US20020110889A1 - Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof - Google Patents
Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof Download PDFInfo
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- US20020110889A1 US20020110889A1 US09/749,588 US74958800A US2002110889A1 US 20020110889 A1 US20020110889 A1 US 20020110889A1 US 74958800 A US74958800 A US 74958800A US 2002110889 A1 US2002110889 A1 US 2002110889A1
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- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/12—Transferases (2.) transferring phosphorus containing groups, e.g. kinases (2.7)
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- C—CHEMISTRY; METALLURGY
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- C12Y—ENZYMES
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- C12Y207/11—Protein-serine/threonine kinases (2.7.11)
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- A—HUMAN NECESSITIES
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- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
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- A61K38/00—Medicinal preparations containing peptides
Definitions
- the present invention is in the field of kinase proteins that are related to the homeodomain-interacting protein kinase subfamily, recombinant DNA molecules, and protein production.
- the present invention specifically provides novel peptides and proteins that effect protein phosphorylation and nucleic acid molecules encoding such peptide and protein molecules, all of which are useful in the development of human therapeutics and diagnostic compositions and methods.
- kinases regulate many different cell proliferation, differentiation, and signaling processes by adding phosphate groups to proteins. Uncontrolled signaling has been implicated in a variety of disease conditions including inflammation, cancer, arteriosclerosis, and psoriasis. Reversible protein phosphorylation is the main strategy for controlling activities of eukaryotic cells. It is estimated that more than 1000 of the 10,000 proteins active in a typical mammalian cell are phosphorylated.
- the high energy phosphate which drives activation, is generally transferred from adenosine triphosphate molecules (ATP) to a particular protein by protein kinases and removed from that protein by protein phosphatases.
- ATP adenosine triphosphate molecules
- Phosphorylation occurs in response to extracellular signals (hormones, neurotransmitters, growth and differentiation factors, etc), cell cycle checkpoints, and environmental or nutritional stresses and is roughly analogous to turning on a molecular switch.
- the appropriate protein kinase activates a metabolic enzyme, regulatory protein, receptor, cytoskeletal protein, ion channel or pump, or transcription factor.
- the kinases comprise the largest known protein group, a superfamily of enzymes with widely varied functions and specificities. They are usually named after their substrate, their regulatory molecules, or some aspect of a mutant phenotype. With regard to substrates, the protein kinases may be roughly divided into two groups; those that phosphorylate tyrosine residues (protein tyrosine kinases, PTK) and those that phosphorylate serine or threonine residues (serine/threonine kinases, STK). A few protein kinases have dual specificity and phosphorylate threonine and tyrosine residues. Almost all kinases contain a similar 250-300 amino acid catalytic domain.
- the N-terminal domain which contains subdomains I-IV, generally folds into a two-lobed structure, which binds and orients the ATP (or GTP) donor molecule.
- the larger C terminal lobe which contains subdomains VI A-XI, binds the protein substrate and carries out the transfer of the gamma phosphate from ATP to the hydroxyl group of a serine, threonine, or tyrosine residue.
- Subdomain V spans the two lobes.
- the kinases may be categorized into families by the different amino acid sequences (generally between 5 and 100 residues) located on either side of, or inserted into loops of, the kinase domain. These added amino acid sequences allow the regulation of each kinase as it recognizes and interacts with its target protein.
- the primary structure of the kinase domains is conserved and can be further subdivided into 11 subdomains. Each of the 11 subdomains contains specific residues and motifs or patterns of amino acids that are characteristic of that subdomain and are highly conserved (Hardie, G. and Hanks, S. (1995) The Protein Kinase Facts Books, Vol I:7-20 Academic Press, San Diego, Calif.).
- the second messenger dependent protein kinases primarily mediate the effects of second messengers such as cyclic AMP (cAMP), cyclic GMP, inositol triphosphate, phosphatidylinositol, 3, 4, 5-triphosphate, cyclic-ADPribose, arachidonic acid, diacylglycerol and calcium-calmodulin.
- cyclic AMP cyclic AMP
- GMP cyclic GMP
- inositol triphosphate phosphatidylinositol
- phosphatidylinositol 3, 4, 5-triphosphate
- cyclic-ADPribose cyclic-ADPribose
- arachidonic acid diacylglycerol
- calcium-calmodulin calcium-calmodulin.
- the cyclic-AMP dependent protein kinases (PKA) are important members of the STK family. Cyclic-AMP is an intracellular mediator of hormone action in all prokaryotic
- Such hormone-induced cellular responses include thyroid hormone secretion, cortisol secretion, progesterone secretion, glycogen breakdown, bone resorption, and regulation of heart rate and force of heart muscle contraction.
- PKA is found in all animal cells and is thought to account for the effects of cyclic-AMP in most of these cells. Altered PKA expression is implicated in a variety of disorders and diseases including cancer, thyroid disorders, diabetes, atherosclerosis, and cardiovascular disease (Isselbacher, K. J. et al. (1994) Harrison's Principles of Internal Medicine, McGraw-Hill, New York, N.Y., pp. 416-431, 1887).
- CaM dependent protein kinases are also members of STK family. Calmodulin is a calcium receptor that mediates many calcium regulated processes by binding to target proteins in response to the binding of calcium. The principle target protein in these processes is CaM dependent protein kinases. CaM-kinases are involved in regulation of smooth muscle contraction (MLC kinase), glycogen breakdown (phosphorylase kinase), and neurotransmission (CaM kinase I and CaM kinase II).
- MLC kinase smooth muscle contraction
- phosphorylase kinase glycogen breakdown
- CaM kinase II neurotransmission
- CaM kinase I phosphorylates a variety of substrates including the neurotransmitter related proteins synapsin I and II, the gene transcription regulator, CREB, and the cystic fibrosis conductance regulator protein, CFTR (Haribabu, B. et al. (1995) EMBO Journal 14:3679-86).
- CaM II kinase also phosphorylates synapsin at different sites, and controls the synthesis of catecholamines in the brain through phosphorylation and activation of tyrosine hydroxylase. Many of the CaM kinases are activated by phosphorylation in addition to binding to CaM.
- the kinase may autophosphorylate itself, or be phosphorylated by another kinase as part of a “kinase cascade”.
- AMPK 5′-AMP-activated protein kinase
- Mammalian AMPK is a regulator of fatty acid and sterol synthesis through phosphorylation of the enzymes acetyl-CoA carboxylase and hydroxymethylglutaryl-CoA reductase and mediates responses of these pathways to cellular stresses such as heat shock and depletion of glucose and ATP.
- AMPK is a heterotrimeric complex comprised of a catalytic alpha subunit and two non-catalytic beta and gamma subunits that are believed to regulate the activity of the alpha subunit.
- Subunits of AMPK have a much wider distribution in non-lipogenic tissues such as brain, heart, spleen, and lung than expected. This distribution suggests that its role may extend beyond regulation of lipid metabolism alone.
- MAP kinases are also members of the STK family. MAP kinases also regulate intracellular signaling pathways. They mediate signal transduction from the cell surface to the nucleus via phosphorylation cascades. Several subgroups have been identified, and each manifests different substrate specificities and responds to distinct extracellular stimuli (Egan, S. E. and Weinberg, R. A. (1993) Nature 365:781-783). MAP kinase signaling pathways are present in mammalian cells as well as in yeast.
- the extracellular stimuli that activate mammalian pathways include epidermal growth factor (EGF), ultraviolet light, hyperosmolar medium, heat shock, endotoxic lipopolysaccharide (LPS), and pro-inflammatory cytokines such as tumor necrosis factor (TNF) and interleukin-1 (IL-1).
- EGF epidermal growth factor
- UV light ultraviolet light
- hyperosmolar medium hyperosmolar medium
- heat shock endotoxic lipopolysaccharide
- pro-inflammatory cytokines such as tumor necrosis factor (TNF) and interleukin-1 (IL-1).
- TNF tumor necrosis factor
- IL-1 interleukin-1
- PRK proliferation-related kinase
- PRK proliferation-related kinase
- PRK is a serum/cytokine inducible STK that is involved in regulation of the cell cycle and cell proliferation in human megakaroytic cells (Li, B. et al. (1996) J. Biol. Chem. 271:19402-8).
- PRK is related to the polo (derived from humans polo gene) family of STKs implicated in cell division.
- PRK is downregulated in lung tumor tissue and may be a proto-oncogene whose deregulated expression in normal tissue leads to oncogenic transformation.
- Altered MAP kinase expression is implicated in a variety of disease conditions including cancer, inflammation, immune disorders, and disorders affecting growth and development.
- CDKs The cyclin-dependent protein kinases
- Cyclins are small regulatory proteins that act by binding to and activating CDKs that then trigger various phases of the cell cycle by phosphorylating and activating selected proteins involved in the mitotic process.
- CDKs are unique in that they require multiple inputs to become activated.
- CDK activation requires the phosphorylation of a specific threonine residue and the dephosphorylation of a specific tyrosine residue.
- Protein tyrosine kinases specifically phosphorylate tyrosine residues on their target proteins and may be divided into transmembrane, receptor PTKs and nontransmembrane, non-receptor PTKs.
- Transmembrane protein-tyrosine kinases are receptors for most growth factors. Binding of growth factor to the receptor activates the transfer of a phosphate group from ATP to selected tyrosine side chains of the receptor and other specific proteins.
- Growth factors (GF) associated with receptor PTKs include; epidermal GF, platelet-derived GF, fibroblast GF, hepatocyte GF, insulin and insulin-like GFs, nerve GF, vascular endothelial GF, and macrophage colony stimulating factor.
- Non-receptor PTKs lack transmembrane regions and, instead, form complexes with the intracellular regions of cell surface receptors.
- Such receptors that function through non-receptor PTKs include those for cytokines, hormones (growth hormone and prolactin) and antigen-specific receptors on T and B lymphocytes.
- PTKs were first identified as the products of mutant oncogenes in cancer cells where their activation was no longer subject to normal cellular controls.
- oncogenes encode PTKs, and it is well known that cellular transformation (oncogenesis) is often accompanied by increased tyrosine phosphorylation activity (Carbonneau H and Tonks N K (1992) Annu. Rev. Cell. Biol. 8:463-93). Regulation of PTK activity may therefore be an important strategy in controlling some types of cancer.
- the novel human protein, and encoding gene, provided by the present invention is related to the family of homeodomain-interacting protein kinases (HIPKs).
- HIPKs are nuclear kinases that act as transcriptional co-repressors for homeodomain transcription factors. HIPKs enhance the repressor functions of NK homeoproteins.
- the HIPK family comprises at least three previously described members: HIPK1, HIPK2, and HIPK3.
- HIPKs comprise a conserved protein kinase domain and a separate homeoprotein/homeodomain interaction domain.
- HIPK2 has been found to significantly increase the DNA binding activity of the NK-3 homeoprotein (Kim et al., J Biol Chem Oct. 2, 1998;273(40):25875-9).
- HIPKs show a high degree of similarity to yeast YAK1 proteins, human PKY (protein kinase YAK1 homolog), and Myak (mouse YAK homolog) proteins, which play important roles in cellular regulation and signaling, multidrug resistance, and in restricting cell growth.
- yeast YAK1 proteins protein kinase YAK1 homolog
- Myak mouse YAK homolog
- Kinase proteins particularly members of the homeodomain-interacting protein kinase subfamily, are a major target for drug action and development. Accordingly, it is valuable to the field of pharmaceutical development to identify and characterize previously unknown members of this subfamily of kinase proteins.
- the present invention advances the state of the art by providing previously unidentified human kinase proteins that have homology to members of the homeodomain-interacting protein kinase subfamily.
- the present invention is based in part on the identification of amino acid sequences of human kinase peptides and proteins that are related to the homeodomain-interacting protein kinase subfamily, as well as allelic variants and other mammalian orthologs thereof. These unique peptide sequences, and nucleic acid sequences that encode these peptides, can be used as models for the development of human therapeutic targets, aid in the identification of therapeutic proteins, and serve as targets for the development of human therapeutic agents that modulate kinase activity in cells and tissues that express the kinase. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- FIG. 1 provides the nucleotide sequence of a CDNA molecule that encodes the kinase protein of the present invention. (SEQ ID NO:1)
- structure and functional information is provided, such as ATG start, stop and tissue distribution, where available, that allows one to readily determine specific uses of inventions based on this molecular sequence.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- FIG. 2 provides the predicted amino acid sequence of the kinase of the present invention. (SEQ ID NO:2) In addition structure and functional information such as protein family, function, and modification sites is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence.
- FIG. 3 provides genomic sequences that span the gene encoding the kinase protein of the present invention.
- SEQ ID NO:3 structure and functional information, such as intron/exon structure, promoter location, etc., is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence.
- SNPs were identified: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at position 14131.
- the present invention is based on the sequencing of the human genome.
- analysis of the sequence information revealed previously unidentified fragments of the human genome that encode peptides that share structural and/or sequence homology to protein/peptide/domains identified and characterized within the art as being a kinase protein or part of a kinase protein and are related to the homeodomain-interacting protein kinase subfamily. Utilizing these sequences, additional genomic sequences were assembled and transcript and/or cDNA sequences were isolated and characterized.
- the present invention provides amino acid sequences of human kinase peptides and proteins that are related to the homeodomain-interacting protein kinase subfamily, nucleic acid sequences in the form of transcript sequences, cDNA sequences and/or genomic sequences that encode these kinase peptides and proteins, nucleic acid variation (allelic information), tissue distribution of expression, and information about the closest art known protein/peptide/domain that has structural or sequence homology to the kinase of the present invention.
- the peptides that are provided in the present invention are selected based on their ability to be used for the development of commercially important products and services. Specifically, the present peptides are selected based on homology and/or structural relatedness to known kinase proteins of the homeodomain-interacting protein kinase subfamily and the expression pattern observed. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. The art has clearly established the commercial importance of members of this family of proteins and proteins that have expression patterns similar to that of the present gene.
- the present invention provides nucleic acid sequences that encode protein molecules that have been identified as being members of the kinase family of proteins and are related to the homeodomain-interacting protein kinase subfamily (protein sequences are provided in FIG. 2, transcript/cDNA sequences are provided in FIG. 1 and genomic sequences are provided in FIG. 3).
- the peptide sequences provided in FIG. 2, as well as the obvious variants described herein, particularly allelic variants as identified herein and using the information in FIG. 3, will be referred herein as the kinase peptides of the present invention, kinase peptides, or peptides/proteins of the present invention.
- the present invention provides isolated peptide and protein molecules that consist of, consist essentially of, or comprise the amino acid sequences of the kinase peptides disclosed in the FIG. 2, (encoded by the nucleic acid molecule shown in FIG. 1, transcript/cDNA or FIG. 3, genomic sequence), as well as all obvious variants of these peptides that are within the art to make and use. Some of these variants are described in detail below.
- a peptide is said to be “isolated” or “purified” when it is substantially free of cellular material or free of chemical precursors or other chemicals.
- the peptides of the present invention can be purified to homogeneity or other degrees of purity. The level of purification will be based on the intended use. The critical feature is that the preparation allows for the desired function of the peptide, even if in the presence of considerable amounts of other components (the features of an isolated nucleic acid molecule is discussed below).
- substantially free of cellular material includes preparations of the peptide having less than about 30% (by dry weight) other proteins (i.e., contaminating protein), less than about 20% other proteins, less than about 10% other proteins, or less than about 5% other proteins.
- the peptide when it is recombinantly produced, it can also be substantially free of culture medium, i.e., culture medium represents less than about 20% of the volume of the protein preparation.
- the language “substantially free of chemical precursors or other chemicals” includes preparations of the peptide in which it is separated from chemical precursors or other chemicals that are involved in its synthesis. In one embodiment, the language “substantially free of chemical precursors or other chemicals” includes preparations of the kinase peptide having less than about 30% (by dry weight) chemical precursors or other chemicals, less than about 20% chemical precursors or other chemicals, less than about 10% chemical precursors or other chemicals, or less than about 5% chemical precursors or other chemicals.
- the isolated kinase peptide can be purified from cells that naturally express it, purified from cells that have been altered to express it (recombinant), or synthesized using known protein synthesis methods.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- a nucleic acid molecule encoding the kinase peptide is cloned into an expression vector, the expression vector introduced into a host cell and the protein expressed in the host cell.
- the protein can then be isolated from the cells by an appropriate purification scheme using standard protein purification techniques. Many of these techniques are described in detail below.
- the present invention provides proteins that consist of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3).
- the amino acid sequence of such a protein is provided in FIG. 2.
- a protein consists of an amino acid sequence when the amino acid sequence is the final amino acid sequence of the protein.
- the present invention further provides proteins that consist essentially of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3).
- a protein consists essentially of an amino acid sequence when such an amino acid sequence is present with only a few additional amino acid residues, for example from about 1 to about 100 or so additional residues, typically from 1 to about 20 additional residues in the final protein.
- the present invention further provides proteins that comprise the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3).
- a protein comprises an amino acid sequence when the amino acid sequence is at least part of the final amino acid sequence of the protein. In such a fashion, the protein can be only the peptide or have additional amino acid molecules, such as amino acid residues (contiguous encoded sequence) that are naturally associated with it or heterologous amino acid residues/peptide sequences. Such a protein can have a few additional amino acid residues or can comprise several hundred or more additional amino acids.
- the preferred classes of proteins that are comprised of the kinase peptides of the present invention are the naturally occurring mature proteins. A brief description of how various types of these proteins can be made/isolated is provided below.
- the kinase peptides of the present invention can be attached to heterologous sequences to form chimeric or fusion proteins.
- Such chimeric and fusion proteins comprise a kinase peptide operatively linked to a heterologous protein having an amino acid sequence not substantially homologous to the kinase peptide.
- “Operatively linked” indicates that the kinase peptide and the heterologous protein are fused in-frame.
- the heterologous protein can be fused to the N-terminus or C-terminus of the kinase peptide.
- the fusion protein does not affect the activity of the kinase peptide per se.
- the fusion protein can include, but is not limited to, enzymatic fusion proteins, for example beta-galactosidase fusions, yeast two-hybrid GAL fusions, poly-His fusions, MYC-tagged, HI-tagged and Ig fusions.
- Such fusion proteins, particularly poly-His fusions can facilitate the purification of recombinant kinase peptide.
- expression and/or secretion of a protein can be increased by using a heterologous signal sequence.
- a chimeric or fusion protein can be produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different protein sequences are ligated together in-frame in accordance with conventional techniques.
- the fusion gene can be synthesized by conventional techniques including automated DNA synthesizers. Alternatively, PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and re-amplified to generate a chimeric gene sequence (see Ausubel et al., Current Protocols in Molecular Biology, 1992).
- many expression vectors are commercially available that already encode a fusion moiety (e.g., a GST protein).
- a kinase peptide-encoding nucleic acid can be cloned into such an expression vector such that the fusion moiety is linked in-frame to the kinase peptide.
- the present invention also provides and enables obvious variants of the amino acid sequence of the proteins of the present invention, such as naturally occurring mature forms of the peptide, allelic/sequence variants of the peptides, non-naturally occurring recombinantly derived variants of the peptides, and orthologs and paralogs of the peptides.
- variants can readily be generated using art-known techniques in the fields of recombinant nucleic acid technology and protein biochemistry. It is understood, however, that variants exclude any amino acid sequences disclosed prior to the invention.
- variants can readily be identified/made using molecular techniques and the sequence information disclosed herein. Further, such variants can readily be distinguished from other peptides based on sequence and/or structural homology to the kinase peptides of the present invention. The degree of homology/identity present will be based primarily on whether the peptide is a functional variant or non-functional variant, the amount of divergence present in the paralog family and the evolutionary distance between the orthologs.
- the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-homologous sequences can be disregarded for comparison purposes).
- at least 30%, 40%, 50%, 60%, 70%, 80%, or 90% or more of the length of a reference sequence is aligned for comparison purposes.
- the amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared.
- amino acid or nucleic acid “identity” is equivalent to amino acid or nucleic acid “homology”.
- the percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, which need to be introduced for optimal alignment of the two sequences.
- the percent identity between two amino acid sequences is determined using the Needleman and Wunsch ( J. Mol. Biol. (48):444-453 (1970)) algorithm which has been incorporated into the GAP program in the GCG software package (available at http://www.gcg.com), using either a Blossom 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5, or 6.
- the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package (Devereux, J., et al., Nucleic Acids Res. 12(1):387 (1984)) (available at http://www.gcg.com), using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70, or 80 and a length weight of 1, 2, 3, 4, 5, or 6.
- the percent identity between two amino acid or nucleotide sequences is determined using the algorithm of E. Myers and W. Miller (CABIOS, 4:11-17 (1989)) which has been incorporated into the ALIGN program (version 2.0), using a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4.
- the nucleic acid and protein sequences of the present invention can further be used as a “query sequence” to perform a search against sequence databases to, for example, identify other family members or related sequences.
- Such searches can be performed using the NBLAST and XBLAST programs (version 2.0) of Altschul, et al. ( J. Mol. Biol. 215:403-10 (1990)).
- Gapped BLAST can be utilized as described in Altschul et al. ( Nucleic Acids Res. 25(17):3389-3402 (1997)).
- the default parameters of the respective programs e.g., XBLAST and NBLAST
- XBLAST and NBLAST can be used.
- Full-length pre-processed forms, as well as mature processed forms, of proteins that comprise one of the peptides of the present invention can readily be identified as having complete sequence identity to one of the kinase peptides of the present invention as well as being encoded by the same genetic locus as the kinase peptide provided herein.
- the gene encoding the novel kinase protein of the present invention is located on a genome component that has been mapped to human chromosome 1 (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data.
- Allelic variants of a kinase peptide can readily be identified as being a human protein having a high degree (significant) of sequence homology/identity to at least a portion of the kinase peptide as well as being encoded by the same genetic locus as the kinase peptide provided herein. Genetic locus can readily be determined based on the genomic information provided in FIG. 3, such as the genomic sequence mapped to the reference human. The gene encoding the novel kinase protein of the present invention is located on a genome component that has been mapped to human chromosome 1 (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data.
- two proteins have significant homology when the amino acid sequences are typically at least about 70-80%, 80-90%, and more typically at least about 90-95% or more homologous.
- a significantly homologous amino acid sequence will be encoded by a nucleic acid sequence that will hybridize to a kinase peptide encoding nucleic acid molecule under stringent conditions as more fully described below.
- FIG. 3 provides information on SNPs that have been found in the gene encoding the kinase protein of the present invention. The following variations were seen: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at position 14131. SNPs in introns, such as these, may affect control/regulatory elements.
- Paralogs of a kinase peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the kinase peptide, as being encoded by a gene from humans, and as having similar activity or function.
- Two proteins will typically be considered paralogs when the amino acid sequences are typically at least about 60% or greater, and more typically at least about 70% or greater homology through a given region or domain.
- Such paralogs will be encoded by a nucleic acid sequence that will hybridize to a kinase peptide encoding nucleic acid molecule under moderate to stringent conditions as more fully described below.
- Orthologs of a kinase peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the kinase peptide as well as being encoded by a gene from another organism.
- Preferred orthologs will be isolated from mammals, preferably primates, for the development of human therapeutic targets and agents.
- Such orthologs will be encoded by a nucleic acid sequence that will hybridize to a kinase peptide encoding nucleic acid molecule under moderate to stringent conditions, as more fully described below, depending on the degree of relatedness of the two organisms yielding the proteins.
- Non-naturally occurring variants of the kinase peptides of the present invention can readily be generated using recombinant techniques.
- Such variants include, but are not limited to deletions, additions and substitutions in the amino acid sequence of the kinase peptide.
- one class of substitutions are conserved amino acid substitution.
- Such substitutions are those that substitute a given amino acid in a kinase peptide by another amino acid of like characteristics.
- conservative substitutions are the replacements, one for another, among the aliphatic amino acids Ala, Val, Leu, and Ile; interchange of the hydroxyl residues Ser and Thr; exchange of the acidic residues Asp and Glu; substitution between the amide residues Asn and Gln; exchange of the basic residues Lys and Arg; and replacements among the aromatic residues Phe and Tyr.
- Guidance concerning which amino acid changes are likely to be phenotypically silent are found in Bowie et al., Science 247:1306-1310 (1990).
- Variant kinase peptides can be fully functional or can lack function in one or more activities, e.g. ability to bind substrate, ability to phosphorylate substrate, ability to mediate signaling, etc.
- Fully functional variants typically contain only conservative variation or variation in non-critical residues or in non-critical regions.
- FIG. 2 provides the result of protein analysis and can be used to identify critical domains/regions.
- Functional variants can also contain substitution of similar amino acids that result in no change or an insignificant change in function. Alternatively, such substitutions may positively or negatively affect function to some degree.
- Non-functional variants typically contain one or more non-conservative amino acid substitutions, deletions, insertions, inversions, or truncation or a substitution, insertion, inversion, or deletion in a critical residue or critical region.
- Amino acids that are essential for function can be identified by methods known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (Cunningham et al., Science 244:1081-1085 (1989)), particularly using the results provided in FIG. 2. The latter procedure introduces single alanine mutations at every residue in the molecule. The resulting mutant molecules are then tested for biological activity such as kinase activity or in assays such as an in vitro proliferative activity. Sites that are critical for binding partner/substrate binding can also be determined by structural analysis such as crystallization, nuclear magnetic resonance or photoaffinity labeling (Smith et al., J. Mol. Biol. 224:899-904 (1992); de Vos et al. Science 255:306-312 (1992)).
- the present invention further provides fragments of the kinase peptides, in addition to proteins and peptides that comprise and consist of such fragments, particularly those comprising the residues identified in FIG. 2.
- the fragments to which the invention pertains are not to be construed as encompassing fragments that may be disclosed publicly prior to the present invention.
- a fragment comprises at least 8, 10, 12, 14, 16, or more contiguous amino acid residues from a kinase peptide.
- Such fragments can be chosen based on the ability to retain one or more of the biological activities of the kinase peptide or could be chosen for the ability to perform a function, e.g. bind a substrate or act as an immunogen.
- Particularly important fragments are biologically active fragments, peptides that are, for example, about 8 or more amino acids in length.
- Such fragments will typically comprise a domain or motif of the kinase peptide, e.g., active site, a transmembrane domain or a substrate-binding domain.
- fragments include, but are not limited to, domain or motif containing fragments, soluble peptide fragments, and fragments containing immunogenic structures.
- Predicted domains and functional sites are readily identifiable by computer programs well known and readily available to those of skill in the art (e.g., PROSITE analysis). The results of one such analysis are provided in FIG. 2.
- Polypeptides often contain amino acids other than the 20 amino acids commonly referred to as the 20 naturally occurring amino acids. Further, many amino acids, including the terminal amino acids, may be modified by natural processes, such as processing and other post-translational modifications, or by chemical modification techniques well known in the art. Common modifications that occur naturally in kinase peptides are described in basic texts, detailed monographs, and the research literature, and they are well known to those of skill in the art (some of these features are identified in FIG. 2).
- Known modifications include, but are not limited to, acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent crosslinks, formation of cystine, formation of pyroglutamate, formylation, gamma carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination.
- the kinase peptides of the present invention also encompass derivatives or analogs in which a substituted amino acid residue is not one encoded by the genetic code, in which a substituent group is included, in which the mature kinase peptide is fused with another compound, such as a compound to increase the half-life of the kinase peptide (for example, polyethylene glycol), or in which the additional amino acids are fused to the mature kinase peptide, such as a leader or secretory sequence or a sequence for purification of the mature kinase peptide or a pro-protein sequence.
- a substituted amino acid residue is not one encoded by the genetic code, in which a substituent group is included, in which the mature kinase peptide is fused with another compound, such as a compound to increase the half-life of the kinase peptide (for example, polyethylene glycol), or in which the additional amino acids are fused to the mature kinase
- the proteins of the present invention can be used in substantial and specific assays related to the functional information provided in the Figures; to raise antibodies or to elicit another immune response; as a reagent (including the labeled reagent) in assays designed to quantitatively determine levels of the protein (or its binding partner or ligand) in biological fluids; and as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in a disease state).
- the protein binds or potentially binds to another protein or ligand (such as, for example, in a kinase-effector protein interaction or kinase-ligand interaction)
- the protein can be used to identify the binding partner/ligand so as to develop a system to identify inhibitors of the binding interaction. Any or all of these uses are capable of being developed into reagent grade or kit format for commercialization as commercial products.
- kinases isolated from humans and their human/mammalian orthologs serve as targets for identifying agents for use in mammalian therapeutic applications, e.g. a human drug, particularly in modulating a biological or pathological response in a cell or tissue that expresses the kinase.
- Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis.
- PCR-based tissue screening panels indicate expression in human liver.
- a large percentage of pharmaceutical agents are being developed that modulate the activity of kinase proteins, particularly members of the homeodomain-interacting protein kinase subfamily (see Background of the Invention).
- the structural and functional information provided in the Background and Figures provide specific and substantial uses for the molecules of the present invention, particularly in combination with the expression information provided in FIG. 1.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. Such uses can readily be determined using the information provided herein, that which is known in the art, and routine experimentation.
- the proteins of the present invention are useful for biological assays related to kinases that are related to members of the homeodomain-interacting protein kinase subfamily.
- assays involve any of the known kinase functions or activities or properties useful for diagnosis and treatment of kinase-related conditions that are specific for the subfamily of kinases that the one of the present invention belongs to, particularly in cells and tissues that express the kinase.
- kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis.
- PCR-based tissue screening panels indicate expression in human liver.
- the proteins of the present invention are also useful in drug screening assays, in cell-based or cell-free systems.
- Cell-based systems can be native, i.e., cells that normally express the kinase, as a biopsy or expanded in cell culture.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- cell-based assays involve recombinant host cells expressing the kinase protein.
- the polypeptides can be used to identify compounds that modulate kinase activity of the protein in its natural state or an altered form that causes a specific disease or pathology associated with the kinase.
- Both the kinases of the present invention and appropriate variants and fragments can be used in high-throughput screens to assay candidate compounds for the ability to bind to the kinase. These compounds can be further screened against a functional kinase to determine the effect of the compound on the kinase activity. Further, these compounds can be tested in animal or invertebrate systems to determine activity/effectiveness. Compounds can be identified that activate (agonist) or inactivate (antagonist) the kinase to a desired degree.
- the proteins of the present invention can be used to screen a compound for the ability to stimulate or inhibit interaction between the kinase protein and a molecule that normally interacts with the kinase protein, e.g. a substrate or a component of the signal pathway that the kinase protein normally interacts (for example, another kinase).
- a molecule that normally interacts with the kinase protein e.g. a substrate or a component of the signal pathway that the kinase protein normally interacts (for example, another kinase).
- Such assays typically include the steps of combining the kinase protein with a candidate compound under conditions that allow the kinase protein, or fragment, to interact with the target molecule, and to detect the formation of a complex between the protein and the target or to detect the biochemical consequence of the interaction with the kinase protein and the target, such as any of the associated effects of signal transduction such as protein phosphorylation, cAMP turnover, and adenylate cyclase activation, etc.
- Candidate compounds include, for example, 1) peptides such as soluble peptides, including Ig-tailed fusion peptides and members of random peptide libraries (see, e.g., Lam et al., Nature 354:82-84 (1991); Houghten et al., Nature 354:84-86 (1991)) and combinatorial chemistry-derived molecular libraries made of D- and/or L- configuration amino acids; 2) phosphopeptides (e.g., members of random and partially degenerate, directed phosphopeptide libraries, see, e.g., Songyang et al., Cell 72:767-778 (1993)); 3) antibodies (e.g., polyclonal, monoclonal, humanized, anti-idiotypic, chimeric, and single chain antibodies as well as Fab, F(ab′) 2 , Fab expression library fragments, and epitope-binding fragments of antibodies); and 4) small organic and inorganic molecules
- One candidate compound is a soluble fragment of the receptor that competes for substrate binding.
- Other candidate compounds include mutant kinases or appropriate fragments containing mutations that affect kinase function and thus compete for substrate. Accordingly, a fragment that competes for substrate, for example with a higher affinity, or a fragment that binds substrate but does not allow release, is encompassed by the invention.
- the invention further includes other end point assays to identify compounds that modulate (stimulate or inhibit) kinase activity.
- the assays typically involve an assay of events in the signal transduction pathway that indicate kinase activity.
- the phosphorylation of a substrate, activation of a protein, a change in the expression of genes that are up- or down-regulated in response to the kinase protein dependent signal cascade can be assayed.
- any of the biological or biochemical functions mediated by the kinase can be used as an endpoint assay. These include all of the biochemical or biochemical/biological events described herein, in the references cited herein, incorporated by reference for these endpoint assay targets, and other functions known to those of ordinary skill in the art or that can be readily identified using the information provided in the Figures, particularly FIG. 2. Specifically, a biological function of a cell or tissues that expresses the kinase can be assayed. Experimental data as provided in FIG.
- kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis.
- PCR-based tissue screening panels indicate expression in human liver.
- Binding and/or activating compounds can also be screened by using chimeric kinase proteins in which the amino terminal extracellular domain, or parts thereof, the entire transmembrane domain or subregions, such as any of the seven transmembrane segments or any of the intracellular or extracellular loops and the carboxy terminal intracellular domain, or parts thereof, can be replaced by heterologous domains or subregions.
- a substrate-binding region can be used that interacts with a different substrate then that which is recognized by the native kinase. Accordingly, a different set of signal transduction components is available as an end-point assay for activation. This allows for assays to be performed in other than the specific host cell from which the kinase is derived.
- the proteins of the present invention are also useful in competition binding assays in methods designed to discover compounds that interact with the kinase (e.g. binding partners and/or ligands).
- a compound is exposed to a kinase polypeptide under conditions that allow the compound to bind or to otherwise interact with the polypeptide.
- Soluble kinase polypeptide is also added to the mixture. If the test compound interacts with the soluble kinase polypeptide, it decreases the amount of complex formed or activity from the kinase target.
- This type of assay is particularly useful in cases in which compounds are sought that interact with specific regions of the kinase.
- the soluble polypeptide that competes with the target kinase region is designed to contain peptide sequences corresponding to the region of interest.
- a fusion protein can be provided which adds a domain that allows the protein to be bound to a matrix.
