WO2001079294A2 - Human proteins, polynucleotides encoding them and methods of using the same - Google Patents

Abstract

The invention provides polypeptides, designated herein as POLYX polypeptides, as well as polynucleotides encoding POLYX polypeptides, and antibodies that immunospecifically-bind to POLYX polypeptide or polynucleotide, or derivatives, variants, mutants, or fragments thereof. The invention additionally provides methods in which the POLYX polypeptide, polynucleotide, and antibody are used in the detection, prevention, and treatment of a broad range of pathological states.

Description

NOVEL HUMAN PROTEINS, POLYNUCLEOTIDES ENCODING THEM AND METHODS OF USING THE SAME

RELATED APPLICATIONS

This application claims priority to USSNs 60/198,293(15966-776), filed April 19, 2000; 60/198,645 (15966-777), filed April 20, 2000; 60/210,809 (15966-778A), filed June 9, 2000; 60/199,476 (15966-778), filed April 26, 2000; 60/200,025 (15966-779), filed April 26, 2000; 60/224,610 (15966-780A), filed August 11, 2000; 60/200,024 (15966-780), filed April 26, 2000; 60/199,880 (15966-781) filed April 26, 2000; 60/218,591(21402-059), filed July 17, 2000; and 60/271,814 (21402-059A), filed February 27, 2001. The contents of this application are incorporated by reference in its entirety.

FIELD OF THE INVENTION

The invention relates to polynucleotides and the polypeptides encoded by such polynucleotides, as well as vectors, host cells, antibodies and recombinant methods for producing the polypeptides and polynucleotides, as well as methods for using the same.

BACKGROUND OF THE INVENTION

The present invention is based in part on nucleic acids encoding proteins that are new members ofthe following protein families: gamma aminobutyric acid (GAB A) receptor, epidermal growth factor (EGF), complement receptor, hematopoietic stem and progenitor cell (HSPC) protein, sulfotransferase (ST), sytaxin and prohibitin. The GAB A receptor family is a related group of ligand-gated chloride channels, where ligand binding results in chloride ion influx and a change in cell polarization. GABA receptors function as the major inhibitory neurotransmitter receptors in the brain, retina and elsewhere in the central nervous system. Alterations in GABA receptors are associated with a number of clinically relevant events and/or pathologies, including e.g. stroke, Huntington's disease, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, epilepsy, alcoholism, cardiomyopathy, and depression. The EGF protein family is a wide category of proteins, often receptors, sharing an EGF-domain important in protein-protein and other interactions. EGF-like receptor proteins are often tyrosine kinases involved in cell proliferation, differentiation, and death. Proteins having EGF domains modulate cell shape and motility, and adhesion. Alterations in EGF-like proteins are associated with a number of clinically relevant events and/or pathologies, including e.g. cancer, aberrant angiogenesis, renal disease, and diabetes.

The complement receptor family of proteins. Complement receptors are found on the extracellular surface of peripheral white blood cells, e.g. neutrophils and eosinophils. Complement receptor proteins are important in cell adhesion and activation. The levels of several complement receptor proteins are elevated on circulating granulocytes in asthmatic individuals.

Members ofthe HSPC protein family are expressed in stem cells and progenitor cells giving rise to several cell types, including hematopoietic cells. HSPC proteins may be modulated by cyclosporin A via inhibition of gamma interferon production by T cells. HSPC proteins may be involved in the progression of leukemia, lupus, and anemia.

The ST family of proteins are a group of related enzymes that catalyze the sulfate conjugation of many substances, e.g. drugs, xenobiotic compounds, hormones and neurotransmitters. ST proteins may share a common structural motif that is important in • enzymatic activity. Alterations in ST proteins may be associated with diseases and/or disorders ofthe liver, intestine and kidney, e.g. primary biliary cirrhosis, cholangitis, hepatitis, ulcers, hyperthyroidism, and developmental disorders.

The sytaxin protein family appear to be involved in the docking of cytoplasmic vesicles with the plasma membrane. These proteins may affect synaptic transmission in the brain and other parts ofthe central nervous system. Sytaxin proteins may be altered in clincally relevant neurological events and/or pathologies such as Lambert-Eaton myasthenic syndrome, asthma, myxoid liposarcoma, acute myeloid leukemia, and diabetes.

The prohibitin family of tumor-suppressor proteins inhibit cell proliferation, and several human cancers, e.g. breast, ovarian, liver and lung, show loss of heterozygosity at the prohibitin gene locus, suggesting mutations in members ofthe prohibitin family are associated with cancer onset and/or progression.

SUMMARY OF THE INVENTION

The invention is based, in part, upon the discovery of novel nucleic acids and secreted polypeptides encoded thereby. The nucleic acids and polypeptides are collectively referred to herein as "POLYX" nucleic acids and polypeptides.

Accordingly, in one aspect, the invention includes an isolated nucleic acid that encodes a POLYX polypeptide, or a fragment, homolog, analog or derivative thereof. For example, the nucleic acid can encode a polypeptide at least 85% identical to a polypeptide comprising the amino acid sequences of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34. The nucleic acid can be, e.g., a genomic DNA fragment or a cDNA molecule. In some embodiments, the invention provides an isolated nucleic acid molecule that includes the nucleic acid sequence of any of SEQ ID NO:l, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31 and/or 33.

Also included within the scope ofthe invention is a vector containing one or more of the nucleic acids described herein, and a cell containing the vectors or nucleic acids described herein.

The invention is also directed to host cells transformed with a vector comprising any of the nucleic acid molecules described above.

In another aspect, the invention includes a pharmaceutical composition that includes a

POLYX nucleic acid and a pharmaceutically acceptable carrier or diluent.

In a further aspect, the invention includes a substantially purified POLYX polypeptide, e.g., any ofthe POLYX polypeptides encoded by a POLYX nucleic acid, and fragments, homologs, analogs, and derivatives thereof. The invention also includes a pharmaceutical composition that includes a POLYX polypeptide and a pharmaceutically acceptable carrier or diluent. In a still a further aspect, the invention provides an antibody that binds specifically to a POLYX polypeptide. The antibody can be, e.g., a monoclonal or polyclonal antibody, and fragments, homologs, analogs, and derivatives thereof. The invention also includes a pharmaceutical composition including POLYX antibody and a pharmaceutically acceptable carrier or diluent. The invention is also directed to isolated antibodies that bind to an epitope on a polypeptide encoded by any ofthe nucleic acid molecules described above.

The invention also includes kits comprising any of he pharmaceutical compositions described above.

The invention further provides a method for producing a POLYX polypeptide by providing a cell containing a POLYX nucleic acid, e.g., a vector that includes a POLYX nucleic acid, and culturing the cell under conditions sufficient to express the POLYX polypeptide encoded by the nucleic acid. The expressed POLYX polypeptide is then recovered from the cell. Preferably, the cell produces little or no endogenous POLYX polypeptide. The cell can be, e.g., a prokaryotic cell or eukaryotic cell.

The invention is also directed to methods of identifying a POLYX polypeptide or nucleic acids in a sample by contacting the sample with a compound that specifically binds to the polypeptide or nucleic acid, and detecting complex formation, if present.

The invention further provides methods of identifying a compound that modulates the activity of a POLYX polypeptide by contacting a POLYX polypeptide with a compound and determining whether the POLYX polypeptide activity is modified.

The invention is also directed to compounds that modulate POLYX polypeptide activity identified by contacting a POLYX polypeptide with the compound and determining whether the compound modifies activity ofthe POLYX polypeptide, binds to the POLYX polypeptide, or binds to a nucleic acid molecule encoding a POLYX polypeptide.

In a another aspect, the invention provides a method of determining the presence of, or predisposition to a POLYX-associated disorder in a subject. The method includes providing a sample from the subject and measuring the amount of POLYX polypeptide in the subject sample. The amount of POLYX polypeptide in the subject sample is then compared to the amount of POLYX polypeptide in a control sample. An alteration in the amount of POLYX polypeptide in the subject protein sample relative to the amount of POLYX polypeptide in the control protein sample indicates the subject has a tissue proliferation-associated condition. A control sample is preferably taken from a matched individual, i. e. , an individual of similar age, sex, or other general condition but who is not suspected of having a tissue proliferation- associated condition. Alternatively, the control sample may be taken from the subject at a time when the subject is not suspected of having a tissue proliferation-associated disorder. In some embodiments, the POLYX is detected using a POLYX antibody.

In a further aspect, the invention provides a method of determining the presence of, or predisposition to, a POLYX-associated disorder in a subject. The method includes providing a nucleic acid sample (e.g., RNA or DNA, or both) from the subject and measuring the amount ofthe POLYX nucleic acid in the subject nucleic acid sample. The amount of POLYX nucleic acid sample in the subject nucleic acid is then compared to the amount of POLYX nucleic acid in a control sample. An alteration in the amount of POLYX nucleic acid in the sample relative to the amount of POLYX in the control sample indicates the subject has a tissue proliferation-associated disorder.

In a still further aspect, the invention provides a method of treating or preventing or delaying a POLYX-associated disorder. The method includes administering to a subject in which such treatment or prevention or delay is desired a POLYX nucleic acid, a POLYX polypeptide, or a POLYX antibody in an amount sufficient to treat, prevent, or delay a tissue proliferation-associated disorder in the subject.

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing ofthe invention, suitable methods and materials are described below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In the case of conflict, the present Specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.

Other features and advantages ofthe invention will be apparent from the following detailed description and claims.

DETAILED DESCRIPTION OF THE INVENTION

The invention provides novel polynucleotides and the polypeptides encoded thereby. The invention is based in part on the discovery of nucleic acids encoding 17 proteins that are novel members ofthe following protein families: gamma aminobutyric acid (GABA) receptor, epidermal growth factor (EGF), complement receptor, hematopoeitic stem and progenitor cell (HSPC), sulfotransferase, syntaxin, and prohibitin. These nucleic acids, and their associated polypeptides, antibodies and other compositions are referred to as POLY1, POLY2, POLY3 through POLY17, respectively. These sequences are collectively referred to as "POLYX nucleic acids" or "POLYX polynucleotides" (where X is an integer between 1 and 17) and the corresponding encoded polypeptide is referred to as a "POLYX polypeptide" or "POLYX protein".

POLY1-4 are novel members ofthe GABA receptor family; POLY5-8 are novel members ofthe EGF family; POLY9-11 are novel members ofthe complement receptor family; POLY12 is a novel member ofthe HSPC family; POLY13 is a novel member ofthe sulfotransferase family; POLY14-16 are novel members ofthe syntaxin family; and POLY17 is a novel member ofthe prohibitin family.

Table 1 provides a cross-reference between a POLYX nucleic acid or polypeptide of the invention, a table disclosing a nucleic acid and encoded polypeptide that is encompassed by an indicated POLYX nucleic acid or polypeptide ofthe invention, and a corresponding sequence identification number (SEQ ID NO:). Also provided is a CuraGen internal Clone Identification Number for the disclosed nucleic acid and encoded polypeptides. Unless indicated otherwise, reference to a "Clone" herein refers to a discrete in silico nucleic acid sequence. TABLE 1.

POLYX nucleic acids, POLYX polypeptides, POLYX antibodies, and related compounds, are useful in a variety of applications and contexts. For example, various POLYX nucleic acids and polypeptides according to the invention are useful, inter alia, as novel members ofthe protein families according to the presence of domains and sequence relatedness to previously described proteins.

POLYX nucleic acids and polypeptides according to the invention can also be used to identify cell types based on the presence or absence of various POLYX nucleic acids according to the invention. Additional utilities for POLYX nucleic acids and polypeptides are discussed below.

POLY1-POLY4

GAMMA AMINOBUTYRIC ACID RECEPTOR-LIKE (GABA) NUCLEIC ACIDS AND PROTEINS

POLY 1-4 nucleic acids and proteins are members ofthe gamma-aminobutyric acid receptor family. GABA receptors are a family of ligand-gated chloride channels that are the major inhibitory neurotransmitter receptors in the nervous system. Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter ofthe brain and acts through binding to GABA(A) receptors, where the ligand causes an influx of chloride ions. Certain GABA receptor sub-types are inhibitory neurotransmitter receptors ofthe brain, the retina, or other parts ofthe CNS.

GABA receptors are molecular substrates for the regulation of vigilance, anxiety, muscle tension, epileptogenic activity, and memory functions. This is evident since GABA receptors are the site of action of a number of important pharmacological agents, including barbiturates, benzodiazepines, and ethanol. Accordingly, benzodiazepino-induced behavioral responses are mediated by specific GABA(A) receptor sub-types in distinct neuronal circuits.

GABA(A) receptors are heterooligomeric, and combinations of different subunits lead to functional diversity. The gene encoding the gamma-3 form ofthe GABA receptor (GABRG3) is located on 15ql l-ql3 in a cluster with GABRA5 and GABRB3. Thus, there is an alpha/beta/gamma cluster of GABA receptor subunit subtype genes on 3 chromosomes, 15, 5, and 3. It has been suggested that these may have originated from chromosome 15 because the centromere of that chromosome is associated with increased amounts of satellite DNA and translocations occur more frequently around such centromeres. Thus, it can be speculated that the ancestral GABA-A receptor gene cluster formed on chromosome 15 and thereafter spawned the clusters on chromosomes 4 and 5. The detailed physical map of this GABAA receptor subunit gene cluster should not only be useful in genetic studies ofthe 15ql l-ql3 region, but will also be important for investigating the evolution and expression ofthe GABAA receptor gene superfamily. Information regarding the known properties ofthe GABA receptor family, to which POLY 1-4 belong, is described in detail below.

Retinal Inhibitory Receptor Properties of GABA receptors

Certain GABA receptor sub-types have been shown to be inhibitory receptors in the retina. Gamma-aminobutyrate is the gamma-aminobutyric acid (GABA) receptor subunit.

GABArholdelta51 is an alternatively spliced form ofthe GABArhol receptor that was recently isolated from human retina cDNA libraries. The rholdelta51 receptor subunit lacks 17 amino acids in the extracellular N-terminal domain and, when expressed in Xenopus oocytes, forms functional homomeric GABA receptors. Unexpectedly, even after a such a big deletion, the fundamental properties ofthe deleted variant receptors are very similar to those ofthe complete GABArhol receptors. For example, both types of receptors are bicuculline resistant, desensitize very little, and are negatively modulated by Zn2+ and positively modulated by La3+. In spite of such similarities, the GABArhol delta51 receptors are more sensitive to GABA, to the specific GABA(C) antagonist (l,2,5,6-tetrahydropyridine-4- yl)methylphosphinic acid and to Zn2+, than the complete GABArhol receptors. The GABArhol delta51 receptors extend the variety of inhibitory receptors in the retina.

GABA receptor rho3 subunit has been localized to rat retina and has been shown to be expressed in rat retina. Digoxigenin-labelled single strand DNA probes was used to examine the expression ofthe mRNA encoding gamma-aminobutyric acid receptor rho 3 subunit in sections ofthe adult rat retina. Transcript for the rho 3 subunit was found in cell somata of a portion of cells lying in the ganglion cell layer.

Additionally, cloned cDNA encoding a putative member of GABA receptor rho- subunit class was isolated from rat-retina-mRNA-derived libraries. The cDNA encodes a signal peptide of 21 amino acids followed by the mature rho 3 subunit sequence of 443 amino acids. The proposed amino acid sequence exhibits 63 and 61% homology to the previously- reported human rho 1 and rat rho 2 sequences, respectively. Northern blot analysis demonstrated the expression of mRNA for rho 3 subunit in retina.

Type A gamma-aminobutyric acid (GABA-A) receptors are a family of ligand- gated chloride channels that are the major inhibitory neurotransmitter receptors in the nervous system. Molecular cloning has revealed diversity in the subunits that compose this heterooligomeric receptor, but each previously elucidated subunit displays amino acid similarity in conserved structural elements. These highly conserved regions were used to identify additional members of this family by using the polymerase chain reaction (PCR). One PCR product was used to isolate a full-length cDNA from a human retina cDNA library. The mature protein predicted from this cDNA sequence is 458 amino acids long and displays between 30 and 38% amino acid similarity to the previously identified GABAA subunits. This gene is expressed primarily in the retina but transcripts are also detected in the brain, lung, and thymus. Injection of Xenopus oocytes with RNA transcribed in vitro produces a GABA- responsive chloride conductance and expression ofthe cDNA in COS cells yields GABA- displaceable muscimol binding. These features are consistent with the identification of a GABA subunit, GABA rho 1, with prominent retinal expression that increases the diversity and tissue specificity of this ligand-gated ion-channel receptor family.

Intracellular Trafficking of GABA(A Receptors

Some ofthe mechanisms that control the intracellular trafficking of GAB A( A) receptors have recently been described. Following the synthesis of alpha, beta, and gamma subunits in the endoplasmic reticulum, ternary receptor complexes assemble slowly and are inefficiently inserted into surface membranes of heterologous cells. While beta3, beta4, and gamma2S subunits appear to contain polypeptide sequences that alone are sufficient for surface targeting, these sequences are neither conserved nor essential for surface expression of heteromeric GABA(A) receptors formed from alphalbeta or alpha lbetagamma subunits. At the neuronal surface, native GAB A(A) receptor clustering and synaptic targeting require a gamma2 subunit and the participation of gephyrin, a clustering protein for glycine receptors. A linker protein, such as the GAB A(A) receptor associated protein (GABARAP), may be necessary for the formation of GABA(A) receptor aggregates containing gephyrin. A substantial fraction of surface receptors are sequestered by endocytosis, another process which requires a GABA(A) receptor gamma2 subunit. In heterologous cells, constitutive endocytosis seems to predominate while, in cortical neurons, internalization is evoked when receptors are occupied by GABA(A) agonists. After constitutive endocytosis, receptors are relatively stable and can be rapidly recycled to the cell surface, a process that may be regulated by protein kinase C. On the other hand, a portion ofthe intracellular GABA(A) receptors derived from ligand-dependent endocytosis is apparently degraded. The clustering of GABA(A) receptors at synapses and at coated pits are two mechanisms that may compete for a pool of diffusable receptors, providing a model for plasticity at inhibitory synapses.

Chromosomal Localizatin of GABA Receptors

The gamma-aminobutyric acid (GABA) receptors are the major inhibitory neurotransmitter receptors in the brain and the site of action of a number of important pharmacological agents including barbiturates, benzodiazepines, and ethanol. The gamma 1 and gamma 2 subunits have been shown to be important in mediating responses to benzodiazepines, and a splicing variant ofthe gamma 2 subunit, gamma 2L, has been shown to be necessary for ethanol actions on the receptor, raising the possibility that the gamma 2 gene may be involved in human genetic predisposition to the development of alcoholism. The human genes encoding the gamma 1 and gamma 2 subunits ofthe GABAA receptor has been mapped to chromosomes 4 and 5, respectively, by PCR amplification of human-specific products from human-hamster somatic cell hybrid DNAs. Using panels of chromosome- specific natural deletion hybrids, the gamma 1 gene (GABRG1) has been further localized to 4pl4-q21.1 and the gamma 2 gene (GABRG2) to 5q31.1-q33.2. This localization indicates that the gamma 1 gene may be clustered together with the previously mapped alpha 2 and beta 1 genes on chromosome 4 and that the gamma 2 gene may be close to the previously localized alpha 1 gene on chromosome 5. To further examine the latter possibility, the alpha 1 gene was mapped using the chromosome 5 deletion hybrids, and was shown to be within the same region as the gamma 2 gene, 5q31.1-q33.2. A PCR-based screening strategy was used to isolate a 450-kilobase human genomic yeast artificial chromosome clone containing both the alpha 1 and gamma 2 genes. Pulsed-field gel restriction mapping ofthe yeast artificial chromosome indicated that the two genes are within 200 kilobases of each other. This demonstrates that members ofthe GABAA receptor gene family often occur in small gene clusters widely distributed in the genome.

Additionally, genes encoding rho2 (GABRR2) and rhol (GABRR1) have been localized to human chromosome 6ql4-q21 and mouse chromosome 4. Two distinct clones have been identified by screening a genomic DNA library with a portion ofthe cDNA encoding the gamma-aminobutyric acid (GABA) receptor subunit rhol. DNA sequencing revealed that one clone contained a single exon from the rhol gene (GABBR1) while the second clone encompassed an exon with 96% identity to the rhol gene. Screening of a human retina cDNA library with oligonucleotides specific for the exon in the second clone identified a 3-kb cDNA with an open reading frame of 1395 bp. The predicted amino acid sequence of this cDNA demonstrated 30 to 38% similarity to alpha, beta, gamma, and delta GABA receptor subunits and 74% similarity to the GABA rhol subunit, suggesting that the newly isolated cDNA encoded a new member ofthe rho subunit family, tentatively named GABA rho2. Polymerase chain reaction (PCR) amplification of rhol and rho2 gene sequences from DNA of three somatic cell hybrid panels mapped both genes to human chromosome 6, bands ql4 to q21. Tight linkage was also demonstrated between restriction fragment length variants (RFLNs) from each rho gene and the Tsha locus on mouse chromosome 4, which is homologous to the CGA locus on human chromosome 6ql2-q21. These two lines of evidence confirmed that GABRR1 and newly identified GABRR2 mapped to the same region on human chromosome 6. This close physical association and high degree of sequence similarity raised the possibility that one rho gene arose from the other by duplication.

Benzodiazepine Actions Mediated by GABA Receptors

When gamma-aminobutyric acid (GABA), the major inhibitory neurotransmitter in vertebrate brain, binds to its receptor, it activates a chloride channel. Neurotransmitter action at the GABAA receptor is potentiated by both benzodiazepines and barbiturates which are therapeutically useful drugs. GABA(A) receptors are therefore molecular substrates for the regulation of vigilance, anxiety, muscle tension, epileptogenic activity and memory functions, which is evident from the spectrum of actions elicited by clinically effective drugs acting at their modulatory benzodiazepine-binding site.

There is strong evidence that this receptor is heterogeneous. Complementary DNAs encoding an alpha- and a beta-subunit have previously isolated. It has been shown that both are needed for expression of a functional GABAA receptor. cDNAs encoding two additional GABAA receptor alpha-subunits have now been isolated, confirming the heterogeneous nature ofthe receptor/chloride channel complex and demonstrating a molecular basis for it. These alpha-subunits are differentially expressed within the CNS and produce, when expressed with the beta-subunit in Xenopus oocytes, receptor subtypes which can be distinguished by their apparent sensitivity to GABA. Highly homologous receptor subtypes which differ functionally are common feature of brain receptors.

Additionally, evidence shows that benzodiazepine actions are mediated by specific

GABA receptor sub-types. By introducing a histidine-to-arginine point mutation at position

101 ofthe murine alpha 1 -subunit gene, it has been shown that alphal-type GABA(A) receptors, which are mainly expressed in cortical areas and thalamus, are rendered insensitive to allosteric modulation by benzodiazepine-site ligands, while regulation by the physiological neurotransmitter gamma-aminobutyric acid is preserved. Alphal(H101R) mice failed to show the sedative, amnesic and partly the anticonvulsant action of diazepam. In contrast, the anxiolytic-like, myorelaxant, motor-impairing and ethanol-potentiating effects were fully retained, and are attributed to the nonmutated GABA(A) receptors found in the limbic system (alpha2, alpha5), in monoaminergic neurons (alpha3) and in motoneurons (alpha2, alpha5). Thus, benzodiazepine-induced behavioural responses are mediated by specific GABA(A) receptor subtypes in distinct neuronal circuits, which is of interest for drug design.

Benzodiazepines have come under scrutiny and attack over recent years because of their abuse liability, withdrawal reactions and development of tolerance. Consequently, practitioners worldwide are discouraged from prescribing them. While some of these risks may have been exaggerated, benzodiazepines remain a useful therapeutic tool, alone or in combination, in a number of psychiatric and medical conditions. Withholding such treatment may be unjustified and detrimental to the patients' health. Further, benzodiazepines have helped researchers in their attempts to elucidate the neurobiological mechanisms underlying anxiety. This, in return, leads to the development of new effective anxiolytic treatments, with fewer problems compared to the traditional benzodiazepine compounds. Such new agents are already available or at the closing stages of clinical trials.

Role of GABA Receptor in Cognitive Function

The role of GABA in cognitive functions was also studied in cats which had received damage to the forebrain basal nuclei. The cognitive functions were studied on experimental model of Alzheimer's disease (destruction ofthe basal nuclei of Meynert in cats) using the stimulation and inhibition of Ach, GABA, and DA brain systems. Ach system was found to be essential to form generalization function, DA system to improve simple learning, and GABA system to involve in formation of complex associations. Novel members ofthe GABA receptor family, POLY 1 -POL Y4, are described in detail below. These nucleic acids and proteins function as described above, and therefore are useful in modulating neurological, e.g. conditions related to brain neurotransmitters, and other disorders.

The protein similarity information, expression pattern, cellular localization, and map location for POLY1-POLY4 discussed below suggest that these GABA Receptor-like proteins have important structural and/or physiological functions characteristic ofthe GABA Receptor family. Therefore, the nucleic acids and proteins ofthe invention are useful in potential diagnostic and therapeutic applications, e.g. diagnosis and therapy of neurological diseases and/or disorders, and as research tools. Additionally, POLY 1 -POL Y4 have applications in the diagnosis and/or treatment of various diseases and disorders. For example, the compositions of POLY 1 -POL Y4 will have efficacy for the treatment of patients suffering from: psychiatric and medical conditions, depression, stroke, Parkinson's disease, Huntington's disease, Tourette's syndrome, amyotrophic lateral sclerosis, head trauma, Alzheimer's disease, alcoholism, vigilance, anxiety, muscle tension, epileptogenic activity and memory functions, cardiomyopathy, and arrhythmogenic right ventricular dysplasia as well as other diseases, disorders and conditions.

These materials are further useful in the generation of antibodies that bind immunospecifically to the novel substances ofthe invention for use in diagnostic and/or therapeutic methods.

POLY1

A novel nucleic acid was identified on chromosome 3 as described in Example 1. The novel nucleic acid of 1875 nucleotides (SEQ ID NO: 1), which encodes a novel gamma aminobutyric acid receptor -like protein is shown in Table 2A. An open reading frame was identified beginning with an ATG initiation codon at nucleotides 10, 11 and 12 and ending with a TGA codon at nucleotides 1411, 1412 and 1413. A putative untranslated region upstream from the initiation codon and downstream from the termination codon is underlined in Table 2A, and the start and stop codons are in bold letters. The encoded protein having 467 amino acid residues (SEQ ID NO:2) is presented using the one-letter code in Table 2B. TABLE 2A: The nucleotide sequence of POLY1.

TTGGAAGAGATGGTCCTGGCTTTCCAGTTAGTCTCCTTCACCTACATCTGGATCATATTGAAACCAAATG TTTGTGCTGCTTCTAACATCAAGATGACACACCAGCGGTGCTCCTCTTCAATGAAACAAACCTGGATGCA AGAAACTAGAATGAAGAAAGATGACAGTACCAAAGCGCGGCCTCAGAAATATGAGCAACTTCTCCATATA GAGGACAACGATTTCGCAATGAGACCTGGATTTGGAGGTTCTCCAGTGCCAGTAGGTATAGATGTCCATG TTGAAAGCATTGACAGCATTTCAGAGACTAACATGGACTTTACAATGACTTTTTATCTCAGGCATTACTG GAAAGACGAGAGGCTCTCCTTTCCTAGCACAGCAAACAAAAGCATGACATTTGATCATAGACACTTGCGG TATTCGTTATTCATCAGAAGGCTGTATCTGTTATACTGCCAGAGGTCTTTCTTCTCACCCTCATCCATAC TTCCCTCATCTCCAGACATCCATGCACCTGGTACATCTAAAAGCAGTTTGTCTGATAGCCTTGTATGTAT ATCTGAAAAAAACTTGCCAGGACACAGTAAAAACACACCTCTTGCAATGTCAGATGTAGCCTACAATGAG GATGACCTAATGCTATACTGGAAACACGGAAACAAGTCCTTAAATACTGAAGAACATATGTCCCTTTCTC AGTTCTTCATTGAAGACTTCAGTGCATCTAGTGGATTAGCTTTCTATAGCAGCACAGGTACAGCATTTTA CATGGGTGATTCATCAGCATTTATTGGACATCTACTGTTTTTGATCTGGAGTTCCAGGAAAAGACCAGGT TTAGAGATGTTGGGTTTGGGAATTCTCAGAATCTGGGTAATAACTAGAGCCATGGATAAGAAAATGGAAA TGGGAATCACCACAGTGCTGACCATGTCCACAATCATCACTGCTGTGAGCGCCTCCATGCCCCAGGTGTC CTACCTCAAGGCTGTGGATGTGTACCTGTGGGTCAGCTCCCTCTTTGTGTTCCTGTCAGTCATTGAGTAT GCAGCTGTGAACTACCTCACCACAGTGGAAGAGCGGAAACAATTCAAAAAAAGTTTTTCAAAGATTTCTA GGATGTACAATATTGATGCAGTTCAAGCTATGGCCTTTGATGGTTGTTACCATGACAGCGAGATTGACAT GGACCAGACTTCCCTCTCTCTAAACTCAGAAGACTTCATGAGAAGAAAATCGATATGCAGCCCCAGCACC GATTCATCTCGGATAAAGAGAAGAAAATCCCTAGGAGGACATGTTGGTAGAATCATTCTGGAAAACAACC ATGTCATTGACACCTATTCTAGGATTTTATTCCCCATTGTGTATATCTTTTTTAATTTGTTTTACTGGGG TGTATATGTATGAAGGGGAATTTCAAATGTATACAACTTTAAAGCCAGATGATGTTTAAAAACAAAACTC TTGAATATGAGTTGGATAGTCCTAGATGGAACTGGGAAAGAGCAAGTCACCTCTCCTGCCCTAATGAAAA TTTGAAAGCTGTCTGATTTACATCTAAGAAAGAGTTTAGGTCCTAGAAAAGTTTGACTCCATAAATAAGA GTCATAGGCATGTGTATTATGGGAAAAACAGTTTTCCATTGGGAAGGGCTTTATAACTACTTCATCTGAA CCCTCCTTCTTTCTTAATGAAATGTTCTTTATTTAACTAGGGAAGAAAGCTGGACTATAACAATAATTCA AAGATATTTTGTTTCTTAGTGCCAGCCAAGTGCCTGGTTATCTACCAGAGCTCAACCGTCCTAGGCAAGA ACATCCACATAGAGGTGGTATCATCCACACTCACACAGCTGAGAATCCTATGAAG (SEQ ID NO:l)

TABLE 2B: Protein sequence encoded by the coding sequence shown in TABLE 2A

MVLAFQLVSFTYI IILKPNVCAASNIKMTHQRCSSS KQTWMQETRMKKDDSTKARPQKYEQLLHIEDNDFAMRPGFGGSPVP VGIDVHVESIDSISETNMDFTMTFYLRHYWKDER SFPSTANKSMTFDHRHLRYS FIRRLYLLYCQRSFFSPSSILPSSPDIH APGTSKSSLSDS VCISEK LPGHSK TPAMSDVAYNEDDLM Y KHGNKSLNTEEHMSLSQFFIEDFSASSGLAFYSSTGTA FY GDSSAFIGHLLFLI SSRKRPGLE GLGILRI VITRAMDKKMEMGITTVLTMSTIITAVSASMPQVSYLKAVDVYLWVS SLFVFLSVIEYAAV YLTTVEERKQFKKSFSKISRMYNIDAVQAMAFDGCYHDSEIDMDQTS SLNSEDFMRRKSICSPSTDSS RIKRRKSLGGHVGRIILENNHVIDTYSRILFPIVYIFFNLFYWGVYV (SEQ ID NO: 2) Similarities

In a search of sequence databases, it was found, for example, that the nucleic acid sequence (SEQ ID NO:l) has 1030 of 1366 bases (75 %) identical to a Rattus norvegicus gamma aminobutyric acid receptor mRNA (GENBANK-ID: D50671). The full amino acid sequence ofthe protein ofthe invention was found to have 296 of 471 amino acid residues (62%) identical to, and 349 of 471 residues 73%) positive with, 464 amino acid gamma aminobutyric acid receptor residue protein from Rattus norvegicus (ptnr:SWISSPROT-ACC: P50573) (Table 2C).

TABLE 2C: BLASTX of POLYl against Gamma-Aminobutyric-Acid Receptor RHO-3 Subunit Precursor tGABA(A)Receptor) (SEQ ID NO:35

>gi| 1730196 |sp|P50573|GAR3_RAT GAMMA-AMINOBUTYRIC-ACID RECEPTOR RHO-3 SUBUNIT PRECURSOR (GABA (A)

RECEPTOR)

Score = 529 bits (1364) , Expect = e-149

Identities = 296/471 (62%) , Positives = 349/471 (73%) , Gaps = 11/471 (2%)

Query: 1 MV AFQ VSFTYI IILKPNVCAASNI MTHQRCSSSMKQTWMQETR KKDDSTKARPQK 60

Mill I III M l + 11 +1 M + l II III ++IIM + MI II I I

Sbjct: 1 MV AFW AFFTYTWIT MLDASAVKEPHQQCLSSPKQTRIRETRMRKDDLTKVWPLK 57

Query: 61 YEQLLHIEDNDFAMRPGFGGSPVPVGIDVHVESIDSISETNMDFT TFYLRHYWKDER S 120 + M + II 1111111111 ! 11 MIIMIII 11 II I II I II II I II 11 II I Sbjct: 58 REQ HIEDHDFSTRPGFGGSPVPVGIDVQVESIDSISEVNMDFT TFYLRHYWKDERLS 117

Query: 121 FPSTANKSMTFDHRH RYSLFIRRLYLLYCQRXXXXXXXXXXXXXDIHAPGTSKSS --S 178 nn in nn i ++ +++ ++ ++ +ι +ι i n +

Sbjct: 118 FPSTTNKSMTFDRR IQ- I VPDIFFVHSKRSFIHDTTVENI RVHPDGNVLFSLRIT 176 Query: 179 DSLVCISΞ-KNLPGHSKNTPLAMSDVAYNEDD MLYWKHGNKSLNTEEHMSLSQFFIEDF 237

I +1 + I ₊₊| I +

Sbjct: 177 VSAMCFMDFSRFP DTQNCS E ESYAYNEEDLMLY KHGNKSLNTEEHISLSQFFIEEF 236 Query: 238 SASSG AFYSSTGTAFYMGDSSAFIGHL FLIWSSRKRPGLEMLG GILRIWVITRAMDK 297

M 111 i 11 ! 1 II I + + + 1+ 1 + + I + 1+ I + 1+ 11+

Sbjct: 237 SASSGLAFYSSTG YYRLFINFVLRRHIFFFVLQTY-FPAMLMV LSWVSFWIDRRAVPA 295

Query: 298 KMEMGITTV T STIITAVSASMPQVSYLKAVDVY VSSLFVFLSVIEYAAVNYLTTVE 357

++ +IMIMMMI + I + +

Sbjct: 296 RVS GITTVLTMSTIVTGVSASMPQVSYVKAVDVYMWVSSLFVFLSVIEYAAVNYLTTVE 355 Query: 358 ERKQFKKSFSKISRMYNIDAVQAMAFDGCYHDSEIDMDQTS SLNS-EDFMRRKSICSPS 416

MI + III IIIII I I+l 111 I+l II II I II Sbjct: 356 EWKQLNRR-GKISGMYNIDAVQAMAFDGCYHDGETDVDQTSFFLHSEEDSMRTKFTGSPC 414 Query: 417 TDSSRIKRRKSLGGHVGRII ENNHVIDTYSRI FPIVYIFFNLFYWGVYV 467

11 I +l I 1111 i I + l ! 111111111111111 I +l ! +l 11 +ll

Sbjct: 415 ADSSQIK-RKSLGGNVGRIILENNHVIDTYSRIVFPWYIIFNLFY GIYV 464 (SEQ ID NO.: 35) In a search of sequence databases, it was also found, for example, that the nucleic acid sequence (SEQ ID NO:l) has 776 of 781 bases (99%) identical to a CuraGen human assembly (s3aq:83055392). The strong (99%) homology between the gene of current invention with the above CuraGen proprietary human assembly strongly suggests that the current invention represents an expressed gene. In a search of sequence databases, it was also found, for example, that the nucleic acid sequence has 623 of 934 bases (66%) identical to a Homo sapiens gamma aminobutyric acid receptor mRNA (GENBANK-ID: M62400). The global sequence homology, as defined by the GAP global sequence alignment program using the full length sequence ofthe best BlastX match and the full length sequence ofthe protein ofthe invention, is 64.6% amino acid identity and 70.2% amino acid homology. In addition, this protein contains the following protein domain, as defined by Interpro, at the indicated amino acid positions: Neurotransmitter-gated ion-channel family domain (IPR001175) at amino acid positions 58-134, 301-361, and 441-463.

It was also found that POLYl had homology to other amino acid sequences shown in the BLASTX data in Table 2D.

Table 2D. BLASTX alignments of POLYl

Sequences producing High-scoring Segment Pairs: Smallest

Sum eading High Prob .

Frame Score P (N) N

R31188 GABA-A receptor beta-2 subunit - Homo sapi. . +1 396 3 7e-43 2

R59866 Human GABA receptor beta2 subunit - Homo s. . +1 396 3 7e-43 2

R93118 Human GABA-A receptor epsilon subunit - Ho. . +1 412 2 Oe-37 1

ΛJ26464 Human GABA-A receptor epsilon subunit - Ho. . +1 412 2 Oe-37 1

B00174 Breast cancer protein BCR3 - Homo sapiens, . . +1 412 2 Oe-37 1

ΛT81634 GABA-gated chloride channel TB -a2 - Helio. . +1 344 5 6e-37 2

High Score is a ranking of homologous polypeptides, and Smallest Sum Prob. Is the likelyhood that the calculated homology occurred by chance.

It was also found that POLYl had homology to other amino acid sequences shown in the BLASTP data in Table 2E.

In a search of CuraGen's human expressed sequence assembly database, assembly(ies) 83055392 (781 nucleotides) was/were identified as having >95% homology to this nucleic acid sequence. This database is composed ofthe expressed sequences (as derived from isolated mRNA) from more than 96 different tissues. The mRNA is converted to cDNA and then sequenced. These expressed DNA sequences are then pooled in a database and those exhibiting a defined level of homology are combined into a single assembly with a common consensus sequence. The consensus sequence is representative of all member components. Since the nucleic acid ofthe described invention has >95% sequence identity with the

CuraGen assembly, the nucleic acid ofthe invention represents an expressed gene sequence. This DNA assembly has 1 component and was found by CuraGen to be expressed in fetal brain.

PSORT analysis predicts the protein ofthe invention to be localized in plasma membrane with a certainty of 0. 64. Using the SIGNALP analysis, it is predicted that the protein ofthe invention has a signal peptide with most likely cleavage site between pos. 24 and 25 of SEQ ID NO.: 2.

POLY2

A novel nucleic acid was identified on chromosome 3. The novel nucleic acid of 1417 nucleotides (SEQ ID NO:3) encodes a novel gamma aminobutyric acid receptor-like protein that is shown in TABLE 3 A. An open reading frame was identified beginning with an ATG initiation codon at nucleotides 8-10 and ending with a TGA codon at nucleotides 1400-1402. A putative untranslated region upstream from the initiation codon and downstream from the termination codon is underlined in TABLE 3 A, and the start and stop codons are in bold letters. The encoded protein having 464 (SEQ ID NO:4) amino acid residues is presented using the one-letter code in TABLE 3B.

TABLE 3A: Nucleotide sequence of POLY2.

GGAAGAGATGGTCCTGGCTTTCCAGTTAGTCTCCTTCACCTACATCTGGATCATATTGGTTTGTGCTGCTTCTAAC ATCAAGATGACACACCAGCGGTGCTCCTCTTCAATGAAACAAACCAGCAAACAAGAAACTAGAATGAAGAAAGATG ACAGTACCAAAGCGCGGCCTCAGAAATATGAGCAACTTCTCCATATAGAGGACAACGATTTCGCAATGAGACCTGG ATTTGGAGGTTCTCCAGTGCCAGTAGGTATAGATGTCCATGTTGAAAGCATTGACAGCATTTCAGAGACTAACATG GACTTTACAATGACTTTTTATCTCAGGCATTACTGGAAAGACGAGAGGCTCTCCTTTCCTAGCACAGCAAACAAAA GCATGACATTTGATCATAGATTGACCAGAAAGATCTGGGTGCCTGATATCTTTTTTGTCCACTCTAAAAGATCCTT CATCCATGATACAACTATGGAGAATATCATGCTGCGCGTACACCCTGATGGAAACGTCCTCCTAAGTCTCAGGATA ACGGTTTCGGCCATGTGCTTTATGGATTTCAGCAGGTTTCCTCTTGACACTCAAAATTGTTCTCTTGAACTGGAAA GCGCCTACAATGAGGATGACCTAATGCTATACTGGAAACACGGAAACAAGTCCTTAAATACTGAAGAACATATGTC CCTTTCTCAGTTCTTCATTGAAGACTTCAGTGCATCTAGTGGATTAGCTTTCTATAGCAGCACAACAGGCTGGTAC AATAGGCTTTTCATCATCTCTGTGCTAAGGAGGCATGTTTTCTTCTTTGTGCTGCCAACCTATTTCCCAGCCATAT TGATGGTGATGCTTTCATGGGTTTCATTTTGGATTGACCGAAGAGCTGTTCCTGCAAGAGTTTCCCTGGGAATCAC CACAGTGCTGACCATGTCCACAATCATCACTGCTGTGAGCGCCTCCATGCCCCAGGTGTCCTACCTCAAGGCTGTG GATGTGTACCTGTGGGTCAGCTCCCTCTTTGTGTTCCTGTCAGTCATTGAGTATGCAGCTGTGAACTACCTCACCA CAGTGGAAGAGCGGAAACAATTCAAGAAGACAGGAAAGATTTCTAGGATGTACAATATTGATGCAGTTCAAGCTAT GGCCTTTGATGGTTGTTACCATGACAGCGAGATTGACATGGACCAGACTTCCCTCTCTCTAAACTCAGAAGACTTC ATGAGAAGAAAATCGATATGCAGCCCCAGCACCGATTCATCTCGGATAAAGAGAAGAAAATCCCTAGGAGGACATG TTGGTAGAATCATTCTGGAAAACAACCATGTCATTGACACCTATTCTAGGATTTTATTCCCCATTGTGTATATTTT ATTTAATTTGTTTTACTGGGGTGTATATGTATGAAGGGGAATTTCAAAT (SEQ ID NO: 3)

TABLE 3B: Protein sequence encoded by the coding sequence shown in TABLE 3A

MVLAFQLVSFTYIWIILVCAASNIKMTHQRCSSSMKQTSKQETRMKKDDSTPARPQKYEQLLHIEDNDFAMRPGFG GSPVPVGIDVHVESIDSISETNMDFT TFYLRHYWKDERLSFPSTANKSMTFDHRLTRKI VPDIFFVHSKRSFIH DTTMENIMLRVHPDGNVLLSLRITVSAMCFMDFSRFPLDTQNCSLELESAYNEDDLMLYWKHGNKSLNTEEHMSLS QFFIEDFSASSGLAFYSSTTG YNRLFIISVLRRHVFFFVLPTYFPAILMVMLSWVSF IDRRAVPARVSLGITTV LTMSTIITAVSASMPQVSYLKAVDVYL VSSLFVFLSVIEYAAVNYLTTVEERKQFKKTGKISRMYNIDAVQAMAF DGCYHDSEIDMDQTSLSLNSEDFMRRKSICSPSTDSSRIKRRKSLGGHVGRIILENNHVIDTYSRILFPIVYILFN LFYWGVYV (SEQ ID NO: ) In a search of sequence databases, it was found, for example, that the nucleic acid sequence has 1208 of 1412 bases (85 %) identical to a Rattus norvegicus gamma aminobutyric acid receptor mRNA (GENBANK-ID: D50671). The full amino acid sequence ofthe protein ofthe invention was found to have 389 of 464 amino acid residues (83%) identical to, and 415 of 464 residues (89 %) positive with, the 464 amino acid residue protein from Rattus norvegicus (ptnr:SWISSPROT-ACC: P50573) (Table 3C).

