gagaagtctg ttactσtatσ 97921 ttσatgcatt tcgggaaaag gaattattta σtσtgaaaσa tttaatgcta actcatttat 97981 attttgtgaa aαgatgagtg tatggσtgga gttσgggggg tagggtggag aggαttgσat 98041 tcctgtgσca tttccccatt cccaccagtg σccaactgga cagtgattag tatcσcctct 98101 ccagactσaa cgtcttcaac attttcgttt ttctttσtσa σagttgagaa aatctaagag 98161 gctσtσgaσa aσatggcatg catctgtgaa aatccσaσtg σccttatatt agtcttcatt 98221 gaccatataa aaaatctttg actcaaatat atgaaaagca gtcagcattt σσctttggcc 98281 actggaaagσ ttgaggctga ataatatcag ttσtgcaaag tgctggcaat gcatcctaat 98341 gaattttσca tgatgcatgt agtgccttgt acacaatgat caagaaatgc ttαattgaat 98401 cagaaattaa tctattttat aaagtgσtta cattgaatct σtttccatac agcctcattt 98461 σttgccσccc ttgagσcttt tgttcσtgtt agaatgaaσt gtgcaattcσ taaagtccσt 98521 gtgσtσtttα ataσctctgt gttttagctc gatgtgtσtc tgtctgaagc agcttggaat 98581 ccccttctta atttttaaga cttaaggtca cttctatgat gacσσtattσ ctσatttσtt 98641 aggtggaaag accσctctct cσtttgagσc ctaaσagtgc tctgaataga atcaatgcct 98701 tttttgtttσ cacatatatσ atσctccact gctactgtga actctgtaaa gtcagaacat 98761 gtgtgactga cctttacatc tgcagtgcca ggtgtgtagt tggtatctag tgagtggttt 98821 tagtgaatga atatactgca gtcatactga gataactgga gggatcaata ggacttactg 98881 σcatacattt aaatccgatc tcattctσtt tttgccagtt aacaggttac ttcaatctgt 98941 tttataaata atctgtgtat caagagtaaa taagtacagt ttcgttttct σtgtttctag 99001 aaggcatttc agttagtgcc tttgtaattc σaσtggagga aaggtagacc atagtatagg 99061 tagcaggttt gatacaatgt tσaggσagcc caaaatagtc ttcσtgcaga aggaaatgga 99121 ggaaacgcac tgggactggc ttσtgataaa ttttctgcσc ccttggcatt gtctctgagc 99181 ttccttccag ctctatagtσ σagtgactct gtgatctgtg attggctgta gatagctatg 99241 cacgggggca aaaggcaaaa gatatgtaac tgtacctcaa aatgaggctg aaaagcctct 99301 atgaatgggg gaaggtggat ctgaσtcctσ aggtttcatc ttatttactg σσgtccaaca 99361 σatgaatata tσacaatttg tttcttgtaa agggttgctc ασattgσtgc ctctttcaaa 99421 ctgcagttgt agcatatgca ggaaacatga atgtctctga gaaaaagttg tgaatttσat 99481 tgtcattttg agatctcagg ctgtatgtcc agaccccatt σatσattttt ttctgtgaat 99541 gccaggatct tactgaaagt ttagaaacta tgcσttagcc actgttatca tttaattcct 99601 tggaaaattσ agtttctttg gaaggttaca gaaaaagtca σttgttttga gtacatttcc 99661 atgtttttca ctgtcatcat ttttcttcag tcaaaaataa ttttactttc cgttcttaaa 99721 agaatagtaa tatgtgagta agctccatag gagttggσσa αctgttctta aaattctgtt 99781 tggtattggt cattctaggt σaactgcatt taccctctσa atgaatgttt caggactatσ 99841 aacacatgca tgtcatgagg agattgσtgg attatgcaaa acacactgσc caagctccag 99901 aatatagtta ttttcttaga gtttaggagg ccaagagtga cacagaggaa ggtcctaggt 99961 acaggatgσt agaaσtσcag aatgtctgaσ tgaaaattca aagggtatca agctggtgag
100021 acatccaaσt tσattgagtt gggggσatct ggcaggtagg gatgggaagg catttgctta 100081 agtgtgtcaa gttcσaggta tgatgagatt agatgcagct cσtctgσtσc taσttaagtc
100141 aaacaσttcc atgttgcaσσ ttgtccctgg ttgtctagtg ggagtaagtg gcagaaσagσ
100201 agagttaaga aaσtσaaaσt ctttctcttt ggatgggaaa gccaσtgggg aσtgaatσct
100261 tctgggacta taggattatg tttccaatgg gagaccσcac aagtagaaaa gagcacttσt
100321 σσσttσctcc cccaaggcca agaaaagcaa agaagatgtc tataatgaag aacatσtata 100381 σatataσσcg gagtttttcc ttttatttaσ aaagσagtaa aσσaaattcc tgtgtgaaca
100441 taaatatcca atataatata atattgcgta tgccatttcc σσσctcaaat atgacttcaa 100501 ttttggσcag ttgttctgac ttaagccaaa aattagtttc atctatatga acatatgatg 100561 gtaagtaacc tatttattac σttaaaatgt ttccccaσat aaaggaaatg gtagagagta 100621 aggggaaaag agaaataaga gatgtgataa aacctattcc acσatσttta tσttcatcca 100681 cagcatgtcc tagacattca gtgcctgggσ σagtσtσtat agtaaacttg ggctgatctg 100741 gaaacgtσtc cacttagctc tgtaaggatg gcacσσttca gggtgcttσa gaggaaactt 100801 actgaattca acσσaagtgt σctgaaagaa attgaagaag ttactcaaag agctgaactt 100861 taaaacaagg agtagctgag ggtgaggcat atcσtatσtt gagtttαtga gcactctggt 100921 aσσatggaat gtσtgtacac tgaccttσgσ σaaagσσaag aaagccσtgg taggagtcac 100981 agcagccatg ggtgagctga aaggcttttσ σtgacttcct ggggtctcag gaatagccag 101041 aggtgaaaag atttgσcttt tttactaσat aattgcacaa aσcatggtat ctattttσtg 101101 atccagattt ccaaaggctt ttσtgaaaaσ tacaagatat acccσttgtg gaσtgtgtga 101161 aaataaattt atσtttatgt atttgaaσag tagccataga tgtgcσtctt ctctaσagat 101221 ttttσtgtca cacacataσa catataaaca cacacataca cacaσagagt ctgtgtggtg 101281 ggccaaacat gσcaaaaata aatactσtca cttσtσtaaa ttatttatag aaσtcatctg 101341 atttttaaaa tatgttaata aataatctaa atgggggagg gagttgaagt gttttttttt 101401 tttttttact tatgttgatg gatagccaca aagσataatc atcttattta caaaaaaσaa 101461 atgccccaaa acctaaaaaa gcccccccag caaccaaaca tcttσtgtaa atatagtttt 101521 taaatgatga gtaaggtaσt gtgcαattgg cσcccatttg gttatgtgσa tσatgttagt 101581 σagcagtagc cattccacga attcctσatg ggtagtgσaa ccagttaaaa agtgtataaa 101641 acattataca tagaaaaaσt ctcaσatcct ttggatgttt gcagttσatσ ataactttgt 101701 ggttacσttt ccgσaaσata aatttaaaaa a'aaaatcaca cacaσaσata σactcacaca 101761 gaσccatata tagaaaσαca ttcatccagt catacaccat ccagagtgta gtgcatggga 101821 ctgaattσca tgaggcacga agggggtgat αccatσσtαa gggtagtσσa tσatcttcaa 101881 ggσttaatgσ σactcgctgg ggagacaaac caaagaattc atcattagat ccataagagt 101941 taσtatttat ttagtattga σaaatcacag acttacgtta ctttaacagg tattagctσa 102001 cataatgttc aaactatcct aagagacagg atttatccta tttattttac agatgagaaa 102061 caaaactcaa tgagcttaag tagggtttgt tctggatcac atagcaagtg gctgaaσtaa 102121 aatttgatσc caggtctgta tgaatccaaa gctgtagatt ttttσatσat tσtgttttgt 102181 atαtttgtaa agaagagttg σaσagatcta aattttctta atσctccctt ataggatttt 102241 aggtttggtc aatttcagtg ggttagcttt ggcaaatgtt aaatttcagg ctatggggtt 102301 acttgtctct agcatgctaa tcacatttag aaaggtaata taσtgcacct tcccaacaga 102361 ttaaaσaσag ttgggaggσa atgσaggtta attaaattσσ atσσσtctct σcσtσaσσcc 102421 tgctttccag tcattaggta gatgctagaσ tcctgtσtgσ σaaaaatggα tgaσσatggg 102481 aaggtgagσσ σactaacσσσ tgaaσcagtc tattccattg tggacaacag atttaaattc 102541 tttcctatat taatgtgaaa tttgtttgtt tatatcttct gacattccct gattccatσt 102601 σagaσtcaga gacagttcta cataggacaa cccttgaaat ttatagatgg tgtttgaatt 102661 cccttccgtt cattctgagt gttttcttct ccagggtaσa σatctaactt tcccαagcta 102721 gtcctgatgt aatσttgttt gcctcttttc catttcccag ataccctσσt ttggaaagaσ 102781 cσtccccagc ttcagtactt ttcctcatag ttatgtgaat ttgggccagc cactttactt 102841 ctσtgagact tagttttatc atσtatcaaa tgggaatagt aacaggacct aσctcaσagg 102901 gttgttgagg aatσaaatga gataatgσaσ agagagtgtt taacatagta cctaaσaaca 102961 catagggcσc agaatatcσt aggtcaacgt aaccaaσata aaatagaatσ agactagtat 103021 ctσccatctc tggaσattct acatatgata aaaagtaact ctactgcctt tcaagtcatc 103081 tttgggttat ctgtagtttt tttatgaatg caatggccat cσtccacσag tgtagatatt 103141 taagaσtatc ttattctagt ctagctacσc tcccaσtctc tctaagacag atctctaggσ 103201 σaaagatagg σcccagtagt gatggtacag ttatccgaga aatggacaga ggagagacag 103261 gttgttgaga atattgattt cσagagσttc aaggctattt aσσtσacgat ataaaggaaa 103321 gagcatgggσ ttttgtgtat atacagactg gagtttgaat tctggttσtg σσacttcctg 103381 gctatgacct taggcaagtt attcaatttc tatgagtctc agtttcctαa tσtgcaaaat 103441 ggggcgaata atatcagctt gataaggtta ttatgaagat taaatgagaa aatatatgta 103501 aaacaσtggg aaσagtgtσt gaσacacagt aggtgσtσac taaatgttga tttccttatt 103561 tctctgcaaσ tggcagaagc ttattacttg gtσcttaaca ctcatcggga gtaactcccσ 103621 ctgagtcatt tctttctctg gaaataatgt caσtttacat gtgcagagtg σtttgtaagt 103681 σaσaaagtgσ tctcacaσgt gσtatσtσac ttgtaαttta taaactcagg aggcaggtag 103741 aatgggggtt gttattctca ttttacaaat aacagtgagc agaaagaagt gactgagatc 103801 acagggcagt ggaaggatgg aactgggagt tttcttattc caagttσagt gσttcttcσa 103861 σtgtgctccc tσtgatcttc aaaaaσtggt σaagσaacta tttttttgga ctggccgagg 103921 ttaaggatσσ tσaaggccat ctgctaaccc tcctcatttg ctccatctca tttcccatgt 103981 ctccσcttca tgaacagttt gcctcagcag σaattσtgtc tgcσctgccσ caaacttgat 104041 tgctttcttc cacatgσσat tcattggtct gtgactaacc catttttctt ctttgcccσa 104101 acaccσagσt tacaatttgc agccttccσa aaσcagaaag cσttσtagga ttggctgcgc 104161 σtgσcttggt tcatgccσtσ actcacσagc ccσtcagaσt tagagtggσa ctgccctacc 104221 ttggatttga cgacaggσag σtσggaaaga gggttσttσg ggagttggtg cagctgtgac 104281 cttggttσcc σcggcaagaσ aaaaagσtσc ttgagggcag gggσtgggtσ ttσcggttσt 104341 σtggtσtσσσ caagacaggg ctctgσccaσ agtgggcgat caaagctgσt gattgcctga 104401 σagggggatg gcactgtgga tgaσσtctga ggtcacaσtc agcσccctga ctgtgctgta 104461 taacagtgac acctgctgtg ccactttgtg gtcctcattc ccccaaaaag ccatgctgtg 104521 ttgtaccttc aagσσtttgσ aσatgcctct atctggaatg σcatttccct ccttσtσtσc 104581 cgggaaaact gctattaatc tttσaaggac atagtccatσ tgtσaccttc tctgtgaggc 104641 attσσttgσc tgattcccσa gaσagaatta atagctcσσt tgttgatgtt tσσatggcat 104701 ctgttcaaσa aatatttgtt gggagtcagc catgσσgtgc taggcatσag gaaaacagat 104761 taatcagaσa gttctgccσt caaggatctt atgggttagt gaggagaαca ctgagtaaaa 104821 gacaagtgga ctacagtgtg acaggggctg tgaggtagag aggσσαagag taσtgtggga 104881 gaacaaagca agσcaaagat agctttctag aagaggggac tcctgagctt ccaccacggc 104941 attcagcaca caattataσc actgtatgtt agtatctcta actcσσtaσσ agcttcttgg 105001 gagcaagσat gttccttatt gacttttgaa taσttgatat σtaatgtggt gσttggσaca 105061 taactggσat aσagtattga aatgaataσa tttgaattaa atggσσacag ttacσcttcc 105121 aggctaaagg ttσtgaaaat ttactgagca gaaagagaga σatttggctt tttttactgc 105181 caggaagagc ctctaggtac aaggtggtcc tgataccttt ttaccttaac cacctaσσcc 105241 agcatttctg tgttccccag ggcσtagaaσ agtgcctgat aαatggtgσg tttttgataa 105301 atgtttgagg aaggaaagaa ggaggaaggg aaggagggag gaaaggaagg aaagaaggaa 105361 agaaaaaaga σagggaggga gggaaggaαg gaaggaaagg agggagggaa ggacggaagg 105421 aaggaaggga gggaagaaag gatgggaagg aagaaaggat gggaggggaa gaaaggatgg 105481 aagggaagat ggtcggaagg taggaattct ccσagtgaga aatacttact gcaggataga 105541 σatggσcaat ctgagcagtt ctccσtatat ggagctcatc ttcgtcttct tcttσtgttg 105601 ttttσctgta gactgggttg tσaaaattσa tgσttttggt gttcttccgc ttccagtttc 105661 tccagatcag gtatccactc atgσacagga gggctatσaσ cactggagga aggacaσagg 105721 aσaσtggaσc tccagcaggc tccaaσσσac tgσtcagaca tctgtacaag gcttgtσaσσ 105781 aσtσcacttt taσtaccctt tgctcctcag gctctgtttσ tgcatgttct tttaσtgσtg 105841 tttgaaagcc σatσtctcat cccttσtttc ctttactaac tattcatcct tσaagatσct 105901 gttcaaatgt gaagtcttcc σcaactgtgg gcagagtcag ttgctctαtc atgtgtgctc 105961 ccagatcaca caσagtatσt tactttatgt atctgtactc ccaactagat agσtσtttσa 106021 aggσagggac tgtgtctttt ttttgttttt aaactctcta cgcccagttσ σtagcactga 106081 ctaggtgcct agtaacatgt gctgaatgaa tgagtgaatt ttaccaσaσc tttgccctaa 106141 tgctgctgct tccctagatt tctctaagaa aacgattctc tcccaaaact ggggggtgga 106201 gagtgggatg gggccaggca gagtgtttat ttccaaaggt gaggctσcaσ ctgaagaaga 106261 acatctctag aaggagacaσ agagggcaac acaagctctg atttagaata aatgactatg 106321 ttaatgatta aaggaggaag σtctσtccaa caσagσtggg taaaaatgga gcaagtagct 106381 ttgtaaggtg attagcagtc actctgagca tcccagtgga ggctgaatga tcaσctatct 106441 aggatgσtat ggaaggggtt tctgttttag taagattaca ataattgata agcattaaag 106501 aσaggaaσaa ggσagttatc attgctaata tttattgtct tagagatcta gctatgcagt 106561 aaggccagaa aaaaatttaa gggtataaat atgggaaagg agcccaggtg cggtggctσa 106621 cgcctgtaat cccaacaσtg tgggaggctg aggcaggcag attacttgag gccaggagtt 106681 σgagaccagc ctggccaaca tggcgaaaac ccatctctac aaaaaataca aagtagttgg 106741 gcatggtggσ gggcacctgt agtσσcagct actcagaagg ctgaggtggg aggattgctt 106801 gagcσtggga ggtcaaggct gcagtgagcc acaatcatgσ cactgcactc cagcσtgggσ 106861 aacagagtga gaccttgtσt caaaaaaaaa aaaaaaaaag taaataaata aatacatatg 106921 agaaaggagg aaacσaaaσt gttattaaca gctatttgta tttttagaaa ctcttaagag 106981 aagctggtga aaaaσtatσa gaaataattt tagttaatca agaatcaaca taaaagatca 107041 ttagccgtct ttttaatσag σaaσaaσσaa ttagaaaatt taacggaggc σaggcaσagt 107101 ggctσacata tgtaatacσa acattttggg aggctgaggσ aggaggattg cttgaaccct 107161 ggagttcaag acσagσccgg gcaagatggt gagcσctggt ctttacaaaa aaattaattt 107221 aaaaaattag ccaggtgtgg tggtgcatgc ctgtagtccc agctactcgg gatgctgagg 107281 σaggagaatσ ccttgagccc aggagttcga ggatgcagtg aactgtgatc gcaccactgc 107341 actσcagcct gggcaagagt gcaagatctt cttgtctctt aaaaagaaaa agaaaaagaa 107401 aaagtaatgg aataaaaata cattcgtaat agcccatcaa aagctataaa atacctagga 107461 aaacctaaga agaaatacgc aagtcσtgtg taatctataa aattctgσtg agggacgtaa 107521 aagaagactg aaataaatag gσcacatttσ tggatgggaa gσtttaatat aataaaaagg 107581 tatattctcc tcacataaac tcatatatct aaaaσaatσt tgataaaaaσ ttcaccaaaa 107641 tttttataga attgataaga ttattctgaa gttcacctag aagagaaact gaataaaaat 107701 agctgagaag atgttgtgag cataacatat catgaagttg tgctaatagt atgtaggaat 107761 atataaatca gtgaaggaaa ataaactgct tagacgcaaa tcaaagtaσg tatgggaggt 107821 agtttataat aaagatgacg tgcaagtcag gagagaagta tggattattc aatgatggtt 107881 ttggggaaaσ tagaσaggta tatagagaaa aaaacagtta aatctctacσ tcatacgata 107941 ctctaaaatt taaattcσaa atagattaat atcctaatac taaaaaaaag tttaaagtag 108001 aaaagaaaaa catcaggaga tattttaata agttagagtg aggσtggσσt tcttaagcaa 108061 gacacaaaac ccagaaatct taaaagattg acaaatctga tacttaaaag tttcatattt 108121 atgcatggca aaagatacca taaacaaact ttaaaaccaa atgtσagaσt ggaagaaaat 108181 atttgtaaca tatattttaa aggtttaata tttgtcatgt ataaatattt σtataaataa 108241 gaaaaagata gσσaatagaa aaataagaaa agactgtgag tgggcgattσ ataacagata 108301 aaatataagt aaaggggσtg ataagcttac gaaaatatac tctacctσaσ agggaaatgt 108361 σagggaaata ataαtcatct ttcactcctc agattagcag aaattaaaaa tattgaatat 108421 ttcagagtga gttatgtcag caaaacagca tatatσtgcc tctttctata gggcaaagga 108481 tggcaagaaa ggggtagatt tatσtttctc cactccaatc aaaataatσσ tggaataatc 108541 acσtcaccat catctttcct ggtgaagcct ttσaaggcca attσaaatgc tgtcttctσc 108601 agaagcgcca cttttactct ggaattaσσt ttσcttctac catccσttσa caagagtatc 108661 atgccactat taσattgttc ctσtgtσtσt atσtatatcc aacatgccσσ tatcatagca 108721 σataatgaσa tgtattaaσa tctaccttaa aggactttat ttttgσctga ttaaagactg 108781 aaagσtctta aagtctttat ttttttcttc cctggatcct tggcaσttgg σacagtcagt 108841 gtcttacaca ggggagaagt ttttaaaaca tttgctgact aaσtcggcat actgaagatt 108901 cccaggataa (aaggacaaag ttσctgtcct tgaagtactc atagccaagt aagggagata 108961 aagσtctgaa tggaσaatca gaatgcaaag atactgctaσ gagatgagaσ tgctaagaga 109021 ggggtgtaca ggataccgtg tggtcatcag ggtggaagag aatgaatcag cccσcatgat 109081 tctctgtgag gtcttaacaa agtgttatac tctggccata ctgatctcct tctagctcta 109141 aacccacccc accctgaccc ttccaggcσa tttσctactc ctggctttac tσatgctgtc 109201 ttcactgctt ggactgttct tgatcσtσcc tcacttggct gaσccagctc aaatatcact 109261 tctgttagga aacctσotct tcσctσttσc ccctcccσσa gccσaagtta agtgtttcσt 109321 cagcactgtσ tσtgaagtca gtgcatgcag σttaacctta ggaσctacca ggtcgtaatg 109381 aacttatctg tgttatgtgg gtctσtctaa caagactata aacttttgta ggacagaacσ 109441 atgtσttatt catctttaac tgcσtttcct σcccttatσa gagtttggca catagtagct 109501 gcttaataaa tacttgttga aaaccaaaca gaaagaaaac aagacagtat gacσtattaa 109561 aggaatggta agσagctcta ttcattaatt σaacaaatcc ttgatatcct acσatgtgct 109621 agacattgσc aggagctggg gagaatggtg agcaagagat accagccctg ttcctaggga 109681 tcataσagtσ gσacttcaca tagctggagt gtagagtgtg aatcgagggg tggggagatg 109741 ggggatgtaσ σtggaaggtc acσtggggcc aggtσctgaa gagccttgtg tgctaggcta 109801 aaaaaccaaa ttaaatcagg actgggaggt gggcaggaag gctgcaaggg cagaacaagt 109861 σaatagggσa ggccaagttσ tσtaασctgc tagcgctσtt ccctaggcct aagcagggtσ 109921 tσtσttttct cttcagtgac tgggggccac actcacctat gggcaσgatg atcccgataa 