- glutathione-S-transferase fusion proteins can be adsorbed onto glutathione sepharose beads (Sigma Chemical, St. Louis, Mo.) or glutathione derivatized microtitre plates, which are then combined with the cell lysates (e.g., 35 S-labeled) and the candidate compound, and the mixture incubated under conditions conducive to complex formation (e.g., at physiological conditions for salt and pH).
- the beads are washed to remove any unbound label, and the matrix immobilized and radiolabel determined directly, or in the supernatant after the complexes are dissociated.
- the complexes can be dissociated from the matrix, separated by SDS-PAGE, and the level of kinase-binding protein found in the bead fraction quantitated from the gel using standard electrophoretic techniques.
- the polypeptide or its target molecule can be immobilized utilizing conjugation of biotin and streptavidin using techniques well known in the art.
- antibodies reactive with the protein but which do not interfere with binding of the protein to its target molecule can be derivatized to the wells of the plate, and the protein trapped in the wells by antibody conjugation.
- Preparations of a kinase-binding protein and a candidate compound are incubated in the kinase protein-presenting wells and the amount of complex trapped in the well can be quantitated.
- Methods for detecting such complexes include immunodetection of complexes using antibodies reactive with the kinase protein target molecule, or which are reactive with kinase protein and compete with the target molecule, as well as enzyme-linked assays which rely on detecting an enzymatic activity associated with the target molecule.
- Agents that modulate one of the kinases of the present invention can be identified using one or more of the above assays, alone or in combination. It is generally preferable to use a cell-based or cell free system first and then confirm activity in an animal or other model system. Such model systems are well known in the art and can readily be employed in this context.
- Modulators of kinase protein activity identified according to these drug screening assays can be used to treat a subject with a disorder mediated by the kinase pathway, by treating cells or tissues that express the kinase.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- These methods of treatment include the steps of administering a modulator of kinase activity in a pharmaceutical composition to a subject in need of such treatment, the modulator being identified as described herein.
- the kinase proteins can be used as “bait proteins” in a two-hybrid assay or three-hybrid assay (see, e.g., U.S. Pat. No. 5,283,317; Zervos et al. (1993) Cell 72:223-232; Madura et al. (1993) J. Biol. Chem. 268:12046-12054; Bartel et al. (1993) Biotechniques 14:920-924; Iwabuchi et al.
- kinase-binding proteins are also likely to be involved in the propagation of signals by the kinase proteins or kinase targets as, for example, downstream elements of a kinase-mediated signaling pathway.
- kinase-binding proteins are likely to be kinase inhibitors.
- the two-hybrid system is based on the modular nature of most transcription factors, which consist of separable DNA-binding and activation domains.
- the assay utilizes two different DNA constructs.
- the gene that codes for a kinase protein is fused to a gene encoding the DNA binding domain of a known transcription factor (e.g., GAL-4).
- a DNA sequence, from a library of DNA sequences, that encodes an unidentified protein (“prey” or “sample”) is fused to a gene that codes for the activation domain of the known transcription factor.
- the DNA-binding and activation domains of the transcription factor are brought into close proximity. This proximity allows transcription of a reporter gene (e.g., LacZ) which is operably linked to a transcriptional regulatory site responsive to the transcription factor. Expression of the reporter gene can be detected and cell colonies containing the functional transcription factor can be isolated and used to obtain the cloned gene which encodes the protein which interacts with the kinase protein.
- a reporter gene e.g., LacZ
- This invention further pertains to novel agents identified by the above-described screening assays. Accordingly, it is within the scope of this invention to further use an agent identified as described herein in an appropriate animal model.
- an agent identified as described herein e.g., a kinase-modulating agent, an antisense kinase nucleic acid molecule, a kinase-specific antibody, or a kinase-binding partner
- an agent identified as described herein can be used in an animal or other model to determine the efficacy, toxicity, or side effects of treatment with such an agent.
- an agent identified as described herein can be used in an animal or other model to determine the mechanism of action of such an agent.
- this invention pertains to uses of novel agents identified by the above-described screening assays for treatments as described herein.
- the kinase proteins of the present invention are also useful to provide a target for diagnosing a disease or predisposition to disease mediated by the peptide. Accordingly, the invention provides methods for detecting the presence, or levels of, the protein (or encoding mRNA) in a cell, tissue, or organism. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. The method involves contacting a biological sample with a compound capable of interacting with the kinase protein such that the interaction can be detected. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.
- One agent for detecting a protein in a sample is an antibody capable of selectively binding to protein.
- a biological sample includes tissues, cells and biological fluids isolated from a subject, as well as tissues, cells and fluids present within a subject.
- the peptides of the present invention also provide targets for diagnosing active protein activity, disease, or predisposition to disease, in a patient having a variant peptide, particularly activities and conditions that are known for other members of the family of proteins to which the present one belongs.
- the peptide can be isolated from a biological sample and assayed for the presence of a genetic mutation that results in aberrant peptide. This includes amino acid substitution, deletion, insertion, rearrangement, (as the result of aberrant splicing events), and inappropriate post-translational modification.
- Analytic methods include altered electrophoretic mobility, altered tryptic peptide digest, altered kinase activity in cell-based or cell-free assay, alteration in substrate or antibody-binding pattern, altered isoelectric point, direct amino acid sequencing, and any other of the known assay techniques useful for detecting mutations in a protein.
- Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.
- peptide detection techniques include enzyme linked immunosorbent assays (ELISAs), Western blots, immunoprecipitations and immunofluorescence using a detection reagent, such as an antibody or protein binding agent.
- a detection reagent such as an antibody or protein binding agent.
- the peptide can be detected in vivo in a subject by introducing into the subject a labeled anti-peptide antibody or other types of detection agent.
- the antibody can be labeled with a radioactive marker whose presence and location in a subject can be detected by standard imaging techniques. Particularly useful are methods that detect the allelic variant of a peptide expressed in a subject and methods which detect fragments of a peptide in a sample.
- the peptides are also useful in pharmacogenomic analysis.
- Pharmacogenomics deal with clinically significant hereditary variations in the response to drugs due to altered drug disposition and abnormal action in affected persons. See, e.g., Eichelbaum, M. ( Clin. Exp. Pharmacol. Physiol. 23(10-11):983-985 (1996)), and Linder, M. W. (Clin. Chem. 43(2):254-266 (1997)).
- the clinical outcomes of these variations result in severe toxicity of therapeutic drugs in certain individuals or therapeutic failure of drugs in certain individuals as a result of individual variation in metabolism.
- the genotype of the individual can determine the way a therapeutic compound acts on the body or the way the body metabolizes the compound.
- the activity of drug metabolizing enzymes effects both the intensity and duration of drug action.
- the pharmacogenomics of the individual permit the selection of effective compounds and effective dosages of such compounds for prophylactic or therapeutic treatment based on the individual's genotype.
- the discovery of genetic polymorphisms in some drug metabolizing enzymes has explained why some patients do not obtain the expected drug effects, show an exaggerated drug effect, or experience serious toxicity from standard drug dosages. Polymorphisms can be expressed in the phenotype of the extensive metabolizer and the phenotype of the poor metabolizer.
- genetic polymorphism may lead to allelic protein variants of the kinase protein in which one or more of the kinase functions in one population is different from those in another population.
- the peptides thus allow a target to ascertain a genetic predisposition that can affect treatment modality.
- polymorphism may give rise to amino terminal extracellular domains and/or other substrate-binding regions that are more or less active in substrate binding, and kinase activation. Accordingly, substrate dosage would necessarily be modified to maximize the therapeutic effect within a given population containing a polymorphism.
- specific polymorphic peptides could be identified.
- the peptides are also useful for treating a disorder characterized by an absence of, inappropriate, or unwanted expression of the protein.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. Accordingly, methods for treatment include the use of the kinase protein or fragments.
- the invention also provides antibodies that selectively bind to one of the peptides of the present invention, a protein comprising such a peptide, as well as variants and fragments thereof.
- an antibody selectively binds a target peptide when it binds the target peptide and does not significantly bind to unrelated proteins.
- An antibody is still considered to selectively bind a peptide even if it also binds to other proteins that are not substantially homologous with the target peptide so long as such proteins share homology with a fragment or domain of the peptide target of the antibody. In this case, it would be understood that antibody binding to the peptide is still selective despite some degree of cross-reactivity.
- an antibody is defined in terms consistent with that recognized within the art: they are multi-subunit proteins produced by a mammalian organism in response to an antigen challenge.
- the antibodies of the present invention include polyclonal antibodies and monoclonal antibodies, as well as fragments of such antibodies, including, but not limited to, Fab or F(ab′) 2 , and Fv fragments.
- an isolated peptide is used as an immunogen and is administered to a mammalian organism, such as a rat, rabbit or mouse.
- a mammalian organism such as a rat, rabbit or mouse.
- the full-length protein, an antigenic peptide fragment or a fusion protein can be used.
- Particularly important fragments are those covering functional domains, such as the domains identified in FIG. 2, and domain of sequence homology or divergence amongst the family, such as those that can readily be identified using protein alignment methods and as presented in the Figures.
- Antibodies are preferably prepared from regions or discrete fragments of the kinase proteins. Antibodies can be prepared from any region of the peptide as described herein. However, preferred regions will include those involved in function/activity and/or kinase/binding partner interaction. FIG. 2 can be used to identify particularly important regions while sequence alignment can be used to identify conserved and unique sequence fragments.
- An antigenic fragment will typically comprise at least 8 contiguous amino acid residues.
- the antigenic peptide can comprise, however, at least 10, 12, 14, 16 or more amino acid residues.
- Such fragments can be selected on a physical property, such as fragments correspond to regions that are located on the surface of the protein, e.g., hydrophilic regions or can be selected based on sequence uniqueness (see FIG. 2).
- Detection on an antibody of the present invention can be facilitated by coupling (i.e., physically linking) the antibody to a detectable substance.
- detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, and radioactive materials.
- suitable enzymes include horseradish peroxidase, alkaline phosphatase, ⁇ -galactosidase, or acetylcholinesterase;
- suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin;
- suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin;
- an example of a luminescent material includes luminol;
- examples of bioluminescent materials include luciferase, luciferin, and aequorin, and examples of suitable radioactive material include 125 I, 131 I, 35 S or 3 H.
- the antibodies can be used to isolate one of the proteins of the present invention by standard techniques, such as affinity chromatography or immunoprecipitation.
- the antibodies can facilitate the purification of the natural protein from cells and recombinantly produced protein expressed in host cells.
- such antibodies are useful to detect the presence of one of the proteins of the present invention in cells or tissues to determine the pattern of expression of the protein among various tissues in an organism and over the course of normal development.
- Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis.
- PCR-based tissue screening panels indicate expression in human liver.
- antibodies can be used to detect protein in situ, in vitro, or in a cell lysate or supernatant in order to evaluate the abundance and pattern of expression.
- antibodies can be used to assess abnormal tissue distribution or abnormal expression during development or progression of a biological condition.
- Antibody detection of circulating fragments of the full length protein can be used to identify turnover.
- the antibodies can be used to assess expression in disease states such as in active stages of the disease or in an individual with a predisposition toward disease related to the protein's function.
- a disorder is caused by an inappropriate tissue distribution, developmental expression, level of expression of the protein, or expressed/processed form
- the antibody can be prepared against the normal protein.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. If a disorder is characterized by a specific mutation in the protein, antibodies specific for this mutant protein can be used to assay for the presence of the specific mutant protein.
- the antibodies can also be used to assess normal and aberrant subcellular localization of cells in the various tissues in an organism.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- the diagnostic uses can be applied, not only in genetic testing, but also in monitoring a treatment modality. Accordingly, where treatment is ultimately aimed at correcting expression level or the presence of aberrant sequence and aberrant tissue distribution or developmental expression, antibodies directed against the protein or relevant fragments can be used to monitor therapeutic efficacy.
- antibodies are useful in pharmacogenomic analysis.
- antibodies prepared against polymorphic proteins can be used to identify individuals that require modified treatment modalities.
- the antibodies are also useful as diagnostic tools as an immunological marker for aberrant protein analyzed by electrophoretic mobility, isoelectric point, tryptic peptide digest, and other physical assays known to those in the art.
- the antibodies are also useful for tissue typing.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- antibodies that are specific for this protein can be used to identify a tissue type.
- the antibodies are also useful for inhibiting protein function, for example, blocking the binding of the kinase peptide to a binding partner such as a substrate. These uses can also be applied in a therapeutic context in which treatment involves inhibiting the protein's function.
- An antibody can be used, for example, to block binding, thus modulating (agonizing or antagonizing) the peptides activity.
- Antibodies can be prepared against specific fragments containing sites required for function or against intact protein that is associated with a cell or cell membrane. See FIG. 2 for structural information relating to the proteins of the present invention.
- kits for using antibodies to detect the presence of a protein in a biological sample can comprise antibodies such as a labeled or labelable antibody and a compound or agent for detecting protein in a biological sample; means for determining the amount of protein in the sample; means for comparing the amount of protein in the sample with a standard; and instructions for use.
- a kit can be supplied to detect a single protein or epitope or can be configured to detect one of a multitude of epitopes, such as in an antibody detection array. Arrays are described in detail below for nuleic acid arrays and similar methods have been developed for antibody arrays.
- the present invention further provides isolated nucleic acid molecules that encode a kinase peptide or protein of the present invention (cDNA, transcript and genomic sequence).
- Such nucleic acid molecules will consist of, consist essentially of, or comprise a nucleotide sequence that encodes one of the kinase peptides of the present invention, an allelic variant thereof, or an ortholog or paralog thereof.
- an “isolated” nucleic acid molecule is one that is separated from other nucleic acid present in the natural source of the nucleic acid.
- an “isolated” nucleic acid is free of sequences which naturally flank the nucleic acid (i.e., sequences located at the 5′ and 3′ ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived.
- flanking nucleotide sequences for example up to about 5KB, 4KB, 3KB, 2KB, or 1KB or less, particularly contiguous peptide encoding sequences and peptide encoding sequences within the same gene but separated by introns in the genomic sequence.
- nucleic acid is isolated from remote and unimportant flanking sequences such that it can be subjected to the specific manipulations described herein such as recombinant expression, preparation of probes and primers, and other uses specific to the nucleic acid sequences.
- an “isolated” nucleic acid molecule such as a transcript/cDNA molecule, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or chemical precursors or other chemicals when chemically synthesized.
- the nucleic acid molecule can be fused to other coding or regulatory sequences and still be considered isolated.
- recombinant DNA molecules contained in a vector are considered isolated.
- isolated DNA molecules include recombinant DNA molecules maintained in heterologous host cells or purified (partially or substantially) DNA molecules in solution.
- isolated RNA molecules include in vivo or in vitro RNA transcripts of the isolated DNA molecules of the present invention.
- Isolated nucleic acid molecules according to the present invention further include such molecules produced synthetically.
- nucleic acid molecules that consist of the nucleotide sequence shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2.
- a nucleic acid molecule consists of a nucleotide sequence when the nucleotide sequence is the complete nucleotide sequence of the nucleic acid molecule.
- the present invention further provides nucleic acid molecules that consist essentially of the nucleotide sequence shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2.
- a nucleic acid molecule consists essentially of a nucleotide sequence when such a nucleotide sequence is present with only a few additional nucleic acid residues in the final nucleic acid molecule.
- the present invention further provides nucleic acid molecules that comprise the nucleotide sequences shown in FIG. 1 or 3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2.
- a nucleic acid molecule comprises a nucleotide sequence when the nucleotide sequence is at least part of the final nucleotide sequence of the nucleic acid molecule.
- the nucleic acid molecule can be only the nucleotide sequence or have additional nucleic acid residues, such as nucleic acid residues that are naturally associated with it or heterologous nucleotide sequences.
- Such a nucleic acid molecule can have a few additional nucleotides or can comprises several hundred or more additional nucleotides. A brief description of how various types of these nucleic acid molecules can be readily made/isolated is provided below.
- FIGS. 1 and 3 both coding and non-coding sequences are provided. Because of the source of the present invention, humans genomic sequence (FIG. 3) and cDNA/transcript sequences (FIG. 1), the nucleic acid molecules in the Figures will contain genomic intronic sequences, 5′ and 3′ non-coding sequences, gene regulatory regions and non-coding intergenic sequences. In general such sequence features are either noted in FIGS. 1 and 3 or can readily be identified using computational tools known in the art. As discussed below, some of the non-coding regions, particularly gene regulatory elements such as promoters, are useful for a variety of purposes, e.g. control of heterologous gene expression, target for identifying gene activity modulating compounds, and are particularly claimed as fragments of the genomic sequence provided herein.
- the isolated nucleic acid molecules can encode the mature protein plus additional amino or carboxyl-terminal amino acids, or amino acids interior to the mature peptide (when the mature form has more than one peptide chain, for instance). Such sequences may play a role in processing of a protein from precursor to a mature form, facilitate protein trafficking, prolong or shorten protein half-life or facilitate manipulation of a protein for assay or production, among other things. As generally is the case in situ, the additional amino acids may be processed away from the mature protein by cellular enzymes.
- the isolated nucleic acid molecules include, but are not limited to, the sequence encoding the kinase peptide alone, the sequence encoding the mature peptide and additional coding sequences, such as a leader or secretory sequence (e.g., a pre-pro or pro-protein sequence), the sequence encoding the mature peptide, with or without the additional coding sequences, plus additional non-coding sequences, for example introns and non-coding 5′ and 3′ sequences such as transcribed but non-translated sequences that play a role in transcription, mRNA processing (including splicing and polyadenylation signals), ribosome binding and stability of mRNA.
- the nucleic acid molecule may be fused to a marker sequence encoding, for example, a peptide that facilitates purification.
- Isolated nucleic acid molecules can be in the form of RNA, such as mRNA, or in the form DNA, including cDNA and genomic DNA obtained by cloning or produced by chemical synthetic techniques or by a combination thereof.
- the nucleic acid, especially DNA can be double-stranded or single-stranded.
- Single-stranded nucleic acid can be the coding strand (sense strand) or the non-coding strand (anti-sense strand).
- the invention further provides nucleic acid molecules that encode fragments of the peptides of the present invention as well as nucleic acid molecules that encode obvious variants of the kinase proteins of the present invention that are described above.
- nucleic acid molecules may be naturally occurring, such as allelic variants (same locus), paralogs (different locus), and orthologs (different organism), or may be constructed by recombinant DNA methods or by chemical synthesis.
- Such non-naturally occurring variants may be made by mutagenesis techniques, including those applied to nucleic acid molecules, cells, or organisms. Accordingly, as discussed above, the variants can contain nucleotide substitutions, deletions, inversions and insertions. Variation can occur in either or both the coding and non-coding regions. The variations can produce both conservative and non-conservative amino acid substitutions.
- the present invention further provides non-coding fragments of the nucleic acid molecules provided in FIGS. 1 and 3.
- Preferred non-coding fragments include, but are not limited to, promoter sequences, enhancer sequences, gene modulating sequences and gene termination sequences. Such fragments are useful in controlling heterologous gene expression and in developing screens to identify gene-modulating agents.
- a promoter can readily be identified as being 5′ to the ATG start site in the genomic sequence provided in FIG. 3.
- a fragment comprises a contiguous nucleotide sequence greater than 12 or more nucleotides. Further, a fragment could at least 30, 40, 50, 100, 250 or 500 nucleotides in length. The length of the fragment will be based on its intended use. For example, the fragment can encode epitope bearing regions of the peptide, or can be useful as DNA probes and primers. Such fragments can be isolated using the known nucleotide sequence to synthesize an oligonucleotide probe. A labeled probe can then be used to screen a cDNA library, genomic DNA library, or mRNA to isolate nucleic acid corresponding to the coding region. Further, primers can be used in PCR reactions to clone specific regions of gene.
- a probe/primer typically comprises substantially a purified oligonucleotide or oligonucleotide pair.
- the oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 12, 20, 25, 40, 50 or more consecutive nucleotides.
- Orthologs, homologs, and allelic variants can be identified using methods well known in the art. As described in the Peptide Section, these variants comprise a nucleotide sequence encoding a peptide that is typically 60-70%, 70-80%, 80-90%, and more typically at least about 90-95% or more homologous to the nucleotide sequence shown in the Figure sheets or a fragment of this sequence. Such nucleic acid molecules can readily be identified as being able to hybridize under moderate to stringent conditions, to the nucleotide sequence shown in the Figure sheets or a fragment of the sequence. Allelic variants can readily be determined by genetic locus of the encoding gene.
- the gene encoding the novel kinase protein of the present invention is located on a genome component that has been mapped to human chromosome 1 (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data.
- FIG. 3 provides information on SNPs that have been found in the gene encoding the kinase protein of the present invention. The following variations were seen: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at position 14131. SNPs in introns, such as these, may affect control/regulatory elements.
- hybridizes under stringent conditions is intended to describe conditions for hybridization and washing under which nucleotide sequences encoding a peptide at least 60-70% homologous to each other typically remain hybridized to each other.
- the conditions can be such that sequences at least about 60%, at least about 70%, or at least about 80% or more homologous to each other typically remain hybridized to each other.
- stringent conditions are known to those skilled in the art and can be found in Current Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), 6.3.1-6.3.6.
- stringent hybridization conditions are hybridization in 6X sodium chloride/sodium citrate (SSC) at about 45 C., followed by one or more washes in 0.2 ⁇ SSC, 0.1% SDS at 50-65 C. Examples of moderate to low stringency hybridization conditions are well known in the art.
- the nucleic acid molecules of the present invention are useful for probes, primers, chemical intermediates, and in biological assays.
- the nucleic acid molecules are useful as a hybridization probe for messenger RNA, transcript/cDNA and genomic DNA to isolate full-length cDNA and genomic clones encoding the peptide described in FIG. 2 and to isolate cDNA and genomic clones that correspond to variants (alleles, orthologs, etc.) producing the same or related peptides shown in FIG. 2.
- the following SNPs were identified: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at position 14131.
- the probe can correspond to any sequence along the entire length of the nucleic acid molecules provided in the Figures. Accordingly, it could be derived from 5′ noncoding regions, the coding region, and 3′ noncoding regions. However, as discussed, fragments are not to be construed as encompassing fragments disclosed prior to the present invention.
- nucleic acid molecules are also useful as primers for PCR to amplify any given region of a nucleic acid molecule and are useful to synthesize antisense molecules of desired length and sequence.
- the nucleic acid molecules are also useful for constructing recombinant vectors.
- Such vectors include expression vectors that express a portion of, or all of, the peptide sequences.
- Vectors also include insertion vectors, used to integrate into another nucleic acid molecule sequence, such as into the cellular genome, to alter in situ expression of a gene and/or gene product.
- an endogenous coding sequence can be replaced via homologous recombination with all or part of the coding region containing one or more specifically introduced mutations.
- nucleic acid molecules are also useful for expressing antigenic portions of the proteins.
- the nucleic acid molecules are also useful as probes for determining the chromosomal positions of the nucleic acid molecules by means of in situ hybridization methods.
- the gene encoding the novel kinase protein of the present invention is located on a genome component that has been mapped to human chromosome 1 (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data.
- nucleic acid molecules are also useful in making vectors containing the gene regulatory regions of the nucleic acid molecules of the present invention.
- nucleic acid molecules are also useful for designing ribozymes corresponding to all, or a part, of the mRNA produced from the nucleic acid molecules described herein.
- nucleic acid molecules are also useful for making vectors that express part, or all, of the peptides.
- nucleic acid molecules are also useful for constructing host cells expressing a part, or all, of the nucleic acid molecules and peptides.
- nucleic acid molecules are also useful for constructing transgenic animals expressing all, or a part, of the nucleic acid molecules and peptides.
- the nucleic acid molecules are also useful as hybridization probes for determining the presence, level, form and distribution of nucleic acid expression.
- Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis.
- PCR-based tissue screening panels indicate expression in human liver. Accordingly, the probes can be used to detect the presence of, or to determine levels of, a specific nucleic acid molecule in cells, tissues, and in organisms.
- the nucleic acid whose level is determined can be DNA or RNA.
- probes corresponding to the peptides described herein can be used to assess expression and/or gene copy number in a given cell, tissue, or organism. These uses are relevant for diagnosis of disorders involving an increase or decrease in kinase protein expression relative to normal results.
- In vitro techniques for detection of mRNA include Northern hybridizations and in situ hybridizations.
- In vitro techniques for detecting DNA includes Southern hybridizations and in situ hybridization.
- Probes can be used as a part of a diagnostic test kit for identifying cells or tissues that express a kinase protein, such as by measuring a level of a kinase-encoding nucleic acid in a sample of cells from a subject e.g., mRNA or genomic DNA, or determining if a kinase gene has been mutated.
- Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis.
- PCR-based tissue screening panels indicate expression in human liver.
- Nucleic acid expression assays are useful for drug screening to identify compounds that modulate kinase nucleic acid expression.
- the invention thus provides a method for identifying a compound that can be used to treat a disorder associated with nucleic acid expression of the kinase gene, particularly biological and pathological processes that are mediated by the kinase in cells and tissues that express it.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- the method typically includes assaying the ability of the compound to modulate the expression of the kinase nucleic acid and thus identifying a compound that can be used to treat a disorder characterized by undesired kinase nucleic acid expression.
- the assays can be performed in cell-based and cell-free systems.
- Cell-based assays include cells naturally expressing the kinase nucleic acid or recombinant cells genetically engineered to express specific nucleic acid sequences.
- the assay for kinase nucleic acid expression can involve direct assay of nucleic acid levels, such as mRNA levels, or on collateral compounds involved in the signal pathway. Further, the expression of genes that are up- or down-regulated in response to the kinase protein signal pathway can also be assayed. In this embodiment the regulatory regions of these genes can be operably linked to a reporter gene such as luciferase.
- modulators of kinase gene expression can be identified in a method wherein a cell is contacted with a candidate compound and the expression of mRNA determined.
- the level of expression of kinase mRNA in the presence of the candidate compound is compared to the level of expression of kinase mRNA in the absence of the candidate compound.
- the candidate compound can then be identified as a modulator of nucleic acid expression based on this comparison and be used, for example to treat a disorder characterized by aberrant nucleic acid expression.
- expression of mRNA is statistically significantly greater in the presence of the candidate compound than in its absence, the candidate compound is identified as a stimulator of nucleic acid expression.
- nucleic acid expression is statistically significantly less in the presence of the candidate compound than in its absence, the candidate compound is identified as an inhibitor of nucleic acid expression.
- the invention further provides methods of treatment, with the nucleic acid as a target, using a compound identified through drug screening as a gene modulator to modulate kinase nucleic acid expression in cells and tissues that express the kinase.
- Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis.
- PCR-based tissue screening panels indicate expression in human liver. Modulation includes both up-regulation (i.e. activation or agonization) or down-regulation (suppression or antagonization) or nucleic acid expression.
- a modulator for kinase nucleic acid expression can be a small molecule or drug identified using the screening assays described herein as long as the drug or small molecule inhibits the kinase nucleic acid expression in the cells and tissues that express the protein.
- Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- the nucleic acid molecules are also useful for monitoring the effectiveness of modulating compounds on the expression or activity of the kinase gene in clinical trials or in a treatment regimen.
- the gene expression pattern can serve as a barometer for the continuing effectiveness of treatment with the compound, particularly with compounds to which a patient can develop resistance.
- the gene expression pattern can also serve as a marker indicative of a physiological response of the affected cells to the compound. Accordingly, such monitoring would allow either increased administration of the compound or the administration of alternative compounds to which the patient has not become resistant. Similarly, if the level of nucleic acid expression falls below a desirable level, administration of the compound could be commensurately decreased.
- the nucleic acid molecules are also useful in diagnostic assays for qualitative changes in kinase nucleic acid expression, and particularly in qualitative changes that lead to pathology.
- the nucleic acid molecules can be used to detect mutations in kinase genes and gene expression products such as mRNA.
- the nucleic acid molecules can be used as hybridization probes to detect naturally occurring genetic mutations in the kinase gene and thereby to determine whether a subject with the mutation is at risk for a disorder caused by the mutation. Mutations include deletion, addition, or substitution of one or more nucleotides in the gene, chromosomal rearrangement, such as inversion or transposition, modification of genomic DNA, such as aberrant methylation patterns or changes in gene copy number, such as amplification. Detection of a mutated form of the kinase gene associated with a dysfunction provides a diagnostic tool for an active disease or susceptibility to disease when the disease results from overexpression, underexpression, or altered expression of a kinase protein
- FIG. 3 provides information on SNPs that have been found in the gene encoding the kinase protein of the present invention. The following variations were seen: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at position 14131. SNPs in introns, such as these, may affect control/regulatory elements.
- the gene encoding the novel kinase protein of the present invention is located on a genome component that has been mapped to human chromosome 1 (as indicated in FIG.
- Genomic DNA can be analyzed directly or can be amplified by using PCR prior to analysis.
- RNA or cDNA can be used in the same way.
- detection of the mutation involves the use of a probe/primer in a polymerase chain reaction (PCR) (see, e.g. U.S. Pat. Nos.
- PCR polymerase chain reaction
- This method can include the steps of collecting a sample of cells from a patient, isolating nucleic acid (e.g., genomic, mRNA or both) from the cells of the sample, contacting the nucleic acid sample with one or more primers which specifically hybridize to a gene under conditions such that hybridization and amplification of the gene (if present) occurs, and detecting the presence or absence of an amplification product, or detecting the size of the amplification product and comparing the length to a control sample. Deletions and insertions can be detected by a change in size of the amplified product compared to the normal genotype. Point mutations can be identified by hybridizing amplified DNA to normal RNA or antisense DNA sequences.
- nucleic acid e.g., genomic, mRNA or both
- mutations in a kinase gene can be directly identified, for example, by alterations in restriction enzyme digestion patterns determined by gel electrophoresis.
- sequence-specific ribozymes can be used to score for the presence of specific mutations by development or loss of a ribozyme cleavage site. Perfectly matched sequences can be distinguished from mismatched sequences by nuclease cleavage digestion assays or by differences in melting temperature.
- Sequence changes at specific locations can also be assessed by nuclease protection assays such as RNase and S1 protection or the chemical cleavage method.
- sequence differences between a mutant kinase gene and a wild-type gene can be determined by direct DNA sequencing.
- a variety of automated sequencing procedures can be utilized when performing the diagnostic assays (Naeve, C. W., (1995) Biotechniques 19:448), including sequencing by mass spectrometry (see, e.g., PCT International Publication No. WO 94/16101; Cohen et al., Adv. Chromatogr. 36:127-162 (1996); and Griffin et al., Appl. Biochem. Biotechnol. 38:147-159 (1993)).
- Other methods for detecting mutations in the gene include methods in which protection from cleavage agents is used to detect mismatched bases in RNA/RNA or RNA/DNA duplexes (Myers et al., Science 230:1242 (1985)); Cotton et al., PNAS 85:4397 (1988); Saleeba et al., Meth. Enzymol. 217:286-295 (1992)), electrophoretic mobility of mutant and wild type nucleic acid is compared (Orita et al., PNAS 86:2766 (1989); Cotton et al., Mutat. Res. 285:125-144 (1993); and Hayashi et al., Genet. Anal. Tech. Appl.
- the nucleic acid molecules are also useful for testing an individual for a genotype that while not necessarily causing the disease, nevertheless affects the treatment modality.
- the nucleic acid molecules can be used to study the relationship between an individual's genotype and the individual's response to a compound used for treatment (pharmacogenomic relationship).
- the nucleic acid molecules described herein can be used to assess the mutation content of the kinase gene in an individual in order to select an appropriate compound or dosage regimen for treatment.
- FIG. 3 provides information on SNPs that have been found in the gene encoding the kinase protein of the present invention.
- SNPs in introns, such as these, may affect control/regulatory elements.
- nucleic acid molecules displaying genetic variations that affect treatment provide a diagnostic target that can be used to tailor treatment in an individual. Accordingly, the production of recombinant cells and animals containing these polymorphisms allow effective clinical design of treatment compounds and dosage regimens.
- the nucleic acid molecules are thus useful as antisense constructs to control kinase gene expression in cells, tissues, and organisms.
- a DNA antisense nucleic acid molecule is designed to be complementary to a region of the gene involved in transcription, preventing transcription and hence production of kinase protein.
- An antisense RNA or DNA nucleic acid molecule would hybridize to the mRNA and thus block translation of mRNA into kinase protein.
- a class of antisense molecules can be used to inactivate mRNA in order to decrease expression of kinase nucleic acid. Accordingly, these molecules can treat a disorder characterized by abnormal or undesired kinase nucleic acid expression.
- This technique involves cleavage by means of ribozymes containing nucleotide sequences complementary to one or more regions in the mRNA that attenuate the ability of the mRNA to be translated. Possible regions include coding regions and particularly coding regions corresponding to the catalytic and other functional activities of the kinase protein, such as substrate binding.
- the nucleic acid molecules also provide vectors for gene therapy in patients containing cells that are aberrant in kinase gene expression.
- recombinant cells which include the patient's cells that have been engineered ex vivo and returned to the patient, are introduced into an individual where the cells produce the desired kinase protein to treat the individual.
- the invention also encompasses kits for detecting the presence of a kinase nucleic acid in a biological sample.
- Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis.
- PCR-based tissue screening panels indicate expression in human liver.
- the kit can comprise reagents such as a labeled or labelable nucleic acid or agent capable of detecting kinase nucleic acid in a biological sample; means for determining the amount of kinase nucleic acid in the sample; and means for comparing the amount of kinase nucleic acid in the sample with a standard.
- the compound or agent can be packaged in a suitable container.
- the kit can further comprise instructions for using the kit to detect kinase protein mRNA or DNA.
- the present invention further provides nucleic acid detection kits, such as arrays or microarrays of nucleic acid molecules that are based on the sequence information provided in FIGS. 1 and 3 (SEQ ID NOS:1 and 3).
- Arrays or “Microarrays” refers to an array of distinct polynucleotides or oligonucleotides synthesized on a substrate, such as paper, nylon or other type of membrane, filter, chip, glass slide, or any other suitable solid support.