TABLE 3C: BLASTX of POLY2 against Gamma-Aminobutyric-Acid Receptor RHO-3 Subunit Precursor (GABA(A)Receptor) (SEQ ID NO:36)

>ptnr:SWISSPROT-ACC:P50573 GAMMA-AMINOBUTYRIC-ACID RECEPTOR RHO-3 SUBUNIT PRECURSOR (GABA(A) RECEPTOR) - Rattus norvegicus (Rat) , 464 aa.

Plus Strand HSPs:

Score = 1992 (701.2 bits), Expect = 4.2e-205, P = 4.2e-205 Identities = 389/464 (83%), Positives = 415/464 (89%), Frame = +2

Query: 8 MVLAFQLVSFTYIWIILVCAASNIKMTHQRCSSSMKQTSKQETR KKDDSTKARPQKYEQ 187 I I I I I I II I I I 1+ II +1 M+l I I II I +1 II I+l I I I I I 1 I I

Sbjct: 1 MVLAFWLAFFTYTWITLMLDASAVKEPHQQCLSSPKQTRIRETRMRKDDLTKVWPLKREQ 60

Query: 188 LLHIEDNDFAMRPGFGGSPVPVGIDVHVESIDSISETNMDFTMTFYLRHYWKDERLSFPS 367

I I I II I+l 1+ II I I I I II I I I II I II II I II II I I I I I II I I Sbjct: 61 LLHIEDHDFSTRPGFGGSPVPVGIDVQVESIDSISEVN DFTMTFYLRHY KDERLSFPS 120

Query: 368 TANKSMTFDHRLTRKIWVPDIFFVHSKRSFIHDTTMENIMLRVHPDGNVLLSLRITVSAM 547

I Mil I II II +111 II III II I I Mil II I I l+ ll I II I I III I II I II II II II I Sbjct: 121 TTNKSMTFDRRLIQKIWVPDIFFVHSKRSFIHDTTVENIMLRVHPDGNVLFSLRITVSAM 180

Query: 548 CF DFSRFPLDTQNCSLELES-AYNEDDL LYWKHGNKSLNTEEHMSLSQFFIEDFSASS 724 I I I II I I I II II II I I II I I I I I I l +ll I I II I 111 I II II lll +l I I II I M +l I I II

Sbjct: 181 CFMDFSRFPLDTQNCSLELESYAYNEEDLMLYWKHGNKSLNTEEHISLSQFFIEEFSASS 240 Query: 725 GLAFYSSTTG YNRLFIISVLRRHVFFFVLPTYFPAILMVMLSWVSFWIDRRAVPARVSL 904 III I Ml I I II I+l III I I I II I+l I I I 1 II II II I II I II II II I I

Sbjct: 241 GLAFYSST-G YYRLFINFVLRRHIFFFVLQTYFPAM VMLSWVSF IDRRAVPARVSL 299

Query: 905 GITTVLTMSTIITAVSASMPQVSYLKAVDVYL VSSLFVFLSVIEYAAVNYLTTVEERKQ 1084 I I I I I I I I II I +1 I I I I I II I I I+1 I I II I+ 1 I II I I I 11 I I I II I II I I I I II I I II

Sbjct: 300 GITTVLTMSTIVTGVSASMPQVSYVKAVDVYM VSSLFVFLSVIEYAAVNYLTTVEE KQ 359

Query: 1085 FKKTGKISR YNIDAVQAMAFDGCYHDSEIDMDQTSLSLNSE-DF RRKSICSPSTDSSR 1261 + I I I I I II I II I III I II II I I I 1 I+ l I I I I+l I I I I I II 111+ Sbjct: 360 LNRRGKISGMYNIDAVQAMAFDGCYHDGETDVDQTSFFLHSEEDSMRTKFTGSPCADSSQ 419

Query: 1262 IKRRKSLGGHVGRIILENNHVIDTYSRILFPIVYILFNLFYWGVYV 1399

111 II 1 I I+l II I MM I I I II II II 1+1 I+l M+l I II II l +ll Sbjct: 420 IKR-KSLGGNVGRIILENNHVIDTYSRIVFPWYIIFNLFY GIYV 464 (SEQ ID NO:36) In a search of sequence databases, it was also found, for example, that the nucleic acid sequence has 339 of 340 bases (99%) identical to a CuraGen Corporation human assembly (s3aq:83055392). The strong (99%) homology between the gene of current invention with the above CuraGen proprietary human assembly strongly suggests that the current invention represents an expressed gene. In a search of sequence databases, it was also found, for example, that the nucleic acid sequence has 888 of 1273 bases (69%) identical to a Homo sapiens gamma aminobutyric acid receptor mRNA (GENBANK-ID: M62400. The global sequence homology, as defined by the GAP global sequence alignment program using the full length sequence ofthe best BlastX match and the full length sequence ofthe protein ofthe invention, is 84% amino acid identity and 86% amino acid homology. In addition, this protein contains the following protein domain, as defined by Interpro, at the indicated amino acid positions: Neurotransmitter-gated ion-channel family domain (IPR001175) at amino acid positions 57 to 361 and 440 to 462.

In a search of CuraGen' s human expressed sequence assembly database, assembly(ies) 83055392 (781 nucleotides) was/were identified as having >95% homology to this predicted gene sequence. The procedure is a differential expression and sequencing procedure that normalizes mRNA species in a sample, and is disclosed in U. S. Ser. No. 09/417,386, filed Oct. 13, 1999, incoφorated herein by reference in its entirety. This database is composed of the expressed sequences (as derived from isolated mRNA) from more than 96 different tissues. The mRNA is converted to cDNA and then sequenced. These expressed DNA sequences are then pooled in a database and those exhibiting a defined level of homology are combined into a single assembly with a common consensus sequence.

PSORT analysis predicts the protein ofthe invention to be localized in plasma membrane with a certainty of 0.68. Using the SIGNALP analysis, it is predicted that the protein ofthe invention has a signal peptide with most likely cleavage site between residues 22 and 23 of SEQ ID NO. 4.

POLY3

A POLY3 nucleic acid was cloned as described in Example 2. The novel nucleic acid of 1444 nucleotides (SEQ ID NO: 5) encodes a novel GABA Receptor-like protein that is shown in TABLE 4. An open reading frame was identified beginning at nucleotides 21-23 and ending at nucleotides 1425-1427. This polypeptide represents a novel functional GABA Receptor-like protein. The start and stop codons ofthe open reading frame are highlighted in bold type. Putative untranslated regions (underlined), are found upstream from the initiation codon and downstream from the termination codon. The encoded protein having 468 amino acid residues (SEQ ID NO:6) is presented using the one-letter code in TABLE 4B. Single nucleotide polymorphisms of a POL Y3 nucleic acid are described in Example 3.

TABLE 4A: Nucleotide sequence of POLY3. GTTTTTTTGTTTTGGAAGAGATGGTCCTGGCTTTCCAGTTAGTCTCCTTCACCTACATCT 60

GGATCATATTGAAACCAAATGTTTGTGCTGCTTCTAACATCAAGATGACACACCAGCGGT 120

GCTCCTCTTCAATGAAACAAACCTGCAAACAAGAAACTAGAATGAAGAAAGATGACAGTA 180

CCAAAGCGCGGCCTCAGAAATATGAGCAACTTCTCCATATAGAGGACAACGATTTCGCAA 240

TGAGACCTGGATTTGGAGGGTCTCCAGTGCCAGTAGGTATAGATGCCCATGTTGAAAGCA 300 TTGACAGCATTTCAGAGACTAACATGGACTTTACAATGACTTTTTATCTCAGGCATTACT 360

GGAAAGACGAGAGGCTCTCCTTTCCTAGCACAGCAAACAAAAGCATGACATTTGATCATA 420

GATTGACCAGAAAGATCTGGGTGCCTGATATCTTTTTTGTCCACTCTAAAAGATCCTTCA 480

TCCATGATACAACTATGGAGAATATCATGCTGCGCGTACACCCTGATGGAAACGTCCTCC 540

TAAGTCTCAGGATAACGGTTTCGGCCATGTGCTTTATGGATTTCAGCAGGTTTCCTCTTG 600 ACGACACTCAAAATTGTTCTCTTGAACTGGAAAGCTGTGCCTACAATGAGGATGACCTAA 660

TGCTATACTGGAAACACGGAAACAAGTCCTTAAATACTGAAGAACATATGTCCCTTTCTC 720

AGTTCTTCATTGAAGACTTCAGTGCATCTAGTGGATTAGCTTTCTATAGCAGCACAGGTT 780

GGTACAATAGGCTTTTCATCAACTTTGTGCTAAGGAGGCATGTTTTCTTCTTTGTGCTGC 840

AAACCTATTTCCCAGCCATATTGATGGTGATGCTTTCATGGGTTTCATTTTGGATTGACC 900 GAAGAGCTGTTCCTGCAAGAGTTTCCCTGGGTATCACCACAGTGCTGACCATGTCCACAA 960

TCATCACTGCTGTGAGCGCCTCCATGCCCCAGGTGTCCTACCTCAAGGCTGTGGATGTGT 1020

ACCTGTGGGTCAGCTCCCTCTTTGTGTTCCTGTCAGTCATTGAGTATGCAGCTGTGAACT 1080

ACCTCACCACAGTGGAAGAGCGGAAACAATTCAAGAAGACAGGAAAGGTATCTAGGATGT 1140

ACAATATTGATGCAGTTCAAGCTATGGCCTTTGATGGTTGTTACCATGACAGCGAGATTG 1200 ACATGGACCAGACTTCCCTCTCTCTAAACTCAGAAGACTTCATGAGAAGAAAATCGATAT 1260

GCAGCCCCAGCACCGATTCATCTCGGATAAAGAGAAGAAAATCCCTAGGAGGACATGTTG 1320

GTAGAATCATTCTGGAAAACAACCATGTCATTGACACCTATTCTAGGATTTTATTCCCCA 1380

TTGTGTATATTTTATTTAATTTGTTTTACTGGGGTGTATATGTATGAAGGGGAATTTCAA 1 40

ATGT (SEQ ID NO:5) 1444 TABLE 4B: Protein sequence encoded by the nucleotide sequence shown in TABLE 4A

MVLAFQLVSFTYIWIILKPNVCAASNI MTHQRCSSSMKQTCKQETRMKKDDSTKARPQK 60 YEQLLHIEDNDFAMRPGFGGSPVPVGIDAHVESIDSISETNMDFTMTFYLRHYWKDERLS 120

FPSTANKSMTFDHRLTRKI VPDIFFVHSKRSFIHDTTMENIMLRVHPDGNVLLSLRITV 180

SAMCFMDFSRFPLDDTQNCSLELESCAYNEDDLM Y KHGNKSLNTEEHMSLSQFFIEDF 240

SASSGLAFYSSTGWYNRLFINFVLRRHVFFFVLQTYFPAILMVMLS VSF IDRRAVPAR 300

VSLGITTVLT STIITAVSASMPQVSYLKAVDVYLWVSSLFVFLSVIEYAAVNY TTVEE 360 RKQFKKTGKVSRMYNIDAVQAMAFDGCYHDSEIDMDQTSLSLNSEDFMRRKSICSPSTDS 420

SRIKRRKSLGGHVGRIILENNHVIDTYSRILFPIVYILFNLFY GVYV (SEQ ID NO: 6) 468

In a search of sequence databases, it was found, for example, that the nucleic acid sequence of this invention has 1169 of 1368 bases (85%) identical to a gb:GENBANK- ID:RATGABA|acc:D50671.1 mRNA from Rattus norvegicus (Rat mRNA for GABA receptor rho-3 subunit, complete cds). The full amino acid sequence ofthe protein ofthe invention was found to have 390 of 468 amino acid residues (83%) identical to, and 417 of 468 amino acid residues (89%) similar to, the 464 amino acid residue ptnr:SWISSPROT-ACC:P50573 protein from Rattus norvegicus (Rat) (GAMMA-AMINOBUTYRIC-ACID RECEPTOR RHO-3 SUBUNIT PRECURSOR (GABA(A) RECEPTOR))(Table 4C).

TABLE 4C: BLASTX of POLY3 against Gamma-Aminobutyric-Acid Receptor RHO-3 Subunit Precursor (GABA(A Receptor) (SEQ ID NO:37

>ptnr:S ISSPROT-ACC:P50573 GAMMA-AMINOBUTYRIC-ACID RECEPTOR RHO-3 SUBUNIT PRECURSOR (GABA(A) RECEPTOR) - Rattus norvegicus (Rat), 464 aa.

Length = 464

Score = 2002 (704.7 bits), Expect = 8.9e-207, P = 8.9e-207 Identities = 390/468 (83%), Positives = 417/468 (89%)

Query: 1 MVLAFQLVSFTYIWIILKPNVCAASNIKMTHQRCSSSMKQTCKQETRMKKDDSTKARPQK 60

I I III I III I I I + M +l M + l II III +1 lll + lll II I I Sbjct: 1 MVLAFWLAFFTYTWITL MLDASAVKEPHQQCLSSPKQTRIRETRMRKDDLTKV PLK 57 Query: 61 YEQLLHIEDNDFAMRPGFGGSPVPVGIDAHVESIDSISETNMDFTMTFYLRHYWKDERLS 120 I MM I I I + l 1+ II I I I I II I II II I I I I II I III III II MM II II I III II I Sbjct: 58 REQLLHIEDHDFSTRPGFGGSPVPVGIDVQVESIDSISEVNMDFTMTFYLRHY KDERLS 117

Query: 121 FPSTANKSMTFDHRLTRKIWVPDIFFVHSKRSFIHDTTMENIMLRVHPDGNVLLSLRITV 180 I || I || I M ] | +M M II II II II II I II II M + l II II II II II I II MMM

Sbjct: 118 FPSTTNKSMTFDRRLIQKI VPDIFFVHSKRSFIHDTTVENIMLRVHPDGNVLFSLRITV 177 Query : 181 SAMCFMDFSRFPLDDTQNCSLELESCAYNEDDLMLY KHGNKSLNTEEHMSLSQFFIEDF 240

I 1 I II I I II I II 1 I lll I lll + l 111 I II I II II I MM I + l I II I II I + l

Sbjct: 178 SAMCFMDFSRFPLD-TQNCSLELESYAYNEEDLMLYWKHGNKSLNTEEHISLSQFFIEEF 236

Query: 241 SASSGLAFYSSTGWYNRLFINFVLRRHVFFFVLQTYFPAILMVMLSWVSF IDRRAVPAR 300

IIIIIIIIIIIIIII I II II I I I I I l + ll II I I III 1 l + ll I I III I I I I I III II I II

Sbjct: 237 SASSGLAFYSSTG YYRLFINFVLRRHIFFFVLQTYFPAMLMVMLSWVSF IDRRAVPAR 296 Query: 301 VSLGITTVLTMSTIITAVSASMPQVSYLKAVDVYLWVSSLFVFLSVIEYAAVNYLTTVEE 360

I I I I II I I II I II I + l I II I I I II M + l II I I l + ll I I II I II III II 1 I I I III I II I Sbjct: 297 VSLGITTVLTMSTIVTGVSASMPQVSYVKAVDVYM VSSLFVFLSVIEYAAVNYLTTVEE 356

Query: 361 RKQFKKTGKVSRMYNIDAVQAMAFDGCYHDSEIDMDQTSLSLNSE-DFMRRKSICSPSTD 419 II + I 1 + ) 11 I II II I I I II I I I Ml I l + ll I I l + ll I II I II I

Sbjct: 357 KQLNRRGKISGMYNIDAVQAMAFDGCYHDGETDVDQTSFFLHSEEDSMRTKFTGSPCAD 416

Query: 420 SSRIKRRKSLGGHVGRIILENNHVIDTYSRILFPIVYILFNLFYWGVYV 468

I I + l II I III I + l I II II I II I I II II II 1 + 1 l + ll I + l II I I ll + ll Sbjct: 417 SSQIKR-KSLGGNVGRIILENNHVIDTYSRIVFPWYIIFNLFY GIYV 464 (SEQ ID NO:37)

Ofthe five families known, four have been shown to form a sequence-related super- family. These are the gamma-aminobutyric acid type A (GABA-A), nicotinic acetylcholine, glycine and the serotonin 5HT3 receptors. The ionotropic glutamate receptors have a distinct primary structure. However, all these receptors posess a pentameric structure (made up of varying subunits), surrounding a central pore. Each of these subunits contains a large extracellular N-terminal ligand-binding region; 3 hydrophobic transmembrane domains; a large intracellular region; and a fourth hydrophobic domain. This indicates that the sequence ofthe invention has properties similar to those of other proteins known to contain this/these domain(s) and similar to the properties of these domains.

PSORT analysis suggests that the GABA Receptor-like protein may be localized in the cytoplasm, although the POLY3 protein (CuraGen Ace. No. CG54683-02) predicted here is similar to the GABA Receptor family, some members of which are membrane localized. Therefore it is likely that this novel GABA Receptor-like protein is localized to the same sub- cellular compartment.

POLY4

A POLY4 nucleic acid was identified as described in Example 4. A POLY4 nucleic acid was localized to human chromosome 3. The novel nucleic acid of 1438 nucleotides (SEQ ID NO:7) encoding a novel GABA Receptor-like protein is shown in TABLE 5. An open reading frame was identified beginning at nucleotides 21-23 and ending at nucleotides 1419- 1421. The encoded polypeptide represents a novel functional GABA Receptor-like protein (TABLE 5B). The start and stop codons ofthe open reading frame are highlighted in bold type. Putative untranslated regions (underlined), are found upstream from the initiation codon and downstream from the termination codon. The encoded protein having 466 (SEQ ID NO: 8) amino acid residues is presented using the one-letter code in TABLE 5B.

TABLE 5A: Nucleotide sequence of POLY4

GTTTTTTTGTTTTGGAAGAGATGGTCCTGGCTTTCCAGTTAGTCTCCTTCACCTACATCT 60

GGATCATATTGAAACCAAATGTTTGTGCTGCTTCTAACATCAAGATGACACACCAGCGGT 120

GCTCCTCTTCAATGAAACAAACCTGCAAACAAGAAACTAGAATGAAGAAAGATGACAGTA 180

CCAAAGCGCGGCCTCAGAAATATGAGCAACTTCTCCATATAGAGGACAACGATTTCGCAA 240 TGAGACCTGGATTTGGAGGGTCTCCAGTGCCAGTAGGTATAGATGTCCATGTTGAAAGCA 300

TTGACAGCATTTCAGAGACTAACATGGACTTTACAATGACTTTTTATCTCAGGCATTACT 360

GGAAAGACGAGAGGCTCTCCTTTCCTAGCACAGCAAACAAAAGCATGACATTTGATCATA 420

GATTGACCAGAAAGATCTGGGTGCCTGATATCTTTTTTGTCCACTCTAAAAGATCCTTCA 480

TCCATGATACAACTATGGAGAATATCATGCTGCGCGTACACCCTGATGGAAACGTCCTCC 540 TAAGTCTCAGGATAACGGTTTCGGCCATGTGCTTTATGGATTTCAGCAGGTTTCCTCTGA 600

CTCAAAATTGTTCTCTTGAACTGGAAAGCTGTGCCTACAATGAGGATGACCTAATGCTAT 660

ACTGGAAACACGGAAACAAGTCCTTAAATACTGAAGAACATATGTCCCTTTCTCAGTTCT 720

TCATTGAAGACTTCAGTGCATCTAGTGGATTAGCTTTCTATAGCAGCACAGGTTGGTACA 780

ATAGGCTTTTCATCAACTTTGTGCTAAGGAGGCATGTTTTCTTCTTTGTGCTGCAAACCT 840 ATTTCCCAGCCATATTGATGGTGATGCTTTCATGGGTTTCATTTTGGATTGACCGAAGAG 900

CTGTTCCTGCAAGAGTTTCCCTGGGTATCACCACAGTGCTGACCATGTCCACAATCATCA 960

CTGCTGTGAGCGCCTCCATGCCCCAGGTGTCCTACCTCAAGGCTGTGGATGTGTACCTGT 1020

GGGTCAGCTCCCTCTTTGTGTTCCTGTCAGTCATTGAGTATGCAGCTGTGAACTACCTCA 1080

CCACAGTGGAAGAGCGGAAACAATTCAAGAAGACAGGAAAGGTATCTAGGATGTACAATA 1140 TTGATGCAGTTCAAGCTATGGCCTTTGATGGTTGTTACCATGACAGCGAGATTGACATGG 1200

ACCAGACTTCCCTCTCTCTAAACTCAGAAGACTTCATGAGAAGAAAATCGATATGCAGCC 1260

CCAGCACCGATTCATCTCGGATAAAGAGAAGAAAATCCCTAGGAGGACATGTTGGTAGAA 1320

TCATTCTGGAAAACAACCATGTCATTGACACCTATTCTAGGATTTTATTCCCCATTGTGT 1380

ATATTTTATTTAATTTGTTTTACTGGGGTGTATATGTATGAAGGGGAATTTCAAATGT 1438 (SEQ ID NO: 7) TABLE 5B:Protein sequence encoded by the nucleotide sequence shown in TABLE 5A

MVLAFQLVSFTYIWIILKPNVCAASNIKMTHQRCSSSMKQTCKQETR KKDDSTKARPQK 60

YEQL HIEDNDFAMRPGFGGSPVPVGIDVHVESIDSISETNMDFTMTFYLRHYWKDER S 120 FPSTANKSMTFDHRLTRKIWVPDIFFVHSKRSFIHDTTMENIMLRVHPDGNVLLSLRITV 180

SAMCFMDFSRFPLTQNCSLELESCAYNEDDLMLYWKHGNKSLNTEEHMSLSQFFIEDFSA 240

SSGLAFYSSTGWYNRLFINFVLRRHVFFFVLQTYFPAILMVMLSWVSFWIDRRAVPARVS 300

LGITTVLTMSTIITAVSASMPQVSYLKAVDVYLWVSSLFVFLSVIEYAAVNYLTTVEERK 360

QFKKTGΪVSRMYNIDAVQAMAFDGCYHDSEIDMDQTSLSLNSEDFMRRKSICSPSTDSSR 420 IKRRKSLGGHVGRIILENNHVIDTYSRILFPIVYILFNLFY GVYV (SEQ ID NO: 8) 466

In a search of sequence databases, it was found, for example, that the POLY4 nucleic acid sequence of this invention has 1218 of 1430 bases (85%) identical to a gb:GENBANK- ID:RATGABA|acc:D50671.1 mRNA from Rattus norvegicus (Rat mRNA for GABA receptor rho-3 subunit, complete cds). The full amino acid sequence ofthe protein ofthe invention was found to have 390 of 466 amino acid residues (83%) identical to, and 417 of 466 amino acid residues (89%) similar to, the 464 amino acid residue ptnr:SWISSPROT-ACC:P50573 protein from Rattus norvegicus (Rat) (GAMMA-AMINOBUTYRIC-ACID RECEPTOR RHO-3 SUBUNIT PRECURSOR (GABA(A) RECEPTOR))(Table 5C). TABLE 5C: BLASTX of POLY4 against Gamma-Aminobutyric-Acid Receptor RHO-3 Subunit Precursor (GABAtA^Receptor) (SEQ ID NO:38^

>ptnr:S ISSPROT-ACC:P50573 GAMMA-AMINOBUTYRIC-ACID RECEPTOR RHO-3 SUBUNIT

PRECURSOR (GABA(A) RECEPTOR) - Rattus norvegicus (Rat), 464 aa. Length = 464

Score = 2000 (704.0 bits), Expect = 1.5e-206, P = 1.5e-206 Identities = 390/466 (83%), Positives = 417/466 (89%) Query: 1 MVLAFQLVSFTYIWIILKPNVCAASNIKMTHQRCSSSMKQTCKQETRMKKDDSTKARPQK 60 I I II I I II I II I + M +l M + l I I I I I +1 I 1 I + l I I II I I

Sbjct: 1 MVLAF LAFFTYTWITL MLDASAVKEPHQQCLSSPKQTRIRETRMRKDDLTKVWPLK 57

Query: 61 YEQLLHIEDNDFAMRPGFGGSPVPVGIDVHVESIDSISETNMDFTMTFYLRHY KDERLS 120 II I I I I 11 + 11+ II II I II II I I MM III III I II I II II I Mill lllll I III

Sbjct: 58 REQLLHIEDHDFSTRPGFGGSPVPVGIDVQVESIDSISEVNMDFTMTFYLRHY KDERLS 117

Query: 121 FPSTANKSMTFDHRLTRKIWVPDIFFVHSKRSFIHDTTMENIMLRVHPDGNVLLSLRITV 180 I III I I I I II I II +1 II I II II I II I I I I I II I M + l II II I I MM 1 I I II I I II Sbjct: 118 FPSTTNKSMTFDRRLIQKI VPDIFFVHSKRSFIHDTTVENIMLRVHPDGNVLFSLRITV 177

Query: 181 SAMCFMDFSRFPL-TQNCSLELESCAYNEDDLMLY KHGNKSLNTEEHMSLSQFFIEDFS 239

I I II I I 1 I II I II I I ll + ll I I II I I I I I III I I M + l I II I lll + l I Sbjct: 178 SAMCFMDFSRFPLDTQNCSLELESYAYNEEDLMLYWKHGNKSLNTEEHISLSQFFIEEFS 237

Query: 240 ASSGLAFYSSTG YNRLFINFVLRRHVFFFVLQTYFPAILMVMLSWVSFWIDRRAVPARV 299

I I II I I I I I I II I I MM I I Ml I I + l III I I I I I M + l I I II I I II I II I M I I II

Sbjct: 238 ASSGLAFYSSTG YYRLFINFVLRRHIFFFVLQTYFPAMLMVMLSWVSF IDRRAVPARV 297

Query: 300 SLGITTVLTMSTIITAVSASMPQVSYLKAVDVYLWVSSLFVFLSVIEYAAVNYLTTVEER 359

Ml I Ml II II M + l MMMMM + MMM + MIMM mmmm M

Sbjct: 298 SLGITTVLTMSTIVTGVSASMPQVSYVKAVDVYM VSSLFVFLSVIEYAAVNYLTTVEE 357

Query: 360 KQFKKTGKVSRMYNIDAVQAMAFDGCYHDSEIDMDQTSLSLNSE-DFMRRKSICSPSTDS 418

I I + I 1 + 1 I I I II I I I I I I I I I I II I 1 I + l I I I l + ll I I I I II II Sbjct: 358 KQLNRRGKISGMYNIDAVQAMAFDGCYHDGETDVDQTSFFLHSEEDSMRTKFTGSPCADS 417 Query: 419 SRIKRRKSLGGHVGRIILENNHVIDTYSRILFPIVYILFNLFYWGVYV 466 l + ll I I I I M + l I II MM I I MM I II I + l I + l I I + l II III l + ll Sbjct: 418 SQIKR-KSLGGNVGRIILENNHVIDTYSRIVFPWYIIFNLFYWGIYV 464 (SEQ ID NO: 38)

This homology indicates that the sequence ofthe invention has properties similar to those of other proteins known to contain this/these domain(s) and similar to the properties of these domains.

POLY5-POLY8:

EPIDERMAL GROWTH FACTOR-LIKE NUCLEIC ACIDS AND PROTEINS

POLY5-POLY8 show significant homologies to human (EGF) proteins. It has a characteristic structure with three disulfide bridges, which are essential for its activity. However, many other proteins, including both growth factors and proteins with unrelated functions, have similar EGF-like domains. EGF-like proteins are important in modulation of cell shape, motility, proliferation and differentiation, and are altered in pathologies, e.g. cancer, aberrant angiogenesis, renal disease, disorders ofthe extracellular matrix, and diabetes.

A number of receptor systems have been implicated in playing an important role in the development and progression of many human cancers. The EGF receptor tyrosine kinase family has been found to consistently play a leading role in tumor progression. Indeed, in human breast cancer cases the prognosis of a patient is inversely correlated with the overexpression and/or amplification of this receptor family. Furthermore, downstream signaling components such as the Src kinases, PI3'K, and the Ras pathway display evidence of deregulation that can accelerate tumor progression. The transgenic mouse system has been ideal in elucidating the biological significance of this receptor family in mammary tumorigenesis. Molecular events involved in mammary tumorigenesis such as ligand binding, receptor dimerization, and the activation of downstream pathways have been addressed using this system. Although there are many molecular steps that appear to drive each stage of tumor development, the EGF receptor family appears to play a causal role in the progression to a transformed phenotype.

POLY5-8 nucleic acids and their encoded polypeptides are useful in a variety of applications and contacts. POLY5-8 are homologous to members ofthe EGF family of proteins that play an important role in the development and progression of many human cancers.

The expression pattern, and protein similarity information for POLY5-8 suggest that the human EGF -like proteins described herein may function as EGF-like proteins. Therefore, POLY5-8 are useful in potential therapeutic applications implicated in, but not limited to, cancer, and other diseases and disorders. The homology to antigenic secreted and membrane proteins suggests that antibodies directed against the novel genes may be useful in treatment and prevention of cancer, tumorigenesis, and other diseases and disorders.

POLY5-8 are useful in potential therapeutic applications implicated in various diseases and disorders described below and/or other pathologies and disorders. For example, but not limited to, a cDNA encoding the human EGF -like protein may be useful in gene therapy of cancer or other cell proliferative diseases and/or disorders, and the human EGF -like proteins may be useful when administered to a subject in need thereof. By way of non-limiting example, the compositions ofthe present invention will have efficacy for treatment of patients suffering from, for example, but not limited to, cancer, and other diseases and disorders. POLY5-8 may further be useful in diagnostic applications, wherein the presence or amount of the nucleic acid or the protein are to be assessed. These materials are further useful in the generation of antibodies that bind immunospecifically to the novel substances ofthe invention for use in therapeutic or diagnostic methods. POLY5

A polynucleotide ofthe present invention has been identified as clone Z97832_B.0.704 (POLY5). POLY5 is a full-length clone of 4400 nucleotides, including the entire coding sequence of a 735 amino acid protein from nucleotides 679 to 2884. The nucleotide sequence of POL Y5 (SEQ ID NO : 9) as presently determined is reported in TABLE 6A. The predicted amino acid sequence ofthe POLY5 protein (SEQ ID NO: 10) corresponding to the foregoing nucleotide sequence is reported in TABLE 6B.

TABLE 6A; The Nucleotide sequence of POLY5

CACGAGCCGGCTTCCGCCCTCCCCTGGCCGCGAGACCGGCCCCGGCGGCTGGGCCGCCAGTAGCTCCAGCCATGGGCTCG GGGCGCGTACCCGGGCTCTGCCTGCTTGTCCTGCTGGTCCACGCCCGCGCCGCCCAGTACAGCAAAGCCGCGCAAGATGT GGATGAGTGTGTGGAGGGGACTGACAACTGCCACATCGATGCTATCTGCCAGAACACCCCGAGGTCATACAAGTGCATCT GCAAGTCTGGCTACACAGGGGACGGCAAACACTGCAAAGACGTGGATGAGTGCGAGCGAGAGGATAATGCAGGTTGTGTG CATGACTGTGTCAACATCCCTGGCAATTACCGGTGTACCTGCTATGATGGATTCCACCTGGCACATGACGGACACAACTG TCTGGATGTGGACGAGTGTGCCGAGGGCAACGGCGGCTGTCAGCAGAGCTGTGTCAACATGATGGGCAGCTATGAGTGCC ACTGCCGGGAAGGCTTCTTCCTCAGCGACAACCAGCATACCTGTATCCAGCGGCCAGAAGAAGGAATGAATTGCATGAAC AAGAACCACGGCTGTGCCCACATTTGCCGGGAGACACCCAAGGGGGGTATTGCCTGTGAATGCCGTCCTGGCTTTGAGCT TACCAAGAACCAACGGGACTGTAAATTGACATGCAACTATGGTAACGGCGGCTGCCAGCACACGTGTGATGACACAGAGC GAGACCTGTGCTGTCAACAACGGGGGCTGTGACAGTAAGTGCCATGATGCAGCGACTGGTGTCCACTGCACCTGCCCTGT GGGCTTCATGCTGCAGCCAGACAGGAAGACGTGCAAAGATATAGATGAGTGCCGCTTAAACAACGGGGGCTGTGACCATA TTTGCCGCAACACAGTGGGCAGCTTCGAATGCAGTTGCAAGAAAGGCTATAAGCTTCTCATCAATGAGAGGAACTGCCAG GATATAGACGAGTGTTCCTTTGATCGAACCTGTGACCACATATGTGTCAACACACCAGGAAGCTTCCAGTGTCTCTGCCA TCGTGGCTACCTGTTGTATGGTATCACCCACTGTGGGGATGTGGATGAATGCAGCATCAACCGGGGAGGTTGCCGCTTTG GCTGCATCAACACTCCTGGCAGCTACCAGTGTACCTGCCCAGCAGGCCAGGGTCGGCTGCACTGGAATGGCAAAGATTGC ACAGAGCCACTGAAGTGTCAGGGCAGTCCTGGGGCCTCGAAAGCCATGCTCAGCTGCAACCGGTCTGGCAAGAAGGACAC CTGTGCCCTGACCTGTCCCTCCAGGGCCCGATTTTTGCCAGAGGCTGCAGTGCTGTCCATTAAACAACGGGCCTCCTTCA AGATCAAGGATGCCAAATGCCGTTTGCACCTGCGAAACAAAGGCAAAACAGAGGAGGCTGGCAGAACCACAGGGCCAGGT GGTGCCCCCTGCTCTGAATGCCAGGTCACCTTCATCCACCTTAAGTGTGACTCCTCTCGGAAGGGCAAGGGCCGACGGGC CCGGACCCCTCCAGGCAAAGAGGTCACAAGGCTCACCCTGGAACTGGAGGCAGAGGTCAGAGCCGAAGAAACCACAGCCA GCTGTGGGCTGCCCTGCCTCCGACAGCGAATGGAACGGCGGCTGAAAGGATCCCTGAAGATGCTCAGAAAGTCCATCAAC CAGGACCGCTTCCTGCTGCGCCTGGCAGGCCTTGATTATGAGCTGGCCCACAAGCCGGGCCTGGTAGCCGGGGAGCGAGC AGAGCCGATGGAGTCCTGTAGGCCCGGGCAGCACCGTGCTGGGACCAAGTGTGTCAGCTGCCCGCAGGGAACGTATTACC ACGGCCAGACGGAGCAGTGTGTGCCATGCCCAGCGGGCACCTTCCAGGAGAGAGAAGGGCAGCTCTCCTGCGACCTTTGC CCTGGGAGTGATGCCCACGGGCCTCTTGGAGCCACCAACGTCACCACGTGTGCAGGTCAGTGCCCACCTGGCCAACACTC TGTAGATGGGTTCAAGCCCTGTCAGCCATGCCCACGTGGCACCTACCAACCTGAAGCAGGACGGACCCTATGCTTCCCTT GTGGTGGGGGCCTCACCACCAAGCATGAAGGGGCCATTTCCTTCCAAGACTGTGACACCAAAGTCCAGTGCTCCCCAGGG CACTACTACAACACCAGCATCCACCGCTGTATTCGCTGTGCCATGGGCTCCTATCAGCCCGACTTCCGTCAGAACTTCTG CAGCCGCTGTCCAGGAAACACAAGCACAGACTTTGATGGCTCTACCAGTGTGGCCCAATGCAAGAATCGTCAGTGTGGTG GGGAGCTGGGTGAGTTCACTGGCTATATTGAGTCCCCCAACTACCCGGGCAACTACCCAGCTGGTGTGGAGTGCATCTGG AACATCAACCCCCCACCCAAGCGCAAGATCCTTATCGTGGTACCAGAGATCTTCCTGCCATCTGAGGATGAGTGTGGGGA CGTCCTCGTCATGAGAAAGAACTCATCCCCATCCTCCATTACCACTTATGAGACCTGCCAGACCTACGAGCGTCCCATTG CCTTCACTGCCCGTTCCAGGAAGCTCTGGATCAACTTCAAGACAAGCGAGGCCAACAGCGCCCGTGGCTTCCAGATTCCC TATGTTACCTATGATGAGGACTATGAGCAGCTGGTAGAAGACATTGTGCGAGATGGCCGGCTCTATGCCTCTGAAAACCA CCAGGAGATTTTAAAGGACAAGAAGCTCATCAAGGCCTTCTTTGAGGTGCTAGCCCACCCCCAGAACTACTTCAAGTACA CAGAGAAACACAAGGAGATGCTGCCAAAATCCTTCATCAAGCTGCTCCGCTCCAAAGTTTCCAGCTTCCTGAGGCCCTAC AAATAGTAACCCTAGGCTCAGAGACCCAATTTTTTAAGCCCCCAGACTCCTTAGCCCTCAGAGCCGGCAGCCCCCTACCC TCAGACAAGGAACTCTCTCCTCTCTTTTTGGAGGGAAAAAAAAATATCACTACACAAACCAGGCACTCTCCCTTTCTGTC TTTCTAGTTTCCTTTCCTTGTCTCTCTCTGCCTGCCTCTCTACTGTTCCCCCTTTTCTAACACACTACCTAGAAAAGCCA TTCAGTACTGGCTCTAGTCCCCGTGAGATGTAAAGAAACAGTACAGCCCCTTCCACTGCCCATTTTACCAGCTCACATTC CCGACCCCATCAGCTTGGAAGGGTGCTAGAGGCCCATCAAGGAAGTGGGTCTGGTGGGAAACGGGGAGGGGAAAGAAGGG CTTCTGCCATTATAGGGTTGTGCCTTGCTAGTCAGGGGCCAAAATGTCCCCTGGCTCTGCTCCCTAGGGTGATTCTAACA GCCCAGGGTCCTGCCAAAGAAGCCTTTGATTTACAGGCTTAATGCCAGCACCAGTCCTCTGGGGCACATGGTTTGAGCTC TGGACTTCCCACATGGCCAGCTTTCTTGTCTATACAGATCCTCTCTTTCTTTCCCTACGTCTGCCTGGGGTCTACTCCAT AAGGGTTTACAAATGGCCCACAACACTGAGTTAGTGGACACCGGCTAAATGAGGAAGAGCAGCAGGCATTGTCATGGTGA ATGCCCCGCTGTAGCTCCCTGAGAGAAAGACTGTAACTCTGCAGGACAGAAACAAGGTTTTAAAGCATTGCCAAAAAAAA AGAAAACAGAAAGAAAAAATGTATCATCTAAAGGTCTAGACACAGAACAATTGGAAGTCAACTTCAAACACTAATCCCTT TTCTTGTCTTCCCTGGCCCAGCCACCTCCTCAGCCCCATGTGATGCTCCCTGGGGGAGCCCTACTCCCCTTGCTACATGT TGTCCTTAAACATGGTTATTGACCTGAAGCCAGCCTAGGCCTTGCCCTACAGTTGTTTTTCCCTTGTAGCCCCAGCTGGC TTGTGGGCTTCACCAAAGAGGACCCCACTCTGAAGCCAGCCTGGAGCCACCTACCTCTGGCCTCAGGCTGTGGGCAGCAA AAGGAATGTGTGTGCACTTGGCGAGCCTCCTGCCCACCCTGTCCACACCTAATAAGTGCAATCATTTTGAGTCTTTCTAT GTTGTCTAGACGGAGGGGTTTTTGTTTTCTGGGTTTGTTTTTTGTTTTTGTTTCTTCTTCCTCTATTAGCAAAACCCTAT TTATAGCTGCCCAAGAGAAAAGAGTGTATGTTTGGAGTGGAAGAAAATCGGTTTTGAATCTCATGAACCTTGAGTGCTGG AGCATCTGATCTGTCTCTATGCCACCACTGGCCACCTAGAGCCCTTGGCTGTGGTAATCCAGGGTAATTGCGCAGAGGCA TCTGATGTGTAGGAAAGTAATTCTGGGGATTTGATGGAGCAGAAAGGAGAGAGACCTATGTTTGCTAAACCAATCTTGCT ATCCCTATGCCTCTCCATGGAGTCAGTGTGGACCTCATGA (SEQ ID NO: 9)

TABLE 6B: The Amino Acid sequence of POLY5

MVTAAASTRVMTQSETCAVNNGGCDSKCHDAATGVHCTCPVGFMLQPDRKTCKDIDECRLNNGGCDHICRNTVGSF ECSCKKGYKLLINERNCQDIDECSFDRTCDHICVNTPGSFQCLCHRGYLLYGITHCGDVDECSINRGGCRFGCINT PGSYQCTCPAGQGRLHWNGKDCTEPLKCQGSPGASKAMLSCNRSGKKDTCALTCPSRARFLPEAAVLSIKQRASFK IKDAKCRLHLRNKGKTEEAGRTTGPGGAPCSECQVTFIHLKCDSSRKGKGRRARTPPGKEVTRLTLELEAEVRAEE TTASCGLPCLRQR ERRLKGSLKMLRKSINQDRFLLRLAGLDYELAHKPGLVAGERAEPMESCRPGQHRAGTKCVS CPQGTYYHGQTEQCVPCPAGTFQEREGQLSCDLCPGSDAHGPLGATNVTTCAGQCPPGQHSVDGFKPCQPCPRGTY QPEAGRTLCFPCGGGLTTKHEGAISFQDCDTKVQCSPGHYYNTSIHRCIRCAMGSYQPDFRQNFCSRCPGNTSTDF DGSTSVAQCKNRQCGGELGEFTGYIESPNYPGNYPAGVECIWNINPPPKRKILIVVPEIFLPSEDECGDVLVMRKN SSPSSITTYETCQTYERPIAFTARSRKLWINFKTSEANSARGFQIPYVTYDEDYEQLVEDIVRDGRLYASENHQEI LKDKKLIKAFFEVLAHPQNYFKYTEKHKEMLPKSFIKLLRSKVSSFLRPYK (SEQ ID NO: 10)

The predicted amino acid sequences was searched in the publicly available GenBank database. POLY5, as disclosed in this invention, has 72 of 160 amino acids (45%) identical to a Caenorhabditis elegans Y64G10A.7 protein (ACC:CAB57911; 1664 aa), and 69 of 169 amino acids (40%) identical and 99 of 169 amino acids (58%) homology to a Homo sapiens fibrillin 5 protein (NCC:CAB56757; 754 aa, fragment). POLY5 also has 273 of 392 amino acids (69%) identical and 322 of 392 amino acids positive to Breast Cancer Protein BCO2 from Homo sapiens (Table 6C).

TABLE 6C: BLASTX of POLY5 against Breast Cancer Protein BCO2 (SEQ ID ΝO:39^

Scδre = 1539 ( 541 . 8 bits ) , Expect = 3 . 9e-157 , P = 3 . 9e-157 Identities = 273/392 ( 69% ) , Positives = 322/392 ( 82 % ) , Frame = +1

Query : 1711 LDYELAHKPGLVAGERAEPMESCRPGQHRAGTKCVSCPQGTYYHGQTEQCVPCPAGTFQE 1890

++ ++1 I I + +11 II II I +1 I I I I I I I I 1 + 1+ I I I I I I

SlbΘct : 1 MNLDVAKKPPRTSERQAE SCGVGQGHAENQCVSCRAGTYYDGARERCILCPNGTFQN 57

Query: 1891 REGQLSCDLCPGSDAHGPLG ATNVTTCAGQCPPGQHSVDGFKPCQPCPRGTYQPEAG 2061

I I I++I+ I I I I 1 I++ I I I I ++1 I I 1 I I I I I +1 I I I I

Sbjct: 58 EEGQMTCEPCPRPGNSGALKTPEAWNMSECGGLCQPTEYSADGFAPCQLCALGXFQPEAG 117

15

Query: 2062 RTLCFPCGGGLTTKHEGAISFQDCDTKVQCSPGHYYNTSIHRCIRCAMGSYQPDFRQNFC 2241

II IIIIIIII I I I + l I 1 I I I l + l + l I I I I I I + l I 1+ I I I I I I +1 + 1 I 1 + 1 +1 I

Sbjct: 118 RTSCFPCGGGLATKHQGATSFQDCETRVQCSPGHFYNTTTHRCIRCPVGTYQPEFGKNNC 177 Q2θry: 2242 SRCPGNTSTDFDGSTSVAQCKNRQCGGELGEFTGYIESPNYPGNYPAGVECIWNINPPPK 2421

I II I 1 + 1 I I I I I I++ I I I I I + l 1 I 1 I I + l I I I I I I I I I I I I 1 I I II I I I I I I 1

Sbjct: 178 VSCPGNTTTDFDGSTNITQCKNRRCGGELGDFTGYIESPNYPGNYPANTECTWTINPPPK 237

Query: 2422 RKILIVVPEIFLPSEDECGDVLVMRKNSSPSSITTYETCQTYERPIAFTARSRKL INFK 2601 25 I + 1 I I I I I I I I I I I I + 1 I I UNI II +I + IIIII11III1IIIII + II + II1I II

Sbjct: 238 RRILIVVPEIFLPIEDDCGDYLVMRKTSSSNSVTTYETCQTYERPIAFTSRSKKL IQFK 297

Query: 2602 TSEANSARGFQIPYVTYDEDYEQLVEDIVRDGRLYASENHQEILKDKKLIKAFFEVLAHP 2781

++I I I I 11 I I + l I I I I I 11 I++I + I I I I I I I I I I I I I I I I 1 I I I I I I I I I I I + l I I I I

Sβ(j)ct: 298 SNEGNSARGFQVPYVTYDEDYQELIEDIVRDGRLYASENHQEILKDKKLIKALFDV AHP 357

Query: 2782 QNYFKYT-EKHKE LPKSFIKLLRSKVSSFLRPYK 2883

I I 1 I I II ++ +1 I I + l I I + l I I I I I I III Ml Sbjct: 358 QNYFKYTAQESRE FPRSFIRLLRSKVSRFLRPYK 392 (SEQIDNO:39)

35

POLY5 also has high homology to the polypeptides shown in the BLASTX data in Table 6D.