109981 σagσggσagt gactgttgag cccatcttac tgtcttcatt tgcatctgσa aaacacaaac 110041 atttgσagaa tgatgctcta tcactgtgtg tccaagcccc tactggσctc aagtggtaag 110101 aaαtaσσσaa σtgctgctca tcσtcattct aaaatgatga tcctggctgt tgcctaataa 110161 ttcagtcttt σcagatccta tσaσaaσtcc tgtgaggσaa gσaggaσaga ggttatσtcc 110221 attttaσagg σaaggaaact gagtcttaaσ tgaggggttt cagaaaagtg gcagagctgg 110281 gacttgaacc σaggactcat gtcccaagtc ccataccctt tccatagcat σatggtagta 110341 ggaagσtggg ggctgtgσat ggσaaagtga gcacttaggt ctttatgttg σtgatggaσt 110401 aggtαatttg σctttttcca tcagtatσtg ttgctttgσc agtattgttt tttgtgaact 110461 gtctgtσcat ctgcattatc agattatttt tcataagtaa ttgaaatggg acatagtata 110521 gtgtagagga atcaaaagcg cagaσttctg tgtcagactt ctgggttσaa gtσσcagctσ 110581 taσtactcac tacccatgtg aσcttgggca aattattata tattataaat acagcacatg 110641 gtattatact tttatatctt taaaatggtg atattaσσta σctcctaggg atatggtaag 110701 gattaaatga aataatttat ctaaaatgaa tataaaatgc ttggcacaac tttgcctagt 110761 tctaagaggg tggagagtgg gatggggttg ttgaataggg tctaaatttt aaaaagatat 110821 gtaaaagcac attttaaact gaaaagtgct tggaaaattt actgtσtttt tgaaaaaσta 110881 tgσcatgcca tctttσtσaσ tσttataacσ atcttcattg taacatttgt gaagcacttt 110941 atagttcaga aagcattttt cccttagatc ctcctgaσag ctccctgtgg tgtgaaaagg 111001 agσtatσatσ tacacttgct gcaggtgaga tgactgtcσc ggcaatggσc caaggcccat 111061 αctctctcaa tgtgactgtt tatccatgtt actccaagag aatctaaσag ttaaggggag 111121 aaaaagσtgc actgσttgct tccagagcta actgtgtcct ccσtgσtgtc ctσσctgctc 111181 tgggccacag cgaaσaσtgg aσagtgatat taaaaσctag agcatgagga agccagtgag 111241 gagaagctgg tgagaggσtσ tgccσtσaga tgagaggaac tggaattcaσ acatgctσca 111301 tctgcctσtg caaacttcgg agtaagtgct ccactccaaa aagcσagσtt σtgctggcaa 111361 ataggaσcag ttaggaagat gttgccaagc agcttggttt ctgggctgtc catgtagggg 111421 aaaaaattaa aaagatagtt tatσσtttta aatgaaσtcc ctctggcagg taactσaatt 111481 aaaaaggtat ttgctgatta atgagataga acatttctag cagtgacaat tactgσtccc 111541 aatgatttaa taagtggtga acttaattat tttcatσcca gggttggaaa gaggtataag 111601 gagaccatgg ttgtagatat tactatctgg ggacσtgσtg tgaactgaga tcagagcttt 111661 ccaaacacaa gggaσaσσtσ ctcatataca σatcagaact ttgtgaaaca tagaσaσaca 111721 caccctcgca gagtcagcaa cggctgtgtg cgtgagσacc tccagttata σcggttacac 111781 σtttgtctat catggcaatc ttgtgaagca ggttgtggaa gggtggttat ttccactttg 111841 taagagaagc aactgaggct cacagggtct cagσttσσta caagacσctc tgtaaggtag 111901 gggcacctat gagtcσtaaa tcgcaggctg gtaσtctacc tccctctcag atatgcagta 111961 acctcctcaa agatatgcag tattcagσtc tggtaggttc tgtσttatσa σataccccct 112021 tσσtggcttc σσtaggagcc ctcccatgtc atgaaagaat gcagaactca tttccttaca 112081 gtgctgggag tggttgctgg ttgcagggct tagggtagac gggctgatgc tgggagσcct 112141 ggggacacta aσtgagcttg ggaσtgcagc tgtcaggctt ggtgtctctg tgctgtggtt 112201 ctggtaggtg gatctgtgga cggtggtcσc gggggctctt gtggtggcag gtactgtcct 112261 cgtσatggta gaagσtaacg tcgtagttga ggtagattga ggtgctggag gggaaataσσ 112321 atggaggtσa σttggacaga taattttgtt gcctaaggta ttgcσtσtga gatataσtta 112381 ggaaσttatσ ttcatggcgt agσtσaaatg σcacttctgt gaagcctttc σtaatσtccc 112441 cagtgggcta tgatσttttσ tttagσtgaa tgσtaagcac ttcaσtttga ttσaataaag 112501 atgagtσatt aaaacattgc tgtggaatta gttgtaagat cagcaataaa aagactgtag 112561 ggaggggaaa tcagataaat ctagaaggat tttacactca tatattgtta taσcaataga 112621 ttgaaattct tattccactt taaaσaattg aaσctgtaaa tσattaataa tgcagtagac 112681 ttaggctcaa atgaaaggcc ttggσtataσ atσaagatta ggaσatgaat σtgtgtatgσ 112741 ggttgaagta ttaactatta gtcccaatta tattgcaaaa gggctgσtgt gtagtgtttg 112801 ttaagttcta ggtgagaaac aggcaaatat atagttatct gcatgtaσct gaagccacgg 112861 cgattaaggg ttcttaactt gaggttttta aagcgttcca gaaactccct gaaactgaat 112921 ttaaaatgtt ttatgtatat gtgcattttt tccttgggag tgagaaaaag ctttggaagg 112981 atσctggggg catgagcatt caaggaaggt aaaaaagaga aaccσσcaaa aggcaaσaag 113041 taaσcaggga agatggaaga aaacσagσag cataσtgtgt σccagaagσc aagggaagat 113101 ttcagcaggg tagggtσtga cactgccagg ggσcatccσt σσtggaaggt ctgcttaσσt 113161 αggtagσacc tcttcatgtc tggacccagc caσattgtgt σaggaσaggc acatgtgtac 113221 ttgggagagt ggctggagat ctgaggagca ggaaggcaσa ggtattcaca gcctccatta 113281 ggctggacac tcagctcaσa ggcatctgga gctaatggca gagagggaga cagσtggggσ 113341 aσagaσagga catgccaggt σttcctgcct cctgaggatg aggcttctcc caσctggctt 113401 gctσaaaaag cttgcσctat actttttttt tcacattttt tttctttttc tttctttttt 113461 tatcccccaa agcttttggg atacacgttt tttgttacat ggatgaatta tatagtggtg 113521 aattctggta ctttagcgca cctgtaaccc aagtgtagtg tacattgtac ctaatgtgta 113581 attttttttt ttttaaatct ctagccccgc tattaccttc tccattttta gtctctaaag 113641 tccattatat gcccctgtgt actσatagct tagctatact ctgtatgccc ctgtgtactc 113701 atagcttagc tcσtgcttat aagtgagagc atatagtttt tggttttcσa ctactatcat 113761 actttactta gaataatggc ttccagctcc atccaagttg ctgcaaaata cattattttg 113821 ttccttttta tggctgagta gtattσcaag gtgtatatat gcσaσacttt ctttattcac 113881 tcattagttg atggacactt aggttggttc cacatσtσtg caattgtgaa gcccttctac 113941 tttttcaatt ttttttatgt tttatgtttt gagacagggt ctcactctgt tgcctagaσt 114001 aagtgσagσa gtgσaatcat agctcactgc agcctcaaac tcctgggctt aagaaatcct 114061 σccaσctcgg cctcccgagt agctggaact ataggcgcat gccaccatac aagggtcatt 114121 tttatagttt ttgtagtgat agagtcttgσ cttcttgccc aggctggtσc caaactcctg 114181 ggσtσaagtg atσσtcctgc gttggcσtσc caaagtgctg gaattgcagg tataagccac 114241 catgσσtggσ σtαcctacta cttttattgg gtaσtttσca gcaccatacc tagtgtttta 114301 tccctaσaσt σtcatttaat ccttgcaaca attctgagag gtggggacgt tacatccσag 114361 aσtgacaaat aaagacacct aggctcaaag agaacaaatt σgtσaaacct atactctagg 114421 aatttttttt ttttttaaga ggtaggggtc ttgctctgtc gcccaggctg gagtgcagta 114481 atgσaatσat agσσσactgc tgcctggagc tcctgtgctc aagggatcct cctgcctσag 114541 σctctcagtg ttgggattac aggcatgagc cacσatgtσt ggactagaga tagaacttaa 114601 attgaggtcg gctgggctcσ aaagcccata agcccgcggt ttttattttt σσctgtgcca 114661 catactatgt ctctcattta aatttctagg tσtagaatσa ggcacσaatσ ttagσtσσtt 114721 aσaσtσσctt gctσtσcctc tttcacσctg gcagσcaaca σttαagttac agttagaatt 114781 aatgtatcct agtgatagag gaggggacaa cσtagtagta ggattσσtag attctattcσ 114841 σaaσcaataa gctgaσttat tatatggccc tcggatacat tagcttataσ tactgcagaa 114901 tggctaσaaa tagσaagtta gatgcagtgt gtcatggtga aagcagσtgt ggaaσcagat 114961 agaσσtgggt ttaggtttσa gttctgccac ctgctaacat tattttacct ctctgagctt 115021 σσgtttcctc aactgttaga agagtaatac ccaσaσtttg taggattggα aaaaacagga 115081 cagttatgta ttcatttata cccagcσtta tttσaσaaag aacttgaggt aaaatgagac 115141 aaaatatatg atgaaaaagt actctaccaa caagagggat tgttgttatt attcσtgggg 115201 ttgσtgagtt gtgacctgaa tgtgaaσaσa gσctgcctgg tgaaaggaga ggacacagtg 115261 acacagtcag gggacctggg acctaggacc agagacagσt σacctσttgg σtgcttcagσ 115321 tcatggaaga tgacaatgtσ atgtgggttg ttgaggttσt σagσcaggat ggagatttcc 115381 aggσcattga gccgatttgc actgaaaatg gcctcgttct ccaggtctgt ccagaacaσc 115441 ttgtcctgtg gggtatagat gcagaggatg ggaggcσtgg agtgtaaatσ σatgacctσa 115501 gtαtgagggg ttggccccaa accatagtca caagaacttc σctgaaatct cccctgatσt 115561 gtcctgtσta tggattcacg gtggggσtσt cagcctctaa tctgtgatgc aσgtσtσctt 115621 gttcccttct atcttagagg attattcagt gattctgtgc tttgaactga cagccacaaσ 115681 attactcatt σatgctgaac taagcctgσt tgσtagagσσ σagcagaaac ccaaggttaa 115741 atσtctatag cattatcatt actggggcct gggaccaaga ttggaaggaa tgtgtgagσt 115801 atgagggtta tgccttgσtg ggcttcctgt agcctctggg tatccacaσg agtccacatg 115861 gttagtσcat ataagcctag atgtgcatct gtcagcaaat σcacaσgtac aggtacaaσt 115921 gtgcatcctc atacacagat ctaaacacat acccaaatgt tcatccacac acaaaaagct 115981 acatttgccc ctaaatatgc agtctatata catcttggta tatgtatgta cacacataag 116041 caσcagcaαt tagaggaatg cacactttta ttctgatgσa tttatattta σccatgσaσa 116101 taσaσatact ttacatgtac atgccatgta tataaacaag σaσaaaσaαt tgtgtaccaa 116161 caσacctgtc ctttaaagca ggggctggac ttagaggtgg agctttgccc acaacttcag 116221 agcagtgctg agtaactttg ctgcaagcaa atσctgccaa tgcccaccaα agaccatcat 116281 ccctttgctt tccctcccσt tggtggtgga gttagttttc gggaagaggt gaaggtgtga 116341 gaccttggtt ggttσtggσt tcttcattcc cggagaagaa aagtσattag ggtcagggσa 116401 σaggagggtc ttcgσtcctc actttgctgg gagσttcttg agactaggat agtgtctgat 116461 tcacttctat gacσσcaggg tctggcagag gtσaataaaa gtgtgσagaa ttgaaαagσa 116521 tσtctcaggc σatttcctcσ agtaaatgat tctaaggata tgtatgttcc ttcttcσttt 116581 cctσccttta σtgggtgσct tttgtatatg ggttacagtg ctgggtgctg agggcacaga 116641 gaggaaacat aσatgcctag cagctcacct gtgagaagtg ctctgggaga ggggtcttgg 116701 gaagagagcg tgggaaaggc tgccaggtgg agagtgggct gcagagcctt tgtgtgcagg 116761 cagctcaαag attgtttaσa aaσaaatσag ttggtttσcc tgttcctgtt ttcatttgaa 116821 caagtctσag ggactcatcc tatttgaaca agcattttct aggcttcagc ttcctagtgg 116881 gσσcttgcct ctσcttacag gaσtσacctc aaacaσagct atcσcaaaag ggtggctσag 116941 gaagtσagtg gaggagatσa gcgtctttct gttgcctσca ctgaagtσaa tgctggacag 117001 ttggtgtagσ ttggagtcta cccagtaσaa gcgctggσtc agσagatσtt gggaaggaag 117061 caggatσagg tcatgaacct gggaσcccag tctggagctσ tgttσctttg tacctσtσcc 117121 tgcccaσatt tctaggcctc acactgaggc cagcctacgg caaccattag gaaacaaagt 117181 cactggcaσc atgagaggac ccagaaacaa gactcatgga gttccagaca gtgatcagga 117241 caaggcacta gaataggccc ccaacccagg aaaggcaggg ctcacccagg gtgattccgt 117301 tgggccattc aatattgtct gacaccagtg tttgccggtσ σaσaσcgttg agcccagatt 117361 tctσaatctt ggcctggtcc ccccagtcag accaatacat gaacctaaaa gacaaaataa 117421 cccaatttgc cttcttgctg gggacatgac σggggtggtσ tgagtcacaa gagctcaata 117481 accσattgac tagttgtggt ttatgtttag tagggactga gaagacctσt aaagttcttt 117541 tgaaccatca aatσttagat ttagcaggca ctttagcσtt cacctσattt gagaacttga 117601 ggaaaactat tctcσgagat tgcacccaga ctcagctgaa tagcσtgtga σcccatctct 117661 ccσaσttσtg gcagtgctaa ctaactagag ccctagggtg tcagtgtggg gaaggcccta 117721 gtaagccctc tcttttctgg tttcagagga gaaagtggat gagcttccta actcaggtaa 117781 ccσtccctgc ttttgtσtσc tcaggcctac tagggccagt agcagcccac tgttactaat 117841 ccaaggtagt aaattagacc taacccactc ctttgtaaat agtcccttta ttaaaccσtσ 117901 σtctgattat cttgagtatg cagtgggttt cctcctggga ccctgacgat ccgσagtgga 117961 ttggggttgg gσtgggtgta actctatgat gtgagggaca ggatgtggσa ggtgσaacac 118021 aaggtctgca tgagaacaga cagagaacag ggatgaagtg agggtaagag gagaggctσc 118081 gtatctgtca gagtgcctag ttctgtgσtg gaagσaσctg acccatgctt agtgaatggc 118141 agctatcagt cacttccσaa ggσσtcacat aacctcccat gtggtactcc σctcacσagα 118201 tgccσttgσt cgaagaagag ggttttctta tccctgttta acaaggaaat agcagtagga 118261 agcagctgtt gattctgtta aacttaacat gatataacgc taaaaaaacc atctcaagat 118321 atσcacactg agggagagag ggagtcctgt tctgttcaga atccctaact cccaaaaσtg 118381 aggggtggσc agagcagggc aacctaggtg gtgagggccc agagaσcata ggcaacaggg 118441 gtagggatgg aggcaggcag tctgaagcag aacagaccag tgatcttggt cctcaaatct 118501 tgctggctct ctcacagggc agggaataga σatgttttat gtaactccag aggccaatgg 118561 aggaagttgc agggagatag atttggcatt atgaggggaa aagaσccact ttctaatgag 118621 cagagctgcc ccacggtgaa acaggcccta tgggaggtaa tgagctaσct gtctttggaa 118681 gtatgtgagσ agctgtcaga tgctcaσcta cagσagσctg aagaaaggct tcctccccca 118741 ggagσttcta tcaggccatc tctagagccc tactctgctc tgagacactc σaattctacg 118801 atataaσgag tgggtgggag agtccaggga gaactttggt gaασaatgcc σagagaacct 118861 tggttgggga ttaaσaagac tttcttcccc atggcctgtg tσtgagtggσ σcagagcttt 118921 ctagaacσct σaagatagcc σttgtgacag acacaagagg actgagcacσ tatggtggga 118981 gaatgggaag ttcagttggg acactcaccc tcgcaggggg tcaacagcga tggcccgggg 119041 ttcactgagg ttacggσtga agagagtgcg tcggcggcca cσatσaaσtg tggccactga 119101 gatggtctta ttgcccgagt cagtσcagta gatgtgcttg tggaccσagt σcactgccag 119161 gccctctgga gagtgσaaσt gctcgtcaat gaggacctcc tgctctttσg ggtσaσtggc 119221 cttgtccatg taggσgσtta agagaaaaca gagatgacca tggggcagat gttσcaccca 119281 tgggcccatσ tggagctacα tgtgσaσσσt tσccctctct tccatσtggg σcatggcaat 119341 agatttttag aggaacgtgg ataatttσca ctσtacacat tccctggggt accagggtag 119401 gggtacagac ttacatgggc cacggtctct ggσtttctaa ggtggggctg ctccacagσt 119461 σtgσccatta gggtgagcca gatataataσ aatgtgatta tggaaagσat tagaggctat 119521 ggcagcagag gcatggagac tgcσtcatcσ gagagggcgg gagaaggctt tatagttgag 119581 tcctgaagga cgagttcacc aggagcatga agtσaccagg acagaaagcc attagggaac 119641 aagaaaggct tgtgcaaatg gσcagaggtg agtctgctct ggaacagtga gatacttagg 119701 ggagσtgσtt atgtgggtgt cagactgcaa gcaggtgtag gcaggaaccc catcttgatg 119761 ggctttgagt accacgσcaa ggaattagga tttctcσσσa gtgataacta gacaggccag 119821 aggatatagt ccaataagca tgttagttca ctgtggcatc tatggagtgg atgggttgga 119881 aggagaggga atgaagcagg gaaactggtt aggaggaσgt taσagσatσt gggtgggaga 119941 ttaagagagt ctgaagaatg accgtgσcag tgagaatgga aagaagggct aagaataσag 120001 tagaσactσa ggaggcaaca ttagcaaaat agcaaatgct gtttcσccag aggttttctt 120061 σttcttgcσc tctctctggg tgattagttσ cttagtgtcc actgccatσa ataactaagt 120121 ctσσaatccc aacagctctc ttacgatcca gaσtgcaaag ctaactagct ccσσttggat 120181 gtσccatgga cacσttgaaσ tcaatatgtc caaaactgtt catσccσatt cccttccσct 120241 cggσσaaσσa gaσggcccaa accctgagcc ctgatcctσσ tσtactgctt cacaσatcag 120301 agaacagσac caccattcat gaaacctσcc aagccaaaaa cσtgaaactc ccaaaattσa 120361 ctatgaagga gtaaatttct tccatσagcc ccatatσtag tσtgtσaσσa aatσctgcσt 120421 σtttσagtta catctcttgg acaggcattg ttctagttat gtttttgggt gtgtgtgaac 120481 ggagtgtctg tatgttgcag ggaggcagga atctagttgt σagtgagtag cacttgctat 120541 atttgcttcc atccactctt ccacccatct gtcccatcat tctttcatσa gtgaσtσagt 120601 gtctaccσag cgcctggtσa tcggcattcc tgccaagtgg atctcaggac aaagaaagga 120661 σatgaσtgcc tgaagagggc ccagacatgc agtggggcag gtgσtggσat ctgagaaagt 120721 cctaggagag aacctσctcσ agtgtgtgaa gagσttccca agcacσaggt ccaσtgaσtg 120781 tggcgtcaaa gacagtgaaa agctggcctt ggggtgatgσ σatccaggaa ggcatgccag 120841 atcagatgcc caggtgggtt cggaggcctσ ctctgtactt tctcatgatc
SEQ ID NO:
DDX5