- the microarray is prepared and used according to the methods described in U.S. Pat. No. 5,837,832, Chee et al., PCT application WO95/11995 (Chee et al.), Lockhart, D. J. et al. (1996; Nat. Biotech. 14: 1675-1680) and Schena, M. et al. (1996; Proc. Natl. Acad. Sci. 93: 10614-10619), all of which are incorporated herein in their entirety by reference.
- such arrays are produced by the methods described by Brown et al, U.S. Pat. No. 5,807,522.
- the microarray or detection kit is preferably composed of a large number of unique, single-stranded nucleic acid sequences, usually either synthetic antisense oligonucleotides or fragments of cDNAs, fixed to a solid support.
- the oligonucleotides are preferably about 6-60 nucleotides in length, more preferably 15-30 nucleotides in length, and most preferably about 20-25 nucleotides in length. For a certain type of microarray or detection kit, it may be preferable to use oligonucleotides that are only 7-20 nucleotides in length.
- the microarray or detection kit may contain oligonucleotides that cover the known 5′, or 3′, sequence, sequential oligonucleotides which cover the full length sequence; or unique oligonucleotides selected from particular areas along the length of the sequence.
- Polynucleotides used in the microarray or detection kit may be oligonucleotides that are specific to a gene or genes of interest.
- the gene(s) of interest (or an ORF identified from the contigs of the present invention) is typically examined using a computer algorithm which starts at the 5′ or at the 3′ end of the nucleotide sequence. Typical algorithms will then identify oligomers of defined length that are unique to the gene, have a GC content within a range suitable for hybridization, and lack predicted secondary structure that may interfere with hybridization. In certain situations it may be appropriate to use pairs of oligonucleotides on a microarray or detection kit.
- the “pairs” will be identical, except for one nucleotide that preferably is located in the center of the sequence.
- the second oligonucleotide in the pair serves as a control.
- the number of oligonucleotide pairs may range from two to one million.
- the oligomers are synthesized at designated areas on a substrate using a light-directed chemical process.
- the substrate may be paper, nylon or other type of membrane, filter, chip, glass slide or any other suitable solid support.
- an oligonucleotide may be synthesized on the surface of the substrate by using a chemical coupling procedure and an ink jet application apparatus, as described in PCT application WO95/251116 (Baldeschweiler et al.) which is incorporated herein in its entirety by reference.
- a “gridded” array analogous to a dot (or slot) blot may be used to arrange and link cDNA fragments or oligonucleotides to the surface of a substrate using a vacuum system, thermal, UV, mechanical or chemical bonding procedures.
- An array such as those described above, may be produced by hand or by using available devices (slot blot or dot blot apparatus), materials (any suitable solid support), and machines (including robotic instruments), and may contain 8, 24, 96, 384, 1536, 6144 or more oligonucleotides, or any other number between two and one million which lends itself to the efficient use of commercially available instrumentation.
- RNA or DNA from a biological sample is made into hybridization probes.
- the mRNA is isolated, and cDNA is produced and used as a template to make antisense RNA (aRNA).
- aRNA is amplified in the presence of fluorescent nucleotides, and labeled probes are incubated with the microarray or detection kit so that the probe sequences hybridize to complementary oligonucleotides of the microarray or detection kit. Incubation conditions are adjusted so that hybridization occurs with precise complementary matches or with various degrees of less complementarity. After removal of nonhybridized probes, a scanner is used to determine the levels and patterns of fluorescence.
- the scanned images are examined to determine degree of complementarity and the relative abundance of each oligonucleotide sequence on the microarray or detection kit.
- the biological samples may be obtained from any bodily fluids (such as blood, urine, saliva, phlegm, gastric juices, etc.), cultured cells, biopsies, or other tissue preparations.
- a detection system may be used to measure the absence, presence, and amount of hybridization for all of the distinct sequences simultaneously. This data may be used for large-scale correlation studies on the sequences, expression patterns, mutations, variants, or polymorphisms among samples.
- the present invention provides methods to identify the expression of the kinase proteins/peptides of the present invention.
- methods comprise incubating a test sample with one or more nucleic acid molecules and assaying for binding of the nucleic acid molecule with components within the test sample.
- assays will typically involve arrays comprising many genes, at least one of which is a gene of the present invention and or alleles of the kinase gene of the present invention.
- FIG. 3 provides information on SNPs that have been found in the gene encoding the kinase protein of the present invention.
- SNPs in introns, such as these, may affect control/regulatory elements.
- Conditions for incubating a nucleic acid molecule with a test sample vary. Incubation conditions depend on the format employed in the assay, the detection methods employed, and the type and nature of the nucleic acid molecule used in the assay.
- One skilled in the art will recognize that any one of the commonly available hybridization, amplification or array assay formats can readily be adapted to employ the novel fragments of the Human genome disclosed herein. Examples of such assays can be found in Chard, T, An Introduction to Radioimmunoassay and Related Techniques, Elsevier Science Publishers, Amsterdam, The Netherlands (1986); Bullock, G. R. et al., Techniques in Immunocytochemistry, Academic Press, Orlando, Fla. Vol. 1 (1 982), Vol. 2 (1983), Vol. 3 (1985); Tijssen, P., Practice and Theory of Enzyme Immunoassays: Laboratory Techniques in Biochemistry and Molecular Biology, Elsevier Science Publishers, Amsterdam, The Netherlands (1985).
- test samples of the present invention include cells, protein or membrane extracts of cells.
- the test sample used in the above-described method will vary based on the assay format, nature of the detection method and the tissues, cells or extracts used as the sample to be assayed. Methods for preparing nucleic acid extracts or of cells are well known in the art and can be readily be adapted in order to obtain a sample that is compatible with the system utilized.
- kits which contain the necessary reagents to carry out the assays of the present invention.
- the invention provides a compartmentalized kit to receive, in close confinement, one or more containers which comprises: (a) a first container comprising one of the nucleic acid molecules that can bind to a fragment of the Human genome disclosed herein; and (b) one or more other containers comprising one or more of the following: wash reagents, reagents capable of detecting presence of a bound nucleic acid.
- a compartmentalized kit includes any kit in which reagents are contained in separate containers.
- Such containers include small glass containers, plastic containers, strips of plastic, glass or paper, or arraying material such as silica.
- Such containers allows one to efficiently transfer reagents from one compartment to another compartment such that the samples and reagents are not cross-contaminated, and the agents or solutions of each container can be added in a quantitative fashion from one compartment to another.
- Such containers will include a container which will accept the test sample, a container which contains the nucleic acid probe, containers which contain wash reagents (such as phosphate buffered saline, Tris-buffers, etc.), and containers which contain the reagents used to detect the bound probe.
- wash reagents such as phosphate buffered saline, Tris-buffers, etc.
- the invention also provides vectors containing the nucleic acid molecules described herein.
- the term “vector” refers to a vehicle, preferably a nucleic acid molecule, which can transport the nucleic acid molecules.
- the vector is a nucleic acid molecule, the nucleic acid molecules are covalently linked to the vector nucleic acid.
- the vector includes a plasmid, single or double stranded phage, a single or double stranded RNA or DNA viral vector, or artificial chromosome, such as a BAC, PAC, YAC, OR MAC.
- a vector can be maintained in the host cell as an extrachromosomal element where it replicates and produces additional copies of the nucleic acid molecules.
- the vector may integrate into the host cell genome and produce additional copies of the nucleic acid molecules when the host cell replicates.
- the invention provides vectors for the maintenance (cloning vectors) or vectors for expression (expression vectors) of the nucleic acid molecules.
- the vectors can function in prokaryotic or eukaryotic cells or in both (shuttle vectors).
- Expression vectors contain cis-acting regulatory regions that are operably linked in the vector to the nucleic acid molecules such that transcription of the nucleic acid molecules is allowed in a host cell.
- the nucleic acid molecules can be introduced into the host cell with a separate nucleic acid molecule capable of affecting transcription.
- the second nucleic acid molecule may provide a trans-acting factor interacting with the cis-regulatory control region to allow transcription of the nucleic acid molecules from the vector.
- a trans-acting factor may be supplied by the host cell.
- a trans-acting factor can be produced from the vector itself. It is understood, however, that in some embodiments, transcription and/or translation of the nucleic acid molecules can occur in a cell-free system.
- the regulatory sequence to which the nucleic acid molecules described herein can be operably linked include promoters for directing mRNA transcription. These include, but are not limited to, the left promoter from bacteriophage ⁇ , the lac, TRP, and TAC promoters from E. coli, the early and late promoters from SV40, the CMV immediate early promoter, the adenovirus early and late promoters, and retrovirus long-terminal repeats.
- expression vectors may also include regions that modulate transcription, such as repressor binding sites and enhancers.
- regions that modulate transcription include the SV40 enhancer, the cytomegalovirus immediate early enhancer, polyoma enhancer, adenovirus enhancers, and retrovirus LTR enhancers.
- expression vectors can also contain sequences necessary for transcription termination and, in the transcribed region a ribosome binding site for translation.
- Other regulatory control elements for expression include initiation and termination codons as well as polyadenylation signals.
- the person of ordinary skill in the art would be aware of the numerous regulatory sequences that are useful in expression vectors. Such regulatory sequences are described, for example, in Sambrook et al., Molecular Cloning: A Laboratory Manual. 2 nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).
- a variety of expression vectors can be used to express a nucleic acid molecule.
- Such vectors include chromosomal, episomal, and virus-derived vectors, for example vectors derived from bacterial plasmids, from bacteriophage, from yeast episomes, from yeast chromosomal elements, including yeast artificial chromosomes, from viruses such as baculoviruses, papovaviruses such as SV40, Vaccinia viruses, adenoviruses, poxviruses, pseudorabies viruses, and retroviruses.
- Vectors may also be derived from combinations of these sources such as those derived from plasmid and bacteriophage genetic elements, e.g.
- the regulatory sequence may provide constitutive expression in one or more host cells (i.e. tissue specific) or may provide for inducible expression in one or more cell types such as by temperature, nutrient additive, or exogenous factor such as a hormone or other ligand.
- host cells i.e. tissue specific
- inducible expression in one or more cell types such as by temperature, nutrient additive, or exogenous factor such as a hormone or other ligand.
- a variety of vectors providing for constitutive and inducible expression in prokaryotic and eukaryotic hosts are well known to those of ordinary skill in the art.
- the nucleic acid molecules can be inserted into the vector nucleic acid by well-known methodology.
- the DNA sequence that will ultimately be expressed is joined to an expression vector by cleaving the DNA sequence and the expression vector with one or more restriction enzymes and then ligating the fragments together. Procedures for restriction enzyme digestion and ligation are well known to those of ordinary skill in the art.
- the vector containing the appropriate nucleic acid molecule can be introduced into an appropriate host cell for propagation or expression using well-known techniques.
- Bacterial cells include, but are not limited to, E. coli, Streptomyces, and Salmonella typhimurium.
- Eukaryotic cells include, but are not limited to, yeast, insect cells such as Drosophila, animal cells such as COS and CHO cells, and plant cells.
- the invention provides fusion vectors that allow for the production of the peptides.
- Fusion vectors can increase the expression of a recombinant protein, increase the solubility of the recombinant protein, and aid in the purification of the protein by acting for example as a ligand for affinity purification.
- a proteolytic cleavage site may be introduced at the junction of the fusion moiety so that the desired peptide can ultimately be separated from the fusion moiety.
- Proteolytic enzymes include, but are not limited to, factor Xa, thrombin, and enterokinase.
- Typical fusion expression vectors include pGEX (Smith et al., Gene 67:31-40 (1988)), pMAL (New England Biolabs, Beverly, Ma.) and pRIT5 (Pharmacia, Piscataway, N.J.) which fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein.
- GST glutathione S-transferase
- suitable inducible non-fusion E. coli expression vectors include pTrc (Amann et al., Gene 69:301-315 (1988)) and pET 11d (Studier et al., Gene Expression Technology: Methods in Enzymology 185:60-89 (1990)).
- Recombinant protein expression can be maximized in host bacteria by providing a genetic background wherein the host cell has an impaired capacity to proteolytically cleave the recombinant protein.
- the sequence of the nucleic acid molecule of interest can be altered to provide preferential codon usage for a specific host cell, for example E. coli. (Wada et al, Nucleic Acids Res. 20:2111-2118 (1992)).
- the nucleic acid molecules can also be expressed by expression vectors that are operative in yeast.
- yeast e.g., S. cerevisiae
- vectors for expression in yeast include pYepSec1 (Baldari, et al., EMBO J 6:229-234 (1987)), pMFa (Kurjan et al., Cell 30:933-943(1982)), pJRY88 (Schultz et al., Gene 54:113-123 (1987)), and pYES2 (Invitrogen Corporation, San Diego, Calif.).
- the nucleic acid molecules can also be expressed in insect cells using, for example, baculovirus expression vectors.
- Baculovirus vectors available for expression of proteins in cultured insect cells include the pAc series (Smith et al., Mol. Cell Biol. 3:2156-2165 (1983)) and the pVL series (Lucklow et al., Virology 1 70:31-39 (1989)).
- the nucleic acid molecules described herein are expressed in mammalian cells using mammalian expression vectors.
- mammalian expression vectors include pCDM8 (Seed, B. Nature 329:840(1987)) and pMT2PC (Kaufman et al., EMBO J 6:187-195 (1987)).
- the expression vectors listed herein are provided by way of example only of the well-known vectors available to those of ordinary skill in the art that would be useful to express the nucleic acid molecules.
- the person of ordinary skill in the art would be aware of other vectors suitable for maintenance propagation or expression of the nucleic acid molecules described herein. These are found for example in Sambrook, J., Fritsh, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual. 2 nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989.
- the invention also relates to recombinant host cells containing the vectors described herein.
- Host cells therefore include prokaryotic cells, lower eukaryotic cells such as yeast, other eukaryotic cells such as insect cells, and higher eukaryotic cells such as mammalian cells.
- the recombinant host cells are prepared by introducing the vector constructs described herein into the cells by techniques readily available to the person of ordinary skill in the art. These include, but are not limited to, calcium phosphate transfection, DEAE-dextran-mediated transfection, cationic lipid-mediated transfection, electroporation, transduction, infection, lipofection, and other techniques such as those found in Sambrook, et al. ( Molecular Cloning: A Laboratory Manual. 2 nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989).
- Host cells can contain more than one vector.
- different nucleotide sequences can be introduced on different vectors of the same cell.
- the nucleic acid molecules can be introduced either alone or with other nucleic acid molecules that are not related to the nucleic acid molecules such as those providing trans-acting factors for expression vectors.
- the vectors can be introduced independently, co-introduced or joined to the nucleic acid molecule vector.
- bacteriophage and viral vectors these can be introduced into cells as packaged or encapsulated virus by standard procedures for infection and transduction.
- Viral vectors can be replication-competent or replication-defective. In the case in which viral replication is defective, replication will occur in host cells providing functions that complement the defects.
- Vectors generally include selectable markers that enable the selection of the subpopulation of cells that contain the recombinant vector constructs.
- the marker can be contained in the same vector that contains the nucleic acid molecules described herein or may be on a separate vector. Markers include tetracycline or ampicillin-resistance genes for prokaryotic host cells and dihydrofolate reductase or neomycin resistance for eukaryotic host cells. However, any marker that provides selection for a phenotypic trait will be effective.
- mature proteins can be produced in bacteria, yeast, mammalian cells, and other cells under the control of the appropriate regulatory sequences, cell-free transcription and translation systems can also be used to produce these proteins using RNA derived from the DNA constructs described herein.
- secretion of the peptide is desired, which is difficult to achieve with multi-transmembrane domain containing proteins such as kinases, appropriate secretion signals are incorporated into the vector.
- the signal sequence can be endogenous to the peptides or heterologous to these peptides.
- the protein can be isolated from the host cell by standard disruption procedures, including freeze thaw, sonication, mechanical disruption, use of lysing agents and the like.
- the peptide can then be recovered and purified by well-known purification methods including ammonium sulfate precipitation, acid extraction, anion or cationic exchange chromatography, phosphocellulose chromatography, hydrophobic-interaction chromatography, affinity chromatography, hydroxylapatitc chromatography, lectin chromatography, or high performance liquid chromatography.
- the peptides can have various glycosylation patterns, depending upon the cell, or maybe non-glycosylated as when produced in bacteria.
- the peptides may include an initial modified methionine in some cases as a result of a host-mediated process.
- the recombinant host cells expressing the peptides described herein have a variety of uses. First, the cells are useful for producing a kinase protein or peptide that can be further purified to produce desired amounts of kinase protein or fragments. Thus, host cells containing expression vectors are useful for peptide production.
- Host cells are also useful for conducting cell-based assays involving the kinase protein or kinase protein fragments, such as those described above as well as other formats known in the art.
- a recombinant host cell expressing a native kinase protein is useful for assaying compounds that stimulate or inhibit kinase protein function.
- Host cells are also useful for identifying kinase protein mutants in which these functions are affected. If the mutants naturally occur and give rise to a pathology, host cells containing the mutations are useful to assay compounds that have a desired effect on the mutant kinase protein (for example, stimulating or inhibiting function) which may not be indicated by their effect on the native kinase protein.
- a desired effect on the mutant kinase protein for example, stimulating or inhibiting function
- a transgenic animal is preferably a mammal, for example a rodent, such as a rat or mouse, in which one or more of the cells of the animal include a transgene.
- a transgene is exogenous DNA which is integrated into the genome of a cell from which a transgenic animal develops and which remains in the genome of the mature animal in one or more cell types or tissues of the transgenic animal. These animals are useful for studying the function of a kinase protein and identifying and evaluating modulators of kinase protein activity.
- Other examples of transgenic animals include non-human primates, sheep, dogs, cows, goats, chickens, and amphibians.
- a transgenic animal can be produced by introducing nucleic acid into the male pronuclei of a fertilized oocyte, e.g., by microinjection, retroviral infection, and allowing the oocyte to develop in a pseudopregnant female foster animal.
- Any of the kinase protein nucleotide sequences can be introduced as a transgene into the genome of a non-human animal, such as a mouse.
- Any of the regulatory or other sequences useful in expression vectors can form part of the transgenic sequence. This includes intronic sequences and polyadenylation signals, if not already included.
- a tissue-specific regulatory sequence(s) can be operably linked to the transgene to direct expression of the kinase protein to particular cells.
- transgenic animals via embryo manipulation and microinjection, particularly animals such as mice, have become conventional in the art and are described, for example, in U.S. Pat. Nos. 4,736,866 and 4,870,009, both by Leder et al., U.S. Pat. No. 4,873,191 by Wagner et al. and in Hogan, B., Manipulating the Mouse Embryo, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986). Similar methods are used for production of other transgenic animals.
- a transgenic founder animal can be identified based upon the presence of the transgene in its genome and/or expression of transgenic mRNA in tissues or cells of the animals.
- transgenic founder animal can then be used to breed additional animals carrying the transgene.
- transgenic animals carrying a transgene can further be bred to other transgenic animals carrying other transgenes.
- a transgenic animal also includes animals in which the entire animal or tissues in the animal have been produced using the homologously recombinant host cells described herein.
- transgenic non-human animals can be produced which contain selected systems that allow for regulated expression of the transgene.
- a system is the cre/loxP recombinase system of bacteriophage P1.
- cre/loxP recombinase system of bacteriophage P1.
- FLP recombinase system of S. cerevisiae (O'Gorman et al. Science 251:1351-1355 (1991).
- mice containing transgenes encoding both the Cre recombinase and a selected protein is required.
- Such animals can be provided through the construction of “double” transgenic animals, e.g., by mating two transgenic animals, one containing a transgene encoding a selected protein and the other containing a transgene encoding a recombinase.
- Clones of the non-human transgenic animals described herein can also be produced according to the methods described in Wilmut, I. et al. Nature 385:810-813 (1997) and PCT International Publication Nos. WO 97/07668 and WO 97/07669.
- a cell e.g., a somatic cell
- the quiescent cell can then be fused, e.g., through the use of electrical pulses, to an enucleated oocyte from an animal of the same species from which the quiescent cell is isolated.
- the reconstructed oocyte is then cultured such that it develops to morula or blastocyst and then transferred to pseudopregnant female foster animal.
- the offspring born of this female foster animal will be a clone of the animal from which the cell, e.g., the somatic cell, is isolated.
- Transgenic animals containing recombinant cells that express the peptides described herein are useful to conduct the assays described herein in an in vivo context. Accordingly, the various physiological factors that are present in vivo and that could effect substrate binding, kinase protein activation, and signal transduction, may not be evident from in vitro cell-free or cell-based assays. Accordingly, it is useful to provide non-human transgenic animals to assay in vivo kinase protein function, including substrate interaction, the effect of specific mutant kinase proteins on kinase protein function and substrate interaction, and the effect of chimeric kinase proteins. It is also possible to assess the effect of null mutations, that is, mutations that substantially or completely eliminate one or more kinase protein functions.
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Abstract
Description
- The present invention is in the field of kinase proteins that are related to the homeodomain-interacting protein kinase subfamily, recombinant DNA molecules, and protein production. The present invention specifically provides novel peptides and proteins that effect protein phosphorylation and nucleic acid molecules encoding such peptide and protein molecules, all of which are useful in the development of human therapeutics and diagnostic compositions and methods.
- Protein Kinases
- Kinases regulate many different cell proliferation, differentiation, and signaling processes by adding phosphate groups to proteins. Uncontrolled signaling has been implicated in a variety of disease conditions including inflammation, cancer, arteriosclerosis, and psoriasis. Reversible protein phosphorylation is the main strategy for controlling activities of eukaryotic cells. It is estimated that more than 1000 of the 10,000 proteins active in a typical mammalian cell are phosphorylated. The high energy phosphate, which drives activation, is generally transferred from adenosine triphosphate molecules (ATP) to a particular protein by protein kinases and removed from that protein by protein phosphatases. Phosphorylation occurs in response to extracellular signals (hormones, neurotransmitters, growth and differentiation factors, etc), cell cycle checkpoints, and environmental or nutritional stresses and is roughly analogous to turning on a molecular switch. When the switch goes on, the appropriate protein kinase activates a metabolic enzyme, regulatory protein, receptor, cytoskeletal protein, ion channel or pump, or transcription factor.
- The kinases comprise the largest known protein group, a superfamily of enzymes with widely varied functions and specificities. They are usually named after their substrate, their regulatory molecules, or some aspect of a mutant phenotype. With regard to substrates, the protein kinases may be roughly divided into two groups; those that phosphorylate tyrosine residues (protein tyrosine kinases, PTK) and those that phosphorylate serine or threonine residues (serine/threonine kinases, STK). A few protein kinases have dual specificity and phosphorylate threonine and tyrosine residues. Almost all kinases contain a similar 250-300 amino acid catalytic domain. The N-terminal domain, which contains subdomains I-IV, generally folds into a two-lobed structure, which binds and orients the ATP (or GTP) donor molecule. The larger C terminal lobe, which contains subdomains VI A-XI, binds the protein substrate and carries out the transfer of the gamma phosphate from ATP to the hydroxyl group of a serine, threonine, or tyrosine residue. Subdomain V spans the two lobes.
- The kinases may be categorized into families by the different amino acid sequences (generally between 5 and 100 residues) located on either side of, or inserted into loops of, the kinase domain. These added amino acid sequences allow the regulation of each kinase as it recognizes and interacts with its target protein. The primary structure of the kinase domains is conserved and can be further subdivided into 11 subdomains. Each of the 11 subdomains contains specific residues and motifs or patterns of amino acids that are characteristic of that subdomain and are highly conserved (Hardie, G. and Hanks, S. (1995)The Protein Kinase Facts Books, Vol I:7-20 Academic Press, San Diego, Calif.).
- The second messenger dependent protein kinases primarily mediate the effects of second messengers such as cyclic AMP (cAMP), cyclic GMP, inositol triphosphate, phosphatidylinositol, 3, 4, 5-triphosphate, cyclic-ADPribose, arachidonic acid, diacylglycerol and calcium-calmodulin. The cyclic-AMP dependent protein kinases (PKA) are important members of the STK family. Cyclic-AMP is an intracellular mediator of hormone action in all prokaryotic and animal cells that have been studied. Such hormone-induced cellular responses include thyroid hormone secretion, cortisol secretion, progesterone secretion, glycogen breakdown, bone resorption, and regulation of heart rate and force of heart muscle contraction. PKA is found in all animal cells and is thought to account for the effects of cyclic-AMP in most of these cells. Altered PKA expression is implicated in a variety of disorders and diseases including cancer, thyroid disorders, diabetes, atherosclerosis, and cardiovascular disease (Isselbacher, K. J. et al. (1994)Harrison's Principles of Internal Medicine, McGraw-Hill, New York, N.Y., pp. 416-431, 1887).
- Calcium-calmodulin (CaM) dependent protein kinases are also members of STK family. Calmodulin is a calcium receptor that mediates many calcium regulated processes by binding to target proteins in response to the binding of calcium. The principle target protein in these processes is CaM dependent protein kinases. CaM-kinases are involved in regulation of smooth muscle contraction (MLC kinase), glycogen breakdown (phosphorylase kinase), and neurotransmission (CaM kinase I and CaM kinase II). CaM kinase I phosphorylates a variety of substrates including the neurotransmitter related proteins synapsin I and II, the gene transcription regulator, CREB, and the cystic fibrosis conductance regulator protein, CFTR (Haribabu, B. et al. (1995)EMBO Journal 14:3679-86). CaM II kinase also phosphorylates synapsin at different sites, and controls the synthesis of catecholamines in the brain through phosphorylation and activation of tyrosine hydroxylase. Many of the CaM kinases are activated by phosphorylation in addition to binding to CaM. The kinase may autophosphorylate itself, or be phosphorylated by another kinase as part of a “kinase cascade”.
- Another ligand-activated protein kinase is 5′-AMP-activated protein kinase (AMPK) (Gao, G. et al. (1996)J. Biol Chem. 15:8675-81). Mammalian AMPK is a regulator of fatty acid and sterol synthesis through phosphorylation of the enzymes acetyl-CoA carboxylase and hydroxymethylglutaryl-CoA reductase and mediates responses of these pathways to cellular stresses such as heat shock and depletion of glucose and ATP. AMPK is a heterotrimeric complex comprised of a catalytic alpha subunit and two non-catalytic beta and gamma subunits that are believed to regulate the activity of the alpha subunit. Subunits of AMPK have a much wider distribution in non-lipogenic tissues such as brain, heart, spleen, and lung than expected. This distribution suggests that its role may extend beyond regulation of lipid metabolism alone.
- The mitogen-activated protein kinases (MAP) are also members of the STK family. MAP kinases also regulate intracellular signaling pathways. They mediate signal transduction from the cell surface to the nucleus via phosphorylation cascades. Several subgroups have been identified, and each manifests different substrate specificities and responds to distinct extracellular stimuli (Egan, S. E. and Weinberg, R. A. (1993)Nature 365:781-783). MAP kinase signaling pathways are present in mammalian cells as well as in yeast. The extracellular stimuli that activate mammalian pathways include epidermal growth factor (EGF), ultraviolet light, hyperosmolar medium, heat shock, endotoxic lipopolysaccharide (LPS), and pro-inflammatory cytokines such as tumor necrosis factor (TNF) and interleukin-1 (IL-1).
- PRK (proliferation-related kinase) is a serum/cytokine inducible STK that is involved in regulation of the cell cycle and cell proliferation in human megakaroytic cells (Li, B. et al. (1996)J. Biol. Chem. 271:19402-8). PRK is related to the polo (derived from humans polo gene) family of STKs implicated in cell division. PRK is downregulated in lung tumor tissue and may be a proto-oncogene whose deregulated expression in normal tissue leads to oncogenic transformation. Altered MAP kinase expression is implicated in a variety of disease conditions including cancer, inflammation, immune disorders, and disorders affecting growth and development.
- The cyclin-dependent protein kinases (CDKs) are another group of STKs that control the progression of cells through the cell cycle. Cyclins are small regulatory proteins that act by binding to and activating CDKs that then trigger various phases of the cell cycle by phosphorylating and activating selected proteins involved in the mitotic process. CDKs are unique in that they require multiple inputs to become activated. In addition to the binding of cyclin, CDK activation requires the phosphorylation of a specific threonine residue and the dephosphorylation of a specific tyrosine residue.
- Protein tyrosine kinases, PTKs, specifically phosphorylate tyrosine residues on their target proteins and may be divided into transmembrane, receptor PTKs and nontransmembrane, non-receptor PTKs. Transmembrane protein-tyrosine kinases are receptors for most growth factors. Binding of growth factor to the receptor activates the transfer of a phosphate group from ATP to selected tyrosine side chains of the receptor and other specific proteins. Growth factors (GF) associated with receptor PTKs include; epidermal GF, platelet-derived GF, fibroblast GF, hepatocyte GF, insulin and insulin-like GFs, nerve GF, vascular endothelial GF, and macrophage colony stimulating factor.
- Non-receptor PTKs lack transmembrane regions and, instead, form complexes with the intracellular regions of cell surface receptors. Such receptors that function through non-receptor PTKs include those for cytokines, hormones (growth hormone and prolactin) and antigen-specific receptors on T and B lymphocytes.
- Many of these PTKs were first identified as the products of mutant oncogenes in cancer cells where their activation was no longer subject to normal cellular controls. In fact, about one third of the known oncogenes encode PTKs, and it is well known that cellular transformation (oncogenesis) is often accompanied by increased tyrosine phosphorylation activity (Carbonneau H and Tonks N K (1992)Annu. Rev. Cell. Biol. 8:463-93). Regulation of PTK activity may therefore be an important strategy in controlling some types of cancer.
- Homeodomain-Interacting Protein Kinases
- The novel human protein, and encoding gene, provided by the present invention is related to the family of homeodomain-interacting protein kinases (HIPKs). HIPKs are nuclear kinases that act as transcriptional co-repressors for homeodomain transcription factors. HIPKs enhance the repressor functions of NK homeoproteins. The HIPK family comprises at least three previously described members: HIPK1, HIPK2, and HIPK3. HIPKs comprise a conserved protein kinase domain and a separate homeoprotein/homeodomain interaction domain. HIPK2 has been found to significantly increase the DNA binding activity of the NK-3 homeoprotein (Kim et al.,J Biol Chem Oct. 2, 1998;273(40):25875-9).
- HIPKs show a high degree of similarity to yeast YAK1 proteins, human PKY (protein kinase YAK1 homolog), and Myak (mouse YAK homolog) proteins, which play important roles in cellular regulation and signaling, multidrug resistance, and in restricting cell growth. For a further review of HIPKs, YAK1, and PKY proteins, see Begley et al.,Gene 200: 35-43, 1997; Nupponen et al., Cytogenet. Cell Genet. 87: 102-103, 1999; and Sampson et al., J. Cell. Biochem. 52: 384-395, 1993.
- Kinase proteins, particularly members of the homeodomain-interacting protein kinase subfamily, are a major target for drug action and development. Accordingly, it is valuable to the field of pharmaceutical development to identify and characterize previously unknown members of this subfamily of kinase proteins. The present invention advances the state of the art by providing previously unidentified human kinase proteins that have homology to members of the homeodomain-interacting protein kinase subfamily.
- The present invention is based in part on the identification of amino acid sequences of human kinase peptides and proteins that are related to the homeodomain-interacting protein kinase subfamily, as well as allelic variants and other mammalian orthologs thereof. These unique peptide sequences, and nucleic acid sequences that encode these peptides, can be used as models for the development of human therapeutic targets, aid in the identification of therapeutic proteins, and serve as targets for the development of human therapeutic agents that modulate kinase activity in cells and tissues that express the kinase. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- FIG. 1 provides the nucleotide sequence of a CDNA molecule that encodes the kinase protein of the present invention. (SEQ ID NO:1) In addition, structure and functional information is provided, such as ATG start, stop and tissue distribution, where available, that allows one to readily determine specific uses of inventions based on this molecular sequence. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- FIG. 2 provides the predicted amino acid sequence of the kinase of the present invention. (SEQ ID NO:2) In addition structure and functional information such as protein family, function, and modification sites is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence.
- FIG. 3 provides genomic sequences that span the gene encoding the kinase protein of the present invention. (SEQ ID NO:3) In addition structure and functional information, such as intron/exon structure, promoter location, etc., is provided where available, allowing one to readily determine specific uses of inventions based on this molecular sequence. As illustrated in FIG. 3, the following SNPs were identified: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at
position 14131. - General Description
- The present invention is based on the sequencing of the human genome. During the sequencing and assembly of the human genome, analysis of the sequence information revealed previously unidentified fragments of the human genome that encode peptides that share structural and/or sequence homology to protein/peptide/domains identified and characterized within the art as being a kinase protein or part of a kinase protein and are related to the homeodomain-interacting protein kinase subfamily. Utilizing these sequences, additional genomic sequences were assembled and transcript and/or cDNA sequences were isolated and characterized. Based on this analysis, the present invention provides amino acid sequences of human kinase peptides and proteins that are related to the homeodomain-interacting protein kinase subfamily, nucleic acid sequences in the form of transcript sequences, cDNA sequences and/or genomic sequences that encode these kinase peptides and proteins, nucleic acid variation (allelic information), tissue distribution of expression, and information about the closest art known protein/peptide/domain that has structural or sequence homology to the kinase of the present invention.
- In addition to being previously unknown, the peptides that are provided in the present invention are selected based on their ability to be used for the development of commercially important products and services. Specifically, the present peptides are selected based on homology and/or structural relatedness to known kinase proteins of the homeodomain-interacting protein kinase subfamily and the expression pattern observed. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. The art has clearly established the commercial importance of members of this family of proteins and proteins that have expression patterns similar to that of the present gene. Some of the more specific features of the peptides of the present invention, and the uses thereof, are described herein, particularly in the Background of the Invention and in the annotation provided in the Figures, and/or are known within the art for each of the known homeodomain-interacting protein kinase family or subfamily of kinase proteins.