Table 6D. BLASTX alignments of POLY5

Sequences producing High-scoring Segment Pairs: Smallest Sum Reading High Prob. Frame Score P(N) N patp:Y07735 Human breast-specific BS200 protein - Homo.+l 732 1 , . 4e-177 1 patp:B00192 Breast cancer protein BC02 - Homo sapiens,. +1 539 3 . . 9e-157 1 patp:B43170 Human ORFX ORF2934 polypeptide sequence SE.+l 682 4 . . 2e-65 1 patp: 99016 Human matrilin-3 - Homo sapiens, 632 aa . +3 382 1 . , 8e-54 2 patp:Y13350 Amino acid sequence of protein PR0219 - Ho.+l 358 2 . .7e-53 2 patp:Y95340 Human PR0219 antitumour protein - Homo sap.+l 358 2.7e-53

PSORT analysis demonstrates that POLY5 is most likely located in the mitochondrial matrix space (certainty=0.7394). SIGNALP analysis is suggests that POLY5 has no N- terminal signal sequence. The predicted molecular weight of POLY5 is 81198.4 daltons.

POLY 6

A polynucleotide ofthe present invention has been identified as clone Z97832_B.0.707 (POLY6). POLY6 is a full-length clone of 4821 nucleotides, including the entire coding sequence of a 845 amino acid protein from nucleotides 730 to 3265. The nucleotide sequence of POLY6 (SEQ ID NO: 11) as presently determined is reported in TABLE 7 A. The predicted amino acid sequence of POLY6 (SEQ ID NO: 12) corresponding to the foregoing nucleotide sequence is reported in TABLE 7B.

TABLE 7A: The Nucleotide sequence of POLY6

TCATGAGGTCCACACTGACTCCATGGAGAGGCATAGGGATAGCAAGATTGGTTTAGCAAACATAGGTCTCTCTCCTTTCT GCTCCATCAAATCCCCAGAATTACTTTCCTACACATCAGATGCCTCTGCGCAATTACCCTGGATTACCACAGCCAAGGGC TCTAGGTGGCCAGTGGTGGCATAGAGACAGATCAGATGCTCCAGCACTCAAGGTTCATGAGATTCAAAACCGATTTTCTT CCACTCCAAACATACACTCTTTTCTCTTGGGCAGCTATAAATAGGGTTTTGCTAATAGAGGAAGAAGAAACAAAAACAAA AAACAAACCCAGAAAACAAAAACCCCTCCGTCTAGACAACATAGAAAGACTCAAAATGATTGCACTTATTAGGTGTGGAC AGGGTGGGCAGGAGGCTCGCCAAGTGCACACACATTCCTTTTGCTGCCCACAGCCTGAGGCCAGAGGTAGGTGGCTCCAG GCTGGCTTCAGAGTGGGGTCCTCTTTGGTGAAGCCCACAAGCCAGCTGGGGCTACAAGGGAAAAACAACTGTAGGGCAAG GCCTAGGCTGGCTTCAGGTCAATAACCATGTTTAAGGACAACATGTAGCAAGGGGAGTAGGGCTCCCCCAGGGAGCATCA CATGGGGCTGAGGAGGTGGCTGGGCCAGGGAAGACAAGAAAAGGGATTAGTGTTTGAAGTTGACTTCCAATTGTTCTGTG TCTAGACCTTTAGATGATACATTTTTTCTTTCTGTTTTCTTTTTTTTTGGCAATGCTTTAAAACCTTGTTTCTGTCCTGC AGAGTTACAGTCTTTCTCTCAGGGAGCTACAGCGGGGCATTCACCATGACAATGCCTGCTGCTCTTCCTCATTTAGCCGG TGTCCACTAACTCAGTGTTGTGGGCCATTTGTAAACCCTTATGGAGTAGACCCCAGGCAGACGTAGGGAAAGAAAGAGAG GATCTGTATAGACAAGAAAGCTGGCCATGTGGGAAGTCCAGAGCTCAAACCATGTGCCCCAGAGGACTGGTGCTGGCATT AAGCCTGTAAATCAAAGGCTTCTTTGGCAGGACCCTGGGCTGTTAGAATCACCCTAGGGAGCAGAGCCAGGGGACATTTT GGCCCCTGACTAGCAAGGCACAACCCTATAATGGCAGAAGCCCTTCTTTCCCCTCCCCGTTTCCCACCAGACCCACTTCC TTGATGGGCCTCTAGCACCCTTCCAAGCTGATGGGGTCGGGAATGTGAGCTGGTAAAATGGGCAGTGGAAGGGGCTGTAC TGTTTCTTTACATCTCACGGGGACTAGAGCCAGTACTGAATGGCTTTTCTAGGTAGTGTGTTAGAAAAGGGGGAACAGTA GAGAGGCAGGCAGAGAGAGACAAGGAAAGGAAACTAGAAAGACAGAAAGGGAGAGTGCCTGGTTTGTGTAGTGATATTTT TTTTTCCCTCCAAAAAGAGAGGAGAGAGTTCCTTGTCTGAGGGTAGGGGGCTGCCGGCTCTGAGGGCTAAGGAGTCTGGG GGCTTAAAAAATTGGGTCTCTGAGCCTAGGGTTACTATTTGTAGGGCCTCAGGAAGCTGGAAACTTTGGAGCGGAGCAGC TTGATGAAGGATTTTGGCAGCATCTCCTTGTGTTTCTCTGTGTACTTGAAGTAGTTCTGGGGGTGGGCTAGCACCTCAAA GAAGGCCTTGATGAGCTTCTTGTCCTTTAAAATCTCCTGGTGGTTTTCAGAGGCATAGAGCCGGCCATCTCGCACAATGT CTTCTACCAGCTGCTCATAGTCCTCATCATAGGTAACATAGGGAATCTGGAAGCCACGGGCGCTGTTGGCCTCGCTTGTC TTGAAGTTGATCCAGAGCTTCCTGGAACGGGCAGTGAAGGCAATGGGACGCTCGTAGGTCTGGCAGGTCTCATAAGTGGT AATGGAGGATGGGGATGAGTTCTTTCTCATGACGAGGACGTCCCCACACTCATCCTCAGATGGCAGGAAGATCTCTGGTA CCACGATAAGGATCTTGCGCTTGGGTGGGGGGTTGATGTTCCAGATGCACTCCACACCAGCTGGGTAGTTGCCCGGGTAG TTGGGGGACTCAATATAGCCAGTGAACTCACCCAGCTCCCCACCACACTGACGATTCTTGCATTGGGCCACACTGGTAGA GCCATCAAAGTCTGTGCTTGTGTTTCCTGGACAGCGGCTGCAGAAGTTCTGACGGAAGTCGGGCTGATAGGAGCCCATGG CACAGCGAATACAGCGGTGGATGCTGGTGTTGTAGTAGTGCCCTGGGGAGCACTGGACTTTGGTGTCACAGTCTTGGAAG GAAATGGCCCCTTCATGCTTGGTGGTGAGGCCCCCACCACAAGGGAAGCATAGGGTCCGTCCTGCTTCAGGTTGGTAGGT GCCACGTGGGCATGGCTGACAGGGCTTGAACCCATCTACAGAGTGTTGGCCAGGTGGGCACTGACCTGCACACGTGGTGA CGTTGGTGGCTCCAAGAGGCCCGTGGGCATCACTCCCAGGGCAAAGGTCGCAGGAGAGCTGCCCTTCTCTCTCCTGGAAG GTGCCCGCTGGGCATGGCACACACTGCTCCGTCTGGCCGTGGTAATACGTTCCCTGCGGGCAGCTGACACACTTGGTCCC AGCACGGTGCTGCCCGGGCCTACAGGACTCCATCGGCTCTGCTCGCTCCCCGGCTACCAGGCCCGGCTTGTGGGCCAGCT CATAATCAAGGCCTGCCAGGCGCAGCAGGAAGCGGTCCTGGTTGATGGACTTTCTGAGCATCTTCAGGGATCCTTTCAGC CGCCGTTCCATTCGCTGTCGGAGGCAGGGCAGCCCACAGCTGGCTGTGGTTTCTTCGGCTCTGACCTCTGCCTCCAGTTC CAGGGTGAGCCTTGTGACCTCTTTGCCTGGAGGGGTCCGGGCCCGTCGGCCCTTGCCCTTCCGAGAGGAGTCACACTTAA GGTGGATGAAGGTGACCTGGCATTCAGAGCAGGGGGCACCACCTGGCCCTGTGGTTCTGCCAGCCTCCTCTGTTTTGCCT TTGTTTCGCAGGTGCAAACGGCATTTGGCATCCTTGATCTTGAAGGAGGCCCGTTGTTTAATGGACAGCACTGCAGCCTC TGGCAAAAATCGGGCCCTGGAGGGACAGGTCAGGGCACAGGTGTCCTTCTTGCCAGACCGGTTGCAGCTGAGCATGGCTT TCGAGGCCCCAGGACTGCCCTGACACTTCAGTGGCTCTGTGCAATCTTTGCCATTCCAGTGCAGCCGACCCTGGCCTGCT GGGCAGGTACACTGGTAGCTGCCAGGAGTGTTGATGCAGCCAAAGCGGCAACCTCCCCGGTTGATGCTGCATTCATCCAC ATCCCCACAGTGGGTGATACCATACAACAGGTAGCCACGATGGCAGAGACACTGGAAGCTTCCTGGTGTGTTGACACATA TGTGGTCACAGGTTCGATCAAAGGAACACTCGTCTATATCCTGGCAGTTCCTCTCATTGATGAGAAGCTTATAGCCTTTC TTGCAACTGCATTCGAAGCTGCCCACTGTGTTGCGGCAAATATGGTCACAGCCCCCGTTGTTTAAGCGGCACTCATCTAT ATCTTTGCACGTCTTCCTGTCTGGCTGCAGCATGAAGCCCACAGGGCAGGTGCAGTGGACACCAGTCGCTGCATCATGGC ACTTACTGTCACAGCCCCCGTTGTTGACAGCACAGGTCTCATTAGAAACGGCTTGAGTGGGGATGTGCTGCTCTAGCCGC CTTTCCCCGATGCATGTCTTCCCGTCGGTATGGAGCACAAACTTGATATGGCAGCCGCACCGGGGACCCTGCTCTGTGTC ATCACACGTGTGCTGGCAGCCGCCGTTACCATAGTTGCATGTCAATTTACAGTCCCGTTGGTTCTTGGTAAGCTCAAAGC CAGGACGGCATTCACAGGCAATACCCCCCTTGGGTGTCTCCCGGCAAATGTGGGCACAGCCGTGGTTCTTGTTCATGCAA TTCATTCCTTCTTCTGGCCGCTGGATACAGGTATGCTGGTTGTCGCTGAGGAAGAAGCCTTCCCGGCAGTGGCACTCATA GCTGCCCATCATGTTGACACAGCTCTGCTGACAGCCGCCGTTGCCCTCGGCACACTCGTCCACATCCAGACAGTTGTGTC CGTCATGTGCCAGGTGGAATCCATCATAGCAGGTACACCGGTAATTGCCAGGGATGTTGACACAGTCATGCACACAACCT GCATTATCCTCTCGCTCGCACTCATCCACGTCTTTGCAGTGTTTGCCGTCCCCTGTGTAGCCAGACTTGCAGATGCACTT GTATGACCTCGGGGTGTTCTGGCAGATAGCATCGATGTGGCAGTTGTCAGTCCCCTCCACACACTCATCCACATCTGGCA GGGGCAGAGGGGGCACATGAGAACCTCTGTTGGCACCTCTTAAGGGGTGTCTTGAAGGTGGGCTTCCAAGGGCAGAATCC CCTCTTCTCTAAAACAGAGGCAGTGACCCCCTCCAGAAACAGGTGCTGTCTCACATCTCTCTGATTTCAGAGTAGGCAGA CACTGATTTTGGGAATTCAGAAGGAACCCCCACTGCCCTCAAAAATACTAAATTCACAGTGACAGCTAAAACTCCATCAT TCGAAACACTCCTTTTTTTATTTGAAAACAAACAAAAAACCCTTAGAGTGGGTAGTACACTTAACTTGATTAGGAATAAT CAACTTAAAGTGAATGAGTTTACGGAGAAGGCTTAGAGGGAAAGTTAAGGGAAAAGGCATGGGAACAGTGGTCTCTGGGA AGGTGGCAGGGTCCAGCAATC (SEQ ID NO: 11)

TABLE 7B: The Amino Acid sequence of POLY6

MMGSYECHCREGFFLSDNQHTCIQRPEEGMNCMNKNHGCAHICRETPKGGIACECRPGFELTKNQRDCK TCNYGN GGCQHTCDDTEQGPRCGCHIKFVLHTDGKTCIGERRLEQHIPTQAVSNETCAVNNGGCDSKCHDAATGVHCTCPVG FMLQPDRKTCKDIDECRLNNGGCDHICRNTVGSFECSC KGYKLLINERNCQDIDECSFDRTCDHICVNTPGSFQC LCHRGYLLYGITHCGDVDECSINRGGCRFGCINTPGSYQCTCPAGQGRLH NGKDCTEPLKCQGSPGASKAMLSCN RSGKKDTCALTCPSRARFLPEAAVLSIKQRASFKIKDAKCRLHLRNKGKTEEAGRTTGPGGAPCSECQVTFIHLKC DSSRKG GRRARTPPGKEVTRLTLELEAEVRAEETTASCGLPCLRQRMERRLKGS KMLRKSINQDRFLLRLAGLD YELAHKPGLVAGERAEPMESCRPGQHRAGTKCVSCPQGTYYHGQTEQCVPCPAGTFQEREGQLSCDLCPGSDAHGP LGATNVTTCAGQCPPGQHSVDGFKPCQPCPRGTYQPEAGRTLCFPCGGGLTTKHEGAISFQDCDT VQCSPGHYYN TSIHRCIRCAMGSYQPDFRQNFCSRCPGNTSTDFDGSTSVAQCKNRQCGGELGEFTGYIESPNYPGNYPAGVECIW NINPPPKRKILIVVPEIFLPSEDECGDVLVMRKNSSPSSITTYETCQTYERPIAFTARSRKLWINFKTSEANSARG FQIPYVTYDEDYEQLVEDIVRDGRLYASENHQEILKDKKLIKAFFEVLAHPQNYFKYTEKHKEM PKSFIKLLRSK VSSFLRPYK (SEQ ID NO: 12)

POLY6 as disclosed in this invention invention has 112 of 280 amino acids (40%) identical to a Caenorhabditis elegans Y64G10A.7 protein (ACC:CAB57911; 1664 aa), and 106 of 304 amino acids (34%) identical and 154 of 304 amino acids (50%) homology to a Homo sapiens hypothetical 82.9 kD protein (ACC:CAB70853; 741 aa, fragment).

PSORT analysis demonstrates that POLY6 is most likely located in the nucleus (certainty= 0.7000). SIGNALP analysis suggests that POLY6 has no N-terminal signal sequence. The predicted molecular weight of POLY6 is 93653.3 daltons.

POLY7

A polynucleotide ofthe present invention has been identified as clone Z97832_B_1 (POLY7). POLY7 is a full-length clone of 4550 nucleotides, including the entire coding sequence of a 974 amino acid protein from nucleotides 72 to 2994. The nucleotide sequence of POLY7 (SEQ ID NO: 13) as presently determined is reported in TABLE 8 A. The predicted amino acid sequence of POLY7 (SEQ ID NO: 14) corresponding to the foregoing nucleotide sequence is reported in TABLE 8B.

TABLE 8A: The nucleotide sequence of POLY7

CACGAGCCGGCTTCCGCCCTCCCCTGGCCGCGAGACCGGCCCCGGCGGCTGGGCCGCCAGTAGCTCCAGCCATGGGCTCG

GGGCGCGTACCCGGGCTCTGCCTGCTTGTCCTGCTGGTCCACGCCCGCGCCGCCCAGTACAGCAAAGCCGCGCAAGATGT GGATGAGTGTGTGGAGGGGACTGACAACTGCCACATCGATGCTATCTGCCAGAACACCCCGAGGTCATACAAGTGCATCT GCAAGTCTGGCTACACAGGGGACGGCAAACACTGCAAAGACGTGGATGAGTGCGAGCGAGAGGATAATGCAGGTTGTGTG CATGACTGTGTCAACATCCCTGGCAATTACCGGTGTACCTGCTATGATGGATTCCACCTGGCACATGACGGACACAACTG TCTGGATGTGGACGAGTGTGCCGAGGGCAACGGCGGCTGTCAGCAGAGCTGTGTCAACATGATGGGCAGCTATGAGTGCC ACTGCCGGGAAGGCTTCTTCCTCAGCGACAACCAGCATACCTGTATCCAGCGGCCAGAAGAAGGAATGAATTGCATGAAC AAGAACCACGGCTGTGCCCACATTTGCCGGGAGACACCCAAGGGGGGTATTGCCTGTGAATGCCGTCCTGGCTTTGAGCT TACCAAGAACCAACGGGACTGTAAATTGACATGCAACTATGGTAACGGCGGCTGCCAGCACACGTGTGATGACACAGAGC AGGGTCCCCGGTGCGGCTGCCATATCAAGTTTGTGCTCCATACCGACGGGAAGACATGCATCGGGGAAAGGCGGCTAGAG CAGCACATCCCCACTCAAGCCGTTTCTAATGAGACCTGTGCTGTCAACAACGGGGGCTGTGACAGTAAGTGCCATGATGC AGCGACTGGTGTCCACTGCACCTGCCCTGTGGGCTTCATGCTGCAGCCAGACAGGAAGACGTGCAAAGATATAGATGAGT GCCGCTTAAACAACGGGGGCTGTGACCATATTTGCCGCAACACAGTGGGCAGCTTCGAATGCAGTTGCAAGAAAGGCTAT AAGCTTCTCATCAATGAGAGGAACTGCCAGGATATAGACGAGTGTTCCTTTGATCGAACCTGTGACCACATATGTGTCAA CACACCAGGAAGCTTCCAGTGTCTCTGCCATCGTGGCTACCTGTTGTATGGTATCACCCACTGTGGGGATGTGGATGAAT GCAGCATCAACCGGGGAGGTTGCCGCTTTGGCTGCATCAACACTCCTGGCAGCTACCAGTGTACCTGCCCAGCAGGCCAG GGTCGGCTGCACTGGAATGGCAAAGATTGCACAGAGCCACTGAAGTGTCAGGGCAGTCCTGGGGCCTCGAAAGCCATGCT CAGCTGCAACCGGTCTGGCAAGAAGGACACCTGTGCCCTGACCTGTCCCTCCAGGGCCCGATTTTTGCCAGAGGCTGCAG TGCTGTCCATTAAACAACGGGCCTCCTTCAAGATCAAGGATGCCAAATGCCGTTTGCACCTGCGAAACAAAGGCAAAACA GAGGAGGCTGGCAGAACCACAGGGCCAGGTGGTGCCCCCTGCTCTGAATGCCAGGTCACCTTCATCCACCTTAAGTGTGA CTCCTCTCGGAAGGGCAAGGGCCGACGGGCCCGGACCCCTCCAGGCAAAGAGGTCACAAGGCTCACCCTGGAACTGGAGG CAGAGGTCAGAGCCGAAGAAACCACAGCCAGCTGTGGGCTGCCCTGCCTCCGACAGCGAATGGAACGGCGGCTGAAAGGA TCCCTGAAGATGCTCAGAAAGTCCATCAACCAGGACCGCTTCCTGCTGCGCCTGGCAGGCCTTGATTATGAGCTGGCCCA CAAGCCGGGCCTGGTAGCCGGGGAGCGAGCAGAGCCGATGGAGTCCTGTAGGCCCGGGCAGCACCGTGCTGGGACCAAGT GTGTCAGCTGCCCGCAGGGAACGTATTACCACGGCCAGACGGAGCAGTGTGTGCCATGCCCAGCGGGCACCTTCCAGGAG AGAGAAGGGCAGCTCTCCTGCGACCTTTGCCCTGGGAGTGATGCCCACGGGCCTCTTGGAGCCACCAACGTCACCACGTG TGCAGGTCAGTGCCCACCTGGCCAACACTCTGTAGATGGGTTCAAGCCCTGTCAGCCATGCCCACGTGGCACCTACCAAC CTGAAGCAGGACGGACCCTATGCTTCCCTTGTGGTGGGGGCCTCACCACCAAGCATGAAGGGGCCATTTCCTTCCAAGAC TGTGACACCAAAGTCCAGTGCTCCCCAGGGCACTACTACAACACCAGCATCCACCGCTGTATTCGCTGTGCCATGGGCTC CTATCAGCCCGACTTCCGTCAGAACTTCTGCAGCCGCTGTCCAGGAAACACAAGCACAGACTTTGATGGCTCTACCAGTG TGGCCCAATGCAAGAATCGTCAGTGTGGTGGGGAGCTGGGTGAGTTCACTGGCTATATTGAGTCCCCCAACTACCCGGGC AACTACCCAGCTGGTGTGGAGTGCATCTGGAACATCAACCCCCCACCCAAGCGCAAGATCCTTATCGTGGTACCAGAGAT CTTCCTGCCATCTGAGGATGAGTGTGGGGACGTCCTCGTCATGAGAAAGAACTCATCCCCATCCTCCATTACCACTTATG AGACCTGCCAGACCTACGAGCGTCCCATTGCCTTCACTGCCCGTTCCAGGAAGCTCTGGATCAACTTCAAGACAAGCGAG GCCAACAGCGCCCGTGGCTTCCAGATTCCCTATGTTACCTATGATGAGGACTATGAGCAGCTGGTAGAAGACATTGTGCG AGATGGCCGGCTCTATGCCTCTGAAAACCACCAGGAGATTTTAAAGGACAAGAAGCTCATCAAGGCCTTCTTTGAGGTGC TAGCCCACCCCCAGAACTACTTCAAGTACACAGAGAAACACAAGGAGATGCTGCCAAAATCCTTCATCAAGCTGCTCCGC TCCAAAGTTTCCAGCTTCCTGAGGCCCTACAAATAGTAACCCTAGGCTCAGAGACCCAATTTTTTAAGCCCCCAGACTCC TTAGCCCTCAGAGCCGGCAGCCCCCTACCCTCAGACAAGGAACTCTCTCCTCTCTTTTTGGAGGGAAAAAAAAATATCAC TACACAAACCAGGCACTCTCCCTTTCTGTCTTTCTAGTTTCCTTTCCTTGTCTCTCTCTGCCTGCCTCTCTACTGTTCCC CCTTTTCTAACACACTACCTAGAAAAGCCATTCAGTACTGGCTCTAGTCCCCGTGAGATGTAAAGAAACAGTACAGCCCC TTCCACTGCCCATTTTACCAGCTCACATTCCCGACCCCATCAGCTTGGAAGGGTGCTAGAGGCCCATCAAGGAAGTGGGT CTGGTGGGAAACGGGGAGGGGAAAGAAGGGCTTCTGCCATTATAGGGTTGTGCCTTGCTAGTCAGGGGCCAAAATGTCCC CTGGCTCTGCTCCCTAGGGTGATTCTAACAGCCCAGGGTCCTGCCAAAGAAGCCTTTGATTTACAGGCTTAATGCCAGCA CCAGTCCTCTGGGGCACATGGTTTGAGCTCTGGACTTCCCACATGGCCAGCTTTCTTGTCTATACAGATCCTCTCTTTCT TTCCCTACGTCTGCCTGGGGTCTACTCCATAAGGGTTTACAAATGGCCCACAACACTGAGTTAGTGGACACCGGCTAAAT GAGGAAGAGCAGCAGGCATTGTCATGGTGAATGCCCCGCTGTAGCTCCCTGAGAGAAAGACTGTAACTCTGCAGGACAGA AACAAGGTTTTAAAGCATTGCCAAAAAAAAAGAAAACAGAAAGAAAAAATGTATCATCTAAAGGTCTAGACACAGAACAA TTGGAAGTCAACTTCAAACACTAATCCCTTTTCTTGTCTTCCCTGGCCCAGCCACCTCCTCAGCCCCATGTGATGCTCCC TGGGGGAGCCCTACTCCCCTTGCTACATGTTGTCCTTAAACATGGTTATTGACCTGAAGCCAGCCTAGGCCTTGCCCTAC AGTTGTTTTTCCCTTGTAGCCCCAGCTGGCTTGTGGGCTTCACC2\AAGAGGACCCCACTCTGAAGCCAGCCTGGAGCCAC CTACCTCTGGCCTCAGGCTGTGGGCAGCAAAAGGAATGTGTGTGCACTTGGCGAGCCTCCTGCCCACCCTGTCCACACCT AATAAGTGCAATCATTTTGAGTCTTTCTATGTTGTCTAGACGGAGGGGTTTTTGTTTTCTGGGTTTGTTTTTTGTTTTTG TTTCTTCTTCCTCTATTAGCAAAACCCTATTTATAGCTGCCCAAGAGAAAAGAGTGTATGTTTGGAGTGGAAGAAAATCG GTTTTGAATCTCATGAACCTTGAGTGCTGGAGCATCTGATCTGTCTCTATGCCACCACTGGCCACCTAGAGCCCTTGGCT GTGGTAATCCAGGGTAATTGCGCAGAGGCATCTGATGTGTAGGAAAGTAATTCTGGGGATTTGATGGAGCAGAAAGGAGA GAGACCTATGTTTGCTAAACCAATCTTGCTATCCCTATGCCTCTCCATGGAGTCAGTGTGGACCTCATGA (SE QID NO: 13)

TABLE 8B: The Amino Acid sequence of POLY7

MGSGRVPGLCLLVLLVHARAAQYSKAAQDVDECVEGTDNCHIDAICQNTPRSYKCICKSGYTGDGKHCKDVDECER EDNAGCVHDCVNIPGNYRCTCYDGFHLAHDGHNCLDVDECAEGNGGCQQSCVN MGSYECHCREGFFLSDNQHTCI QRPEEGMNCMNKNHGCAHICRETPKGGIACECRPGFELTKNQRDCKLTCNYGNGGCQHTCDDTEQGPRCGCHIKFV HTDGKTCIGERRLEQHIPTQAVSNETCAVNNGGCDSKCHDAATGVHCTCPVGFMLQPDRKTCKDIDECRLNNGGC DHICRNTVGSFECSCKKGYKLLINERNCQDIDECSFDRTCDHICVNTPGSFQCLCHRGYLLYGITHCGDVDECSIN RGGCRFGCINTPGSYQCTCPAGQGRLHWNGKDCTEPLKCQGSPGASKAMLSCNRSGKKDTCALTCPSRARFLPEAA VLSIKQRASFKIKDAKCRLHLRNKGKTEEAGRTTGPGGAPCSECQVTFIHLKCDSSRKGKGRRARTPPGKEVTRLT LELEAEVRAEETTASCGLPCLRQRMERRLKGSLKMLRKSINQDRFLLRLAGLDYELAHKPGLVAGERAEPMESCRP GQHRAGTKCVSCPQGTYYHGQTEQCVPCPAGTFQEREGQLSCDLCPGSDAHGPLGATNVTTCAGQCPPGQHSVDGF KPCQPCPRGTYQPEAGRTLCFPCGGGLTTKHEGAISFQDCDTKVQCSPGHYYNTSIHRCIRCAMGSYQPDFRQNFC SRCPGNTSTDFDGSTSVAQCKNRQCGGELGEFTGYIESPNYPGNYPAGVECI NINPPPKRKILIVVPEIFLPSED ECGDVLVMRKNSSPSSITTYETCQTYERPIAFTARSRKLWINFKTSEANSARGFQIPYVTYDEDYEQLVEDIVRDG RLYASENHQEILKDKKLIKAFFEVLAHPQNYFKYTEKHKEMLPKSFIKLLRSKVSSFLRPYK (SEQ ID NO:14)

POLY7 as disclosed in this invention has 145 of 355 amino acids (40%) identical to a Rattus norvegicus MEGF6 protein (ACC:O88281 ; 1574 aa), and 151 of 404 amino acids

(37%) identical and 205 of 404 amino acids (50%) homology to a Homo sapiens hypothetical 82.9 kD protein (ACC:CAB70853; 741 aa, fragment).

PSORT analysis demonstrates that POLY7 is most likely located outside ofthe cell (certainty^ 0.3700). SIGNALP analysis suggests that POLY7 has a cleavable N-term signal sequence with a most likely cleavage site between positions 21 and 22 of SEQ ID NO. 14. The predicted molecular weight of POLY7 is 107538.6 daltons. POLY 8

A polynucleotide ofthe present invention has been identified as clone CG55096-04 (POLY8). POLY8 is a full-length clone of 3177 nucleotides, including a coding sequence of a 1009 amino acid protein. The nucleotide sequence of POLY8 (SEQ ID NO: 15) as presently determined is reported in TABLE 9 A. The predicted amino acid sequence of POLY8 (SEQ ID NO: 16) corresponding to the foregoing nucleotide sequence is reported in TABLE 9B.

TABLE 9A The nucleotide sequence of POLY8.

CCCCTCCCCTCCCCCTCCTGCGAGCTGGGATCCGGCCGGCTTCCGCCCTCCCCTGGCCGCGAGACCGGCC CCGGCGGCTGGGCCGCCAGTAGCTCCAGCCATGGGCTCGGGGCGCGTACCCGGGCTCTGCCTGCTTGTCC TGCTGGTCCACGCCCGCGCCGCCCAGTACAGCAAAGCCGCGCAAGATGTGGATGAGTGTGTGGAGGGGAC TGACAACTGCCACATCGATGCTATCTGCCAGAACACCCCGAGGTCATACAAGTGCATCTGCAAGTCTGGC TACACAGGGGACGGCAAACACTGCAAAGACGTGGATGAGTGCGAGCGAGAGGATAATGCAGGTTGTGTGC ATGACTGTGTCAACATCCCTGGCAATTACCGGTGTACCTGCTATGATGGATTCCACCTGGCACATGACGG ACACAACTGTCTGGATGTGGACGAGTGTGCCGAGGGCAACGGCGGCTGTCAGCAGAGCTGTGTCAACATG ATGGGCAGCTATGAGTGCCACTGCCGGGAAGGCTTCTTCCTCAGCGACAACCAGCATACCTGTATCCAGC GGCCAGAAGAAGGAATGAATTGCATGAACAAGAACCACGGCTGTGCCCACATTTGCCGGGAGACACCCAA GGGGGGTATTGCCTGTGAATGCCGTCCTGGCTTTGAGCTTACCAAGAACCAACGGGACTGTAAATTGACA TGCAACTATGGTAACGGCGGCTGCCAGCACACGTGTGATGACACAGAGCAGGGTCCCCGGTGCGGCTGCC ATATCAAGTTTGTGCTCCATACCGACGGGAAGACATGCATCGGGGAAAGGCGGCTAGAGCAGCACATCCC CACTCAAGCCGTTTCTAATGAGACCTGTGCTGTCAACAACGGGGGCTGTGACAGTAAGTGCCATGATGCA GCGACTGGTGTCCACTGCACCTGCCCTGTGGGCTTCATGCTGCAGCCAGACAGGAAGACGTGCAAAGATA TAGATGAGTGCCGCTTAAACAACGGGGGCTGTGACCATATTTGCCGCAACACAGTGGGCAGCTTCGAATG CAGTTGCAAGAAAGGCTATAAGCTTCTCATCAATGAGAGGAACTGCCAGGATATAGACGAGCGTTCCTTT GATCGAACCTGTGACCACATATGTGTCAACACACCAGGAAGCTTCCAGTGTCTCTGCCATCGTGGCTACC TGTTGTATGGTATCACCCACTGTGGGGATGTGGATGAATGCAGCATCAACCGGGGAGGTTGCCGCTTTGG CTGCATCAACACTCCTGGCAGCTACCAGTGTACCTGCCCAGCAGGCCAGGGTCGGCTGCACTGGAATGGC AAAGATTGCACAGAGCCACTGAAGTGTCAGGGCAGTCCTGGGGCCTCGAAAGCCATGCTCAGCTGCAACC GGTCTGGCAAGAAGGACACCTGTGCCCTGACCTGTCCCTCCAGGGCCCGATTTTTGCCAGAGTCTGAGAA TGGCTTCACGGTGAGCTGTGGGACCCCCAGCCCCAGGGCTGCTCCAGCCCGAGCTGGCCACAATGGGAAC AGCACCAACTCCAACCACTGCCATGAGGCTGCAGTGCTGTCCATTAAACAACGGGCCTCCTTCAAGATCA AGGATGCCAAATGCCGTTTGCACCTGCGAAACAAAGGCAAAACAGAGGAGGCTGGCAGAATCACAGGGCC AGGTGGTGCCCCCTGCTCTGAATGCCAGGTCACCTTCATCCACCTTAAGTGTGACTCCTCTCGGAAGGGC AAGGGCCGACGGGCCCGGACCCCTCCAGGCAAAGAGGTCACAAGGCTCACCCTGGAACTGGAGGCAGAGG TCAGAGCCGAAGAAACCACAGCCAGCTGTGGGCTGCCCTGCCTCCGACAGCGAATGGAACGGCGGCTGAA AGGATCCCTGAAGATGCTCAGAAAGTCCATCAACCAGGACCGCTTCCTGCTGCGCCTGGCAGGCCTTGAT TATGAGCTGGCCCACAAGCCGGGCCTGGTAGCCGGGGAGCGAGCAGAGCCGATGGAGTCCTGTAGGCCCG GGCAGCACCGTGCTGGGACCAAGTGTGTCAGCTGCCCGCAGGGAACGTATTACCACGGCCAGACGGAGCA GTGTGTGCCATGCCCAGCGGGCACCTTCCAGGAGAGAGAAGGGCAGCTCTCCTGCGACCTTTGCCCTGGG AGTGATGCCCACGGGCCTCTTGGAGCCACCAACGTCACCACGTGTGCAGGTCAGTGCCCACCTGGCCAAC ACTCTGTAGATGGGTTCAAGCCCTGTCAGCCATGCCCACGTGGCACCTACCAACCTGAAGCAGGACGGAC CCTATGCTTCCCTTGTGGTGGGGGCCTCACCACCAAGCATGAAGGGGCCATTTCCTTCCAAGACTGTGAC ACCAAAGTCCAGTGCTCCCCAGGGCACTACTACAACACCAGCATCCACCGCTGTATTCGCTGTGCCATGG GCTCCTATCAGCCCGACTTCCGTCAGAACTTCTGCAGCCGCTGTCCAGGAAACACAAGCACAGACTTTGA TGGCTCTACCAGTGTGGCCCAATGCAAGAATCGTCAGTGTGGTGGGGAGCTGGGTGAGTTCACTGGCTAT ATTGAGTCCCCCAACTACCCGGGCAACTACCCAGCTGGTGTGGAGTGCATCTGGAACATCAACCCCCCAC CCAAGCGCAAGATCCTTATCGTGGTACCAGAGATCTTCCTGCCATCTGAGGATGAGTGTGGGGACGTCCT CGTCATGAGAAAGAACTCATCCCCATCCTCCATTACCACTTATGAGACCTGCCAGACCTACGAGCGTCCC ATTGCCTTCACTGCCCGTTCCAGGAAGCTCTGGATCAACTTCAAGACAAGCGAGGCCAACAGCGCCCGTG GCTTCCAGATTCCCTATGTTACCTATGATGAGGACTATGAGCAGCTGGTAGAAGACATTGTGCGAGATGG CCGGCTCTATGCCTCTGAAAACCACCAGGAGATTTTAAAGGACAAGAAGCTCATCAAGGCCTTCTTTGAG GTGCTAGCCCACCCCCAGAACTACTTCAAGTACACAGAGAAACACAAGGAGATGCTGCCAAAATCCTTCA TCAAGCTGCTCCGCTCCAAAGTTTCCAGCTTCCTGAGGCCCTACAAATAGTAACCCTAGGCTCAGAGACC CAATTTTTTAAGCCCCCAGACTCCTTA (SEQ ID NO. 15)

TABLE 9B The amino acid sequence ofPOLY8. GSGRVPGLCLLVLLVHARAAQYSKAAQDVDECVEGTDNCHIDAICQNTPRSYKCICKSG YTGDGKHCKDVDECEREDNAGCVHDCVNIPGNYRCTCYDGFHLAHDGHNCLDVDECAEGN GGCQQSCVNMMGSYECHCREGFFLSDNQHTCIQRPEEGMNCMNKNHGCAHICRETPKGGI ACECRPGFELTKNQRDCKLTCNYGNGGCQHTCDDTEQGPRCGCHIKFVLHTDGKTCIGER RLEQHIPTQAVSNETCAVNNGGCDSKCHDAATGVHCTCPVGFMLQPDRKTCKDIDECRLN NGGCDHICRNTVGSFECSCKKGYKLLINERNCQDIDERSFDRTCDHICVNTPGSFQCLCH RGYLLYGITHCGDVDECSINRGGCRFGCINTPGSYQCTCPAGQGRLHWNGKDCTEPLKCQ GSPGASKAMLSCNRSGKKDTCALTCPSRARFLPESENGFTVSCGTPSPRAAPARAGHNGN STNSNHCHEAAVLSIKQRASFKIKDAKCRLHLRNKGKTEEAGRITGPGGAPCSECQVTFI HLKCDSSRKGKGRRARTPPGKEVTRLTLELEAEVRAEETTASCGLPCLRQR ERRLKGSL KMLRKSINQDRFLLRLAGLDYELAHKPGLVAGERAEPMESCRPGQHRAGTKCVSCPQGTY YHGQTEQCVPCPAGTFQEREGQLSCDLCPGSDAHGPLGATNVTTCAGQCPPGQHSVDGFK PCQPCPRGTYQPEAGRTLCFPCGGGLTTKHEGAISFQDCDTKVQCSPGHYYNTSIHRCIR CAMGSYQPDFRQNFCSRCPGNTSTDFDGSTSVAQCKNRQCGGELGEFTGYIESPNYPGNY PAGVECIWNINPPPKRKILIVVPEIFLPSEDECGDVLVMRKNSSPSSITTYETCQTYERP IAFTARSRKL INFKTSEANSARGFQIPYVTYDEDYEQLVEDIVRDGRLYASENHQEILK DKKLIKAFFEVLAHPQNYFKYTEKHKEMLPKSFIKLLRSKVSSFLRPYK (SEQ ID NO. 16)

POLY5-8 represent novel members ofthe EGF family. Based on homology described above, they all share the activity of members ofthe EGF family and thus are useful in modulating tumor progression.

POLY9-11:

COMPLEMENT RECEPTOR 1 NUCLEIC ACIDS AND PROTEINS

POLY9-11 show significant homology to complement receptor proteins. Complement receptors on neutrophils and eosinophils play a role in activation and adhesion. During asthmatic reactions these receptors have been found elevated on circulating granulocytes. The expression of CD35 (complement receptor type 1) and CDl lb (complement receptor type 3) on neutrophils and eosinophils from asthmatic and non-asthmatic children was different. These results indicate that the inducible expression of CDl lb on neutrophils and eosinophils from allergic asthmatic children is primed in vivo.

The expression pattern, and protein similarity information for the invention suggest that the human complement receptor 1 -like proteins described in this invention may function as human complement receptor 1 -like proteins. Therefore, the nucleic acid and protein ofthe invention are useful in potential therapeutic applications implicated, for example but not limited to, lung diseases, such as asthma, viral diseases, and other diseases and disorders. The homology to antigenic secreted and membrane proteins suggests that antibodies directed against the novel genes may be useful in treatment and prevention of lung diseases, such as asthma, viral diseases, and other diseases and disorders, and other diseases and disorders.

The nucleic acids and proteins ofthe invention are useful in potential therapeutic applications implicated in lung diseases, such as asthma, viral diseases, and other diseases and disorders. For example, but not limited to, a cDNA encoding the human complement receptor 1 -like proteins may be useful in gene therapy for lung diseases such as asthma, and the human complement receptor 1 -like proteins may be useful when administered to a subject in need thereof. By way of non-limiting example, the compositions ofthe present invention will have efficacy for treatment of patients suffering from, for example, but not limited to, asthma, and other diseases and disorders. The novel nucleic acid encoding the human complement receptor 1 -like proteins, and the human complement receptor 1 -like proteins, or fragments thereof, may further be useful in diagnostic applications, wherein the presence or amount ofthe nucleic acid or the protein are to be assessed. These materials are further useful in the generation of antibodies that bind immunospecifically to the novel substances ofthe invention for use in therapeutic or diagnostic methods.

POLY9

The novel nucleic acid of 1709 nucleotides, POLY9 (designated CuraGen Ace. No.

10327789.0.16, SEQ ID NO: 17), encodes a novel complement receptor 1 -like protein as shown in TABLE 10. A POLY9 nucleic acid is expressed in mammary tissue. An open reading frame was identified beginning with an ATG initiation codon at nucleotide 413 and ending with a stop codon at nucleotide 1444. The encoded protein having 344 amino acid residues (SEQ ID NO: 18) is presented using the one-letter code in TABLE 10B.