NM_004396.2| Homo sapiens DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 5 (RNA helicase, 68kDa) (DDX5) , mRNA 1 acctcattca tttctaccgg tctctagtag tgcagcttcg gctggtgtca tcggtgtcct 61 tcσtσcgctg ccgcccccgc aaggcttcgc cgtcatcgag gσσatttcca gcgacttgtc 121 gσacgctttt ctatatactt cgttcσσcgc caacσgσaac cattgacgcc atgtcgggtt 181 attcgagtga cσgagaccgc ggccgggacc gagggtttgg tgσacctcga tttggaggaa 241 gtagggcagg gccσttatσt ggaaagaagt ttggaaaσcc tggggagaaa ttagttaaaa 301 agaagtggaa tcttgatgag ctgcctaaat ttgagaagaa tttttatcaa gagcaccctg 361 atttggctag gcgcacagca caagaggtgg aaaσataσag aagaagσaag gaaattacag 421 ttagaggtca caactgcσcg aagccagttc taaattttta tgaagcσaat ttccctgcaa 481 atgtcatgga tgttattgσa agacagaatt tcactgaacc cactgctatt caagctcagg 541 gatggccagt tgctctaagt ggattggata tggttggagt ggcaσagact ggatctggga 601 aaacattgtσ ttatttgσtt σσtgσσattg tσσacatcaa tcatcagcσa ttcctagaga 661 gaggcgatgg gcctatttgt ttggtgctgg cacσaactcg ggaaσtggcc caacaggtgc 721 agcaagtagc tgctgaatat tgtagagcat gtσgcttgaa gtσtacttgt atctacggtg 781 gtgσtcctaa gggaccaσaa atacgtgatt tggagagagg tgtggaaatσ tgtattgσaa 841 cacctggaag actgattgaσ tttttagagt gtggaaaaac caatctgaga agaacaacct 901 accttgtcct tgatgaagca gatagaatgc ttgatatggg ctttgaaccc σaaataagga 961 agattgtgga tcaaataaga cctgataggc aaactσtaat gtggagtgcg acttggccaa 1021 aagaagtaag acagcttgct gaagatttcc tgaaagacta tattcatata aacattggtg 1081 cacttgaact gagtgcaaac cacaacattc ttcagattgt ggatgtgtgt catgaσgtag 1141 aaaaggatga aaaaσttatt cgtctaatgg aagagatcat gagtgagaag gagaataaaa 1201 ccattgtttt tgtggaaaσσ aaaagaagat gtgatgagσt taccagaaaa atgaggagag 1261 atgggtggσσ tgccatgggt atσσatggtg acaagagtca aσaagagσgt gactgggttc 1321 taaatgaatt caaacatgga aaagctσσta ttctgattgc tacagatgtg gcctccagag 1381 ggσtagatgt ggaagatgtg aaatttgtσa tcaattatga ctaσσαtaac tcctcagagg 1441 attatattca tσgaattgga agaactgctc gcagtaccaa aacaggcaca gcatacactt 1501 tctttacacc taataacata aagcaagtga gcgacσttat σtσtgtgctt cgtgaagcta 1561 atcaagcaat taatcccaag ttgcttcagt tggtcgaaga cagaggttca ggtcgttcca 1621 ggggtagagg aggcatgaag gatgaσcgtc gggacagata σtctgcgggc aaaaggggtg 1681 gatttaatac ctttagagac agggaaaatt atgacagagg ttactctagc ctgcttaaaa 1741 gagattttgg ggcaaaaact σagaatggtg tttaσagtgc tgcaaattac accaatggga 1801 gσtttggaag taattttgtg tctgctggta tacagacσag ttttaggact ggtaatccaa 1861 cagggactta cσagaatggt tatgatagσa σtσagcaata cggaagtaat gttccaaata 1921 tgcacaatgg tatgaaccaa caggσatatg σatatcctgc tactgcagct gcacctatga 1981 ttggttatcσ aatgσσaaσa ggatattccσ aataagaσtt tagaagtata tgtaaatgtc 2041 tgtttttcat aattgσtctt tatattgtgt gttatctgaσ aagatagtta tttaagaaac 2101 atgggaattg cagaaatgaσ tgσagtgcag cagtaattat ggtgcacttt ttcgctattt 2161 aagttggata tttctctaca ttcctgaaac aatttttagg ttttttttgt aσtagaaaat 2221 gcaggcagtg ttttσaσaaa agtaaatgta σagtgatttg aaataσaata atgaaggcaa 2281 tgcatggcct tcσaataaaa aatatttgaa gactgaaaaa aaaaa
SEQ ID NO: 5 CAMKK2
NM_006549 Homo sapiens calcium/calmodulin-dependent protein kinase kinase 2, beta (CAMKK2) , transcript variant 1, mRNA gi I 27437014 I ref |NM__006549.3 | [27437014] 1 gagcctgggg aggtcgaggg tgcagcgagσ σgtgatσgtg σtaσtgcact ccagcctggg 61 caacacagag agaccctgtc tcaaaacaaa σaaaσaaaσa aaσaaaσaaa caaacaaaaa 121 aaacaaagaa aaaaaaatgg gagtgggccg ggcgcggtga σtσaσacctg taatccσagc 181 actttcggag gccaaggcgg gtggatcacg aggtcaggaa ttcaagatta gσ'ctggacaa 241 σatggtgaaa cσccatctct acgaaaaata caaaaattag σσaagtatgg tggccggcgc 301 ctgtaatσcσ agσtactcgg gagactgagg cagagaactg cttgaacctg ggaggcagag 361 gttgcagtga tccgagatcg cgtcactgσa σtσcagcgtg ggcgacagag cgagactccg 421 tttcagaaaa gaaaaaaaaa aaaaaaaaaa agggagtcgg ggtggagctc tcattggσtc 481 gttgcatgtg agtgtσccta cggcctagaa atacaagaga agcaσatcgg aacgggctgg 541 aaatccaccc agttaactag agggctttga acσttttatt aaσttggagg ttgactctcc 601 tgtcaactcg attcσctttt ggctgtttgg cagggtcagt gagaσatccc ctgggtcgct 661 σgaασccgta ggacggttσa gggagσcctσ σaggtσttcg tttctcctct tcccσgcaca 721 gtgσtgttat ccagctgggg gatccaacgc aσaσttaagg σtccagcaaa gtggctccgc 781 tgccggatgg gagtgcccca gtgtgσtgga tgaagctggc gcatgcacca tgtcatcatg 841 tgtctctagc σagσσcagca gcaaccgggσ cgcσccσcag gatgagctgg ggggcagggg 901 cagcagcagc agcgaaagcc agaagccctg tgaggcσctg cggggcctct catccttgag 961 σatσcacctg ggcatggagt cσttσattgt ggtαaσcgag tgtgagccgg gctgtgctgt 1021 ggacctcggc ttggcgcggg aσcggcccct ggaggσcgat ggccaagagg tσccccttga 1081 cacσtσσggg tσccaggσσc ggcσσσacct ctccggtcgc aagctgtctc tgcaagagcg 1141 gtcccagggt gggctggcag ccggtggσag cctggacatg aacggacgct gcatctgσσc 1201 gtccσtgccσ taσtσaσccg tσagσtσσcc gcagtcctcg cσtαggctgc cccggcggcc 1261 gacagtggag tctcacσaσg tσtσσatσaσ gggtatgcag gactgtgtgc agctgaatσa 1321 gtataccctg aaggatgaaa ttggaaaggg ctcctatggt gtcgtcaagt tggcctacaa 1381 tgaaaatgac aatacctact atgcaatgaa ggtgctgtcc aaaaagaagc tgatccggca 1441 ggσcggcttt ccaσgtcgcc σtσcaccccg aggcacσσgg σσagctcσtg gaggctgcat 1501 ccagcccagg ggccσcattg agcaggtgta σcaggaaatt gccatσσtca agaagctgga 1561 ccacccσaat gtggtgaagσ tggtggaggt cctggatgac cccaatgagg accatctgta 1621 catggtgttc gaactggtca accaagggcc cgtgatggaa gtgcccaccc tcaaaccact 1681 ctctgaagac caggσccgtt tσtacttσσa ggatctgatc aaaggcatcg agtacttaσa 1741 ctaccagaag atcatcσacc gtgacatσaa accttccaaσ ctcctggtcg gagaagatgg 1801 gcacatcaag atcgctgaσt ttggtgtgag σaatgaattc aagggcagtg acgcgctcσt 1861 ctccaaσacc gtgggcacgc ccgσcttcat ggcacccgag tcgctctσtg agaσccgcaa 1921 gatσttctct gggaaggcct tggatgtttg ggccatgggt gtgacactat actgctttgt 1981 ctttggccag tgcccattca tggacgagcg gatcatgtgt ttacacagta agatσaagag 2041 tσaggcσctg gaatttccag accagcccga catagctgag gacttgaagg acctgatcac 2101 cσgtatgσtg gacaagaacσ ccgagtcgag gatσgtggtg ccggaaatca agctgcaσcc 2161 ctgggtcaσg aggσatgggg cggagccgtt gccgtcggag gatgagaact gσacgσtggt 2221 cgaagtgact gaagaggagg tcgagaactc agtcaaacaσ attσccagct tggcaaccgt 2281 gatcctggtg aagaccatga tacgtaaacg ctσctttggg aacσσattcg agggcagccg 2341 gσgggaggaa σgctcactgt cagσgσctgg aaacttgctc accaaaaaac caacσaggga 2401 atgtgagtσσ σtgtctgagc tcaaggaagc aaggcagcga agaσaaσctc cagggcaccg 2461 acccgccccc cgtgggggag gaggaagtgc tcttgtgaga ggσagtσcct gcgtggaaag 2521 ttgctgggσc cσcgcccccg gctcccccgc acgcatgcat ccaσtgcggc σggaggaggσ 2581 catggagccc gagtagctgc ctggatcgct cgacctcgca tgcgcgccgc gtσgcctctg 2641 gggggctgct gcaccgcgtt tccatagcag catgtσctac ggaaacccag caσgtgtgta 2701 gagσσtσgat cgtcatctct ggttatttgt tttttccttt gttgttttaa aggggacaaa 2761 aaaaaaaaaa ggacttgaσt σcatgacgtc gaccgtggcc gctggctggc tggacaggcg 2821 ggtgtgagga gttgcagacc caaacσcacg tgcattttgg gacaattgct ttttaaaacg 2881 tttttatgcc aaaaatcctt cattgtgatt ttσagaacca cgtcagatat aσcaagtgac 2941 tgtgtgtggg gtttgacaac tgtggaaagg cgagcagaaa actccggσgg tctgaggcσa 3001 tggaggtggt tgσtgσattt gagagggagt agggggctag atgtggctcc tagtgσaaaσ 3061 σggaaaσcat ggcaccttcc agagccgtgg tctcaaggag tcagagcagg gctggccctσ 3121 agtagσtgca gggagctttg atgcaactta tttgtaagaa ggatttttaa attttttatg 3181 ggtagaattg tagtcaggaa aacagaaagg gcttgaaatt taataagtgα tgctggaagg 3241 ggattttcca agcctggaag ggtattcagc agσtgtggtg gggaaaσatt tctcctgaaa 3301 gaαtgaacgt gtttσttσat gacagctgct caaagcaggt ttctgagata gctgaccgag 3361 ctctggtaaa tctctttgtc aaattacgaa aacttcaggg tgaaatccta tgcttccatg 3421 tacattacat ggcttaagat taaacaaaaa catttttcaa gtctctaaσt agagtgaaσt 3481 σtagagσaσa gtagttcaga aactatttag agcttccagg atatatttca cagcttσagg 3541 catgtgatca gttagagσcg atgaaacσta tgcccgσctg tatatatatt agcagσttag 3601 ctagttcata acctgtatat tσtaaagact gctaaggttt tgttttcatt ttaaatccta 3661 gσtgattgtt gtggtcaatg aaatacσσag tttσtggagg gccaggtggg aaatgctttc 3721 actggaccaa σacacaaatg atcatcctga ggatctgagc ttccctagac tccacacaat 3781 aaccttgggg caccctttta gagaagaσtg ttgaaaccca cagσaσtcgt tggggtatga 3841 ggaaaccagg gσttggcaca ggaagttccc ctttgtagct aaaagtccag aaagaaaggg 3901 ttσatσtttt tgacttccaa ctgatattgg gaagtttggt tgaggttcaa gtgtgactcc 3961 ttσσagagcc acaggtaggg gagtgtgaag ttgaggggga ggaaagctgg aaggactctg 4021 σcttgggaga ttσccagctσ tgσtttccag cgcttggtgg aatctgggσt ggggaaagac 4081 ggcaσσggga aaσtctgctt cσccattgtt tccatσtgat σagctgtggt gtgaggactt 4141 ctcagacaaa ggcaaggcct σgtgcccctg cccagcccat tcatggagσσ σtgggccttσ 4201 ttggσttσca tagatcσtaa gctcttgact gtagtttagc cagacttgtt ttgctatctt 4261 ataagcagtt cagaattagg gaatgσtggt tttgaagagσ aaaggacagg tagtctagag 4321 agggtcgtct ggcctgcttg ctgggtcttt gtaaσσσagc acttcσtctt gcσctcctgg 4381 ctttatgttt atggggagag gactcaatag ctσcaccσct tctggcacca gatggggctt 4441 ggttagtttg caataagcac cttgcagagg ttaaagccag cgggtσααta gtσttaggσc 4501 cagcctgσtt gtgtgggctc tggσctggcc tggtggσtgg σσcagggggc agσagtgctt 4561 agagcttctg cagggcttσt cttgtttaca cagctgcatc agacaatgcσ atttctσcσc 4621 aσσaσggaac cttσcatcta agatttcttc cagggaatgc cagσaatcag gcagcaccca 4681 gσtgtggggg cagtggggtg ggggagaccc acattgatga cttttttttt ttσttttaat 4741 gaagaaacac caaagaaagc tgtggaaagg acctgσccσa σatgaaaagg ataagαcaag 4801 atggctgtaa acacagagca tttgagctgσ σaσtσttgga gσacattgat ttttcaaaag 4861 ccagctctgt caggaaagga ggtgctgtta tgagσagσtσ ttσσagtggg σaaagaggac 4921 gcccataatt tcttcσattg σtagctcatσ tgtgggaσca atttggtgta agcaaσσtgt 4981 ggσctgcaσt tgtggσctcg aaggaagcac aaaσσctcca tccaσttccc atttcctctg 5041 cccttttcca cctccccσtt ccatσσcacc agctgccagt ggctcccaga aagccttatt1 5101 gagccccttg ttgaσacttg gggctgσgga ggσσtctccc tactggtctg gσσtttσctg 5161 agaggcaggt cttcσgtcct cagagcσttt σtggaaσaag gagaatgcct gtgσaggtgg 5221 aσacacaggc ctggσctgtc gctσtσactt gtcttccagσ ggggagcttc acgttgcσga 5281 gtggaagaac catgacctcσ aσttgσttσc aaggtgctag ggaagtttca gggtacgσtg 5341 gttσσσσtct cσagσtggag gσσgagtttσ tggggactgc agatttttσt actctgtgat 5401 cgattcaatg σσσgatgσtt σtgtttσatt cccgaccσtt tσtactatgc attttccttt 5461 tatcaggtgt ataaagttaa atactgtgta tttatcacta aaaagtacat gaacttaaga 5521 gaσaaσtaag cctttcgtgt ttttccacag gtgtttaagc ttctctgtac agttgaaata 5581 aaσagaσagc aaaatggtgc σaaaaaaaaa aaaaaaaaaa
SEQ ID NO: 6
ACAAl NM_001607 Homo sapiens acetyl-Coenzyme A acyltransferase 1 (peroxisomal 3- oxoacyl-Coenzyme A thiolase) (ACAAl) , nuclear gene encoding mitochondrial protein, mRNA gi | 6598316 | ref |NM_001607.2 | [6598316]
1 atgtggttct gcgcgtgtgc ggacggctgt σtgttaactc cgcggtcagt tccσggaσtg 61 gtggσtggtc tgcagggttg acctgσgcaa tgσagaggσt gσaggtagtg αtgggσcacc 121 tgaggggtcc ggccgattcc ggσtggatgσ σgσaggσcgc gcσttgσctg agcggtgccc 181 cgcaggcσtσ ggccgcggac gtggtggtgg tgcaσgggcg gcgcacggcc atctgccggg 241 cgggccgcgg cggcttcaag gacaccaσσσ σσgaσgagσt tσtσtcggca gtσatgaσσg 301 cggttctcaa ggacgtgaat ctgaggσσgg aaσagσtggg ggaσatσtgt gtσggaaatg 361 tgctgσagcc tggggccggg gcaatcatgg ccσgaatσgc cσagtttσtg agtgacatcc 421 cggagaσtgt gσctttgtcc actgtcaata gaσagtgttσ gtcggggcta caggcagtgg 481 σσagσatagc aggtggcatc agaaatgggt cttatgacat tggcatggcσ tgtggggtgg 541 agtσσatgtc cctggctgac agagggaacc ctggaaatat tacttcgcgσ ttgatggaga 601 aggagaaggc cagagattgc ctgattσcta tggggataac ctctgagaat gtggctgagσ 661 ggtttggcat ttσaσgggag aagσaggata cctttgσcct ggαttcccag cagaaggcag 721 σaagagσσσa gagσaagggc tgtttccaag ctgagattgt gcctgtgacc aσσaσggtσc 781 atgatgacaa gggσaσcaag aggagcatca σtgtgaccca ggatgagggt atccgcccca 841 gcaccaccat ggagggcctg gccaaactga agcσtgcctt caagaaagat ggttctacca 901 cagctggaaa ctσtagccag gtgagtgatg gggcagctgc catcσtgσtg gσccggaggt 961 ccaaggcaga agagttgggc σttσσcatcσ ttggggtcσt gaggtcttat gcagtggttg 1021 gggtcccacc tgacatcatg ggcattggaσ ctgcctatgc catcσσagta gσtttgcaaa 1081 aagcagggct gacagtgagt gacgtggaca tσttσgagat caatgaggσσ tttgcaagcc 1141 aggσtgccta ctgtgtggag aagctacgac tcccσσctga gaaggtgaaσ cccctggggg 1201 gtgcagtggc cttagggσaσ σcactgggct gσactggggc acgacaggtσ atcacgctgc 1261 tσaatgagct gaagcgccgt gggaagaggg σataσggagt ggtgtccatg tgcatcggga 1321 ctggaatggg agσcgctgcc gtctttgaat acσctgggaa ctgagtgagg tcσcaggctg 1381 gaggσgctac gcagacagtc σtgctgctσt agσagσaagg cagtaacacc aσaaaagσaa 1441 aaσcaσatgg gaaaactσag σactggtggt ggtggcagtg gacagatcaa ggcacttcaa 1501 σtσatttgga aaatgtgaaσ aσtgatgaσa tggtatagga gtgggtgggg tgttgagσca 1561 cσcatcagaσ σctctttagc tgtgcaagat aaaagcagcc tgggtσaσcc aggσσacaag 1621 gcσatggtta attcttaagg caaggcaaat ασatggatga gaagtgcaat gggσatagta 1681 aaagtgσatg aattt
SEQ ID NO: 7
GNPI NM_005471 Homo sapiens glucosamine-6-phosphate deaminase 1 (GNPDAl) , mRNA gi I 315428511 ref |NM_005471. | [31542851]
1 cggggacctt cctcgcgggc cggagcgcgg agcgctgccc cagσσσtaσg gcactcgggg 61 tcgggacccc ggggagccgc cctcacacat tttccaggag ggatcggagg ggcgatgggg 121 tggtaatggg ggtgggggac aσgσtgtaσσ ccaccgacga ccgσgcgggc σaccttcgcc 181 tctttccttc aσactcccac taacσgcagt gctgggggaa caaaatgtcc tσcttctgga 241 gcgattacct tttcσctttt gtgctttggg ggaaactgaa gacccagagg ggttcgcaaa 301 gcaagtctgt gaagtaggta ctattgtσcc aatttttaca taggaggaaa σggctcagag 361 agaacttagg tσctttgacc gaggtσσtgσ aggtggaσaa gatgaagσtc atcatσctgg 421 agcaσtattc tcaggσgagσ gagtgggcgg σtaaatacat caggaaccgt atcatccagt 481 ttaacccagg gσcagagaag tacttcaσcc tggggσtσσc caσtgggagt aσαccacttg 541 gσtgσtacaa gaagctgatt gaatactata agaatgggga σσtgtccttt aaatatgtga 601 agaccttcaa catggatgag tacgtgggcσ ttcctσgaga σcacccggag agttaccaσt 661 σσttσatgtg gaacaacttσ ttcaagcaca ttgacatσσa σccagaaaac aσσcaσattc 721 tggatgggaa tgcagtσgaσ σtacaggcag aatgtgatgc ctttgaagag aagatcaagg 781 ctgσaggtgg gatσgagσta tttgttggag gσatcggcσc tgatggacac attgcσttσa 841 aσgagσσagg ctccagtctg gtgtccagga σccgtgtgaa gacgctggcc atggatacca 901 tcσtggσσaa tgctaggttc ttcgatggag aactcaccaa ggtgcccacc atggcσttga 961 σggtgggggt gggσactgtσ atggatgcta gagaggtgat gatcσttatc acaggtgctc 1021 acaaggcatt tgctctgtac aaggσσatσg aggagggagt gaaσσacatg tggaccgtgt 1081 ctgccttcσa gσagcatcσc cgcaccgtgt ttgtgtgtga σgaggatgσσ aσcttggagc 1141 tgaaagtgaa gaσtgtcaag tatttcaaag gtttaatgσt tgttσataaσ aagttggtgg 1201 accccttgta cagtatcaaa gagaaagaaa ctgagaaaag ccaatcttcg aagaaaσcat 1261 acagcgatta gcctgtgctg ggacctagtg tcaagtaccc atagggaaag gcaggtcttt 1321 ctggaaattg tctttagaag aaagaattgt atttσtttaa tctagtatgg ttactccaga 1381 taagtgggtg aacttattgt tcttggccat gaggctggga gσctagtcac ggagtttagc 1441 tatagggaga atgtttgtaa cttaatcaga aaaaaaatat ctgcaaaatg tactccatca 1501 ttctgatgtc tgccaaacσσ aggttgggag ttttaaaσtt tttgttσtgα ttcagccatg 1561 gttcacaσat atgaσaσaσt σccgtcagga atttctctσc ttacacgσaσ tgattttσaa 1621 gtgggaggga attaggggσt tatgtatatt ggataσcacc tcttgagagt ccttcttgca 1681 caggcσtgcc ccttggttga gaacσattgt tαcaagtgaa ggcaσaaact ctcaatatσt 1741 aaaataagtg σaaggaagca gtctotttgg tcagtaacaa gtgcaatgga aagaaaacga 1801 tσσcttcctt cttccacttt cacagctttt ttctgaaσta ggagaaσσtg ggggtggatt 1861 tgggtgggtg gggσσaaaga ggaggσttσt attgataaat σσagagσσtc aaggggcσca 1921 gccaσgtσaa acttctσtσc ctcagggact ctσσagcacc aaaaggσaga aggtggaagσ 1981 cgtttttccc cσagagσcct gtgtttttgt gaaaggcctc aσtgtggσtc ctctgtttta 2041 catactσatt agtaagtggg aggtcσaσtg gggσaaσaga σaσtgccaca atttcagtgt 2101 tgtgttcagc caaggggaσg gtctggacag gcagcttaag tgtgagttta gtcacaaσtσ 2161 ctgagtgtσc cgctctσctg cttacσtagg aggtgagtgσ caggaaaata caccaaatgc 2221 ttctagtatt gtttσcccac ttaaaatagt σctgcttaaa ttcaσatggt gtggtctgat 2281 gttσtgagag σatσaggaaa taσaaσσctt ttgcccattt aσσcttctσσ σcggatccca 2341 aggtggtσtg ttgσtσtggσ ttσctttcat tgtcttaggc cttcatggag tggatgctgσ 2401 ctcσtcctgg ctgtttttgt gcctgtttga agctactgσt gcctσcattt ctgggaaaga 2461 cσtttgagag σσtagσccag gcctaagggc tatgtttggt acσagtattt tgtctttagc 2521 ttttctatgt gattgtgccg tcattctgtt ttaagσtσat ggatσaatgg atttgtttac 2581 aatgtgatat tttctattaa atσσagtatt ttg
SEQ ID NO: 8
DHCR24
NM_014762 Homo sapiens 24-dehydrocholesterol reductase (DHCR24) , mRNA gi 113375617 I ref |NM_014762.11 [13375617]