- Specific Embodiments
- Peptide Molecules
- The present invention provides nucleic acid sequences that encode protein molecules that have been identified as being members of the kinase family of proteins and are related to the homeodomain-interacting protein kinase subfamily (protein sequences are provided in FIG. 2, transcript/cDNA sequences are provided in FIG. 1 and genomic sequences are provided in FIG. 3). The peptide sequences provided in FIG. 2, as well as the obvious variants described herein, particularly allelic variants as identified herein and using the information in FIG. 3, will be referred herein as the kinase peptides of the present invention, kinase peptides, or peptides/proteins of the present invention.
- The present invention provides isolated peptide and protein molecules that consist of, consist essentially of, or comprise the amino acid sequences of the kinase peptides disclosed in the FIG. 2, (encoded by the nucleic acid molecule shown in FIG. 1, transcript/cDNA or FIG. 3, genomic sequence), as well as all obvious variants of these peptides that are within the art to make and use. Some of these variants are described in detail below.
- As used herein, a peptide is said to be “isolated” or “purified” when it is substantially free of cellular material or free of chemical precursors or other chemicals. The peptides of the present invention can be purified to homogeneity or other degrees of purity. The level of purification will be based on the intended use. The critical feature is that the preparation allows for the desired function of the peptide, even if in the presence of considerable amounts of other components (the features of an isolated nucleic acid molecule is discussed below).
- In some uses, “substantially free of cellular material” includes preparations of the peptide having less than about 30% (by dry weight) other proteins (i.e., contaminating protein), less than about 20% other proteins, less than about 10% other proteins, or less than about 5% other proteins. When the peptide is recombinantly produced, it can also be substantially free of culture medium, i.e., culture medium represents less than about 20% of the volume of the protein preparation.
- The language “substantially free of chemical precursors or other chemicals” includes preparations of the peptide in which it is separated from chemical precursors or other chemicals that are involved in its synthesis. In one embodiment, the language “substantially free of chemical precursors or other chemicals” includes preparations of the kinase peptide having less than about 30% (by dry weight) chemical precursors or other chemicals, less than about 20% chemical precursors or other chemicals, less than about 10% chemical precursors or other chemicals, or less than about 5% chemical precursors or other chemicals.
- The isolated kinase peptide can be purified from cells that naturally express it, purified from cells that have been altered to express it (recombinant), or synthesized using known protein synthesis methods. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. For example, a nucleic acid molecule encoding the kinase peptide is cloned into an expression vector, the expression vector introduced into a host cell and the protein expressed in the host cell. The protein can then be isolated from the cells by an appropriate purification scheme using standard protein purification techniques. Many of these techniques are described in detail below.
- Accordingly, the present invention provides proteins that consist of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). The amino acid sequence of such a protein is provided in FIG. 2. A protein consists of an amino acid sequence when the amino acid sequence is the final amino acid sequence of the protein.
- The present invention further provides proteins that consist essentially of the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). A protein consists essentially of an amino acid sequence when such an amino acid sequence is present with only a few additional amino acid residues, for example from about 1 to about 100 or so additional residues, typically from 1 to about 20 additional residues in the final protein.
- The present invention further provides proteins that comprise the amino acid sequences provided in FIG. 2 (SEQ ID NO:2), for example, proteins encoded by the transcript/cDNA nucleic acid sequences shown in FIG. 1 (SEQ ID NO:1) and the genomic sequences provided in FIG. 3 (SEQ ID NO:3). A protein comprises an amino acid sequence when the amino acid sequence is at least part of the final amino acid sequence of the protein. In such a fashion, the protein can be only the peptide or have additional amino acid molecules, such as amino acid residues (contiguous encoded sequence) that are naturally associated with it or heterologous amino acid residues/peptide sequences. Such a protein can have a few additional amino acid residues or can comprise several hundred or more additional amino acids. The preferred classes of proteins that are comprised of the kinase peptides of the present invention are the naturally occurring mature proteins. A brief description of how various types of these proteins can be made/isolated is provided below.
- The kinase peptides of the present invention can be attached to heterologous sequences to form chimeric or fusion proteins. Such chimeric and fusion proteins comprise a kinase peptide operatively linked to a heterologous protein having an amino acid sequence not substantially homologous to the kinase peptide. “Operatively linked” indicates that the kinase peptide and the heterologous protein are fused in-frame. The heterologous protein can be fused to the N-terminus or C-terminus of the kinase peptide.
- In some uses, the fusion protein does not affect the activity of the kinase peptide per se. For example, the fusion protein can include, but is not limited to, enzymatic fusion proteins, for example beta-galactosidase fusions, yeast two-hybrid GAL fusions, poly-His fusions, MYC-tagged, HI-tagged and Ig fusions. Such fusion proteins, particularly poly-His fusions, can facilitate the purification of recombinant kinase peptide. In certain host cells (e.g., mammalian host cells), expression and/or secretion of a protein can be increased by using a heterologous signal sequence.
- A chimeric or fusion protein can be produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different protein sequences are ligated together in-frame in accordance with conventional techniques. In another embodiment, the fusion gene can be synthesized by conventional techniques including automated DNA synthesizers. Alternatively, PCR amplification of gene fragments can be carried out using anchor primers which give rise to complementary overhangs between two consecutive gene fragments which can subsequently be annealed and re-amplified to generate a chimeric gene sequence (see Ausubel et al.,Current Protocols in Molecular Biology, 1992). Moreover, many expression vectors are commercially available that already encode a fusion moiety (e.g., a GST protein). A kinase peptide-encoding nucleic acid can be cloned into such an expression vector such that the fusion moiety is linked in-frame to the kinase peptide.
- As mentioned above, the present invention also provides and enables obvious variants of the amino acid sequence of the proteins of the present invention, such as naturally occurring mature forms of the peptide, allelic/sequence variants of the peptides, non-naturally occurring recombinantly derived variants of the peptides, and orthologs and paralogs of the peptides. Such variants can readily be generated using art-known techniques in the fields of recombinant nucleic acid technology and protein biochemistry. It is understood, however, that variants exclude any amino acid sequences disclosed prior to the invention.
- Such variants can readily be identified/made using molecular techniques and the sequence information disclosed herein. Further, such variants can readily be distinguished from other peptides based on sequence and/or structural homology to the kinase peptides of the present invention. The degree of homology/identity present will be based primarily on whether the peptide is a functional variant or non-functional variant, the amount of divergence present in the paralog family and the evolutionary distance between the orthologs.
- To determine the percent identity of two amino acid sequences or two nucleic acid sequences, the sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-homologous sequences can be disregarded for comparison purposes). In a preferred embodiment, at least 30%, 40%, 50%, 60%, 70%, 80%, or 90% or more of the length of a reference sequence is aligned for comparison purposes. The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position (as used herein amino acid or nucleic acid “identity” is equivalent to amino acid or nucleic acid “homology”). The percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, which need to be introduced for optimal alignment of the two sequences.
- The comparison of sequences and determination of percent identity and similarity between two sequences can be accomplished using a mathematical algorithm. (Computational Molecular Biology, Lesk, A. M., ed., Oxford University Press, New York, 1988; Biocomputing: Informatics and Genome Projects, Smith, D. W., ed., Academic Press, New York, 1993; Computer Analysis of Sequence Data,
Part 1, Griffin, A. M., and Griffin, H. G., eds., Humana Press, New Jersey, 1994; Sequence Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; and Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press, New York, 1991). In a preferred embodiment, the percent identity between two amino acid sequences is determined using the Needleman and Wunsch (J. Mol. Biol. (48):444-453 (1970)) algorithm which has been incorporated into the GAP program in the GCG software package (available at http://www.gcg.com), using either a Blossom 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5, or 6. In yet another preferred embodiment, the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package (Devereux, J., et al., Nucleic Acids Res. 12(1):387 (1984)) (available at http://www.gcg.com), using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70, or 80 and a length weight of 1, 2, 3, 4, 5, or 6. In another embodiment, the percent identity between two amino acid or nucleotide sequences is determined using the algorithm of E. Myers and W. Miller (CABIOS, 4:11-17 (1989)) which has been incorporated into the ALIGN program (version 2.0), using a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4. - The nucleic acid and protein sequences of the present invention can further be used as a “query sequence” to perform a search against sequence databases to, for example, identify other family members or related sequences. Such searches can be performed using the NBLAST and XBLAST programs (version 2.0) of Altschul, et al. (J. Mol. Biol. 215:403-10 (1990)). BLAST nucleotide searches can be performed with the NBLAST program, score=100, wordlength=12 to obtain nucleotide sequences homologous to the nucleic acid molecules of the invention. BLAST protein searches can be performed with the XBLAST program, score=50, wordlength=3 to obtain amino acid sequences homologous to the proteins of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilized as described in Altschul et al. (Nucleic Acids Res. 25(17):3389-3402 (1997)). When utilizing BLAST and gapped BLAST programs, the default parameters of the respective programs (e.g., XBLAST and NBLAST) can be used.
- Full-length pre-processed forms, as well as mature processed forms, of proteins that comprise one of the peptides of the present invention can readily be identified as having complete sequence identity to one of the kinase peptides of the present invention as well as being encoded by the same genetic locus as the kinase peptide provided herein. The gene encoding the novel kinase protein of the present invention is located on a genome component that has been mapped to human chromosome 1 (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data.
- Allelic variants of a kinase peptide can readily be identified as being a human protein having a high degree (significant) of sequence homology/identity to at least a portion of the kinase peptide as well as being encoded by the same genetic locus as the kinase peptide provided herein. Genetic locus can readily be determined based on the genomic information provided in FIG. 3, such as the genomic sequence mapped to the reference human. The gene encoding the novel kinase protein of the present invention is located on a genome component that has been mapped to human chromosome 1 (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data. As used herein, two proteins (or a region of the proteins) have significant homology when the amino acid sequences are typically at least about 70-80%, 80-90%, and more typically at least about 90-95% or more homologous. A significantly homologous amino acid sequence, according to the present invention, will be encoded by a nucleic acid sequence that will hybridize to a kinase peptide encoding nucleic acid molecule under stringent conditions as more fully described below.
- FIG. 3 provides information on SNPs that have been found in the gene encoding the kinase protein of the present invention. The following variations were seen: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at
position 14131. SNPs in introns, such as these, may affect control/regulatory elements. - Paralogs of a kinase peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the kinase peptide, as being encoded by a gene from humans, and as having similar activity or function. Two proteins will typically be considered paralogs when the amino acid sequences are typically at least about 60% or greater, and more typically at least about 70% or greater homology through a given region or domain. Such paralogs will be encoded by a nucleic acid sequence that will hybridize to a kinase peptide encoding nucleic acid molecule under moderate to stringent conditions as more fully described below.
- Orthologs of a kinase peptide can readily be identified as having some degree of significant sequence homology/identity to at least a portion of the kinase peptide as well as being encoded by a gene from another organism. Preferred orthologs will be isolated from mammals, preferably primates, for the development of human therapeutic targets and agents. Such orthologs will be encoded by a nucleic acid sequence that will hybridize to a kinase peptide encoding nucleic acid molecule under moderate to stringent conditions, as more fully described below, depending on the degree of relatedness of the two organisms yielding the proteins.
- Non-naturally occurring variants of the kinase peptides of the present invention can readily be generated using recombinant techniques. Such variants include, but are not limited to deletions, additions and substitutions in the amino acid sequence of the kinase peptide. For example, one class of substitutions are conserved amino acid substitution. Such substitutions are those that substitute a given amino acid in a kinase peptide by another amino acid of like characteristics. Typically seen as conservative substitutions are the replacements, one for another, among the aliphatic amino acids Ala, Val, Leu, and Ile; interchange of the hydroxyl residues Ser and Thr; exchange of the acidic residues Asp and Glu; substitution between the amide residues Asn and Gln; exchange of the basic residues Lys and Arg; and replacements among the aromatic residues Phe and Tyr. Guidance concerning which amino acid changes are likely to be phenotypically silent are found in Bowie et al.,Science 247:1306-1310 (1990).
- Variant kinase peptides can be fully functional or can lack function in one or more activities, e.g. ability to bind substrate, ability to phosphorylate substrate, ability to mediate signaling, etc. Fully functional variants typically contain only conservative variation or variation in non-critical residues or in non-critical regions. FIG. 2 provides the result of protein analysis and can be used to identify critical domains/regions. Functional variants can also contain substitution of similar amino acids that result in no change or an insignificant change in function. Alternatively, such substitutions may positively or negatively affect function to some degree.
- Non-functional variants typically contain one or more non-conservative amino acid substitutions, deletions, insertions, inversions, or truncation or a substitution, insertion, inversion, or deletion in a critical residue or critical region.
- Amino acids that are essential for function can be identified by methods known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (Cunningham et al.,Science 244:1081-1085 (1989)), particularly using the results provided in FIG. 2. The latter procedure introduces single alanine mutations at every residue in the molecule. The resulting mutant molecules are then tested for biological activity such as kinase activity or in assays such as an in vitro proliferative activity. Sites that are critical for binding partner/substrate binding can also be determined by structural analysis such as crystallization, nuclear magnetic resonance or photoaffinity labeling (Smith et al., J. Mol. Biol. 224:899-904 (1992); de Vos et al. Science 255:306-312 (1992)).
- The present invention further provides fragments of the kinase peptides, in addition to proteins and peptides that comprise and consist of such fragments, particularly those comprising the residues identified in FIG. 2. The fragments to which the invention pertains, however, are not to be construed as encompassing fragments that may be disclosed publicly prior to the present invention.
- As used herein, a fragment comprises at least 8, 10, 12, 14, 16, or more contiguous amino acid residues from a kinase peptide. Such fragments can be chosen based on the ability to retain one or more of the biological activities of the kinase peptide or could be chosen for the ability to perform a function, e.g. bind a substrate or act as an immunogen. Particularly important fragments are biologically active fragments, peptides that are, for example, about 8 or more amino acids in length. Such fragments will typically comprise a domain or motif of the kinase peptide, e.g., active site, a transmembrane domain or a substrate-binding domain. Further, possible fragments include, but are not limited to, domain or motif containing fragments, soluble peptide fragments, and fragments containing immunogenic structures. Predicted domains and functional sites are readily identifiable by computer programs well known and readily available to those of skill in the art (e.g., PROSITE analysis). The results of one such analysis are provided in FIG. 2.
- Polypeptides often contain amino acids other than the 20 amino acids commonly referred to as the 20 naturally occurring amino acids. Further, many amino acids, including the terminal amino acids, may be modified by natural processes, such as processing and other post-translational modifications, or by chemical modification techniques well known in the art. Common modifications that occur naturally in kinase peptides are described in basic texts, detailed monographs, and the research literature, and they are well known to those of skill in the art (some of these features are identified in FIG. 2).
- Known modifications include, but are not limited to, acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent crosslinks, formation of cystine, formation of pyroglutamate, formylation, gamma carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination.
- Such modifications are well known to those of skill in the art and have been described in great detail in the scientific literature. Several particularly common modifications, glycosylation, lipid attachment, sulfation, gamma-carboxylation of glutamic acid residues, hydroxylation and ADP-ribosylation, for instance, are described in most basic texts, such asProteins—Structure and Molecular Properties, 2nd Ed., T. E. Creighton, W. H. Freeman and Company, New York (1993). Many detailed reviews are available on this subject, such as by Wold, F., Posttranslational Covalent Modification of Proteins, B. C. Johnson, Ed., Academic Press, New York 1-12 (1983); Seifter et al. (Meth. Enzymol. 182: 626-646 (1990)) and Rattan et al. (Ann. N.Y. Acad. Sci. 663:48-62 (1992)).
- Accordingly, the kinase peptides of the present invention also encompass derivatives or analogs in which a substituted amino acid residue is not one encoded by the genetic code, in which a substituent group is included, in which the mature kinase peptide is fused with another compound, such as a compound to increase the half-life of the kinase peptide (for example, polyethylene glycol), or in which the additional amino acids are fused to the mature kinase peptide, such as a leader or secretory sequence or a sequence for purification of the mature kinase peptide or a pro-protein sequence.
- Protein/Peptide Uses
- The proteins of the present invention can be used in substantial and specific assays related to the functional information provided in the Figures; to raise antibodies or to elicit another immune response; as a reagent (including the labeled reagent) in assays designed to quantitatively determine levels of the protein (or its binding partner or ligand) in biological fluids; and as markers for tissues in which the corresponding protein is preferentially expressed (either constitutively or at a particular stage of tissue differentiation or development or in a disease state). Where the protein binds or potentially binds to another protein or ligand (such as, for example, in a kinase-effector protein interaction or kinase-ligand interaction), the protein can be used to identify the binding partner/ligand so as to develop a system to identify inhibitors of the binding interaction. Any or all of these uses are capable of being developed into reagent grade or kit format for commercialization as commercial products.
- Methods for performing the uses listed above are well known to those skilled in the art. References disclosing such methods include “Molecular Cloning: A Laboratory Manual”, 2d ed., Cold Spring Harbor Laboratory Press, Sambrook, J., E. F. Fritsch and T. Maniatis eds., 1989, and “Methods in Enzymology: Guide to Molecular Cloning Techniques”, Academic Press, Berger, S. L. and A. R. Kimmel eds., 1987.
- The potential uses of the peptides of the present invention are based primarily on the source of the protein as well as the class/action of the protein. For example, kinases isolated from humans and their human/mammalian orthologs serve as targets for identifying agents for use in mammalian therapeutic applications, e.g. a human drug, particularly in modulating a biological or pathological response in a cell or tissue that expresses the kinase. Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in human liver. A large percentage of pharmaceutical agents are being developed that modulate the activity of kinase proteins, particularly members of the homeodomain-interacting protein kinase subfamily (see Background of the Invention). The structural and functional information provided in the Background and Figures provide specific and substantial uses for the molecules of the present invention, particularly in combination with the expression information provided in FIG. 1. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. Such uses can readily be determined using the information provided herein, that which is known in the art, and routine experimentation.
- The proteins of the present invention (including variants and fragments that may have been disclosed prior to the present invention) are useful for biological assays related to kinases that are related to members of the homeodomain-interacting protein kinase subfamily. Such assays involve any of the known kinase functions or activities or properties useful for diagnosis and treatment of kinase-related conditions that are specific for the subfamily of kinases that the one of the present invention belongs to, particularly in cells and tissues that express the kinase. Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in human liver.
- The proteins of the present invention are also useful in drug screening assays, in cell-based or cell-free systems. Cell-based systems can be native, i.e., cells that normally express the kinase, as a biopsy or expanded in cell culture. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. In an alternate embodiment, cell-based assays involve recombinant host cells expressing the kinase protein.
- The polypeptides can be used to identify compounds that modulate kinase activity of the protein in its natural state or an altered form that causes a specific disease or pathology associated with the kinase. Both the kinases of the present invention and appropriate variants and fragments can be used in high-throughput screens to assay candidate compounds for the ability to bind to the kinase. These compounds can be further screened against a functional kinase to determine the effect of the compound on the kinase activity. Further, these compounds can be tested in animal or invertebrate systems to determine activity/effectiveness. Compounds can be identified that activate (agonist) or inactivate (antagonist) the kinase to a desired degree.
- Further, the proteins of the present invention can be used to screen a compound for the ability to stimulate or inhibit interaction between the kinase protein and a molecule that normally interacts with the kinase protein, e.g. a substrate or a component of the signal pathway that the kinase protein normally interacts (for example, another kinase). Such assays typically include the steps of combining the kinase protein with a candidate compound under conditions that allow the kinase protein, or fragment, to interact with the target molecule, and to detect the formation of a complex between the protein and the target or to detect the biochemical consequence of the interaction with the kinase protein and the target, such as any of the associated effects of signal transduction such as protein phosphorylation, cAMP turnover, and adenylate cyclase activation, etc.
- Candidate compounds include, for example, 1) peptides such as soluble peptides, including Ig-tailed fusion peptides and members of random peptide libraries (see, e.g., Lam et al.,Nature 354:82-84 (1991); Houghten et al., Nature 354:84-86 (1991)) and combinatorial chemistry-derived molecular libraries made of D- and/or L- configuration amino acids; 2) phosphopeptides (e.g., members of random and partially degenerate, directed phosphopeptide libraries, see, e.g., Songyang et al., Cell 72:767-778 (1993)); 3) antibodies (e.g., polyclonal, monoclonal, humanized, anti-idiotypic, chimeric, and single chain antibodies as well as Fab, F(ab′)2, Fab expression library fragments, and epitope-binding fragments of antibodies); and 4) small organic and inorganic molecules (e.g., molecules obtained from combinatorial and natural product libraries).
- One candidate compound is a soluble fragment of the receptor that competes for substrate binding. Other candidate compounds include mutant kinases or appropriate fragments containing mutations that affect kinase function and thus compete for substrate. Accordingly, a fragment that competes for substrate, for example with a higher affinity, or a fragment that binds substrate but does not allow release, is encompassed by the invention.
- The invention further includes other end point assays to identify compounds that modulate (stimulate or inhibit) kinase activity. The assays typically involve an assay of events in the signal transduction pathway that indicate kinase activity. Thus, the phosphorylation of a substrate, activation of a protein, a change in the expression of genes that are up- or down-regulated in response to the kinase protein dependent signal cascade can be assayed.
- Any of the biological or biochemical functions mediated by the kinase can be used as an endpoint assay. These include all of the biochemical or biochemical/biological events described herein, in the references cited herein, incorporated by reference for these endpoint assay targets, and other functions known to those of ordinary skill in the art or that can be readily identified using the information provided in the Figures, particularly FIG. 2. Specifically, a biological function of a cell or tissues that expresses the kinase can be assayed. Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in human liver.
- Binding and/or activating compounds can also be screened by using chimeric kinase proteins in which the amino terminal extracellular domain, or parts thereof, the entire transmembrane domain or subregions, such as any of the seven transmembrane segments or any of the intracellular or extracellular loops and the carboxy terminal intracellular domain, or parts thereof, can be replaced by heterologous domains or subregions. For example, a substrate-binding region can be used that interacts with a different substrate then that which is recognized by the native kinase. Accordingly, a different set of signal transduction components is available as an end-point assay for activation. This allows for assays to be performed in other than the specific host cell from which the kinase is derived.
- The proteins of the present invention are also useful in competition binding assays in methods designed to discover compounds that interact with the kinase (e.g. binding partners and/or ligands). Thus, a compound is exposed to a kinase polypeptide under conditions that allow the compound to bind or to otherwise interact with the polypeptide. Soluble kinase polypeptide is also added to the mixture. If the test compound interacts with the soluble kinase polypeptide, it decreases the amount of complex formed or activity from the kinase target. This type of assay is particularly useful in cases in which compounds are sought that interact with specific regions of the kinase. Thus, the soluble polypeptide that competes with the target kinase region is designed to contain peptide sequences corresponding to the region of interest.
- To perform cell free drug screening assays, it is sometimes desirable to immobilize either the kinase protein, or fragment, or its target molecule to facilitate separation of complexes from uncomplexed forms of one or both of the proteins, as well as to accommodate automation of the assay.
- Techniques for immobilizing proteins on matrices can be used in the drug screening assays. In one embodiment, a fusion protein can be provided which adds a domain that allows the protein to be bound to a matrix. For example, glutathione-S-transferase fusion proteins can be adsorbed onto glutathione sepharose beads (Sigma Chemical, St. Louis, Mo.) or glutathione derivatized microtitre plates, which are then combined with the cell lysates (e.g.,35S-labeled) and the candidate compound, and the mixture incubated under conditions conducive to complex formation (e.g., at physiological conditions for salt and pH). Following incubation, the beads are washed to remove any unbound label, and the matrix immobilized and radiolabel determined directly, or in the supernatant after the complexes are dissociated. Alternatively, the complexes can be dissociated from the matrix, separated by SDS-PAGE, and the level of kinase-binding protein found in the bead fraction quantitated from the gel using standard electrophoretic techniques. For example, either the polypeptide or its target molecule can be immobilized utilizing conjugation of biotin and streptavidin using techniques well known in the art. Alternatively, antibodies reactive with the protein but which do not interfere with binding of the protein to its target molecule can be derivatized to the wells of the plate, and the protein trapped in the wells by antibody conjugation. Preparations of a kinase-binding protein and a candidate compound are incubated in the kinase protein-presenting wells and the amount of complex trapped in the well can be quantitated. Methods for detecting such complexes, in addition to those described above for the GST-immobilized complexes, include immunodetection of complexes using antibodies reactive with the kinase protein target molecule, or which are reactive with kinase protein and compete with the target molecule, as well as enzyme-linked assays which rely on detecting an enzymatic activity associated with the target molecule.
- Agents that modulate one of the kinases of the present invention can be identified using one or more of the above assays, alone or in combination. It is generally preferable to use a cell-based or cell free system first and then confirm activity in an animal or other model system. Such model systems are well known in the art and can readily be employed in this context.
- Modulators of kinase protein activity identified according to these drug screening assays can be used to treat a subject with a disorder mediated by the kinase pathway, by treating cells or tissues that express the kinase. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. These methods of treatment include the steps of administering a modulator of kinase activity in a pharmaceutical composition to a subject in need of such treatment, the modulator being identified as described herein.
- In yet another aspect of the invention, the kinase proteins can be used as “bait proteins” in a two-hybrid assay or three-hybrid assay (see, e.g., U.S. Pat. No. 5,283,317; Zervos et al. (1993)Cell 72:223-232; Madura et al. (1993) J. Biol. Chem. 268:12046-12054; Bartel et al. (1993) Biotechniques 14:920-924; Iwabuchi et al. (1993) Oncogene 8:1693-1696; and Brent WO94/10300), to identify other proteins, which bind to or interact with the kinase and are involved in kinase activity. Such kinase-binding proteins are also likely to be involved in the propagation of signals by the kinase proteins or kinase targets as, for example, downstream elements of a kinase-mediated signaling pathway. Alternatively, such kinase-binding proteins are likely to be kinase inhibitors.
- The two-hybrid system is based on the modular nature of most transcription factors, which consist of separable DNA-binding and activation domains. Briefly, the assay utilizes two different DNA constructs. In one construct, the gene that codes for a kinase protein is fused to a gene encoding the DNA binding domain of a known transcription factor (e.g., GAL-4). In the other construct, a DNA sequence, from a library of DNA sequences, that encodes an unidentified protein (“prey” or “sample”) is fused to a gene that codes for the activation domain of the known transcription factor. If the “bait” and the “prey” proteins are able to interact, in vivo, forming a kinase-dependent complex, the DNA-binding and activation domains of the transcription factor are brought into close proximity. This proximity allows transcription of a reporter gene (e.g., LacZ) which is operably linked to a transcriptional regulatory site responsive to the transcription factor. Expression of the reporter gene can be detected and cell colonies containing the functional transcription factor can be isolated and used to obtain the cloned gene which encodes the protein which interacts with the kinase protein.
- This invention further pertains to novel agents identified by the above-described screening assays. Accordingly, it is within the scope of this invention to further use an agent identified as described herein in an appropriate animal model. For example, an agent identified as described herein (e.g., a kinase-modulating agent, an antisense kinase nucleic acid molecule, a kinase-specific antibody, or a kinase-binding partner) can be used in an animal or other model to determine the efficacy, toxicity, or side effects of treatment with such an agent. Alternatively, an agent identified as described herein can be used in an animal or other model to determine the mechanism of action of such an agent. Furthermore, this invention pertains to uses of novel agents identified by the above-described screening assays for treatments as described herein.
- The kinase proteins of the present invention are also useful to provide a target for diagnosing a disease or predisposition to disease mediated by the peptide. Accordingly, the invention provides methods for detecting the presence, or levels of, the protein (or encoding mRNA) in a cell, tissue, or organism. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. The method involves contacting a biological sample with a compound capable of interacting with the kinase protein such that the interaction can be detected. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.
- One agent for detecting a protein in a sample is an antibody capable of selectively binding to protein. A biological sample includes tissues, cells and biological fluids isolated from a subject, as well as tissues, cells and fluids present within a subject.
- The peptides of the present invention also provide targets for diagnosing active protein activity, disease, or predisposition to disease, in a patient having a variant peptide, particularly activities and conditions that are known for other members of the family of proteins to which the present one belongs. Thus, the peptide can be isolated from a biological sample and assayed for the presence of a genetic mutation that results in aberrant peptide. This includes amino acid substitution, deletion, insertion, rearrangement, (as the result of aberrant splicing events), and inappropriate post-translational modification. Analytic methods include altered electrophoretic mobility, altered tryptic peptide digest, altered kinase activity in cell-based or cell-free assay, alteration in substrate or antibody-binding pattern, altered isoelectric point, direct amino acid sequencing, and any other of the known assay techniques useful for detecting mutations in a protein. Such an assay can be provided in a single detection format or a multi-detection format such as an antibody chip array.
- In vitro techniques for detection of peptide include enzyme linked immunosorbent assays (ELISAs), Western blots, immunoprecipitations and immunofluorescence using a detection reagent, such as an antibody or protein binding agent. Alternatively, the peptide can be detected in vivo in a subject by introducing into the subject a labeled anti-peptide antibody or other types of detection agent. For example, the antibody can be labeled with a radioactive marker whose presence and location in a subject can be detected by standard imaging techniques. Particularly useful are methods that detect the allelic variant of a peptide expressed in a subject and methods which detect fragments of a peptide in a sample.
- The peptides are also useful in pharmacogenomic analysis. Pharmacogenomics deal with clinically significant hereditary variations in the response to drugs due to altered drug disposition and abnormal action in affected persons. See, e.g., Eichelbaum, M. (Clin. Exp. Pharmacol. Physiol. 23(10-11):983-985 (1996)), and Linder, M. W. (Clin. Chem. 43(2):254-266 (1997)). The clinical outcomes of these variations result in severe toxicity of therapeutic drugs in certain individuals or therapeutic failure of drugs in certain individuals as a result of individual variation in metabolism. Thus, the genotype of the individual can determine the way a therapeutic compound acts on the body or the way the body metabolizes the compound. Further, the activity of drug metabolizing enzymes effects both the intensity and duration of drug action. Thus, the pharmacogenomics of the individual permit the selection of effective compounds and effective dosages of such compounds for prophylactic or therapeutic treatment based on the individual's genotype. The discovery of genetic polymorphisms in some drug metabolizing enzymes has explained why some patients do not obtain the expected drug effects, show an exaggerated drug effect, or experience serious toxicity from standard drug dosages. Polymorphisms can be expressed in the phenotype of the extensive metabolizer and the phenotype of the poor metabolizer. Accordingly, genetic polymorphism may lead to allelic protein variants of the kinase protein in which one or more of the kinase functions in one population is different from those in another population. The peptides thus allow a target to ascertain a genetic predisposition that can affect treatment modality. Thus, in a ligand-based treatment, polymorphism may give rise to amino terminal extracellular domains and/or other substrate-binding regions that are more or less active in substrate binding, and kinase activation. Accordingly, substrate dosage would necessarily be modified to maximize the therapeutic effect within a given population containing a polymorphism. As an alternative to genotyping, specific polymorphic peptides could be identified.
- The peptides are also useful for treating a disorder characterized by an absence of, inappropriate, or unwanted expression of the protein. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. Accordingly, methods for treatment include the use of the kinase protein or fragments.
- Antibodies
- The invention also provides antibodies that selectively bind to one of the peptides of the present invention, a protein comprising such a peptide, as well as variants and fragments thereof. As used herein, an antibody selectively binds a target peptide when it binds the target peptide and does not significantly bind to unrelated proteins. An antibody is still considered to selectively bind a peptide even if it also binds to other proteins that are not substantially homologous with the target peptide so long as such proteins share homology with a fragment or domain of the peptide target of the antibody. In this case, it would be understood that antibody binding to the peptide is still selective despite some degree of cross-reactivity.
- As used herein, an antibody is defined in terms consistent with that recognized within the art: they are multi-subunit proteins produced by a mammalian organism in response to an antigen challenge. The antibodies of the present invention include polyclonal antibodies and monoclonal antibodies, as well as fragments of such antibodies, including, but not limited to, Fab or F(ab′)2, and Fv fragments.
- Many methods are known for generating and/or identifying antibodies to a given target peptide. Several such methods are described by Harlow, Antibodies, Cold Spring Harbor Press, (1989).
- In general, to generate antibodies, an isolated peptide is used as an immunogen and is administered to a mammalian organism, such as a rat, rabbit or mouse. The full-length protein, an antigenic peptide fragment or a fusion protein can be used. Particularly important fragments are those covering functional domains, such as the domains identified in FIG. 2, and domain of sequence homology or divergence amongst the family, such as those that can readily be identified using protein alignment methods and as presented in the Figures.
- Antibodies are preferably prepared from regions or discrete fragments of the kinase proteins. Antibodies can be prepared from any region of the peptide as described herein. However, preferred regions will include those involved in function/activity and/or kinase/binding partner interaction. FIG. 2 can be used to identify particularly important regions while sequence alignment can be used to identify conserved and unique sequence fragments.
- An antigenic fragment will typically comprise at least 8 contiguous amino acid residues. The antigenic peptide can comprise, however, at least 10, 12, 14, 16 or more amino acid residues. Such fragments can be selected on a physical property, such as fragments correspond to regions that are located on the surface of the protein, e.g., hydrophilic regions or can be selected based on sequence uniqueness (see FIG. 2).
- Detection on an antibody of the present invention can be facilitated by coupling (i.e., physically linking) the antibody to a detectable substance. Examples of detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, and radioactive materials. Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, β-galactosidase, or acetylcholinesterase; examples of suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin; examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin; an example of a luminescent material includes luminol; examples of bioluminescent materials include luciferase, luciferin, and aequorin, and examples of suitable radioactive material include125I, 131I, 35S or 3H.
- Antibody Uses
- The antibodies can be used to isolate one of the proteins of the present invention by standard techniques, such as affinity chromatography or immunoprecipitation. The antibodies can facilitate the purification of the natural protein from cells and recombinantly produced protein expressed in host cells. In addition, such antibodies are useful to detect the presence of one of the proteins of the present invention in cells or tissues to determine the pattern of expression of the protein among various tissues in an organism and over the course of normal development. Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in human liver. Further, such antibodies can be used to detect protein in situ, in vitro, or in a cell lysate or supernatant in order to evaluate the abundance and pattern of expression. Also, such antibodies can be used to assess abnormal tissue distribution or abnormal expression during development or progression of a biological condition. Antibody detection of circulating fragments of the full length protein can be used to identify turnover.