TABLE 10A: The Nucleotide Sequence of POLY9

CAGAGTCTTGCTCTGTCTCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG TGATTCTCCTGCCTCAGCTTCCCAAATGGCTGAGATTACAGGCACATACCACCATGCCTAGCTAATTTTTGTACAGGTTT CACCATGTTGGCCAGGCTGGTCTCGAACTCCTAACCTCAAGTGTTCCTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGT AGGCATGAATCGTCATGCCGAGCCTAAGTTGACTTTCTACTATCATTTTCACTTATTTAAAAAAATAGAATGGATCTATT GGAAAAACCATAAATCATTATTTGCTTACTTCCTAATTGATTCATTTTAACATAGACCTTTTAGTTTTTTTCACTATCCA AGGATTTAGTTAATGCTATCATCTGTTATACAAATCGC^CTCΑCTTGCTTTCTTCCTGTTGCACAGCATACAACTGGCAG GATCTTTGAGAGTGAAGTGAGGTATCAGTGTAACCCGGGCTATAAGTCAGTCGGAAGTCCTGTATTTGTCTGCCAAGCCA ATCGCCACTGGCACAGTGAATCCCCTCTGATGTGTGTTCCTCTCGACTGTGGAAAACCTCCCCCGATCCAGAATGGCTTC ATGAAAGGAGAAAACTTTGAAGTAGGGTCCAAGGTTCAGTTTTTCTGTAATGAGGGTTATGAGCTTGTTGGGGACAGTTC TTGGACATGTCAGAAATCTGGCAAATGGAATAAGAAGTCAAATCCAAAGTGCATGCCTGCCAAGTGCCCAGAGCCGCCCC TCTTGGAAAACCAGCTAGTATTAAAGGAGTTGACCACCGAGGTAGGAGTTGTGACATTTTCCTGTAAAGAAGGGCATGTC CTGCAAGGCCCCTCTGTCCTGAAATGCTTGCCATCCCAGCAATGGAATGACTCTTTCCCTGTTTGTAAGATTGTTCTTTG TACCCCACCTCCCCTAATTTCCTTTGGTGTCCCCATTCCTTCTTCTGCTCTTCATTTTGGAAGTACTGTCAAGTATTCTT GTGTAGGTGGGTTTTTCCTAAGAGGAAATTCTACCACCCTCTGCCAACCTGATGGCACCTGGAGCTCTCCACTGCCAGAA TGTGTTCCAGTAGAATGTCCCCAACCTGAGGAAATCCCCAATGGAATCATTGATGTGCAAGGCCTTGCCTATCTCAGCAC AGCTCTCTATACCTGCAAGCCAGGCTTTGAATTGGTGGGAAATACTACCACCCTTTGTGGAGAAAATGGTCACTGGCTTG GAGGAAAACCAACATGTAAAGCCATTGAGTGCCTGAAACCCAAGGAGATTTTGAATGGCAAATTCTCTTACACGGACCTA CACTATGGACAGACCGTTACCTACTCTTGCAACCGAGGCTTTCGGCTCGAAGGGTCCCAGTGCCTTGACCTGTTTAGAGA CAGGTGATTGGGATGTAGATGCCCCATCTTGCAATGCCATCCACTGTGATTCCCCACAACCCATTGAAAATGGTTTTGTA GAAGGTGCAGATTACAGCTATGGTGCCATAATCATCTACAGTTGCTTCCCTGGGTTTCAGGTGGCTGGTCATGCCATGCA GACCTGTGAAGAGTCAGGATGGTCACTCGTGCCCCCAACATGTATGCCAATAGACTGTGGCCTCCCTCCTCATATAGATT TTGGAGACTGTACTAAACTCAAAGATGAC (SEQ ID NO: 17)

TABLE 10B: The Amino Acid sequence of POLY9

MLSSVIQIALTCFLPVAQHTTGRIFESEVRYQCNPGYKSVGSPVFVCQANRH HSESPL CVPLDCGKPPPIQNGF MKGENFEVGSKVQFFCNEGYELVGDSS TCQKSGK NKKSNPKCMPAKCPEPPLLENQLVLKELTTEVGVVTFSCK EGHVLQGPSVLKCLPSQQWNDSFPVCKIVLCTPPPLISFGVPIPSSALHFGSTVKYSCVGGFFLRGNSTTLCQPDG TWSSPLPECVPVECPQPEEIPNGIIDVQGLAYLSTALYTCKPGFELVGNTTTLCGENGH LGGKPTCKAIECLKPK EILNGKFSYTDLHYGQTVTYSCNRGFRLEGSQCLDLFRDR (SEQ ID NO: 18)

In a search of sequence databases, it was found, for example, that POLY9 has 152 of

299 amino acids (35 %) identical to a Pan troglodytes (chimpanzee) complement receptor 1 (ACC:Q29530). The full amino acid sequence ofthe protein ofthe invention was found to have 105 of 299 amino acid esidues (35 %) identical to, and 152 of 299 residues (50 %) similar to, the 2039 amino acid residue complement receptor 1 from Homo sapiens (human) (ACC:Q16745). POLY9 also has homology to a number of other proteins shown in BLASTX data in Table IOC. Table IOC. BLASTX alignments of POLY9

Sequences producing High-scoring Segment Pairs : Smalles t Sum

Reading High Prob . Frame Score P (N) N

Datp : B43122 Human ORFX ORF2886 polypeptide sequence SE . . +2 481 2 le-60 2 :>atp : R36743 CR1 - Homo sapiens , 2039 aa . +2 414 2 . 2e-48 3, 3atp : R11982 Partial human complement type 1 receptor - . . +2 412 8 . 8e-48 3 3atp : W45899 Human complememt receptor 1 ( residues 1-19 . . +2 414 1 . 2e-47 3 3atp : Y55751 Human C3b/C4b receptor (CR1 ) protein - Horn . . +2 414 1 5e-47 3 natp : R11810 Human complement type 1 receptor - Homo sa . . +2 414 1 5e-47 3

SignalP, Psort and/or hydropathy suggest that POLY9 may be localized outside ofthe cell (Certainty=0.3700) with a most likely cleavage site between positions 22 and 23 of SEQ ID NO.: 18. Since POLY9 is similar to the "complement receptor family", it is likely that POLY9 is available at the appropriate sub-cellular localization and hence accessible for the therapeutic uses described in this application.

POLY10

A novel nucleic acid of 1952 nucleotides, POLYl 0 (designated CuraGen Ace. No. 10327789.0.140, SEQ ID NO: 19), encodes a novel complement receptor 1 -like protein as shown in TABLE 11 A. A POLYl 0 nucleic acid is expressed in human mammary tissue. An open reading frame was identified beginning with an ATG initiation codon at nucleotides 470 and ending with a stop codon at nucleotide 1687. The encoded protein having 406 amino acid residues (SEQ ID NO: 20) is presented using the one-letter code in TABLE 1 IB.

TABLE 11 A: The Nucleotide sequence of POLY10

TTCAGGAACACCGTCACTTACACTTGCAAAGAAGGCTATACTCTTGCTGGTCTTGACACCATTGAATGCCTGGCCGACGG CAAGTGGAGTAGAAGTGACCAGCAGTGCCTGGCTGTCTCCTGTGATGAGCCACCCATTGTGGACCACGCCTCTCCAGAGA CTGCCCATCGGCTCTTTGGAGACATTGCATTCTACTACTGCTCTGATGGTTACAGCCTAGCAGACAATTCCCAGCTTCTC TGCAATGCCCAGGGCAAGTGGGTACCCCCAGAAGGTCAAGACATGCCCCGTTGTATAGCTCATTTCTGTGAAAAACCTCC ATCGGTTTCCTATAGCATCTTGGAATCTGTGAGCAAAGCAAAATTTGCAGCTGGCTCAGTTGTGAGCTTTAAATGCATGG AAGGCTTTGTACTGAACACCTCAGCAAAGATTGAATGTATGAGAGGTGGGCAGTGGAACCCTTCCCCCCATGTCCATCCA GTGCATCCCTGTGCGGTGTGGAGAGCCACCAAGCATCATGAATGGCTATGCAAGTGGATCAAACTACAGTTTTGGAGCCA TGGTGGCTTACAGCTGCAACAAGGGGTTCTACATCAAAGGGGAAAAGAAGAGCACCTGCGAAGCCACAGGGCAGTGGAGT AGTCCTATACCGACGTGCCACCCGGTATCTTGTGGTGAACCACCTAAGGTTGAGAATGGCTTTCTGGAGCATACAACTGG CAGGATCTTTGAGAGTGAAGTGAGGTATCAGTGTAACCCGGGCTATAAGTCAGTCGGAAGTCCTGTATTTGTCTGCCAAG CCAATCGCCACTGGCACAGTGAATCCCCTCTGATGTGTGTTCCTCTCGACTGTGGAAAACCTCCCCCGATCCAGAATGGC TTCATGAAAGGAGAAAACTTTGAAGTAGGGTCCAAGGTTCAGTTTTTCTGTAATGAGGGTTATGAGCTTGTTGGGGACAG TTCTTGGACATGTCAGAAATCTGGCAAATGGAATAAGAAGTCAAATCCAAAGTGCATGCCTGCCAAGTGCCCAGAGCCGC CCCTCTTGGAAAACCAGCTAGTATTAAAGGAGTTGACCACCGAGGTAGGAGTTGTGACATTTTCCTGTAAAGAAGGGCAT GTCCTGCAAGGCCCCTCTGTCCTGAAATGCTTGCCATCCCAGCAATGGAATGACTCTTTCCCTGTTTGTAAGATTGTTCT TTGTACCCCACCTCCCCTAATTTCCTTTGGTGTCCCCATTCCTTCTTCTGCTCTTCATTTTGGAAGTACTGTCAAGTATT CTTGTGTAGGTGGGTTTTTCCTAAGAGGAAATTCTACCACCCTCTGCCAACCTGATGGCACCTGGAGCTCTCCACTGCCA GAATGTGTTCCAGTAGAATGTCCCCAACCTGAGGAAATCCCCAATGGAATCATTGATGTGCAAGGCCTTGCCTATCTCAG CACAGCTCTCTATACCTGCAAGCCAGGCTTTGAATTGGTGGGAAATACTACCACCCTTTGTGGAGAAAATGGTCACTGGC TTGGAGGAAAACCAACATGTAAAGCCATTGAGTGCCTGAAACCCAAGGAGATTTTGAATGGCAAATTCTCTTACACGGAC CTACACTATGGACAGACCGTTACCTACTCTTGCAACCGAGGCTTTCGGCTCGAAGGGTCCCAGTGCCTTGACCTGTTTAG AGACAGGTGATTGGGATGTAGATGCCCCATCTTGCAATGCCATCCACTGTGATTCCCCACAACCCATTGAAAATGGTTTT GTAGAAGGTGCAGATTACAGCTATGGTGCCATAATCATCTACAGTTGCTTCCCTGGGTTTCAGGTGGCTGGTCATGCCAT GCAGACCTGTGAAGAGTCAGGATGGTCACTCGTGCCCCCAACATGTATGCCAATAGACTGTGGCCTCCCTCCTCATATAG ATTTTGGAGACTGTACTAAACTCAAAGATGAC (SEQ ID NO: 19)

TABLE 11B: The Amino Acid sequence of POLY10 MSIQCIPVRCGEPPSIMNGYASGSNYSFGAMVAYSCNKGFYIKGEKKSTCEATGQ SSPIPTCHPVSCGΞPPKVE NGF EHTTGRIFESΞVRYQCNPGYKSVGSPVFVCQANRH HSESPLMCVPLDCGKPPPIQNGFMKGENFEVGSKV QFFCNEGYELVGDSS TCQKSGKWNKKSNPKCMPAKCPEPP ENQ VLKE TTEVGWTFSCKEGHV QGPSVL KCLPSQQWNDSFPVCKIVLCTPPPLISFGVPIPSSALHFGSTVKYSCVGGFFLRGNSTT CQPDGTWSSPLPECV PVECPQPEEIPNGIIDVQG AYLSTALYTCKPGFELVGNTTTLCGENGHW GGKPTCKAIEC KPKEI NGKFSY TDLHYGQTVTYSCNRGFRLEGSQC D FRDR (SEQ ID NO:20)

In a search of sequence databases, it was found, for example, that POLYl 0 has 101 of 298 amino acids (33 %) identical to a Pan troglodytes (chimpanzee) complement receptor 1 (ACC:Q29530). The full amino acid sequence of POLY10 was found to have 105 of 299 amino acid residues (35 %) identical to, and 152 of 299 residues (50 %) similar to, the 2039 amino acid residue complement receptor type 1 precursor (C3B/C4B receptor) (CD35 antigen) from Homo sapiens (human) (ACC:P17927). SignalP, Psort and/or hydropathy suggest that the protein may be localized in the cytoplasm ofthe cell (Certainty=0.6500). Since POLYl 0 is similar to the "complement receptor family", it is likely that POLYl 0 is available at the appropriate sub-cellular localization and hence accessible for the therapeutic uses described in this application. POLYl 1

A novel nucleic acid of 6153 nucleotides, POLYl 1 (designated CuraGen Ace. No. 10327789_1, SEQ ID NO: 21) encodes a novel human complement receptor-like protein as shown in TABLE 12A. APOLY11 nucleic acid is expressed in the following tissues: mammary gland, hypothalamus, lymph node, fetal liver, pooled adrenal gland/placenta, placenta, cervix, testicular tumor, adipose, ovary, ascending colon, lymph node, bone marrow, stomach, and fetal lung. An open reading frame was identified beginning with an ATG initiation codon at nucleotides 1-3 and ending with a stop codon at nucleotides 6151-6153. The encoded protein having 2050 amino acid residues (SEQ ID NO: 22) is presented using the one-letter code in TABLE 12B. The predicted molecular weight ofthe protein is 224498.2 Da.

TABLE 12A: The Nucleotide sequence of POLY11

ATGGCGGGCGCCCCTCCCCCAGCCTCGTTGCCGCCTTGCAGTTTGATCTCAGACTGCTGTGCTAGCAATCAGCGAG ATTCCGTGGGCGTAGGACCCTCTGAGCCAGGTGTGGGATATAGTCTCGTGGTGCGCCGTTTCTTAAGCCGGTCTGA AAAGCGCAATATTCGGGTGGGAGTGACCCGATTTTCCAGCTATACTCTTGCTGGTCTTGACACCATTGAATGCCTG GCCGACGGCAAGTGGAGTAGAAGTGACCAGCAGTGCCTGGCTGTCTCCTGTGATGAGCCACCCATTGTGGACCACG CCTCTCCAGAGACTGCCCATCGGCTCTTTGGAGACATTGCATTCTACTACTGCTCTGATGGTTACAGCCTAGCAGA CAATTCCCAGCTTCTCTGCAATGCCCAGGGCAAGTGGGTACCCCCAGAAGGTCAAGACATGCCCCGTTGTATAGCT CATTTCTGTGAAAAACCTCCATCGGTTTCCTATAGCATCTTGGAATCTGTGAGCAAAGCAAAATTTGCAGCTGGCT CAGTTGTGAGCTTTAAATGCATGGAAGGCTTTGTACTGAACACCTCAGCAAAGATTGAATGTATGAGAGGTGGGCA GTGGAACCCTTCCCCCATGTCCATCCAGTGCATCCCTGTGCGGTGTGGAGAGCCACCAAGCATCATGAATGGCTAT GCAAGTGGATCAAACTACAGTTTTGGAGCCATGGTGGCTTACAGCTGCAACAAGGGGTTCTACATCAAAGGGGAAA AGAAGAGCACCTGCGAAGCCACAGGGCAGTGGAGTAGTCCTATACCGACGTGCCACCCGGTATCTTGTGGTGAACC ACCTAAGGTTGAGAATGGCTTTCTGGAGCATACAACTGGCAGGATCTTTGAGAGTGAAGTGAGGTATCAGTGTAAC CCGGGCTATAAGTCAGTCGGAAGTCCTGTATTTGTCTGCCAAGCCAATCGCCACTGGCACAGTGAATCCCCTCTGA TGTGTGTTCCTCTCGACTGTGGAAAACCTCCCCCGATCCAGAATGGCTTCATGAAAGGAGAAAACTTTGAAGTAGG GTCCAAGGGTCAGTTTTTCTGTAATGAAGGGTTATNGAGCTTTGTTGGGGACAGTTCTTGGACATGTCAGAAATCT GGCAAATGGAATAAGAAGTCAAATCCAAAGTGCATGCCTGCCAAGTGCCCAGAGCCGCCCCTCTTGGAAAACCAGC TAGTATTAAAGGAGTTGACCACCGAGGTAGGAGTTGTGACATTTTCCTGTAAAGAAAGGCATGTCCTGCAAGGCCC CTCTGTCCTGAAATGCTTGCCATCCCAGCAATGGAATGACTCTTTCCCTGTTTGTAAGATTGTTCTTTGTACCCCA CCTCCCCTAATTTCCTTTGGTGTCCCCATTCCTTCTTCTGCTCTTCATTTTGGAAGTACTGTCAAGTATTCTTGTG TAGGTGGGTTTTTCCTAAGAGGAAATTCTACCACCCTCTGCCAACCTGATGGCACCTGGAGCTCTCCACTGCCAGA ATGTGTTCCAGTAGAATGTCCCCAACCTGAGGAAATCCCCAATGGAATCATTGATGTGCAAGGCCTTGCCTATCTC AGCACAGCTCTCTATACCTGCAAGCCAGGCTTTGAATTGGTGGGAAATACTACCACCCTTTGTGGAGAAAATGGTC ACTGGCTTGGAGGAAAACCAACATGTAAAGCCATTGAGTGCCTGAAACCCAAGGAGATTTTGAATGGCAAATTCTC TTACACGGACCTACACTATGGACAGACCGTTACCTACTCTTGCAACCGAGGCTTTCGGCTCGAAGGTCCCAGTGCC TTGACCTGTTTAGAGACAGGTGATTGGGATGTAGATGCCCCATCTTGCAATGCCATCCACTGTGATTCCCCACAAC CCATTGAAAATGGTTTTGTAGAAGGTGCAGATTACAGCTATGGTGCCATAATCATCTACAGTTGCTTCCCTGGGTT TCAGGTGGCTGGTCATGCCATGCAGACCTGTGAAGAGTCAGGATGGTCAAGTTCCATCCCAACATGTATGCCAATA GACTGTGGCCTCCCTCCTCATATAGATTTTGGAGACTGTACTAAACTCAAAGATGACCAGGGATATTTTGAGCAAG AAGACGACATGATGGAAGTTCCATATGTGACTCCTCACCCTCCTTATCATTTGGGAGCAGTGGCTAAAACCTGGGA AAATACAAAGGAGTCTCCTGCTACACATTCATCAAACTTTCTGTATGGTACCATGGTTTCATACACCTGTAATCCA GGATATGAACTTCTGGGGAACCCTGTGCTGATCTGCCAGGAAGATGGAACTTGGAATGGCAGTGCACCATCCTGCA TTTCAATTGAATGTGACTTGCCTACTGCTCCTGAAAATGGCTTTTTGCGTTTTACAGAGACTAGCATGGGAAGTGC TGTGCAGTATAGCTGTAAACCTGGACACATTCTAGCAGGCTCTGACTTAAGGCTTTGTCTAGAGAATAGAAAGTGG AGTGGTGCCTCCCCACGCTGTGAAGCCATTTCATGCAAAAAGCCAAATCCAGTCATGAATGGATCCATCAAAGGAA GCAACTACACATACCTGAGCACGTTGTACTATGAGTGTGACCCCGGATATGTGCTGAATGGCACTGAGAGGAGAAC ATGCCAGGATGACAAAAACTGGGATGAGGATGAGCCCATTTGCATTCCTGTGGACTGCAGTTCACCCCCAGTCTCA GCCAATGGCCAGGTGAGAGGAGACGAGTACACATTCCAAAAAGAGATTGAATACACTTGCAATGAAGGGTTCTTGC TTGAGGGAGCCAGGAGTCGGGTTTGTCTTGCCAATGGAAGTTGGAGTGGAGCCACTCCCGACTGTGTGCCTGTCAG ATGTGCCACCCCGCCACAACTGGCCAATGGGGTGACGGAAGGCCTGGACTATGGCTTCATGAAGGAAGTAACATTC CACTGTCACGAGGGCTACATCTTGCACGGTGCTCCAAAACTCACCTGTCAGTCAGATGGCAACTGGGATGCAGAGA TTCCTCTCTGTAAACCAGTCAACTGTGGACCTCCTGAAGATCTTGCCCATGGTTTCCCTAATGGTTTTTCCTTTAT TCATGGGGGCCATATACAGTATCAGTGCTTTCCTGGTTATAAGCTCCATGGAAATTCATCAAGAAGGTGCCTCTCC AATGGCTCCTGGAGTGGCAGCTCACCTTCCTGCCTGCCTTGCAGATGTTCCACACCAGTAATTGAATATGGAACTG TCAATGGGACAGATTTTGACTGTGGAAAGGCAGCCCGGATTCAGTGCTTCAAAGGCTTCAAGCTCCTAGGACTTTC TGAAATCACCTGTGAAGCCGATGGCCAGTGGAGCTCTGGGTTCCCCCACTGTGAACACACTTCTTGTGGTTCTCTT CCAATGATACCAAATGCGTTCATCAGTGAGACCAGCTCTTGGAAGGAAAATGTGATAACTTACAGCTGCAGGTCTG GATATGTCATACAAGGCAGTTCAGATCTGATTTGTACAGAGAAAGGGGTATGGAGCCAGCCTTATCCAGTCTGTGA GCCCTTGTCCTGTGGGTCCCCACCGTCTGTCGCCAATGCAGTGGCAACTGGAGAGGCACACACCTATGAAAGTGAA GTGAAACTCAGATGTCTGGAAGGTTATACGATGGATACAGATACAGATACATTCACCTGTCAGAAAGATGGTCGCT GGTTCCCTGAGAGAATCTCCTGCAGTCCTAAAAAATGTCCTCTCCCGGAAAACATAACACATATACTTGTACATGG GGACGATTTCAGTGTGAATAGGCAAGTTTCTGTGTCATGTGCAGAAGGGTATACCTTTGAGGGAGTTAACATATCA GTATGTCAGCTTGATGGAACCTGGGAGCCACCATTCTCCGATGAATCTTGCAGTCCAGTTTCTTGTGGGAAACCTG AAAGTCCAGAACATGGATTTGTGGTTGGCAGTAAATACACCTTTGAAAGCACAATTATTTATCAGTGTGAGCCTGG CTATGAACTAGAGAATTTGGCTGTGAATCCATCTGGTCCTGGACTTTTCTTGGTTGACAGGACCCTCAGCTGCAGG TCGGAGTTGGCTAGAGGTCCAATCCAGACCCTGTTTGCCTGGGTATCAGCAGCAGAGGGTGCAGAACAGCGGATAT TGGTGAACCGCAAATGCTGCTGCCTGATCATTCCTCTGGAAGTTTTGTCTCAGAGGAATACCCGGCCATGTGAGGT GTCAGTCCGCCCCTACTGGGGGGGGAACAGGGAACGTGTCTGCCAGGAGAACAGACAGTGGAGTGGAGGGGTGGCA ATATGCAAAGAGACCAGGTGTGAAACTCCACTTGAATTTCTCAATGGGAAAGCTGACATTGAAAACAGGACGACTG GACCCAACGTGGTATATTCCTGCAACAGAGGCTACAGTCTTGAAGGGCCATCTGAGGCACACTGCACAGAAAATGG AACCTGGAGCCACCCAGTCCCTCTCTGCAAACCAAATCCATGCCCTGTTCCTTTTGTGATTCCCGAGAATGCTCTG CTGTCTGAAAAGGAGTTTTATGTTGATCAGAATGTGTCCATCAAATGTAGGGAAGGTTTTCTGCTGCAGGGCCACG GCATCATTACCTGCAACCCCGACGAGACGTGGACACAGACAAGCGCCAAATGTGAAAGAAGATATACACAACAGCC CAAGTCCCTGAATTTTCAGCTAGCAGCTTATTGCAGTATTAGAATGTTTATTTTGCGGGGAGGGGTTCAAGATGGC CAACTAGAAACAGCTGTGGCCGGAGCCTCCCACCGAGAAGAACAAAAACAAAAGCGAGAAAAAGCAAGGTGGTACA ACGGCCCACCTGGGAGCCACATGGGGCAAGCAGAGCTCCCACCCCCAGCCAAAGGAGGTGGACCTCCCTGCGGGAA TTTCAGCAACTCCAGCCAGGGGTTTATGAACAGACCTCTGATCTCCCTGAGATGGAGCCCCTGGGGCTCCATGTGG CCATGGTCTCCACAGATCAGCAGGCTTAGTCCTTCCCCTGCTGGCTCTGAGGAATCCAGGCAGGCTGGACTAGTGG GATTCCCCACAGCACAGTTTACCTGCTCTGCCAAGGGGCAGCTAGAGCGCTTTGTTAAGCGAGTCCCTGATCCCAT GCCTCCTGATTGGGATGAGACCCCCCCACAACAGGGGTCACGGATGAGACCCCCCCACAACAGGGGTCACCAGACA CCTTATACAAGGGTGTTCCTGCTAGCATCAGGTCAGTGCCCCTCTGGGACAGAGCTCCCAGAGGAAAGAGCAGGCA GCCATCTTTGCTGTTCTGCAGCGTCCGCTGGAAAAGCACAGAATTGGGCAGAGGCTAGGATTGATGAATTGAAAGA AGTAGGCTTCAGAAAGTGGGTAATAATGAAGTTCGCTGAGCTAAAGGAACATGTTCTAAACCAATGCAAAGACGCC AAGAACCAGGATAAAACATTACAGGATCCGTTAACCAGAATAACCAGTTTAGAAAGGAATGTAAATGACCTGATGG AGCTGAAAAACACAACACGAGAACTTCACAATGCAACAACAAAACAAGGCCAACATTCCAGTTCAGGAAATCCAGA GAACCCCAGTAAGATACTCCATGAGAAGATCAACCCCAAGACACATAATCCTCAGGTTCTCCAAGAAATCTCATGT GGTCCACCAGCTCACGTAGAAAATGCAATTGCTCGAGGCGTACATTATCAATATGGAGACATGATCACCTACTCAT GTTACAGTGGATACATGTTGGAGGGTTTCCTGAGGAGTGTTTGTTTAGAAAATGGAACATGGACATCACCTCCTAT TTGCAGAGCTGTCTGTCGATTTCCATGTCAGAATGGGGGCATCTGCCAACGCCCAAATGCTTGTTCCTGTCCAGAG GGCTGGATGGGGCGCCTCTGTGAAGAACCAATCTGCATTCTTCCCTGTCTGAACGGAGGTCGCTGTGTGGCCCCTT ACCAGTGTGACTGCCCGCCTGGCTGGACGGGGTCTCGCTGTCATACAGGTAGGCCTCTTTCATGGTTTGTTTTCTT GGTGGCTCAGGCCCATGAAACTCCAGAGGACATTGAAGAGTGTGACTTAGACTCAGAAGTGGTGGCAAAATGA (SEQ ID NO:21)

TABLE 12B: The Amino Acid sequence of POLY11

MAGAPPPASLPPCSLISDCCASNQRDSVGVGPSEPGVGYSLVVRRFLSRSEKRNIRVGVTRFSSYTLAGLDTIECL ADGK SRSDQQCLAVSCDEPPIVDHASPETAHRLFGDIAFYYCSDGYSLADNSQLLCNAQGKWVPPEGQDMPRCIA HFCEKPPSVSYSILESVSKAKFAAGSVVSFKCMEGFVLNTSAKIECMRGGQ NPSPMSIQCIPVRCGEPPSIMNGY ASGSNYSFGAMVAYSCNKGFYIKGEKKSTCEATGQWSSPIPTCHPVSCGEPPKVENGFLEHTTGRIFESEVRYQCN PGYKSVGSPVFVCQANRHWHSESPLMCVPLDCGKPPPIQNGFMKGENFEVGSKGQFFCNEGLXSFVGDSSWTCQKS GKWNKKSNPKCMPAKCPEPPLLENQLVLKELTTEVGVVTFSCKERHVLQGPSVLKCLPSQQ NDSFPVCKIVLCTP PPLISFGVPIPSSALHFGSTVKYSCVGGFFLRGNSTTLCQPDGTWSSPLPECVPVECPQPEEIPNGIIDVQGLAYL STALYTCKPGFELVGNTTTLCGENGH LGGKPTCKAIECLKPKEILNGKFSYTDLHYGQTVTYSCNRGFRLEGPSA LTCLETGD DVDAPSCNAIHCDSPQPIENGFVEGADYSYGAIIIYSCFPGFQVAGHAMQTCEESGWSSSIPTCMPI DCGLPPHIDFGDCTKLKDDQGYFEQEDD MEVPYVTPHPPYHLGAVAKTWENTKESPATHSSNFLYGTMVSYTCNP GYELLGNPVLICQEDGTWNGSAPSCISIECD PTAPENGFLRFTETSMGSAVQYSCKPGHILAGSDLR CLENRK SGASPRCEAISCKKPNPVMNGSIKGSNYTYLSTLYYECDPGYVLNGTERRTCQDDKNWDEDEPICIPVDCSSPPVS ANGQVRGDEYTFQKEIEYTCNEGF LEGARSRVCLANGSWSGATPDCVPVRCATPPQLANGVTEGLDYGFMKEVTF HCHEGYILHGAPKLTCQSDGNWDAEIPLCKPVNCGPPEDLAHGFPNGFSFIHGGHIQYQCFPGYKLHGNSSRRCLS NGSWSGSSPSCLPCRCSTPVIEYGTVNGTDFDCGKAARIQCFKGFKLLGLSEITCEADGQ SSGFPHCEHTSCGSL PMIPNAFISETSS KENVITYSCRSGYVIQGSSDLICTEKGV SQPYPVCEPLSCGSPPSVANAVATGEAHTYESE VKLRCLEGYTMDTDTDTFTCQKDGR FPERISCSPKKCPLPENITHILVHGDDFSVNRQVSVSCAEGYTFEGVNIS VCQLDGT EPPFSDESCSPVSCGKPESPEHGFVVGSKYTFESTIIYQCEPGYELENLAVNPSGPGLFLVDRTLSCR SELARGPIQTLFA VSAAEGAEQRILVNRKCCCLIIPLEVLSQRNTRPCEVSVRPYWGGNRERVCQENRQ SGGVA ICKETRCETPLEFLNGKADIENRTTGPNVVYSCNRGYSLEGPSEAHCTENGT SHPVPLCKPNPCPVPFVIPENAL LSEKEFYVDQNVSIKCREGFLLQGHGIITCNPDET TQTSAKCERRYTQQPKSLNFQLAAYCSIR FILRGGVQDG QLETAVAGASHREEQKQKREKARWYNGPPGSHMGQAELPPPAKGGGPPCGNFSNSSQGF NRPLISLR SPWGSMW PWSPQISR SPSPAGSEESRQAGLVGFPTAQFTCSAKGQLERFVKRVPDPMPPDWDETPPQQGSRMRPPHNRGHQT PYTRVFLLASGQCPSGTELPEERAGSHLCCSAASAGKAQN AEARIDELKEVGFRKVIMKFAELKEHVLNQCKDA KNQDKTLQDPLTRITSLERNVNDLMELKNTTRELHNATTKQGQHSSSGNPENPSKILHEKINPKTHNPQV QEISC GPPAHVENAIARGVHYQYGDMITYSCYSGYM EGFLRSVCLENGTWTSPPICRAVCRFPCQNGGICQRPNACSCPE G MGR CEEPICILPCLNGGRCVAPYQCDCPPGWTGSRCHTGRPLSWFVFLVAQAHETPEDIEECDLDSEVVAK (SEQ ID NO:22)

In a search of sequence databases, it was found, for example, that the amino acid sequence of POLYl 1 has 136 of 427 amino acid residues (31%) identical and 195 of 427 amino acid residues (45%) positive with the 2489 amino acid residue human complement receptor-1 (ACC:Q16744).

The POLYl 1 sequence disclosed in the present application includes within it shorter sequences having nearly 100% identity ofthe nucleotide sequence in the respective comparisons (see POLYl 0 and POLY9) and SeqListing#6077 in US Ser. No. 09/540,763 filed March 30, 2000. SignalP, Psort and/or hydropathy suggest that the protein may be localized in the cytoplasm with a certainty-0.4500. No signal peptide is predicted. The expression pattern of a POLYl 1 nucleic acid in various cells and tissues described in Example 5; POLYl 1 is highly expressed in normal adipose, cerebellum, lung, mammary gland and placenta.

POLY12: HEMATOPOIETIC STEM AND PROGENITOR CELLS (HSPC) POLY 12 shows significant homology to hematopoietic stem and proginitor cells (HSPC).

The direct effects of cyclosporin A on proliferation of hematopoietic stem and progenitor cells (HSPC)have been well known. Perry et al., Cell Transplant 1999 Jul- Aug;8(4):339-44. Cyclosporin A (Cy A) has been reported to both stimulate and inhibit bone marrow colony assays in a dose-dependent manner. The observation that anti-gamma-IFN antibodies stimulate hematopoiesis to the same degree as Cy A has led several groups to propose that the stimulatory effects of Cy A are due to inhibition of gamma-IFN production by T cells. They show that Cy A can stimulate hematopoietic stem cell growth independent of mediation by T cells. Consequently, these results argue for a direct positive effect of Cy A on the signal transduction pathways in HSPC. There is also direct evidence of selectin ligands on HSPC under physiologic flow conditions and are the first to show a correlation between the maturity of HSPC during development and rolling efficiency on selectins, suggesting a mechanism by which HSPC subsets may differentially home to the extravascular spaces of the bone marrow. Furthermore, it has been discovered that cell cycle progression by itself cannot account for the decrease in repopulating potential that is observed after ex vivo expansion. Other determinants of engraftment must be identified to facilitate the transplantation of cultured HSPC.

The POLYl 2 nucleic acid and its encoded polypeptide are useful in a variety of applications and contexts. POLY12 is homologous to members ofthe HSPC family of proteins that are important in hematopoietic cell proliferation and differentiation. Therefore, POLYl 2 nucleic acids, proteins, antibodies and other compositions ofthe present invention are useful in diagnostic and therapeutic applications in disorders ofthe hematopoietic system, e.g. leukemia, systemic lupus erythematosus, and chronic aplastic anemia. POLYl 2 also has utility as a marker for alterations in gene expression in cells following cyclosporin A and gamma-interferon.d

POLY12

The novel nucleic acid of 2216 nucleotides, POLYl 2 (designated CuraGen Ace. No.

AC016030_A.0.82 ) encodes a novel hematopoietic stem and progenitor cell-like protein as shown in TABLE 13 A. An open reading frame was identified beginning with an ATG initiation codon at nucleotides 720 and ending with a stop codon at nucleotides 2090. The encoded protein having 457 amino acid residues is presented using the one-letter code in TABLE 13B.

TABLE 13A: The Nucleotide sequence of POLY12

CCCACGCGTCCGCCCACGCGTCCGCCCACGCGTCCGCCCACGCGTCCGCCCACGCGTCCG CCCACGCGTCCGCCCACGCGTCCGGTGCAAGCTCGCGCCGCACACTGCCTGGTGGAGGGA AGGAGCCCGGGCGCCTCTCGCCGCTCCCCGCGCCGCCGTCCGCACCTCCCCACCGCCCGC CGCCCGCCGCCCGCCGCCCGCAAAGCATGAGTGAGCCCGCTCTCTGCAGCTGCCCGGGGC GCGA GGCAGGCTGTTTCCGCGGAG AAAAGGTGGCGCCGGTCAGTGGTCGTTTCCAAT GACGGACATTAACCAGACTGTCAGATCCTGGGGAGTCGCGAGCCCCGAGTTTGGAGTTTT TTCCCCCCACAACGTCACAGTCCGAACTGCAGAGGGAAAGGAAGGCGGCAGGAAGGCGAA GCTCGGGCTCCGGCACGTAGTTGGGAAACTTGCGGGTCCTAGAAGTCGCCTCCCCGCCTT GCCGGCCGCCCTTGCAGCCCCGAGCCGAGCAGCAAAGTGAGACATTGTGCGCCTGCCAGA CCGCCGGCCGCGGACCGGGGCTGCCTCGGAAACACAGAGGGGTCTTCTCTCGCCCTGCA TATAATTAGCCTGCACACAAAGGGAGCAGCTGAATGGAGGTTGTCACTCTCTGGAAAAGG ATTTCTGACCGAGCGCTTCCAATGGACATTCTCCAGTCTCTCTGGAAAGATTCTCGCTAA TGGATTTCCTGCTGCTCGGTCTCTGTCTATACTGGCTGCTGAGGAGGCCCTCGGGGGTGG TCTTGTGTCTGCTGGGGGCCTGCTTTCAGATGCTGCCCGCCGCCCCCAGCGGGTGCCCGC AGCTGTGCCGGTGCGAGGGGCGGCTGCTGTACTGCGAGGCGCTCAACCTCACCGAGGCGC CCCACAACCTGTCCGGCCTGCTGGGCTTGTCCCTGCGCTACAACAGCCTCTCGGAGCTGC GCGCCGGCCAGTTCACGGGGTTAATGCAGCTCACGTGGCTCTATCTGGATCACAATCACA TCTGCTCCGTGCAGGGGGACGCCTTTCAGAAACTGCGCCGAGTTAAGGAACTCACGCTGA GTGCCTACCGGAGCTGCGGTGGCGTCTCCACACGCAACCATGAAGTTGAAGGACACAAAA TCAAGGCCAAAGCAGTCAAGCTGTGGCAAATTTCAGACAAAGGGAATCAAAGTTGTGGGA AAATGGAAGGAAATGGACAGATGGATGACTTGGTGTGCTTTGAGGAATTGACAGATTACC AGTTGGTCTCCCCTGCCAAGAATCCCTCCAGTCTCTTCTCAAAGGAAGCACCCAAGAGAA AGGCACAAGCTGTTTCAGAAGAAGAGGAGGAGGAGGAGGGAAAGTCTAGCTCACCAAAGA AAAAGATCAAGTTGAAGAAAAGTAAAAATGTAGCAACTGAAGGAACCAGTACCCAGAAAG ATTTGAAGTGAAAGATCCTGAGCTGGAGGCCCAGGGAGATGACATGGTTTGTGATGATC CGGAGGCTGGGGAGATGACATCAGAAAACCTGGTCCAAACTGCTCCAAAAAAGAΆGAAAA

ATAAAGGGAAAAAAGGGTTGGAGCCTTCTC GAGC CTGCTGCCAAGGTGCCCAAAAAAG

CGAAGACATGGATTCCTGAAGTTCATGATCAGAAAGCAGATGTGTCAGCT GGAAGGACC

TGTTTGTTCCCAGGCCGGTTCTCCGAGCACTCAGCTTTCTAGGCTTCTCTGCACCCACAC CAATCCAAGCCCTGACCTTGGCACCTGCCATCCGTGACAAACTGG CATCCTTGGGGCTG CTGAGACAGGAAGTGGGAAAACTCTTGCCTTTGCCATCCCAATGATTCATGCGGTGTTGC AGTGGCAGAAGAGGAATGCTGCCCCTCCTCCAAGTAACACCGAAGCACCACCTGGAGAGA CCAGAACTGAGGCCGGAGCTGAGACTAGATTACCAGGCAAGGCTGAAGCTGAGTCTGATG CATTGCCTGACGATACTGTAATTGAGAGTGAAGCACTGCCCAGTGATATTGCAGCCGAGG CCAGAGCCAAGACTGGAGGCACTGTCTCAGACCAGGCGTTGCTCTT GAGTGACGATGAT GCTGGTGAAGGGCCTTCTTCCCTGATCAGGGAGAAACCTGTTCCCAAACAGAATGGGAAT

GAAGAGGAAAATCTTTGATAAGAGCAGACTGGAAGTCTAAAACAGGAGTTGGATGA ( SEQ ID NO : 23 )

TABLE 13B: The Amino Acid sequence of POLY12

MDFL LGLCLY LLRRPSGW C LGACFQM PAAPSGCPQLCRCEGRLLYCΞALN TEAPHNLSGLLGLSLRYN SLSE RAGQFTGLMQLT LYLDHNHICSVQGDAFQKLRRVKELTLSAYRSCGGVSTRNHEVEGHKIKAKAVKLWQ ISDKGNQSCGKMEGNGQMDD VCFEELTDYQLVSPAKNPSSLFSKEAPKRKAQAVSEΞEEEEEGKSSSPKKKIKL KKSKNVATEGTSTQKEFEVKDPELEAQGDDMVCDDPEAGEMTSENLVQTAPKKKKNKGKKGLEPSQSTAAKVPKK AKT IPEVHDQKADVSAWKD FVPRPVLRALSFLGFSAPTPIQA TLAPAIRDK DILGAAETGSGKTLAFAIPM IHAV QWQKRNAAPPPSNTEAPPGETRTEAGAETR PGKAΞAESDALPDDTVIESEALPSDIAAEARAKTGGTVS DQA LFE (SEQ ID NO: 24)

In a search of sequence databases, it was found, for example, that POLYl 2 had 129 of 171 amino acid residues (75 %) identical to, and 135 of 171 residues (78%) similar to, the 172 amino acid (fragment) hematopoietic stem and progenitor cell 328 (HSPC328) protein from Homo sapiens (human) (ACC:AAF29006). SignalP, Psort and/or hydropathy suggest that POLY12 may be localized outside ofthe cell (Certainty= 0.6520) with a most likely cleavage site between positions 34 and 35 of SEQ ID NO.: 24. Since POLY12 is a member ofthe HSPC family, it is likely that this novel HSPC -like protein is available at the appropriate sub- cellular localization and hence accessible for the therapeutic uses described in this application.

A POLYl 2 nucleic acid is expressed in the following cells and tissues: kidney, skin, uterus, adrenal gland, placenta, hypothalamus, lymph node, fetal liver, bone marrow, fetal brain, fetal thymus, brain, HUNEC, salivary gland, testis, HuNec, CAEC, UtMNEC- myo, thyroid, PA-1 , HEPG2, A204, HFDPC, stomach, trachea, SK-PΝ-DW, ovary tumor, breast carcinoma, CADMECJLA, small intestine, hippocampus, Burkett's lymphoma, mammary gland, ONCAR-3, K-562, fetal lung, thalamus, spleen, and heart. The expression pattern, and protein similarity information for the invention suggest that the human HSPC-like protein described in this invention may function a human HSPC- like protein. Therefore, the nucleic acid and protein ofthe invention are useful in potential therapeutic applications implicated, for example but not limited to immune responses such as transplantation and inflammation and other diseases and disorders. The homology to antigenic secreted and membrane proteins suggests that antibodies directed against the novel genes may be useful in treatment and prevention of immune responses such as transplantation and inflammation, viral diseases, and other diseases and disorders, and other diseases and disorders.

The nucleic acids and proteins ofthe invention are useful in potential therapeutic applications implicated in immune responses such as transplantation and inflammation, viral diseases, and other diseases and disorders. For example, but not limited to, a cDNA encoding the human HSPC-like protein may be useful in gene therapy for hematopoietic disorders such as leukemia, and the human HSPC-like protein may be useful when administered to a subject in need thereof. By way of non-limiting example, the compositions ofthe present invention will have efficacy for treatment of patients suffering from, for example, but not limited to, cancer, and other diseases and disorders. The novel nucleic acid encoding the human HSPC- like protein, and the human HSPC-like protein ofthe invention, or fragments thereof, may further be useful in diagnostic applications, wherein the presence or amount ofthe nucleic acid or the protein are to be assessed. These materials are further useful in the generation of antibodies that bind immunospecifically to the novel substances ofthe invention for use in therapeutic or diagnostic methods.

POLY13

SULFOTRANSFERASE-LIKE PROTEINS AND NUCLEIC ACIDS

Sulfation is an important pathway in the biotransformation of steroid hormones such as estrogens. Human liver contains two different types of sulfotransf erases, dehydroepiandrosterone (DHEA) sulfotransferase and phenol sulfotransferase. Estrogen preferring sulfotransferases are cytosolic proteins present in liver, intestine, and in kidney (at lower concentrations). Functionally, the enzyme is believed to control the level ofthe estrogen receptor by sulfurylating free estradiol. It maximally sulfates beta-estradiol and estrone at concentrations of 20 nm, and dehydroepiandrosterone, pregnenolone, ethinylestradiol, equalenin, diethylstilbesterol, and 1-naphthol at significantly higher concentrations. However, cortisol, testosterone, and dopamine are not sulfated by the estrogen preferring sulfotransferases .

Cytosolic sulfotransferase (ST) enzymes catalyze the sulfate conjugation of many drugs, xenobiotic compounds, hormones, and neurotransmitters. There are a several STs with highly conserved regions among STs.

Estrone sulfate is the predominant form of estrogen found in the circulation in women and could thus serve as precursor for active estrogens in target tissues by removal ofthe sulfate group through the action of endogenous steroid sulfatase. A cDNA encoding human placental estrogen sulfotransferase was used as a probe for isolating a clone containing almost the whole genomic sequence. The gene contains nine short exons separated by eight introns in an expanse of approximately 7.7 kb. The first two exons, named exon la and exon lb, are noncoding and correspond to the 5 -prime untranslated sequences of human brain and human placental estrogen sulfotransferase cDNAs, respectively. Transfection of chloramphenicol acetyltransf erase reporter gene vectors containing the 5 -prime flanking sequence upstream from exon la and exon lb into human adrenal adenocarcinoma cells indicated that both sequences possess promoter activity. The results were interpreted as indicating that human brain aryl sulfotransferase and placental estrogen sulfotransferase mRNA species are transcribed from a single gene by alternate exon la and exon lb promoters, respectively. Using DNA from panels of human-rodent somatic cell hybrids and amplification ofthe gene by PCR, the placental estrogen sulfotransferase gene was assigned to chromosome 16, while liver estrogen sulfotransferase cDNA was mapped to 4q 13.1 by fluorescence in situ hybridization, suggesting that these may be two separate genes. The liver STE gene spans approximately 20 kb and consists of eight exons, ranging in length from 95 to 181 bp. The locations of most exon-intron splice junctions within STE were identical to those found in a human phenol ST gene. The STM gene maps to chromosome lόpl l .2. Indeed, STM is the same as the 'placental estrogen sulfotransferase' gene mapped to chromosome 16. The locations of five STE introns were conserved in the human DHEA-sulfotransferase gene, which is located on chromosome 19. The Ste gene is located on mouse chromosome 5. All three known human STP genes, STP1, STP2, and STM, are located on 16p. STP1 is located approximately 45 kb 5-prime to STP2, and the 2 genes are aligned 'head-to-tail.' These 2 genes, in turn, are located approximately 100 kb telomeric to the gene for the monoamine- preferring sulfotransferase, STM. These three STP genes on 16p may be originated as a result of gene duplication events or gene duplication plus recombination. A mouse sulfotransferase gene, Stp, is located on mouse chromosome 7 in an area syntenic with human 16p.