1 cccgggctgt gggctacagg cgcagagcgg gccaggcgcg gagctggσgg σagtgaσagg 61 aggcgcgaaσ σcgcagcgct taccgσgσgg σgσcgcaσca tggagcccgσ σgtgtσgctg 121 gccgtgtgcg cgctgctctt σctgctgtgg gtgcgcctga aggggctgga gttcgtgctc 181 atccaσσagσ gσtgggtgtt σgtgtgcctc ttσctcctgσ σgσtσtσgσt tatcttcgat 241 atctactact acgtgcgcgc ctgggtggtg ttσaagctca gcagσgσtσσ gcgcctgcaσ 301 gagcagcgαg tgσgggaσat ccagaagσag gtgcgggaat ggaaggagca gggtagσaag 361 aσcttcatgt gcacggggcg cσctggctgg ctcaσtgtct cactacgtgt σgggaagtaσ 421 aagaagacac acaaaaacat catgatcaac ctgatggaca ttctggaagt ggacaσσaag 481 aaaσagattg tcσgtgtgga gcccttggtg accatgggσc aggtgactgα σctgctgacc 541 tccattggct ggactctccc cgtgttgcct gagcttgatg acctcaσagt ggggggσttg 601 atσatgggca caggσatσga gtσatcatcc cacaagtacg gcctgttcca acacatctgc 661 actgcttacg agctggtcct ggctgatggc agctttgtgc gatgcactcσ gtccgaaaac 721 tσagaσσtgt tctatgccgt accctggtcc tgtgggacgc tgggtttcct ggtggσcgct 781 gagatccgca tcatccctgc caagaagtaσ gtcaagctgc gtttcgagσσ agtgcggggc 841 ctggaggcta tctgtgccaa gttcacαcac gagtαccagc ggcaggagaa ccacttcgtg 901 gaagggσtgc tctactcσct ggatgaggct gtcattatga caggggtcat gacagatgag 961 gcagagccca gcaagctgaa tagcattggc aattactaca agccgtggtt σtttaagcat 1021 gtggagaact atctgaagac aaaccgagag ggσσtggagt aσattσαctt gagacactac 1081 tacσaσcgcc acacgcgcag catcttctgg gagctccagg aσatcatccσ ctttggcaac 1141 aaccccatct tccgσtacct ctttggctgg atggtgσctc ccaagatctc σctcctgaag 1201 ctgacccagg gtgagaccct gcgσaagctg tacgagcagσ acσaσgtggt gcaggacatg 1261 ctggtgσσσa tgaagtgcct gcagcaggσc ctgcacacσt tccaaaacga catσcacgtc 1321 tacσcσatct ggctgtgtcc gttcatcctg cccagccagc σaggσσtagt gcaccccaaa 1381 ggaaatgagg cagagctcta catcgacatt ggagcatatg gggagccgσg tgtgaaaσaσ 1441 tttgaagcca ggtcctgcat gaggcagctg gagaagtttg tccgcagcgt gcatggcttσ 1501 σagatgctgt atgcσgactg ctacatgaac cgggaggagt tctgggagat gtttgatggc 1561 tccttgtacc acaagσtgcg agagaagctg ggttgccagg acgccttccc cgaggtgtaσ 1621 gaσaagatct gσaaggσcgc caggcactga gσtggagccσ gσσtggagag acagacacgt 1681 gtgagtggtc aggcatcttc ccttcactca agcttggctg ctttσctaga tccaσaσttt 1741 σaaagagaaa ccσσtccaga actcccacσc tgacagσcca acaccaσctt cctcctggct 1801 tccagggggc agcccagtgg aatggaaaga atgtgggatt tggagtcaga σaagcctgag 1861 tcσagttccc cgtttagaac tσattagctg tgtgactctg ggtgagtασσ ttaacccσtσ 1921 tgagcccggg tctcttcatt agttgaaagg gatagtaata σσtacttgca ggttgttgtc 1981 atctgagttg agcactggtc acattgaagg tgσtgggtaa gtggtagctc ttgttgσttσ 2041 ccgttcagcg tcaσatctgc agtggagσct gaaaaggσtc caσattaggt cacctgtgca 2101 cagccatggc tggaatgatg aaggggatac gctggagttg ccctgccatσ gcctσcatca 2161 gccagacgag gtcσtcacag gagaaggaca gσtcttcccc acσσtgggat σtσaggaggg 2221 cagccacgga gtggggaggc ccσagatgσg ctgtgccaaa gσcaggtccg aggccaaagt 2281 tctccctgcc atccttggtg ccgtcctgcσ ccttcσtσct tcatgσσtgg gσσtgcaggc 2341 ccaccσσagc caccactgag tσσactcgga gtgccctgtg ttσctggaga aggcattcca 2401 gggttgaatc ttgtcccagc ctcagcctgg gacacσtagg tggagagagt ggtσtccgct 2461 ctgaattgga tccaggggaσ ctgggctcat tcttcttggσ tcaccaaccc tgcaggcctc 2521 atctttccca aaacσσaσtt tgtσttggtg ggagtgggtσ cgcgσtgctc tgcagcaggg 2581 gctggggagt ggacagcatσ aggtgggaaa gtggagtσσa σσctcatgtt tσtgtaggat 2641 tσtcaccgtg gggσtggaag aaaagagcat cgaσttgatt tσtσσaacca ctcatccctc 2701 tttttctttc ttccaccact cσccaσccca gctgtagtta atttcagtgc cttacaaatc 2761 ctaagctcag agaaagttcc atttσcgttc σagagggaag ggaaσctccc taggtcσttc 2821 cctggcttgt tataacgσaa agσttggttg tttatgcaac tσtatσttaa gaactgccca 2881 gcctcagctg aaaaσσcgaa tctgagaagg aattgσgtσa tgtaagggaa gctggaatta 2941 agggagctga gccagtcatg gttgtggcgt gtgagtcagg agacctaggt ttcagcσcct 3001 σtctactgtc agσgagσtgt gσaaσgtggg σaagtcattg tcctctgagc tgcagtttcc 3061 tcatctgtca catcgctaca gacaagaσσt ccctggaacσ cttctgattg tcttagacac 3121 tgtggttgca aaacccacgg aaagcσtcat ttgtgtggaa agtcagagga aaaatgatσc 3181 agtggacact tggggattat ctgtcattca agatccttcc ttcaaccσσa aggccagctc 3241 ccatctcatt tccagaaagg ctcatacctg gσttgcaggg aagcatσtgt cttgtcattσ 3301 caggtgccag aatcctctσa gagtcattga agggtgttca cccatccσac cσaaggσttg 3361 gcacaσtgσc agtgtcttag cagggtcttg tgagggctgg gggcatccag gσaσtσagaa 3421 ggcaaaggaa ccaccctacc σatttggσσt σtggaggggg σagaagaaag aaagaaacct 3481 catcctatat tttaσaaagσ atgtgaattσ tggcattagc tctcatagga gacccatgtg 3541 cttcσttgσt cagtgcaaaa ctgatgattc tacttgσtgt agatgaatgg ttaacacgag 3601 ctagttaaac agtgcσattg ttttgccagt gaagσctcca acσσtaagcc actgggacgg 3661 tggσσagaga tgccagσagσ σtctgtcgcc cttagtcata taacσaaaat σσagacctta 3721 tccacaaσcc ggggcttgga aaggaaggta ttttggaatσ aσaσσσtσcg gttatgttgc 3781 tccagtaaaa tcttgcσtgg aaagaggσag tcttcttagσ atggtgagct gagttcatgg 3841 cttttttttg tagσσagtσc tgtccctggc catccatgtg atggttttgg atggagttaa 3901 aσttgatgσc agtgggcagt gσatgtggaa agtatσagag taagcctσtσ σσσtccagag 3961 ccctgagttt cttggctgca tgaaggtttt σtttagaatc agaattgtag ccagtttctt 4021 tggccagaag gatgaatact tggatattac tgaaagggag gggtggagat gggtgtggca 4081 gtgtatggtg tgtgattttt attttcttσt ttggtcatgg gggccaagga gaaaggcatg 4141 aatcttσcct gtcaggctct tacagccaσa ggσaσtgtgt σtactgtctg gaagacatgt 4201 ccccgtggct gtggggccgc tgcttctgtt taaataaaag tggcctgg
SEQ ID NO:9
SELT
BC026350 Homo sapiens selenoprotein T, mRNA (σDNA clone MGC:26803 IMAGE : 4796883) , complete eds gi | 20070974 |gb|BC026350.1 | [20070974]
1 gσtσctgggc tttgggctgg σtgσagtσtg tctgagggcg gcσgaagtgg σtggσtcatt 61 taagatgagg cttσtgσtgσ ttσtcctagt ggcggcgtct gcgatggtcc ggagcgaggσ 121 ctcggccaat ctgggcggcg tgcσcagσaa gagattaaag atgσagtacg cσaσggggσc 181 gctgσtcaag ttccagattt gtgtttσctg aggttatagg cgggtgtttg aggagtacat 241 gcgggttatt agccagcggt acσcagacat σcgcattgaa ggagagaatt acctccctσa 301 aσcaatatat agacaσatag σatctttcct gtσagtcttc aaactagtat taataggctt 361 aataattgtt ggcaaggatc cttttgcttt ctttggcatg caagctccta gcatσtggca 421 gtggggccaa gaaaataagg tttatgcatg tatgatggtt ttcttcttga gcaacatgat 481 tgagaaσcag tgtatgtcaa caggtgσatt tgagataact ttaaatgatg tacctgtgtg 541 gtctaagctg gaatctggtc acσttccatσ σatgσaaσaa cttgttcaaa ttσttgacaa 601 tgaaatgaag σtcaatgtgc atatggattc aatcccaσaσ catcgatcat agcaccacct 661 atcagcaαtg aaaactcttt tgcattaagg gatcattgca agagcagcgt gactgacatt 721 atgaaggcct gtaσtgaaga σagσaagσtg ttagtaσaga cσagatgctt tcttggcagg 781 ctcgttgtac ctcttggaaa acctcaatgc aagatagtgt ttcagtgctg gcatattttg 841 gaattctgca σattcatgga gtgσaataat actgtatagc tttσσccaσσ tccσacaaaa 901 tcaσccagtt aatgtgtgtg tgtgtgtttt ttttaaggta aaσattacta cttgtaactt 961 tttttcttag tcatatttga aaaagtagaa aattgagtta caatttgatt ttttttσcaa 1021 agatgtctgt taaatctgtt gtgcttttat atgaatattt gttttttata gtttaaaatt 1081 gatcσtttgg gaatccagtt gaagttccσa aataσtttat aagagtttat σagacatσtσ 1141 taatttggσσ atgtccagtt tataσagttt acaaaatata gcagatgσaa gattatgggg 1201 gaaatσctat attcagagta ctctataaat ttttgtgtat gtgtgtatgt gσgtgtgatt 1261 aσcagagaac tactaaaaaa accaactgct ttttaaatcc tattgtgtag ttaaagtgtc 1321 atgσσttgac caatctaatg aattgattaa ttaaσtgggσ σtttatactt aactaaataa 1381 aaaactaagc agatatgagt taaatttaaa agtttσaatt tattgctcag tgtacctgtt 1441 aacattatat ttaaσaattg σttaaatttt tgtttttgat ttatggataa tttσttaaga 1501 gtaσaσactt tagatacaca aataatcgtt catttacσat σtttaggatc attgaaactc 1561 atctcactaa agaaagttca cttgaacctσ tttatagσat tgataσtagg tgaacagaaa 1621 ttaσctgact aataatttgt ctaaσatσat atatcagaat tttattgtat atgatgaaca 1681 aaaσttaaaa ttttttaaat ttaattttta aataσtgttt σagagttcta aaaaggcagt 1741 tttttaaaaa acttaagttg ataaaaactg taagaataat ttagσagaaa tagaaσσaga 1801 atgtagaaga gtagtσatgt aacagcagta ataaσatact tcagcttcca tataggaata 1861 gaagtggtag agσσaaaagt gatttaggag aagttataag gtaσaggttg agtatαcctt 1921 ttccaaaaat gcttgggaca agaagtattt cagatttcat aatttttttc aaagtttgga 1981 atatttgcat tatacttaσσ agttgggcat cccaaatctg aaatctgaaa tgttccatga 2041 gcatttcctt tgagtgtσat gttggσactc aaaaaggttσ aacattgagt ccacttaaσa 2101 cttaggtgtt agaagaccta actttctgta acaattaacc ttatactttg tttgtcatcg 2161 aatatttgtt gaatgcatgt caggtaatgg tcttgattgt gatagσttca aggtggaaca 2221 tactgtaatc tccagatgct aggaagttag tctaataatt cactgcagaa aattgattaa 2281 gtggctgtcc ttttaattaa gagtgtggag tcataaaσtt aagttσttca tatagtgaca 2341 agagtcctta gagattgtta ttσaagttcc ttagaaattg ttatttaggt ataatatcat 2401 cttgtctttg actagagσtt gaaaccttgt tatctgattg tgtaccactc caaattσσct 2461 gcσttσtgσa agttgaatgt σttgctgaat gtgtctaggg gttcatσttc agtaatcgaσ 2521 attσσactag tgcσatagtt aaσttcatga catgtagaσa ttσaaaaσtt gagccttgga 2581 tgttcctgtg gaσσtgacag ttaaaaatat aaagaaccta ggattσaatt ccaactttct 2641 ctgtttgcct tgggttgaat aacttatctt ttggagaata gctttaagtg gσttagaσaσ 2701 tgataaaatt cagctgtgtt gttgacgctc atctcttttg tσttaσgσtt agσσatattt 2761 aaatσttgaa tttaatagag tctagtgaaa aaaatgagtg ggaagaatga atataaaagt 2821 aataatataa ggaaaaaggg aagtaaacta tttagaatgt agttttgtta tattσccagc 2881 atttcaatat ttattagtta cttgtaaatt aσtgtggσtg tgtagtttat aaatgtσtgt 2941 gcactatatt aattagaaga ccatagaaca tgccagσagg ttggctaatg ctatgggggt 3001 ttttaccaca gttgσcattg tggaagaaat tatttggtac attaataaaa aaagttggta 3061 aaacatggtt ttatacctca gtgtataaga tgtgσaagaα aaatatgctt atttcctttt 3121 ctagaatata agtgatatta tttgcttatg acaσtaaσaσ tattaatgaσ aggagtσaat 3181 cagcctttaσ agctatcaaa atataatgag atcccaatga tgattσtttt ttaσtttgaa 3241 tgttaattag tttgggactt tgattggctg gσaaaσattt tatσattgtσ agaatttaat 3301 ttagatttca aaaatagctt acaggatttt aaacatggtg tggtattcta aagcσttttt 3361 tttaaaaaaa gagatσtttt tgagagaaaσ aaatgaggat tgtaaagttt ggggacttac 3421 ctctgtagca ttgtgaaaat aaactttgat taagcaaaaa aaaaaaaaaa a
SEQ ID NO: 10
SELT
NM_016275 Homo sapiens selenoprotein T (SELT) , mRNA gi I 7706470 I ref |NM_016275.11 [7706470] 1 tgcagtctgt σtgagggσgg σσgaagtggσ tggctcattt aagatgaggσ ttctgctgct 61 tctcctagtg gcggcgtctg cgatggtσcg gagσgaggσc tσggσσaatc tgggcggcgt 121 gccagcaaga gattaaagat gσagtaσgcc acggggcσgc tgσtσaagtt σcagatttgt 181 gtttcctgag gttataggcg ggtgtttgag gagtaσatgc gggttattag σcagcggtac 241 ccagacatcc gcattgaagg agagaattaσ σtccctcaac σaatatatag aσacatagca 301 tctttcctgt cagtcttσaa actagtatta ataggcttaa taattgttgg σaaggatσσt 361 tttgσtttct ttggcatgca agctσαtagσ atσtggσagt ggggσcaaga aaataaggtt 421 tatgcatgta tgatggtttt cttcttgagc aacatgattg agaaσcagtg tatgtcaaσa 481 ggtgσatttg agataacttt aaatgatgta σσtgtgtggt ctaagctgga atctggtσac 541 cttccatσca tgcaacaact tgttcaaatt cttgaσaatg aaatgaagct caatgtgcat 601 atggattcaa tcccacacca tσgatcatag caσσaσctat cagcactgaa aactcttttg 661 cattaaggga tcattgcaag agcagcgtga ctgacattat gaaggcctgt aσtgaagaσa 721 gσaagctgtt agtacagacc agatgctttc ttggcaggct cgttgtacct cttggaaaac 781 ctcaatgcaa gatagtgttt cagtgctggc atattttgga attσtgcaca ttσatggagt 841 gσaataataσ tgtatagσtt tσσσσcacct cccaσaaaat caccσagtta atgtgtgtgt 901 gtgtgttttt tttaaggtaa acattactac ttgtaacttt ttttctttag tcatatttgg 961 aaaaagtaga aaattggagt tacatttgga ttttttttσσ aa SEQ ID NO: 11
PTPRB
NM_002837 Homo sapiens protein tyrosine phosphatase, reσeptor type, B (PTPRB) , mRNA gi 118491009 I ref |NM_002837.2 | [18491009]
1 gtσtσctctg gatcttaact aσtgagσgσa atgσtgagσσ atggagσcgg gttggcσttg 61 tggatcacac tgagσctgct gcagaσtgga σtggcggagc cagagagatg taacttcacc 121 ctggcggagt ccaaggcctσ σagccattct gtgtσtatcc agtggagaat tttgggctca 181 ccσtgtaact ttagcσtσat σtatagσagt gacaccctgg gggccgcgtt gtgccctaσc 241 tttcggatag aσaaσaccac atacggatgt aaσσttσaag atttaσaagσ aggaaσαatσ 301 tataacttca agattatttc tσtggatgaa gagagaactg tggtcttgαa aaσagatσσt 361 ttaσσtσctg ctaggtttgg agtcagtaaa gagaagacga cttσaaccgg cttgcatgtt 421 tggtggactc σttcttccgg aaaagtcaσc tcatatgagg tgcaattatt tgatgaaaat 481 aaσcaaaaga tacagggggt tσaaattcaa gaaagtactt catggaatga atacaσtttt 541 ttcaatctca ctgσtggtag taaataσaat attgσσatca cagσtgtttσ tggaggaaaa 601 cgttcttttt σagtttatac caatggatca acagtgcσat σtccagtgaa agatattggt 661 atttccacaa aagcσaattσ tctαctgatt tcctggtσcc atggttctgg gaatgtggaa 721 cgataccggc tgatgσtaat ggataaaggg atσσtagttc atggcggtgt tgtggacaaa 781 catgctaσtt σctatgcttt tcacgggctg tcccctggσt acctσtacaa cσtcaσtgtt 841 atgaσtgagg σtgσagggσt gσaaaaσtac aggtggaaac tagtcaggac agccccσatg 901 gaagtσtσaa atctgaaggt gacaaatgat ggcagtttga σctctσtaaa agtcaaatgg 961 σaaagacctσ σtggaaatgt ggattcttac aatatσaσσc tgtctσacaa agggaσcatc 1021 aaggaatσca gagtattagc accttggatt actgaaactc actttaaaga gttagtcccc 1081 ggtcgacttt atcaagttac tgtcagctgt gtctctggtg aactgtσtgc tcagaagatg 1141 gcagtgggca gaacatttcc agacaaagtt gcaaacctgg aggσaaacaa taatggcagg 1201 atgaggtctσ ttgtagtgag σtggtcgccc cctgctggag actgggagσa gtatcggatc 1261 ctactcttca atgattctgt ggtgσtgctc aaσatσaσtg tgggaaagga agaaaσacag 1321 tatgtcatgg atgaσaσggg gσtcgtaccg ggaagacagt atgaggtgga agtcattgtt 1381 gagagtggaa atttgaagaa ttctgagcgt tgccaaggσa ggaσagtσσσ σσtggσtgtc 1441 ctccagcttc gtgtcaaaca tgccaatgaa acctcactga gtatσatgtg gσagacccσt 1501 gtagcagaat gggagaaata catcatttcc σtagctgaca gagaσσtσtt aσtgatcσac 1561 aagtcactct cσaaagatgc caaagaattc acttttactg acctggtgσσ tggaσgaaaa 1621 taσatggcta cagtcacσag tattagtgga gaσttaaaaa attcctcttc agtaaaagga 1681 agaaσagtgσ σtgcccaagt gactgacttg catgtggcσa aσσaaggaat gaσcagtagt 1741 ctgtttaαta aσtggaσσσa ggσaσaagga gacgtagaat tttaccaagt cttactgatc 1801 catgaaaatg tggtσattaa aaatgaaagc atctccagtg agaccagσag ataσagcttc 1861 caσtσtσtσa agtσcggcag σctgtaσtcc gtggtggtaa σaacagtgag tggagggatc 1921 tcttcσσgac aagtggttgt ggagggaaga acagtccctt ccagtgtgag tggagtaaσg 1981 gtgaaσaatt σcggtcgtaa tgactacσtσ agσgtttσct ggctgσtggc gcσσggagat 2041 gtggataact atgaggtaac attgtσtcat gacggcaagg tggttcagtσ σσttgtσatt 2101 gccaagtctg tσagagaatg ttccttσagσ tσσσtσaσcc caggccgcσt ctacaσσgtg 2161 accataacta caaggagtgg caagtatgaa aatσaσtcct tσagccaaga gσggacagtg 2221 cctgaσaaag tσcagggagt σagtgttagσ aaσtcagcca ggagtgacta tttaagggta 2281 tcctgggtgc atgccactgg agactttgat cactatgaag tcaccattaa aaacaaaaaσ 2341 aacttcattc aaactaaaag cattσσσaag tcagaaaacg aatgtgtatt tgttcagcta 2401 gtccctggac ggttgtaσag tgtcactgtt actacaaaaa gtggacaata tgaagccaat 2461 gaacaaggga atgggagaac aattcσagag cctgttaagg atctaaσatt gcgcaacagg 2521 agσactgagg acttgcatgt gacttggtca ggagctaatg gggatgtcga ccaatatgag 2581 atccagctgc tcttcaatga σatgaaagta tttcctcctt ttcaccttgt aaataσσgca 2641 accgagtatc gatttacttc cctaaσaσca ggcσgccaat acaaaattct tgtcttgacg 2701 attagσgggg atgtaσagσa gtcagccttc attgagggct tσaσagttσc tagtgctgtc 2761 aaaaatattc acatttctcσ σaatggagσa acagatagcc tgacggtgaa ctggactσσt 2821 ggtgggggag aσgttgattc ctaσaσggtg tcggcattca ggcacagtσa aaaggttgaσ 2881 tσtcagacta ttcccaagσa σgtσtttgag σacacgttcc acagactgga ggσcggggag 2941 cagtacσaga tcatgattgc σtcagtcagc gggtccctga agaatσagat aaatgtggtt 3001 gggσggacag ttccagcatc tgtσσaagga gtaattgσag acaatgcata σagcagttat 3061 tccttaatag taagttggca aaaagctgct ggtgtggcag aaagatatga tatcσtgσtt 3121 ctaaσtgaaa atggaatσσt tσtgσgσaac acatcagagc σagσcaccaσ taagcaacaσ 3181 aaatttgaag atσtaacacc aggσaagaaa taσaagataσ agatcσtaaσ tgtcagtgga 3241 ggcctcttta gcaaggaagc ccagactgaa ggcσgaaσag tσcσagσagα tgtcaσσgac -3301 ctgaggatca cagagaaσtc caccaggcaσ σtgtccttcc gctggaccgσ σtcagagggg 3361 gagctσagct ggtacaacat ctttttgtaσ aaσσcagatg ggaatctcca ggagagagσt 3421 caagttgacc cactagtcca gagcttctct ttcσagaact tgctacaagg σagaatgtaσ 3481 aagatggtga ttgtaactca cagtggggag ctgtctaatg agtctttcat atttggtaga 3541 acagtσσcag cσtσtgtgag tσatσtσagg gggtσcaatc ggaacacgac agacagcctt 3601 tggttσaact ggagtccagc σtσtggggaσ tttgaσtttt atgagσtgat tctctataat 3661 ccσaatggca caaagaagga aaactggaaa gacaaggacc tgacggagtg gcggtttcaa 3721 ggccttgttσ σtggaaggaa gtacgtgctg tgggtggtaa ctcaσagtgg agatctcagc 3781 aataaagtca cagσggagag σagaacagct ccaagtcctc ccagtcttat gtcatttgct 3841 gacattgcaa acaσatcctt ggccatcaσg tggaaagggc ccασagactg gacagactac 3901 aaσgaσtttg agσtgσagtg gttgσccaga gatgcactta ctgtσttcaa cσσσtacaac 3961 aaσagaaaat cagaaggacg cattgtgtat ggtcttcgtc cagggagatc σtatcaattc 4021 aaσgtσaaga