- Further, the antibodies can be used to assess expression in disease states such as in active stages of the disease or in an individual with a predisposition toward disease related to the protein's function. When a disorder is caused by an inappropriate tissue distribution, developmental expression, level of expression of the protein, or expressed/processed form, the antibody can be prepared against the normal protein. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. If a disorder is characterized by a specific mutation in the protein, antibodies specific for this mutant protein can be used to assay for the presence of the specific mutant protein.
- The antibodies can also be used to assess normal and aberrant subcellular localization of cells in the various tissues in an organism. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. The diagnostic uses can be applied, not only in genetic testing, but also in monitoring a treatment modality. Accordingly, where treatment is ultimately aimed at correcting expression level or the presence of aberrant sequence and aberrant tissue distribution or developmental expression, antibodies directed against the protein or relevant fragments can be used to monitor therapeutic efficacy.
- Additionally, antibodies are useful in pharmacogenomic analysis. Thus, antibodies prepared against polymorphic proteins can be used to identify individuals that require modified treatment modalities. The antibodies are also useful as diagnostic tools as an immunological marker for aberrant protein analyzed by electrophoretic mobility, isoelectric point, tryptic peptide digest, and other physical assays known to those in the art.
- The antibodies are also useful for tissue typing. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. Thus, where a specific protein has been correlated with expression in a specific tissue, antibodies that are specific for this protein can be used to identify a tissue type.
- The antibodies are also useful for inhibiting protein function, for example, blocking the binding of the kinase peptide to a binding partner such as a substrate. These uses can also be applied in a therapeutic context in which treatment involves inhibiting the protein's function. An antibody can be used, for example, to block binding, thus modulating (agonizing or antagonizing) the peptides activity. Antibodies can be prepared against specific fragments containing sites required for function or against intact protein that is associated with a cell or cell membrane. See FIG. 2 for structural information relating to the proteins of the present invention.
- The invention also encompasses kits for using antibodies to detect the presence of a protein in a biological sample. The kit can comprise antibodies such as a labeled or labelable antibody and a compound or agent for detecting protein in a biological sample; means for determining the amount of protein in the sample; means for comparing the amount of protein in the sample with a standard; and instructions for use. Such a kit can be supplied to detect a single protein or epitope or can be configured to detect one of a multitude of epitopes, such as in an antibody detection array. Arrays are described in detail below for nuleic acid arrays and similar methods have been developed for antibody arrays.
- Nucleic Acid Molecules
- The present invention further provides isolated nucleic acid molecules that encode a kinase peptide or protein of the present invention (cDNA, transcript and genomic sequence). Such nucleic acid molecules will consist of, consist essentially of, or comprise a nucleotide sequence that encodes one of the kinase peptides of the present invention, an allelic variant thereof, or an ortholog or paralog thereof.
- As used herein, an “isolated” nucleic acid molecule is one that is separated from other nucleic acid present in the natural source of the nucleic acid. Preferably, an “isolated” nucleic acid is free of sequences which naturally flank the nucleic acid (i.e., sequences located at the 5′ and 3′ ends of the nucleic acid) in the genomic DNA of the organism from which the nucleic acid is derived. However, there can be some flanking nucleotide sequences, for example up to about 5KB, 4KB, 3KB, 2KB, or 1KB or less, particularly contiguous peptide encoding sequences and peptide encoding sequences within the same gene but separated by introns in the genomic sequence. The important point is that the nucleic acid is isolated from remote and unimportant flanking sequences such that it can be subjected to the specific manipulations described herein such as recombinant expression, preparation of probes and primers, and other uses specific to the nucleic acid sequences.
- Moreover, an “isolated” nucleic acid molecule, such as a transcript/cDNA molecule, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or chemical precursors or other chemicals when chemically synthesized. However, the nucleic acid molecule can be fused to other coding or regulatory sequences and still be considered isolated.
- For example, recombinant DNA molecules contained in a vector are considered isolated. Further examples of isolated DNA molecules include recombinant DNA molecules maintained in heterologous host cells or purified (partially or substantially) DNA molecules in solution. Isolated RNA molecules include in vivo or in vitro RNA transcripts of the isolated DNA molecules of the present invention. Isolated nucleic acid molecules according to the present invention further include such molecules produced synthetically.
- Accordingly, the present invention provides nucleic acid molecules that consist of the nucleotide sequence shown in FIG. 1 or3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule consists of a nucleotide sequence when the nucleotide sequence is the complete nucleotide sequence of the nucleic acid molecule.
- The present invention further provides nucleic acid molecules that consist essentially of the nucleotide sequence shown in FIG. 1 or3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule consists essentially of a nucleotide sequence when such a nucleotide sequence is present with only a few additional nucleic acid residues in the final nucleic acid molecule.
- The present invention further provides nucleic acid molecules that comprise the nucleotide sequences shown in FIG. 1 or3 (SEQ ID NO:1, transcript sequence and SEQ ID NO:3, genomic sequence), or any nucleic acid molecule that encodes the protein provided in FIG. 2, SEQ ID NO:2. A nucleic acid molecule comprises a nucleotide sequence when the nucleotide sequence is at least part of the final nucleotide sequence of the nucleic acid molecule. In such a fashion, the nucleic acid molecule can be only the nucleotide sequence or have additional nucleic acid residues, such as nucleic acid residues that are naturally associated with it or heterologous nucleotide sequences. Such a nucleic acid molecule can have a few additional nucleotides or can comprises several hundred or more additional nucleotides. A brief description of how various types of these nucleic acid molecules can be readily made/isolated is provided below.
- In FIGS. 1 and 3, both coding and non-coding sequences are provided. Because of the source of the present invention, humans genomic sequence (FIG. 3) and cDNA/transcript sequences (FIG. 1), the nucleic acid molecules in the Figures will contain genomic intronic sequences, 5′ and 3′ non-coding sequences, gene regulatory regions and non-coding intergenic sequences. In general such sequence features are either noted in FIGS. 1 and 3 or can readily be identified using computational tools known in the art. As discussed below, some of the non-coding regions, particularly gene regulatory elements such as promoters, are useful for a variety of purposes, e.g. control of heterologous gene expression, target for identifying gene activity modulating compounds, and are particularly claimed as fragments of the genomic sequence provided herein.
- The isolated nucleic acid molecules can encode the mature protein plus additional amino or carboxyl-terminal amino acids, or amino acids interior to the mature peptide (when the mature form has more than one peptide chain, for instance). Such sequences may play a role in processing of a protein from precursor to a mature form, facilitate protein trafficking, prolong or shorten protein half-life or facilitate manipulation of a protein for assay or production, among other things. As generally is the case in situ, the additional amino acids may be processed away from the mature protein by cellular enzymes.
- As mentioned above, the isolated nucleic acid molecules include, but are not limited to, the sequence encoding the kinase peptide alone, the sequence encoding the mature peptide and additional coding sequences, such as a leader or secretory sequence (e.g., a pre-pro or pro-protein sequence), the sequence encoding the mature peptide, with or without the additional coding sequences, plus additional non-coding sequences, for example introns and non-coding 5′ and 3′ sequences such as transcribed but non-translated sequences that play a role in transcription, mRNA processing (including splicing and polyadenylation signals), ribosome binding and stability of mRNA. In addition, the nucleic acid molecule may be fused to a marker sequence encoding, for example, a peptide that facilitates purification.
- Isolated nucleic acid molecules can be in the form of RNA, such as mRNA, or in the form DNA, including cDNA and genomic DNA obtained by cloning or produced by chemical synthetic techniques or by a combination thereof. The nucleic acid, especially DNA, can be double-stranded or single-stranded. Single-stranded nucleic acid can be the coding strand (sense strand) or the non-coding strand (anti-sense strand).
- The invention further provides nucleic acid molecules that encode fragments of the peptides of the present invention as well as nucleic acid molecules that encode obvious variants of the kinase proteins of the present invention that are described above. Such nucleic acid molecules may be naturally occurring, such as allelic variants (same locus), paralogs (different locus), and orthologs (different organism), or may be constructed by recombinant DNA methods or by chemical synthesis. Such non-naturally occurring variants may be made by mutagenesis techniques, including those applied to nucleic acid molecules, cells, or organisms. Accordingly, as discussed above, the variants can contain nucleotide substitutions, deletions, inversions and insertions. Variation can occur in either or both the coding and non-coding regions. The variations can produce both conservative and non-conservative amino acid substitutions.
- The present invention further provides non-coding fragments of the nucleic acid molecules provided in FIGS. 1 and 3. Preferred non-coding fragments include, but are not limited to, promoter sequences, enhancer sequences, gene modulating sequences and gene termination sequences. Such fragments are useful in controlling heterologous gene expression and in developing screens to identify gene-modulating agents. A promoter can readily be identified as being 5′ to the ATG start site in the genomic sequence provided in FIG. 3.
- A fragment comprises a contiguous nucleotide sequence greater than 12 or more nucleotides. Further, a fragment could at least 30, 40, 50, 100, 250 or 500 nucleotides in length. The length of the fragment will be based on its intended use. For example, the fragment can encode epitope bearing regions of the peptide, or can be useful as DNA probes and primers. Such fragments can be isolated using the known nucleotide sequence to synthesize an oligonucleotide probe. A labeled probe can then be used to screen a cDNA library, genomic DNA library, or mRNA to isolate nucleic acid corresponding to the coding region. Further, primers can be used in PCR reactions to clone specific regions of gene.
- A probe/primer typically comprises substantially a purified oligonucleotide or oligonucleotide pair. The oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 12, 20, 25, 40, 50 or more consecutive nucleotides.
- Orthologs, homologs, and allelic variants can be identified using methods well known in the art. As described in the Peptide Section, these variants comprise a nucleotide sequence encoding a peptide that is typically 60-70%, 70-80%, 80-90%, and more typically at least about 90-95% or more homologous to the nucleotide sequence shown in the Figure sheets or a fragment of this sequence. Such nucleic acid molecules can readily be identified as being able to hybridize under moderate to stringent conditions, to the nucleotide sequence shown in the Figure sheets or a fragment of the sequence. Allelic variants can readily be determined by genetic locus of the encoding gene. The gene encoding the novel kinase protein of the present invention is located on a genome component that has been mapped to human chromosome 1 (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data.
- FIG. 3 provides information on SNPs that have been found in the gene encoding the kinase protein of the present invention. The following variations were seen: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at
position 14131. SNPs in introns, such as these, may affect control/regulatory elements. - As used herein, the term “hybridizes under stringent conditions” is intended to describe conditions for hybridization and washing under which nucleotide sequences encoding a peptide at least 60-70% homologous to each other typically remain hybridized to each other. The conditions can be such that sequences at least about 60%, at least about 70%, or at least about 80% or more homologous to each other typically remain hybridized to each other. Such stringent conditions are known to those skilled in the art and can be found inCurrent Protocols in Molecular Biology, John Wiley & Sons, N.Y. (1989), 6.3.1-6.3.6. One example of stringent hybridization conditions are hybridization in 6X sodium chloride/sodium citrate (SSC) at about 45 C., followed by one or more washes in 0.2×SSC, 0.1% SDS at 50-65 C. Examples of moderate to low stringency hybridization conditions are well known in the art.
- Nucleic Acid Molecule Uses
- The nucleic acid molecules of the present invention are useful for probes, primers, chemical intermediates, and in biological assays. The nucleic acid molecules are useful as a hybridization probe for messenger RNA, transcript/cDNA and genomic DNA to isolate full-length cDNA and genomic clones encoding the peptide described in FIG. 2 and to isolate cDNA and genomic clones that correspond to variants (alleles, orthologs, etc.) producing the same or related peptides shown in FIG. 2. As illustrated in FIG. 3, the following SNPs were identified: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at
position 14131. - The probe can correspond to any sequence along the entire length of the nucleic acid molecules provided in the Figures. Accordingly, it could be derived from 5′ noncoding regions, the coding region, and 3′ noncoding regions. However, as discussed, fragments are not to be construed as encompassing fragments disclosed prior to the present invention.
- The nucleic acid molecules are also useful as primers for PCR to amplify any given region of a nucleic acid molecule and are useful to synthesize antisense molecules of desired length and sequence.
- The nucleic acid molecules are also useful for constructing recombinant vectors. Such vectors include expression vectors that express a portion of, or all of, the peptide sequences. Vectors also include insertion vectors, used to integrate into another nucleic acid molecule sequence, such as into the cellular genome, to alter in situ expression of a gene and/or gene product. For example, an endogenous coding sequence can be replaced via homologous recombination with all or part of the coding region containing one or more specifically introduced mutations.
- The nucleic acid molecules are also useful for expressing antigenic portions of the proteins.
- The nucleic acid molecules are also useful as probes for determining the chromosomal positions of the nucleic acid molecules by means of in situ hybridization methods. The gene encoding the novel kinase protein of the present invention is located on a genome component that has been mapped to human chromosome 1 (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data.
- The nucleic acid molecules are also useful in making vectors containing the gene regulatory regions of the nucleic acid molecules of the present invention.
- The nucleic acid molecules are also useful for designing ribozymes corresponding to all, or a part, of the mRNA produced from the nucleic acid molecules described herein.
- The nucleic acid molecules are also useful for making vectors that express part, or all, of the peptides.
- The nucleic acid molecules are also useful for constructing host cells expressing a part, or all, of the nucleic acid molecules and peptides.
- The nucleic acid molecules are also useful for constructing transgenic animals expressing all, or a part, of the nucleic acid molecules and peptides.
- The nucleic acid molecules are also useful as hybridization probes for determining the presence, level, form and distribution of nucleic acid expression. Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in human liver. Accordingly, the probes can be used to detect the presence of, or to determine levels of, a specific nucleic acid molecule in cells, tissues, and in organisms. The nucleic acid whose level is determined can be DNA or RNA. Accordingly, probes corresponding to the peptides described herein can be used to assess expression and/or gene copy number in a given cell, tissue, or organism. These uses are relevant for diagnosis of disorders involving an increase or decrease in kinase protein expression relative to normal results.
- In vitro techniques for detection of mRNA include Northern hybridizations and in situ hybridizations. In vitro techniques for detecting DNA includes Southern hybridizations and in situ hybridization.
- Probes can be used as a part of a diagnostic test kit for identifying cells or tissues that express a kinase protein, such as by measuring a level of a kinase-encoding nucleic acid in a sample of cells from a subject e.g., mRNA or genomic DNA, or determining if a kinase gene has been mutated. Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in human liver.
- Nucleic acid expression assays are useful for drug screening to identify compounds that modulate kinase nucleic acid expression.
- The invention thus provides a method for identifying a compound that can be used to treat a disorder associated with nucleic acid expression of the kinase gene, particularly biological and pathological processes that are mediated by the kinase in cells and tissues that express it. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver. The method typically includes assaying the ability of the compound to modulate the expression of the kinase nucleic acid and thus identifying a compound that can be used to treat a disorder characterized by undesired kinase nucleic acid expression. The assays can be performed in cell-based and cell-free systems. Cell-based assays include cells naturally expressing the kinase nucleic acid or recombinant cells genetically engineered to express specific nucleic acid sequences.
- The assay for kinase nucleic acid expression can involve direct assay of nucleic acid levels, such as mRNA levels, or on collateral compounds involved in the signal pathway. Further, the expression of genes that are up- or down-regulated in response to the kinase protein signal pathway can also be assayed. In this embodiment the regulatory regions of these genes can be operably linked to a reporter gene such as luciferase.
- Thus, modulators of kinase gene expression can be identified in a method wherein a cell is contacted with a candidate compound and the expression of mRNA determined. The level of expression of kinase mRNA in the presence of the candidate compound is compared to the level of expression of kinase mRNA in the absence of the candidate compound. The candidate compound can then be identified as a modulator of nucleic acid expression based on this comparison and be used, for example to treat a disorder characterized by aberrant nucleic acid expression. When expression of mRNA is statistically significantly greater in the presence of the candidate compound than in its absence, the candidate compound is identified as a stimulator of nucleic acid expression. When nucleic acid expression is statistically significantly less in the presence of the candidate compound than in its absence, the candidate compound is identified as an inhibitor of nucleic acid expression.
- The invention further provides methods of treatment, with the nucleic acid as a target, using a compound identified through drug screening as a gene modulator to modulate kinase nucleic acid expression in cells and tissues that express the kinase. Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in human liver. Modulation includes both up-regulation (i.e. activation or agonization) or down-regulation (suppression or antagonization) or nucleic acid expression.
- Alternatively, a modulator for kinase nucleic acid expression can be a small molecule or drug identified using the screening assays described herein as long as the drug or small molecule inhibits the kinase nucleic acid expression in the cells and tissues that express the protein. Experimental data as provided in FIG. 1 indicates expression in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, colon, and liver.
- The nucleic acid molecules are also useful for monitoring the effectiveness of modulating compounds on the expression or activity of the kinase gene in clinical trials or in a treatment regimen. Thus, the gene expression pattern can serve as a barometer for the continuing effectiveness of treatment with the compound, particularly with compounds to which a patient can develop resistance. The gene expression pattern can also serve as a marker indicative of a physiological response of the affected cells to the compound. Accordingly, such monitoring would allow either increased administration of the compound or the administration of alternative compounds to which the patient has not become resistant. Similarly, if the level of nucleic acid expression falls below a desirable level, administration of the compound could be commensurately decreased.
- The nucleic acid molecules are also useful in diagnostic assays for qualitative changes in kinase nucleic acid expression, and particularly in qualitative changes that lead to pathology. The nucleic acid molecules can be used to detect mutations in kinase genes and gene expression products such as mRNA. The nucleic acid molecules can be used as hybridization probes to detect naturally occurring genetic mutations in the kinase gene and thereby to determine whether a subject with the mutation is at risk for a disorder caused by the mutation. Mutations include deletion, addition, or substitution of one or more nucleotides in the gene, chromosomal rearrangement, such as inversion or transposition, modification of genomic DNA, such as aberrant methylation patterns or changes in gene copy number, such as amplification. Detection of a mutated form of the kinase gene associated with a dysfunction provides a diagnostic tool for an active disease or susceptibility to disease when the disease results from overexpression, underexpression, or altered expression of a kinase protein.
- Individuals carrying mutations in the kinase gene can be detected at the nucleic acid level by a variety of techniques. FIG. 3 provides information on SNPs that have been found in the gene encoding the kinase protein of the present invention. The following variations were seen: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at
position 14131. SNPs in introns, such as these, may affect control/regulatory elements. The gene encoding the novel kinase protein of the present invention is located on a genome component that has been mapped to human chromosome 1 (as indicated in FIG. 3), which is supported by multiple lines of evidence, such as STS and BAC map data. Genomic DNA can be analyzed directly or can be amplified by using PCR prior to analysis. RNA or cDNA can be used in the same way. In some uses, detection of the mutation involves the use of a probe/primer in a polymerase chain reaction (PCR) (see, e.g. U.S. Pat. Nos. 4,683,195 and 4,683,202), such as anchor PCR or RACE PCR, or, alternatively, in a ligation chain reaction (LCR) (see, e.g., Landegran et al., Science 241:1077-1080 (1988); and Nakazawa et al., PNAS 91:360-364 (1994)), the latter of which can be particularly useful for detecting point mutations in the gene (see Abravaya et al., Nucleic Acids Res. 23:675-682 (1995)). This method can include the steps of collecting a sample of cells from a patient, isolating nucleic acid (e.g., genomic, mRNA or both) from the cells of the sample, contacting the nucleic acid sample with one or more primers which specifically hybridize to a gene under conditions such that hybridization and amplification of the gene (if present) occurs, and detecting the presence or absence of an amplification product, or detecting the size of the amplification product and comparing the length to a control sample. Deletions and insertions can be detected by a change in size of the amplified product compared to the normal genotype. Point mutations can be identified by hybridizing amplified DNA to normal RNA or antisense DNA sequences. - Alternatively, mutations in a kinase gene can be directly identified, for example, by alterations in restriction enzyme digestion patterns determined by gel electrophoresis.
- Further, sequence-specific ribozymes (U.S. Pat. No. 5,498,531) can be used to score for the presence of specific mutations by development or loss of a ribozyme cleavage site. Perfectly matched sequences can be distinguished from mismatched sequences by nuclease cleavage digestion assays or by differences in melting temperature.
- Sequence changes at specific locations can also be assessed by nuclease protection assays such as RNase and S1 protection or the chemical cleavage method. Furthermore, sequence differences between a mutant kinase gene and a wild-type gene can be determined by direct DNA sequencing. A variety of automated sequencing procedures can be utilized when performing the diagnostic assays (Naeve, C. W., (1995)Biotechniques 19:448), including sequencing by mass spectrometry (see, e.g., PCT International Publication No. WO 94/16101; Cohen et al., Adv. Chromatogr. 36:127-162 (1996); and Griffin et al., Appl. Biochem. Biotechnol. 38:147-159 (1993)).
- Other methods for detecting mutations in the gene include methods in which protection from cleavage agents is used to detect mismatched bases in RNA/RNA or RNA/DNA duplexes (Myers et al.,Science 230:1242 (1985)); Cotton et al., PNAS 85:4397 (1988); Saleeba et al., Meth. Enzymol. 217:286-295 (1992)), electrophoretic mobility of mutant and wild type nucleic acid is compared (Orita et al., PNAS 86:2766 (1989); Cotton et al., Mutat. Res. 285:125-144 (1993); and Hayashi et al., Genet. Anal. Tech. Appl. 9:73-79 (1992)), and movement of mutant or wild-type fragments in polyacrylamide gels containing a gradient of denaturant is assayed using denaturing gradient gel electrophoresis (Myers et al., Nature 313:495 (1985)). Examples of other techniques for detecting point mutations include selective oligonucleotide hybridization, selective amplification, and selective primer extension.
- The nucleic acid molecules are also useful for testing an individual for a genotype that while not necessarily causing the disease, nevertheless affects the treatment modality. Thus, the nucleic acid molecules can be used to study the relationship between an individual's genotype and the individual's response to a compound used for treatment (pharmacogenomic relationship). Accordingly, the nucleic acid molecules described herein can be used to assess the mutation content of the kinase gene in an individual in order to select an appropriate compound or dosage regimen for treatment. FIG. 3 provides information on SNPs that have been found in the gene encoding the kinase protein of the present invention. The following variations were seen: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at
position 14131. SNPs in introns, such as these, may affect control/regulatory elements. - Thus nucleic acid molecules displaying genetic variations that affect treatment provide a diagnostic target that can be used to tailor treatment in an individual. Accordingly, the production of recombinant cells and animals containing these polymorphisms allow effective clinical design of treatment compounds and dosage regimens.
- The nucleic acid molecules are thus useful as antisense constructs to control kinase gene expression in cells, tissues, and organisms. A DNA antisense nucleic acid molecule is designed to be complementary to a region of the gene involved in transcription, preventing transcription and hence production of kinase protein. An antisense RNA or DNA nucleic acid molecule would hybridize to the mRNA and thus block translation of mRNA into kinase protein.
- Alternatively, a class of antisense molecules can be used to inactivate mRNA in order to decrease expression of kinase nucleic acid. Accordingly, these molecules can treat a disorder characterized by abnormal or undesired kinase nucleic acid expression. This technique involves cleavage by means of ribozymes containing nucleotide sequences complementary to one or more regions in the mRNA that attenuate the ability of the mRNA to be translated. Possible regions include coding regions and particularly coding regions corresponding to the catalytic and other functional activities of the kinase protein, such as substrate binding.
- The nucleic acid molecules also provide vectors for gene therapy in patients containing cells that are aberrant in kinase gene expression. Thus, recombinant cells, which include the patient's cells that have been engineered ex vivo and returned to the patient, are introduced into an individual where the cells produce the desired kinase protein to treat the individual.
- The invention also encompasses kits for detecting the presence of a kinase nucleic acid in a biological sample. Experimental data as provided in FIG. 1 indicates that kinase proteins of the present invention are expressed in humans in testis, brain medulloblastomas, infant brain, schizophrenic brain, retina, germinal center B cells, and colon, as indicated by virtual northern blot analysis. In addition, PCR-based tissue screening panels indicate expression in human liver. For example, the kit can comprise reagents such as a labeled or labelable nucleic acid or agent capable of detecting kinase nucleic acid in a biological sample; means for determining the amount of kinase nucleic acid in the sample; and means for comparing the amount of kinase nucleic acid in the sample with a standard. The compound or agent can be packaged in a suitable container. The kit can further comprise instructions for using the kit to detect kinase protein mRNA or DNA.
- Nucleic Acid Arrays
- The present invention further provides nucleic acid detection kits, such as arrays or microarrays of nucleic acid molecules that are based on the sequence information provided in FIGS. 1 and 3 (SEQ ID NOS:1 and 3).
- As used herein “Arrays” or “Microarrays” refers to an array of distinct polynucleotides or oligonucleotides synthesized on a substrate, such as paper, nylon or other type of membrane, filter, chip, glass slide, or any other suitable solid support. In one embodiment, the microarray is prepared and used according to the methods described in U.S. Pat. No. 5,837,832, Chee et al., PCT application WO95/11995 (Chee et al.), Lockhart, D. J. et al. (1996; Nat. Biotech. 14: 1675-1680) and Schena, M. et al. (1996; Proc. Natl. Acad. Sci. 93: 10614-10619), all of which are incorporated herein in their entirety by reference. In other embodiments, such arrays are produced by the methods described by Brown et al, U.S. Pat. No. 5,807,522.
- The microarray or detection kit is preferably composed of a large number of unique, single-stranded nucleic acid sequences, usually either synthetic antisense oligonucleotides or fragments of cDNAs, fixed to a solid support. The oligonucleotides are preferably about 6-60 nucleotides in length, more preferably 15-30 nucleotides in length, and most preferably about 20-25 nucleotides in length. For a certain type of microarray or detection kit, it may be preferable to use oligonucleotides that are only 7-20 nucleotides in length. The microarray or detection kit may contain oligonucleotides that cover the known 5′, or 3′, sequence, sequential oligonucleotides which cover the full length sequence; or unique oligonucleotides selected from particular areas along the length of the sequence. Polynucleotides used in the microarray or detection kit may be oligonucleotides that are specific to a gene or genes of interest.
- In order to produce oligonucleotides to a known sequence for a microarray or detection kit, the gene(s) of interest (or an ORF identified from the contigs of the present invention) is typically examined using a computer algorithm which starts at the 5′ or at the 3′ end of the nucleotide sequence. Typical algorithms will then identify oligomers of defined length that are unique to the gene, have a GC content within a range suitable for hybridization, and lack predicted secondary structure that may interfere with hybridization. In certain situations it may be appropriate to use pairs of oligonucleotides on a microarray or detection kit. The “pairs” will be identical, except for one nucleotide that preferably is located in the center of the sequence. The second oligonucleotide in the pair (mismatched by one) serves as a control. The number of oligonucleotide pairs may range from two to one million. The oligomers are synthesized at designated areas on a substrate using a light-directed chemical process. The substrate may be paper, nylon or other type of membrane, filter, chip, glass slide or any other suitable solid support.
- In another aspect, an oligonucleotide may be synthesized on the surface of the substrate by using a chemical coupling procedure and an ink jet application apparatus, as described in PCT application WO95/251116 (Baldeschweiler et al.) which is incorporated herein in its entirety by reference. In another aspect, a “gridded” array analogous to a dot (or slot) blot may be used to arrange and link cDNA fragments or oligonucleotides to the surface of a substrate using a vacuum system, thermal, UV, mechanical or chemical bonding procedures. An array, such as those described above, may be produced by hand or by using available devices (slot blot or dot blot apparatus), materials (any suitable solid support), and machines (including robotic instruments), and may contain 8, 24, 96, 384, 1536, 6144 or more oligonucleotides, or any other number between two and one million which lends itself to the efficient use of commercially available instrumentation.
- In order to conduct sample analysis using a microarray or detection kit, the RNA or DNA from a biological sample is made into hybridization probes. The mRNA is isolated, and cDNA is produced and used as a template to make antisense RNA (aRNA). The aRNA is amplified in the presence of fluorescent nucleotides, and labeled probes are incubated with the microarray or detection kit so that the probe sequences hybridize to complementary oligonucleotides of the microarray or detection kit. Incubation conditions are adjusted so that hybridization occurs with precise complementary matches or with various degrees of less complementarity. After removal of nonhybridized probes, a scanner is used to determine the levels and patterns of fluorescence. The scanned images are examined to determine degree of complementarity and the relative abundance of each oligonucleotide sequence on the microarray or detection kit. The biological samples may be obtained from any bodily fluids (such as blood, urine, saliva, phlegm, gastric juices, etc.), cultured cells, biopsies, or other tissue preparations. A detection system may be used to measure the absence, presence, and amount of hybridization for all of the distinct sequences simultaneously. This data may be used for large-scale correlation studies on the sequences, expression patterns, mutations, variants, or polymorphisms among samples.
- Using such arrays, the present invention provides methods to identify the expression of the kinase proteins/peptides of the present invention. In detail, such methods comprise incubating a test sample with one or more nucleic acid molecules and assaying for binding of the nucleic acid molecule with components within the test sample. Such assays will typically involve arrays comprising many genes, at least one of which is a gene of the present invention and or alleles of the kinase gene of the present invention. FIG. 3 provides information on SNPs that have been found in the gene encoding the kinase protein of the present invention. The following variations were seen: T4452A, A5330G, A9256C, A11773G, G12886A, and a T insertion/deletion (“indel”) at
position 14131. SNPs in introns, such as these, may affect control/regulatory elements. - Conditions for incubating a nucleic acid molecule with a test sample vary. Incubation conditions depend on the format employed in the assay, the detection methods employed, and the type and nature of the nucleic acid molecule used in the assay. One skilled in the art will recognize that any one of the commonly available hybridization, amplification or array assay formats can readily be adapted to employ the novel fragments of the Human genome disclosed herein. Examples of such assays can be found in Chard, T,An Introduction to Radioimmunoassay and Related Techniques, Elsevier Science Publishers, Amsterdam, The Netherlands (1986); Bullock, G. R. et al., Techniques in Immunocytochemistry, Academic Press, Orlando, Fla. Vol. 1 (1 982), Vol. 2 (1983), Vol. 3 (1985); Tijssen, P., Practice and Theory of Enzyme Immunoassays: Laboratory Techniques in Biochemistry and Molecular Biology, Elsevier Science Publishers, Amsterdam, The Netherlands (1985).
- The test samples of the present invention include cells, protein or membrane extracts of cells. The test sample used in the above-described method will vary based on the assay format, nature of the detection method and the tissues, cells or extracts used as the sample to be assayed. Methods for preparing nucleic acid extracts or of cells are well known in the art and can be readily be adapted in order to obtain a sample that is compatible with the system utilized.
- In another embodiment of the present invention, kits are provided which contain the necessary reagents to carry out the assays of the present invention.
- Specifically, the invention provides a compartmentalized kit to receive, in close confinement, one or more containers which comprises: (a) a first container comprising one of the nucleic acid molecules that can bind to a fragment of the Human genome disclosed herein; and (b) one or more other containers comprising one or more of the following: wash reagents, reagents capable of detecting presence of a bound nucleic acid.
- In detail, a compartmentalized kit includes any kit in which reagents are contained in separate containers. Such containers include small glass containers, plastic containers, strips of plastic, glass or paper, or arraying material such as silica. Such containers allows one to efficiently transfer reagents from one compartment to another compartment such that the samples and reagents are not cross-contaminated, and the agents or solutions of each container can be added in a quantitative fashion from one compartment to another. Such containers will include a container which will accept the test sample, a container which contains the nucleic acid probe, containers which contain wash reagents (such as phosphate buffered saline, Tris-buffers, etc.), and containers which contain the reagents used to detect the bound probe. One skilled in the art will readily recognize that the previously unidentified kinase gene of the present invention can be routinely identified using the sequence information disclosed herein can be readily incorporated into one of the established kit formats which are well known in the art, particularly expression arrays.
- Vectors/host cells
- The invention also provides vectors containing the nucleic acid molecules described herein. The term “vector” refers to a vehicle, preferably a nucleic acid molecule, which can transport the nucleic acid molecules. When the vector is a nucleic acid molecule, the nucleic acid molecules are covalently linked to the vector nucleic acid. With this aspect of the invention, the vector includes a plasmid, single or double stranded phage, a single or double stranded RNA or DNA viral vector, or artificial chromosome, such as a BAC, PAC, YAC, OR MAC.
- A vector can be maintained in the host cell as an extrachromosomal element where it replicates and produces additional copies of the nucleic acid molecules. Alternatively, the vector may integrate into the host cell genome and produce additional copies of the nucleic acid molecules when the host cell replicates.
- The invention provides vectors for the maintenance (cloning vectors) or vectors for expression (expression vectors) of the nucleic acid molecules. The vectors can function in prokaryotic or eukaryotic cells or in both (shuttle vectors).
- Expression vectors contain cis-acting regulatory regions that are operably linked in the vector to the nucleic acid molecules such that transcription of the nucleic acid molecules is allowed in a host cell. The nucleic acid molecules can be introduced into the host cell with a separate nucleic acid molecule capable of affecting transcription. Thus, the second nucleic acid molecule may provide a trans-acting factor interacting with the cis-regulatory control region to allow transcription of the nucleic acid molecules from the vector. Alternatively, a trans-acting factor may be supplied by the host cell. Finally, a trans-acting factor can be produced from the vector itself. It is understood, however, that in some embodiments, transcription and/or translation of the nucleic acid molecules can occur in a cell-free system.
- The regulatory sequence to which the nucleic acid molecules described herein can be operably linked include promoters for directing mRNA transcription. These include, but are not limited to, the left promoter from bacteriophage λ, the lac, TRP, and TAC promoters fromE. coli, the early and late promoters from SV40, the CMV immediate early promoter, the adenovirus early and late promoters, and retrovirus long-terminal repeats.
- In addition to control regions that promote transcription, expression vectors may also include regions that modulate transcription, such as repressor binding sites and enhancers. Examples include the SV40 enhancer, the cytomegalovirus immediate early enhancer, polyoma enhancer, adenovirus enhancers, and retrovirus LTR enhancers.