A POLY 13 nucleic acid was identified on chromosome 2 as described in Example 1. A nucleic acid of 921 nucleotides, POLYl 3 (designated CuraGen Ace. No. h_nh0443k08_A) encodes a novel Sulfotransferase-like protein as shown in TABLE 14. An open reading frame was identified beginning with an ATG initiation codon at nucleotides 1-3 and ending with a TGA codon at nucleotides 916-918. A putative untranslated region upstream from the initiation codon and downstream from the termination codon is underlined in TABLE 14 A, and the start and stop codons are in bold letters. The encoded protein having 305 amino acid residues is presented using the one-letter code in TABLE 14B.

TABLE 14A: The Nucleic Acid sequence of POLY13.

ATGGCGAAGATTGAGAAAAACGCTCCCACGATGGAAAAAAAGCCAGAACTGTTTAACATCATGGAAGTAG ATGGAGTCCCTACGTTGATATTATCAAAAGAATGGTGGGAAAAAGTATGTAATTTCCAAGCCAAGCCTGA

TGATCTTATTCTGGCAACTTACCCAAAGTCAGGTACAACATGGATGCATGAAATTTTAGACATGATTCTA

AATGATGGTGATGTGGAGAAATGCAAAAGAGCCCAGACTCTAGATAGACACGCTTTCCTTGAACTGAAAT

TTCCCCATAAAGAAAAACCAGATTTGGAGTTCGTTCTTGAAATGTCCTCACCACAACTGATAAAAACACA

TCTCCCTTCACATCTGATTCCACCATCTATCTGGAAAGAAAACTGCAAGATTGTCTATGTGGCCAGAAAT CCCAAGGATTGCCTGGTGTCCTACTACCACTTTCACAGGATGGCTTCCTTTATGCCTGATCCTCAGAACT

TAGAGGAATTTTATGAGAAATTCATGTCCGGAAAAGGTGAGTTCGGGTCCTGGTTTGACCATGTGAAAGG

ATGGTGGGCTGCAAAAGACATGCACCGGATCCTCTACCTCTTCTACGAGGATATTAAACAGAATCCAAAA

CATGAGATCCACAAGGTGTTGGAATTCTTGGAGAAAACTTGGTCAGGTGATGTTATAAACAAGATTGTCC

ACCATACCTCATTTGATGTAATGAAGGATAATCCCATGGCCAACCATACTGCGGTACCTGCTCACATATT CAATCACTCCATCTCAAAATTTATGAGGAAAGGTGGGATGCCTGGAGACTGGAAGAACCACTTTACTGTG

GCTTTGAATGAGAACTTTGATAAGCATTATGAAAAGAAGATGGCAGGGTCCACACTGAACTTCTGCCTGG

AGATCTGAGAG (SEQ ID NO:25)

TABLE 14B: The Amino Acid sequence of POLY13.

MAKIEKNAPTMEKKPELFNIMEVDGVPT I SKE EKVCNFQAKPDDLILATYPKSGTT MHEI DMIL NDGDVEKCKRAQT DRHAFLELKFPHKEKPD EFVLEMSSPQ IKTH PSHLIPPSI KENCKIVYVARN PKDC VSYYHFHRMASFMPDPQNLEEFYEKFMSGKGEFGS FDHVKG WAAKDMHRILYLFYEDIKQNPK HEIHKVLEF EKTWSGDVINKIVHHTSFDVMKDNPMANHTAVPAHI FNHSISKFMRKGGMPGDWKNHFTV ALNENFDKHYEKKMAGST NFCLEI (SEQ ID NO :26)

In a search of sequence databases, it was found, for example, that the nucleic acid sequence has 647 of 920 bases (70%) identical to a Mus musculus Sulfotransferase mRNA (GENBANK-ID: AF033653|acc:AF033653). The full amino acid sequence ofthe protein of the invention was found to have 173 of 284 amino acid residues (60%) identical to, and 219 of 284 residues (77%) positive with, the 304 amino acid residue sulfotransferase protein from Rattus norvegicus (ptnr: SWISSPROT-ACC:P50237) (Table 14C).

TABLE 14C: BLASTX of POLY13 against N-Hvdroxyarylamine Sulfotransferase (SEO ID NO:40) Length = 304

Score = 971 (341.8 bits), Expect = 3.5e-97, P = 3.5e-97 Identities = 173/284 (60%), Positives = 219/284 (77%), Frame = +1 Query: 64 EVDGVPTLILSKEWWEKVCNFQAKPDDLILATYPKSGTT MHEILDMILNDGDVEKCKRA 243

11 +1+ I + 1 +1+ IIIMIIII++III l +llll ll +lll lllll +ll +ll

Sbjct: 22 EVNGILMSKLMSDNWDKIW FQAKPDDLLIATYAKAGTT TQEIVDMIQNDGDVQKCQRA 81 Query: 244 QTLDRHAFLELKFPHKEKPDLEFVLEMSSPQLIKTHLPSHLIPPSIWKENCKIVYVAR P 423 I III | ₊| I |+ ₊| ||₊ +||||| |++||| MM ll +IIIM

Sbjct: 82 NTYDRHPFIEWTLPSPLNSGLDLANKMPSPRTLKTHLPVHMLPPSFWKENSKIIYVARA 141 Query: 424 KDCLVSYYHFHRMASFMPDPQNLEEFYEKFMSGKGEFGS FDHVKGWAAKDMHRILYLF 603 + l II +111 I 1+ I + l +11 +IM + IIIIIM II MiM Sbjct: 142 KDCLVSYYYFSRM KMLPDPGTLGEYIEQFKAGKVLWGS YDHVKGW DVKDQHRILYLF 201 Query: 604 YΞDI QNPKHEIHKVLEFLEKTWSGDVINKIVHHTSFDVMKDNPMANHTAVPAHIFNHSI 783

III+I++II II 1+ +1111 I +1+ I +111

Sbjct: 202 YΞDMKEDPKREI KIAKFLEKDISEEVLNKIIYHTSFDV KENPMANYTTLPSSIMDHSI 261

Query: 784 SKFMRKGGMPGD KNHFTVALNENFDKHYEKKMAGSTLNFCLEI 915

I Mill Mlllll + llll +1 + 11+ I +IIIII + I II

Sbjct: 262 SPFMRKG- PGD KNYFTVAQSEDFDEDYRRKMAGSNITFRTEI 304 (SEQ ID NO. : 40)

POLYl 3 also has significant homology to the proteins shown in the BLASTX data in

Table 14D. Table 14D. BLASTX alignments of POLY13

Sequences producing High-scoring Segment Pairs : Smallest Sum Reading High Prob . Frame Score P(N) N patp:W40498 Human EST protein - Homo sapiens, 294 aa.+l 769 1. .5e-75 1 patp: 44247 Human oestrogen sulphotransferase - Homo.+l 769 1. ,5e-75 1 patp:W23657 E6AP-binding protein cln25 - Homo sapien.+l 762 8. ,5e-75 1 patp:Y67294 Human STP2 (phenol sulphotransferase 2) .+1 744 6. .8e-73 1 patp:Y45080 Wheat N-hydroxyarylamine sulphotransfera. +1 468 1. .2e-43 1

The global sequence homology (as defined by FASTA alignment with the full length sequence of this protein) is 61% amino acid identity and 71% amino acid homology. In addition, this protein contains the following protein domains (as defined by Interpro) at the indicated amino acid positions: Sulfotransfer domain (IPR000863) at amino acid positions 24 to 293. PSORT analysis predicts the protein ofthe invention to be localized in the peroxisome with a certainty of 0.75. Based on the SIGNALP analysis, no signal peptide could be predicted for the protein of the invention.

The POLYl 3 nucleic acids and proteins ofthe invention are useful in potential therapeutic applications implicated in liver, intestine and kidney disorders including but not limited to primary biliary cirrhosis, primary sclerosing cholangitis, chronic active hepatitis and alcoholic cirrhosis, detoxification, ulcers, hyperthyroidism, developmental disorders, immune response, and/or other pathologies and disorders. For example, a cDNA encoding the Sulfotransferase-like protein may be useful in gene therapy in primary biliary cirrhosis, and the Sulfotransferase-like protein may be useful when administered to a subject in need thereof. By way of nonlimiting example, the compositions ofthe present invention will have efficacy for treatment of patients suffering from liver, intestine and kidney disorders including but not limited to primary biliary cirrhosis, primary sclerosing cholangitis, chronic active hepatitis and alcoholic cirrhosis, detoxification, ulcers, hyperthyroidism, developmental disorders, various forms of immune response. The novel nucleic acid encoding Sulfotransferase-like protein, and the Sulfotransferase-like protein ofthe invention, or fragments thereof, may further be useful in diagnostic applications, wherein the presence or amount ofthe nucleic acid or the protein are to be assessed. These materials are further useful in the generation of antibodies that bind immunospecifically to the novel substances ofthe invention for use in therapeutic or diagnostic methods.

POLY14-16

NOVEL SYNTAXIN-LIKE PROTEINS AND NUCLEIC ACIDS

Syntaxins belong to a family of proteins that appear to be involved in the docking vesicles with the plasma membrane during transmitter release. One of these proteins, designated syntaxin IB (STX1B), is directly implicated in the process of calcium-dependent synaptic transmission in rat brain. The expression of this protein is transiently induced by long-term potentiation of synaptic responses in the rat hippocampus. The protein may play an important role in the excitatory pathway of synaptic transmission, which is known to be implicated in several neurologic diseases.The human STX1B gene was mapped to 16pl 1.2 by fluorescence in situ hybridization. The gene was found at a single locus. Chromosome rearrangements with breaks in 16pl 1 are observed in myxoid liposarcoma and in acute myeloid leukemia. A tumor that displays neuroendocrine properties, small cell lung cancer, has been observed in about 60% of patients with Lambert-Eaton myasthenic syndrome , an autoimmune disease of neurotransmission that is characterized by muscle weakness. Autoantibodies from these patients recognize the presynaptic N-type calcium channel and synaptotagmin, two proteins that are involved in synaptic transmission and interact with syntaxin.

Synaptic vesicles store neurotransmitters that are released during calcium-regulated exocytosis. The specificity of neurotransmitter release requires the localization of both synaptic vesicles and calcium channels to the presynaptic active zone. Syntaxins function in this vesicle fusion process. Syntaxins also serve as a substrate for botulinum neurotoxin type C, a metalloprotease that blocks exocytosis and has high affinity for a molecular complex that includes the alpha-latrotoxin receptor which produces explosive exocytosis.

By PCR analysis of human/rodent somatic cell hybrid panels and fluorescence in situ hybridization, the STX1A gene was mapped to chromosome 7ql 1.2. Syntaxin 1A is expressed in airway epithelial cells, and is not a neural-specific protein and syntaxin 1 A regulates CFTR activity in airway epithelial cells.

Both syntaxin4 and NAMP2 are implicated in insulin regulation of glucose transporter- 4 (GLUT4) trafficking in adipocytes as target (t) soluble Ν-ethylmaleimide-sensitive factor attachment protein receptors (SNARE) and vesicle (v)-SNARE proteins, respectively, which mediate fusion of GLUT4-containing vesicles with the plasma membrane. Synaptosome- associated 23-kDa protein (SNAP23) is a widely expressed isoform of SNAP25, the principal t-SNARE of neuronal cells, and colocalizes with syntaxin4 in the plasma membrane of 3T3- Ll adipocytes. In the present study, two SNAP23 mutants, SNAP23-DeltaC8 (amino acids 1 to 202) and SNAP23-DeltaC49 (amino acids 1 to 161), were generated to determine whether SNAP23 is required for insulin-induced translocation of GLUT4 to the plasma membrane in 3T3-L1 adipocytes. Wild-type SNAP23 (SNAP23-WT) promoted the interaction between syntaxin4 and NAMP2 both in vitro and in vivo. Although SΝAP23-DeltaC49 bound to neither syntaxin4 nor NAMP2, the SΝAP23-DeltaC8 mutant bound to syntaxin4 but not to NAMP2. In addition, although SΝAP23-DeltaC8 bound to syntaxin4, it did not mediate the interaction between syntaxin4 and NAMP2. Moreover, overexpression of SΝAP23-DeltaC8 in 3T3-L1 adipocytes by adeno virus-mediated gene transfer inhibited insulin-induced translocation of GLUT4 but not that of GLUTI. In contrast, overexpression of neither SNAP23-WT nor SNAP23-DeltaC49 in 3T3-L1 adipocytes affected the translocation of GLUT4 or GLUTI. Together, these results demonstrate that SNAP23 contributes to insulin- dependent trafficking of GLUT4 to the plasma membrane in 3T3-L1 adipocytes by mediating the interaction between t-SNARE (syntaxin4) and v-SNARE (VAMP2).

POLY14

A novel POLY14 nucleic acid was identified as described in Example 1. A POLY14 nucleic acid is found on chromosome 1. The novel nucleic acid of 893 nucleotides, POLYl 4 (designated CuraGen Ace. No. h_nh0778pl7_A), encodes a novel Syntaxin-like protein as shown in TABLE 15. An open reading frame was identified beginning with an ATG initiation codon at nucleotides 5-7 and ending with a TAA codon at nucleotides 887-889. A putative untranslated region upstream from the initiation codon and downstream from the termination codon is underlined in TABLE 15 A, and the start and stop codons are in bold letters. The encoded protein having 294 amino acid residues is presented using the one-letter code in TABLE 15B.

TABLE 15A: The Nucleotide sequence of POLY14 GAAGATGAAAGACCGACTTCAAGAACTAAAGCAGAGAACAAAGGAAATTGAACTCTCTAGAGACAGTCAT GTATCAACTACAGAAACAGAGGAACAAGGGGTGTTTCTACAGCAAGCTGTTATTTATGAAAGAGAGCCTG TAGCTGAGAGACACCTACATGAAATCCAAAAACTACAGGAAAGTATTAACAATTTGGCAGATAATGTTCA AAAATTTGGGCAGCAACAGAAAAGTCTGGTGGCTTCAATGAGAAGGTTTAGTCTACTTAAGAGAGAGTCT ACCATTACAAAGGAGATAAAAATTCAGGCAGAATACATCAACAGAAGTTTGAATGATTTAGTTAAAGAAG TTAAAAAGTCAGAGGTTGAAAATGGTCCATCTTCAGTGGTCACAAGGATACTTAAATCTCAGCATGCTGC AATGTTCCGCCATTTTCAGCAAATCATGTTTATATACAATGACACAATAGCAGCAAAGCAAGAGAAGTGC AAGACATTTATTTTACGTCAGCTTGAAGTTGCTGGAAAAGAGATGTCTGAAGAAGATGTAAATGATATGC TTCATCAAGGAAAATGGGAAGTTTTTAATGAAAGCTTACTTACAGAAATCAATATCACTAAAGCACAACT TTCAGAGATTGAACAGAGACACAAGGAACTTGTTAATTTGGAGAACCAAATAAAGGATTTAAGGGATCTT TTCATTCAGATATCTCTTTTAGTAGAGGAACAAGG GAGAGCATCAACAATATTGAAATGACAGTGAATA GTACAAAAGAGTATGTTAACAATACTAAAGAGAAATTTGGACTAGCTGTAAAATACAAAAAAAGAAATCC TTGCAGAGTACTGTGTTGTTGGTGCTGTCCATGCTGTAGCTCAAAATAAAGAA (SEQ ID NO: 27)

TABLE 15B: The Amino Acid sequence of POLY14 MKDR QELKQRTKEIELSRDSHVSTTETEEQGVFLQQAVIYEREPVAERHLHEIQKLQESINN ADNVQK FGQQQKS VASMRRFS LKRESTITKEIKIQAEYINRSLNDLVKEVKKSEVENGPSSWTRI KSQHAAM FRHFQQIMFIYNDTIAAKQΞKCKTFILRQLEVAGKEMSEEDVNDM HQGKWEVFNES TEINITKAQLS EIEQRHKE VNLENQIKDLRD FIQISLLVEEQGESINNIEMTVNSTKEYVNNTKΞKFGLAVKYKKRNPC RVLCCWCCPCCSSK (SEQ ID NO :28)

In a search of sequence databases, it was found, for example, that the nucleic acid sequence has 363 of 622 bases (58%) identical to a Caenorhabditis elegans Syntaxin mRNA (GENBANK-ID: AB008842|acc:AB008842). The full amino acid sequence ofthe protein of the invention was found to have 108 of 290 amino acid residues (37%) identical to, and 184 of 290 residues (63%) positive with, the 287 amino acid residue SYNTAXIN 11 protein from Homo sapiens (ptnr: SWISSNEW-ACC:O75558) (Table 15C).

TABLE 15C: BLASTX of POLY14 against Syntaxin 11 (SEO ID NO:41)

Length = 287

Score = 553 (194.7 bits), Expect = 6.9e-53, P = 6.9e-53 Identities = 108/290 (37%) , Positives = 184/290 (63%) , Frame = +2

Query: 5 MKDRLQELKQRTKEIELSRDSHVSTTETΞEQGVFLQQAVIYEREPVAERHLHEIQ LQES 184 IMM M ++II+ + +++ + +++I + + I +|+ +| + Sbj ct : 1 MKDRLAEL- -LDLSKQYDQQFPDGDDEFDSPHEDIVFETDHILESLYRDIRDIQ.DE 54

Query: 185 I LADNVQKFGQQQKSLVASMRRFSLLKRES-TITKEIKIQAEYINRSLNDLVKEVKKS 361

I +I++ |₊| + mi I +||₊₊ +| i II + I |₊ I + ₊ + + Sbjct: 55 NQLLVADVKRLGKQNARFLTSMRRLSSIKRDTNSIAKAIKARGEVIHCKLRAMKELSEAA 114 Query: 362 EVENGPSSWTRILKSQHAAMFRHFQQIMFIYNDTIAAKQEKCKTFILRQLEVAGKEMSE 541

I ++II I I II ++I+ 1+ 11+ I II +++ II I Mil- lll+l

Sbjct: 115 EAQHGPHSAVARISRAQY ALTLTFQRAMHDYNQAEMKQRDNCKIRIQRQLEIMGKEVSG 174

Query: 542 EDVNDMLHQGKWEVFNESLLTEINITKAQLSEIEQRHKELV LENQIKDLRDLFIQISLL 721

+ + II llll+ll+l+ll ++ +1 I +l 11 11+11+ II++I+I+ +II+I+++I

Sbjct: 175 DQIEDMFEQGK DVFSENLLADVKGARAALNEIESRHRELLRLESRIRDVHELFLQMAVL 234 Query: 722 VEEQGESINNIEMTVNSTKEYVNNTKEKFGLAVKYKKRNPCRVLCC CCPC 874

M+l +++I 11+ I I +1 I + II+I+++IIII lll+llll

Sbjct: 235 VEKQADTLNVIELNVQKTVDYTGQAKAQVRKAVQYEEKNPCRTLCCFCCPC 285 (SEQ ID NO.41)

POLYl 4 also has significant homology to the proteins shown in the BLASTX data in Table 15D.

Table 15D. BLASTX alignments of POLY14

Sequences producing High-scoring Segment Pairs : Smalles t Sum

Reading High Prob . Frame Score P (N) N patp : R44916 Rat post-synaptic NMDA receptor GR33 - Rat . +2 381 2 Oe-34 1 patp : W43419 Rat syntaxin IB protein - Rattus sp, 288 aa+2 381 2 Oe-34 1 patp : R96421 Rat syntaxin 1A - Rattus rattus , 288 aa . +2 379 3 3e-34 1 patp : W30105 Rat syntaxin - Rattus sp, 288 aa . +2 379 3 3e-34 1 patp : W24927 Rat syntaxin 1A - Rattus rattus , 288 aa . +2 379 3 3e-34 1 patp : B12822 Rat syntaxin 1A amino acid sequence - Ratt . +2 379 3 3e-34 1

The global sequence homology (as defined by FASTA alignment with the full length sequence of this protein) is 51% amino acid identity and 37% amino acid homology. In addition, this protein contains the following protein domain (as defined by Interpro) at the indicated amino acid positions: syntaxin family (IPR000017) at amino acid positions 1-292. PSORT analysis predicts the protein ofthe invention to be localized in the plasma membrane with a certainty of 0.6. Based on the SIGNALP analysis, no signal peptide could be predicted for the protein ofthe invention. POLY15

In the present invention, the target sequence identified previously, POLY 14, was subjected to the exon linking process as described in Example 6. The novel nucleic acid of 892 nucleotides, POLYl 5 (designated CuraGen Ace. No. h_nh0778pl7_Al), encodes a novel Syntaxin-like protein as shown in TABLE 16. An open reading frame was identified beginning with an ATG initiation codon at nucleotides 4-6 and ending with a TAA codon at nucleotides 887-889. A putative untranslated region upstream from the initiation codon and downstream from the termination codon is underlined in TABLE 16A, and the start and stop codons are in bold letters. The encoded protein having 294 amino acid residues is presented using the one-letter code in TABLE 16B. The molecular weight of POLYl 5 is 3.4324 kDa.

TABLE 16A: The Nucleotide sequence ofPOLY15

AAGATGAAAGACCGACTTCAAGAACTAAAGCAGAGAACAAAGGAAATTGAACTCTCTAGAGACAGTCATGTATCAA CTACAGAAACAGAGGAACAAGGGGTGTTTCTACAGCAAGCTGTTATTTATGAAAGAGAGCCTGTAGCTGAGAGACA CCTACATGAAATCCAAAAACTACAGGAAAGTATTAACAATTTGGCAGATAATGTTCAAAAATTTGGGCAGCAACAG AAAAGTCTGGTGGCTTCAATGAGAAGGTTTAGTCTACTTAAGAGAGAGTCTACCATTACAAAGGAGATAAAAATTC AGGCAGAATACATCAACAGAAGTTTGAATGATTTAGTTAAAGAAGTTAAAAAGTCAGAGGTTGAAAATGGTCCATC TTCAGTGGTCACAAGGATACTTAAATCTCAGCATGCTGCAATGTTCCGCCATTTTCAGCAAATCATGTTTATATAC AATGACACAATAGCAGCAAAGCAAGAGAAGTGCAAGACATTTATTTTACGTCAGCTTGAAGTTGCTGGAAAAGAGA TGTCTGAAGAΆGATGTAΆATGATATGCTTCATCAAGGAΆAATGGGAAGTTTTTAATGAAAGCTTACTTACAGAAAT CAATATCACTAAAGCACAACTTTCAGAGATTGAACAGAGACACAAGGAACTTGTTAATTTGGAGAACCAAATAAAG GATTTAΆGGGATCTTTTCATTCAGATATCTCTTTTAGTAGAGGAACAAGGAGAGAGCATCAACAATATTGAΆATGA CAGTGAATAGTACAAAAGAGTATGTTAACAATACTAAΆGAGAAATTTGGACTAGCTGTAAAATACAAAAAAAGAAA

TCCTTGCAGAGTACTGTGTTGTTGGTGCTGTCCATGCTGTAGCTCAAAATAAAGAA ( SEQ ID NO : 29 )

TABLE 16B: The Amino Acid sequence of POLY15

MKDRLQELKQRTKEIELSRDSHVSTTETEEQGVFLQQAVIYEREPVAERHLHEIQK QESINNLADNVQKFGQQQK SLVASMRRFSLLKRESTITKEIKIQAEYINRSLNDLVKEVKKSEVENGPSSVVTRILKSQHAAMFRHFQQIMFIYN DTIAAKQEKCKTFILRQLEVAGKEMSEEDVNDMLHQGKWEVFNESLLTEINITKAQLSEIEQRHKELVNLENQIKD LRDLFIQISLLVEEQGESINNIEMTVNSTKEYVNNTKEKFGLAVKYKKRNPCRVLCC CCPCCSSK (SEQ ID NO :30)

The full amino acid sequence ofthe protein ofthe invention was found to have 108 of 290 amino acid residues (37%) identical to, and 184 of 290 residues (63%) positive with, the 287 amino acid residue SYNTAXIN 11 protein from Homo sapiens (ptnr: SWISSNEW- ACC:O75558) (Table 16C). TABLE 16C: BLASTX of POLY15 against Syntaxin 11 (SEO ID NO:42)

Length = 287

Score = 553 (194.7 bits), Expect = 6.9e-53, P = 6.9e-53 Identities = 108/290 (37%) , Positives = 184/290 (63%) , Frame = +2

Query: 5 MKDRLQELKQRTKEIELSRDSHVSTTETEEQGVFLQQAVIYEREPVAERHLHEIQ LQES 184

M i l l I I ++ I I + + +++ + +++ I + + I + 1 + + 1 +

Sbjct: 1 MKDRLAEL LDLSKQYDQQFPDGDDEFDSPHEDIVFETDHILESLYRDIRDIQDE 54

Query: 185 INNLADNVQKFGQQQKSLVASMRRFSLLKRES-TITKEIKIQAEYINRSLNDLVKEVKKS 361

I +I++ I+l + MM I +II++ +1 I II + I 1+ I + + + +

Sbj ct : 55 NQLLVADVKRLGKQNARFLTSMRRLSSIKRDTNSIAKAIKARGEVIHCKLRAMKELSEAA 114

Query: 362 EVENGPSSWTRILKSQHAA FRHFQQIMFIYNDTIAAKQEKCKTFILRQLEVAGKEMSE 541

I ++M I I II ++I+ 1+ 11+ I II +++ II I 1111+ lll+l

Sbj ct : 115 EAQHGPHSAVARISRAQY ALTLTFQRAMHDYNQAEMKQRDNCKIRIQRQLEIMG EVSG 174

Query: 542 EDVNDMLHQG EVFNESLLTEINITKAQLSEIEQRHKELVNLENQIKDLRDLFIQISLL 721

+ + I I M M + M + I + I I ++ + 1 l + l l l 1 1 + 1 1 + M ++ I + I + + M + I +++ I

Sbj ct : 175 DQIEDMFEQGK DVFSENLLADVKGARAALNEIESRHRELLRLESRIRDVHELFLQMAVL 234

Query: 722 VEEQGESINNIEMTVNSTKEYVNNTKEKFGLAVKYKKRNPCRVLCCWCCPC 874

M + l +++ I 1 1 + I I + 1 I + I I + I +++ M M l l l + I I M

Sbj ct : 235 VEKQADTL VIELNVQKTVDYTGQAKAQVRKAVQYEEK PCRTLCCFCCPC 285 (SEQ ID NO . 42 )

The global sequence homology (as defined by FASTA alignment with the full length sequence of this protein) is 51% amino acid identity and 37% amino acid homology. In addition, this protein contains the following protein domain (as defined by Interpro) at the indicated amino acid positions: syntaxin family (IPR000017) at amino acid positions 1-292.

PSORT analysis predicts the protein ofthe invention to be localized in the cytoplasm with a certainty of 0.6500. Based on the SIGNALP analysis, no N-terminal signal peptide could be predicted for the protein ofthe invention.

POLY16 In the present invention, the target sequence identified previously, POLYl 4, was subjected to the exon linking process as described in Example 6. The novel nucleic acid of 892 nucleotides, POLYl 6 (designated CuraGen Ace. No. CG55655-02), encodes a novel Syntaxin-like protein as shown in TABLE 17. An open reading frame was identified beginning with an ATG initiation codon at nucleotides 4-6 and ending with a TAA codon at nucleotides 887-889. A putative untranslated region upstream from the initiation codon and downstream from the termination codon is underlined in TABLE 17 A, and the start and stop codons are in bold letters. The encoded protein having 294 amino acid residues is presented using the one-letter code in TABLE 17B. The molecular weight of POLYl 6 is 3.4324 kDa.

TABLE 17A: The Nucleotide sequence of POLY16

5. AAGATGAAAGACCGACTTCAAGAACTAAAGCAGAGAACAAAGGAAATTGAACTCTCTAGAGACAGTCATGTATCAA CTACAGAAACAGAGGAACAAGGGGTGTTTCTACAGCAAGCTGTTATTTATGAAAGAGAGCCTGTAGCTGAGAGACA CCTACATGAAATCCAAAAACTACAGGAAAGTATTAACAATTTGGCAGATAATGTTCAAAAATTTGGGCAGCAACAG AAAAGTCTGGTGGCTTCAATGAGAAGGTTTAGTCTACTTAAGAGAGAGTCTACCATTACAAAGGAGATAAAAATTC AGGCAGAATACATCAACAGAAGTTTGAATGATTTAGTTAAAGAAGTTAAAAAGTCAGAGGTTGAAAATGGTCCATC 0 TTCAGTGGTCACAAGGATACTTAAATCTCAGCATGCTGCAATGTTCCGCCATTTTCAGCAAATCATGTTTATATAC AATGACACAATAGCAGCAAAGCAAGAGAAGTGCAAGACATTTATTTTACGTCAGCTTGAAGTTGCTGGAAAAGAGA TGTCTGAAGAAGATGTAAATGATATGCTTCATCAAGGAAAATGGGAAGTTTTTAATGAAAGCTTACTTACAGAAAT CAATATCACTAAAGCACAACTTTCAGAGATTGAACAGAGACACAAGGAACTTGTTAATTTGGAGAACCAAATAAAG GATTTAAGGGATCTTTTCATTCAGATATCTCTTTTAGTAGAGGAACAAGGAGAGAGCATCAACAATATTGAAATGA 5 CAGTGAATAGTACAAAAGAGTATGTTAACAATACTAAAGAGAAATTTGGACTAGCTGTAAAATACAAAAAAAGAAA TCCTTGCAGAGTACTGTGTTGTTGGTGCTGTCCATGCTGTAGCTCAAAATAAAGAA (SEQ ID NO: 29)

TABLE 17B: The Amino Acid sequence of POLY16

MKDRLQELKQRTKEIELSRDSHVSTTETEEQGVFLQQAVIYEREPVAERHLHEIQKLQESINNLADNVQKFGQQQK 0 SLVASMRRFSLLKRESTITKEIKIQAEYINRSLNDLVKEVKKSEVENGPSSVVTRILKSQHAAMFRHFQQIMFIYN DTIAAKQEKCKTFILRQLEVAGKEMSEEDVNDMLHQGKWEVFNESLLTEINITKAQLSEIEQRHKELVN ENQIKD LRDLFIQISL VEEQGESINNIEMTVNSTKEYVNNTKEKFGLAVKYKKRNPCRVLCCWCCPCCSSK (SEQ ID NO :30)

5 The full amino acid sequence ofthe protein ofthe invention was found to have 108 of

290 amino acid residues (37%) identical to, and 184 of 290 residues (63%) positive with, the 287 amino acid residue SYNTAXIN 11 protein from Homo sapiens (ptnr: SWISSNEW- ACC:O75558). The global sequence homology (as defined by FASTA alignment with the full length sequence of this protein) is 51% amino acid identity and 37% amino acid homology. In 0 addition, this protein contains the following protein domain (as defined by Interpro) at the indicated amino acid positions: syntaxin family (IPR000017) at amino acid positions 1-292.

PSORT analysis predicts the protein ofthe invention to be localized in the cytoplasm with a certainty of 0.6500. Based on the SIGNALP analysis, no N-terminal signal peptide could be predicted for POLYl 6.

5 This Syntaxin-like protein may function as a member of a "Syntaxin family".

Therefore, the POLYl 4- 16 novel nucleic acids and proteins identified here may be useful in potential therapeutic applications implicated in (but not limited to) various pathologies and disorders such as various forms of cancers, neurologic disorders, autoimmune disease, CFTR, Lambert-Eaton myasthenic syndrome, small cell lung cancer, myxoid liposarcoma and in acute myeloid leukemia, Type I and II diabetes, obesity, skin disorders, degenerative disorders affecting epithelial-derived tissues and/or other pathologies and disorders. For example, a cDNA encoding the Syntaxin-like protein may be useful in gene therapy, and the Syntaxin- like protein may be useful when administered to a subject in need thereof. By way of nonlimiting example, the compositions ofthe present invention will have efficacy for treatment of patients suffering from various forms of cancers, neurologic disorders, autoimmune disease, CFTR, Lambert-Eaton myasthenic syndrome, small cell lung cancer, myxoid liposarcoma and in acute myeloid leukemia, Type I and II diabetes, obesity, skin disorders, and various degenerative disorders affecting epithelial-derived tissues. The novel nucleic acid encoding Syntaxin-like protein, and the Syntaxin-like protein ofthe invention, or fragments thereof, may further be useful in diagnostic applications, wherein the presence or amount ofthe nucleic acid or the protein are to be assessed. These materials are further useful in the generation of antibodies that bind immunospecifically to the novel substances ofthe invention for use in therapeutic or diagnostic methods.

POLY17

PROHIBITIN-LIKE PROTEINS AND NUCLEIC ACIDS

Prohibitin (PHB) is a 30-kD intracellular, antiproliferative protein. The gene was mapped to chromosome 17 by analysis of human-mouse somatic cell hybrid cell lines using a genomic fragment of human prohibitin DNA isolated from a library using the rat prohibitin cDNA clone. The PHB gene was located in the 17ql 1.2-q23 region where a gene responsible for hereditary breast cancer is localized. The human homolog ofthe rat prohibitin gene mapped to 17ql2-q21 by in situ hybridization. The human prohibitin gene family consists of one functional PHB gene on 17q21 and four processed pseudogenes, each on a different chromosome: PHBP1 on 6q25, PHBP2 on 1 lpl 1.2, PHBP3 on lp31.3, and PHBP4 on 2q21. DNA sequence analysis of two exons in this gene in 23 sporadic breast cancers, which showed loss of heterozygosity on the long arm of chromosome 17 (17q) or developed in patients 35 years old or younger, identified four cases of somatic mutation; two of these were missense mutations; one showed a two-base deletion resulting in truncation ofthe gene product due to a frame shift; the other had a C to T transition in an intron adjacent to an intron- exon boundary. These results suggest that this gene may be a tumor suppressor gene and is associated with tumor development and/or progression of at least some breast cancers. Mutations in the PHB gene were not detected in other forms of tumors, namely, those of ovary, liver, and lung.

The retinoblastoma tumor suppressor protein and its family members, p 107 and p 130, are major regulators ofthe mammalian cell cycle. They exert their growth suppressive effects at least in part by binding the E2F family of transcription factors and inhibiting their transcriptional activity. Agents that disrupt the interaction between Rb family proteins and E2F promote cell proliferation. Prohibitin physically interacts with all three Rb family proteins in vitro and in vivo, and was very effective in repressing E2F-mediated transcription.

Prohibitin could inhibit the activity of E2Fs 1, 2, 3, 4 and 5, but could not affect the activity of promoters lacking an E2F site. Prohibitin-mediated repression of E2F could not be reversed by adenovirus El A protein. A prohibitin mutant that could not bind to Rb was impaired in its ability to repress E2F activity and inhibit cell proliferation. Prohibitin may be a novel regulator of E2F activity that responds to specific signaling cascades.

A POLYl 7 nucleic acid was identified as described in Example 1. A POLYl 7 nucleic acid of 967 nucleotides (designated CuraGen Ace. No. GM_11817402_A) encoding a novel Prohibitin -like protein is shown in TABLE 18. An open reading frame was identified beginning with an ATG initiation codon at nucleotides 75-77 and ending with a TGA codon at nucleotides 888-890. A putative untranslated region upstream from the initiation codon and downstream from the termination codon is underlined in TABLE 18 A, and the start and stop codons are in bold letters. The encoded protein having 271 amino acid residues is presented using the one-letter code in TABLE 18B.

TABLE 18A: The Nucleic Acid sequence of POLY17. TCAGAAATCAATGATAAAGGGACGGAATTCATGTGGGGGGTTGGAGTGGACGCAGGCGTGAGTGGGTCCAGCA GATGGAAACACAGCTGCCAAGTCTGCCCCTGTCCTTAGCTTCTGCAGGAGGTGTGGGGAACTCTGCCTTCTAC AATGTGATGCTGCACAGAGAGCTGTCTGTCATCTTCGACCAATTCCATGGCATTCAGGACACTGTGATAGGGG AAGGAACGCACTTTCTCATCCCATGGGAAAAGAAACCAATTATTTTTGACTGCTGCTCTCGACCACATTATGC ACCAATCATCACTGTGAGCAAAGATTGTCACCATGTCACCATCACACTGGGCGTCCTCTTCCCGCCTTGTTGC TGGCCAGGTCCTTGCATCTTCCAATTACTGGAGAAGCCAATGAAGAATGTGCTGCCATCCATCACTGCGGAGC TCCTCAAGCTGGGGGCGGCTCAGGCTGACGCTGGAGAACTGATCACGCAGGGAGAGCTGGGCTCCAGACAGGT GAGCGAGCAATTAACTGAGCAAGCAGCAACCTTTGGGTTCCTCCTGGATGCTGTGACCTTGGATCTGACCTTC GGGAAGGAATTTGCAGAAGCAGTGGAACCAAAGGAGGTGGCTCAGCAGGAAGAAGAGAGGGCCAGATCTGTGG TGGCAAGGGCTGAGCAGCAGAAGACGGCGGCCATCATCTCTGCCGAGGGCGACTCCAAGGCCACGGAGTTCAT CGCCAGCTCAGTGGCCACCGCAGGTGACGGCCTGATCAAGGCCCACAAGCTGGAACCATGGAGGACACTGGCC CTCCAGCTCTCAGAACTCATCCACCTCATCCACCTGCCCGTGGGGACATCTGTGCTCCTCCAGCTGCCCCAGC GCAGGCCGCCCTGACCTGCACCTCCTCCAGCCAACTGGGCCACAGCACCAATGACTTTTACTACCGCCTTCCT TCTGTCCCCACTCCAGAA (SEQ ID NO:33)

TABLE 18B: The Amino Acid sequence ofPOLY17.

METQLPSLPLSLASAGGVGNSAFYNVMLHRELSVIFDQFHGIQDTVIGEGTHFLIP EKKPII FDCCSRPHYAPIITVSKDCHHVTITLGVLFPPCCWPGPCIFQLLEKPMKNVLPSITAELLKLG AAQADAGELITQGELGSRQVSEQLTEQAATFGFLLDAVTLDLTFGKEFAEAVEPKEVAQQEEE RARSVVARAEQQKTAAIISAEGDSKATEFIASSVATAGDGLIKAHKLEPWRTLALQLSELIHL IHLPVGTSVLLQLPQRRPP (SEQ ID NO: 34) In a search of sequence databases, it was found, for example, that the nucleic acid sequence has 737 of 936 bases (78%) identical to Homo sapiens Prohibitin mRNA (GENBANK-ID: S85655). The full amino acid sequence ofthe protein ofthe invention was found to have 168 of 259 amino acid residues (64%) identical to, and 194 of 259 residues (74 %) positive with, the 272 amino acid residue Prohibitin protein from Homo sapiens (ptnr:SPTREMBL-ACC:P35232).

POLYl 7 also has high homology to the proteins in the BLAST data shown in Table 18C.

Table 18C. BLASTP results for POLY17

Gene Index/ Protein/ Organism Length Identity Positives Expect Identifier (aa) (%) (%>

POLYl 7 also has high homology to the amino acid sequences presented in the BLASTX data shown in Table 18D.

Table 18D. BLASTX alignments of POLY17

Sequences producing High-scoring Segment Pairs : Smallest Sum Reading High Prob . Frame Score P (N) N patp : R13467 Cc protein - Drosophila, 276 aa . +3 613 5 . 2e-59 1 patp : B65735 Prohibitin-related protein #1 - Pinus radi . +3 473 3 . 6e-44 1

The global sequence homology (as defined by FASTA alignment with the full length sequence of this protein) is 68% amino acid identity and 63% amino acid homology. In addition, this protein contains the following protein domains (as defined by Interpro) at the indicated amino acid positions: SPFH domain / Band 7 family (IPR001107) at amino acid positions from 8 to 202.

In a search of CuraGen' s proprietary human expressed sequence assembly database, assembly 11817402 (309 nucleotides) was/were identified as having >95% homology to this predicted gene sequence. This database is composed ofthe expressed sequences (as derived from isolated mRNA) from more than 96 different tissues. The mRNA is converted to cDNA and then sequenced. These expressed DNA sequences are then pooled in a database and those exhibiting a defined level of homology are combined into a single assembly with a common consensus sequence. The consensus sequence is representative of all member components. Since the nucleic acid ofthe described invention has >95% sequence identity with the CuraGen assembly, the nucleic acid ofthe invention represents an expressed gene sequence. This DNA assembly has one component and was found by CuraGen to be expressed in the endocrine system, for example in the thyroid.

PSORT analysis predicts the protein ofthe invention to be localized in the cytoplasm with a certainty of 0.4500. Using the SIGNALP analysis, it is predicted that the protein ofthe invention has a signal peptide with most likely cleavage site between pos. 19 and 20 of SEQ ID NO.: 34.

POLYl 7 is a new member ofthe prohibitin-like family of proteins, and is therefor useful as a marker to detect binding proteins ofthe probibitin-like protein family. POLYl 7 is also useful to detect tissues ofthe endocrine system, e.g. the thyroid, and activated B-cells, e.g. PMA-treated chronic leukemic B-cells. The above defined information for POLY 17 suggests that this Prohibitin -like protein may function as a member of a "Prohibitin family". Therefore, the novel nucleic acids and proteins identified here may be useful in potential therapeutic applications implicated in (but not limited to) various pathologies and disorders such as breast and ovarian cancer, tumor suppression, senescence, growth regulation, modulation of apotosis, reproductive control and associated disorder^'s of reproduction, endometrial hyperplasia and adenocarcinoma, and/or other pathologies and disorders. For example, a cDNA encoding the Prohibitin -like protein may be useful in gene therapy for leukemia, and the Prohibitin -like protein may be useful when administered to a subject in need thereof. By way of nonlimiting example, the compositions ofthe present invention will have efficacy for treatment of patients suffering from cancers including but not limited to breast and ovarian cancer, tumor suppression, senescence, growth regulation, modulation of apotosis, reproductive control and associated disorders of reproduction, endometrial hyperplasia and adenocarcinoma. The novel nucleic acid encoding Prohibitin -like protein, and the Prohibitin -like protein ofthe invention, or fragments thereof, may further be useful in diagnostic applications, wherein the presence or amount ofthe nucleic acid or the protein are to be assessed. These materials are further useful in the generation of antibodies that bind immunospecifically to the novel substances ofthe invention for use in therapeutic or diagnostic methods. POLYX Nucleic Acids

The novel nucleic acids ofthe invention include those that encode a POLYX or POLYX-like protein, or biologically-active portions thereof. The nucleic acids include nucleic acids encoding polypeptides that include the amino acid sequence of one or more of SEQ ID NO:2rø (wherein n = 1 to 17). The encoded polypeptides can thus include, e.g., the amino acid sequences of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 3414, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34.

In some embodiments, a nucleic acid encoding a polypeptide having the amino acid sequence of one or more of SEQ ID NO:2« (wherein n = 1 to 17) includes the nucleic acid sequence of any of SEQ ID NO:2«-l (wherein n = 1 to 17), or a fragment thereof, and can thus include, e.g., the nucleic acid sequences of SEQ ID NO:l, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31 and/or 33. Additionally, the invention includes mutant or variant nucleic acids of any of SEQ ID NO:2«-l (wherein n = 1 to 17), or a fragment thereof, any of whose bases may be changed from the disclosed sequence while still encoding a protein that maintains its POLYX-like biological activities and physiological functions. The invention further includes the complement ofthe nucleic acid sequence of any of SEQ ID NO:2«-l (wherein n = 1 to 17), including fragments, derivatives, analogs and homologs thereof. The invention additionally includes nucleic acids or nucleic acid fragments, or complements thereto, whose structures include chemical modifications.