σtgtσagtgg tgattcctgg aaaacttaca gσaaaccaat ttttggatct 4081 gtgaggacaa agcσtgacaa gatacaaaac ctgcattgcc ggcctσagaa ctccaσggσc 4141 attgcctgtt σttggatccc tcctgattct gaσtttgatg gttatagtat tgaatgccgg 4201 aaaatggaca cccaagaagt tgagttttcc agaaagσtgg agaaagaaaa atctctgctc 4261 aacatcatga tgσtagtgσc σσataagagg tacσtggtgt ccatσaaagt gσagtσggσc 4321 ggcatgacca gcgaggtggt tgaagacagσ actatcacaa tgatagaccg σccσcctσσt 4381 σcacccccac acattcgtgt gaatgaaaag gatgtgctaa ttagcaagtc ttccatcaac 4441 tttactgtσa aσtgcagctg gttcagσgaσ accaatggag ctgtgaaata cttσaσagtg 4501 gtggtgagag aggσtgatgg σagtgatgag ctgaagcσag aaσagαagca ccσtσtccct 4561 tcctacctgg agtacaggca caatgσσtcc attcgggtgt atcagactaa ttattttgcc 4621 agcaaatgtg ccgaaaatcc taacagcaaσ tccaagagtt ttaaσattaa gσttggagσa 4681 gagatggaga gσttaggtgg aaaaσgσgat , cccactcagσ aaaaattσtg tgatggaασa 4741 σtgaagccac acaσtgσcta cagaatcagσ attσgagσtt ttaσaαagct ctttgatgag 4801 gacσtgaagg aattcaσaaa gσσaσtctat tcagacaσat ttttttcttt acσcatcaσt 4861 actgaatcag agcccttgtt tggagσtatt gaaggtgtga gtgctggtct gtttttaatt 4921 ggcatgctag tggctgttgt tgcσttattg atσtgσagaσ agaaagtgag σσatggtcga 4981 gaaagaccct ctgcccgtct gagσattσgt agggatσgaσ σattatctgt ccacttaaac 5041 ctgggσcaga aaggtaacσg gaaaacttct tgtcσaataa aaataaatσa gtttgaaggg 5101 σatttσatga agctacaggc tgaσtσcaac taσcttctat ccaaggaata σgaggagtta 5161 aaagacgtgg gccgaaacca gtσatgtgac attgσaσtσt tgccggagaa tagagggaaa 5221 aatσgataσa acaatatatt gcσctatgat gccacgcgag tgaagctctc caatgtagat 5281 gatgatcctt gctctgacta catσaatgcc agctaσatσσ σtggσaaσaa σttσagaaga 5341 gaataσattg tcactcaggg accgcttcct ggcaccaagg atgacttσtg gaaaatggtg 5401 tgggaacaaa acgttcacaa catcgtcatg gtgaccσagt gtgttgagaa gggccgagta 5461 aagtgtgacc attactggcc agcggaccag gattccσtct actatgggga cctcatσσtg 5521 cagatgctσt σagagtccgt cctgcctgag tggacσatσσ gggagtttaa gatatgσggt 5581 gaggaaσagc ttgatgcaσa σagactcatc σgσαaσtttσ aσtatacggt gtggccagac 5641 σatggagtσc cagaaaccac ccagtσtσtg atσσagtttg tgagaaσtgt σagggactac 5701 atcaaσagaa gσccgggtgσ tgggcccact gtggtgσaσt gσagtgσtgg tgtgggtagg 5761 actggaacσt ttattgσatt ggaσcgaatc ctσcagcagt tagactcσaa agactctgtg 5821 gacatttatg gagcagtgca cgacctaaga cttcacaggg ttcacatggt σcagactgag 5881 tgtcagtatg tctacctaσa tσagtgtgta agagatgtcc tσagagσaag aaagctacgg 5941 agtgaacaag aaaaσccctt gtttccaatc tatgaaaatg tgaatccaga gtatcacaga 6001 gatccagtct attcaaggca ttgagaatgt aσσtgaagag σtσctggata aaaattattc 6061 aσtgtgtgat ttgtttttaa aaacttgctt σatgccctac agaggtgcca gctatttctg 6121 ttgatactat gtataattta ttaatctgga gaatgtttaa aattttatat aatttaaagg 6181 taacagatat tattgtacat agttgtattt tgtagtttct tctgtaaata tgtatttttσ 6241 ataatgttta atattaagct ttatataata ctatttttσσ aσaσtaaagt gttσatgaσt 6301 tgttσtacat aaaactaatt σaaσctgtaa a
SEQ ID NO-.12
GBA
NM_000157 Homo sapiens glucosidase, beta; acid (includes glucosylσeramidase) (GBA), mRNA gi I 4503934 I ref |NM_000157.11 [4503934]
1 gσtaacctag tgcctatagc taaggcaggt acctgcatcσ ttgtttttgt ttagtggatσ 61 ctctatcctt cagagactct ggaaσccctg tggtcttctc ttcatctaat gacασtgagg 121 ggatggagtt ttσaagtσαt tσcagagagg aatgtσccaa gσctttgagt agggtaagca 181 tσatggctgg cagcctcaca ggtttgcttc tacttcaggc agtgtcgtgg gcatαaggtg 241 ccσgσccctg catccctaaa agcttcggct acagctcggt ggtgtgtgtc tgcaatgcσa 301 catactgtga ctcctttgac σcccσgacct ttcctgccct tggtaccttσ agσcgctatg 361 agagtacacg cagtgggcga σggatggagc tgagtatggg gcccatσcag gctaatcaσa 421 cgggcacagg cctgctactg accctgσagc cagaacagaa gttσcagaaa gtgaagggat 481 ttggaggggc catgacagat gctgctgctc tcaaσatcct tgσcctgtca cccσctgcσσ 541 aaaatttgct acttaaatcg tacttctctg aagaaggaat σggatataaσ atσatσcggg 601 tacαcatggc cagctgtgac ttctσcatcc gcacctaσaσ αtatgcagac aσσσctgatg 661 atttccagtt gcacaacttc agcctcσcag aggaagatac caagσtcaag atacccctga 721 ttcaccgagσ σσtgσagttg gcccagcgtc ccgtttcaσt σcttgccagσ ccctggaσat 781 σaσccaσttg gctcaagacc aatggagcgg tgaatgggaa ggggtcactσ aagggaσagσ 841 σcggagacat ctaccaccag acctgggcca gatactttgt gaagttcσtg gatgσctatg 901 ctgagcacaa gttacagttc tgggcagtga cagctgaaaa tgagccttct gctgggσtgt 961 tgagtggata ccccttccag tgσctgggct tcacccctga aσatσagσga gaσttσattg 1021 cccgtgacct aggtcσtaσc ctcgccaaca gtactcaσσa σaatgtccgσ ctactcatgc 1081 tggatgacca acgcttgσtg ctgccccaσt gggcaaaggt ggtactgaca gacccagaag 1141 cagσtaaata tgttσatggc attgctgtac attggtacσt ggaσtttctg gctσcagcσa 1201 aagccaσσct aggggagaca σaccgcctgt tccσσaacac σatgctcttt gcctσagagg 1261 cctgtgtggg ctσσaagttc tgggagcaga gtgtgcggσt aggσtσσtgg gatαgaggga 1321 tgσagtaσag c-cacagcatc atσaσgaaσc tcctgtaσσa tgtggtσggσ tggaαcgact 1381 ggaaσcttgσ cctgaaccσσ gaaggaggac ccaattgggt gcgtaacttt gtσgaσagtc 1441 σcatcattgt agaσatcaσσ aaggaσacgt tttacaaaca gccσatgttσ taσσaccttg 1501 gccacttσag caagttcatt cctgagggαt σαcagagagt ggggctggtt gcσagtσaga 1561 agaacgacct ggacgσagtg gcactgatgc atcσcgatgg ctctgσtgtt gtggtσgtgc 1621 taaaccgctα σtσtaaggat gtgcctctta ccatcaagga tcctgσtgtg ggσttσctgg 1681 agacaatσtc acσtggctac tcσattcaca cctacσtgtg gcatcgccag tgatggagca 1741 gataαtσaag gaggσactgg gσtcagcctg ggcattaaag ggaσagagtσ agσtcacaσg 1801 ctgtctgtga ctaaagaggg cacagcaggg ccagtgtgag cttacagcga cgtaagσcca 1861 ggggσaatgg tttgggtgac tσactttcσσ ctctaggtgg tgcccagggc tggaggcccσ 1921 tagaaaaaga tσagtaagcc ccagtgtccc σccagccccc atgcttatgt gaacatgcgc 1981 tgtgtgσtgσ ttgσtttgga aaσtngcctg ggtcσaggσc tagggtgagc tcactgtccg 2041 tacaaacaσa agatσagggσ tgagggtaag gaaaagaaga gaσtaggaaa gctgggccca 2101 aaactggaga σtgtttgtct ttcσtagaga tgσagaaσtg ggcccgtgga gcagcagtgt 2161 cagcatσagg gσggaagσct taaagcagσa gcgggtgtgc ccaggσaccc agatgattcc 2221 tatggcacca gσcaggaaaa atggcagctσ ttaaaggaga aaatgtttga gccca
SEQ ID NO: 13
UAPl
NM_003115 Homo sapiens UDP-N-aσteylgluσosamine pyrophosphorylase 1 (UAPl) , mRNA gi I 34147515 I ref |NM_003115.3 | [34147515] 1 σtgtgσtσcc ggcgctgaσg tgtctgggcg gtcggcttcc aσtccttcag gcgtcggcag 61 ccaσtagtcg tggcgagagg ggcggggtgg ccggggctgg cgσtσσaσtt ggσσccσgσt 121 σccggcccgc σσcgcσgσσg σggcccσσcg gatgagggta tatattcgga gcgagcgcgg 181 gacgccgatg agtggccgσg cggaaggagc tggagacggt cgtagctgcg gtcgcgccga 241 gaaaggttta caggtacata σattaαaσcc ctatttctac aaagcttggc tattagagσa 301 ttatgaacat taatgacαtc aaactcacgt tgtccaaagc tgggcaagag σaσσtaσtaσ 361 gtttσtggaa tgagcttgaa gaagcccaac aggtagaaσt ttatgσagag σtσσaggσca 421 tgaactttga ggagσtgaaσ ttctttttcc aaaaggccat tgaaggtttt aaccagtctt 481 cttaσσaaaa gaatgtggat gσacgaatgg aacctgtgσc tcgagaggta ttaggσagtg 541 σtaσaaggga tσaagatσag σtαcaggcct gggaaagtga aggacttttc σagatttσtc 601 agaataaagt agcagttctt cttctagctg gtgggcaggg gaσaagactc ggcgttgσat 661 atσctaaggg gatgtatgat gttggtttgc catcccgtaa gaαaσttttt cagattcaag 721 cagagσgtat σσtgaagσta σagσaggttg σtgaaaaata ttatggcaac aaatgcatta 781 ttcσatggta tataatgaσc agtggσagaa caatggaatc tacaaaggag ttσttσaσca 841 agcacaagta ctttggttta aaaaaagaga atgtaatctt ttttσagσaa ggaatgctcc 901 ccgccatgag ttttgatggg aaaattattt tggaagagaa gaacaaagtt tctatggctc 961 cagatgggaa tggtggtctt tatcgggcac ttgσagccca gaatattgtg gaggatatgg 1021 agcaaagagg σatttggagσ attcatgtct attgtgttga caacatatta gtaaaagtgg 1081 cagaccσaσg gttσattgga ttttgσattσ agaaaggagσ agaσtgtgga gσaaaggtgg 1141 tagagaaaaσ gaaccctaca gaaccagttg gagtggtttg ccgagtggat ggagtttaσc 1201 aggtggtaga atatagtgag atttσσctgg caacagσtca aaaacgaagα tcagacggac 1261 gaσtgσtgtt σaatgσgggg aaσattgcca aσcatttctt cactgtaσca tttctgagag 1321 atgttgtcaa tgtttatgaa cctσagttgσ agcacσatgt ggctσaaaag aagattcctt 1381 atgtggatac cσaaggacag ttaattaagc cagaσaaaσσ σaatggaata aagatggaaa 1441 aatttgtctt tgacatσttσ cagtttgcaa agaagtttgt ggtatatgaa gtattgcgag 1501 aagatgagtt ttccccacta aagaatgctg atagtcagaa tgggaaagac aaσσctacta 1561 ctgcaaggσa tgσtttgatg tσccttσatc attgctgggt αctcaatgca gggggccatt 1621 tσatagatga aaatggctct cgccttσcag caattσccσg cttgaaggat gccaatgatg 1681 taccaatcca atgtgaaatσ tσtσctctta tσtσσtatgc tggagaagga ttagaaagtt 1741 atgtggcaga taaagaattσ σatgcacctc taatcatσga tgagaatgga gttcatgagc 1801 tggtgaaaaa tggtatttga aσcagatacc aagttttgtt tgσcacgata ggaatagctt 1861 ttatttttga tagaccaaσt , gtgaacctac aagacgtctt ggacaaσtga agtttaaata 1921 tσcacagggt tttattttgc ttgttgaact cttagagcta ttgcaaactt cccaagatcc 1981 agatgaσtga atttcagata gcatttttat gattσσcaac tσattgaagg tσttatttat 2041 ataatttttt σcaagccaag gagaccattg gccatcσagg aaatttcgta cagctgaaat 2101 ataggcagga tgttcaacat cagtttactt gcagσtggaa gσatttgttt ttgaagttgt 2161 acatagtaat aatatgtcat tgtacatgtt gaaaggtttc tatggtacta aaagtttgtt 2221 ttattttatc aaaσattaag σttttttaag aaaataattg ggσagtgaaa taaatgtatc 2281 ttcttgtctc tggaaaaaaa aaaaaaaaaa aaaaaaaaaa aaa
SEQ ID NO: 14 MRPL30
NM_145212.l| Homo sapiens mitochondrial ribosomal protein L30 (MRPL30) , nuclear gene encoding mitochondrial protein, transcript variant 1, mRNA
1 gccggaaσaa aaatgσctca gtttggaggt cgcgctcact gcgacggcag gctttgagtg 61 tagcaσttgg tagttσttσc tctgctσtgc ttcccttcgg aggaaaattt caggctgaag 121 gtttagcggg tgcσgσσtσt aaagagagσa atcactacaσ ttatggσtgg gattttgσgα 181 ttagtagttc aatggcσσcc aggcagacta cagactgtga caaaaggtgt ggagtctσtt 241 atttgtaσag attggattσg tcacaaattc accagatcaa gaattccaga aaaagtgttt 301 caggσσtσac ctgaagatσa tgaaaaatac ggtggggatc caσagaaσσσ tcataaactg 361 σatattgtta ccagaataaa aagtaσaaga agacgtccat attgggaaaa agatataata 421 aagatgσttg gattagaaaa agcacatacc cctcaagttc acaagaatat cccttσagtg 481 aatgσaaaat tgaaagtagt taagσatttg ataagaatca agcccttgaa gttgcσaσaa 541 ggaσttccag cagaggagaa σatgtσtaac acgtgcctca aaagcaσtgg ggagttagta 601 gtgcagtggc atctgaaacc tgtggagcag aaagσaσatg agtσctaatg ccccagcagc 661 ttccgattgg aaaatgcaaa ttgtttttat ttaaagatgg tgagaaagtg ttttcattaa 721 aatatgtttt σaaaaccatt ttcaggccgg gcacggtggc tσacctgtaa tccσagcact 781 ttgggaggcc aaggσgggσa gatcacctga ggtσaagagt tcgagaccag cctgaσcaac 841 atggagaaac σσσcatctct aσtgaaaata σagaattagc caggcatggt ggcacatgcc 901 tgtaacccag ctactcggga ggctgaagσa ggagaatσac ttgaaσoσgg gaggσagagg 961 ttgcagtgag ctgagatggt gccactgtac tcσagcctgg gtgataggat gagactccat 1021 ctcaggggaa aaaaaaaaaa tttttttttc actgactaaa cσtgσtgσag σtσtctttta 1081 ctacagactt ggagatttta gtttaatttg gtttaattσt σtgtσσtttσ αctttcactg 1141 tttcactcca aaacatgtaa gaatggcaat gtttgaacat σtgcgtttgg gtctaσtgcc 1201 accttagcaa gσctcattaa cσattttata aaaattgcgt tagtattgtt gttgttgttt 1261 ttgagacagg gtcttgctct gtcaσσcaag ctggaataca gtggcatgat ttσagttσac 1321 tgcagcctcg acctσccagg ctcaagtgat cσtccσaσct cagcctccag agtagctagg 1381 actacaggσa gtgtgσσaσσ acatccagct aattttttaa agttttttca tagagaσagg 1441 gactcactat gttgtcσaag σtggtctcaa aσtcctgggt tσaagccatσ ctcσσacctσ 1501 agσctcccaa aatgctggga ttacaggcat gagccactgt acccagσσaa aattgttttσ 1561 ttttttaagt gaattσaaσa atttctgtga gtggσtcttt gcatgaacac tgtgcaaggt 1621 gttggagaaa tccaaagctg accaaaacat ggtccccacσ ttttggagσt tacagtctgt 1681 tσtggggaac agagattcag cσaaagtσaa gaaaσaσtgg atgσσagσta gattatσtgt 1741 tctgtgcttt ggtgtctata agtacatatg tggatatggg ttcattttat σσσtaaactt 1801 agtacσaaac cagcatttaa tatσtaatta taaatctaat ttggcctaaa σtttattatt 1861 gcaσactgcc tgaacaaaaσ σtatttgtct ctatgtaaat tttttcσtσa tggaacaagg 1921 gtgtgaaatg aaaatatttt aggatttatt caaaaacaga σtattσtgtt ttσagcttca 1981 gaattgttσt ttgaatccta aggaacσtσt gtσaacagtt gaggttgctg ttgaaaagaa 2041 agaagaagga ggcggaaatc tctcagggag aattatttcc tttcttttσt attttagata 2101 cctggagggg tggggagaag taagaattgt aagggaggtt cagtagtggg gaattσtgtg 2161 acagctgatt gaagatgatg atgaagaaσc tctgcattσt agttaσcctt tgcttccctt 2221 cacσtcttgt aaaatttggc ttggσaaσaa tgacattgtc atgσttattg tcccaatatc 2281 catcctgtcg tagatσttaa tgtttttgat σgttgcgtta aagtggaagt gccacccaca 2341 gtgaaaccag atσσcattaa taaataagct taaaggcgaa aaaaaaaaaa aaaaaaaaaa 2401 aaaaaaaa
SEQ ID NO:15
MRPL30
NM_016503 Homo sapiens mitoσhondrial ribosomal protein L30 (MRPL30) , nuσlear gene encoding mitochondrial protein, transcript variant 2, mRNA gi I 217356011 ref |NM_016503.2 | [21735601]
1 gcσggaaσaa aaatgσctca gtttggaggt cgcgctσact gcgaσggcag gctttgagtg 61 tagσaσttgg tagttσttcc tctgctctgc ttccσttσgg aggaaaattt caggctgaag 121 gtttagcggg tgσσgσσtσt aaagagagσa atcactaσaσ ttatggσtgg gattttgσgσ 181 ttagtagttσ aatggσccσc aggcagacta cagaσtgtga caaaaggtgt ggagtctσtt 241 atttgtaσag attggattσg tcacaaattc aσcagatcaa gaattccaga aaaagtgttt 301 σaggσctcac ctgaagatca tgaaaaatac ggtggggatc cacagaaσσσ tσataaaσtg 361 σatattgtta ccagaataaa aagtacaaga agacgtcσat attgggaaaa agatataata 421 aagatgcttg gattagaaaa agcacatacc σσtcaagttc acaagaatat cccttcagtg 481 aatgcaaaat tgaaagtagt taagcatttg ataaggtttg ttgtttcttc tcagctcttt 541 ttaaaatgta ttgcctagtg taattctaaa tgcatttttc ttttttcgtt aatgttctga 601 aaaaaacttt ttaaaaaaσt aaaaaaaaaa aaaaaaaaaa aaaaaaaaa
SEQ ID NO: 16
CCT3 AL833197.1|HSM804508 Homo sapiens mRNA; σDNA DKFZp667A196 (from clone DKFZp667A196) (Chaperonin, containing TCP-1, HSP60)
1 agcgttttct gggcttσtgt σtggttσtct ctctcσagaa ggttσtgσcg gttcccccag 61 σtctgggtac ccggctctgc atσgσgtcgc catgatgggc catcgtccag tgσtσgtgct 121 cagcσagaaσ acaaagcgtg aatσσggaag aaaagttcaa tctggaaaca tcaatgctgc 181 caagactatt gcagatatca tccgaaσatg tttgggaσcc aagtccatga tgaagatgσt 241 tttggaσcca atgggaggσa ttgtgatgaσ caatgatggc aatgccattc ttcgagagat 301 tcaagtccag catccagcgg cσaagtccat gatcgaaatt agccggaccσ aggatgaaga 361 ggttggagat gggaccacat cagtaattat tcttgσaggg gaaatgσtgt σtgtagσtga 421 gcacttcctg gagcagcaga tgcacccaac agtggtgatc agtgcttacc gσaaggσatt 481 ggatgatatg atσagcaccc taaagaaaat aagtatccca gtcgacatca gtgacagtga 541 tatgatgσtg aaσatσatσa acagctctat taσtaσcaaa gcσatcagtc ggtggtσatσ 601 tttggcttgc aacattgccc tggatgctgt caagatggta cagtttgagg agaatggtσg 661 gaaagagatt gaσataaaaa aatatgσaag agtggaaaag ataσctggag gcatσattga 721 agactcctgt gtcttgcgtg gagtcatgat taacaaggat gtgacccatσ σacgtatgcg 781 gσgσtatatσ aagaaccctc gcattgtgct gctggattct tctctggaat acaagaaagg 841 agaaagcσag actgacattg agattaαacg agaggaggac ttcacccgaa ttctccagat 901 ggaggaagag tacatccagσ agctctgtga ggacattatc caaσtgaagσ αcgatgtggt 961 catcaσtgaa aagggcatct cagatttagc tcagcactac cttatgcggg σσaatatcac 1021 agccatccgσ agagtσcgga agacagacaa taatcgσatt gctagagcct gtggggσccg 1081 gatagtcagc cgaccagagg aactgagaga agatgatgtt ggaacaggag caggσctgtt 1141 ggaaatcaag aaaattggag atgaatactt tactttσatσ aσtgaσtgca aagacσσσaa 1201 ggσctgcacσ attctcctcc ggggggctag caaagagatt ctctσggaag tagaaσgcaa 1261 cctccaggat gσσatgcaag tgtgtcgcaa tgttctcσtg gaccσtσagc tggtgcσagg 1321 gggtggggσσ tσσgagatgg ctgtggccca tgccttgaσa gaaaaatcσa aggccatgac 1381 tggtgtggaa caatggccat acagggctgt tgcccaggcc ctagaggtσa ttcctσgtaσ 1441 cctgatcσag aaσtgtgggg σσagσaαcat ccgtctaσtt acctcσσttσ gggccaagσa 1501 cacccaggag aactgtgaga cctggggtgt aaatggtgag acgggtactt tggtggacat 1561 gaaggaactg ggcatatggg agccattggσ tgtgaagσtg σagaσttata agacagcagt 1621 ggagaσggca gttσtgctac tgcgaattga tgacatcgtt tσaggσcaca aaaagaaagg 1681 cgatgaσcag agccggcaag gcggggσtσc tgatgctggσ σaggagtgag tgctaggcaa 1741 ggctaσttca atgσacagaa ccagcagagt σtcccctttt σσtgagαcag agtgccagga 1801 aσaσtgtgga σgtctttgtt cagaagggat caggttgggg ggcagcccσσ agtccσtttσ 1861 tgtσccagct cagttttcca aaagacactg acatgtaatt σttσtctatt gtaaggtttc 1921 catttagttt gσttσcgatg attaaatσta agtcattcaa aaaaaaaaaa aaaaa