- In addition to containing sites for transcription initiation and control, expression vectors can also contain sequences necessary for transcription termination and, in the transcribed region a ribosome binding site for translation. Other regulatory control elements for expression include initiation and termination codons as well as polyadenylation signals. The person of ordinary skill in the art would be aware of the numerous regulatory sequences that are useful in expression vectors. Such regulatory sequences are described, for example, in Sambrook et al.,Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).
- A variety of expression vectors can be used to express a nucleic acid molecule. Such vectors include chromosomal, episomal, and virus-derived vectors, for example vectors derived from bacterial plasmids, from bacteriophage, from yeast episomes, from yeast chromosomal elements, including yeast artificial chromosomes, from viruses such as baculoviruses, papovaviruses such as SV40, Vaccinia viruses, adenoviruses, poxviruses, pseudorabies viruses, and retroviruses. Vectors may also be derived from combinations of these sources such as those derived from plasmid and bacteriophage genetic elements, e.g. cosmids and phagemids. Appropriate cloning and expression vectors for prokaryotic and eukaryotic hosts are described in Sambrook et al.,Molecular Cloning: A Laboratory Manual. 2nd. ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., (1989).
- The regulatory sequence may provide constitutive expression in one or more host cells (i.e. tissue specific) or may provide for inducible expression in one or more cell types such as by temperature, nutrient additive, or exogenous factor such as a hormone or other ligand. A variety of vectors providing for constitutive and inducible expression in prokaryotic and eukaryotic hosts are well known to those of ordinary skill in the art.
- The nucleic acid molecules can be inserted into the vector nucleic acid by well-known methodology. Generally, the DNA sequence that will ultimately be expressed is joined to an expression vector by cleaving the DNA sequence and the expression vector with one or more restriction enzymes and then ligating the fragments together. Procedures for restriction enzyme digestion and ligation are well known to those of ordinary skill in the art.
- The vector containing the appropriate nucleic acid molecule can be introduced into an appropriate host cell for propagation or expression using well-known techniques. Bacterial cells include, but are not limited to,E. coli, Streptomyces, and Salmonella typhimurium. Eukaryotic cells include, but are not limited to, yeast, insect cells such as Drosophila, animal cells such as COS and CHO cells, and plant cells.
- As described herein, it may be desirable to express the peptide as a fusion protein. Accordingly, the invention provides fusion vectors that allow for the production of the peptides. Fusion vectors can increase the expression of a recombinant protein, increase the solubility of the recombinant protein, and aid in the purification of the protein by acting for example as a ligand for affinity purification. A proteolytic cleavage site may be introduced at the junction of the fusion moiety so that the desired peptide can ultimately be separated from the fusion moiety. Proteolytic enzymes include, but are not limited to, factor Xa, thrombin, and enterokinase. Typical fusion expression vectors include pGEX (Smith et al.,Gene 67:31-40 (1988)), pMAL (New England Biolabs, Beverly, Ma.) and pRIT5 (Pharmacia, Piscataway, N.J.) which fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein. Examples of suitable inducible non-fusion E. coli expression vectors include pTrc (Amann et al., Gene 69:301-315 (1988)) and pET 11d (Studier et al., Gene Expression Technology: Methods in Enzymology 185:60-89 (1990)).
- Recombinant protein expression can be maximized in host bacteria by providing a genetic background wherein the host cell has an impaired capacity to proteolytically cleave the recombinant protein. (Gottesman, S.,Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. (1990) 119-128). Alternatively, the sequence of the nucleic acid molecule of interest can be altered to provide preferential codon usage for a specific host cell, for example E. coli. (Wada et al, Nucleic Acids Res. 20:2111-2118 (1992)).
- The nucleic acid molecules can also be expressed by expression vectors that are operative in yeast. Examples of vectors for expression in yeast e.g.,S. cerevisiae include pYepSec1 (Baldari, et al., EMBO J 6:229-234 (1987)), pMFa (Kurjan et al., Cell 30:933-943(1982)), pJRY88 (Schultz et al., Gene 54:113-123 (1987)), and pYES2 (Invitrogen Corporation, San Diego, Calif.).
- The nucleic acid molecules can also be expressed in insect cells using, for example, baculovirus expression vectors. Baculovirus vectors available for expression of proteins in cultured insect cells (e.g.,
Sf 9 cells) include the pAc series (Smith et al., Mol. Cell Biol. 3:2156-2165 (1983)) and the pVL series (Lucklow et al.,Virology 1 70:31-39 (1989)). - In certain embodiments of the invention, the nucleic acid molecules described herein are expressed in mammalian cells using mammalian expression vectors. Examples of mammalian expression vectors include pCDM8 (Seed, B.Nature 329:840(1987)) and pMT2PC (Kaufman et al., EMBO J 6:187-195 (1987)).
- The expression vectors listed herein are provided by way of example only of the well-known vectors available to those of ordinary skill in the art that would be useful to express the nucleic acid molecules. The person of ordinary skill in the art would be aware of other vectors suitable for maintenance propagation or expression of the nucleic acid molecules described herein. These are found for example in Sambrook, J., Fritsh, E. F., and Maniatis, T.Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989.
- The invention also encompasses vectors in which the nucleic acid sequences described herein are cloned into the vector in reverse orientation, but operably linked to a regulatory sequence that permits transcription of antisense RNA. Thus, an antisense transcript can be produced to all, or to a portion, of the nucleic acid molecule sequences described herein, including both coding and non-coding regions. Expression of this antisense RNA is subject to each of the parameters described above in relation to expression of the sense RNA (regulatory sequences, constitutive or inducible expression, tissue-specific expression).
- The invention also relates to recombinant host cells containing the vectors described herein. Host cells therefore include prokaryotic cells, lower eukaryotic cells such as yeast, other eukaryotic cells such as insect cells, and higher eukaryotic cells such as mammalian cells.
- The recombinant host cells are prepared by introducing the vector constructs described herein into the cells by techniques readily available to the person of ordinary skill in the art. These include, but are not limited to, calcium phosphate transfection, DEAE-dextran-mediated transfection, cationic lipid-mediated transfection, electroporation, transduction, infection, lipofection, and other techniques such as those found in Sambrook, et al. (Molecular Cloning: A Laboratory Manual. 2nd, ed., Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989).
- Host cells can contain more than one vector. Thus, different nucleotide sequences can be introduced on different vectors of the same cell. Similarly, the nucleic acid molecules can be introduced either alone or with other nucleic acid molecules that are not related to the nucleic acid molecules such as those providing trans-acting factors for expression vectors. When more than one vector is introduced into a cell, the vectors can be introduced independently, co-introduced or joined to the nucleic acid molecule vector.
- In the case of bacteriophage and viral vectors, these can be introduced into cells as packaged or encapsulated virus by standard procedures for infection and transduction. Viral vectors can be replication-competent or replication-defective. In the case in which viral replication is defective, replication will occur in host cells providing functions that complement the defects.
- Vectors generally include selectable markers that enable the selection of the subpopulation of cells that contain the recombinant vector constructs. The marker can be contained in the same vector that contains the nucleic acid molecules described herein or may be on a separate vector. Markers include tetracycline or ampicillin-resistance genes for prokaryotic host cells and dihydrofolate reductase or neomycin resistance for eukaryotic host cells. However, any marker that provides selection for a phenotypic trait will be effective.
- While the mature proteins can be produced in bacteria, yeast, mammalian cells, and other cells under the control of the appropriate regulatory sequences, cell-free transcription and translation systems can also be used to produce these proteins using RNA derived from the DNA constructs described herein.
- Where secretion of the peptide is desired, which is difficult to achieve with multi-transmembrane domain containing proteins such as kinases, appropriate secretion signals are incorporated into the vector. The signal sequence can be endogenous to the peptides or heterologous to these peptides.
- Where the peptide is not secreted into the medium, which is typically the case with kinases, the protein can be isolated from the host cell by standard disruption procedures, including freeze thaw, sonication, mechanical disruption, use of lysing agents and the like. The peptide can then be recovered and purified by well-known purification methods including ammonium sulfate precipitation, acid extraction, anion or cationic exchange chromatography, phosphocellulose chromatography, hydrophobic-interaction chromatography, affinity chromatography, hydroxylapatitc chromatography, lectin chromatography, or high performance liquid chromatography.
- It is also understood that depending upon the host cell in recombinant production of the peptides described herein, the peptides can have various glycosylation patterns, depending upon the cell, or maybe non-glycosylated as when produced in bacteria. In addition, the peptides may include an initial modified methionine in some cases as a result of a host-mediated process.
- Uses of vectors and host cells
- The recombinant host cells expressing the peptides described herein have a variety of uses. First, the cells are useful for producing a kinase protein or peptide that can be further purified to produce desired amounts of kinase protein or fragments. Thus, host cells containing expression vectors are useful for peptide production.
- Host cells are also useful for conducting cell-based assays involving the kinase protein or kinase protein fragments, such as those described above as well as other formats known in the art. Thus, a recombinant host cell expressing a native kinase protein is useful for assaying compounds that stimulate or inhibit kinase protein function.
- Host cells are also useful for identifying kinase protein mutants in which these functions are affected. If the mutants naturally occur and give rise to a pathology, host cells containing the mutations are useful to assay compounds that have a desired effect on the mutant kinase protein (for example, stimulating or inhibiting function) which may not be indicated by their effect on the native kinase protein.
- Genetically engineered host cells can be further used to produce non-human transgenic animals. A transgenic animal is preferably a mammal, for example a rodent, such as a rat or mouse, in which one or more of the cells of the animal include a transgene. A transgene is exogenous DNA which is integrated into the genome of a cell from which a transgenic animal develops and which remains in the genome of the mature animal in one or more cell types or tissues of the transgenic animal. These animals are useful for studying the function of a kinase protein and identifying and evaluating modulators of kinase protein activity. Other examples of transgenic animals include non-human primates, sheep, dogs, cows, goats, chickens, and amphibians.
- A transgenic animal can be produced by introducing nucleic acid into the male pronuclei of a fertilized oocyte, e.g., by microinjection, retroviral infection, and allowing the oocyte to develop in a pseudopregnant female foster animal. Any of the kinase protein nucleotide sequences can be introduced as a transgene into the genome of a non-human animal, such as a mouse.
- Any of the regulatory or other sequences useful in expression vectors can form part of the transgenic sequence. This includes intronic sequences and polyadenylation signals, if not already included. A tissue-specific regulatory sequence(s) can be operably linked to the transgene to direct expression of the kinase protein to particular cells.
- Methods for generating transgenic animals via embryo manipulation and microinjection, particularly animals such as mice, have become conventional in the art and are described, for example, in U.S. Pat. Nos. 4,736,866 and 4,870,009, both by Leder et al., U.S. Pat. No. 4,873,191 by Wagner et al. and in Hogan, B.,Manipulating the Mouse Embryo, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1986). Similar methods are used for production of other transgenic animals. A transgenic founder animal can be identified based upon the presence of the transgene in its genome and/or expression of transgenic mRNA in tissues or cells of the animals. A transgenic founder animal can then be used to breed additional animals carrying the transgene. Moreover, transgenic animals carrying a transgene can further be bred to other transgenic animals carrying other transgenes. A transgenic animal also includes animals in which the entire animal or tissues in the animal have been produced using the homologously recombinant host cells described herein.
- In another embodiment, transgenic non-human animals can be produced which contain selected systems that allow for regulated expression of the transgene. One example of such a system is the cre/loxP recombinase system of bacteriophage P1. For a description of the cre/loxP recombinase system, see, e.g., Lakso et al.PNAS 89:6232-6236 (1992). Another example of a recombinase system is the FLP recombinase system of S. cerevisiae (O'Gorman et al. Science 251:1351-1355 (1991). If a cre/loxP recombinase system is used to regulate expression of the transgene, animals containing transgenes encoding both the Cre recombinase and a selected protein is required. Such animals can be provided through the construction of “double” transgenic animals, e.g., by mating two transgenic animals, one containing a transgene encoding a selected protein and the other containing a transgene encoding a recombinase.
- Clones of the non-human transgenic animals described herein can also be produced according to the methods described in Wilmut, I. et al.Nature 385:810-813 (1997) and PCT International Publication Nos. WO 97/07668 and WO 97/07669. In brief, a cell, e.g., a somatic cell, from the transgenic animal can be isolated and induced to exit the growth cycle and enter G0 phase. The quiescent cell can then be fused, e.g., through the use of electrical pulses, to an enucleated oocyte from an animal of the same species from which the quiescent cell is isolated. The reconstructed oocyte is then cultured such that it develops to morula or blastocyst and then transferred to pseudopregnant female foster animal. The offspring born of this female foster animal will be a clone of the animal from which the cell, e.g., the somatic cell, is isolated.
- Transgenic animals containing recombinant cells that express the peptides described herein are useful to conduct the assays described herein in an in vivo context. Accordingly, the various physiological factors that are present in vivo and that could effect substrate binding, kinase protein activation, and signal transduction, may not be evident from in vitro cell-free or cell-based assays. Accordingly, it is useful to provide non-human transgenic animals to assay in vivo kinase protein function, including substrate interaction, the effect of specific mutant kinase proteins on kinase protein function and substrate interaction, and the effect of chimeric kinase proteins. It is also possible to assess the effect of null mutations, that is, mutations that substantially or completely eliminate one or more kinase protein functions.
- All publications and patents mentioned in the above specification are herein incorporated by reference. Various modifications and variations of the described method and system of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the above-described modes for carrying out the invention which are obvious to those skilled in the field of molecular biology or related fields are intended to be within the scope of the following claims.
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1 4 1 3565 DNA Human 1 ttcttccttt ctctcaatat aggtatggca tcacagctgc aagtgttttc gcccccatca 60 gtgtcgtcga gtgccttctg cagtgcgaag aaactgaaaa tagagccctc tggctgggat 120 gtttcaggac agagtagcaa cgacaaatat tatacccaca gcaaaaccct cccagccaca 180 caagggcaag ccaactcctc tcaccaggta gcaaatttca acatccctgc ttacgaccag 240 ggcctcctcc tcccagctcc tgcagtggaa catattgttg taacagccgc tgatagctcg 300 ggcagtgctg ctacatcaac cttccaaagc agccagaccc tgactcacag aagcaacgtt 360 tctttgcttg agccatatca aaaatgtgga ttgaaacgaa aaagtgagga agttgacagc 420 aacggtagtg tgcagatcat agaagaacat ccccctctca tgctgcaaaa caggactgtg 480 gtgggtgctg ctgccacaac caccactgtg accacaaaga gtagcagttc cagcggagaa 540 ggggattacc agctggtcca gcatgagatc ctttgctcta tgaccaatag ctatgaagtc 600 ttggagttcc taggccgggg gacatttgga caggtggcta agtgctggaa gaggagcacc 660 aaggaaattg tggctattaa aatcttgaag aaccacccct cctatgccag acaaggacag 720 attgaagtga gcatcctttc ccgcctaagc agtgaaaatg ctgatgagta taattttgtc 780 cgttcatacg agtgctttca gcataagaat cacacctgcc ttgtttttga aatgttggag 840 cagaacttat atgattttct aaagcaaaac aaatttagcc cactgccact caagtacatc 900 agaccaatct tgcagcaggt ggccacagcc ttgatgaagc tcaagagtct tggtctgatc 960 cacgctgacc ttaagcctga aaacatcatg ctggttgatc cagttcgcca gccctaccga 1020 gtgaaggtca ttgactttgg ttctgctagt cacgtttcca aagctgtgtg ctcaacctac 1080 ttacagtcac gttactacag agctcctgaa attattcttg ggttaccatt ttgtgaagct 1140 attgatatgt ggtcactggg ctgtgtgata gctgagctgt tcctgggatg gcctctttat 1200 cctggtgctt cagaatatga tcagacacct gaagaacacg aactggagac tggaataaaa 1260 tcaaaagaag ctcggaagta catttttaat tgcttagatg acatggctca ggtgaatatg 1320 tctacagacc tggagggaac agacatgttg gcagagaagg cagaccgaag agaatacatt 1380 gatctgttaa agaaaatgct cacaattgat gcagataaga gaattacccc tctaaaaact 1440 cttaaccatc agtttgtgac aatgactcac cttttggatt ttccacatag caatcatgtt 1500 aagtcttgtt ttcagaacat ggagatctgc aagcggaggg ttcacatgta tgatacagtg 1560 aatcagatca agagtccctt cactacacat gttgccccaa atacaagcac aaatctaacc 1620 atgagcttca gcaatcagct caatacagtg cacaatcagg ccagtgttct agcttccagt 1680 tctactgcag cagctgctac tctttctctg gctaattcag atgtctcact actaaactac 1740 cagtcagctt tgtacccatc atctgctgca ccagttcctg gagttgccca gcagggtgtt 1800 tccttgcagc ctggaaccac ccagatttgc actcagacag atccattcca acagacattt 1860 atagtatgtc cacctgcgtt tcaaactgga ctacaagcaa caacaaagca ttctggattc 1920 cctgtgagga tggataatgc tgtaccgatt gtaccccagg caccagctgc tcagccacta 1980 cagattcagt caggagttct cacgcaggga agctgtacac cactaatggt agcaactctc 2040 caccctcaag tagccaccat cacgccgcag tatgcggtgc cctttactct gagctgcgca 2100 gccggccggc cggcgctggt tgaacagact gccgctgtac tgcaggcgtg gcctggaggg 2160 actcagcaaa ttctcctgcc ttcaacttgg caacagttgc ctggggtagc tctacacaac 2220 tctgtccagc ccacagcaat gattccagag gccatgggga gtggacagca gctagctgac 2280 tggaggaatg cccactctca tggcaaccag tacagcacta tcatgcagca gccatccttg 2340 ctgactaacc atgtgacatt ggccactgct cagcctcaat gttggtgttg cccatgttgt 2400 ctgacaacaa caatccagtt ccctcccttc gaagaagaat aagcagtcag ctccagtctc 2460 ttccaagtcc tctctagatg ttctgccttc ccaagtctat tctctggttg ggagcagtcc 2520 cctccgcacc acatcttctt ataattcctt ggtccctgtc caagatcagc atcagcccat 2580 catcattcca gatactccca gccctcctgt gagtgtcatc actatccgaa gtgacactga 2640 tgaggaagag gacaacaaat acaagcccag tagctctgga ctgaagccaa ggtctaatgt 2700 catcagttat gtcactgtca atgattctcc agactctgac tcttctttga gcagccctta 2760 ttccactgat accctgagtg ctctccgagg caatagtgga tccgttttgg aggggcctgg 2820 cagagttgtg gcagatggca ctggcacccg cactatcatt gtgcctccac tgaaaactca 2880 gcttggtgac tgcactgtag caacccaggc ctcaggtctc ctgagcaata agactaagcc 2940 agtcgcttca gtgagtgggc agtcatctgg atgctgtatc acccccacag ggtatcgagc 3000 tcaacgcggg gggaccagtg cagcacaacc actcaatctt agccagaacc agcagtcatc 3060 ggcggctcca acctcacagg agagaagcag caacccagcc ccccgcaggc agcaggcatt 3120 tgtggcccct ctctcccaag ccccctacac cttccagcat ggcagcccgc tacactcgac 3180 agggcaccca caccttgccc cggcccctgc tcacctgcca agccaggctc atctgtatac 3240 gtatgctgcc ccgacttctg ctgctgcact gggctcaacc agctccattg ctcatctttt 3300 ctccccacag ggttcctcaa ggcatgctgc agcctatacc actcacccta gcactttggt 3360 gcaccaggtc cctgtcagtg ttgggcccag cctcctcact tctgccagcg tggcccctgc 3420 tcagtaccaa caccagtttg ccacccaatc ctacattggg tcttcccgag gctcaacaat 3480 ttacactgga tacccgctga gtcctaccaa gatcagccag tattcctact tatagttggt 3540 gagcatgagg aagggcgaat tctgt 3565 2 1170 PRT Human 2 Met Ala Ser Gln Leu Gln Val Phe Ser Pro Pro Ser Val Ser Ser Ser 1 5 10 15 Ala Phe Cys Ser Ala Lys Lys Leu Lys Ile Glu Pro Ser Gly Trp Asp 20 25 30 Val Ser Gly Gln Ser Ser Asn Asp Lys Tyr Tyr Thr His Ser Lys Thr 35 40 45 Leu Pro Ala Thr Gln Gly Gln Ala Asn Ser Ser His Gln Val Ala Asn 50 55 60 Phe Asn Ile Pro Ala Tyr Asp Gln Gly Leu Leu Leu Pro Ala Pro Ala 65 70 75 80 Val Glu His Ile Val Val Thr Ala Ala Asp Ser Ser Gly Ser Ala Ala 85 90 95 Thr Ser Thr Phe Gln Ser Ser Gln Thr Leu Thr His Arg Ser Asn Val 100 105 110 Ser Leu Leu Glu Pro Tyr Gln Lys Cys Gly Leu Lys Arg Lys Ser Glu 115 120 125 Glu Val Asp Ser Asn Gly Ser Val Gln Ile Ile Glu Glu His Pro Pro 130 135 140 Leu Met Leu Gln Asn Arg Thr Val Val Gly Ala Ala Ala Thr Thr Thr 145 150 155 160 Thr Val Thr Thr Lys Ser Ser Ser Ser Ser Gly Glu Gly Asp Tyr Gln 165 170 175 Leu Val Gln His Glu Ile Leu Cys Ser Met Thr Asn Ser Tyr Glu Val 180 185 190 Leu Glu Phe Leu Gly Arg Gly Thr Phe Gly Gln Val Ala Lys Cys Trp 195 200 205 Lys Arg Ser Thr Lys Glu Ile Val Ala Ile Lys Ile Leu Lys Asn His 210 215 220 Pro Ser Tyr Ala Arg Gln Gly Gln Ile Glu Val Ser Ile Leu Ser Arg 225 230 235 240 Leu Ser Ser Glu Asn Ala Asp Glu Tyr Asn Phe Val Arg Ser Tyr Glu 245 250 255 Cys Phe Gln His Lys Asn His Thr Cys Leu Val Phe Glu Met Leu Glu 260 265 270 Gln Asn Leu Tyr Asp Phe Leu Lys Gln Asn Lys Phe Ser Pro Leu Pro 275 280 285 Leu Lys Tyr Ile Arg Pro Ile Leu Gln Gln Val Ala Thr Ala Leu Met 290 295 300 Lys Leu Lys Ser Leu Gly Leu Ile His Ala Asp Leu Lys Pro Glu Asn 305 310 315 320 Ile Met Leu Val Asp Pro Val Arg Gln Pro Tyr Arg Val Lys Val Ile 325 330 335 Asp Phe Gly Ser Ala Ser His Val Ser Lys Ala Val Cys Ser Thr Tyr 340 345 350 Leu Gln Ser Arg Tyr Tyr Arg Ala Pro Glu Ile Ile Leu Gly Leu Pro 355 360 365 Phe Cys Glu Ala Ile Asp Met Trp Ser Leu Gly Cys Val Ile Ala Glu 370 375 380 Leu Phe Leu Gly Trp Pro Leu Tyr Pro Gly Ala Ser Glu Tyr Asp Gln 385 390 395 400 Thr Pro Glu Glu His Glu Leu Glu Thr Gly Ile Lys Ser Lys Glu Ala 405 410 415 Arg Lys Tyr Ile Phe Asn Cys Leu Asp Asp Met Ala Gln Val Asn Met 420 425 430 Ser Thr Asp Leu Glu Gly Thr Asp Met Leu Ala Glu Lys Ala Asp Arg 435 440 445 Arg Glu Tyr Ile Asp Leu Leu Lys Lys Met Leu Thr Ile Asp Ala Asp 450 455 460 Lys Arg Ile Thr Pro Leu Lys Thr Leu Asn His Gln Phe Val Thr Met 465 470 475 480 Thr His Leu Leu Asp Phe Pro His Ser Asn His Val Lys Ser Cys Phe 485 490 495 Gln Asn Met Glu Ile Cys Lys Arg Arg Val His Met Tyr Asp Thr Val 500 505 510 Asn Gln Ile Lys Ser Pro Phe Thr Thr His Val Ala Pro Asn Thr Ser 515 520 525 Thr Asn Leu Thr Met Ser Phe Ser Asn Gln Leu Asn Thr Val His Asn 530 535 540 Gln Ala Ser Val Leu Ala Ser Ser Ser Thr Ala Ala Ala Ala Thr Leu 545 550 555 560 Ser Leu Ala Asn Ser Asp Val Ser Leu Leu Asn Tyr Gln Ser Ala Leu 565 570 575 Tyr Pro Ser Ser Ala Ala Pro Val Pro Gly Val Ala Gln Gln Gly Val 580 585 590 Ser Leu Gln Pro Gly Thr Thr Gln Ile Cys Thr Gln Thr Asp Pro Phe 595 600 605 Gln Gln Thr Phe Ile Val Cys Pro Pro Ala Phe Gln Thr Gly Leu Gln 610 615 620 Ala Thr Thr Lys His Ser Gly Phe Pro Val Arg Met Asp Asn Ala Val 625 630 635 640 Pro Ile Val Pro Gln Ala Pro Ala Ala Gln Pro Leu Gln Ile Gln Ser 645 650 655 Gly Val Leu Thr Gln Gly Ser Cys Thr Pro Leu Met Val Ala Thr Leu 660 665 670 His Pro Gln Val Ala Thr Ile Thr Pro Gln Tyr Ala Val Pro Phe Thr 675 680 685 Leu Ser Cys Ala Ala Gly Arg Pro Ala Leu Val Glu Gln Thr Ala Ala 690 695 700 Val Leu Gln Ala Trp Pro Gly Gly Thr Gln Gln Ile Leu Leu Pro Ser 705 710 715 720 Thr Trp Gln Gln Leu Pro Gly Val Ala Leu His Asn Ser Val Gln Pro 725 730 735 Thr Ala Met Ile Pro Glu Ala Met Gly Ser Gly Gln Gln Leu Ala Asp 740 745 750 Trp Arg Asn Ala His Ser His Gly Asn Gln Tyr Ser Thr Ile Met Gln 755 760 765 Gln Pro Ser Leu Leu Thr Asn His Val Thr Leu Ala Thr Ala Gln Pro 770 775 780 Leu Asn Val Gly Val Ala His Val Val Arg Gln Gln Gln Ser Ser Ser 785 790 795 800 Leu Pro Ser Lys Lys Asn Lys Gln Ser Ala Pro Val Ser Ser Lys Ser 805 810 815 Ser Leu Asp Val Leu Pro Ser Gln Val Tyr Ser Leu Val Gly Ser Ser 820 825 830 Pro Leu Arg Thr Thr Ser Ser Tyr Asn Ser Leu Val Pro Val Gln Asp 835 840 845 Gln His Gln Pro Ile Ile Ile Pro Asp Thr Pro Ser Pro Pro Val Ser 850 855 860 Val Ile Thr Ile Arg Ser Asp Thr Asp Glu Glu Glu Asp Asn Lys Tyr 865 870 875 880 Lys Pro Ser Ser Ser Gly Leu Lys Pro Arg Ser Asn Val Ile Ser Tyr 885 890 895 Val Thr Val Asn Asp Ser Pro Asp Ser Asp Ser Ser Leu Ser Ser Pro 900 905 910 Tyr Ser Thr Asp Thr Leu Ser Ala Leu Arg Gly Asn Ser Gly Ser Val 915 920 925 Leu Glu Gly Pro Gly Arg Val Val Ala Asp Gly Thr Gly Thr Arg Thr 930 935 940 Ile Ile Val Pro Pro Leu Lys Thr Gln Leu Gly Asp Cys Thr Val Ala 945 950 955 960 Thr Gln Ala Ser Gly Leu Leu Ser Asn Lys Thr Lys Pro Val Ala Ser 965 970 975 Val Ser Gly Gln Ser Ser Gly Cys Cys Ile Thr Pro Thr Gly Tyr Arg 980 985 990 Ala Gln Arg Gly Gly Thr Ser Ala Ala Gln Pro Leu Asn Leu Ser Gln 995 1000 1005 Asn Gln Gln Ser Ser Ala Ala Pro Thr Ser Gln Glu Arg Ser Ser Asn 1010 1015 1020 Pro Ala Pro Arg Arg Gln Gln Ala Phe Val Ala Pro Leu Ser Gln Ala 1025 1030 1035 1040 Pro Tyr Thr Phe Gln His Gly Ser Pro Leu His Ser Thr Gly His Pro 1045 1050 1055 His Leu Ala Pro Ala Pro Ala His Leu Pro Ser Gln Ala His Leu Tyr 1060 1065 1070 Thr Tyr Ala Ala Pro Thr Ser Ala Ala Ala Leu Gly Ser Thr Ser Ser 1075 1080 1085 Ile Ala His Leu Phe Ser Pro Gln Gly Ser Ser Arg His Ala Ala Ala 1090 1095 1100 Tyr Thr Thr His Pro Ser Thr Leu Val His Gln Val Pro Val Ser Val 1105 1110 1115 1120 Gly Pro Ser Leu Leu Thr Ser Ala Ser Val Ala Pro Ala Gln Tyr Gln 1125 1130 1135 His Gln Phe Ala Thr Gln Ser Tyr Ile Gly Ser Ser Arg Gly Ser Thr 1140 1145 1150 Ile Tyr Thr Gly Tyr Pro Leu Ser Pro Thr Lys Ile Ser Gln Tyr Ser 1155 1160 1165 Tyr Leu 1170 3 36159 DNA Human misc_feature (1)...