Also included are nucleic acid fragments sufficient for use as hybridization probes to identify POLYX-encoding nucleic acids (e.g., POLYX mRNA) and fragments for use as polymerase chain reaction (PCR) primers for the amplification or mutation of POLYX nucleic acid molecules. As used herein, the term "nucleic acid molecule" is intended to include DNA molecules (e.g., cDNA or genomic DNA), RNA molecules (e.g., mRNA), analogs ofthe DNA or RNA generated using nucleotide analogs, and derivatives, fragments, and homologs thereof. The nucleic acid molecule can be single-stranded or double-stranded, but preferably is double-stranded DNA. As utilized herein, the term "probes" refer to nucleic acid sequences of variable length, preferably between at least about 1 nucleotides (nt), 100 nt, or as many as about, e.g., 6,000 nt, depending upon the specific use. Probes are used in the detection of identical, similar, or complementary nucleic acid sequences. Longer length probes are usually obtained from a natural or recombinant source, are highly specific and much slower to hybridize than oligomers. Probes may be single- or double-stranded, and may also be designed to have specificity in PCR, membrane-based hybridization technologies, or ELISA-like technologies.

As utilized herein, the term "isolated" nucleic acid molecule is a nucleic acid that is separated from other nucleic acid molecules that are present in the natural source ofthe nucleic acid. Examples of isolated nucleic acid molecules include, but are not limited to, recombinant DNA molecules contained in a vector, recombinant DNA molecules maintained in a heterologous host cell, partially or substantially purified nucleic acid molecules, and synthetic DNA or RNA molecules. Preferably, an "isolated" nucleic acid is free of sequences which naturally flank the nucleic acid (i.e., sequences located at the 5'- and 3 '-termini ofthe nucleic acid) in the genomic DNA ofthe organism from which the nucleic acid is derived. For example, in various embodiments, the isolated POLYX nucleic acid molecule can contain less than approximately 50 kb, 25 kb, 5 kb, 4 kb, 3 kb, 2 kb, 1 kb, 0.5 kb or 0.1 kb of nucleotide sequences which naturally flank the nucleic acid molecule in genomic DNA ofthe cell from which the nucleic acid is derived. Moreover, an "isolated" nucleic acid molecule, such as a cDNA molecule, can be substantially free of other cellular material or culture medium when produced by recombinant techniques, or of chemical precursors or other chemicals when chemically synthesized.

As used herein, a "mature" form of a polypeptide or protein disclosed in the present invention is the product of a naturally occurring polypeptide or precursor form or proprotein. The naturally occurring polypeptide, precursor or proprotein includes, by way of nonlimiting example, the full length gene product, encoded by the corresponding gene. Alternatively, it may be defined as the polypeptide, precursor or proprotein encoded by an open reading frame described herein. The product "mature" form arises, again by way of nonlimiting example, as a result of one or more naturally occurring processing steps as they may take place within the cell, or host cell, in which the gene product arises. Examples of such processing steps leading to a "mature" form of a polypeptide or protein include the cleavage ofthe N-terminal methionine residue encoded by the initiation codon of an open reading frame, or the proteolytic cleavage of a signal peptide or leader sequence. Thus a mature form arising from a precursor polypeptide or protein that has residues 1 to N, where residue 1 is the N-terminal methionine, would have residues 2 through N remaining after removal of the N-terminal methionine. Alternatively, a mature form arising from a precursor polypeptide or protein having residues 1 to N, in which an N-terminal signal sequence from residue 1 to residue M is cleaved, would have the residues from residue M+l to residue N remaining. Further as used herein, a "mature" form of a polypeptide or protein may arise from a step of post-translational modification other than a proteolytic cleavage event. Such additional processes include, by way of non-limiting example, glycosylation, myristoylation or phosphorylation. In general, a mature polypeptide or protein may result from the operation of only one of these processes, or a combination of any of them.

A nucleic acid molecule ofthe invention, e.g., a nucleic acid molecule having the nucleotide sequence of SEQ ID NO:2«-l (wherein n = 1 to 17), or a complement of any of these nucleotide sequences, can be isolated using standard molecular biology techniques and the sequence information provided herein. Using all or a portion ofthe nucleic acid sequence of any of SEQ ID NO:2R-1 (wherein n=l to 17) as a hybridization probe, POLYX nucleic acid sequences can be isolated using standard hybridization and cloning techniques (e.g., as described in Sambrook et αl., eds., MOLECULAR CLONING: A LABORATORY MANUAL 2^nd Ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1989; and Ausubel, et αl., eds., CURRENT PROTOCOLS IN MOLECULAR BIOLOGY, John Wiley & Sons, New York, NY, 1993.)

A nucleic acid ofthe invention can be amplified using cDNA, mRNA or alternatively, genomic DNA, as a template and appropriate oligonucleotide primers according to standard PCR amplification techniques. The nucleic acid so amplified can be cloned into an appropriate vector and characterized by DNA sequence analysis. Furthermore, oligonucleotides corresponding to POLYX nucleotide sequences can be prepared by standard synthetic techniques, e.g., using an automated DNA synthesizer. As used herein, the term "oligonucleotide" refers to a series of linked nucleotide residues, which oligonucleotide has a sufficient number of nucleotide bases to be used in a PCR reaction. A short oligonucleotide sequence may be based on, or designed from, a genomic or cDNA sequence and is used to amplify, confirm, or reveal the presence of an identical, similar or complementary DNA or RNA in a particular cell or tissue.

Oligonucleotides comprise portions of a nucleic acid sequence having about 10 nt, 50 nt, or 100 nt in length, preferably about 15 nt to 30 nt in length. In one embodiment, an oligonucleotide comprising a nucleic acid molecule less than 100 nt in length would further comprise at lease 6 contiguous nucleotides of any of SEQ ID NO:2«-l (wherein n = 1 to 17), or a complement thereof. Oligonucleotides may be chemically synthesized and may also be used as probes.

In another embodiment, an isolated nucleic acid molecule ofthe invention comprises a nucleic acid molecule that is a complement ofthe nucleotide sequence shown in any of SEQ ID NO:2n-l (wherein n = 1 to 17). In still another embodiment, an isolated nucleic acid molecule ofthe invention comprises a nucleic acid molecule that is a complement ofthe nucleotide sequence shown in any of SEQ ID NO:2rø-l (wherein n = 1 to 17), or a portion of this nucleotide sequence. A nucleic acid molecule that is complementary to the nucleotide sequence shown in any of SEQ ID NO:2n-l (wherein n = 1 to 17) is one that is sufficiently complementary to the nucleotide sequence shown that it can hydrogen bond with little or no mismatches to the nucleotide sequence shown in of any of SEQ ID NO:2rø-l (wherein n = 1 to 17), thereby forming a stable duplex.

As used herein, the term "complementary" refers to Watson-Crick or Hoogsteen base- pairing between nucleotides units of a nucleic acid molecule, whereas the term "binding" is defined as the physical or chemical interaction between two polypeptides or compounds or associated polypeptides or compounds or combinations thereof. Binding includes ionic, non-ionic, Non der Waals, hydrophobic interactions, and the like. A physical interaction can be either direct or indirect. Indirect interactions may be through or due to the effects of another polypeptide or compound. Direct binding refers to interactions that do not take place through, or due to, the effect of another polypeptide or compound, but instead are without other substantial chemical intermediates. Additionally, the nucleic acid molecule ofthe invention can comprise only a portion of the nucleic acid sequence of any of SEQ ID NO:2«-l (wherein n = 1 to 17), e.g., a fragment that can be used as a probe or primer, or a fragment encoding a biologically active portion of POLYX. Fragments provided herein are defined as sequences of at least 6 (contiguous) nucleic acids or at least 4 (contiguous) amino acids, a length sufficient to allow for specific hybridization in the case of nucleic acids or for specific recognition of an epitope in the case of amino acids, respectively, and are at most some portion less than a full length sequence. Fragments may be derived from any contiguous portion of a nucleic acid or amino acid sequence of choice. Derivatives are nucleic acid sequences or amino acid sequences formed from the native compounds either directly or by modification or partial substitution. Analogs are nucleic acid sequences or amino acid sequences that have a structure similar to, but not identical to, the native compound but differs from it in respect to certain components or side chains. Analogs may be synthetic or from a different evolutionary origin and may have a similar or opposite metabolic activity compared to wild-type.

Derivatives and analogs may be full-length or other than full-length, if the derivative or analog contains a modified nucleic acid or amino acid, as described infr . Derivatives or analogs ofthe nucleic acids or proteins ofthe invention include, but are not limited to, molecules comprising regions that are substantially homologous to the nucleic acids or proteins ofthe invention, in various embodiments, by at least about 70%, 80%, 85%, 90%, 95%, 98%, or even 99% identity (with a preferred identity of 80-99%) over a nucleic acid or amino acid sequence of identical size or when compared to an aligned sequence in which the alignment is done by a computer homology program known in the art, or whose encoding nucleic acid is capable of hybridizing to the complement of a sequence encoding the aforementioned proteins under stringent, moderately stringent, or low stringent conditions. See e.g. Ausubel, et αl., CURRENT PROTOCOLS IN MOLECULAR BIOLOGY, John Wiley & Sons, New York, NY, 1993, and below. An exemplary program is the Gap program (Wisconsin Sequence Analysis Package, Version 8 for UNIX, Genetics Computer Group, University Research Park, Madison, WI) using the default settings, which uses the algorithm of Smith and Waterman (Adv. Appl. Math., 1981, 2: 482-489), which is incoφorated herein by reference in its entirety. As utilized herein, the term "homologous nucleic acid sequence" or "homologous amino acid sequence," or variations thereof, refer to sequences characterized by a homology at the nucleotide level or amino acid level as discussed supra. Homologous nucleotide sequences encode those sequences coding for isoforms of POLYX polypeptide. Isoforms can be expressed in different tissues ofthe same organism as a result of, e.g., alternative splicing of RNA. Alternatively, isoforms can be encoded by different genes. In the invention, homologous nucleotide sequences include nucleotide sequences encoding for a POLYX polypeptide of species other than humans, including, but not limited to, mammals, and thus can include, e.g., mouse, rat, rabbit, dog, cat cow, horse, and other organisms. Homologous nucleotide sequences also include, but are not limited to, naturally occurring allelic variations and mutations ofthe nucleotide sequences set forth herein. A homologous nucleotide sequence does not, however, include the nucleotide sequence encoding human POLYX protein. Homologous nucleic acid sequences include those nucleic acid sequences that encode conservative amino acid substitutions (see below) in any of SEQ ID NO:2« (wherein n = 1 to 17) as well as a polypeptide having POLYX activity. Biological activities ofthe POLYX proteins are described below. A homologous amino acid sequence does not encode the amino acid sequence of a human POLYX polypeptide.

The nucleotide sequence determined from the cloning ofthe human POLYX gene allows for the generation of probes and primers designed for use in identifying the cell types disclosed and/or cloning POLYX homologues in other cell types, e.g., from other tissues, as well as POLYX homologues from other mammals. The probe/primer typically comprises a substantially-purified oligonucleotide. The oligonucleotide typically comprises a region of nucleotide sequence that hybridizes under stringent conditions to at least about 12, 25, 50, 100, 150, 200, 250, 300, 350 or 400 or more consecutive sense strand nucleotide sequence of SEQ ID NO:2rø-l (wherein n = 1 to 17); or an anti-sense strand nucleotide sequence of SEQ ID NO:2«-l (wherein n = 1 to 17); or of a naturally occurring mutant of SEQ ID NO:2«-l (wherein n = 1 to 17).

Probes based upon the human POLYX nucleotide sequence can be used to detect transcripts or genomic sequences encoding the same or homologous proteins. In various embodiments, the probe further comprises a label group attached thereto, e.g., the label group can be a radioisotope, a fluorescent compound, an enzyme, or an enzyme co-factor. Such probes can be used as a part of a diagnostic test kit for identifying cells or tissue which mis- express a POLYX protein, such as by measuring a level of a POLYX-encoding nucleic acid in a sample of cells from a subject e.g., detecting POLYX mRNA levels or determining whether a genomic POLYX gene has been mutated or deleted.

As utilized herein, the term "a polypeptide having a biologically-active portion of POLYX refers to polypeptides exhibiting activity similar, but not necessarily identical to, an activity of a polypeptide ofthe invention, including mature forms, as measured in a particular biological assay, with or without dose dependency. A nucleic acid fragment encoding a "biologically-active portion of POLYX can be prepared by isolating a portion of SEQ ID NO:2«-l (wherein n = 1 to 17), that encodes a polypeptide having a POLYX biological activity , expressing the encoded portion of POLYX protein (e.g., by recombinant expression in vitro), and assessing the activity ofthe encoded portion of POLY.

POLYX Variants

The invention further encompasses nucleic acid molecules that differ from the disclosed POLYX nucleotide sequences due to degeneracy ofthe genetic code. These nucleic acids therefore encode the same POLYX protein as those encoded by the nucleotide sequence shown in SEQ ID NO:2«-l (wherein n = 1 to 17). In another embodiment, an isolated nucleic acid molecule ofthe invention has a nucleotide sequence encoding a protein having an amino acid sequence shown in any of SEQ ID NO:2« (wherein n = 1 to 17).

In addition to the human POLYX nucleotide sequence shown in any of SEQ ID

NO:2rø-l (wherein n = 1 to 17), it will be appreciated by those skilled in the art that DNA sequence polymorphisms that lead to changes in the amino acid sequences of POLYX may exist within a population (e.g., the human population). Such genetic polymoφhism in the POLYX gene may exist among individuals within a population due to natural allelic variation.

As used herein, the terms "gene" and "recombinant gene" refer to nucleic acid molecules comprising an open reading frame encoding a POLYX protein, preferably a mammalian

POLYX protein. Such natural allelic variations can typically result in 1-5% variance in the nucleotide sequence ofthe POLYX gene. Any and all such nucleotide variations and resulting amino acid polymoφhisms in POLYX that are the result of natural allelic variation and that do not alter the functional activity of POLYX are intended to be within the scope ofthe invention.

Additionally, nucleic acid molecules encoding POLYX proteins from other species, and thus that have a nucleotide sequence that differs from the human sequence of any of SEQ ID NO:2rø-l (wherein n = 1 to 17), are intended to be within the scope ofthe invention. Nucleic acid molecules corresponding to natural allelic variants and homologues ofthe POLYX cDNAs ofthe invention can be isolated based on their homology to the human POLYX nucleic acids disclosed herein using the human cDNAs, or a portion thereof, as a hybridization probe according to standard hybridization techniques under stringent hybridization conditions.

In another embodiment, an isolated nucleic acid molecule ofthe invention is at least 6 nucleotides in length and hybridizes under stringent conditions to the nucleic acid molecule comprising the nucleotide sequence of any of SEQ ID NO:2rø-l (wherein n = 1 to 17). In another embodiment, the nucleic acid is at least 10, 25, 50, 100, 250, 500 or 750 nucleotides in length. In yet another embodiment, an isolated nucleic acid molecule ofthe invention hybridizes to the coding region. As used herein, the term "hybridizes under stringent conditions" is intended to describe conditions for hybridization and washing under which nucleotide sequences at least 60% homologous to each other typically remain hybridized to each other.

Homologs (i.e., nucleic acids encoding POLYX proteins derived from species other than human) or other related sequences (e.g., paralogs) can be obtained by low, moderate or high stringency hybridization with all or a portion ofthe particular human sequence as a probe using methods well known in the art for nucleic acid hybridization and cloning.

As used herein, the phrase "stringent hybridization conditions" refers to conditions under which a probe, primer or oligonucleotide will hybridize to its target sequence, but to no other sequences. Stringent conditions are sequence-dependent and will be different in different circumstances. Longer sequences hybridize specifically at higher temperatures than shorter sequences. Generally, stringent conditions are selected to be about 5°C lower than the thermal melting point (T_m) for the specific sequence at a defined ionic strength and pH. The T_m is the temperature (under defined ionic strength, pH and nucleic acid concentration) at which 50% ofthe probes complementary to the target sequence hybridize to the target sequence at equilibrium. Since the target sequences are generally present at excess, at T_m, 50% ofthe probes are occupied at equilibrium. Typically, stringent conditions will be those in which the salt concentration is less than about 1.0 M sodium ion, typically about 0.01 to 1.0 M sodium ion (or other salts) at pH 7.0 to 8.3 and the temperature is at least about 30°C for short probes, primers or oligonucleotides (e.g., 10 nt to 50 nt) and at least about 60°C for longer probes, primers and oligonucleotides. Stringent conditions may also be achieved with the addition of destabilizing agents, such as formamide.

Stringent conditions are known to those skilled in the art and can be found in CURRENT

PROTOCOLS IN MOLECULAR BIOLOGY, John Wiley & Sons, NN. (1989), 6.3.1-6.3.6. Preferably, the conditions are such that sequences at least about 65%, 70%, 75%, 85%, 90%, 95%), 98%, or 99% homologous to each other typically remain hybridized to each other. A non-limiting example of stringent hybridization conditions is hybridization in a high salt buffer comprising 6X SSC, 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 0.02% PVP, 0.02%

Ficoll, 0.02% BSA, and 500 mg/ml denatured salmon sperm DΝA at 65°C. This hybridization is followed by one or more washes in 0.2X SSC, 0.01% BSA at 50°C. An isolated nucleic acid molecule ofthe invention that hybridizes under stringent conditions to the sequence of any of SEQ ID ΝO:2«-l (wherein n = 1 to 17) corresponds to a naturally occurring nucleic acid molecule. As used herein, a "naturally-occurring" nucleic acid molecule refers to an RNA or DNA molecule having a nucleotide sequence that occurs in nature (e.g., encodes a natural protein).

In a second embodiment, a nucleic acid sequence that is hybridizable to the nucleic acid molecule comprising the nucleotide sequence of any of SEQ ID NO:2«-l (wherein n = 1 to 17), or fragments, analogs or derivatives thereof, under conditions of moderate stringency is provided. A non-limiting example of moderate stringency hybridization conditions are hybridization in 6X SSC, 5X Denhardt's solution, 0.5% SDS and 100 mg/ml denatured salmon sperm DNA at 55°C, followed by one or more washes in IX SSC, 0.1% SDS at 37°C. Other conditions of moderate stringency that may be used are well known in the art. See, e.g., Ausubel et al. feds.), 1993, CURRENT PROTOCOLS IN MOLECULAR BIOLOGY, John Wiley & Sons, NY, and Kriegler, 1990. GENE TRANSFER AND EXPRESSION, A LABORATORY MANUAL, Stockton Press, NY.

In a third embodiment, a nucleic acid that is hybridizable to the nucleic acid molecule comprising the nucleotide sequence of any of SEQ ID NO:2w-l (wherein n = 1 to 17), or fragments, analogs or derivatives thereof, under conditions of low stringency, is provided. A non-limiting example of low stringency hybridization conditions are hybridization in 35% formamide, 5X SSC, 50 mM Tris-HCl (pH 7.5), 5 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.2% BSA, 100 mg/ml denatured salmon sperm DNA, 10% (wt/vol) dextran sulfate at 40°C, followed by one or more washes in 2X SSC, 25 mM Tris-HCl (pH 7.4), 5 mM EDTA, and 0.1% SDS at 50°C. Other conditions of low stringency that may be used are well known in the art (e.g., as employed for cross-species hybridizations). See, e.g., Ausubel, et al, feds.), 1993. CURRENT PROTOCOLS IN MOLECULAR BIOLOGY, John Wiley & Sons, NY, and Kriegler, 1990. GENE TRANSFER AND EXPRESSION, A LABORATORY MANUAL, Stockton Press, NY; Shilo and Weinberg, 1981. Proc. Natl. Acad. Sci. USA 78: 6789-6792.

Conservative Mutations

In addition to naturally-occurring allelic variants ofthe POLYX sequence that may exist in the population, the skilled artisan will further appreciate that changes can be introduced by mutation into the nucleotide sequence of any of SEQ ID NO:2«-l (wherein n = 1 to 17), thereby leading to changes in the amino acid sequence ofthe encoded POLYX protein, without altering the functional ability ofthe POLYX protein. For example, nucleotide substitutions leading to amino acid substitutions at "non-essential" amino acid residues can be made in the sequence of any of SEQ ID NO:2n-l (wherein n = 1 to 17). A "non-essential" amino acid residue is a residue that can be altered from the wild-type sequence of POLYX without altering the biological activity, whereas an "essential" amino acid residue is required for biological activity. For example, amino acid residues that are conserved among the POLYX proteins ofthe invention, are predicted to be particularly non-amenable to such alteration.

Amino acid residues that are conserved among members of a POLYX family are predicted to be less amenable to alteration. For example, a POLYX protein according to the invention can contain at least one domain that is a typically conserved region in a POLYX family member. As such, these conserved domains are not likely to be amenable to mutation. Other amino acid residues, however, (e.g., those that are not conserved or only semi-conserved among members ofthe POLYX family) may not be as essential for activity and thus are more likely to be amenable to alteration.

Another aspect ofthe invention pertains to nucleic acid molecules encoding POLYX proteins that contain changes in amino acid residues that are not essential for activity. Such POLYX proteins differ in amino acid sequence from any of any of SEQ ID NO:2« (wherein n = 1 to 17), yet retain biological activity. In one embodiment, the isolated nucleic acid molecule comprises a nucleotide sequence encoding a protein, wherein the protein comprises an amino acid sequence at least about 75% homologous to the amino acid sequence of any of SEQ ID NO:2« (wherein n = 1 to 17). Preferably, the protein encoded by the nucleic acid is at least about 80% homologous to any of SEQ ID NO:2« (wherein n = 1 to 17), more preferably at least about 90%, 95%, 98%, and most preferably at least about 99% homologous to SEQ ID NO :2n (wherein n = 1 to 17).

An isolated nucleic acid molecule encoding a POLYX protein homologous to the protein of any of SEQ ID NO:2TΪ (wherein n = 1 to 17) can be created by introducing one or more nucleotide substitutions, additions or deletions into the corresponding nucleotide sequence (i.e., SEQ ID NO:2n-l for the corresponding n), such that one or more amino acid substitutions, additions or deletions are introduced into the encoded protein.

Mutations can be introduced into SEQ ID NO:2«-l (wherein n = 1 to 17) by standard techniques, such as site-directed mutagenesis and PCR-mediated mutagenesis. Preferably, conservative amino acid substitutions are made at one or more predicted non-essential amino acid residues. A "conservative amino acid substitution" is one in which the amino acid residue is replaced with an amino acid residue having a similar side chain. Families of amino acid residues having similar side chains have been defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), β-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). Thus, a predicted nonessential amino acid residue in POLYX is replaced with another amino acid residue from the same side chain family. Alternatively, in another embodiment, mutations can be introduced randomly along all or part of a POLYX coding sequence, such as by saturation mutagenesis, and the resultant mutants can be screened for POLYX biological activity to identify mutants that retain activity. Following mutagenesis of SEQ ID NO:2«-l (wherein n = 1 to 17)_α the encoded protein can be expressed by any recombinant technology known in the art and the activity ofthe protein can be determined.

In one embodiment, a mutant POLYX protein can be assayed for: (/) the ability to form proteimprotein interactions with other POLYX proteins, other cell-surface proteins, or biologically-active portions thereof; (ii) complex formation between a mutant POLYX protein and a POLYX receptor; (iii) the ability of a mutant POLYX protein to bind to an intracellular target protein or biologically active portion thereof; (e.g., avidin proteins); (iv) the ability to bind BRA protein; or (v) the ability to specifically bind an anti-POLYX protein antibody.

Antisense Nucleic Acids

Another aspect ofthe invention pertains to isolated antisense nucleic acid molecules that are hybridizable to or complementary to the nucleic acid molecule comprising the nucleotide sequence of SEQ ID NO:2«-l (wherein n = 1 to 17), or fragments, analogs or derivatives thereof. An "antisense" nucleic acid comprises a nucleotide sequence that is complementary to a "sense" nucleic acid encoding a protein, e.g., complementary to the coding strand of a double-stranded cDNA molecule or complementary to an mRNA sequence. In specific aspects, antisense nucleic acid molecules are provided that comprise a sequence complementary to at least about 10, 25, 50, 100, 250 or 500 nucleotides or an entire POLYX coding strand, or to only a portion thereof. Nucleic acid molecules encoding fragments, homologs, derivatives and analogs of a POLYX protein of any of SEQ ID NO:2« (wherein n = 1 to 17) or antisense nucleic acids complementary to a POLYX nucleic acid sequence of SEQ ID NO:2n-l (wherein n = 1 to 17) are additionally provided. In one embodiment, an antisense nucleic acid molecule is antisense to a "coding region" ofthe coding strand of a nucleotide sequence encoding POLY. The term "coding region" refers to the region ofthe nucleotide sequence comprising codons which are translated into amino acid residues (e.g., the protein coding region of a human POLYX that corresponds to any of SEQ ID NO:2« (wherein n = 1 to 17)). In another embodiment, the antisense nucleic acid molecule is antisense to a "non-coding region" ofthe coding strand of a nucleotide sequence encoding POLY. The term "non-coding region" refers to 5' and 3' sequences which flank the coding region that are not translated into amino acids (i.e., also referred to as 5' and 3' non-translated regions).

Given the coding strand sequences encoding POLYX disclosed herein (e.g., SEQ ID

NO:2«-l (wherein n = 1 to 17) ), antisense nucleic acids ofthe invention can be designed according to the rules of Watson and Crick or Hoogsteen base-pairing. The antisense nucleic acid molecule can be complementary to the entire coding region of POLYX mRNA, but more preferably is an oligonucleotide that is antisense to only a portion ofthe coding or non-coding region of POLYX mRNA. For example, the antisense oligonucleotide can be complementary to the region surrounding the translation start site of POLYX mRNA. An antisense oligonucleotide can be, for example, about 5, 10, 15, 20, 25, 30, 35, 40, 45 or 50 nucleotides in length. An antisense nucleic acid ofthe invention can be constructed using chemical synthesis or enzymatic ligation reactions using procedures known in the art. For example, an antisense nucleic acid (e.g., an antisense oligonucleotide) can be chemically synthesized using naturally- occurring nucleotides or variously modified nucleotides designed to increase the biological stability ofthe molecules or to increase the physical stability ofthe duplex formed between the antisense and sense nucleic acids, e.g., phosphorothioate derivatives and acridine-substituted nucleotides can be used.

Examples of modified nucleotides that can be used to generate the antisense nucleic acid include: 5-fluorouracil, 5-bromouracil, 5-chlorouracil, 5-iodouracil, hypoxanthine, xanthine, 4-acetylcytosine, 5-(carboxyhydroxylmethyl) uracil, 5-carboxymethylaminomethyl-

2-thiouridine, 5-carboxymethylaminomethyluracil, dihydrouracil, beta-D-galactosylqueosine, inosine, N6-isopentenyladenine, 1-methylguanine, 1-methylinosine, 2,2-dimethylguanine, 2-methyladenine, 2-methylguanine, 3-methylcytosine, 5-methylcytosine, N6-adenine, 7-methylguanine, 5-methylaminomethyluracil, 5-methoxyaminomethyl-2-thiouracil, beta-D-mannosylqueosine, 5'-methoxycarboxymethyluracil, 5-methoxyuracil, 2-methylthio-N6-isopentenyladenine, uracil-5-oxyacetic acid (v), wybutoxosine, pseudouracil, queosine, 2-thiocytosine, 5-methyl-2-thiouracil, 2-thiouracil, 4-thiouracil, 5-methyluracil, uracil-5-oxyacetic acid methylester, uracil-5-oxyacetic acid (v), 5-methyl-2-thiouracil,

3-(3-amino-3-N-2-carboxypropyl) uracil, (acp3)w, and 2,6-diaminopurine. Alternatively, the antisense nucleic acid can be produced biologically using an expression vector into which a nucleic acid has been subcloned in an antisense orientation (i.e., RNA transcribed from the inserted nucleic acid will be of an antisense orientation to a target nucleic acid of interest, described further in the following subsection).

The antisense nucleic acid molecules ofthe invention are typically administered to a subject or generated in situ such that they hybridize with or bind to cellular mRNA and/or genomic DNA encoding a POLYX protein to thereby inhibit expression ofthe protein, e.g., by inhibiting transcription and/or translation. The hybridization can be by conventional nucleotide complementarity to form a stable duplex, or, for example, in the case of an antisense nucleic acid molecule that binds to DNA duplexes, through specific interactions in the major groove ofthe double helix. An example of a route of administration of antisense nucleic acid molecules ofthe invention includes direct injection at a tissue site. Alternatively, antisense nucleic acid molecules can be modified to target selected cells and then administered systemically. For example, for systemic administration, antisense molecules can be modified such that they specifically bind to receptors or antigens expressed on a selected cell surface (e.g., by linking the antisense nucleic acid molecules to peptides or antibodies that bind to cell surface receptors or antigens). The antisense nucleic acid molecules can also be delivered to cells using the vectors described herein. To achieve sufficient intracellular concentrations of antisense molecules, vector constructs in which the antisense nucleic acid molecule is placed under the control of a strong pol II or pol III promoter are preferred.

In yet another embodiment, the antisense nucleic acid molecule ofthe invention is an α-anomeric nucleic acid molecule. An α-anomeric nucleic acid molecule forms specific double-stranded hybrids with complementary RNA in which, contrary to the usual α-units, the strands run parallel to each other (Gaultier, et al., 1987. Nucl. Acids Res. 15: 6625-6641). The antisense nucleic acid molecule can also comprise a 2'-o-methylribonucleotide (Inoue, et al., 1987. Nucl. Acids Res. 15: 6131-6148) or a chimeric RNA-DNA analogue (Inoue, et al, 1987. FEBSLett. 215: 327-330).

Ribozymes and PNA Moieties

Such modifications include, by way of non-limiting example, modified bases, and nucleic acids whose sugar phosphate backbones are modified or derivatized. These modifications are carried out at least in part to enhance the chemical stability ofthe modified nucleic acid, such that they may be used, for example, as antisense binding nucleic acids in therapeutic applications in a subject.

In still another embodiment, an antisense nucleic acid ofthe invention is a ribozyme.

Ribozymes are catalytic RNA molecules with ribonuclease activity that are capable of cleaving a single-stranded nucleic acid, such as an mRNA, to which they have a complementary region. Thus, ribozymes (e.g., hammerhead ribozymes; described by Haselhoff and Gerlach, 1988. Nature 334: 585 -591) can be used to catalytically-cleave POLYX mRNA transcripts to thereby inhibit translation of POLYX mRNA. A ribozyme having specificity for a POLYX-encoding nucleic acid can be designed based upon the nucleotide sequence of a POLYX DNA disclosed herein (i.e., SEQ ID NO:2rø-l (wherein n = 1 to 17)). For example, a derivative of a Tetrahymena L-19 IVS RNA can be constructed in which the nucleotide sequence ofthe active site is complementary to the nucleotide sequence to be cleaved in a POLYX-encoding mRNA. See, e.g., Cech, et ah, U.S. Patent No.

4,987,071 ; and Cech, et al, U.S. Patent No. 5,116,742. Alternatively, POLYX mRNA can be used to select a catalytic RNA having a specific ribonuclease activity from a pool of RNA molecules (Bartel, et al, 1993. Science 261: 1411-1418).

Alternatively, POLYX gene expression can be inhibited by targeting nucleotide sequences complementary to the regulatory region ofthe POLYX (e.g., the POLYX promoter and/or enhancers) to form triple helical structures that prevent transcription ofthe POLYX gene in target cells. See, e.g., Helene, 1991. Anticancer DrugDes. 6: 569-84; Helene, et al, 1992. Ann. NY. Acad. Sci. 660: 27-36; and Maher, 1992. Bioassays 14: 807-15. In various embodiments, the nucleic acids of POLYX can be modified at the base moiety, sugar moiety or phosphate backbone to improve, e.g., the stability, hybridization, or solubility ofthe molecule. For example, the deoxyribose phosphate backbone ofthe nucleic acids can be modified to generate peptide nucleic acids (Hyrup, et al, 1996. Bioorg. Med. Chem. 4: 5-23). As used herein, the terms "peptide nucleic acids" or "PNAs" refer to nucleic acid mimics, e.g., DNA mimics, in which the deoxyribose phosphate backbone is replaced by a pseudopeptide backbone and only the four natural nucleobases are retained. The neutral backbone of PNAs has been shown to allow for specific hybridization to DNA and RNA under conditions of low ionic strength. The synthesis of PNA oligomers can be performed using standard solid phase peptide synthesis protocols as described in Hyrup, et al, 1996. supra; Perry-O'Keefe, et al, 1996. Proc. Natl. Acad. Sci. USA 93: 14670-14675.

PNAs of POLYX can be used in therapeutic and diagnostic applications. For example, PNAs can be used as antisense or antigene agents for sequence-specific modulation of gene expression by, e.g., inducing transcription or translation arrest or inhibiting replication. PNAs of POLYX can also be used, e.g. , in the analysis of single base pair mutations in a gene by, e.g., PNA directed PCR clamping; as artificial restriction enzymes when used in combination with other enzymes, e.g., Sl nucleases (see, Hyrup, 1996., supra); or as probes or primers for DNA sequence and hybridization (see, Hyrup, et al, 1996.; Perry-O'Keefe, 1996., supra).

In another embodiment, PNAs of POLYX can be modified, e.g., to enhance their stability or cellular uptake, by attaching lipophilic or other helper groups to PNA, by the formation of PNA-DNA chimeras, or by the use of liposomes or other techniques of drug delivery known in the art. For example, PNA-DNA chimeras of POLYX can be generated that may combine the advantageous properties of PNA and DNA. Such chimeras allow DNA recognition enzymes, e.g., RNase H and DNA polymerases, to interact with the DNA portion while the PNA portion would provide high binding affinity and specificity. PNA-DNA chimeras can be linked using linkers of appropriate lengths selected in terms of base stacking, number of bonds between the nucleobases, and orientation (see, Hyrup, 1996., supra). The synthesis of PNA-DNA chimeras can be performed as described in Finn, et al, (1996. Nucl.

Acids Res. 24: 3357-3363). For example, a DNA chain can be synthesized on a solid support using standard phosphoramidite coupling chemistry, and modified nucleoside analogs, e.g., 5'-(4-methoxytrityl)amino-5'-deoxy-thymidine phosphoramidite, can be used between the PNA and the 5' end of DNA (Mag, et al, 1989. Nucl. Acid Res. 17: 5973-5988). PNA monomers are then coupled in a stepwise manner to produce a chimeric molecule with a 5' PNA segment and a 3' DNA segment (see, Finn, et al, 1996., supra). Alternatively, chimeric molecules can be synthesized with a 5' DNA segment and a 3' PNA segment. See, e.g., Petersen, et al, 1975. Bioorg. Med. Chem. Lett. 5: 1119-11124.

In other embodiments, the oligonucleotide may include other appended groups such as peptides (e.g., for targeting host cell receptors in vivo), or agents facilitating transport across the cell membrane (see, e.g., Letsinger, et al, 1989. Proc. Natl. Acad. Sci. U.S.A. 86: 6553-6556; Lemaitre, et al, 1987. Proc. Natl. Acad. Sci. 84: 648-652; PCT Publication No. WO88/09810) or the blood-brain barrier (see, e.g., PCT Publication No. WO 89/10134). In addition, oligonucleotides can be modified with hybridization triggered cleavage agents (see, e.g., Krol, et a , 1988. BioTechniques 6:958-976) or intercalating agents (see, e.g., Zon, 1988. Pharm. Res. 5: 539-549). To this end, the oligonucleotide may be conjugated to another molecule, e.g., a peptide, a hybridization triggered cross-linking agent, a transport agent, a hybridization-triggered cleavage agent, and the like.

Characterization of POLYX Polypeptides

A polypeptide according to the invention includes a polypeptide including the amino acid sequence of POLYX polypeptides whose sequences are provided in any SEQ ID NO:2« (wherein n - 1 to 17) and includes SEQ ID NOS:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34. The invention also includes a mutant or variant protein any of whose residues may be changed from the corresponding residues shown in SEQ ID NOS: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34, while still encoding a protein that maintains its POLYX activities and physiological functions, or a functional fragment thereof.

In general, a POLYX variant that preserves POLYX-like function includes any variant in which residues at a particular position in the sequence have been substituted by other amino acids, and further include the possibility of inserting an additional residue or residues between two residues ofthe parent protein as well as the possibility of deleting one or more residues from the parent sequence. Any amino acid substitution, insertion, or deletion is encompassed by the invention. In favorable circumstances, the substitution is a conservative substitution as defined above.

One aspect ofthe invention pertains to isolated POLYX proteins, and biologically- active portions thereof, or derivatives, fragments, analogs or homologs thereof. Also provided are polypeptide fragments suitable for use as immunogens to raise anti-POLYX antibodies. In one embodiment, native POLYX proteins can be isolated from cells or tissue sources by an appropriate purification scheme using standard protein purification techniques. In another embodiment, POLYX proteins are produced by recombinant DNA techniques. Alternative to recombinant expression, a POLYX protein or polypeptide can be synthesized chemically using standard peptide synthesis techniques.

An "isolated" or "purified" polypeptide or protein or biologically-active portion thereof is substantially free of cellular material or other contaminating proteins from the cell or tissue source from which the POLYX protein is derived, or substantially free from chemical precursors or other chemicals when chemically synthesized. The language "substantially free of cellular material" includes preparations of POLYX proteins in which the protein is separated from cellular components ofthe cells from which it is isolated or recombinantly- produced. In one embodiment, the language "substantially free of cellular material" includes preparations of POLYX proteins having less than about 30% (by dry weight) of non-POLYX proteins (also referred to herein as a "contaminating protein"), more preferably less than about 20% of non-POLYX proteins, still more preferably less than about 10% of non-POLYX proteins, and most preferably less than about 5% of non-POLYX proteins. When the POLYX protein or biologically-active portion thereof is recombinantly-produced, it is also preferably substantially free of culture medium, i.e., culture medium represents less than about 20%, more preferably less than about 10%, and most preferably less than about 5% ofthe volume of the POLYX protein preparation.

As utilized herein, the phrase "substantially free of chemical precursors or other chemicals" includes preparations of POLYX protein in which the protein is separated from chemical precursors or other chemicals that are involved in the synthesis ofthe protein. In one embodiment, the language "substantially free of chemical precursors or other chemicals" includes preparations of POLYX protein having less than about 30% (by dry weight) of chemical precursors or non-POLYX chemicals, more preferably less than about 20% chemical precursors or non-POLYX chemicals, still more preferably less than about 10% chemical precursors or non-POLYX chemicals, and most preferably less than about 5% chemical precursors or non-POLYX chemicals.

Biologically-active portions of a POLYX protein include peptides comprising amino acid sequences sufficiently homologous to or derived from the amino acid sequence ofthe POLYX protein which include fewer amino acids than the full-length POLYX proteins, and exhibit at least one activity of a POLYX protein. Typically, biologically-active portions comprise a domain or motif with at least one activity ofthe POLYX protein. A biologically- active portion of a POLYX protein can be a polypeptide which is, for example, 10, 25, 50, 100 or more amino acids in length.

A biologically-active portion of a POLYX protein ofthe invention may contain at least one ofthe above-identified conserved domains. Moreover, other biologically active portions, in which other regions ofthe protein are deleted, can be prepared by recombinant techniques and evaluated for one or more ofthe functional activities of a native POLYX protein.

In an embodiment, the POLYX protein has an amino acid sequence shown in any of SEQ ID NO:2τ? (wherein n = 1 to 17). In other embodiments, the POLYX protein is substantially homologous to any of SEQ ID NO:2« (wherein n = 1 to 17) and retains the functional activity ofthe protein of any of SEQ ID NO:2« (wherein n = 1 to 17), yet differs in amino acid sequence due to natural allelic variation or mutagenesis, as described in detail below. Accordingly, in another embodiment, the POLYX protein is a protein that comprises an amino acid sequence at least about 45% homologous, and more preferably about 55, 65, 70, 75, 80, 85, 90, 95, 98 or even 99% homologous to the amino acid sequence of any of SEQ ID NO:2τ? (wherein n = 1 to 17) and retains the functional activity ofthe POLYX proteins ofthe corresponding polypeptide having the sequence of SEQ ID NO:2τ? (wherein n = 1 to 17). Determining Homology Between Two or More Sequences

To determine the percent homology of two amino acid sequences or of two nucleic acids, the sequences are aligned for optimal comparison puφoses (e.g., gaps can be introduced in the sequence of a first amino acid or nucleic acid sequence for optimal alignment with a second amino or nucleic acid sequence). 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 homologous at that position (i.e., as used herein amino acid or nucleic acid "homology" is equivalent to amino acid or nucleic acid "identity").

The nucleic acid sequence homology may be determined as the degree of identity between two sequences. The homology may be determined using computer programs known in the art, such as GAP software provided in the GCG program package. See, Needleman and Wunsch, 1970. J. Mol. Biol. 48: 443-453. Using GCG GAP software with the following settings for nucleic acid sequence comparison: GAP creation penalty of 5.0 and GAP extension penalty of 0.3, the coding region ofthe analogous nucleic acid sequences referred to above exhibits a degree of identity preferably of at least 70%, 75%, 80%, 85%, 90%, 95%, 98%, or 99%, with the CDS (encoding) part ofthe DNA sequence shown in SEQ ID NO:2«-l (wherein n = 1 to 17), e.g., SEQ ID NOS:l, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31 and/or 33.

The term "sequence identity" refers to the degree to which two polynucleotide or polypeptide sequences are identical on a residue-by-residue basis over a particular region of comparison. The term "percentage of sequence identity" is calculated by comparing two optimally aligned sequences over that region of comparison, determining the number of positions at which the identical nucleic acid base (e.g., A, T, C, G, U, or I, in the case of nucleic acids) occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the region of comparison (i.e., the window size), and multiplying the result by 100 to yield the percentage of sequence identity. The term "substantial identity" as used herein denotes a characteristic of a polynucleotide sequence, wherein the polynucleotide comprises a sequence that has at least 80 percent sequence identity, preferably at least 85 percent identity and often 90 to 95 percent sequence identity, more usually at least 99 percent sequence identity as compared to a reference sequence over a comparison region.

Chimeric and Fusion Proteins

The invention also provides POLYX chimeric or fusion proteins. As used herein, a POLYX "chimeric protein" or "fusion protein" comprises a POLYX polypeptide operatively- linked to a non-POLYX polypeptide. An "POLYX polypeptide" refers to a polypeptide having an amino acid sequence corresponding to a POLYX protein shown in SEQ ID NO:2n (wherein n = 1 to 17), [e.g., SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34], whereas a "non-POLYX polypeptide" refers to a polypeptide having an amino acid sequence corresponding to a protein that is not substantially homologous to the POLYX protein (e.g., a protein that is different from the POLYX protein and that is derived from the same or a different organism). Within a POLYX fusion protein the POLYX polypeptide can correspond to all or a portion of a POLYX protein. In one embodiment, a POLYX fusion protein comprises at least one biologically-active portion of a POLYX protein. In another embodiment, a POLYX fusion protein comprises at least two biologically-active portions of a POLYX protein. In yet another embodiment, a POLYX fusion protein comprises at least three biologically-active portions of a POLYX protein. Within the fusion protein, the term "operatively-linked" is intended to indicate that the POLYX polypeptide and the non-POLYX polypeptide are fused in-frame with one another. The non-POLYX polypeptide can be fused to the amino-terminus or carboxyl-terminus ofthe POLYX polypeptide.

In one embodiment, the fusion protein is a GST-POL YX fusion protein in which the POLYX sequences are fused to the carboxyl-terminus ofthe GST (glutathione S-transferase) sequences. Such fusion proteins can facilitate the purification of recombinant POLYX polypeptides.

In another embodiment, the fusion protein is a POLYX protein containing a heterologous signal sequence at its amino-terminus. In certain host cells (e.g., mammalian host cells), expression and/or secretion of POLYX can be increased through use of a heterologous signal sequence.