SEQ ID NO: 17
CCT3
NM_005998 Homo sapiens chaperonin containing TCPl, subunit 3 (gamma) (CCT3) , mRNA gi I 315422911 ref |NM_005998.2 | [31542291] 1 gtctggttct ctctctccag aaggttσtgσ cggttccccc agctctgggt accσggctct 61 gσatcgcgtc gccatgatgg gccatcgtσσ agtgctcgtg σtαagccaga acacaaagcg 121 tgaatcσgga agaaaagttσ aatctggaaa catσaatgct gccaagacta ttgcagatat 181 catccgaaca tgtttgggac ccaagtccat gatgaagatg cttttggaσσ σaatgggagg 241 σattgtgatg aσcaatgatg gcaatgccat tcttcgagag attcaagtcc agcatccagc 301 ggccaagtσc atgatcgaaa ttagccggaσ σσaggatgaa gaggttggag atgggaσσac 361 atcagtaatt attcttgcag gggaaatgct gtctgtagct gagcacttσc tggagcagσa 421 gatgσaσαca acagtggtga tcagtgctta ccgcaaggca ttggatgata tgatcagcaσ 481 σctaaagaaa ataagtatcσ σagtσgacat cagtgacagt gatatgatgc tgaacatσat 541 σaacagctct attactacca aagσcatcag tcggtggtca tctttggctt gcaacattgc 601 σσtggatgct gtcaagatgg tacagtttga ggagaatggt σggaaagaga ttgacataaa 661 aaaatatgca agagtggaaa agataσctgg aggcatσatt gaagaσtσσt gtgtσttgσg 721 tggagtσatg attaacaagg atgtgacσca tccaσgtatg cggcgσtata tσaagaaσσσ 781 tσgcattgtg ctgctggatt σttσtσtgga ataσaagaaa ggagaaagσσ agactgacat 841 tgagattaca cgagaggagg acttcacccg aattctσcag atggaggaag agtacatcσa 901 gcagctσtgt gaggaσatta tσcaactgaa gcccgatgtg gtσatcactg aaaagggσat 961 ctcagattta gσtσagσact aσcttatgcg ggccaatatσ acagccatcc gσagagtccg 1021 gaagacagac aataatcgca ttgctagagc σtgtggggσc cggatagtca gccgaccaga 1081 ggaactgaga gaagatgatg ttggaacagg agσaggσctg ttggaaatca agaaaattgg 1141 agatgaataσ tttaσtttca tcactgactg caaagaσccc aaggσσtgσa ccattctασt 1201 ccggggggct agσaaagaga ttctctcgga agtagaacgc aacσtccagg atgccatgca 1261 agtgtgtσgσ aatgttσtcc tggaccσtca gctggtgcca gggggtgggg cctccgagat 1321 ggctgtggcc σatgσcttga cagaaaaatσ σaaggσσatg actggtgtgg aaσaatggσα 1381 ataαagggct gttgccσagg ccctagaggt cattcctcgt acσσtgatσc agaactgtgg 1441 ggccagcacc atσσgtctac ttacctσσσt tcgggccaag σacacσcagg agaactgtga 1501 gacctggggt gtaaatggtg agacgggtac tttggtggac atgaaggaaσ tgggcatatg 1561 ggagcσattg gσtgtgaagc tgcagactta taagacagca gtggagacgg cagttctgct 1621 actgcgaatt gatgacatcg tttcaggcca σaaaaagaaa ggσgatgaσσ agagccggca 1681 aggcggggct cctgatgσtg gccaggagtg agtgctaggc aaggctactt caatgcaσag 1741 aaccagcaga gtctσσcctt ttcctgagcc agagtgccag gaaσaσtgtg gaσgtctttg 1801 ttcagaaggg atcaggttgg ggggcagccc σcagtcσctt tctgtcccag ctcagttttσ 1861 σaaaagaσaσ tgaσatgtaa ttcttctcta ttgtaaggtt tccatttagt ttgcttσσga 1921 tgattaaatc taagtcattt gaaaaaaaaa aaaaaaaaaa aaaaa
SEQ ID NO: 18
HSPA8 NM_006597 Homo sapiens heat shoσk 70kDa protein 8 (HSPA8) , transαript variant 1, mRNA gi I 24234684 I ref |NM_006597.3 | [24234684]
1 σtσattgaaα tσgσctgcag σtcttgggtt ttttgtggct tσσttσgtta ttggagσcag 61 gcσtaσaσcc cagcaacσat gtccaaggga cctgcagttg gtattgatσt tggσaccacc 121 tactcttgtg tgggtgtttt σσagσaσgga aaagtcgaga taattgcσaa tgatcaggga 181 aaccgaaσca ctccaagcta tgtcgccttt acggacaσtg aaσggttgat cggtgatgcc 241 gσaaagaatc aagttgcaat gaaccσcacc aacaσagttt ttgatgccaa acgtctgatt 301 ggacgcagat ttgatgatgσ tgttgtσcag tctgatatga aacattggσσ ctttatggtg 361 gtgaatgatg ctggcaggσσ σaaggtccaa gtagaataca agggagagaσ caaaagcttc 421 tatσσagagg aggtgtσttc tatggttctg acaaagatga aggaaattgc agaagcctaσ 481 σttgggaaga σtgttaσcaa tgctgtggtc acagtgcσag cttactttaa tgactctcag 541 cgtcaggcta ccaaagatgσ tggaaσtatt gctggtctσa atgtaσttag aattattaat 601 gagccaaσtg σtgσtgctat tgcttacggc ttagaσaaaa aggttggagσ agaaagaaaσ 661 gtgctcatct ttgaσctggg aggtggcact tttgatgtgt caatcctcac tattgaggat 721 ggaatσtttg aggtσaagtα taσagσtgga gaσaσσcact tgggtggaga agattttgac 781 aacσgaatgg tσaaσcattt tattgctgag tttaagcgca agσataagaa ggacatcagt 841 gagaacaaga gagctgtaag acgcctccgt actgcttgtg aaσgtgctaa gcgtaccctc 901 tcttσσagca cσcaggccag tattgagatc gattσtctct atgaaggaat cgacttσtat 961 aσctcσatta σσcgtgcccg atttgaagaa σtgaatgσtg aσσtgttσσg tggcaccctg 1021 gacccagtag agaaagccσt tσgagatgσσ aaaσtagaσa agtcacagat tσatgatatt 1081 gtcctggttg gtggttctaσ tσgtatσσσc aagattcaga agcttctσca agacttcttc 1141 aatggaaaag aactgaataa gagcatcaac cctgatgaag ctgttgctta tggtgcagσt 1201 gtσσaggcag cσatσttgtc tggagacaag tctgagaatg ttσaagattt gσtgctcttg 1261 gatgtσactσ σtctttccct tggtattgaa actgctggtg gagtσatgac tgtcctcatσ 1321 aagσgtaata σσaσσattcc taccaagcag aσacagacct tσaσtaccta ttctgaσaaσ 1381 σagcctggtg tgcttattca ggtttatgaa ggcgagcgtg ccatgaσaaa ggataacaac 1441 ctgσttggca agtttgaact caσaggσata σσtσctgcac cσσgaggtgt tcctcagatt 1501 gaagtcactt ttgacattga tgccaatggt atactcaatg tctσtgσtgt ggaσaagagt 1561 acgggaaaag agaacaagat tactatcaσt aatgacaagg gcσgtttgag σaaggaagaσ 1621 attgaacgta tggtcσagga agσtgagaag tacaaagctg aagatgagaa gcagagggac 1681 aaggtgtcat cσaagaattσ aσttgagtσc tatgccttσa aσatgaaagc aactgttgaa 1741 gatgagaaaσ ttcaaggcaa gattaacgat gaggaσaaac agaagattct ggaσaagtgt 1801 aatgaaatta tσaaσtggσt tgataagaat σagaσtgσtg agaaggaaga atttgaacat 1861 caacagaaag agctggagaa agtttgcaaσ σσσatσatσa σσaagσtgta ccagagtgσa 1921 ggaggσatgσ σaggaggaat gcctggggga tttcctggtg gtggagσtσσ tσσσtctggt 1981 ggtgσttcct cagggcσσaσ cattgaagag gttgattaag σcaaccaagt gtagatgtag 2041 cattgttcca cacatttaaa acatttgaag gacctaaatt cgtagcaaat tctgtggcag 2101 ttttaaaaag ttaagctgct atagtaagtt aσtgggcatt ctσaataσtt gaatatggaa 2161 σatatgσaca ggggaaggaa ataacattgc actttataaa cactgtattg taagtggaaa 2221 atgcaatgtσ ttaaataaaa σtatttaaaa ttggcaccat aaaaaaaaaa aaaaaa
SEQ ID NO: 19
SLC16A1
NM_003051.2| Homo sapiens solute carrier family 16 (monocarboxylic acid transporters) , member 1 (SLC16A1) , mRNA
1 tgcgaσgtga σtggσtagct gcgtgggtac tggaacaagc aaaσgaggσa gcgagcgaag 61 gaσgggagcc ggaccctggg σσccgtggaa ctccagσctg cgσσaσσaσg tσaσgcacaσ 121 gσtcggcgct gcgatσσgσg σatataacga tatttggatt tgacctgσat tttggaattt 181 atctacaσtt aaaatgccac cagcagttgg aggtccagtt ggataσaσσc ccccagatgg 241 aggctggggc tgggcagtgg taattggagc tttσatttcc atcggcttct σttatgσatt 301 tccσaaatca attactgtσt tcttcaaaga gattgaaggt atattcσatg σσaccacσag 361 σgaagtgtσa tggatatσσt ccataatgtt ggctgtcatg tatggtggag gtσσtatσag 421 σagtatσctg gtgaataaat atggaagtcg tatagtcatg attgttggtg gσtgσttgtc 481 aggσtgtggσ ttgattgcag cttσtttctg taacaccgta cagσaaσtat acgtctgtat 541 tggagtcatt ggaggtcttg ggcttgσσtt σaacttgaat ccagctσtga σcatgattgg 601 caagtatttc tacaagaggc gaccattggσ caacggactg gccatggcag gσagccctgt 661 gttcctσtgt aσtσtggσcc ccctcaatca ggttttcttc ggtatσtttg gatggagagg 721 aagσtttcta attcttgggg gσttgctact aaactgctgt gttgctggag ccσtcatgcg 781 accaatσggg ccσaagccaa σσaaggcagg gaaagataag tctaaagcat σccttgagaa 841 agσtggaaaa tctggtgtga aaaaagatct gcatgatgca aatacagatc ttattggaag 901 acacσσtaaa σaagagaaaσ gatσagtctt ccaaacaatt aatσagttcc tggaσttaaσ 961 cctattσacc cacagaggσt ttttgσtata cctctctgga aatgtgatσa tgttttttgg 1021 aσtσtttgσa cctttggtgt ttcttagtag ttatgggaag agtcagcatt attctagtga 1081 gaagtctgcσ ttσσttσttt ccattctggc ttttgttgac atggtagσσc gacσatσtat 1141 gggaαttgta gccaacacaa agccaataag acctσgaatt σagtatttσt ttgσggcttc 1201 cgttgttgca aatggagtgt gtcatatgct agcaσσttta tσcactaσct atgttggatt 1261 ctgtgtctat gcgggattct ttggatttgc σttcgggtgg ctσagσtccg tattgtttga 1321 aaσattgatg gaσσttgttg gaccccagag gttσtσσagc gctgtgggat tggtgaccat 1381 tgtggaatgc tgtσctgtcc tcctggggcc aσσaσtttta ggtσggctca atgacatgta 1441 tggagactaσ aaataσacat actgggcatg tggcgtσgtc ctaattattt caggtatcta 1501 tσtcttcatt ggcatgggca tcaattatcg acttttggca aaagaacaga aagcaaaσga 1561 gσagaaaaag gaaagtaaag aggaagagac cagtatagat gttgctggga agccaaatga 1621 agttacσaaa gσagσagaat σtccggacca gaaagaσaσa gaaggagggc cσaaggagga 1681 ggaaagtσca gtσtgaatcc atggggσtga agggtaaatt gagcagttca tgaσccagga 1741 tatctgaaaa tattctaσtg gcctgtaatc taσσagtggt gctcaatgσa aatagtagac 1801 atttgtgtgg aaatcatacc agttgttcat tgatgggatt tttgtttgac tccttaσσaa 1861 tagcctgaat ttgaggaggg aatgattggt agσaaaggat gggggaaaga agtaggttct 1921 gttttgtttt gttttaatσt tagcttttaa tagtgtcata aagattataa tatgtgcσtt 1981 aagttttagt σtttagaact ctagagagσσ ttaacttctt aaaccatttt tgσtgaattσ 2041 atctatttcg agtgttgtgt taaaaggaaa aataacaaσt aaσttgtttg aggσaaatσt 2101 aaaatttaaa attaatσttg σttcattgtt acatgtaata tatttcagac attttcactg 2161 gaagatttat gaaσagaaat attggttgaa agttagagat tttacaaaat gctgacaaaa 2221 atattttcct agcatσagta gatttctggc atatgtttct gctagctata tatttaggaa 2281 attσaaagca taaaactttg gσaacatctt ggctgttσta gaσaσagtgt aσttgtσaaσ 2341 ccσtσtσagg taccttttct tgggatgctt attagaagcc aagtaaagtg cttaaggttt 2401 gttttcatta aattagσtat ttctgctccc ctgttσaaag atgσattttg agtgtttata 2461 gatσaσtgcc ctttttgaaa tcacctggta ttatttttct taαtggaaaa gttagtatta 2521 aaatctacag aactacatat ttgtgcctcc ttggtaaata caacacatσt aattaaatgt 2581 agacagatat ttcaaacatc agctgaattc aαttaagttt ttσσaaaacc tσagttaaaσ 2641 tgtgaagσta ttggaatttt tttttcctgg aatttttσcc ctttgattca cagtggtcσc 2701 atttatatct gcttσtagct tagtgctatg tgtgagatat gtgtgtgttt ggtgtttttg 2761 tttttttgtt tttttttttt taaggtttgσ aaattaaaaa gggccagaaa aatttggσaσ 2821 σaggcaaacg aataaagata ggattgggaa agaagttgct aagtgtgσtt agttttaata 2881 agtaattσct tctσtttttt σagagaaggσ σttaσagaaa attgttgtgσ ttagaattgα 2941 tggatgcatt tttacσσtcc acacaaacct aaaaattttg tgaccσσttt cacttaσσtg 3001 aaaagtagag aaatggattc agtataagga taaggaggga aggtggacca gaatgaaaac 3061 tgtaaatatt tttttaaσct aatatcactt aaatcgaggc agaaagatat agacattcaa 3121 tgaattatat tcaatgcatt taaaatacca ctgtaattga cagagtaaaa gtatagatac 3181 aaaaσσttgt gtaagaggct gacttttcca aataaacatt ttttaagaaa aσatttαttσ 3241 tcccaaatgt ctattttctt gaggaaaata ttgσtgtgtc ttcattttσa ttaσcaggtt 3301 tcattttggg ccttgctaaa ttgattgaat taaatcctcc agcttttgaa ccttgaaaaa 3361 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa agaaaaaaaa aaaaaaaaag
SEQ ID NO: 20 SH2 of Abl AK074067.l| Homo sapiens mRNA for FLJ00138 protein
1 ggacaagggc aagattatta agcagαaaga gaσggtcatc attttagaag actatgctga 61 cccttatgat gσcaaacgga caaagggtca aagggatgσa gagagagtcg gagagaacga 121 cggttacatg gaaccatatg atgcacagca aatgataaσa gaaattagaσ gacggggttc 181 σaaagatσcσ σtggtgaagg σtσtσσagσt gcttgacagt cσctgtgaac σσgσagaσgg 241 tggσσtgaaa tσagagaσct tggccaaaag acggagttσc aaggacctcc tggggaagσc 301 gccaσagσta tacgacactσ σσtacgagcc tgcagaaggg gggcccaggg cagaggggaa 361 ggcgcggccc ccagacagσσ ggσtgσσcga gaacgaσgag aggcccgcgg cagagtaσga 421 gcagccatgg gagtggaaga aggagσagat σgtgcgggct ctgtcagtcc agtttgaagg 481 agctgagcga cσttσcttca gggaggagaσ agtgaggcag caccaccggc agaagagctg 541 gaσccagaag atcctgaagσ σagcσσtctc ggaσcacagt gagggagaga aagtggacσσ 601 gggσσtgσcc ctggagaagc agccctggta tcatggtgcc atσagccgtg ctgaggctga 661 gagtcgacta cagccσtgσa aagaagctgg ttacctggtt cgaaatagtg agtσagggaa 721 σagσaggtaσ tσσattgσcc taaagactag tcaaggatgt gtcσacatca tagtggctca 781 gaσcaaagac aacaaataσa cactgaatσa gaαaagcgct gtgtttgaca gσatccctga 841 agtggtacaσ tattattcca atgaaaagtt gcctttσaaa ggggcagaac acatgacttt 901 actctaσσca gtgcacagca agσttσacta agattcagcc actgcaagcc ctgggcctct 961 ggσaσσttca agggcatcat cagcgcacaa ccagcatctσ agaggaσaag gctggactag
1021 caaσtgσtag aaaatgggag tσttccttga aaagtσagag agtgatttgt tttgttttgt
1081 ttgagaσgaa gtσtσgσtgt gttgcccagg ctggagtgca atggcgσagt σttggσtσaσ 1141 tgcaacatct gactσσtggg ttσaagcagt tcttccccat cagcctccσa agtaggtggg
1201 aσtataggtt σgcaccaσca σtcccagcta attttttttt tgtattttta gtagagatgg
1261 ggtttcgccg tσttσgtσag gσtggtctca aactcσtgac ctσaaatgat σσaσccaσσt
1321 σagtσtcccc gagtgσσtgg attacaggca tgagcσaσtg αaσσcggcσa agtσtttggt
1381 σttaaagtga ttccatgaσa ctttgtttgt ggcσtgtσcc ttgtttcσtt gcaagtagtt 1441 ctaσaataag aaatσatgat ttagσtgttg cσtσcagctc tggggtaggg tgttcttttt
1501 atggtgtgac cctσaggaag gttaagtcag gagttcagga gcatcagagt tctctagaaa
1561 tgtgcσtact tgttacctgg aatacctggt σtαtaaaσaa acσagcaaaa aatccacgtg
1621 gcttttσσac atgatggtgc agactggaag aggatgttat attggactcg ttattgggga
1681 aatgaatgag σgggagaaaa tgtgaatgac gggcaagaag gtggtctttc tαcctcagaa 1741 gtcctaattc agctctggag ttcatggaaa tσσgcaactt cagagtgtgg σctaaggatt
1801 attttgttgg tcagσctttc caagaaagtg tgtgttσtσt σaatσtσtgt ggattttctc
1861 attttttagσ aaatσagtga gataagσata aataggaagg aagataccσσ aggtttaaga
1921 atσacσaata tσattaggσa ttggcatcat tattagaatt ctgaattata gaataaaagg
1981 tacaaσaaaa atttcatttc tgaattttaa aattctggaa atttgcaaag ctccacaaσt 2041 gtttttttaσ tgaattaatt aσatagaaσt tcgatgtctt ttgtttσatσ atcattgggc
2101 attttagttg σtatggaata atttttaatt tttgtσtcta aaattagatt tgσtttgtag
2161 taaatttttt aaaaatgcaa ccctaagatc tgattatatg aactgggtct ctaaagccta
2221 caaagattct ctσgttσtgt aσcaagcaga σtgccttgta σtatacagaa gtgtttgaaa
2281 agacctagag gttttctctt aaataccatt acttaagatt σatagtatta ggatσtttat 2341 gatttatσat gagσttatat σaσσagttta tttaαtgtga aaaaaaσσat gggaatggσa
2401 taσtgtgaga agagtaσtat ggtgaatggσ tσcagaatta aaattcagαa gatgtgtσtg
2461 tattctgggg ttggtcattt gggtctσaaa aσtgccσσat atgσaaatgt aσtgaσtgtc
2521 atcaatgaaa agttaacctt tgtagcttat aaataσacac aaaatgttga tttggttaat
2581 tttttaggaa agtatacσtt tgtagttaσt agttaσattt gactgtaaga tttagaggtt 2641 agtaaatttt tgcttcttta ttcagataag atctcagcσa aaaggttgtg tgatσtttga
2701 ttttaaaaat ttaagaggaa σttttσctca σtggaaσaσa atgattttat taataaagaa
2761 tgtaggσtgg gtgσggtggc tcatgσacgt aatcσσaaσa atttgggagg ctgaggcagg
2821 cagatcacgt gaggtcagga gtttgggacσ ggcctggσσa acatggtgaa acσσtgtαtσ
2881 tagtaaaaat acaaaaatta gctgggcacg gtggσgggσa σσtgtagttσ σagctgcttg 2941 ggaggσtgag gcacgagaat cacttgagcσ caggaggtgg aggttgcagt gagccaagat