(36159) n = A,T,C or G 3 aaagtgggga gatgttggaa ggcagcaagc agattttgga gtgcatttta aggcaggttg 60 agacaggttt tttttttgag ataggatcta gctctgttgc ccaggctaga gtgcaatgga 120 gtaatcacaa ctcactgtag cctcaatgtc ccagactcag atgattttcc tgcttcagcc 180 tcctgagtag ctgggaccac aggcatgtgc cacttacact tggctttttt tttttttttt 240 tcccggtaga gatggagtct ccccatgttg ctctggctgg tcttgaactc gtggactcaa 300 gtgatccttc caccttgggt tcctaaagtg ccaggattac aggcgtgagc caccacatct 360 ggcctaattt ttcttttctt ttcttttttt tttttgttaa tgcttcccag gctgatcttg 420 aactcctgag ctcaagtgat cctcctgcct gggcctccca aagtgcggga attacaggct 480 tgagcgacca tggccagcca agttgagaat cttggacatt atctccaaag caatgagaaa 540 ccccgggaga aggggaagca agatggttaa gaagagagag cagttatctg atttgcattg 600 tttaaaagca aagatctact gagtggattt aaggagatta gtttggaagc tactggcagt 660 ttgaactaga atggtgccaa taagggtagg gaaaaagggc tgatttgaaa tatacttagg 720 aggccagggg cagtggctca cgcctgtaat cccagcactt tgggagggtg aggggggtgg 780 atcacttgag ctcaggagtt tgagaccacc caggcaacat ggtgaaaacc catctctact 840 aaaaatacaa agaaattaac tgggtgtggt cgtgcacgcc tctactctca gctacttggg 900 aggctgaggc aggagaattg cttgagcccc agaggtgaag gttgcagcga gccaagattg 960 caccattgca ctccagcttg ggctacagag tgagactctg tctcaaaaaa aaaaaaaaaa 1020 aatatacaca cacacacaca cacacacaca cacacacaca cacacacact taggagatgg 1080 aatggataag atagagatta gatgtggagg aataagggag aggaatgagc caggataata 1140 gtattaaata tgtggtagac actatcattt tacatgtatt aaattattta attctcagaa 1200 caaccccatg aggtaggtat tgctatcacc attatgtagc tgaggaaaca gacatcccta 1260 attttttttc ttttttttga gacagggtgt cattctttca ccctggctgg agtgcagtgg 1320 cacgatcaca gctcactgca gcctctacct ctgggctcag gtgatcactt ctgccttctg 1380 agtagctagg actacaggca tgtgccacca tgcctggcta actttttttt ctgttttttt 1440 ttttttttgt tgttgttgtt gtttgtttgt tttagagacg gtttcaccat gttgcccagg 1500 ctggagctcc ctgatttctg gcttgaggcg ttggatgtgt gatggcatct cataattaag 1560 atagaaaact gaaggtgggg tggaggctcg taagtttaat tctgaatgta ttgaatatga 1620 ggtgtttgtg aaatgtccaa gttgcagggt taagtagtca tttggatata gggtttggag 1680 ttcaaagcga gagaatcctg ggttagagat agagatttta gtcttttgaa gatgactaat 1740 tttgaggagt aattattaaa aaggggcaaa gggtagagca aggaaagagg gattactata 1800 gagccccaag gcatatgaga tcggatggtt gaaaatggag aagataaata tgaaatggct 1860 tgtgtgctat gtcagatgtt tggactttat tctgaaaaaa tagctttcag tttaatctgt 1920 gggcttattg agctggaagt gtctgtggga tattcaggga cagaaagctg gactgttctt 1980 acatcctttc ctcatatttt tctgctaact ttcctcggtt cttcagaata tactctagct 2040 ttctcatcat cctggttact tttttttttt tttttttcaa ttttagtatt tttagagaca 2100 gggtctcact acattgccta ggctggtctc gaactcctca gctcaggaga tcttcctgcc 2160 ttggcctccc aaagtgctgg aattaaaggc ttgagccact gtgcctggcc catactggtt 2220 acttttttat cttaaaatgt ggtagacaat tgaatgcatt ttatgtatga cctgagcaga 2280 gtggataatc ttcactttgt ccagcacgtt ctgtacactg tttctatgaa tataggtcaa 2340 gattgaatta gtttttgaga agaggagaac attattacat catgtttctt ttatcaagta 2400 aaagtgtgtg tgtgtgtttg tgtgttttaa atctaagcct tgtatctttt atccttgtgg 2460 tctaattctt cctttctctc aatataggta tggcatcaca gctgcaagtg ttttcgcccc 2520 catcagtgtc gtcgagtgcc ttctgcagtg cgaagaaact gaaaatagag ccctctggct 2580 gggatgtttc aggacagagt agcaacgaca aatattatac ccacagcaaa accctcccag 2640 ccacacaagg gcaagccaac tcctctcacc aggtagcaaa tttcaacatc cctgcttacg 2700 accagggcct cctcctccca gctcctgcag tggagcatat tgttgtaaca gccgctgata 2760 gctcgggcag tgctgctaca tcaaccttcc aaagcagcca gaccctgact cacagaagca 2820 acgtttcttt gcttgagcca tatcaaaaat gtggattgaa acgaaaaagt gaggaagttg 2880 acagcaacgg tagtgtgcag atcatagaag aacatccccc tctcatgctg caaaacagga 2940 ctgtggtggg tgctgctgcc acaaccacca ctgtgaccac aaagagtagc agttccagcg 3000 gagaagggga ttaccagctg gtccagcatg agatcctttg ctctatgacc aatagctatg 3060 aagtcttgga gttcctaggc cgggggacat ttggacaggt ggctaagtgc tggaagagga 3120 gcaccaagga aattgtggct attaaaatct tgaagaacca cccctcctat gccagacaag 3180 gacagattga agtgagcatc ctttcccgcc taagcagtga aaatgctgat gagtataatt 3240 ttgtccgttc atacgagtgc tttcagcata agaatcacac ctgccttgtt tttgaaatgt 3300 tggagcagaa cttatatgat tttctaaagc aaaacaaatt tagcccactg ccactcaagt 3360 acatcagacc aatcttgcag caggtggcca cagccttgat gaagctcaag agtcttggtc 3420 tgatccacgc tgaccttaag cctgaaaaca tcatgctggt tgatccagtt cgccagccct 3480 accgagtgaa ggtcattgac tttggttctg ctagtcacgt ttccaaagct gtgtgctcaa 3540 cctacttaca gtcacgttac tacaggcaag tggcaaatgc tgaaaatcgt atcttaggct 3600 agagttctgt ccttatattt aacatatacc ccgtaggcta catatagcaa tgaatttgtt 3660 tatagattct gagatagaaa taggatatgt tttagctcat tctatgtgtg tggcattcct 3720 atatatgaca tttatttctg aaattttatc tagcactgga aaaattaact cagtctgatt 3780 ctgaaagttg ttactagttg aattatacta gcacctggtt ctttagtatt attttacctc 3840 attttcccat tttatttatt ttatttattt atttatttat ttagagacag aatctcgctc 3900 tgtcgcccag gctggagtgc agtggcgtga tatcagctca ctgcaagccc cacctcctgg 3960 gttcacgcca ttctcctgcc tcagcctcct gagtagctgg gaccacaggc acccgccatc 4020 acgcccggct aatttttttt gtatttttag tagagacggg gtttcaccgt gttagccagg 4080 atggtctcga tatcctgacc tcgtgatcca cccgtctcgg cctcccaaag cgctgggatt 4140 acaggcgtga gccaccgtgc ccagcctatt tatttatttt tttaagatgg agtttcactt 4200 gccacccagg ctagagtgca gtggtgtgac attgactcac ggcagcctcc acctcctggg 4260 gtcaagtgat ttctcctgca actcctgtcc tgagtagctg ggactacagg cacctgctac 4320 cacgcccggc taattttttt gtttttaata gagatggggt ttcaccatgt tgaccgggct 4380 ggttttgaac tcctgacctc aggtgatcca cccgcctcag cctcccaaag tgattagagg 4440 cgtgagccac catgcccagc cattttccca ttttgaagag tcttgaaata cacaaagata 4500 tttacttatt tgtaatgaat ctgagcatat gttgctgttt tttcgaacct cttatcttgg 4560 caggtaaaat aacgtgggaa taactctagg tttaactcta gtaacatttt attcttttac 4620 attttcttct gtagtagcat gaattgaatt acatggttgc tacaatctct tcctgtttta 4680 actttctcta aatactttga acttaatggg ttatcctaga atggccttga cccaagtacc 4740 ttatacttta atgatatata tttctagatt gatactttta atgtagctac cattttaata 4800 tataataatt attgggacag tatgtaaatg ctgatatata caattttgtc tgtaccataa 4860 ccaaggcttt taaaatgtgc tttttatcag cacccattta cttacttgcc tagttattaa 4920 ttttaaggaa tctaatattt agttttaatg gccatacatt aaatacaaat catgtaagca 4980 tccaatcaag aagtgaaata ataaaaacat agataaccta taaaatatgt ttataaggag 5040 ctatacatgc cagatgcctg taataaaatt tgaggaaata gaaattctga attaagaatt 5100 ttatattatg tgtgaaaata atgtgaggat attttaaccc atacaaggac tcagaaaaaa 5160 tgtcatctgc atgtttcctt ttttaaaaac attgtggtaa gatgtttata ataggaaatt 5220 tacaatttta accatttggt accactcatt gtgttaagta cattcatagt gttgtgtaac 5280 catcactgct gtctgttaag tatattcaca atgttgtgta accatcacca ctatttccaa 5340 atgttttcat cacccaaaac agaaattcta accattaagc aataactccc tattctctct 5400 tcttcctacc actggtaatc ttgatttgac tttctgtctc tatgaatttg cctattctag 5460 atactgcatg taagtggaat catacaatat ttgtcttttt gtgtctagtt tatttcactt 5520 agtgtaatgc ttttgaggct aatccatgct gtaacatgta tcagaacttc attcctttta 5580 tggctgtata atattccatt gtttgtatat accacatttt gtttatgcat tcatctgttg 5640 gtagatattt gggttgttgc tacctttagg ctgttgtgaa taatgctgct atgaacattg 5700 gtgtacaagt atcctagtcc ctattttcag ttactttggg gatatagcta ggagggaatt 5760 gctgggtcac atgataattc tatgtttaac tttttgcaga attaccaaat tattttccac 5820 agaggctgca ctattttaca ttcctaccag cagtggatgt gcattccaaa tttctccaca 5880 ttttctctaa catttgttat tttttttatt taaaaatatt gtttgtttat ttttacagag 5940 acaggggctg cctctattgc tcatgctgga gtacagtggc acgatcatag ttcactgtag 6000 cctccaactc ctggacttga gcagtcctcc cacttcagcc tcccaagtag ctaggactgc 6060 agtcacactc caccatacct ggctaattac tattatttta ttttttgtgg cgacagtgtt 6120 ttgagggtct cattttgttg cccaatctgg tctcaaacta ctggcctcaa gccatcctcc 6180 tgcctcagtc tcccaaagtt ctgggattac aggtgtgaac taccactcct ggccttgttt 6240 tgttttttaa ataatagcca tgggtttttt tttttttttt tttttttttt ttttttttgg 6300 aaagggagtt tcacttttgt tgcctaggct ggagggcagg ggggcaatct cggttaactg 6360 gaacctttgc ctcccaggat tttcctgcct aaacctccca agtagctggg attacagggg 6420 cctgccacca cacccagtta atttttgttt ttttaaaaaa aatggggttt taccatgttg 6480 gccagggggg gctccaactc ctgacctcag gggatctgcc caccttggcc tcccaaagtg 6540 ctgggattac aggcatgagc cactatgcct ggccaataat agtttttttt tgtttttttt 6600 ttgttttttt tttgagatgg agtcttgctc tgttgccagg ctggagtgca gtggcacaat 6660 ctcggttcac tgcaacctcc acctcacagg ttcaagcagt tctcctagct tggcctcctg 6720 agtagctggg aatacaggtg ccaccatgcc cagctaattt ttgtattttt agtagagaca 6780 gggtttcacc atgttggccg ggatggtctc gatctcttga cctcgtgatg aagtgctggg 6840 attacaggca tgagccaccg ggcccggtca ataatagcca ttcttatggg tgtgaagtgg 6900 tatctcattg tggttttgat ttgtatttcc ctaatgatta atgatgttga gcatttgttt 6960 tattttgttt gtttgagaca gagtcccact ttgtcaccca ggctggggtg cagttgtgca 7020 atcatggctt actgcagcca tgacctctca ggctcaagca gtcctcccac cttagccttt 7080 cgggtacctg agactacggg catgcacccc cacacctgac tagtgttttg tatttttagt 7140 agagacgggg tttcactgtg ttgcccaggc tggtctcaaa ctcataggct caagtgatat 7200 gcccgcctcg gcaacccaaa gtgctgggat tacagacatg agccaccatg cccagcctgg 7260 cattttttta tgtgcccgac atctgtatat cttctttgga gaaatgtcta tttaagtcct 7320 ttcctcattt cttgaattgg gctttttgtt gttgagttgt atactctata tacttaattt 7380 tcatctattc cttgggttgc ctttttacct gttgatagtg tttgacacag aaaagttttt 7440 aactttggtg aagtgcagtt tgtctacttt ttctttggtt gcttgtgctt ttggtgacat 7500 atccaagaag tcactgttaa gtcgaaatca tacagatttt cccctatgtt ttctgctaag 7560 agttttatag ttttagctct tatattttgg tctttgattc tttgttgatt tttgtctatg 7620 gtccaaggta caaatccagt gtaattcttt ggcatgtgac tattcagttc ttcaaacacc 7680 atttgctaag aagattgtcc tttctgcatt gggtggtttg ggcacccttg ttggaatcat 7740 ttgaacatat atacaaataa ttcttatctt ctattgcttt cccattttca atgttgggct 7800 ctctattcca ttaatctata tatgtcttta tgccagtacc acattgtttt gattattgta 7860 gctttgtagt aagtttgaaa tcaggaagtg tgagacctcc aactttgttc tttttcaaga 7920 ttgttttggc tatttggggt ctttgagggt ccatataaat tttaggatgg gtttttctat 7980 tttatacaaa aaccataatt gctttttatt aaggatagcg atgaatctgt agatgacttt 8040 gggtagtatt gacagcttaa tagtaagtca gtccatcctt atttctttat atcttttcac 8100 agttttataa aactggtatt ttttacttga ggtaaggtaa ataaactctt agagcctttg 8160 ttttctggtt ttatgctgcc ctaggcaacc ttggctaact ttaagaatgt catctccatt 8220 tatttattta tgccttggga gatttaggtt ccaactacat ttgcttttta atgctctcct 8280 ttgagcagtc tcaccaccag ccacaccaac ataacatata tataacatac tctacaggtg 8340 cactgaagaa ttcagcgcag catcccattt tgagtcctca ggagggacta ggcagaccac 8400 agctgaagga agagggctga tcagctcttc ctttctgtct tgactctgtg cctgcaggtg 8460 ttctttaact atttgtttgc cctgtcaaag acaaagtgca ttctcttgtg ataccagagt 8520 agtttttaaa ttgaaaaagg gagagcaata ggagataaaa attatttggc tttgttataa 8580 ttggggcatg ttaatacaaa ataaaatgaa ttatttggct gcttagcttt ctgtaatgtg 8640 taattcattt gaataatttt cagtgttagg ttgctgatct ttgtattttt tatcctttta 8700 atttaagctg tcaattgatt cattttggtt ttgtttttta tagaaactaa ggttttcaaa 8760 tcttcaaagt tacccttcga caaagctttc tttaaattca ctgcaatata gttgttgact 8820 ataattttaa gtggagctaa gtttgcctct taaaaacagg agttcattct gtgtattact 8880 gagtaattac tctgtatact gaagttcagt gcccagggct tgacagtgtt taggatttaa 8940 catgagtgtt ctgttgtgtc acagtaatac ttgataatga gcctaaggca gatggaacag 9000 cagctcaggc attccttctt tatcactagt tttacccgca gtggtcctct taagcttctt 9060 tgatgttgct ttgttgccat attagagtcc attaagtcct cacccttctg tctttcaaaa 9120 aacctctgtg aaatctgttt ggctggtgaa gcattttgac tccaaagcta gtccttctct 9180 tacccacctt tttagtttac cttgctttgt ctttctgata atatgccagt attatcagct 9240 cacataaatt tgccaccttg ctgtgtccat tggccctggg catggctaaa tgattcaggc 9300 agtggaaata atatacttta ctctctggct cactgtaaat gtgcacagac tccaagcaaa 9360 gctcctgtct ttcgggcttg agttttagag acaaaggttt gccatgctta caggctgaat 9420 gtttttccct actgaacaaa ctagccagcc tttatttcaa gctgaatcac tttgttactt 9480 acggaaggaa aaggtctaga gaaggaaaac gtatcttcca tttatcctag acaaacaaat 9540 aatctaattt cctctggcag tcaaaatata gtttcaccta agccactgat gcaggaagtt 9600 aggttttatg taacctctct aattggtaag taagtaggtt tgatgtctct gagataggaa 9660 gaaagaaacg aaaatgttca tgaaaataat cagagtgatt tgtgttaagt gatcctaacc 9720 ttagcttgct ctgggtgcca gtgaaattaa cctcaacaat gttggttgga agaatttttc 9780 aacttaaaga agtttgaagt tggggaatca aaaggcaggg attgttgttt ctatcactta 9840 gctgtaataa ccagagcctg tttagtattt gttttttaag gatgggatgt gtcttcaaag 9900 aggagacttg ccatgttcaa agcacaatta atgccatttt cctactgaag tgaacactgc 9960 cagtttttaa cagtttcttt cactttcctg tgcttctgta gataaccttt tttactgccc 10020 agttgttgga atgttacagc tggaaaggga cctagaagag taattatcta actctgtttc 10080 cttattacac aaatgaggta gaaccagagt tttacgtgtc tatagagtnn nnnnnnnnnn 10140 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnca gtggcgcaat catggctcac 10200 tgcagccttg acctcctggg ctcaagtgat ccttccacct cagcttcctg agtagctaga 10260 actgcaggca tgcaccacca tacctggcta attttttaaa tttttttggt agagattggg 10320 tcttgctgtg ttgcctaggc tggtctcaaa ctcctgctca agtgatcctc ctgccttggc 10380 ttcccaaagt gctgggatta taggtgtgaa ccgccgtttc tggccgtatt tttttttttt 10440 ttaaactgct ttcctttttt tgtttttcct tttgctattt gcctttttat aaggtagata 10500 cggtagagtt gctgttttga ctgagctttt gctggaagtc cttagctgct tttgtcactc 10560 caaaagcagg gtgagaccaa atgaaaaaac tttcagctaa tcttcagttt ttttttttaa 10620 ttaaatggga cttgggggct gtggaagtga tattttcctt aatttcccag aaaactttaa 10680 gctcgagaca gttatcatat attattgcta ccttttttat ttttttctga gacggagttt 10740 cgctcttacg cccagtctgg agtgaattga cgtaatcttg gctcactgca acctctgccc 10800 cccgggttca agcgattctc ctgcctcagc ctctggagta gttgggatta caggcgcctg 10860 ccaccatgcc cagctaattt ttgtattttt agtagagact gggtttcatc atgttggcca 10920 ggctggactt gaactcctga cctcaggcca tccacgtgcc ttggccaccc acagtgctag 10980 gattataggc gtgagccacc gcgcctggcc tgttatcgct accttttaaa gaagaaagtt 11040 atagagtggc ctggccattc tctgtgacct accttttgga ctttaaaatg tctttctagt 11100 atggtaggaa tagcaaaatc aatatgctgc cctccaattg atgctttgga atgttctaaa 11160 cccagttttt attttggctc attgccagtt gtgctccccc tgccagctat ttttggcatt 11220 gtcatgaact tggaaattaa tgattctgct cactaggagt agaaaatttt gttccttttc 11280 aattttagaa aagcttttat gttgtttctg ggtagtctta ctagcttatt aatgcgcctg 11340 tcaaacttgt gcagtgttga aaacatgcca ttatggttga gatttcactg aactctgaaa 11400 ttccatcagt aatatgtgcc tctagccacc tgcaacagga atatcacttt tgagggttac 11460 ttcttttctt ttcttttttt tttttttttg agacagagtc ttactctgtc acccaggctg 11520 gagtgcagtg gcactgtgtc agctcactgc aacctccgtc tcctgggttc aagcaattct 11580 cctgcctcag cctcctgagt agctgggatt acaggtgccc gccaccacac ctggctgatt 11640 ttttatattt ttagtagaga tggggtttca ccatgttggc caggctggtc tcaaactcct 11700 gacttcaggt gatccagcct cctcggcctc ccaaagtgct tgtattacag gcatgagcca 11760 ccgcacccgg ccagttattt ctttggtaaa caaaaccaca gttcaaatta aatactacaa 11820 aaactgatga tattggtggt tccacccata gctgttaaaa agtgtaagcc cgaagaggcc 11880 tgggtcgact gctatttgta tttaaggatc agaaaagctt tcaggccctg tggagtcccc 11940 agatttactg ttttctaagg gccactattt atgtataaat actaggggag gatttttttt 12000 ttcttctatg cctagtttgc ttagatgggg agggatattc ttatttaggg aaattatatt 12060 ctccttgctt aatccttgcc ttccctcaac cccctgcaca tatacacaaa acaacaataa 12120 gcacatatca cttgaaagta gtttgagaaa cctgggtatt ctgtgaggag acacggccag 12180 ttagatggtt cttcacggaa agatctgttt tccatttaac tcctgtaaca tgaggaatct 12240 gaatctggat ctggatctgg atctggagtg tccttataga ttataattcc atgacttgta 12300 agaaagaaag gaaattattt ggagaagatg atccagtgcc taagagctga aatcttggat 12360 ccaaatagct tgggtaccat cctttttctt ttgttgagat ggagtctcgc tctgtcgccc 12420 aggctggagt gcagtggcag atctcaactc attgcaactt atgcctccca agtttaagta 12480 attctcttgc ctcagcctct gagtagttgg gattacagct gcccgccacc atgcccagct 12540 aatttttgta tttttagtag agatggagtt tcaccgtgtt gaccaggctg ttctcgaact 12600 cgtgacctca agcaatccac tcaccttggc ttcccaaagt gctgggatta caggtgtgag 12660 ccactgcgct ggccaagggc accatctttt agtagttatg tagccttggg caagttactt 12720 taacctctta gtgccagttt cttcatctgt aaaatggagg taatactttt attgcataga 12780 atctaacatg ccattgatta taagatacat tatttttgta ccacttaaaa aaggaaaagc 12840 gctgccatta aactaaaata taccatcatt tgtaagaatc ttcttaattt cagaggtgct 12900 aacatgtaaa aagatgtgta tcttagaatt gatgacatca taataatact ttgataggat 12960 tgttgtaagg attaagtgac tcaacattta taaagaactt agaacagtgc atggcacata 13020 gtaggcaata tttatgtgtc atttattatt attgctatta gtgttaccta ttattttctt 13080 tttgaaccca cttattgcct aattagtcat agtttgacaa ttgcccttgt attccaccat 13140 gtcaaatata aatttacata gatgagtatg tacttttact tattgagaaa cagtgtaata 13200 tataatatac tcaattctgg agccagattg cagggattca aatcctagct ctgccactta 13260 tttgactgtg actctaggcc aataacttaa tctttctttt tctcagtttc ttcttctgta 13320 atggggataa taattctatt ttagatgtgt tcgtatatat aaacgtctga gttatggatt 13380 accttagtca tctctttaaa gttccctagc attttatttc tcacttggac tgttaatgaa 13440 tatttctaaa aagcacacta agagttcaaa gttttaaaat aatggtaaca taatactgtt 13500 attatatcta acacctacta gtatttacca tgtgccatgc actggtctaa aagctttcat 13560 atatttattt aagcttcaca acaactctat gtggtgggaa ctcttactgt ctccatttta 13620 tagatgagga acctgaggca cagagagatc aagtaatata cctgcagcta ttaaatgatg 13680 gaactaggat tcagaccctg acaggctggc tctagagagt gtgctgtcaa caccatgtct 13740 cttcagaagg catttctttt tctttttttt ttttccagaa ggcatttctg tcatgaaggg 13800 gttatttatt gaccagggct tttttttttt tttttggact gtcttgggtc tcctaggctg 13860 gagtgtagtg gtgtgatctt ggcttactgc aacctctacc tcctgggttc aagcgattct 13920 tttgtctcaa cctcctgagt agctgggatt acaggcgccc accaccacac ctgactcatt 13980 tttgtatttt tagtagattt ggggtttcac catattggcc aagctggtct tgaacttctg 14040 acctcaggtg atccacccgc ttcggcttcc caaagtgctg ggattacagg catgagccac 14100 tgtgcccagt tgaccaggcc ttttaattga tttttttttt ttatgattga aatggtgcta 14160 ggaataataa taaaaaaaat ctattatccc ttatctgtga ttgcaaaatt cagaaagctc 14220 tcataaatga aaatttttct ttaagtttgg tataaattca tttaattggc aagacctgac 14280 ttgaaccatt gttaagctat ttgaagtctt tatttagcca acttagtatg actgttccca 14340 tgttttgttg cagaaatatt aatgtgtttg attatagtgc actgccctga actccactgg 14400 gattattata taatgtgtac tttgtgttct gcattacctt tctgaaattc aaaatattct 14460 gaattccaaa acacatctgg ccctgagctt cagatgatgg attgtatacc aaagattttt 14520 tttccatttc attgaataaa tgttccttta gctaatacta aaacaggact tagtcatgta 14580 gttaattttc ccaaataatg tttttttttt tttaatctga tattttttgt ttttgctaga 14640 gctcctgaaa ttattcttgg gttaccattt tgtgaagcta ttgatatgtg gtcactgggc 14700 tgtgtgatag ctgagctgtt cctgggatgg cctctttatc ctggtgcttc agaatatgat 14760 caggtaaaag tgtttatttg aatggaaata gaatgcaaat agttacttgt gaattagatt 14820 ctggagaaag agaagtacta agtactactg aagtatttag ataataggga aagagtagtc 14880 caattgctac taaagaactt tttaaagaat agtataattt tctcttcctg cttcttaggc 14940 taaagtatgt ttgcaattct ataataaaaa aaagaatttt attttatatt aaggttgata 15000 ctttgctaga tctgtaatga tttattagag acttaacttt cattaactta tgtgctttgt 15060 gagttaggaa agtagagtaa agatgaggaa ctggaatttt aaaagagaac ttctacttac 15120 tcggagctat tataatttac ttttacgcat gacacactga agtactttct tcagactgaa 15180 acacttcagg tcccagaagc tgtgacatac tgggtcgcta agataggatt tagaaaggaa 15240 atcatcctga gttgtagtaa tatatgatct gtatctaaaa atagacaaac ttaggagata 15300 tggtataatt tcctaaggaa ttggtccgtt aagggaaaat gttttactat ggaagtaaat 15360 tgtgaattct catttcttgt tattttttct tttttctttt tatttgtttg agatggagtc 15420 ttgctctgtc acccaggctg gagtgcagtg gcgcgatctc ggctcactgc aacctctgcc 15480 tccctggttc aagcgattct cctgcctcag cctcctgagt agctgggatt acaggtgcct 15540 gccaccatga ccaactaatt tttgtatttt ttagtagaga cggggtttca ccatgttggc 15600 caggctggtt tcgaactcct gacttcaggt gatccacctg cctcagcctc ccaaagtgtt 15660 gggattacag gtgtgagtca ccgtgcctgg ccttcttctt attttttaaa aatgttcctg 15720 ccctttatga tgtaagctcc ttgagggtag agattgtttc acatcaccag tgtatcctca 15780 gctcctaaca ctgtgtctgg tacacagtaa gtacaccagt ttttttgttg tggtttttaa 15840 gtttttattt ttttagagac agagtcttgc tcagtcaccc aggctggcat gtaggcctgt 15900 cacagcttac tgtaacctct agctcctggg cttaagtgat cctcccacct cagcctccca 15960 ggtagatggg actataggtg catgccacct tgcctagcta attcttttat tttttgtaga 16020 gtcggggatc ttgctatatc agcctagggt ggtctcaaac tcccaggctc aagctatcct 16080 cctaccttgg cctcccaaag tactgggatt acaggtgtga gccaccatgc ctggcctata 16140 ttgtcaaata tctttacttg tccgtaaata cacttctacc ttgtcattta caatgtctgc 16200 atggtatttt ggtttccagc tacaggattt agaaaggaag ttatctgagt tgtagtagat 16260 tccacagatt tgaagtatta gaagtcaaca ggaaaagcaa aaaagattat agccaaaatt 16320 ttcaaaactg gatttccttg taaataatag atacagtagc tgtggatgga ttagtatata 16380 taggtattta cagataaatt tcagttgtat tgattaaaga tttgatttct tcctttgcct 16440 aaagttaatg atgttttagt gtaaaagcct ttaataattt cccttttcac tccaaatagt 16500 tgtttgatgg ttttgatgtt tcagattcgt tatatttcac aaacacaagg cttgccagct 16560 gaatatctta tcagtgccgg aacaaaaaca accaggtttt tcaacagaga tcctaatttg 16620 gggtacccac tgtggaggct taaggtctgt cttccctact atgcttccga ctcctgtact 16680 ccacccctca ctccccaatt ttgaattcaa agtttagtta ttaaattctt caggtagaga 16740 agggaaagga gagggggaag cattttgaaa aattatttct ttgtacctgt ttggccttat 16800 cctcagttga aaaacaaaac attaattgct agttcagttg gctgaggtta ttttgtatat 16860 gttcaatcca cagctgatag aaagtttgga gggtagtgct caccattaag cgatagaact 16920 agagacatat agtaatgact gatttttaga gaattctcaa tgaacatgat aaaatcacaa 16980 attttctaac tgcccacatt caggacttct atattttttc ttgaaacaaa tacctgcttt 17040 ttacttctga gcctactctg tcaggttcag aaatatctga gtaatttgac taaccctgtg 17100 actgtgtgtc tgagtctgtt gaacagttag catttgagat atcgatttat ttgaaagtag 17160 ctttaagaga acaatggtag tgtccccttt tacctgacat tctttaggaa ctgtgctgta 17220 tcattacttg catgtttatc actgttgaaa gggtagctag atatcaaggt cacatctctc 17280 cactggaaga ttttctggtt gtgaattact ttcatgtttg ccatctatgg ttggcaaggt 17340 gaccacactt gtctcttgta ttctggcttt ggttttgaat aaaatgtgaa aataacatac 17400 agatggaatt taaggaggaa aatctttatt ttatagacac ctgaagaaca tgaactggag 17460 actggaataa aatcaaaaga agctcggaag tacattttta attgcttaga tgacatggct 17520 caggtgagta cggaaagttt cagaaagtca gacatttatt tttaatcaga gacacttctg 17580 ttgattatac taaagacaaa tttaatgtta tctttctagt atttgttttc agtttttata 17640 aaaaatgcat taatattcca ccatgtagta aaggaacatt taaatcctaa ccaagtatat 17700 ttttagaatt acatatttct ctcttgcttt acttgtcttg ttacatagca gtgttttaaa 17760 atattactta tgaaagtttc ttgtcccatt ttctctatta aatacttaag aattatattt 17820 attgagcgcc tattatgtta cgaactctga acacttcaca cttatgtcat ttaatttttt 17880 caacagtaga agcttttata tttaggtagt aacaatcact attgcttagc tacttgttcc 17940 attttttttt tttttttttt tttttttgag acagagtctc actctattgc ccaggctgga 18000 gtgcagtggc gtaatctcag ctcactgcaa cctctgcctc ccgggttcaa gcgattctcc 18060 tgcctcagcc tcccaagtag ctgggattac aggcacgtgc caccatgccc ggctaatttt 18120 tgtatttttt ttagtagaga cggggttttg ccatgttggc caggctgggt ctcaaactcc 18180 tgacctcagg tgatccacct gccttggctt cccaaaatgc tgggattaca ggcatgagcc 18240 accgcgccca gcccccaaat ttttaatgac aagaaattgt ttagctttct tctaccactc 18300 aatttagatg aagattttaa ttaaacagca taaaaagagc ttcctcctct gaaaatgatt 18360 agattttcat aaaaagaatt tccccaggtt tctcttttga ttacatatat acacacacac 18420 atagtttgga gggaaagcag ctatgtagtg tcagtgccaa aggttaagtg aagaagtata 18480 attctgaatt ttctttggaa ggtgaatatg tctacagacc tggagggaac agacatgttg 18540 gcagagaagg cagaccgaag agaatacatt gatctgttaa agaaaatgct cacaattgat 18600 gcagataaga gaattacccc tctaaaaact cttaaccatc agtttgtgac aatgactcac 18660 cttttggatt ttccacatag caatcagtga gtatggaata ttctggggct tttgccatgt 18720 ggttctttgt tgagttaccg ccttatcaat ggcactatca aatgagcccg ccactttggt 18780 gcttataaat ctggctcagc agtgcttttc tttctcattg aaacatcata agataaaaat 18840 tagatgtgta tttttcttcc ctatgattat acaaattctt gatttatttt atctgaaagt 18900 gattgggaaa aaaagctttg atccatgttc atcttgagtt atttgctgtc tgtttaaatc 18960 tcagcattca tttaatgaat ctttaatctc cttttcagtg ttaagtcttg ttttcagaac 19020 atggagatct gcaagcggag ggttcacatg tatgatacag tgagtcagat caagagtccc 19080 ttcactacac atgttgcccc aaatacaagc acaaatctaa ccatgagctt cagcaatcag 19140 ctcaatacag tgcacaatca ggtattcaat aaataatttt ggaaactcaa gcttaagtgg 19200 gatagaaact agtaagaata cagggcaagg taaagaacca atttttgttt tggtggtctt 19260 gttgcttctt agaaattctc cacttgacaa aagttgatgg aaaacagggt agactgataa 19320 tacttaccag gcacaggcta actaaagtta aatataaagg cctaatccat gccctcatat 19380 gttcagcatc gtcaaataaa tggggtctga ctattatgct acttactgct gttagtttta 19440 ctgactttag ccaaatgact ttctccctgt taggagaagg attttatatc tcttgttact 19500 gtattgaaag gtttccagtc attaacttta agggtggttt tgcatttgtt tgctagccag 19560 tgatatttgc atttaggttt atttctgaag atgtaagctt cccagtttct tggctgggtc 19620 tactttttta atggaagagc ctatgagatt tggtgggatc ttccatccag taattttttg 19680 tgcagaagta gttggggttt gtgtagccac agccaacata ggaccattcg tttttttttt 19740 tttatttgct tatttgacca tataatatgc cttcaattta gggactaggg aagtttctta 19800 agcagagagt tatttcagag gcagttaaca ttacatttta aaacattatt ctacgttttt 19860 ctggataaat tctgtatata taaaattatt gtgtgtctct acttaataca agtgtacaaa 19920 tataatcctt ttgtttttag gccagtgttc tagcttccag ttctactgca gcagctgcta 19980 ctctttctct ggctaattca gatgtctcac tactaaacta ccagtcagct ttgtacccat 20040 catctgctgc accagttcct ggagttgccc agcagggtgt ttccttgcag cctggaacca 20100 cccagatttg cactcagaca gatccattcc aacagacatt tatagtatgt ccacctgcgt 20160 ttcaaagtaa gtggggaaac tcctgtatca tatggtattg tatcagacct acctgcttta 20220 ggcagctcta gttgtttagt tctgatcttt acaagtttaa actctgtctc tgatgaagaa 20280 ggtaactaaa attgggtaat atcgcaaaat ggattttctc tttttacata ggctatttat 20340 ctaattatga tgctatctga tgcattgtaa gagctcactt tatgtttcct taattgaatt 20400 gcctgatacc agttttcttg cccattgagt ccttgtgtca atgtcgtacg tcttgtataa 20460 gcatgtatct gtcaatatgc aaaatctata caacttgaaa aaatttgttg taagcagaat 20520 tgctaaatan nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 20580 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 20640 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 20700 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 20760 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 20820 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 20880 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 20940 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21000 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21060 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21120 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21180 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21240 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21300 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21360 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21420 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21480 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21540 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21600 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21660 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21720 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21780 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21840 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21900 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 21960 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22020 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22080 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22140 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22200 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22260 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22320 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22380 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22440 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22500 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22560 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22620 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22680 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22740 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22800 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22860 