In yet another embodiment, the fusion protein is a POLYX-immunoglobulin fusion protein in which the POLYX sequences are fused to sequences derived from a member ofthe immunoglobulin protein family. The POLYX-immunoglobulin fusion proteins ofthe invention can be incoφorated into pharmaceutical compositions and administered to a subject to inhibit an interaction between a POLYX ligand and a POLYX protein on the surface of a cell, to thereby suppress POLYX-mediated signal transduction in vivo. The POLYX- immunoglobulin fusion proteins can be used to affect the bioavailability of a POLYX cognate ligand. Inhibition ofthe POLYX ligand/POLYX interaction may be useful therapeutically for both the treatment of proliferative and differentiative disorders, as well as modulating (e.g., promoting or inhibiting) cell survival. Moreover, the POLYX-immunoglobulin fusion proteins ofthe invention can be used as immunogens to produce anti-POLYX antibodies in a subject, to purify POLYX ligands, and in screening assays to identify molecules that inhibit the interaction of POLYX with a POLYX ligand.

A POLYX chimeric or fusion protein ofthe invention can be produced by standard recombinant DNA techniques. For example, DNA fragments coding for the different polypeptide sequences are ligated together in-frame in accordance with conventional techniques, e.g., by employing blunt-ended or stagger-ended termini for ligation, restriction enzyme digestion to provide for appropriate termini, filling-in of cohesive ends as appropriate, alkaline phosphatase treatment to avoid undesirable joining, and enzymatic ligation. 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 that give rise to complementary overhangs between two consecutive gene fragments that can subsequently be annealed and reamplified to generate a chimeric gene sequence (see, e.g., Ausubel, et al. (eds.) CURRENT PROTOCOLS IN MOLECULAR

BIOLOGY, John Wiley & Sons, 1992). Moreover, many expression vectors are commercially available that already encode a fusion moiety (e.g., a GST polypeptide). A POLYX-encoding nucleic acid can be cloned into such an expression vector such that the fusion moiety is linked in-frame to the POLYX protein. POLYX Agonists and Antagonists

The invention also pertains to variants ofthe POLYX proteins that function as either POLYX agonists (i.e., mimetics) or as POLYX antagonists. Variants ofthe POLYX protein can be generated by mutagenesis (e.g., discrete point mutation or truncation ofthe POLYX protein). An agonist of a POLYX protein can retain substantially the same, or a subset of, the biological activities ofthe naturally-occurring form of a POLYX protein. An antagonist of a POLYX protein can inhibit one or more ofthe activities ofthe naturally occurring form of a POLYX protein by, for example, competitively binding to a downstream or upstream member of a cellular signaling cascade which includes the POLYX protein. Thus, specific biological effects can be elicited by treatment with a variant of limited function. In one embodiment, treatment of a subject with a variant having a subset ofthe biological activities ofthe naturally occurring form ofthe protein has fewer side effects in a subject relative to treatment with the naturally occurring form ofthe POLYX proteins.

Variants ofthe POLYX proteins that function as either POLYX agonists (i.e., mimetics) or as POLYX antagonists can be identified by screening combinatorial libraries of mutants (e.g., truncation mutants) ofthe POLYX proteins for POLYX protein agonist or antagonist activity. In one embodiment, a variegated library of POLYX variants is generated by combinatorial mutagenesis at the nucleic acid level and is encoded by a variegated gene library. A variegated library of POLYX variants can be produced by, for example, enzymatically-ligating a mixture of synthetic oligonucleotides into gene sequences such that a degenerate set of potential POLYX sequences is expressible as individual polypeptides, or alternatively, as a set of larger fusion proteins (e.g., for phage display) containing the set of POLYX sequences therein. There are a variety of methods which can be used to produce libraries of potential POLYX variants from a degenerate oligonucleotide sequence. Chemical synthesis of a degenerate gene sequence can be performed in an automatic DNA synthesizer, and the synthetic gene then ligated into an appropriate expression vector. Use of a degenerate set of genes allows for the provision, in one mixture, of all ofthe sequences encoding the desired set of potential POLYX sequences. Methods for synthesizing degenerate oligonucleotides are well-known within the art. See, e.g., Narang, 1983. Tetrahedron 39: 3; Itakura, et al, 1984. Annu. Rev. Biochem. 53: 323; Itakura, et al, 1984. Science 198: 1056; Ike, et al, 1983. Nucl. Acids Res. 11 : 477.

Polypeptide Libraries

In addition, libraries of fragments ofthe POLYX protein coding sequences can be used to generate a variegated population of POLYX fragments for screening and subsequent selection of variants of a POLYX protein. In one embodiment, a library of coding sequence fragments can be generated by treating a double-stranded PCR fragment of a POLYX coding sequence with a nuclease under conditions wherein nicking occurs only about once per molecule, denaturing the double stranded DNA, renaturing the DNA to form double-stranded DNA that can include sense/antisense pairs from different nicked products, removing single stranded portions from reformed duplexes by treatment with S] nuclease, and ligating the resulting fragment library into an expression vector. By this method, expression libraries can be derived which encodes amino-terminal and internal fragments of various sizes ofthe POLYX proteins.

Various techniques are known in the art for screening gene products of combinatorial libraries made by point mutations or truncation, and for screening cDNA libraries for gene products having a selected property. Such techniques are adaptable for rapid screening ofthe gene libraries generated by the combinatorial mutagenesis of POLYX proteins. The most widely used techniques, which are amenable to high throughput analysis, for screening large gene libraries typically include cloning the gene library into replicable expression vectors, transforming appropriate cells with the resulting library of vectors, and expressing the combinatorial genes under conditions in which detection of a desired activity facilitates isolation ofthe vector encoding the gene whose product was detected. Recursive ensemble mutagenesis (REM), a new technique that enhances the frequency of functional mutants in the libraries, can be used in combination with the screening assays to identify POLYX variants. See, e.g., Arkin and Yourvan, 1992. Proc. Natl. Acad. Sci. USA 89: 7811-7815; Delgrave, et al, 1993. Protein Engineering 6:327-331. Anti-POLYX Antibodies

The invention encompasses antibodies and antibody fragments, such as F_ab or (F_ab)_2, that bind immunospecifically to any ofthe POLYX polypeptides of said invention.

An isolated POLYX protein, or a portion or fragment thereof, can be used as an immunogen to generate antibodies that bind to POLYX polypeptides using standard techniques for polyclonal and monoclonal antibody preparation. The full-length POLYX proteins can be used or, alternatively, the invention provides antigenic peptide fragments of POLYX proteins for use as immunogens. The antigenic POLYX peptides comprises at least 4 amino acid residues ofthe amino acid sequence shown in SEQ ID NO:2« (wherein n = 1 to 17) and encompasses an epitope of POLYX such that an antibody raised against the peptide forms a specific immune complex with POLY. Preferably, the antigenic peptide comprises at least 6, 8, 10, 15, 20, or 30 amino acid residues. Longer antigenic peptides are sometimes preferable over shorter antigenic peptides, depending on use and according to methods well known to someone skilled in the art.

In certain embodiments ofthe invention, at least one epitope encompassed by the antigenic peptide is a region of POLYX that is located on the surface ofthe protein (e.g., a hydrophilic region). As a means for targeting antibody production, hydropathy plots showing regions of hydrophilicity and hydrophobicity may be generated by any method well known in the art, including, for example, the Kyte-Doolittle or the Hopp- Woods methods, either with or without Fourier transformation (see, e.g., Hopp and Woods, 1981. Proc. Nat. Acad. Sci. USA 78: 3824-3828; Kyte and Doolittle, 1982. J Mol. Biol. 157: 105-142, each incoφorated herein by reference in their entirety).

As disclosed herein, POLYX protein sequences of SEQ ID NO:2« (wherein n = 1 to

17), or derivatives, fragments, analogs, or homologs thereof, may be utilized as immunogens in the generation of antibodies that immunospecifically-bind these protein components. The term "antibody" as used herein refers to immunoglobulin molecules and immunologically- active portions of immunoglobulin molecules, i.e., molecules that contain an antigen binding site that specifically-binds (immunoreacts with) an antigen, such as POLY. Such antibodies include, but are not limited to, polyclonal, monoclonal, chimeric, single chain, F_ab and F_(ab'₎2 fragments, and an F_ab expression library. In a specific embodiment, antibodies to human POLYX proteins are disclosed. Various procedures known within the art may be used for the production of polyclonal or monoclonal antibodies to a POLYX protein sequence of SEQ ID NO:2« (wherein n = 1 to 17), or a derivative, fragment, analog, or homolog thereof. Some of these proteins are discussed, infra.

For the production of polyclonal antibodies, various suitable host animals (e.g., rabbit, goat, mouse or other mammal) may be immunized by injection with the native protein, or a synthetic variant thereof, or a derivative ofthe foregoing. An appropriate immunogenic preparation can contain, for example, recombinantly-expressed POLYX protein or a chemically-synthesized POLYX polypeptide. The preparation can further include an adjuvant. Various adjuvants used to increase the immunological response include, but are not limited to, Freund's (complete and incomplete), mineral gels (e.g., aluminum hydroxide), surface active substances (e.g., lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, dinitrophenol, etc.), human adjuvants such as Bacille Calmette-Guerin and Corynebacterium parvum, or similar immunostimulatory agents. If desired, the antibody molecules directed against POLYX can be isolated from the mammal (e.g., from the blood) and further purified by well known techniques, such as protein A chromatography to obtain the IgG fraction.

The term "monoclonal antibody" or "monoclonal antibody composition", as used herein, refers to a population of antibody molecules that contain only one species of an antigen binding site capable of immunoreacting with a particular epitope of POLY. A monoclonal antibody composition thus typically displays a single binding affinity for a particular POLYX protein with which it immunoreacts. For preparation of monoclonal antibodies directed towards a particular POLYX protein, or derivatives, fragments, analogs or homologs thereof, any technique that provides for the production of antibody molecules by continuous cell line culture may be utilized. Such techniques include, but are not limited to, the hybridoma technique (see, e.g., Kohler & Milstein, 1975. Nature 256: 495-497); the trioma technique; the human B-cell hybridoma technique (see, e.g., Kozbor, et al, 1983. Immunol. Today 4: 72) and the EBV hybridoma technique to produce human monoclonal antibodies (see, e.g., Cole, et al,

1985. In: MONOCLONAL ANTIBODIES AND CANCER THERAPY, Alan R. Liss, Inc., pp. 11-96). Human monoclonal antibodies may be utilized in the practice ofthe invention and may be produced by using human hybridomas (see, e.g., Cote, et al, 1983. Proc. Natl. Acad. Sci. USA 80: 2026-2030) or by transforming human B-cells with Epstein Barr Virus in vitro (see, e.g., Cole, et al, 1985. In: MONOCLONAL ANTIBODIES AND CANCER THERAPY, Alan R. Liss, Inc., pp. 77-96). Each ofthe above citations is incoφorated herein by reference in their entirety.

According to the invention, techniques can be adapted for the production of single-chain antibodies specific to a POLYX protein (see, e.g., U.S. Patent No. 4,946,778). In addition, methods can be adapted for the construction of F_ab expression libraries (see, e.g., Huse, et al, 1989. Science 246: 1275-1281) to allow rapid and effective identification of monoclonal F_ab fragments with the desired specificity for a POLYX protein or derivatives, fragments, analogs or homologs thereof. Non-human antibodies can be "humanized" by techniques well known in the art. See, e.g., U.S. Patent No. 5,225,539. Antibody fragments that contain the idiotypes to a POLYX protein may be produced by techniques known in the art including, but not limited to: (i) an F_(ab')2 fragment produced by pepsin digestion of an antibody molecule; (ii) an F_ab fragment generated by reducing the disulfide bridges of an F_(ab')2 fragment; (iii) an F_ab fragment generated by the treatment ofthe antibody molecule with papain and a reducing agent and (iv) F_v fragments.

Additionally, recombinant anti-POLYX antibodies, such as chimeric and humanized monoclonal antibodies, comprising both human and non-human portions, which can be made using standard recombinant DNA techniques, are within the scope ofthe invention. Such chimeric and humanized monoclonal antibodies can be produced by recombinant DNA techniques known in the art, for example using methods described in International Application No. PCT/US86/02269; European Patent Application No. 184,187; European Patent Application No. 171,496; European Patent Application No. 173,494; PCT International Publication No. WO 86/01533; U.S. Patent No. 4,816,567; U.S. Pat. No. 5,225,539; European Patent Application No. 125,023; Better, et al, 1988. Science 240: 1041-1043; Liu, et al, 1987.

Proc. Natl. Acad. Sci. USA 84: 3439-3443; Liu, et al, 1987. J. Immunol. 139: 3521-3526; Sun, et al, 1987. Proc. Natl. Acad. Sci. USA 84: 214-218; Nishimura, et al, 1987. Cancer Res. 47:

999-1005; Wood, et al, 1985. Nature 314 :446-449; Shaw, et al, 1988. J. Natl. Cancer Inst.

80: 1553-1559); Morrison(1985) Science 229:1202-1207; Oi, et al. (1986) BioTechniques 4:214; Jones, et al, 1986. Nature 321 : 552-525; Verhoeyan, et al, 1988. Science 239: 1534; and Beidler, et al, 1988. J Immunol. 141 : 4053-4060. Each ofthe above citations are incoφorated herein by reference in their entirety.

In one embodiment, methods for the screening of antibodies that possess the desired specificity include, but are not limited to, enzyme-linked immunosorbent assay (ELISA) and other immunologically-mediated techniques known within the art. In a specific embodiment, selection of antibodies that are specific to a particular domain of a POLYX protein is facilitated by generation of hybridomas that bind to the fragment of a POLYX protein possessing such a domain. Thus, antibodies that are specific for a desired domain within a POLYX protein, or derivatives, fragments, analogs or homologs thereof, are also provided herein.

Anti-POLYX antibodies may be used in methods known within the art relating to the localization and/or quantitation of a POLYX protein (e.g., for use in measuring levels ofthe POLYX protein within appropriate physiological samples, for use in diagnostic methods, for use in imaging the protein, and the like). In a given embodiment, antibodies for POLYX proteins, or derivatives, fragments, analogs or homologs thereof, that contain the antibody derived binding domain, are utilized as pharmacologically-active compounds (hereinafter "Therapeutics").

An anti-POLYX antibody (e.g., monoclonal antibody) can be used to isolate a POLYX polypeptide by standard techniques, such as affinity chromatography or immunoprecipitation. An anti-POLYX antibody can facilitate the purification of natural POLYX polypeptide from cells and of recombinantly-produced POLYX polypeptide expressed in host cells. Moreover, an anti-POLYX antibody can be used to detect POLYX protein (e.g., in a cellular lysate or cell supernatant) in order to evaluate the abundance and pattern of expression ofthe POLYX protein. Anti-POLYX antibodies can be used diagnostically to monitor protein levels in tissue as part of a clinical testing procedure, e.g., to, for example, determine the efficacy of a given treatment regimen. Detection 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 include ¹²⁵I, ¹³¹L ³⁵S or ³H.

POLYX Recombinant Expression Vectors and Host Cells

Another aspect ofthe invention pertains to vectors, preferably expression vectors, containing a nucleic acid encoding a POLYX protein, or derivatives, fragments, analogs or homologs thereof. As used herein, the term "vector" refers to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. One type of vector is a "plasmid", which refers to a circular double stranded DNA loop into which additional DNA segments can be ligated. Another type of vector is a viral vector, wherein additional DNA segments can be ligated into the viral genome. Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g., bacterial vectors having a bacterial origin of replication and episomal mammalian vectors). Other vectors (e.g., non-episomal mammalian vectors) are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome. Moreover, certain vectors are capable of directing the expression of genes to which they are operatively-linked. Such vectors are referred to herein as "expression vectors". In general, expression vectors of utility in recombinant DNA techniques are often in the form of plasmids. In the present Specification, "plasmid" and "vector" can be used interchangeably, as the plasmid is the most commonly used form of vector. However, the invention is intended to include such other forms of expression vectors, such as viral vectors (e.g., replication defective retroviruses, adenoviruses and adeno-associated viruses), which serve equivalent functions.

The recombinant expression vectors ofthe invention comprise a nucleic acid ofthe invention in a form suitable for expression ofthe nucleic acid in a host cell, which means that the recombinant expression vectors include one or more regulatory sequences, selected on the basis ofthe host cells to be used for expression, that is operative! y-linked to the nucleic acid sequence to be expressed. Within a recombinant expression vector, "operably-linked" is intended to mean that the nucleotide sequence of interest is linked to the regulatory sequence(s) in a manner that allows for expression ofthe nucleotide sequence (e.g., in an in vitro transcription translation system or in a host cell when the vector is introduced into the host cell).

As utilized herein, the phrase "regulatory sequence" is intended to includes promoters, enhancers and other expression control elements (e.g., polyadenylation signals). Such regulatory sequences are described, for example, in Goeddel, GENE EXPRESSION TECHNOLOGY: METHODS IN ENZYMOLOGY 185, Academic Press, San Diego, CA (1990). Regulatory sequences include those that direct constitutive expression of a nucleotide sequence in many types of host cell and those that direct expression ofthe nucleotide sequence only in certain host cells (e.g., tissue-specific regulatory sequences). It will be appreciated by those skilled in the art that the design ofthe expression vector can depend on such factors as the choice ofthe host cell to be transformed, the level of expression of protein desired, etc. The expression vectors ofthe invention can be introduced into host cells to thereby produce proteins or peptides, including fusion proteins or peptides, encoded by nucleic acids as described herein (e.g., POLYX proteins, mutant forms of POLYX proteins, fusion proteins, etc.).

The recombinant expression vectors ofthe invention can be designed for expression of

POLYX proteins in prokaryotic or eukaryotic cells. For example, POLYX proteins can be expressed in bacterial cells such as Escherichia coli, insect cells (using baculovirus expression vectors) yeast cells or mammalian cells. Suitable host cells are discussed further in Goeddel, GENE EXPRESSION TECHNOLOGY: METHODS IN ENZYMOLOGY 185, Academic Press, San Diego, Calif. (1990). Alternatively, the recombinant expression vector can be transcribed and translated in vitro, for example using T₇ promoter regulatory sequences and T₇ polymerase.

Expression of proteins in prokaryotes is most often carried out in Escherichia coli with vectors containing constitutive or inducible promoters directing the expression of either fusion or non-fusion proteins. Fusion vectors add a number of amino acids to a protein encoded therein, usually to the amino terminus ofthe recombinant protein. Such fusion vectors typically serve three puφoses: (i) to increase expression of recombinant protein; (if) to increase the solubility ofthe recombinant protein; and (iii) to aid in the purification ofthe recombinant protein by acting as a ligand in affinity purification. Often, in fusion expression vectors, a proteolytic cleavage site is introduced at the junction ofthe fusion moiety and the recombinant protein to enable separation ofthe recombinant protein from the fusion moiety subsequent to purification ofthe fusion protein. Such enzymes, and their cognate recognition sequences, include Factor X_a, thrombin, and enterokinase. Typical fusion expression vectors include pGEX (Pharmacia Biotech Inc; Smith and Johnson, 1988. Gene 61: 31-40), pMAL (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia, Piscataway, NJ) that fuse glutathione S-transferase (GST), maltose E binding protein, or protein A, respectively, to the target recombinant protein.

Examples of suitable inducible non-fusion Escherichia coli expression vectors include pTrc (Amrann et al, (1988) Gene 69:301-315) and pET l id (Srudier, et al, GENE EXPRESSION TECHNOLOGY: METHODS IN ENZYMOLOGY 185, Academic Press, San Diego, Calif. (1990) 60-89).

One strategy to maximize recombinant protein expression in Escherichia coli is to express the protein in a host bacteria with an impaired capacity to proteolytically-cleave the recombinant protein. See, e.g., Gottesman, GENE EXPRESSION TECHNOLOGY: METHODS IN ENZYMOLOGY 185, Academic Press, San Diego, Calif. (1990) 119-128. Another strategy is to alter the nucleic acid sequence ofthe nucleic acid to be inserted into an expression vector so that the individual codons for each amino acid are those preferentially utilized in Escherichia coli (see, e.g., Wada, et al, 1992. Nucl. Acids Res. 20: 2111-2118). Such alteration of nucleic acid sequences ofthe invention can be carried out by standard DNA synthesis techniques.

In another embodiment, the POLYX expression vector is a yeast expression vector.

Examples of vectors for expression in yeast Saccharomyces cerivisae include pYepSecl (Baldari, et al, 1987. EMBO J. 6: 229-234), pMFa (Kurjan and Herskowitz, 1982. Cell 30: 933-943), pJRY88 (Schultz et al, 1987. Gene 54: 113-123), pYES2 (Invitrogen Coφoration, San Diego, Calif.), and picZ (InVitrogen Coφ, San Diego, Calif). Alternatively, POLYX can be expressed in insect cells using baculovirus expression vectors. Baculovirus vectors available for expression of proteins in cultured insect cells (e.g., SF9 cells) include the pAc series (Smith, et al, 1983. Mol. Cell. Biol. 3: 2156-2165) and the pVL series (Lucklow and Summers, 1989. Virology 170: 31-39).

In yet another embodiment, a nucleic acid ofthe invention is expressed in mammalian cells using a mammalian expression vector. Examples of mammalian expression vectors include pCDM8 (Seed, 1987. Nature 329: 840) and pMT2PC (Kaufman, et al, 1987. EMBO J. 6: 187-195). When used in mammalian cells, the expression vector's control functions are often provided by viral regulatory elements. For example, commonly used promoters are derived from polyoma, adenovirus 2, cytomegalovirus, and simian virus 40. For other suitable expression systems for both prokaryotic and eukaryotic cells see, e.g., Chapters 16 and 17 of 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.

In another embodiment, the recombinant mammalian expression vector is capable of directing expression ofthe nucleic acid preferentially in a particular cell type (e.g., tissue-specific regulatory elements are used to express the nucleic acid). Tissue-specific regulatory elements are known in the art. Non-limiting examples of suitable tissue-specific promoters include the albumin promoter (liver-specific; see, Pinkert, et al, 1987. Genes Dev. 1 : 268-277), lymphoid-specific promoters (see, Calame and Eaton, 1988. Adv. Immunol. 43: 235-275), in particular promoters of T cell receptors (see, Winoto and Baltimore, 1989. EMBO J. 8: 729-733) and immunoglobulins (see, Banerji, et al, 1983. Cell 33: 729-740; Queen and Baltimore, 1983. Cell 33: 741-748), neuron-specific promoters (e.g., the neurofilament promoter; see, Byrne and Ruddle, 1989. Proc. Natl. Acad. Sci. USA 86: 5473-5477), pancreas-specific promoters (see, Edlund, et al, 1985. Science 230: 912-916), and mammary gland-specific promoters (e.g., milk whey promoter; U.S. Pat. No. 4,873,316 and European Application Publication No. 264,166). Developmentally-regulated promoters are also encompassed, e.g., the murine hox promoters (Kessel and Grass, 1990. Science 249: 374-379) and the -fetoprotein promoter (see, Campes and Tilghman, 1989. Genes Dev. 3: 537-546). The invention further provides a recombinant expression vector comprising a DNA molecule ofthe invention cloned into the expression vector in an antisense orientation. That is, the DNA molecule is operatively-linked to a regulatory sequence in a manner that allows for expression (by transcription ofthe DNA molecule) of an RNA molecule that is antisense to POLYX mRNA. Regulatory sequences operatively linked to a nucleic acid cloned in the antisense orientation can be chosen that direct the continuous expression ofthe antisense RNA molecule in a variety of cell types, for instance viral promoters and/or enhancers, or regulatory sequences can be chosen that direct constitutive, tissue specific or cell type specific expression of antisense RNA. The antisense expression vector can be in the form of a recombinant plasmid, phagemid or attenuated virus in which antisense nucleic acids are produced under the control of a high efficiency regulatory region, the activity of which can be determined by the cell type into which the vector is introduced. For a discussion ofthe regulation of gene expression using antisense genes see, e.g., Weintraub, et al, "Antisense RNA as a molecular tool for genetic analysis," Reviews-Trends in Genetics, Vol. 1(1) 1986.

Another aspect ofthe invention pertains to host cells into which a recombinant expression vector ofthe invention has been introduced. The terms "host cell" and "recombinant host cell" are used interchangeably herein. It is understood that such terms refer not only to the particular subject cell but also to the progeny or potential progeny of such a cell. Because certain modifications may occur in succeeding generations due to either mutation or environmental influences, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope ofthe term as used herein.

A host cell can be any prokaryotic or eukaryotic cell. For example, POLYX protein can be expressed in bacterial cells such as Escherichia coli, insect cells, yeast or mammalian cells (such as Chinese hamster ovary cells (CHO) or COS cells). Other suitable host cells are known to those skilled in the art.

Vector DNA can be introduced into prokaryotic or eukaryotic cells via conventional transformation or transfection techniques. As used herein, the terms "transformation" and "transfection" are intended to refer to a variety of art-recognized techniques for introducing foreign nucleic acid (e.g., DNA) into a host cell, including calcium phosphate or calcium chloride co-precipitation, DEAE-dextran-mediated transfection, lipofection, or electroporation. Suitable methods for transforming or transfecting host cells can be 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), and other laboratory manuals.

For stable transfection of mammalian cells, it is known that, depending upon the expression vector and transfection technique used, only a small fraction of cells may integrate the foreign DNA into their genome. In order to identify and select these integrants, a gene that encodes a selectable marker (e.g., resistance to antibiotics) is generally introduced into the host cells along with the gene of interest. Various selectable markers include those that confer resistance to drugs, such as G418, hygromycin, and methotrexate. Nucleic acid encoding a selectable marker can be introduced into a host cell on the same vector as that encoding POLYX or can be introduced on a separate vector. Cells stably-transfected with the introduced nucleic acid can be identified by drug selection (e.g., cells that have incoφorated the selectable marker gene will survive, while the other cells die).

A host cell ofthe invention, such as a prokaryotic or eukaryotic host cell in culture, can be used to produce (i.e., express) POLYX protein. Accordingly, the invention further provides methods for producing POLYX protein using the host cells ofthe invention. In one embodiment, the method comprises culturing the host cell of invention (i.e., into which a recombinant expression vector encoding POLYX protein has been introduced) in a suitable medium such that POLYX protein is produced. In another embodiment, the method further comprises isolating POLYX protein from the medium or the host cell.

Transgenic Animals

The host cells ofthe invention can also be used to produce non-human transgenic animals. For example, in one embodiment, a host cell ofthe invention is a fertilized oocyte or an embryonic stem cell into which POLYX protein-coding sequences have been introduced.

These host cells can then be used to create non-human transgenic animals in which exogenous

POLYX sequences have been introduced into their genome or homologous recombinant animals in which endogenous POLYX sequences have been altered. Such animals are useful for studying the function and/or activity of POLYX protein and for identifying and/or evaluating modulators of POLYX protein activity. As used herein, a "transgenic animal" is a non-human animal, preferably a mammal, more preferably a rodent such as a rat or mouse, in which one or more ofthe cells ofthe animal includes a transgene. Other examples of transgenic animals include non-human primates, sheep, dogs, cows, goats, chickens, amphibians, etc.

A transgene is exogenous DNA that is integrated into the genome of a cell from which a transgenic animal develops and that remains in the genome ofthe mature animal, thereby directing the expression of an encoded gene product in one or more cell types or tissues ofthe transgenic animal. As used herein, a "homologous recombinant animal" is a non-human animal, preferably a mammal, more preferably a mouse, in which an endogenous POLYX gene has been altered by homologous recombination between the endogenous gene and an exogenous DNA molecule introduced into a cell ofthe animal, e.g., an embryonic cell ofthe animal, prior to development ofthe animal.

A transgenic animal ofthe invention can be created by introducing POLYX-encoding nucleic acid into the male pronuclei of a fertilized oocyte (e.g., by micro-injection, retro viral infection) and allowing the oocyte to develop in a pseudopregnant female foster animal. The human POLYX cDNA sequences of SEQ ID NO:2??-l (wherein n = 1 to 17), can be introduced as a transgene into the genome of a non-human animal. Alternatively, a non- human homologue ofthe human POLYX gene, such as a mouse POLYX gene, can be isolated based on hybridization to the human POLYX cDNA (described further supra) and used as a transgene. Intronic sequences and polyadenylation signals can also be included in the transgene to increase the efficiency of expression ofthe transgene. A tissue-specific regulatory sequence(s) can be operably-linked to the POLYX transgene to direct expression of POLYX protein to particular cells. Methods for generating transgenic animals via embryo manipulation and micro-injection, particularly animals such as mice, have become conventional in the art and are described, for example, in U.S. Patent Nos. 4,736,866; 4,870,009; and 4,873,191; and Hogan, 1986. In: MANIPULATING THE MOUSE EMBRYO, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NN. Similar methods are used for production of other transgenic animals. A transgenic founder animal can be identified based upon the presence ofthe POLYX transgene in its genome and/or expression of POLYX mRNA in tissues or cells ofthe animals. A transgenic founder animal can then be used to breed additional animals carrying the transgene. Moreover, transgenic animals carrying a transgene-encoding POLYX protein can further be bred to other transgenic animals carrying other transgenes.

To create a homologous recombinant animal, a vector is prepared which contains at least a portion of a POLYX gene into which a deletion, addition or substitution has been introduced to thereby alter, e.g., functionally disrupt, the POLYX gene. The POLYX gene can be a human gene (e.g., the cDNA of SEQ ID NO:2τ?-l (wherein n = 1 to 17)), but more preferably, is a non-human homologue of a human POLYX gene. For example, a mouse homologue of human POLYX gene of SEQ ID NO:2«-l (wherein n = 1 to 17), can be used to construct a homologous recombination vector suitable for altering an endogenous POLYX gene in the mouse genome. In one embodiment, the vector is designed such that, upon homologous recombination, the endogenous POLYX gene is functionally disrupted (i.e., no longer encodes a functional protein; also referred to as a "knock out" vector).

Alternatively, the vector can be designed such that, upon homologous recombination, the endogenous POLYX gene is mutated or otherwise altered but still encodes functional protein (e.g., the upstream regulatory region can be altered to thereby alter the expression of the endogenous POLYX protein). In the homologous recombination vector, the altered portion ofthe POLYX gene is flanked at its 5'- and 3'-termini by additional nucleic acid ofthe POLYX gene to allow for homologous recombination to occur between the exogenous POLYX gene carried by the vector and an endogenous POLYX gene in an embryonic stem cell. The additional flanking POLYX nucleic acid is of sufficient length for successful homologous recombination with the endogenous gene. Typically, several kilobases (Kb) of flanking DNA (both at the 5'- and 3'-termini) are included in the vector. See, e.g., Thomas, et al, 1987. Cell 51: 503 for a description of homologous recombination vectors. The vector is ten introduced into an embryonic stem cell line (e.g., by electroporation) and cells in which the introduced POLYX gene has homologously-recombined with the endogenous POLYX gene are selected. See, e.g., Li, et al, 1992. Cell 69: 915. The selected cells are then micro-injected into a blastocyst of an animal (e.g., a mouse) to form aggregation chimeras. See, e.g., Bradley, 1987. In: TERATOCARCINOMAS AND EMBRYONIC STEM CELLS: A PRACTICAL APPROACH, Robertson, ed. IRL, Oxford, pp. 113-152. A chimeric embryo can then be implanted into a suitable pseudopregnant female foster animal and the embryo brought to term. Progeny harboring the homologously-recombined DNA in their germ cells can be used to breed animals in which all cells ofthe animal contain the homologously-recombined DNA by germline transmission ofthe transgene. Methods for constructing homologous recombination vectors and homologous recombinant animals are described further in Bradley, 1991. Curr. Opin. Biotechnol. 2: 823-829; PCT International Publication Nos.: WO 90/11354; WO 91/01140; WO 92/0968; and WO 93/04169.

In another embodiment, transgenic non-human animals can be produced that contain selected systems that allow for regulated expression ofthe transgene. One example of such a system is the cre/loxP recombinase system of bacteriophage PI . For a description ofthe cre/loxP recombinase system, See, e.g., Lakso, et αl, 1992. Proc. Nαtl. Acαd. Sci. USA 89: 6232-6236. Another example of a recombinase system is the FLP recombinase system of

Sαcchαromyces cerevisiαe. See, O'Gorman, et αl, 1991. Science 251:1351-1355. If a cre/loxP recombinase system is used to regulate expression ofthe transgene, animals containing transgenes encoding both the Cre recombinase and a selected protein are 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 ofthe non-human transgenic animals described herein can also be produced according to the methods described in Wilmut, et αl, 1997. Nature 385: 810-813. 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 ofthe same species from which the quiescent cell is isolated. The reconstructed oocyte is then cultured such that it develops to morula or blastocyte, and then transferred to pseudopregnant female foster animal. The offspring borne of this female foster animal will be a clone ofthe animal from which the cell (e.g., the somatic cell) is isolated. Pharmaceutical Compositions

The POLYX nucleic acid molecules, POLYX proteins, and anti-POLYX antibodies (also referred to herein as "active compounds") ofthe invention, and derivatives, fragments, analogs and homologs thereof, can be incoφorated into pharmaceutical compositions suitable for administration. Such compositions typically comprise the nucleic acid molecule, protein, or antibody and a pharmaceutically-acceptable carrier. As used herein, "pharmaceutically- acceptable carrier" is intended to include any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absoφtion delaying agents, and the like, compatible with pharmaceutical administration. Suitable carriers are described in the most recent edition of Remington's Pharmaceutical Sciences, a standard reference text in the field, which is incoφorated herein by reference. Preferred examples of such carriers or diluents include, but are not limited to, water, saline, finger's solutions, dextrose solution, and 5% human serum albumin. Liposomes and other non-aqueous (i.e., lipophilic) vehicles such as fixed oils may also be used. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active compound, use thereof in the compositions is contemplated. Supplementary active compounds can also be incoφorated into the compositions.

A pharmaceutical composition ofthe invention is formulated to be compatible with its intended route of administration. Examples of routes of administration include parenteral, e.g., intravenous, intradermal, subcutaneous, oral (e.g., inhalation), transdermal (i.e., topical), transmucosal, and rectal administration. Solutions or suspensions used for parenteral, intradermal, or subcutaneous application can include the following components: a sterile diluent such as water for injection, saline solution, fixed oils, polyethylene glycols, glycerine, propylene glycol or other synthetic solvents; antibacterial agents such as benzyl alcohol or methyl parabens; antioxidants such as ascorbic acid or sodium bisulfite; chelating agents such as ethylenediaminetetraacetic acid (EDTA); buffers such as acetates, citrates or phosphates, and agents for the adjustment of tonicity such as sodium chloride or dextrose. The pH can be adjusted with acids or bases, such as hydrochloric acid or sodium hydroxide. The parenteral preparation can be enclosed in ampoules, disposable syringes or multiple dose vials made of glass or plastic. Pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. For intravenous administration, suitable carriers include physiological saline, bacteriostatic water, Cremophor EL (BASF, Parsippany, N.J.) or phosphate buffered saline (PBS). In all cases, the composition must be sterile and should be fluid to the extent that easy syringeability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance ofthe required particle size in the case of dispersion and by the use of surfactants. Prevention ofthe action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as manitol, sorbitol, sodium chloride in the composition. Prolonged absoφtion ofthe injectable compositions can be brought about by including in the composition an agent which delays absoφtion, for example, aluminum monostearate and gelatin.

Sterile injectable solutions can be prepared by incoφorating the active compound (e.g., a POLYX protein or anti-POLYX antibody) in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incoφorating the active compound into a sterile vehicle that contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, methods of preparation are vacuum drying and freeze-drying that yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.

Oral compositions generally include an inert diluent or an edible carrier. They can be enclosed in gelatin capsules or compressed into tablets. For the pmpose of oral therapeutic administration, the active compound can be incoφorated with excipients and used in the form of tablets, troches, or capsules. Oral compositions can also be prepared using a fluid carrier for use as a mouthwash, wherein the compound in the fluid carrier is applied orally and swished and expectorated or swallowed. Pharmaceutically compatible binding agents, and/or adjuvant materials can be included as part ofthe composition. The tablets, pills, capsules, troches and the like can contain any ofthe following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate or Sterotes; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.

For administration by inhalation, the compounds are delivered in the form of an aerosol spray from pressured container or dispenser which contains a suitable propellant, e.g., a gas such as carbon dioxide, or a nebulizer.

Systemic administration can also be by transmucosal or transdermal means. For transmucosal or transdermal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives. Transmucosal administration can be accomplished through the use of nasal sprays or suppositories. For transdermal administration, the active compounds are formulated into ointments, salves, gels, or creams as generally known in the art.

The compounds can also be prepared in the form of suppositories (e.g., with conventional suppository bases such as cocoa butter and other glycerides) or retention enemas for rectal delivery.

In one embodiment, the active compounds are prepared with carriers that will protect the compound against rapid elimination from the body, such as a controlled release formulation, including implants and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Methods for preparation of such formulations will be apparent to those skilled in the art. The materials can also be obtained commercially from Alza Coφoration and Nova Pharmaceuticals, Inc. Liposomal suspensions (including liposomes targeted to infected cells with monoclonal antibodies to viral antigens) can also be used as pharmaceutically acceptable carriers. These can be prepared according to methods known to those skilled in the art, for example, as described in U.S. Patent No. 4,522,811.

It is especially advantageous to formulate oral or parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subject to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. The specification for the dosage unit forms ofthe invention are dictated by and directly dependent on the unique characteristics ofthe active compound and the particular therapeutic effect to be achieved, and the limitations inherent in the art of compounding such an active compound for the treatment of individuals.

The nucleic acid molecules ofthe invention can be inserted into vectors and used as gene therapy vectors. Gene therapy vectors can be delivered to a subject by, for example, intravenous injection, local administration (see, e.g., U.S. Patent No. 5,328,470) or by stereotactic injection (see, e.g., Chen, et al, 1994. Proc. Natl. Acad. Sci. USA 91: 3054-3057). The pharmaceutical preparation ofthe gene therapy vector can include the gene therapy vector in an acceptable diluent, or can comprise a slow release matrix in which the gene delivery vehicle is imbedded. Alternatively, where the complete gene delivery vector can be produced intact from recombinant cells, e.g., retro viral vectors, the pharmaceutical preparation can include one or more cells that produce the gene delivery system.

The pharmaceutical compositions can be included in a container, pack, or dispenser together with instructions for administration. Screening and Detection Methods

The nucleic acid molecules, proteins, protein homologues, and antibodies described herein can be used in one or more ofthe following methods: (t) screening assays; (ii) detection assays (e.g., chromosomal mapping, cell and tissue typing, forensic biology), (iii) predictive medicine (e.g. , diagnostic assays, prognostic assays, monitoring clinical trials, and pharmacogenomics); and (zv) methods of treatment (e.g., therapeutic and prophylactic).

The isolated nucleic acid molecules ofthe present invention can be used to express POLYX protein (e.g., via a recombinant expression vector in a host cell in gene therapy applications), to detect POLYX mRNA (e.g., in a biological sample) or a genetic lesion in an POLYX gene, and to modulate POLYX activity, as described further, infra. In addition, the POLYX proteins can be used to screen drugs or compounds that modulate the POLYX protein activity or expression as well as to treat disorders characterized by insufficient or excessive production of POLYX protein or production of POLYX protein forms that have decreased or aberrant activity compared to POLYX wild-type protein. In addition, the anti-POLYX antibodies ofthe present invention can be used to detect and isolate POLYX proteins and modulate POLYX activity.

The invention further pertains to novel agents identified by the screening assays described herein and uses thereof for treatments as described, supra.

Screening Assays

The invention provides a method (also referred to herein as a "screening assay") for identifying modulators, i.e., candidate or test compounds or agents (e.g., peptides, peptidomimetics, small molecules or other drugs) that bind to POLYX proteins or have a stimulatory or inhibitory effect on, e.g., POLYX protein expression or POLYX protein activity. The invention also includes compounds identified in the screening assays described herein.

In one embodiment, the invention provides assays for screening candidate or test compounds which bind to or modulate the activity ofthe membrane-bound form of a POLYX protein or polypeptide or biologically-active portion thereof. The test compounds ofthe invention can be obtained using any ofthe numerous approaches in combinatorial library methods known in the art, including: biological libraries; spatially addressable parallel solid phase or solution phase libraries; synthetic library methods requiring deconvolution; the "one-bead one-compound" library method; and synthetic library methods using affinity chromatography selection. The biological library approach is limited to peptide libraries, while the other four approaches are applicable to peptide, non-peptide oligomer or small molecule libraries of compounds. See, e.g., Lam, 1997. Anticancer Drug Design 12: 145.

A "small molecule" as used herein, is meant to refer to a composition that has a molecular weight of less than about 5 kD and most preferably less than about 4 kD. Small molecules/can be, e.g., nucleic acids, peptides, polypeptides, peptidomimetics, carbohydrates, lipids or other organic or inorganic molecules. Libraries of chemical and/or biological mixtures, such as fungal, bacterial, or algal extracts, are known in the art and can be screened with any ofthe assays ofthe invention.

Examples of methods for the synthesis of molecular libraries can be found in the art, for example in: DeWitt, et al, 1993. Proc. Natl Acad. Sci. U.S.A. 90: 6909; Erb, et al, 1994. Proc. Natl. Acad. Sci. U.S.A. 91: 11422; Zuckermann, et al, 1994. J. Med. Chem. 37: 2678; Cho, et al, 1993. Science 261 : 1303; Carrell, et al, 1994. Angew. Chem. Int. Ed. Engl. 33: 2059; Carell, et al, 1994. Angew. Chem. Int. Ed. Engl. 33: 2061; and Gallop, et al, 1994. J. Med. Chem. 37: 1233.

Libraries of compounds may be presented in solution (e.g., Houghten, 1992. Biotechniques 13: 412-421), or on beads (Lam, 1991. Nature 354: 82-84), on chips (Fodor, 1993. Nature 364: 555-556), bacteria (Ladner, U.S. Patent No. 5,223,409), spores (Ladner, U.S. Patent 5,233,409), plasmids (Cull, et al, 1992. Proc. Natl. Acad. Sci. USA 89: 1865-1869) or on phage (Scott and Smith, 1990. Science 249: 386-390; Devlin, 1990. Science 249: 404-406; Cwirla, et al, 1990. Proc. Natl. Acad. Sci. U.S.A. 87: 6378-6382; Felici, 1991. J. Mol. Biol. 222: 301-310; Ladner, U.S. Patent No. 5,233,409.).

In one embodiment, an assay is a cell-based assay in which a cell which expresses a membrane-bound form of POLYX protein, or a biologically-active portion thereof, on the cell surface is contacted with a test compound and the ability ofthe test compound to bind to a POLYX protein determined. The cell, for example, can of mammalian origin or a yeast cell. Determining the ability ofthe test compound to bind to the POLYX protein can be accomplished, for example, by coupling the test compound with a radioisotope or enzymatic label such that binding ofthe test compound to the POLYX protein or biologically-active portion thereof can be determined by detecting the labeled compound in a complex. For example, test compounds can be labeled with ¹²⁵1, ³⁵S, ¹⁴C, or ³H, either directly or indirectly, and the radioisotope detected by direct counting of radioemission or by scintillation counting. Alternatively, test compounds can be enzymatically-labeled with, for example, horseradish peroxidase, alkaline phosphatase, or luciferase, and the enzymatic label detected by determination of conversion of an appropriate substrate to product. In one embodiment, the assay comprises contacting a cell which expresses a membrane-bound form of POLYX protein, or a biologically-active portion thereof, on the cell surface with a known compound which binds POLYX to form an assay mixture, contacting the assay mixture with a test compound, and determining the ability ofthe test compound to interact with a POLYX protein, wherein determining the ability ofthe test compound to interact with a POLYX protein comprises determining the ability ofthe test compound to preferentially bind to POLYX protein or a biologically-active portion thereof as compared to the known compound.

In another embodiment, an assay is a cell-based assay comprising contacting a cell expressing a membrane-bound form of POLYX protein, or a biologically-active portion thereof, on the cell surface with a test compound and determining the ability ofthe test compound to modulate (e.g., stimulate or inhibit) the activity ofthe POLYX protein or biologically-active portion thereof. Determining the ability ofthe test compound to modulate the activity of POLYX or a biologically-active portion thereof can be accomplished, for example, by determining the ability ofthe POLYX protein to bind to or interact with a POLYX target molecule. As used herein, a "target molecule" is a molecule with which a POLYX protein binds or interacts in nature, for example, a molecule on the surface of a cell which expresses a POLYX interacting protein, a molecule on the surface of a second cell, a molecule in the extracellular milieu, a molecule associated with the internal surface of a cell membrane or a cytoplasmic molecule. An POLYX target molecule can be a non-POLYX molecule or a POLYX protein or polypeptide ofthe invention. In one embodiment, a POLYX target molecule is a component of a signal transduction pathway that facilitates transduction of an extracellular signal (e.g. a signal generated by binding of a compound to a membrane-bound POLYX molecule) through the cell membrane and into the cell. The target, for example, can be a second intercellular protein that has catalytic activity or a protein that facilitates the association of downstream signaling molecules with POLY.