3001 tgtgtcactg caσtccatcc tgggtgacaa gagcgaaact ccatctcaaa aaaaaaaaaa 3061 aaaaaaaagc ctggcctggt ggtggatgcc tgtggttσσa gctattcggg aggctgaggt 3121 aggtggatca σctctgσtca ggtcaaggct gcagcgagcc atgatcgcac cattgcactσ 3181 σagσσtgagt gaσagagtga gaccctgtct σaaσaagσaa gσaaaσaaaa aaσσaaaagg 3241 aatgtttttt tcagatactg atagaatgtt ttcagtgtgt attggttcat ttactatatσ 3301 tttagtgtaa gattttaaaa ggttttttσa gcatcσattc aacaaatatt tattatσttt 3361 atacaaatta ttcattgtgt taaaσttatt tttagtttaa cattctagaa atgaaacgtt 3421 tttacttaaσ σttattσtac aaagggaata cagσagttat tσtaatttta ataaatgcta 3481 aaagctttat acaatttttc tttgtgcact aaatgatttt tggccσatac cσagσaaαtg 3541 tgatgaatgt ataatgaaat aacatcttga aaaαaggcσa gatacattaa gtatttattg 3601 agcttσtgtσ atatgccσag tattatgctt cttctatact gtttctctgt gacaagtσat 3661 actatattct ttatagaatt aaaagtagag gagaggcaga gtttacatat tgtccagttg 3721 ctttacagtt gtacaggagg ttataagaag aaatatagta aattagtggg aagtσagagg 3781 tgggggcgtt agtgagctat tttcttcttg aggttgtgac acaagctgac aaaagccagg 3841 gagttσaσag σtgtgtggtg gcacaaagtt ccatatgttc taaaaacaat taggσccagσ 3901 agggtgtαcc taatggcttσ σttgttaaaσ ctcσatggcc agσtgatσtg aagσtctgtg 3961 acatgttctc tgagctctga atgctctggc tttttgtcat tttgtσttga gacaagtatt 4021 ttαctgtagt σσtσattcσt tσgagttatt ccatctσσσa ggatattσtc tggtgagaag 4081 aatgtσtttc agtgaatttg cccttgaatt tagcatccat agagctgtgt cagtgttctt 4141 cttgatcaαa σσttctttaa aaaaaatact tgcttgσgat gaσtggaσaa gttσagttgg 4201 ttagtttσag gσσtataaga agagagagta aaggaccttg ctatttactt tgataccata 4261 gttgtatctc aggatggcct gcaaaσcact ggccttgtgt gtatttaagc taggaataaa 4321 ataatggaga agtgttaata tgtatacaaa aaggtaaata ttgatatatc tactctctgt 4381 tgggggσaga agtgtcattt taagttattc aaagσaσttt σttaagcatt ttagaaagcc 4441 tttattσttt gσtgttggaa gtαtccgtaα tttgσagaat tggtatttgt gtactagcαt 4501 σtgσσgσagg atggggaggt gggσaggtag ctgatagggg cagσσaggag tttttgaggσ 4561 aggtggtggg aaattgtσσt aatttgttaa ttggattatg taactctgtt actagtctgt 4621 tattggσtgt tgttactgga tgcatσttga tattcagaag aataactgtg aggσattσtt 4681 cagttgcggg ttaagtgggg ttagtttσtg ttσtgtcaga tgcσcttttt tcagtσaaag 4741 gttagccσct tgtttctccc tccttccagg gtttagggag tgσagtgatg tσgatttσat 4801 ttσσσttσσσ σgσacccctt gacactσagσ aggattgσaσ tgaaaσcctt cacaatctσt 4861 σgttσaσtag ttgtctcσta tttttσσata actagcacta gtttggcctt atgacctggt 4921 tagaatcact σttctgtatt ctcatttcσa atttttgtgc ccσactaacg tggactagag 4981 aaacttggcc tgσtgtgσag tgggσcttct gttσaactta ccσtσσaσσg σtgacσσtgt 5041 gtgaagagag atggtgσgtt actgcσatσt aatgggaaaa gagaaaactg cagttgggaa 5101 aagcagctgt gcatttaagg gtagggcttt αtgaaggatt tσtgataαag tσσagaaaag 5161 ggaaaatgat gaσaσagσag ttgσσatσtt gaaaaatgcc σtttσctgcg gaaagggtgt 5221 tttgaagtσt aatacaacta tcatcacaag gtσσctggac taaggσtgga tσgtgtaatt 5281 tagaatctca aattgtattt taattaatat gctggcaaσa gaatcattga aacaggcatc 5341 tcattttgtα aagttcttag ccgttcagtt tgtcaggggc tttaatattt tagatatcaa 5401 ctaatacata gtttcaactt ttaaaaatgt ttgaagattg tatgtaatat aggtgcctat 5461 σtatagtgcc ttagtaattt aaatσagaaa tattttataa aaσttσtggt tgttttgcag 5521 tagccaatat aggcttcatg ccctcσtgaa gatagtttcc tctgaaatgt aactttaaat 5581 aaacattatt σσaag SEQ ID NO:21 SH2 Of Abl XM_060121[gi: 20539061] 1 ggaσaagggc aagattatta agcagσaaga gacggtcatc attttagaag actatgctga 61 cσcttatgat gccaaacgga caaagggtσa aagggatgσa gagagagtσg gagagaaσga 121 cggttacatg gaaccatatg atgcacagσa aatgataaca gaaattagac gaσggggttσ 181 caaagatcσσ σtggtgaagg σtctccagct gcttgacagt ccctgtgaac σσgcagacgg 241 tggcctgaaa tcagagacct tggccaaaag acggagttcc aaggaσσtσσ tggggaagcc 301 gαcacagσta taαgaσactc σctacgagcc tgcagaaggg gggσσcaggg cagaggggaa 361 ggσgcggccc σcagacagcc ggσtgσσcga gaacgacgag aggcσσgcgg σagagtacga 421 gcagccatgg gagtggaaga aggagcagat cgtgσgggct ctgtcagtcc agtttgaagg 481 agctgagσga σσttσσttσa gggaggagaσ agtgaggσag σaccaccggc agaagagctg 541 gacσcagaag atcσtgaagσ σagccctσtσ ggaσσaσagt gagggagaga aagtggaσcc 601 gggcσtgσσσ σtggagaagσ agccctggta tcatggtgcc atcagcαgtg σtgaggctga 661 gagtcgaσta σagσσctgca aagaagσtgg ttacctggtt σgaaatagtg agtcagggaa 721 cagcaggtac tσcattgcσc taaagactag tcaaggatgt gtccacatσa tagtggσtσa 781 gaσσaaagaσ aaσaaataσa σaσtgaatσa gacaagcgct gtgtttgaca gσatccctga 841 agtggtacaσ tattattσσa atgaaaagtt gcσtttσaaa ggggσagaac acatgacttt 901 aσtctaccca gtgcacagca agσttσacta agattcagcc aσtgσaagσσ σtgggcctct 961 ggcaccttca agggcatσat cagcgcaσaa ccagcatσtc agaggacaag gσtggactag 1021 caaσtgσtag aaaatgggag tσttccttga aaagtσagag agtgatttgt tttgttttgt 1081 ttgagacgaa gtctcgctgt gttgccσagg σtggagtgca atggcgσaat cttggctcaσ 1141 tgcaacatct gactσσtggg ttσaagσagt tσttσασσat σagσctccca agtaggtggg 1201 aσtataggtt cgcaσσaσca ctcccagcta attttttttt ttgtattttt agtagagatg 1261 gggtttcgcc gtcttσgtσa ggctggtctc aaactcctga cctcaaatga tσσaccσacc 1321 tσagtctccc cgagtgcctg gattacaggc atgagcσact gσaccσggσc aagtctttgg 1381 tcttaaagtg attcσatgaσ aσtttgtttg tggcctgtcc σttgtttσσt tgctaagtag 1441 ttctacaata agaaatσatg atttagctgt tgcctσσagc tctggggtag ggtgttcttt 1501 ttatggtgtg aσσctcagga aggttaagtc aggagttcag gagσatσaga gttσtσtaga 1561 aatgtgccta cttgttacσt ggaatacctg gtσtσtaaac aaaccaaσaa aaaatσσaσg 1621 tggcttttcc aσatgatggt gσagaσtgga agaggatgtt atattggaσt σgttattggg 1681 gaaatgaatg agσgggagaa aatgtgaatg aσgggcaaga aggtggtctt tσtσcctσag 1741 aagtσσtaat tσagσtσtgg agttcatgga aatccgcaac ttcagagtgt ggcσtaagga 1801 ttattttgtt ggtcagcσtt tσσaagaaag tgtgtgttct ctcaatσtct gtggattttc 1861 tcatttttta gcaaatσagt gagataagσa taaataggaa ggaagataσc ccaggtttaa 1921 gaatcacσaa tatσattagg σattggcatc attattagaa ttctgaatta tagaataaaa 1981 ggtaσaaσaa aaatttσatt tσtgaatttt aaaattσtgg aaatttgσaa agσtcσacaa 2041 ctgttttttt actgaattaa ttacatagaa σttcgatgtc ttttgtttca tcatcattgg 2101 gcattttagt tgctatggaa taatttttaa tttttgtctc taaaattaga tttgctttgt 2161 agtaaatttt ttaaaaatgc aaccctaaga tctgattata tgaaσtgggt σtσtaaagσσ 2221 taσaaagatt ctctσgttct gtaccaagca gaσtgσσttg taσtatacag aagtgtttga 2281 aaagacctag aggttttctσ ttaaata'σσa ttaσttaaga ttσatagtat taggatσttt 2341 atgatttatσ atgagcttat atcaccagtt tatttaσtgt gaaaaaaaσc atgggaatgg 2401 cataσtgtga gaagagtact atggtgaatg gctccagaat taaaattσag cagatgtgtc 2461 tgtattctgg ggttggtcat ttgggtctσa aaaσtgσσσc atatgcaaat gtactgactg 2521 tcatcaatga aaagttaacc tttgtagctt ataaatacac acaaaatgtt gatttggtta 2581 attttttagg aaagtataσσ tttgtagtta σtagttaσat ttgactgtaa gatttagagg 2641 ttagtaaatt tttgcttσtt tattσagata agatctcagc caaaaggttg tgtgatσttt 2701 gattttaaaa atttaagagg aacttttcσt cactggaaσa aaatgatttt attaataaag 2761 aatgtaggct gggtgcggtg gσtcatgcaσ gtaatσσcaa caatttggga ggctgaggca 2821 ggcagatcac gtgaggtcag gagtttgaga ccagcctggc caaσatggtg aaaσcctgtc 2881 tgtagtaaaa ataσaaaaat tagctgggσa σggtggσggg cacσtgtagt tccagctgct 2941 tgggaggσtg aggcacgaga atσaσttgag σccaggaggt ggaggttgσa gtgagccaag 3001 attatgtσaσ tgσaσtcσat σσtgggtgaσ aagagσgaaa σtccatctca aaaaaaaaaa 3061 aaaaaaaaag cctggσσtgg tggtggatgσ σtgtggttσc agctattσgg gaggctgagg 3121 taggtggatc acctσtgσtσ aggtσaaggc tgcagσgagc catgatcgca σcattgcact 3181 σcagcσtgag tgaσagagtg agaccctgtc tcaacaagca agσaaaσaaa aaaccaaaag 3241 gaatgttttt ttcagataσt gatagaatgt tttcagtgtg tattggttca tttactatat 3301 ctttagtgta agattttaaa aggttttttσ agcatccatt σaaσaaatat ttattatσtt 3361 tatacaaatt attcattgtg ttaaacttat ttttagttta acattσtaga aatgaaaσgt 3421 ttttacttaa ccttattcta σaaagggaat acagcagtta ttctaatttt aataaatgσt 3481 aaaagσttta taσaattttt σtttgtgcac taaatgattt ttggcσcata cσcagcaact 3541 gtgatgaatg tataatgaaa taacatcttg aaaaσaggσc agataσatta agtatttatt 3601 gagσttctgt catatgcσσa gtattatgσt tσttσtatac tgtttσtσtg tgaσaagtσa 3661 taσtatattσ tttatagaat taaaagtaga ggagaggσag agtttacata ttgtccagtt 3721 gctttaσagt tgtaσaggag gttataagaa gaaatatagt aaattagtgg gaagtcagag 3781 gtgggggcgt tagtgagcta ttttcttctt gaggttgtga caσaagσtga σaaaagσσag 3841 ggagttσaca gctgtgtggt ggcacaaagt tσσatatgtt σtaaaaaσaa ttaggccσag 3901 cagggtgtcc σtaatggσtt σσttgttaaa σσtccatggc σagσtgatct gaagσtctgt 3961 gaσatgttσt σtgagctctg aatgctctgg ctttttgtσa ttttgtcttg agacaagtat 4021 tttσσtgtag tcσtcattcσ ttcgagttat tccatctccc aggatattct ctggtgagaa 4081 gaatgtσttt σagtgaattt gσcttgaatt tagcatcσat agagctgtgt cagtgttσtt 4141 σttgatσaσa σσttσtttaa aaaaaatact tgcttgcgat gaσtggacaa gttcagttgg 4201 ttagtttσag gσσtataaga agagagagta aaggaσcttg ctatttaσtt tgataσσata 4261 gttgtatctc aggatggcct gσaaaccact ggccttgtgt gtatttaagc taggaataaa 4321 ataatggaga agtgttaata tgtatacaaa aaggtaaata ttgatatatc tactctctgt 4381 tgggggcaga agtgtcattt taagttattc aaagσaσttt cttaagcatt ttagaaagcσ 4441 tttattcttt gctgttggaa gtctccgtac tttgcagaat tggtatttgt gtactagcct 4501 ctgccgσagg atggggaggt gggσaggtag σtgatagggg cagccaggag tttttgaggc 4561 aggtggtggg aaattgtcσt aatttgttaa ttggattatg taaσtσtgtt aσtagtctgt 4621 tattggctgt tgttactgga tgcatcttga tattcagaag aataaσtgtg aggσattσtt 4681 σagttgσggg ttaagtgggg ttagtttctg ttσtgtσaga tgσccttttt cagtcaaagg 4741 ttagcσcctt gtttσtσσct ccttcσaggg tttagggagt gσagtgatgt σgatttσatt 4801 tσccttσccc gσaσσccttg aσactcagca ggattgcact gaaacccttc aαagatσtσt 4861 σgttσaσtag ttgtσtccta tttttσσata aσtagσaσta gtttggcctt atgacctggt 4921 tagaatσaσt σttσtgtatt σtcatttcca atttttgtgc cccactaacg tggaσtagag 4981 aaacttggcσ tgctgtgcag tgggccttct gttcaactta cσctcσaσσg ctgacσctgt 5041 gtgaagagag atggtgcgtt actgccatct aatgggaaaa gagaaaactg σagttgggaa 5101 aagcagctgt gcatttaagg gtagggcttt ctgaaggatt tctgataσag tσcagaaaag 5161 ggaaaatgat gacacagcag ttgccatctt gaaaaatgcc ctttcctgcg gaaagggtgt 5221 tttgaagtct aataσaacta tcatcacaag gtσcctggac taaggctgga tcgtgtaatt 5281 tagaatctca aattgtattt taattaatat gctggσaaca gaatcattga aacaggcgtc 5341 tσattttgtσ aagttcttag ccgttσagtt tgtcaggggc tttaatattt tagatatcaa 5401 ctaataσata gtttcaactt ttaaaaatgt ttgaagattg tatgtaatat aggtgtctat 5461 σtatagtgσc ttagtaattt aaatcagaaa tattttataa aacttctggt tgttttgcag 5521 tagcσaatat aggcttcatg ccctσctgaa gatagtttcc tctgaaatgt aaσtttaaat 5581 aaaσattatt σσaag
SEQ ID NO: 22 ubiquitin hydrolase (USP37) NM_020935 Homo sapiens ubiquitin speσifiσ protease 37 (USP37) , mRNA gi I 32698743 I ref |NM_020935.11 [32698743] 1 σatσagσσgc tctccαtgac taggggtagc tagcggcctc cctσσtttgg gttσtgtatσ 61 σctacttcca ttaσσσtcgg ctcctcccac tcctcggggg ctccgtgctt tccgcgggtc 121 tgtσσggggg σtccggaσcc tcggcgcagc tgagttgatg gcttσσggag aaσtggcata 181 gccgcagaat atgagtagtg tcccaagaag agtgctttgc ctttggcaσa aggatcagaa 241 taaaggtgaa ttgctattaσ atagggtttt tσggtaaaag tσactgaaaa ttatttgcσa 301 tacagtaacc agagacctcc aactaggggc cccσaaaσtg tatασtgσσt gtagccagaa 361 gσaattttta aagaaaatat gtctcctctg aagatacatg gtcσtatσag aattcgaagt 421 atgcagactg ggattacaaa gtggaaagaa ggatcctttg aaattgtaga aaaagagaat 481 aaagtσagcc tagtagttσa ctacaatact ggaggaattc caaggatatt tcagctaagt 541 cataaσatta aaaatgtggt gσttcgaccc agtggagcga aacaaagccg cσtaatgtta 601 aσtσtgσaag ataaσagctt cttgtctatt gacaaagtac caagtaagga tgcagaggaa 661 atgaggttgt ttctagatgc agtccatcaa aaσagacttc ctgcagσσat gaaacσgtσt 721 σaggggtσtg gtagttttgg agσcattctg ggcagcagga cctσacagaa ggaaacσagc 781 aggcagσttt σttaσtcaga caatcaggct tctgcaaaaa gaggaagttt ggaaactaaa 841 gatgatattc catttcgaaa agttcttggt aatccgggta gaggatcgat taagaσtgta 901 gσaggaagtg gaatagσtσg gaσgattασt tσtttgaσat ctacttcaac acctcttaga 961 tcagggttgσ tagaaaatσg tactgaaaag aggaaaagaa tgatatcaaσ tggctcagaa 1021 ttgaatgaag attaσcctaa ggaaaatgat tcatcatcga aσaaσaaggσ σatgacagat 1081 ccσtccagaa agtatttaaσ cagcagtaga gaaaagcagc tgagtttgaa acagtσagaa 1141 gagaatagga σatσagggσt tttaσcttta cagtσatαat ccttttatgg tagσagagct 1201 ggatcσaagg aacactcttc tggtggcact aaσttagaσa ggactaatgt ttcaagccag 1261 actcσctctg cσaaaagaag tttgggattt σttσσtcagc cagttσαtσt ttσtgttaaa 1321 aaaσtgaggt gtaaσcagga ttacactggc tggaataaac caagagtgcc cσtttσctct 1381 cacσaaσagσ agcaactgσa gggcttctcc aagttgggaa atacctgcta tatgaatgct 1441 attσtaσaat αtαtattttc actccagtca tttgσaaatg aattgattaa acaaggtatc 1501 ccatggaaga aaattccact caatgcactt atcagacgct ttgcacactt gcttgttaaa 1561 aaagatatct gtaattcaga gaccaaaaag gatttactca agaaggttaa aaatgccatt 1621 tσagctaσag cagagagatt σtctggttat atgcagaatg atgctcatga atttttaagt 1681 cagtgtttgg accagctgaa agaagatatg gaaaaattaa ataaaacttg gaagactgaa 1741 cctgtttσtg gagaagaaaa ttcaccagat atttαagota ccagagcata cacttgccct 1801 gttattacta atttggagtt tgaggttcag caσtσσatσa tttgtaaagσ atgtggggag 1861 attatcccσa aaagagaaσa gtttaatgac ctctσtattg aσσttσσtσg taggaaaaaa 1921 σσactccctc ctσgttσaat tσaagattσt cttgatcttt tctttagggα σgaagaaσtg 1981 gagtattσtt gtgagaagtg tggtgggaag tgtgσtcttg tcaggcacaa atttaaσagg 2041 σttσσtaggg tcctσattσt σαatttgaaa σgatatagσt tσaatgtggσ tσtσtσgσtt 2101 aacaataaga ttgggcagca agtcatσatt ccaagataσσ tgaσσσtgtσ atσtσattgσ 2161 actgaaaata caaaaccacσ ttttaccctt ggttggagtg cacatatggc aatttctaga 2221 σcattgaaag cσtαtcaaat ggtgaattcc tgcatcacσa gσσσttctac aσσttσaaag 2281 aaattcacσt tσaaatccaa gagctσσttg gctttatgcσ ttgattcaga cagtgaggat 2341 gagctaaaac gttctgtggc cctcagσσag agactttgtg aaatgttagg caacgaacag 2401 cagσaggaag aσσtggaaaa agattσaaaa ttatgσccaa tagagcctga caagtσtgaa 2461 ttggaaaact caggatttga cagaatgagc gaagaagagc ttαtagcagc tgtcttggag 2521 ataagtaaga gagatgcttc accatctctg agtcatgaag atgatgatga gccaaσtagc 2581 agccσagata σcggatttgc agaagatgat attcaagaaa tgσσagaaaa tσcagacact 2641 atggaaactg agaagcσcaa aacaatcaca gagctggatc ctgccagttt tactgagata 2701 aσtaaagaσt gtgatgagaa taaagaaaac aaaactσcag aaggatctca gggagaagtt 2761 gattggσtσσ agσagtatga tatggagσgt gaaagggaag agσaagagσt tσagσaggσa 2821 σtggctcaga gccttcaaga gcaagaggct tgggaaσaga aagaagatga tgaσσtσaaa 2881 agagctacσg agttaagtσt tσaagagttt aaαaaαtσσt ttgtggatgc attgggttct 2941 gatgaggact ctggaaatga ggatgttttt gatatggagt aσacagaagc tgaagσtgag 3001 gaaσtgaaaa gaaatgctga gacaggaaat ctgcctσatt σgtaccggσt σatσagtgtt 3061 gtcagtcaσa ttggtagcac ttσttcttca gatcattaca ttagtgatgt atatgaσatt 3121 aagaagcaag cgtggtttac ttacaatgac ctggaggtat caaaaatcca agaggctgcσ 3181 gtgσagagtg atσgagatcg gagtggctac atcttctttt atatgσaσaa ggagatσttt 3241 gatgagctgc tggaaaσaga aaagaactct cagtcactta gσaσggaagt ggggaagact 3301 acccgtσagg σσtσgtgagg aacaaactcσ tgggttggσa gσatgσaσtg σatatttgtt 3361 actgctgσσσ aσσtσaσctt tcσtσtgσtg aaggagaatt tggaattσta σttgatgcgg 3421 gagcaacaaa σagσtcaggg ccaaaccaaa agacaaaaat tggagtaacg tagaatgσtσ 3481 σatgσtattt tatggaaact ttggtctcaσ atσcgtagct gattatcctσ tttttσtσσt 3541 atgagtggσa cttcttttgt σttaggaata catgttgtaa atatatatct gtgtatgtgt 3601 gtataσaσaσ aσaσagacac acacaαaσaσ aσacgggatg aatggagcct taaagagtta 3661 ggatgagcαa ccagaatatg σctgctσaaa attaatagσa σagcagtttg gagaagaaat 3721 gaaggtgtca aagagtccat tcaσσtgaga aatgtgtgaa gaσatactta tcagttggct 3781 tttagσtttt atgttccttg agtagtttσa ctcaagtσtg taaσσttttg tgttσσttat 3841 tagtaaaatt cactggaaag σcagctcttc atgttacaσt aatgacagtt tgttctcttt 3901 gcaagagagg ggσattactg tσaσσtgact tgaggagctg ttttgttgtt gttgttgtσt 3961 gσaaatttca tgaatttgtg atgtctttgσ tgtttaσatg σagtcσcaag aaatggattg 4021 ttggtgcttt ggaatatgtt acagtσσσaσ atttgatatt tσttatataσ tttgttttct 4081 ctaaggagat ttσttcacac agtatgttca tcatatatca tcatσattat tatggtggta 4141 aagatagaat σttttttctt ttttgtcatt ctgccatgga gcagcattaσ cctaatggat 4201 tgσaaσσaaa aσtttaaaca agtagaaaga taatatttct σcaattggga ctcσccagαa 4261 ggaatactta gggataagga agaatgctag catctctgtσ tσtcaaacat agggaggata 4321 agaagagtgt tcttctggta aagctaaaat tctggaσcac tgaagσtaaa agccctattg 4381 σaagtatgaa attaagtaσt tgagctatag gacaaaσσtt gggcatttaa ccatttactg 4441 tσtggσtttg σσcttaaaat agggttgcaa ttaaaatgtg attggσttag gtaatσσcaa 4501 aaactaaσaa ataaσaaagg tgαataattt atttatctac tttttaggtg ctctgagttg 4561 aggσaaagta gagσggσaaσ attaagtgσt atgctagtca cttagctgaσ gtaaσσagσt 4621 tggttaagσa gσttatgaaa σcatataaag aattcttttg aggatggaat tσtgtccaca 4681 aaataatttt gtgagcccag atatcattag gatcacacag agttaaatat agaaaaatga 4741 aacαatcatt atattctttc gtgttttttc ttttattata aacaagggga ttattσttta 4801 gttσtσagag gtagggacaa aaccacatca ggttttσaga aggaaaaaac atttaaaaac 4861 ccacσatcac atgagagaat σacttgaacσ σaggaggcag aggttgcagt gagσtgagat 4921 cgcatcattg cactgσagtc tgagtgacag agtgagaσtc catctcatta aaaaaaacga 4981 aaacaaaaac aaaaaaaaca σaaaσcatσa tcacagaaga tgcaacatct tttctgaaag 5041 attgccttaa gagagctcca gtσctactct tggaaσttgg atgtattσta atgtagtaaa 5101 ctattctaag ttttcattct ttgaattata aatggσσtca gcagttttgc tcaactactg 5161 ataaatgσtt tgcctcctac σatctaccta tatacσttat tgtaatgaat gttσcaaaat 5221 ggtagagtgg