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22920 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 22980 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23040 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23100 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23160 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23220 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23280 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23340 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23400 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23460 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23520 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23580 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23640 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23700 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23760 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23820 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23880 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 23940 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24000 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24060 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24120 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24180 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24240 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24300 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24360 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24420 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24480 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24540 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24600 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24660 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24720 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 24780 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn ncaagttttt 24840 tttccaccta gtggattaaa aagtgaataa tgctgggcac agtggctcac acctgtaatc 24900 ccggcacttt gggaggccaa gatgggcaga tcatgaggtc aggagttcga gaccagcctg 24960 gccaacatgg tgaaaccccg tctctactga aaatataaaa attagacggg cgtggtggcg 25020 cactcctgta gtcgcagcta cttgggaggc tgtggcagaa gaatcgcttg aacttgggag 25080 cagagtttgc agtgagccca gatagcatca ctgcactcca gcctgggtga cagagcgaga 25140 ctccatctca naaaaaaaaa aaaaaaaaaa aaaaaaaatg aaagtgaatt taatttacta 25200 agtgaagatt tttttgtttt tgcctgtact cttaatggag atgggatgaa tattgtgttt 25260 taaattttgt agcataaaaa aaatttagaa ttcttttaaa ccatccctca ctatatcaaa 25320 catctttcca ttaacctaac ctgaggggaa gtctcccttt tcttaacttc caagacttct 25380 atgaatgaaa cttctttgtc ttaagtgtct aggattaaaa cctgaacagt ggattatttg 25440 aacagagaag ctgaaaacaa aataatctta aaacagtact cccagacctt gcaaaactat 25500 ttaactgtga tgctgttttc aatagctgga ctacaagcaa caacaaagca ttctggattc 25560 cctgtgagga tggataatgc tgtaccgatt gtaccgcagg caccagctgc tcagccacta 25620 cagattcagt caggagttct cacgcaggta aaagctagag caatgtggat actcagtatt 25680 gctaaacact attgagattc agatattttg tcctagaaaa tggtatttcc tttgactata 25740 agatctttct tggtcatgat tcagtggact taaaatgaaa catctctatg gaacaatata 25800 ctaattccta acactattgc aactctgcca ttgtcttcct tagacttgca gggaaaaaat 25860 atccagacat tcttgagaaa tggtcttctg agtaagttta ctctaatttt gcggggtgaa 25920 gcgttttttt ttgttgttgt ttgtttttta aatgttggag ctcatataaa gataagtata 25980 tatgtagcat tttgattcta aaatataagc ttccactttt gcaccctttg tgtccctttt 26040 gctcactctt ttagaatttc atcacagttg agaggctgga tcacatcagg atgcctcttc 26100 acatattaca ttccttcatt ccgtgtgttt aaccatattg tagaaagctt taaaacttta 26160 tacttgctat ggaacattcg actaagatga tagagaaaat tgtaaagtat ttaaatagca 26220 acaaacagta tattttatat tttatatata aatgtttgtg gcctatgaca cataggaaat 26280 tctcaaatcc aaaaactcta ttttgtgaac aggaggaaga attcttaata aatgtctctg 26340 tttcatagaa ctgatcccct gaatctagcc caaggaggat tcctatactt ctttgtttta 26400 ggccattggc atttgacttt gtgggccaat gccatacaaa gttgaagggg gaaagttgtg 26460 tttggtatat gcattttaga tgctatcaaa ttactgttca ttgtcagtaa taacttgggg 26520 ggaatgagaa cccttctgaa tccagatatc ctgcctccgt gtttgtttca ctcacctgcc 26580 taatctacgt ttcagggaag ctgtacacca ctaatggtag caactctcca ccctcaagta 26640 gccaccatca caccgcagta tgcggtgccc tttactctga gctgcgcagc cggccggccg 26700 gcgctggttg aacagactgc cgctgtactg gtaattcccc tcacttgatt gtgttactaa 26760 cggagtttct ttggtttctt tcttttttgt tttttcctgt ttgtttttgt tctgtttttt 26820 tctggtttat ttttcaaaaa aattttttag cttagtcttt gcagagggca tggaagcatg 26880 tgccatcttg tggctgtgtt cttgctacat cttttaatgt ctcattgttt tcctccccca 26940 acatttgctg tagcactgtc tgactgatgg ttatgtggct ctgtaaggag ccagatccct 27000 tgattcttct ttgccagcct agtgtgataa aagctctcga tgtagcctca gaagagcttc 27060 aacactgtta cttgttttct gccttttacc ctctgatcct tgagaatgaa ggaaatggcc 27120 tttaatttgg ctcagctaca ggtacccgga tggccaaaat tgagctcgtt ggcaagatag 27180 ctttctcctt tttttgctgt tttaaggttc taaaactttt ctgcatgtgg aaatgcttaa 27240 gatgctctta atttattgct ttctcagttg atactaacca tccttctatg gacacatgaa 27300 gatagctctt tttgccactc atgatcagtg gcagcttata tcttacattt aaagatattc 27360 cctttagaat gtagatcata ttgtaggtca tattgttggt tgaaattaaa agtggacaca 27420 tttttaggag ttttgggagg aattaattat tttacaaata ggtctttata caaaggttga 27480 aagtatggcc aacaaactat gcaaatacaa tatctttgtt attaaaagtc atggggaata 27540 gttacttaat gtagctgcaa ttgtagtact gggcttagag atagaaaaaa caaccaagac 27600 tttgaggtgt gtttcaggat ttgtaacctt aagagtgatt ttttggatgt gttttggttt 27660 atatggggag ttagaattgt ttattggata tccagcattt tctcatttga aatttaaaat 27720 taggtaagca tccaaaaacc tgaaaggcac tattgaatcc tgttatttct ctgttttcaa 27780 agttgcttta aatttctttt gttgtttctt aagtattcat gtgagtgaaa acacttccag 27840 aaacatactt tggttggaat ttggttttca ttttaaaagt ctttgtcact tccagattaa 27900 ttttcttgta agcagaaaac ctgagtgtga gggagtcaga tatatttcca acttgattga 27960 tccaagccaa tggttttaac tcactcatct gtagtttcga ggttggaatg ttagttgaca 28020 cttctccttt gctgcttctc ttaagtttgc actagccatt tgctaagctt tgcatatttt 28080 tgttcttcct ctgtcaaaac agttcgtcgc ttggaacgcc agatttctgc ctcacattgg 28140 aatgttattt cttgctttgt attaaactac atgctttgtc ttgtgcaggt gttggcttat 28200 ggaaagacgc atggtgtgac ttaacatact tcttttattt tttgttttgt tttattttgt 28260 tttaaattct gcttatggta gcagacgtgt ttgcagtttc tctgctttga aggcttcttg 28320 tttggaacca gtatttgtaa caagtagatc tgttacttgc agaaatattt ttaaaacagt 28380 gtgttgatgg ccttgcaatt tgaaattcaa gaaacagaac catatgtacc caagcattgt 28440 aggtaattgt actgcagaat tcaagtttaa aaaggaaact tccaaatccg ttcccatttt 28500 ttttttcaaa aaatgccaga atttctgtga ggaagaagta cagaaaacat ttgttgctca 28560 gtttattgca agtgacatgg cttttttaaa actagaaatc atgtattttc ttgtagtgat 28620 tagtttttat gtggaaatat tcctgcaaat gatacataaa aacatatttt aggtaactat 28680 tagaaacaaa gtatgatgct ttctgcttct aaaacatctt actttttgcc ttattttgaa 28740 attccattat gtggctataa atgatgaatt agctttttct tgctggcata agattttttc 28800 cccaaaagga ttaggccttt ggtcatccac atctggctcc attttccaaa tactaccctt 28860 ttaaaaaagg gaacagttct gccttttgtt ttatgggttg aattgatctg ataccttatc 28920 tgattggcag tcagattaaa aaattttaat ctccagggag tcctcttaac tctttctagg 28980 gatttatttt agaattgttg caaaaatgaa actccagcat ttaaccagct cttatctctg 29040 aactctcaga ctccttttct ctacagtata atagaagctc ttaaccgcag ggatcttctt 29100 ttctttaata cccgggtggt caggttatgg gggtgagcaa gagaaagcag tatgttttct 29160 ttccccattc ataagacttg tagcttgagc ccctctgacc tttctttttt aatctctgca 29220 agttaacaat ctacaagcaa cttcttttaa gatatgaatt tttctttctt taaaaaaaca 29280 gaagaaaaag ccaagaatga atcaagtctg gatgtttttt atgtgtgttt ccttacagca 29340 ggcgtggcct ggagggactc agcaaattct cctgccttca acttggcaac agttgcctgg 29400 ggtagctcta cacaactctg tccagcccac agcaatgatt ccagaggcca tggggagtgg 29460 acagcagcta gctgactgga ggcaagtgtc ctgtgttact ctgggagatt tgtaagggcc 29520 gatcccatag ggtgggagca cttggtaata aggagagaga ctagtaagaa aataaaggaa 29580 aatttgacac tgttggaatc ctttaagaac ccatatcagg ctaggagatg gtgttataag 29640 aaaactttga atataggaaa gcagtaggtt ctgaaggtca ggaatcattt cttctagatt 29700 ttttaaagag agtcttaagt gattagaaac catacagtga gatcctaaag ccttgtaatc 29760 taggtcccca actttatctt ttataatgaa aattcttttt ttctaatgtt taatttttgt 29820 gattacatac taggtatata tatttatggg gtacatgaga tgttttgaca caggcatgta 29880 atgtgaaata agcacatcat ggaaaagggg gtgtccatcc cctcaagcat ttatcctttg 29940 agttacaaat aatccaatta cactctttaa gtcatttaaa aatgtacaat taagttatta 30000 ctgactataa tcacctattg cgctatcaaa tagtagttct tattcttttt tttttttttt 30060 tgtacccatt aaccatccct acctccccac tagccctcca ctactcttac cagcctctgg 30120 taaccatcct actctctatg tccatgaatt aaattgtttt gatttttaga tcccataaat 30180 aagtgagaac atgtggtttg tctttctgtg tctggcttat ttcacttaac atgatgatct 30240 tgagttccat ccatgttgtt gcaaatgaca acgtgtactt tttgtggctg agtagtactc 30300 cattgtgtat atgtaccata ttttctttat ccattcatct gttgatggac acttaggctg 30360 cttccaaatc ttactgtgaa cagtgctgca acataggagt gcaggtatct ctttgatata 30420 ctgatttcct ttcttttggg tatataccca gcagtgggat tgctggatca tatggtagct 30480 caatttttag tttttacagg aacctccaaa ctgttctcca taatagttgt actaacttac 30540 attcctacca acagtgtaca attgttccct tttttccata tccttggcag tgtttattat 30600 tgcttgtctt ttggatataa gccattttaa ctggggtgag ataatatctc attgcagttt 30660 tgatctgcat ttctctaatg atcagagatg ttgagcacct tttcatatgc ctgtttgtca 30720 tttgtaagtc atcttttgga aaatgtctat tcaattcttt tgcccatttt ttgatcgtat 30780 tattagattt ttttccatag agttgtttga gctgcttacg tattctggtt attaatccct 30840 tatcagatgg taggtgctca actttaaaaa aataaaatgc agctgcattt tggctaattg 30900 cttttgatgt ctgtttggtc ctgattcttc agtggttttg gaattcactc ttctctttct 30960 ttctgttggt acaggaatgc ccactctcat ggcaaccagt acagcactat catgcagcag 31020 ccatccttgc tgactaacca tgtgacattg gccactgctc agcctctgaa tgttggtgtt 31080 gcccatgttg tcagacaaca acaatccagt tccctccctt cgaagaagaa taagcagtca 31140 gctccagtct cttccaagtg agtctgtgtt acagctgata gttaaaactg tgccagtttg 31200 agagatatgt tgccttgcat ttggaatatt gtatagacat ataatataga tatgaagcag 31260 caagtagctg ccaaattgag gaagagcaaa tcatttcatc tgggcatgta caccaggtgt 31320 gtcctggttt tatgatggtc ctttgtctct gctgccactt tgaatctagg gcattttatg 31380 atgtttttat tttactttac agagtgaaat ttaatcctgg gataaagggc ttataaaagt 31440 aaaatgtctt ttgtattttg gtgttcttgt ccctggaaac tcttgccagc atggtgctta 31500 ttttcactgg aacttatata gttaaatgta tttgcttaat gattatgtaa aaaggaatca 31560 atgagtaaat tggaaagcag tctggggaaa agatacacaa tttggaaggc caaggactga 31620 atcatctttc catgtgaact tttcctacag gtcctctcta gatgttctgc cttcccaagt 31680 ctattctctg gttgggagca gtcccctccg caccacatct tcttataatt ccttggtccc 31740 tgtccaagat cagcatcagc ccatcatcat tccagatact cccagccctc ctgtgagtgt 31800 catcactatc cgaagtgaca ctgatgagga agaggacaac aaatacaagc ccagtaggta 31860 agataagtga atggttcctg gctctattgg ttttagactg ttggcctcag gcaagtgggc 31920 ccagtttggc ctgtgaaaga aaggaccggt ggggcatggt ggctcacgcc tgtaatccca 31980 gcactttggg aggttgaggc cagcagatca cctgaggtga ggagttcaag accagcctgg 32040 ccaacatggc acaaccctgt ctctactaaa aatacaaaaa ttagcagggc cgtggtggca 32100 catgtttgta tcccagctac tcgggaggct gaggcaggag aatcacttga acccaggagg 32160 cggaggttac agtgagctga gatcgtgcca ctgtactcca gcctgagtga cagagcaaga 32220 ctgcatcccc tcccgccccc acccaaaaaa aagggccgaa gaaaaannnn nnnnnnnnnn 32280 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnncaat ggtaagaaat aaaggctagg 32340 aaaaattcaa atttactgac gccagaatag ggtgagttga gtcaccagtt attaacttgc 32400 aggagtgggg aaccctatga tctcttgatt ctccctcttc ctgtcatact tacaagcaaa 32460 atgctgttac ctgagccaga ttaggatcta tcttgctaag aggcagaagg aggggtggct 32520 gatttctgac agcattcaat gccagtgtgg gagattatgt gctataccca ttcgaaaaca 32580 gtacaagtca gaacctgagc tcttaacttg gcctttggtg ccctgagctg gagtgacctc 32640 aggattcctc acttcttcct tctttcttcc agaaccagca gtcatcggcg gctccaacct 32700 cacaggagag aagcagcaac ccagcccccc gcaggcagca ggcgtttgtg gcccctctct 32760 cccaagcccc ctacaccttc cagcatggca gcccgctaca ctcgacaggg cacccacacc 32820 ttgccccggc ccctgctcac ctgccaagcc aggctcatct gtatacgtat gctgccccga 32880 cttctgctgc tgcactgggc tcaaccagct ccattgctca tcttttctcc ccacagggtt 32940 cctcaaggca tgctgcagcc tataccactc accctagcac tttggtgcac caggtccctg 33000 tcagtgttgg gcccagcctc ctcacttctg ccagcgtggc ccctgctcag taccaacacc 33060 agtttgccac ccaatcctac attgggtctt cccgaggctc aacaatttac actggatacc 33120 cgctgagtcc taccaagatc agccagtatt cctacttata gttggtgagc atgagggagg 33180 aggaatcatg gctaccttct cctggccctg cgttcttaat attgggctat ggagagatcc 33240 tcctttaccc tcttgaaatt tcttagccag caacttgttc tgcaggggcc cactgaagca 33300 gaaggttttt ctctggggga acctgtctca gtgttgactg cattgttgta gtcttcccaa 33360 agtttgccct atttttaaat tcattatttt tgtgacagta attttggtac ttggaagagt 33420 tcagatgccc atcttctgca gttaccaagg aagagagatt gttctgaagt taccctctga 33480 aaaatatttt gtctctctga cttgatttct ataaatgctt ttaaaaacaa gtgaagcccc 33540 tctttatttc attttgtgtt attgtgattg ctggtcagga aaaatgctga tagaaggagt 33600 tgaaatctga tgacaaaaaa agaaaaatta ctttttgttt gtttataaac tcagacttgc 33660 ctattttatt ttaaaagcgg cttacacaat ctcccttttg tttattggac atttaaactt 33720 acagagtttc agttttgttt taatgtcata ttatacttaa tgggcaattg ttatttttgc 33780 aaaactggtt acgtattact ctgtgttact attggagatt ctctcaattg ctcctgtgtt 33840 tgttataaag tagtgtttaa aaggcagctc accatttgct ggtaacttaa tgtgagagaa 33900 tccatatctg cgtgaaaaca ccaagtattc tttttaaatg aagcaccatg aattcttttt 33960 taaattattt tttaaaagtc tttctctctc tgattcagct taaatttttt tatcgaaaaa 34020 gccattaagg tggttattat tacatggtgg tggtggtttt attatatgca aaatctctgt 34080 ctattatgag atactggcat tgatgagctt tgcctaaaga ttagtatgaa ttttcagtaa 34140 tacacctctg ttttgctcat ctctcccttc tgttttatgt gatttgtttg gggagaaagc 34200 taaaaaaacc tgaaaccaga taagaacatt tcttgtgtat agcttttata cttcaaagta 34260 gcttcctttg tatgccagca gcaaattgaa tgctctctta ttaagactta tataataagt 34320 gcatgtagga attgcaaaaa atattttaaa aatttattac tgaatttaaa aatattttag 34380 aagttttgta atggtggtgt tttaatattt tacataatta aatatgtaca tattgattag 34440 aaaaatataa caagcaattt ttcctgctaa cccaaaatgt tatttgtaat caaatgtgta 34500 gtgattacac ttgaattgtg tacttagtgt gtatgtgatc ctccagtgtt atcccggaga 34560 tggattgatg tctccattgt atttaaacca aaatgaactg atacttgttg gaatgtatgt 34620 gaactaattg caattatatt agagcatatt actgtagtgc tgaatgagca ggggcattgc 34680 ctgcaaggag aggagaccct tggaattgtt ttgcacaggt gtgtctggtg aggagttttt 34740 cagtgtgtgt ctcttccttc cctttcttcc tccttccctt attgtagtgc cttatatgat 34800 aatgtagtgg ttaatagagt ttacagtgag cttgccttag gatggaccag caagcccccg 34860 tggaccctaa gttgttcacc gggatttatc agaacaggat tagtagctgt attgtgtaat 34920 gcattgttct cagtttccct gccaacattg aaaaataaaa acagcagctt ttctccttta 34980 ccaccacctc tacccctttc cattttggat tctcggctga gttctcacag aagcattttc 35040 cccatgtggc tctctcactg tgcgttgcta ccttgcttct gtgagaattc aggaagcagg 35100 tgagaggagt caagccaata ttaaatatgc attcttttaa agtatgtgca atcactttta 35160 gaatgaattt ttttttcctt ttcccatgtg gcagtccttc ctgcacatag ttgacattcc 35220 tagtaaaata tttgcttgtt gaaaaaaaca tgttaacaga tgtgtttata ccaaagagcc 35280 tgttgtattg cttaccatgt ccccatacta tgaggagaag ttttgtggtg ccgctggtga 35340 caaggaactc acagaaaggt ttcttagctg gtgaagaata tagagaagga accaaagcct 35400 gttgagtcat tgaggctttt gaggtttctt ttttaacagc ttgtatagtc ttggggccct 35460 tcaagctgtg aaattgtcct tgtactctca gctcctgcat ggatctgggt caagtagaag 35520 gtactgggga tggggacatt cctgcccata aaggatttgg ggaaagaaga ttaatcctaa 35580 aatacaggtg tgttccatct gaattgaaaa tgatatattt gagatataat tttaggactg 35640 gttctgtgta gatagagatg gtgtcaagga ggtgcaggat ggagatggga gatttcatgg 35700 agcctggtca gccagctctg taccaggttg aacaccgagg agctgtcaaa gtatttggag 35760 tttcttcatt gtaaggagta agggcttcca agatggggca ggtagtccgt acagcctacc 35820 aggaacatgt tgtgttttcn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 35880 nnnnnnnnna agatgggagg atagcttgag cccagaggtt gaggtcgcag cgagctgtga 35940 tcactccact gcactccagc ctgggtgaca gaacaagacg ctgtcacaca cacaaaaaag 36000 aacaattcaa ttttcatgta tttttctttt cctcagctct ggactgaagc caaggtctaa 36060 tgtcatcagt tatgtcactg tcaatgattc tccagactct gactcttctt tgagcagccc 36120 ttattccact gataccctga gtgctctccg aggcaatag 36159 4 1209 PRT Mus musculus 4 Met Ala Ser Gln Leu Gln Val Phe Ser Pro Pro Ser Val Ser Ser Ser 1 5 10 15 Ala Phe Cys Ser Ala Lys Lys Leu Lys Ile Glu Pro Ser Gly Trp Asp 20 25 30 Val Ser Gly Gln Ser Ser Asn Asp Lys Tyr Tyr Thr His Ser Lys Thr 35 40 45 Leu Pro Ala Thr Gln Gly Gln Ala Ser Ser Ser His Gln Val Ala Asn 50 55 60 Phe Asn Leu Pro Ala Tyr Asp Gln Gly Leu Leu Leu Pro Ala Pro Ala 65 70 75 80 Val Glu His Ile Val Val Thr Ala Ala Asp Ser Ser Gly Ser Ala Ala 85 90 95 Thr Ala Thr Phe Gln Ser Ser Gln Thr Leu Thr His Arg Ser Asn Val 100 105 110 Ser Leu Leu Glu Pro Tyr Gln Lys Cys Gly Leu Lys Arg Lys Ser Glu 115 120 125 Glu Val Glu Ser Asn Gly Ser Val Gln Ile Ile Glu Glu His Pro Pro 130 135 140 Leu Met Leu Gln Asn Arg Thr Val Val Gly Ala Ala Ala Thr Thr Thr 145 150 155 160 Thr Val Thr Thr Lys Ser Ser Ser Ser Ser Gly Glu Gly Asp Tyr Gln 165 170 175 Leu Val Gln His Glu Ile Leu Cys Ser Met Thr Asn Ser Tyr Glu Val 180 185 190 Leu Glu Phe Leu Gly Arg Gly Thr Phe Gly Gln Val Ala Lys Cys Trp 195 200 205 Lys Arg Ser Thr Lys Glu Ile Val Ala Ile Lys Ile Leu Lys Asn His 210 215 220 Pro Ser Tyr Ala Arg Gln Gly Gln Ile Glu Val Ser Ile Leu Ser Arg 225 230 235 240 Leu Ser Ser Glu Asn Ala Asp Glu Tyr Asn Phe Val Arg Ser Tyr Glu 245 250 255 Cys Phe Gln His Lys Asn His Thr Cys Leu Val Phe Glu Met Leu Glu 260 265 270 Gln Asn Leu Tyr Asp Phe Leu Lys Gln Asn Lys Phe Ser Pro Leu Pro 275 280 285 Leu Lys Tyr Ile Arg Pro Ile Leu Gln Gln Val Ala Thr Ala Leu Met 290 295 300 Lys Leu Lys Ser Leu Gly Leu Ile His Ala Asp Leu Lys Pro Glu Asn 305 310 315 320 Ile Met Leu Val Asp Pro Val Arg Gln Pro Tyr Arg Val Lys Val Ile 325 330 335 Asp Phe Gly Ser Ala Ser His Val Ser Lys Ala Val Cys Ser Thr Tyr 340 345 350 Leu Gln Ser Arg Tyr Tyr Arg Ala Pro Glu Ile Ile Leu Gly Leu Pro 355 360 365 Phe Cys Glu Ala Ile Asp Met Trp Ser Leu Gly Cys Val Ile Ala Glu 370 375 380 Leu Phe Leu Gly Trp Pro Leu Tyr Pro Gly Ala Ser Glu Tyr Asp Gln 385 390 395 400 Ile Arg Tyr Ile Ser Gln Thr Gln Gly Leu Pro Ala Glu Tyr Leu Leu 405 410 415 Ser Ala Gly Thr Lys Thr Thr Arg Phe Phe Asn Arg Asp Pro Asn Leu 420 425 430 Gly Tyr Pro Leu Trp Arg Leu Lys Thr Pro Glu Glu His Glu Leu Glu 435 440 445 Thr Gly Ile Lys Ser Lys Glu Ala Arg Lys Tyr Ile Phe Asn Cys Leu 450 455 460 Asp Asp Met Ala Gln Val Asn Met Ser Thr Asp Leu Glu Gly Thr Asp 465 470 475 480 Met Leu Ala Glu Lys Ala Asp Arg Arg Glu Tyr Ile Asp Leu Leu Lys 485 490 495 Lys Met Leu Thr Ile Asp Ala Asp Lys Arg Ile Thr Pro Leu Lys Thr 500 505 510 Leu Asn His Gln Phe Val Thr Met Ser His Leu Leu Asp Phe Pro His 515 520 525 Ser Ser His Val Lys Ser Cys Phe Gln Asn Met Glu Ile Cys Lys Arg 530 535 540 Arg Val His Met Tyr Asp Thr Val Ser Gln Ile Lys Ser Pro Phe Thr 545 550 555 560 Thr His Val Ala Pro Asn Thr Ser Thr Asn Leu Thr Met Ser Phe Ser 565 570 575 Asn Gln Leu Asn Thr Val His Asn Gln Ala Ser Val Leu Ala Ser Ser 580 585 590 Ser Thr Ala Ala Ala Ala Thr Leu Ser Leu Ala Asn Ser Asp Val Ser 595 600 605 Leu Leu Asn Tyr Gln Ser Ala Leu Tyr Pro Ser Ser Ala Ala Pro Val 610 615 620 Pro Gly Val Ala Gln Gln Gly Val Ser Leu Gln Pro Gly Thr Thr Gln 625 630 635 640 Ile Cys Thr Gln Thr Asp Pro Phe Gln Gln Thr Phe Ile Val Cys Pro 645 650 655 Pro Ala Phe Gln Thr Gly Leu Gln Ala Thr Thr Lys His Ser Gly Phe 660 665 670 Pro Val Arg Met Asp Asn Ala Val Pro Ile Val Pro Gln Ala Pro Ala 675 680 685 Ala Gln Pro Leu Gln Ile Gln Ser Gly Val Leu Thr Gln Gly Ser Cys 690 695 700 Thr Pro Leu Met Val Ala Thr Leu His Pro Gln Val Ala Thr Ile Thr 705 710 715 720 Pro Gln Tyr Ala Val Pro Phe Thr Leu Ser Cys Ala Gly Arg Pro Ala 725 730 735 Leu Val Glu Gln Thr Ala Ala Val Leu Gln Ala Trp Pro Gly Gly Thr 740 745 750 Gln Gln Ile Leu Leu Pro Ser Ala Trp Gln Gln Leu Pro Gly Val Ala 755 760 765 Leu His Asn Ser Val Gln Pro Ala Ala Val Ile Pro Glu Ala Met Gly 770 775 780 Ser Ser Gln Gln Leu Ala Asp Trp Arg Asn Ala His Ser His Gly Asn 785 790 795 800 Gln Tyr Ser Thr Ile Met Gln Gln Pro Ser Leu Leu Thr Asn His Val 805 810 815 Thr Leu Ala Thr Ala Gln Pro Leu Asn Val Gly Val Ala His Val Val 820 825 830 Arg Gln Gln Gln Ser Ser Ser Leu Pro Ser Lys Lys Asn Lys Gln Ser 835 840 845 Ala Pro Val Ser Ser Lys Ser Ser Leu Glu Val Leu Pro Ser Gln Val 850 855 860 Tyr Ser Leu Val Gly Ser Ser Pro Leu Arg Thr Thr Ser Ser Tyr Asn 865 870 875 880 Ser Leu Val Pro Val Gln Asp Gln His Gln Pro Ile Ile Ile Pro Asp 885 890 895 Thr Pro Ser Pro Pro Val Ser Val Ile Thr Ile Arg Ser Asp Thr Asp 900 905 910 Glu Glu Glu Asp Asn Lys Tyr Glu Pro Asn Ser Ser Ser Leu Lys Ala 915 920 925 Arg Ser Asn Val Ile Ser Tyr Val Thr Val Asn Asp Ser Pro Asp Ser 930 935 940 Asp Ser Ser Leu Ser Ser Pro His Ser Thr Asp Thr Leu Ser Ala Leu 945 950 955 960 Arg Gly Asn Ser Gly Thr Leu Leu Glu Gly Pro Gly Arg Pro Ala Ala 965 970 975 Asp Gly Ile Gly Thr Arg Thr Ile Ile Val Pro Pro Leu Lys Thr Gln 980 985 990 Leu Gly Asp Cys Thr Val Ala Thr Gln Ala Ser Gly Leu Leu Ser Ser 995 1000 1005 Lys Thr Lys Pro Val Ala Ser Val Ser Gly Gln Ser Ser Gly Cys Cys 1010 1015 1020 Ile Thr Pro Thr Gly Tyr Arg Ala Gln Arg Gly Gly Ala Ser Ala Val 1025 1030 1035 1040 Gln Pro Leu Asn Leu Ser Gln Asn Gln Gln Ser Ser Ser Ala Ser Thr 1045 1050 1055 Ser Gln Glu Arg Ser Ser Asn Pro Ala Pro Arg Arg Gln Gln Ala Phe 1060 1065 1070 Val Ala Pro Leu Ser Gln Ala Pro Tyr Ala Phe Gln His Gly Ser Pro 1075 1080 1085 Leu His Ser Thr Gly His Pro His Leu Ala Pro Ala Pro Ala His Leu 1090 1095 1100 Pro Ser Gln Pro His Leu Tyr Thr Tyr Ala Ala Pro Thr Ser Ala Ala 1105 1110 1115 1120 Ala Leu Gly Ser Thr Ser Ser Ile Ala His Leu Phe Phe Pro Gln Gly 1125 1130 1135 Ser Ser Arg His Ala Ala Ala Tyr Thr Thr His Pro Ser Thr Leu Val 1140 1145 1150 His Gln Val Pro Val Ser Val Gly Pro Ser Leu Leu Thr Ser Ala Ser 1155 1160 1165 Val Ala Pro Ala Gln Tyr Gln His Gln Phe Ala Thr Gln Ser Tyr Ile 1170 1175 1180 Gly Ser Ser Arg Gly Ser Thr Ile Tyr Thr Gly Tyr Pro Leu Ser Pro 1185 1190 1195 1200 Thr Lys Ile Ser Gln Tyr Ser Tyr Leu 1205
Claims (23)
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/749,588 US6423521B1 (en) | 2000-12-28 | 2000-12-28 | Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof |
AU2002232599A AU2002232599A1 (en) | 2000-12-28 | 2001-12-19 | Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof |
CA002433559A CA2433559A1 (en) | 2000-12-28 | 2001-12-19 | Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof |
EP01992126A EP1348022A2 (en) | 2000-12-28 | 2001-12-19 | Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof |
JP2002555227A JP2005503757A (en) | 2000-12-28 | 2001-12-19 | Isolated human kinase protein, nucleic acid molecule encoding human kinase protein, and methods of use thereof |
PCT/US2001/048534 WO2002053717A2 (en) | 2000-12-28 | 2001-12-19 | Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof |
US10/135,687 US6689597B2 (en) | 2000-12-28 | 2002-05-01 | Isolated human kinase proteins |
US10/635,535 US20040266679A1 (en) | 2000-12-28 | 2003-08-07 | Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US09/749,588 US6423521B1 (en) | 2000-12-28 | 2000-12-28 | Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof |
Related Child Applications (1)
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US10/135,687 Division US6689597B2 (en) | 2000-12-28 | 2002-05-01 | Isolated human kinase proteins |
Publications (2)
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US6423521B1 US6423521B1 (en) | 2002-07-23 |
US20020110889A1 true US20020110889A1 (en) | 2002-08-15 |
Family
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US09/749,588 Expired - Fee Related US6423521B1 (en) | 2000-12-28 | 2000-12-28 | Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof |
US10/135,687 Expired - Fee Related US6689597B2 (en) | 2000-12-28 | 2002-05-01 | Isolated human kinase proteins |
US10/635,535 Abandoned US20040266679A1 (en) | 2000-12-28 | 2003-08-07 | Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof |
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Application Number | Title | Priority Date | Filing Date |
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US10/135,687 Expired - Fee Related US6689597B2 (en) | 2000-12-28 | 2002-05-01 | Isolated human kinase proteins |
US10/635,535 Abandoned US20040266679A1 (en) | 2000-12-28 | 2003-08-07 | Isolated human kinase proteins, nucleic acid molecules encoding human kinase proteins, and uses thereof |
Country Status (6)
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US (3) | US6423521B1 (en) |
EP (1) | EP1348022A2 (en) |
JP (1) | JP2005503757A (en) |
AU (1) | AU2002232599A1 (en) |
CA (1) | CA2433559A1 (en) |
WO (1) | WO2002053717A2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030224460A1 (en) * | 2000-09-22 | 2003-12-04 | Pedersen Finn Skou | Novel compositions and methods for lymphoma and leukemia |
US20070098728A1 (en) * | 2001-09-24 | 2007-05-03 | Pedersen Finn S | Novel compositions and methods in cancer |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1891965A1 (en) * | 2006-08-16 | 2008-02-27 | Bayer Schering Pharma Aktiengesellschaft | Hip-Kinase for fertility controll |
EP1889626A1 (en) * | 2006-08-16 | 2008-02-20 | Bayer Schering Pharma AG | Hip kinase for fertility control |
AR070498A1 (en) * | 2008-02-29 | 2010-04-07 | Procter & Gamble | DETERGENT COMPOSITION THAT LIPASA INCLUDES |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1077991A1 (en) * | 1998-05-07 | 2001-02-28 | Genetics Institute, Inc. | Secreted proteins and polynucleotides encoding them |
WO2001055387A1 (en) * | 2000-01-31 | 2001-08-02 | Human Genome Sciences, Inc. | Nucleic acids, proteins, and antibodies |
WO2001081555A2 (en) * | 2000-04-20 | 2001-11-01 | Incyte Genomics, Inc. | Human kinases |
AU2001263287A1 (en) * | 2000-05-19 | 2001-12-03 | Millennium Pharmaceuticals, Inc. | Human protein kinase "13305" and uses therefor |
US20030224460A1 (en) * | 2000-09-22 | 2003-12-04 | Pedersen Finn Skou | Novel compositions and methods for lymphoma and leukemia |
-
2000
- 2000-12-28 US US09/749,588 patent/US6423521B1/en not_active Expired - Fee Related
-
2001
- 2001-12-19 AU AU2002232599A patent/AU2002232599A1/en not_active Abandoned
- 2001-12-19 EP EP01992126A patent/EP1348022A2/en not_active Withdrawn
- 2001-12-19 WO PCT/US2001/048534 patent/WO2002053717A2/en not_active Application Discontinuation
- 2001-12-19 JP JP2002555227A patent/JP2005503757A/en not_active Withdrawn
- 2001-12-19 CA CA002433559A patent/CA2433559A1/en not_active Abandoned
-
2002
- 2002-05-01 US US10/135,687 patent/US6689597B2/en not_active Expired - Fee Related
-
2003
- 2003-08-07 US US10/635,535 patent/US20040266679A1/en not_active Abandoned
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030224460A1 (en) * | 2000-09-22 | 2003-12-04 | Pedersen Finn Skou | Novel compositions and methods for lymphoma and leukemia |
US20070059724A1 (en) * | 2000-09-22 | 2007-03-15 | Pedersen Finn S | Novel compositions and methods for lymphoma and leukemia |
US20070098728A1 (en) * | 2001-09-24 | 2007-05-03 | Pedersen Finn S | Novel compositions and methods in cancer |
Also Published As
Publication number | Publication date |
---|---|
US6423521B1 (en) | 2002-07-23 |
AU2002232599A1 (en) | 2002-07-16 |
US20020123120A1 (en) | 2002-09-05 |
CA2433559A1 (en) | 2002-07-11 |
US20040266679A1 (en) | 2004-12-30 |
EP1348022A2 (en) | 2003-10-01 |
WO2002053717A3 (en) | 2003-03-27 |
WO2002053717A2 (en) | 2002-07-11 |
US6689597B2 (en) | 2004-02-10 |
JP2005503757A (en) | 2005-02-10 |
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