tagaaaacgc cagagtagtt tagagcagag gaaaatattt gttttaaaac 5281 tagσtttaaa gttttgtttσ atttctacca ggagcctctt tggtttggtt tgattttgct 5341 tggaaataat tggttttctt ataaatgagt gaagcggtga taaaattctt tggctagtta 5401 ttaattσttt taσgtgtσtt tgσatttgag aggσaαtgtt aaaaattatt gggaaagatt 5461 taaagtgσag gσtgcaatta aaacatggag aaaagtagaa ataatgccat aagtctagat 5521 tgσctcatga agcagαctca tttgaattgc tttσatagct ttcatgtgtg tatggtttag 5581 aagtacactt acctcagaaa cctgatttga tcttcatgtc ttgggσagga gttgttgaaa 5641 ataggttatt ggaatatata agttatctca ctgσtcatgt aσttgσatgt ttgggactca 5701 aattttactt gatgtctgtc cattcttgtg gccctatcag ccttctσctt cctttactcσ 5761 tttaatσtac ttctttgact accagtggag atttcagctg gactatgttg atggggtttg 5821 ttgttgtttt tgagctggct gtatatattt taaaattata aatagataat atattatttt 5881 ttgcacattg tgatcagttt gcσσagaatt ggggatgggg σagttagαat gttggggσσa 5941 ggaagggaσa agttagataa ggactgagtg cttcσgttgσ aggcagtttg cacaatacσt 6001 aattaacctt cctattgaaa ataccaaatg tgtggttaca ttactttaaa tgaσattgaa 6061 ttggaaσttg atggcaatta gttctagata caacσttttg atσtttgttg gaattttaag 6121 ggaaaaatga aσtaaaσttσ atatttgttg attttaatca cctaatagta ctgaaggttg 6181 gaaagttgσa tgtggσtgga tgσtgttaat ttσtttaata gσσatgaσta taatttaagσ 6241 σtatgagaag atagaσtgtt tcgtagggat atatttacat gtgtgtgαaσ aσtσatgagt 6301 tttgtσtσag σaggatagaa taagcaaatc catgaactgg tcttctatta atactttgat 6361 tctaaaaatt atttgtttac ttgctatggt ctgttσattσ tgggcctaac σσtaaaggσt 6421 σaataacaaa tacaaσaaat gtaaatatgt ttacatttta agacatatgσ agtggttσtt 6481 acagatcagt taattaactc cagaaagcaa atgttagaσt acacatttat ttttσtcσtt 6541 gatσaagtgt aaaattctga aaσagaggσt ttaaaattta aaaσσtcagσ aaaataatσc 6601 atgaatttac tgattcttct gtatcgtgtg tagttaccat tatgtaaσta taσaσacata 6661 cagσtatgga tatagttgta taatgaaaat tatσtgcaaa cacctaaatt aaagagaaaa 6721 aaaagtagtt tgtaaactca tttgtgatσt actgaaaaga ggttatatta aagcaaatta 6781 aaatattttc σttσtσtgtσ σtσtgaaatg aσtgσagtag ataσtαttag ttatcccatt 6841 tagggtggtt ggagggcctt tttaatttaa ttgaccccσσ gaggtggtσt tttgttttaa 6901 aσagggggσa aσagctggat ctccaagtac atatggattt tgtatatata ggagattttt 6961 agaaaaatca aσaaσσtaaσ aσσagattσa agtσaσataa aagtgttσca ataaaatgga 7021 tggatgtctt tttσσtcσσσ attttgcttt ataσtgagta atgcactσtt gcaagtgtat 7081 acaaaaacta aatagacttc tgccctccaa catcttttta ttgcattact tcaaaatcct 7141 aattttgtct ctactgatat gtcttattaa catctgaaaa aatatatatt ttttattgga 7201 aaattctaat ttgttaggσσ ttgaaagttt tgtgaσaatt attttgctgt gtttaacσaσ 7261 aatσattcac cttatggσat gctttgatta σtagaσttca ggcagtσtca ttcattgtat 7321 σataσttaσa σaσaattagt aagttgtσtc catgtgtgct atatgtctga ggtgtatgga 7381 gtttttattt aaaaagtgtg σcagtctgaa tataagσatt tgattttgta acattggact 7441 tttcttaaaa gtaσagaggt tσaaagtata ggtatgtσσa ttggcataag aatagagtgg 7501 gtgagggtct ggaccaggtt σcaggttggt ccagtcagat gσcagaacaa agaagaaσag 7561 tcaactaaaσ tggtσtactt caaaaatagt gggcctgtgt gaagaatgag aσσaσatgtg 7621 ggtgtgcaσa σσtσttgtσσ σcaggtttcσ σtσσσtttga gσttttσttt σσctcσctaa 7681 cttctctggσ σtattgtσat tgttgtttσt ttaaacttaa ggagagaaaa acaaaaatga 7741 gattcctaca σtttgσσtaa ttgagσσaσt aσcaggtttt ctggcagσtg tggccaσatt 7801 atttgtgaga tgattttttt tσtttatgtt σagagtgaσt tttgattctg attctttatg 7861 ttttgtatgg agcggσactt ttatctgtgt tttagcagaa ctgttcctct gtatσσttta 7921 cggtttttct ttgtttttgt ttccttttta aattatgcat agagtttttt tgtgtgtatg 7981 aaattaaagc σtttattaac cttσaaaaaa aaaaa
SEQ ID NO: 23 ubiquitin hydrolase
AB046814 Homo sapiens mRNA for KIAA1594 protein, partial σds gi 110047262 I dbj |AB046814.l| [10047262] 1 caaggatatt tcagctaagt cataacatta aaaatgtggt gσttcgaccσ agtggagσga 61 aacaaagcσg cctaatgtta actctgσaag ataaσagσtt σttgtσtatt gacaaagtac 121 σaagtaagga tgcagaggaa atgaggttgt ttctagatgc agtcσatσaa aacagacttc 181 ctgcag'σσat gaaaσcgtct σaggggtσtg gtagttttgg agccattctg ggcagcagga 241 cσtσaσagaa ggaaaccagσ aggcagcttt cttactcaga caatcaggct tctgcaaaaa 301 gaggaagttt ggaaactaaa gatgatattc catttcgaaa agttσttggt aatσσgggta 361 gaggatcgat taagactgta gcaggaagtg gaatagctσg gacgattcσt tσtttgacat 421 ctacttcaaσ aαctcttaga tcagggttgσ tagaaaatcg tactgaaaag aggaaaagaa 481 tgatatcaac tggσtcagaa ttgaatgaag attaccctaa ggaaaatgat tcatcatσga 541 aσaaσaaggc catgacagat ccctσσagaa agtatttaac cagcagtaga gaaaagcagc 601 tgagtttgaa aσagtcagaa gagaatagga catcagggct tttacσttta cagtcatσat 661 ccttttatgg tagcagagct ggatccaagg aacaσtσttc tggtggcact aacttagaca 721 ggactaatgt ttcaagcσag actccctσtg ccaaaagaag tttgggattt cttcσtσagc 781 cagttcσtσt ttctgttaaa aaactgaggt gtaaccagga ttacaσtggσ tggaataaaσ 841 σaagagtgcc ασtttcctct caσσaaσagσ agσaaσtgca gggcttctcσ aatttgggaa 901 ataσσtgσta tatgaatgct attctaαaat ctctattttc actccagtσa tttgσaaatg 961 aσttgcttaa acaaggtatσ σcatggaaga aaattccaσt σaatgαactt atcagaσgσt 1021 ttgσacactt gσttgttaaa aaagatatct gtaattcaga gacσaaaaag gatttaαtσa 1081 agaaggttaa aaatgccatt tcagctacag cagagagatt ctσtggttat atgσagaatg 1141 atgσtσatga atttttaagt σagtgtttgg aασagαtgaa agaagatatg gaaaaattaa 1201 ataaaaσttg gaagactgaa cσtgtttσtg gagaagaaaa ttσaσσagat atttcagcta 1261 σcagagcata cacttgccct gttattacta atttggagtt tgaggttσag cactccatca 1321 tttgtaaagc atgtggagag attatcσσca aaagagaaca gtttaatgac ctctctattg 1381 accttcctcg taggaaaaaa σσaσtccσtσ ctcgttcaat tcaagattct cttgatσttt 1441 tctttagggc σgaagaactg gagtattctt gtgagaagtg tggtgggaag tgtgctcttg 1501 tσaggσaσaa atttaaσagg cttcσtaggg tσctcattσt σcatttgaaa cgatatagct 1561 tcaatgtggα tctctcgσtt aaσaataaga ttgggσagσa agtcatcatt ccaagatacc 1621 tgaccσtgtc atctcattgσ aσtgaaaata caaaaccacc ttttacσσtt ggttggagtg 1681 σacatatggc aatttctaga σσattgaaag cctσtσaaat ggtgaattσσ tgcatcacσa 1741 gσσσttctac accttcaaag aaattcaσσt tσaaatccaa gagσtccttg gctttatgcσ 1801 ttgattcaga cagtgaggat gagctaaaac gttctgtggc cctcagσσag agactttgtg 1861 aaatgttagg caacgaacag cagcaggaag acσtggaaaa .agattσaaaa ttatgσσσaa 1921 tagagσctga caagtσtgaa ttggaaaaσt caggatttga cagaatgagc gaagaagagc 1981 ttctagcagc tgtcttggag ataagtaaga gagatgcttc aσcatctαtg agtσatgaag 2041 atgatgataa gσσaactagc agcccagata ccggatttgc agaagatgat attσaagaaa 2101 tgσcagaaaa tccagaσaσt atggaaaσtg agaagασcaa aacaatαaσa gagσtggatc 2161 ctgσcagttt tactgagata actaaagaσt gtgatgagaa taaagaaaaσ aaaactcσag 2221 aaggatσtca gggagaagtt gattggctcc agcagtatga tatggagσgt gaaagggaag 2281 agσaagagct tcagσaggσa σtggctcaga gcσttσaaga gσaagaggσt tgggaaσaga 2341 aagaagatga tgaσσtcaaa agagctaσcg agttaagtct tσaagagttt aaσaaσtσσt 2401 ttgtggatgc attgggttσt gatgaggaσt σtggaaatga ggatgttttt gatatggagt 2461 acacagaagc tgaagctgag gaactgaaaa gaaatgctga gacaggaaat ctgcctcatt 2521 σgtaσσggct catcagtgtt gtσagtcaca ttggtagcac ttcttcttca ggtcattaca 2581 ttagtgatgt atatgaσatt aagaagcaag cgtggtttac ttacaatgac ctggaggtat 2641 σaaaaatσca agaggctgcc gtgcagagtg atcgagatcg gagtggσtaα atσttσtttt 2701 atatgσacaa ggagatcttt gatgagctgc tggaaacaga aaagaactct cagtcactta 2761 gαaσggaagt ggggaagaσt aσσcgtcagg cctcgtgagg aaσaaaσtσc tgggttggca 2821 gσatgcactg σatatttgtt aσtgσtgσσc acctcacctt tσσtσtgσtg aaggagaatt 2881 tggaattcta cttgatgcgg gagcaacaaa cagctcaggg ccaaaσcaaa agacaaaaat 2941 tggagtaacg tagaatgctc catgσtattt tatggaaaαt ttggtσtσac atcσgtagct 3001 gattatcσtc tttttctcσt atgagtggσa σttσttttgt σttaggaata σatgttgtaa 3061 atatatatσt gtgtatgtgt gtatacacac acacagaσac acacacaσac acacgggatg 3121 aatggagcct taaagagtta ggatgagcσa ccagaatatg cctgσtσaaa attaatagσa 3181 σagcagtttg gagaagaaat gaaggtgtca aagagtσσat tcacctgaga aatgtgtgaa 3241 gacatactta tcagttggσt tttagσtttt atgttσcttg agtagtttca σtσaagtctg 3301 taaccttttg tgtttcctta ttagtaaaat tcactggaaa gccagσtσtt σatgttaσaσ 3361 taatgaσagt ttgttσtσtt tgcaagagag gggcattact gtcacctgaσ ttgaggagσt 3421 gttttgttgt tgttgttgtc tgcaaatttσ atgaatttgt gatgtσtttg σtgtttaσat 3481 gσagtσσcaa gaaatggatt gttggtgctt tggaatatgt tacagtccca catttgatat 3541 ttσttatata σtttgttttσ tctaaggaga tttcttcaca σagtatgttc atcatatatc 3601 atσatσatta ttatggtggt aaagatagaa tcttttttct tttttgtcat tctgσcatgg 3661 agcagcatta σσσtaatgga ttgcaaσcaa aaσtttaaac aagtagaaag ataatatttc 3721 tccaattggg actccccagc aggaatactt agggataagg aagaatgcta gσatctctgt 3781 σtσtσaaaσa tagggaggat aagaagagtg ttσttσtggt aaagσtaaaa ttctggacca 3841 ctgaagctaa aagccctatt gcaagtatga aattaagtaσ ttgagσtata ggaσaaaσσt 3901 tgggσattta aσσatttact gtctggcttt gcccttaaaa tagggttgca attaaaatgt 3961 gattggσtta ggtaatσcca aaaactaaca aataacaaag gtgcataatt tatttatcta 4021 σtttttaggt gσtctgagtt gaggcaaagt agagσggcaa cattaagtgc tatgctagtc 4081 aσttagσtga cgtaaccagσ ttggttaagc agcttatgaa aσσatataaa gaattσtttt 4141 gaggatggaa ttσtgtσσaσ aaaataattt tgtgagσσσa gatatσatta ggatσaσaσa 4201 gagttaaata tagaaaaatg aaaσσatσat tatattσttt αgtgtttttt cttttattat 4261 aaacaagggg attattσttt agttctcaga ggtagggaca aaaccacatc aggttttcag 4321 aaggaaaaaa σatttaaaaa cccacσatca catgagagaa tσaσttgaac cσaggaggσa 4381 gaggttgσag tgagctgaga tcgcatcatt gcactgσagt σtgagtgaσa gagtgagaσt 4441 σσatctcatt

Claims

WHAT IS CLAIMED IS: 1. A method for identifying a compound that modulates angiogenesis, the method comprising the steps of: (i) contacting the compound with an angiogenesis polypeptide selected from the group consisting ofubiquitin hydrolase (USP37), calcium/calmodulin-dependent protein kinase β (CAMKK2), methionine adenosyltransferase II α (Mat2A), camitine palmitoyltransferase II (CPT-2), DDX5 RNA helicase, acetyl-coenzyme A acyltransferase (ACAAl), glucosamine-6-phosphate isomerase (GNPI), 24- dehydrocholesterol reductase (DHCR24), selenoprotein T (SELT), protein tyrosine phosphatase, receptor type, B (PTPRB), glucosidase β acid (GBA), UDP-N- acteylglucosamine pyrophosphorylase 1 (UAPl), mitochondrial ribosomal protein L30 (MRPL30), chaperonin containing TCP 1 , subunit 3 γ (CCT3), HSP A8, solute carrier family 16 (monocarboxylic acid transporters), and member 1 (SLC16A1), SH2 of Abl; and (ii) determining the functional effect ofthe compound upon the angiogenesis polypeptide.
2. The method of claim 1 , wherein the functional effect is determined in vitro.
3. The method of claim 2, wherein the functional effect is a physical effect.
4. The method of claim 2, wherein the functional effect is determined by measuring ligand binding to the polypeptide.
5. The method ofclaim 2, wherein the functional effect is a chemical effect.
6. The method of claim 1 , wherein the polypeptide is expressed in a eukaryotic host cell.
7. The method of claim 6, wherein the functional effect is a physical effect.
8. The method of claim 7, wherein the functional effect is determined by measuring ligand binding to the polypeptide.
9. The method of claim 1 , wherein the functional effect is a chemical or phenotypic effect.
10. The method ofclaim 10, wherein the polypeptide is expressed in a eukaryotic host cell.
11. The method of claim 10, wherein the host cell is an endothelial cell.
12. The method of claim 11 , wherein the functional effect is determined by measuring VEGF-R2 surface expression, avβ3 expression, or haptotaxis.
13. The method of claim 1 , wherein modulation is inhibition of angiogenesis.
14. The method of claim 1, wherein the polypeptide is recombinant.
15 . The method ofclaim 1, wherein the compound is an antibody.
16 . The method ofclaim 1, wherein the compound is an antisense molecule.
17 . The method of claim 1 , wherein the compound is an RNAi molecule.
18 . The method of claim 1, wherein the compound is a small organic molecule.
19 . A method for identifying a compound that modulates angiogenesis, the method comprising the steps of: (i) contacting the compound with an angiogenesis polypeptide selected from the group consisting ofubiquitin hydrolase (USP37), calcium/calmodulin-dependent protein kinase β (CAMK 2), methionine adenosyltransferase α (Mat2A), camitine palmitoyltransferase II (CPT-2), DDX5 RNA helicase, acetyl-coenzyme A acyltransferase (ACAAl), glucosamine-6-phosphate isomerase (GNPI), 24- dehydrocholesterol reductase (DHCR24), selenoprotein T (SELT), protein tyrosine phosphatase, receptor type, B (PTPRB), glucosidase β acid (GBA), UDP-N- acteylglucosamine pyrophosphorylase 1 (UAPl), mitochondrial ribosomal protein L30 (MRPL30), chaperonin containing TCP 1 , subunit 3 γ (CCT3), HSPA8, solute carrier family 16 (monocarboxylic acid transporters), and member 1 (SLC16A1), SH2 of Abl; (ii) determining the physical effect of the compound upon the target polypeptide or fragment thereof or inactive variant thereof; and (iii) determining the chemical or phenotypic effect ofthe compound upon a cell compnsing the target polypeptide or fragment thereof or inactive variant thereof, thereby identifying a compound that modulates cell cycle aπest.
20. A method of modulating angiogenesis in a subject, the method comprising the step of administering to the subject a therapeutically effective amount of a compound identified using the method of claim 1.
21. The method ofclaim 20, wherein the subject is a human.
22. The method of claim 20, wherein the compound is an antibody.
23. The method of claim 20, wherein the compound is an antisense molecule.
24. The method of claim 20, wherein the compound is an RNAi molecule.
25. The method ofclaim 20, wherein the compound is a small organic molecule.
26. The method of claim 20, wherein the compound inhibits angiogenesis.
PCT/US2005/001194 2004-01-13 2005-01-13 Modulators of angiogenesis WO2005069855A2 (en)

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US8207185B2 (en) 2006-10-12 2012-06-26 Duke University CaMKKβ as a target for treating obesity
US8741581B2 (en) 2009-04-27 2014-06-03 Technion Research And Development Foundation Ltd. Markers for cancer detection
WO2011008641A1 (en) 2009-07-13 2011-01-20 Beth Israel Deaconess Medical Center, Inc. Methids of modulating angiogenesis and treatment of angiogenesis-related diseases
EP2606130B1 (en) 2010-08-16 2019-03-13 Duke University Camkk-beta as a marker in prostate cancer
EP2654793B1 (en) 2010-12-21 2017-09-13 Leidos, Inc. Methods and compositions for wound treatment
US20240325506A1 (en) * 2021-06-23 2024-10-03 Avrobio, Inc. Compositions and methods for treatment of gaucher disease

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EP1204764A2 (en) * 1999-08-11 2002-05-15 EOS Biotechnology, Inc. Methods of screening for angiogenesis modulators
CA2389751A1 (en) 1999-11-01 2001-05-10 Curagen Corporation Differentially expressed genes involved in angiogenesis, the polypeptides encoded thereby, and methods of using the same
EP1418943A1 (en) 2001-02-14 2004-05-19 Protein Design Labs, Inc. Methods of diagnosis of angiogenesis, compositions and methods of screening for angiogenesis modulators
US20030232400A1 (en) * 2002-12-20 2003-12-18 Susan Radka Methods of screening subjects for expression of soluble receptors of vascular endothelial growth factor (VEGF) for use in managing treatment and determining prognostic outcome

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