Determining the ability ofthe POLYX protein to bind to or interact with a POLYX target molecule can be accomplished by one ofthe methods described above for determining direct binding. In one embodiment, determining the ability ofthe POLYX protein to bind to or interact with a POLYX target molecule can be accomplished by determining the activity ofthe target molecule. For example, the activity ofthe target molecule can be determined by detecting induction of a cellular second messenger ofthe target (i.e. intracellular Ca²⁺, diacylglycerol, IP₃, etc.), detecting catalytic/enzymatic activity ofthe target an appropriate substrate, detecting the induction of a reporter gene (comprising a POLYX-responsive regulatory element operatively linked to a nucleic acid encoding a detectable marker, e.g., luciferase), or detecting a cellular response, for example, cell survival, cellular differentiation, or cell proliferation.

In yet another embodiment, an assay ofthe invention is a cell-free assay comprising contacting a POLYX protein or biologically-active portion thereof with a test compound and determining the ability ofthe test compound to bind to the POLYX protein or biologically- active portion thereof. Binding ofthe test compound to the POLYX protein can be determined either directly or indirectly as described above. In one such embodiment, the assay comprises contacting the POLYX protein or biologically-active portion thereof with a known compound which binds POLYX to form an assay mixture, contacting the assay mixture with a test compound, and determining the ability ofthe test compound to interact with a POLYX protein, wherein determining the ability ofthe test compound to interact with a POLYX protein comprises determining the ability ofthe test compound to preferentially bind to POLYX or biologically-active portion thereof as compared to the known compound.

I l l In still another embodiment, an assay is a cell-free assay comprising contacting POLYX protein or biologically-active portion thereof with a test compound and determining the ability ofthe test compound to modulate (e.g. stimulate or inhibit) the activity ofthe POLYX protein or biologically-active portion thereof. Determining the ability ofthe test compound to modulate the activity of POLYX can be accomplished, for example, by determining the ability ofthe POLYX protein to bind to a POLYX target molecule by one of the methods described above for determining direct binding. In an alternative embodiment, determining the ability ofthe test compound to modulate the activity of POLYX protein can be accomplished by determining the ability ofthe POLYX protein further modulate a POLYX target molecule. For example, the catalytic/enzymatic activity ofthe target molecule on an appropriate substrate can be determined as described, supra.

In yet another embodiment, the cell-free assay comprises contacting the POLYX protein or biologically-active portion thereof with a known compound which binds POLYX protein to form an assay mixture, contacting the assay mixture with a test compound, and determining the ability ofthe test compound to interact with a POLYX protein, wherein determining the ability ofthe test compound to interact with a POLYX protein comprises determining the ability ofthe POLYX protein to preferentially bind to or modulate the activity of a POLYX target molecule.

The cell-free assays ofthe invention are amenable to use of both the soluble form or the membrane-bound form of POLYX protein. In the case of cell-free assays comprising the membrane-bound form of POLYX protein, it may be desirable to utilize a solubilizing agent such that the membrane-bound form of POLYX protein is maintained in solution. Examples of such solubilizing agents include non-ionic detergents such as n-octylglucoside, n-dodecylglucoside, n-dodecylmaltoside, octanoyl-N-methylglucamide, decanoyl-N-methylglucamide, Triton^® X-100, Triton^® X-l 14, Thesit^®,

Isotridecypoly(ethylene glycol ether)_n, N-dodecyl~N,N-dimethyl-3-ammonio-l -propane sulfonate, 3-(3-cholamidopropyl) dimethylamminiol-1 -propane sulfonate (CHAPS), or 3-(3-cholamidopropyl)dimethylamminiol-2-hydroxy-l -propane sulfonate (CHAPSO). In more than one embodiment ofthe above assay methods ofthe invention, it may be desirable to immobilize either POLYX protein or its target molecule to facilitate separation of complexed from uncomplexed forms of one or both ofthe proteins, as well as to accommodate automation ofthe assay. Binding of a test compound to POLYX protein, or interaction of POLYX protein with a target molecule in the presence and absence of a candidate compound, can be accomplished in any vessel suitable for containing the reactants. Examples of such vessels include microtiter plates, test tubes, and micro-centrifuge tubes. In one embodiment, a fusion protein can be provided that adds a domain that allows one or both ofthe proteins to be bound to a matrix. For example, GST-POL YX fusion proteins or GST-target fusion proteins can be adsorbed onto glutathione sepharose beads (Sigma Chemical, St. Louis, MO) or glutathione derivatized microtiter plates, that are then combined with the test compound or the test compound and either the non-adsorbed target protein or POLYX protein, and the mixture is incubated under conditions conducive to complex formation (e.g., at physiological conditions for salt and pH). Following incubation, the beads or microtiter plate wells are washed to remove any unbound components, the matrix immobilized in the case of beads, complex determined either directly or indirectly, for example, as described, supra. Alternatively, the complexes can be dissociated from the matrix, and the level of POLYX protein binding or activity determined using standard techniques.

Other techniques for immobilizing proteins on matrices can also be used in the screening assays ofthe invention. For example, either the POLYX protein or its target molecule can be immobilized utilizing conjugation of biotin and streptavidin. Biotinylated POLYX protein or target molecules can be prepared from biotin-NHS (N-hydroxy-succinimide) using techniques well-known within the art (e.g., biotinylation kit, Pierce Chemicals, Rockford, 111.), and immobilized in the wells of streptavidin-coated 96 well plates (Pierce Chemical). Alternatively, antibodies reactive with POLYX protein or target molecules, but which do not interfere with binding ofthe POLYX protein to its target molecule, can be derivatized to the wells ofthe plate, and unbound target or POLYX protein trapped in the wells by antibody conjugation. 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 POLYX protein or target molecule, as well as enzyme-linked assays that rely on detecting an enzymatic activity associated with the POLYX protein or target molecule.

In another embodiment, modulators of POLYX protein expression are identified in a method wherein a cell is contacted with a candidate compound and the expression of POLYX mRNA or protein in the cell is determined. The level of expression of POLYX mRNA or protein in the presence ofthe candidate compound is compared to the level of expression of POLYX mRNA or protein in the absence ofthe candidate compound. The candidate compound can then be identified as a modulator of POLYX mRNA or protein expression based upon this comparison. For example, when expression of POLYX mRNA or protein is greater (i.e., statistically significantly greater) in the presence ofthe candidate compound than in its absence, the candidate compound is identified as a stimulator of POLYX mRNA or protein expression. Alternatively, when expression of POLYX mRNA or protein is less (statistically significantly less) in the presence ofthe candidate compound than in its absence, the candidate compound is identified as an inhibitor of POLYX mRNA or protein expression. The level of POLYX mRNA or protein expression in the cells can be determined by methods described herein for detecting POLYX mRNA or protein.

In yet another aspect ofthe invention, the POLYX proteins can be used as "bait proteins" in a two-hybrid assay or three hybrid assay (see, e.g., U.S. Patent No. 5,283,317; Zervos, et al, 1993. Ce// 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 WO 94/10300), to identify other proteins that bind to or interact with POLYX ("POLYX-binding proteins" or "POLYX-bp") and modulate POLYX activity. Such POLYX-binding proteins are also likely to be involved in the propagation of signals by the POLYX proteins as, for example, upstream or downstream elements ofthe POLYX pathway.

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 POLYX 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 ofthe known transcription factor._. If the "bait" and the "prey" proteins are able to interact, in vivo, forming a POLYX-dependent complex, the DNA-binding and activation domains ofthe transcription factor are brought into close POLYX imity. This POLYX imity allows transcription of a reporter gene (e.g., LacZ) that is operably linked to a transcriptional regulatory site responsive to the transcription factor. Expression ofthe reporter gene can be detected and cell colonies containing the functional transcription factor can be isolated and used to obtain the cloned gene that encodes the protein which interacts with POLY.

The invention further pertains to novel agents identified by the aforementioned screening assays and uses thereof for treatments as described herein.

Detection Assays

Portions or fragments ofthe cDNA sequences identified herein (and the corresponding complete gene sequences) can be used in numerous ways as polynucleotide reagents. By way of example, and not of limitation, these sequences can be used to: (i) map their respective genes on a chromosome; and, thus, locate gene regions associated with genetic disease; (ii) identify an individual from a minute biological sample (tissue typing); and ( / ) aid in forensic identification of a biological sample. Some of these applications are described in the subsections, infra.

Chromosome Mapping

Once the sequence (or a portion ofthe sequence) of a gene has been isolated, this sequence can be used to map the location ofthe gene on a chromosome. This process is called chromosome mapping. Accordingly, portions or fragments ofthe POLYX sequences shown in SEQ ID NO:2«-l (wherein n = 1 to 17), or fragments or derivatives thereof, can be used to map the location ofthe POLYX genes, respectively, on a chromosome. The mapping ofthe POLYX sequences to chromosomes is an important first step in correlating these sequences with genes associated with disease. Briefly, POLYX genes can be mapped to chromosomes by preparing PCR primers (preferably 15-25 bp in length) from the POLYX sequences. Computer analysis ofthe POLY, sequences can be used to rapidly select primers that do not span more than one exon in the genomic DNA, thus complicating the amplification process. These primers can then be used for PCR screening of somatic cell hybrids containing individual human chromosomes. Only those hybrids containing the human gene corresponding to the POLYX sequences will yield an amplified fragment.

Somatic cell hybrids are prepared by fusing somatic cells from different mammals (e.g., human and mouse cells). As hybrids of human and mouse cells grow and divide, they gradually lose human chromosomes in random order, but retain the mouse chromosomes. By using media in which mouse cells cannot grow, because they lack a particular enzyme, but in which human cells can, the one human chromosome that contains the gene encoding the needed enzyme will be retained. By using various media, panels of hybrid cell lines can be established. Each cell line in a panel contains either a single human chromosome or a small number of human chromosomes, and a full set of mouse chromosomes, allowing easy mapping of individual genes to specific human chromosomes. See, e.g., D'Eustachio, et al, 1983. Science 220: 919-924. Somatic cell hybrids containing only fragments of human chromosomes can also be produced by using human chromosomes with translocations and deletions.

PCR mapping of somatic cell hybrids is a rapid procedure for assigning a particular sequence to a particular chromosome. Three or more sequences can be assigned per day using a single thermal cycler. Using the POLYX sequences to design oligonucleotide primers, sub- localization can be achieved with panels of fragments from specific chromosomes.

Fluorescence in situ hybridization (FISH) of a DNA sequence to a metaphase chromosomal spread can further be used to provide a precise chromosomal location in one step. Chromosome spreads can be made using cells whose division has been blocked in metaphase by a chemical like colcemid that disrupts the mitotic spindle. The chromosomes can be treated briefly with trypsin, and then stained with Giemsa. A pattern of light and dark bands develops on each chromosome, so that the chromosomes can be identified individually. The FISH technique can be used with a DNA sequence as short as 500 or 600 bases. However, clones larger than 1 ,000 bases have a higher likelihood of binding to a unique chromosomal location with sufficient signal intensity for simple detection. Preferably 1 ,000 bases, and more preferably 2,000 bases, will suffice to get good results at a reasonable amount of time. For a review of this technique, see, Verma, et al, HUMAN CHROMOSOMES: A MANUAL OF BASIC TECHNIQUES (Pergamon Press, NY 1988).

Reagents for chromosome mapping can be used individually to mark a single chromosome or a single site on that chromosome, or panels of reagents can be used for marking multiple sites and/or multiple chromosomes. Reagents corresponding to non-coding regions ofthe genes actually are preferred for mapping puφoses. Coding sequences are more likely to be conserved within gene families, thus increasing the chance of cross hybridizations during chromosomal mapping.

Once a sequence has been mapped to a precise chromosomal location, the physical position ofthe sequence on the chromosome can be correlated with genetic map data. Such data are found, e.g., in McKusick, MENDELIAN INHERITANCE IN MAN, available on-line through Johns Hopkins University Welch Medical Library). The relationship between genes and disease, mapped to the same chromosomal region, can then be identified through linkage analysis (co-inheritance of physically adjacent genes), described in, e.g., Egeland, et al, 1987. Nature, 325: 783-787.

Additionally, differences in the DNA sequences between individuals affected and unaffected with a disease associated with the POLYX gene, can be determined. If a mutation is observed in some or all ofthe affected individuals but not in any unaffected individuals, then the mutation is likely to be the causative agent ofthe particular disease. Comparison of affected and unaffected individuals generally involves first looking for structural alterations in the chromosomes, such as deletions or translocations that are visible from chromosome spreads or detectable using PCR based on that DNA sequence. Ultimately, complete sequencing of genes from several individuals can be performed to confirm the presence of a mutation and to distinguish mutations from polymoφhisms. Tissue Typing

The POLYX sequences ofthe invention can also be used to identify individuals from minute biological samples. In this technique, an individual's genomic DNA is digested with one or more restriction enzymes, and probed on a Southern blot to yield unique bands for identification. The sequences ofthe invention are useful as additional DNA markers for RFLP ("restriction fragment length polymoφhisms," as described in U.S. Patent No. 5,272,057).

Furthermore, the sequences ofthe invention can be used to provide an alternative technique that determines the actual base-by-base DNA sequence of selected portions of an individual's genome. Thus, the POLYX sequences described herein can be used to prepare two PCR primers from the 5'- and 3'-termini ofthe sequences. These primers can then be used to amplify an individual's DNA and subsequently sequence it.

Panels of corresponding DNA sequences from individuals, prepared in this manner, can provide unique individual identifications, as each individual will have a unique set of such DNA sequences due to allelic differences. The sequences ofthe invention can be used to obtain such identification sequences from individuals and from tissue. The POLYX sequences ofthe invention uniquely represent portions ofthe human genome. Allelic variation occurs to some degree in the coding regions of these sequences, and to a greater degree in the non- coding regions. It is estimated that allelic variation between individual humans occurs with a frequency of about once per each 500 bases. Much ofthe allelic variation is due to single nucleotide polymoφhisms (SNPs), which include restriction fragment length polymoφhisms (RFLPs).

Each ofthe sequences described herein can, to some degree, be used as a standard against which DNA from an individual can be compared for identification puφoses. Because greater numbers of polymoφhisms occur in the non-coding regions, fewer sequences are necessary to differentiate individuals. The non-coding sequences can comfortably provide positive individual identification with a panel of perhaps 10 to 1,000 primers that each yield a non-coding amplified sequence of 100 bases. If predicted coding sequences, such as those in

SEQ ID NO:2«-l (wherein n = 1 to 17) are used, a more appropriate number of primers for positive individual identification would be 500-2,000. Use of Partial POLYX Sequences in Forensic Biology

DNA-based identification techniques can also be used in forensic biology. Forensic biology is a scientific field employing genetic typing of biological evidence found at a crime scene as a means for positively identifying, e.g., a peφetrator of a crime. To make such an identification, PCR technology can be used to amplify DNA sequences taken from very small biological samples such as tissues (e.g., hair or skin, or body fluids, e.g., blood, saliva, or semen found at a crime scene). The amplified sequence can then be compared to a standard, thereby allowing identification ofthe origin ofthe biological sample.

The sequences ofthe invention can be used to provide polynucleotide reagents, e.g., PCR primers, targeted to specific loci in the human genome, that can enhance the reliability of DNA-based forensic identifications by, for example, providing another "identification marker" (i.e. another DNA sequence that is unique to a particular individual). As mentioned above, actual base sequence information can be used for identification as an accurate alternative to patterns formed by restriction enzyme generated fragments. Sequences targeted to non-coding regions of SEQ ID NO:2«-l (where n - 1 to 17) are particularly appropriate for this use as greater numbers of polymoφhisms occur in the non-coding regions, making it easier to differentiate individuals using this technique. Examples of polynucleotide reagents include the POLYX sequences or portions thereof, e.g., fragments derived from the non-coding regions of one or more of SEQ ID NO:2rø-l (where n = 1 to 17), having a length of at least 20 bases, preferably at least 30 bases.

The POLYX sequences described herein can further be used to provide polynucleotide reagents, e.g., labeled or label-able probes that can be used, for example, in an in situ hybridization technique, to identify a specific tissue (e.g., brain tissue, etc). This can be very useful in cases where a forensic pathologist is presented with a tissue of unknown origin. Panels of such POLYX probes can be used to identify tissue by species and/or by organ type.

In a similar fashion, these reagents, e.g., POLYX primers or probes can be used to screen tissue culture for contamination (i.e., screen for the presence of a mixture of different types of cells in a culture). Predictive Medicine

The invention also pertains to the field of predictive medicine in which diagnostic assays, prognostic assays, pharmacogenomics, and monitoring clinical trials are used for prognostic (predictive) puφoses to thereby treat an individual prophylactically. Accordingly, one aspect ofthe invention relates to diagnostic assays for determining POLYX protein and/or nucleic acid expression as well as POLYX activity, in the context of a biological sample (e.g., blood, serum, cells, tissue) to thereby determine whether an individual is afflicted with a disease or disorder, or is at risk of developing a disorder, associated with aberrant POLYX expression or activity. The invention also provides for prognostic (or predictive) assays for determining whether an individual is at risk of developing a disorder associated with POLYX protein, nucleic acid expression or activity. For example, mutations in a POLYX gene can be assayed in a biological sample. Such assays can be used for prognostic or predictive puφose to thereby prophylactically treat an individual prior to the onset of a disorder characterized by or associated with POLYX protein, nucleic acid expression, or biological activity.

Another aspect of the invention provides methods for determining POLYX protein, nucleic acid expression or activity in an individual to thereby select appropriate therapeutic or prophylactic agents for that individual (referred to herein as "pharmacogenomics"). Pharmacogenomics allows for the selection of agents (e.g., drugs) for therapeutic or prophylactic treatment of an individual based on the genotype ofthe individual (e.g., the genotype ofthe individual examined to determine the ability ofthe individual to respond to a particular agent.)

Yet another aspect ofthe invention pertains to monitoring the influence of agents (e.g., drugs, compounds) on the expression or activity of POLYX in clinical trials. These and other agents are described in further detail in the following sections.

Diagnostic Assays

An exemplary method for detecting the presence or absence of POLYX in a biological sample involves obtaining a biological sample from a test subject and contacting the biological sample with a compound or an agent capable of detecting POLYX protein or nucleic acid (e.g., mRNA, genomic DNA) that encodes POLYX protein such that the presence of POLYX is detected in the biological sample. An agent for detecting POLYX mRNA or genomic DNA is a labeled nucleic acid probe capable of hybridizing to POLYX mRNA or genomic DNA. The nucleic acid probe can be, for example, a full-length POLYX nucleic acid, such as the nucleic acid of SEQ ID NO:2 -l (wherein n = 1 to 17), or a portion thereof, such as an oligonucleotide of at least 15, 30, 50, 100, 250 or 500 nucleotides in length and sufficient to specifically hybridize under stringent conditions to POLYX mRNA or genomic DNA. Other suitable probes for use in the diagnostic assays ofthe invention are described herein.

An agent for detecting POLYX protein is an antibody capable of binding to POLYX protein, preferably an antibody with a detectable label. Antibodies can be polyclonal, or more preferably, monoclonal. An intact antibody, or a fragment thereof (e.g., F_ab or F_(ab)2) can be used. As utilized herein, the term "labeled", with regard to the probe or antibody, is intended to encompass direct labeling ofthe probe or antibody by coupling (i.e., physically linking) a detectable substance to the probe or antibody, as well as indirect labeling ofthe probe or antibody by reactivity with another reagent that is directly labeled. Examples of indirect labeling include detection of a primary antibody using a fluorescently-labeled secondary antibody and end-labeling of a DNA probe with biotin such that it can be detected with fluorescently-labeled streptavidin. As utilized herein, the term "biological sample" is intended to include tissues, cells and biological fluids isolated from a subject, as well as tissues, cells and fluids present within a subject. That is, the detection method ofthe invention can be used to detect POLYX mRNA, protein, or genomic DNA in a biological sample in vitro as well as in vivo. For example, in vitro techniques for detection of POLYX mRNA include Northern hybridizations and in situ hybridizations. In vitro techniques for detection of POLYX protein include enzyme linked immunosorbent assays (ELISAs), Western blots, immunoprecipitations, and immunofluorescence. In vitro techniques for detection of POLYX genomic DNA include Southern hybridizations. Furthermore, in vivo techniques for detection of POLYX protein include introducing into a subject a labeled anti-POLYX antibody. 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. In one embodiment, the biological sample contains protein molecules from the test subject. Alternatively, the biological sample can contain mRNA molecules from the test subject or genomic DNA molecules from the test subject. A preferred biological sample is a peripheral blood leukocyte sample isolated by conventional means from a subject.

In another embodiment, the methods further involve obtaining a control biological sample from a control subject, contacting the control sample with a compound or agent capable of detecting POLYX protein, mRNA, or genomic DNA, such that the presence of POLYX protein, mRNA or genomic DNA is detected in the biological sample, and comparing the presence of POLYX protein, mRNA or genomic DNA in the control sample with the presence of POLYX protein, mRNA or genomic DNA in the test sample.

The invention also encompasses kits for detecting the presence of POLYX in a biological sample. For example, the kit can comprise: a labeled compound or agent capable of detecting POLYX protein or mRNA in a biological sample; means for determining the amount of POLYX in the sample; and means for comparing the amount of POLYX 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 POLYX protein or nucleic acid.

Prognostic Assays

The diagnostic methods described herein can furthermore be utilized to identify subjects having or at risk of developing a disease or disorder associated with aberrant POLYX expression or activity. For example, the assays described herein, such as the preceding diagnostic assays or the following assays, can be utilized to identify a subject having or at risk of developing a disorder associated with POLYX protein, nucleic acid expression or activity. Alternatively, the prognostic assays can be utilized to identify a subject having or at risk for developing a disease or disorder. Thus, the invention provides a method for identifying a disease or disorder associated with aberrant POLYX expression or activity in which a test sample is obtained from a subject and POLYX protein or nucleic acid (e.g., mRNA, genomic

DNA) is detected, wherein the presence of POLYX protein or nucleic acid is diagnostic for a subject having or at risk of developing a disease or disorder associated with aberrant POLYX expression or activity. As used herein, a "test sample" refers to a biological sample obtained from a subject of interest. For example, a test sample can be a biological fluid (e.g., serum), cell sample, or tissue.

Furthermore, the prognostic assays described herein can be used to determine whether a subject can be administered an agent (e.g., an agonist, antagonist, peptidomimetic, protein, peptide, nucleic acid, small molecule, or other drug candidate) to treat a disease or disorder associated with aberrant POLYX expression or activity. For example, such methods can be used to determine whether a subject can be effectively treated with an agent for a disorder. Thus, the invention provides methods for determining whether a subject can be effectively treated with an agent for a disorder associated with aberrant POLYX expression or activity in which a test sample is obtained and POLYX protein or nucleic acid is detected (e.g., wherein the presence of POLYX protein or nucleic acid is diagnostic for a subject that can be administered the agent to treat a disorder associated with aberrant POLYX expression or activity).

The methods ofthe invention can also be used to detect genetic lesions in a POLYX gene, thereby determining if a subject with the lesioned gene is at risk for a disorder characterized by aberrant cell proliferation and/or differentiation. In various embodiments, the methods include detecting, in a sample of cells from the subject, the presence or absence of a genetic lesion characterized by at least one of an alteration affecting the integrity of a gene encoding a POLYX-protein, or the mis-expression ofthe POLYX gene. For example, such genetic lesions can be detected by ascertaining the existence of at least one of: (i) a deletion of one or more nucleotides from a POLYX gene; (if) an addition of one or more nucleotides to a

POLYX gene; (iii) a substitution of one or more nucleotides of a POLYX gene, (iv) a chromosomal rearrangement of a POLYX gene; (v) an alteration in the level of a messenger

RNA transcript of a POLYX gene; (vf) aberrant modification of a POLYX gene, such as ofthe methylation pattern ofthe genomic DNA; (vii) the presence of a non- wild-type splicing pattern of a messenger RNA transcript of a POLYX gene; (viii) a non- wild-type level of a POLYX protein, (ix) allelic loss of a POLYX gene; and (x) inappropriate post-translational modification of a POLYX protein. As described herein, there are a large number of assay techniques known in the art which can be used for detecting lesions in a POLYX gene. A preferred biological sample is a peripheral blood leukocyte sample isolated by conventional means from a subject. However, any biological sample containing nucleated cells may be used, including, for example, buccal mucosal cells.

In certain embodiments, detection ofthe lesion involves the use of a probe/primer in a polymerase chain reaction (PCR) (see, e.g., U.S. Patent 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, 1988. Science 241: 1077-1080; and Nakazawa, et al, 1994. Proc. Natl. Acad. Sci. USA 91: 360-364), the latter of which can be particularly useful for detecting point mutations in the POLYX-gene (see, Abravaya, et al, 1995. Nucl. Acids Res. 23: 675-682). 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 ofthe sample, contacting the , nucleic acid sample with one or more primers that specifically hybridize to a POLYX gene under conditions such that hybridization and amplification ofthe POLYX gene (if present) occurs, and detecting the presence or absence of an amplification product, or detecting the size ofthe amplification product and comparing the length to a control sample. It is anticipated that PCR and/or LCR may be desirable to use as a preliminary amplification step in conjunction with any ofthe techniques used for detecting mutations described herein.

Alternative amplification methods include: self sustained sequence replication (see, Guatelli, et al, 1990. Proc. Natl. Acad. Sci. USA 87: 1874-1878), transcriptional amplification system (see, Kwoh, et al, 1989. Proc. Natl. Acad. Sci. USA 86: 1173-1177); Qβ Replicase (see, Lizardi, et al, 1988. BioTechnology 6: 1197), or any other nucleic acid amplification method, followed by the detection ofthe amplified molecules using techniques well known to those of skill in the art. These detection schemes are especially useful for the detection of nucleic acid molecules if such molecules are present in very low numbers.

In an alternative embodiment, mutations in a POLYX gene from a sample cell can be identified by alterations in restriction enzyme cleavage patterns. For example, sample and control DNA is isolated, amplified (optionally), digested with one or more restriction endonucleases, and fragment length sizes are determined by gel electrophoresis and compared. Differences in fragment length sizes between sample and control DNA indicates mutations in the sample DNA. Moreover, the use of sequence specific ribozymes (see, e.g., U.S. Patent No. 5,493,531) can be used to score for the presence of specific mutations by development or loss of a ribozyme cleavage site.

In other embodiments, genetic mutations in POLYX can be identified by hybridizing a sample and control nucleic acids, e.g., DNA or RNA, to high-density arrays containing hundreds or thousands of oligonucleotides probes. See, e.g., Cronin, et al, 1996. Human Mutation 1: 244-255; Kozal, et al, 1996. Nat. Med. 2: 753-759. For example, genetic mutations in POLYX can be identified in two dimensional arrays containing light-generated DNA probes as described in Cronin, et al, supra. Briefly, a first hybridization array of probes can be used to scan through long stretches of DNA in a sample and control to identify base changes between the sequences by making linear arrays of sequential overlapping probes. This step allows the identification of point mutations. This is followed by a second hybridization array that allows the characterization of specific mutations by using smaller, specialized probe arrays complementary to all variants or mutations detected. Each mutation array is composed of parallel probe sets, one complementary to the wild-type gene and the other complementary to the mutant gene.

In yet another embodiment, any of a variety of sequencing reactions known in the art can be used to directly sequence the POLYX gene and detect mutations by comparing the sequence ofthe sample POLYX with the corresponding wild-type (control) sequence. Examples of sequencing reactions include those based on techniques developed by Maxim and Gilbert, 1977. Proc. Natl. Acad. Sci. USA 74: 560 or Sanger, 1977. Proc. Natl Acad. Sci. USA 74: 5463. It is also contemplated that any of a variety of automated sequencing procedures can be utilized when performing the diagnostic assays (see, e.g., Naeve, et al, 1995. BioTechniques 19: 448), including sequencing by mass spectrometry (see, e.g., PCT International Publication No. WO 94/16101; Cohen, et al, 1996. Adv. Chromatography 36: 127-162; and Griffin, et al, 1993. Appl. Biochem. Biotechnol. 38: 147-159).

Other methods for detecting mutations in the POLYX gene include methods in which protection from cleavage agents is used to detect mismatched bases in RNNRNA or RNA/DNA heteroduplexes. See, e.g., Myers, et al, 1985. Science 230: 1242. In general, the art technique of "mismatch cleavage" starts by providing heteroduplexes of formed by hybridizing (labeled) RNA or DNA containing the wild-type POLYX sequence with potentially mutant RNA or DNA obtained from a tissue sample. The double-stranded duplexes are treated with an agent that cleaves single-stranded regions ofthe duplex such as which will exist due to basepair mismatches between the control and sample strands. For instance, RNA/DNA duplexes can be treated with RNase and DNA/DNA hybrids treated with Si nuclease to enzymatically digesting the mismatched regions. In other embodiments, either DNA/DNA or RNA/DNA duplexes can be treated with hydroxylamine or osmium tetroxide and with piperidine in order to digest mismatched regions. After digestion ofthe mismatched regions, the resulting material is then separated by size on denaturing polyacrylamide gels to determine the site of mutation. See, e.g., Cotton, et al, 1988. Proc. Natl. Acad. Sci. USA 85: 4397; Saleeba, et al, 1992. Methods Enzymol. 217: 286-295. In an embodiment, the control DNA or RNA can be labeled for detection.

In still another embodiment, the mismatch cleavage reaction employs one or more proteins that recognize mismatched base pairs in double-stranded DNA (so called "DNA mismatch repair" enzymes) in defined systems for detecting and mapping point mutations in POLYX cDNAs obtained from samples of cells. For example, the mutY enzyme of E. coli cleaves A at G/A mismatches and the thymidine DNA glycosylase from HeLa cells cleaves T at G/T mismatches. See, e.g., Hsu, et al, 1994. Carcinogenesis 15: 1657-1662. According to an exemplary embodiment, a probe based on a POLYX sequence, e.g., a wild-type POLYX sequence, is hybridized to a cDNA or other DNA product from a test cell(s). The duplex is treated with a DNA mismatch repair enzyme, and the cleavage products, if any, can be detected from electrophoresis protocols or the like. See, e.g., U.S. Patent No. 5,459,039.

In other embodiments, alterations in electrophoretic mobility will be used to identify mutations in POLYX genes. For example, single strand conformation polymoφhism (SSCP) may be used to detect differences in electrophoretic mobility between mutant and wild type nucleic acids. See, e.g., Orita, et al, 1989. Proc. Natl. Acad. Sci. USA: 86: 2766; Cotton,

1993. Mutat. Res. 285: 125-144; Hayashi, 1992. Genet. Anal. Tech. Appl. 9: 73-79.

Single-stranded DNA fragments of sample and control POLYX nucleic acids will be denatured and allowed to renature. The secondary structure of single-stranded nucleic acids varies according to sequence, the resulting alteration in electrophoretic mobility enables the detection of even a single base change. The DNA fragments may be labeled or detected with labeled probes. The sensitivity ofthe assay may be enhanced by using RNA (rather than DNA), in which the secondary structure is more sensitive to a change in sequence. In one embodiment, the subject method utilizes heteroduplex analysis to separate double stranded heteroduplex molecules on the basis of changes in electrophoretic mobility. See, e.g., Keen, et al, 1991. Trends Genet. 1: 5.

In yet another embodiment, the movement of mutant or wild-type fragments in polyacrylamide gels containing a gradient of denaturant is assayed using denaturing gradient gel electrophoresis (DGGE). See, e.g., Myers, et al, 1985. Nature 313: 495. When DGGE is used as the method of analysis, DNA will be modified to insure that it does not completely denature, for example by adding a GC clamp of apPOL YXimately 40 bp of high-melting GC-rich DNA by PCR. In a further embodiment, a temperature gradient is used in place of a denaturing gradient to identify differences in the mobility of control and sample DNA. See, e.g., Rosenbaum and Reissner, 1987. Biophys. Chem. 265: 12753.

Examples of other techniques for detecting point mutations include, but are not limited to, selective oligonucleotide hybridization, selective amplification, or selective primer extension. For example, oligonucleotide primers may be prepared in which the known mutation is placed centrally and then hybridized to target DNA under conditions that permit hybridization only if a perfect match is found. See, e.g., Saiki, et al, 1986. Nature 324: 163; Saiki, et al, 1989. Proc. Natl. Acad. Sci. USA 86: 6230. Such allele specific oligonucleotides are hybridized to PCR amplified target DNA or a number of different mutations when the oligonucleotides are attached to the hybridizing membrane and hybridized with labeled target DNA.

Alternatively, allele specific amplification technology that depends on selective PCR amplification may be used in conjunction with the instant invention. Oligonucleotides used as primers for specific amplification may carry the mutation of interest in the center ofthe molecule (so that amplification depends on differential hybridization; see, e.g., Gibbs, et al, 1989. Nucl. Acids Res. 17: 2437-2448) or at the extreme 3'-terminus of one primer where, under appropriate conditions, mismatch can prevent, or reduce polymerase extension (see, e.g., Prossner, 1993. Tibtech. 11 : 238). In addition it may be desirable to introduce a novel restriction site in the region ofthe mutation to create cleavage-based detection. See, e.g., Gasparini, et al, 1992. Mol. Cell Probes 6: 1. It is anticipated that in certain embodiments amplification may also be performed using Taq ligase for amplification. See, e.g., Barany, 1991. Proc. Natl. Acad. Sci. USA 88: 189. In such cases, ligation will occur only if there is a perfect match at the 3'-terminus ofthe 5' sequence, making it possible to detect the presence of a known mutation at a specific site by looking for the presence or absence of amplification.

The methods described herein may be performed, for example, by utilizing pre-packaged diagnostic kits comprising at least one probe nucleic acid or antibody reagent described herein, which may be conveniently used, e.g., in clinical settings to diagnose patients exhibiting symptoms or family history of a disease or illness involving a POLYX gene.

Furthermore, any cell type or tissue, preferably peripheral blood leukocytes, in which POLYX is expressed may be utilized in the prognostic assays described herein. However, any biological sample containing nucleated cells may be used, including, for example, buccal mucosal cells.

Pharmacogenomics

Agents, or modulators that have a stimulatory or inhibitory effect on POLYX activity (e.g., POLYX gene expression), as identified by a screening assay described herein can be administered to individuals to treat (prophylactically or therapeutically) disorders (e.g., cancer or immune disorders associated with aberrant POLYX activity. In conjunction with such treatment, the pharmacogenomics (i.e., the study ofthe relationship between an individual's genotype and that individual's response to a foreign compound or drug) ofthe individual may be considered. Differences in metabolism of therapeutics can lead to severe toxicity or therapeutic failure by altering the relation between dose and blood concentration ofthe pharmacologically active drug. Thus, the pharmacogenomics ofthe individual permits the selection of effective agents (e.g., drugs) for prophylactic or therapeutic treatments based on a consideration ofthe individual's genotype. Such pharmacogenomics can further be used to determine appropriate dosages and therapeutic regimens. Accordingly, the activity of POLYX protein, expression of POLYX nucleic acid, or mutation content of POLYX genes in an individual can be determined to thereby select appropriate agent(s) for therapeutic or prophylactic treatment ofthe individual.

Pharmacogenomics deals with clinically significant hereditary variations in the response to drags due to altered drag disposition and abnormal action in affected persons. See e.g., Eichelbaum, 1996. Clin. Exp. Pharmacol Physiol. 23: 983-985; Linder, 1997. Clin. Chem., 43: 254-266. In general, two types of pharmacogenetic conditions can be differentiated. Genetic conditions transmitted as a single factor altering the way drugs act on the body (altered drag action) or genetic conditions transmitted as single factors altering the way the body acts on drags (altered drug metabolism). These pharmacogenetic conditions can occur either as rare defects or as polymoφhisms. For example, glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common inherited enzymopathy in which the main clinical complication is hemolysis after ingestion of oxidant drags (anti-malarials, sulfonamides, analgesics, nitrofurans) and consumption of fava beans.

As an illustrative embodiment, the activity of drug metabolizing enzymes is a major determinant of both the intensity and duration of drug action. The discovery of genetic polymoφhisms of drag metabolizing enzymes (e.g., N-acetyltransferase 2 (NAT 2) and cytochrome P450 enzymes CYP2D6 and CYP2C19) has provided an explanation as to why some patients do not obtain the expected drug effects or show exaggerated drug response and serious toxicity after taking the standard and safe dose of a drag. These polymoφhisms are expressed in two phenotypes in the population, the extensive metabolizer (EM) and poor metabolizer (PM). The prevalence of PM is different among different populations. For example, the gene coding for CYP2D6 is highly polymoφhic and several mutations have been identified in PM, which all lead to the absence of functional CYP2D6. Poor metabolizers of CYP2D6 and CYP2C19 quite frequently experience exaggerated drag response and side effects when they receive standard doses. If a metabolite is the active therapeutic moiety, PM show no therapeutic response, as demonstrated for the analgesic effect of codeine mediated by its CYP2D6-formed metabolite moφhine. At the other extreme are the so called ultra-rapid metabolizers who do not respond to standard doses. Recently, the molecular basis of ultra-rapid metabolism has been identified to be due to CYP2D6 gene amplification. Thus, the activity of POLYX protein, expression of POLYX nucleic acid, or mutation content of POLYX genes in an individual can be determined to thereby select appropriate agent(s) for therapeutic or prophylactic treatment ofthe individual. In addition, pharmacogenetic studies can be used to apply genotyping of polymoφhic alleles encoding drug-metabolizing enzymes to the identification of an individual's drug responsiveness phenotype. This knowledge, when applied to dosing or drag selection, can avoid adverse reactions or therapeutic failure and thus enhance therapeutic or prophylactic efficiency when treating a subject with a POLYX modulator, such as a modulator identified by one ofthe exemplary screening assays described herein.

Monitoring of Effects During Clinical Trials

Monitoring the influence of agents (e.g., drugs, compounds) on the expression or activity of POLYX (e.g., the ability to modulate aberrant cell proliferation and/or differentiation) can be applied not only in basic drug screening, but also in clinical trials. For example, the effectiveness of an agent determined by a screening assay as described herein to increase POLYX gene expression, protein levels, or upregulate POLYX activity, can be monitored in clinical trails of subjects exhibiting decreased POLYX gene expression, protein levels, or downregulated POLYX activity. Alternatively, the effectiveness of an agent determined by a screening assay to decrease POLYX gene expression, protein levels, or downregulate POLYX activity, can be monitored in clinical trails of subjects exhibiting increased POLYX gene expression, protein levels, or upregulated POLYX activity. In such clinical trials, the expression or activity of POLYX and, preferably, other genes that have been implicated in, for example, a cellular proliferation or immune disorder can be used as a "read out" or markers ofthe immune responsiveness of a particular cell.

By way of example, and not of limitation, genes, including POLY, that are modulated in cells by treatment with an agent (e.g., compound, drag or small molecule) that modulates POLYX activity (e.g., identified in a screening assay as described herein) can be identified. Thus, to study the effect of agents on cellular proliferation disorders, for example, in a clinical trial, cells can be isolated and RNA prepared and analyzed for the levels of expression of POLYX and other genes implicated in the disorder. The levels of gene expression (i.e., a gene expression pattern) can be quantified by Northern blot analysis or RT-PCR, as described herein, or alternatively by measuring the amount of protein produced, by one ofthe methods as described herein, or by measuring the levels of activity of POLYX or other genes. In this manner, the gene expression pattern can serve as a marker, indicative ofthe physiological response ofthe cells to the agent. Accordingly, this response state may be determined before, and at various points during, treatment ofthe individual with the agent.

In one embodiment, the invention provides a method for monitoring the effectiveness of treatment of a subject with an agent (e.g., an agonist, antagonist, protein, peptide, peptidomimetic, nucleic acid, small molecule, or other drag candidate identified by the screening assays described herein) comprising the steps of (i) obtaining a pre-administration sample from a subject prior to administration ofthe agent; (if) detecting the level of expression of a POLYX protein, mRNA, or genomic DNA in the pre-administration sample; (Hi) obtaining one or more post-administration samples from the subject; (iv) detecting the level of expression or activity ofthe POLYX protein, mRNA, or genomic DNA in the post-administration samples; (v) comparing the level of expression or activity ofthe POLYX protein, mRNA, or genomic DNA in the pre-administration sample with the POLYX protein, mRNA, or genomic DNA in the post administration sample or samples; and (vi) altering the administration ofthe agent to the subject accordingly. For example, increased administration ofthe agent may be desirable to increase the expression or activity of POLYX to higher levels than detected, i.e., to increase the effectiveness ofthe agent. Alternatively, decreased administration ofthe agent may be desirable to decrease expression or activity of POLYX to lower levels than detected, i.e., to decrease the effectiveness ofthe agent.

Methods of Treatment

The invention provides for both prophylactic and therapeutic methods of treating a subject at risk of (or susceptible to) a disorder or having a disorder associated with aberrant POLYX expression or activity. These methods of treatment will be discussed more fully, infra. Disease and Disorders

Diseases and disorders that are characterized by increased (relative to a subject not suffering from the disease or disorder) levels or biological activity may be treated with Therapeutics that antagonize (i.e., reduce or inhibit) activity. Therapeutics that antagonize activity may be administered in a therapeutic or prophylactic manner. Therapeutics that may be utilized include, but are not limited to: (/) an aforementioned peptide, or analogs, derivatives, fragments or homologs thereof; (ii) antibodies to an aforementioned peptide; (iii) nucleic acids encoding an aforementioned peptide; (iv) administration of antisense nucleic acid and nucleic acids that are "dysfunctional" (i.e., due to a heterologous insertion within the coding sequences of coding sequences to an aforementioned peptide) that are utilized to "knockout" endoggenous function of an aforementioned peptide by homologous recombination (see, e.g., Capecchi, 1989. Science 244: 1288-1292); or (v) modulators ( i.e., inhibitors, agonists and antagonists, including additional peptide mimetic ofthe invention or antibodies specific to a peptide ofthe invention) that alter the interaction between an aforementioned peptide and its binding partner.

Diseases and disorders that are characterized by decreased (relative to a subject not suffering from the disease or disorder) levels or biological activity may be treated with Therapeutics that increase (i.e., are agonists to) activity. Therapeutics that upregulate activity may be administered in a therapeutic or prophylactic manner. Therapeutics that may be utilized include, but are not limited to, an aforementioned peptide, or analogs, derivatives, fragments or homologs thereof; or an agonist that increases bioavailability.

Increased or decreased levels can be readily detected by quantifying peptide and/or RNA, by obtaining a patient tissue sample (e.g., from biopsy tissue) and assaying it in vitro for RNA or peptide levels, structure and/or activity ofthe expressed peptides (or mRNAs of an aforementioned peptide). Methods that are well-known within the art include, but are not limited to, immunoassays (e.g., by Western blot analysis, immunoprecipitation followed by sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis, immunocytochemistry, etc.) and/or hybridization assays to detect expression of mRNAs (e.g., Northern assays, dot blots, in situ hybridization, and the like). Prophylactic Methods

In one aspect, the invention provides a method for preventing, in a subject, a disease or condition associated with an aberrant POLYX expression or activity, by administering to the subject an agent that modulates POLYX expression or at least one POLYX activity. Subjects at risk for a disease that is caused or contributed to by aberrant POLYX expression or activity can be identified by, for example, any or a combination of diagnostic or prognostic assays as described herein. Administration of a prophylactic agent can occur prior to the manifestation of symptoms characteristic ofthe POLYX aberrancy, such that a disease or disorder is prevented or, alternatively, delayed in its progression. Depending upon the type of POLYX aberrancy, for example, a POLYX agonist or POLYX antagonist agent can be used for treating the subject. The appropriate agent can be determined based on screening assays described herein.

Therapeutic Methods

Another aspect ofthe invention pertains to methods of modulating POLYX expression or activity for therapeutic puφoses. The modulatory method ofthe invention involves contacting a cell with an agent that modulates one or more ofthe activities of POLYX protein activity associated with the cell. An agent that modulates POLYX protein activity can be an agent as described herein, such as a nucleic acid or a protein, a naturally-occurring cognate ligand of a POLYX protein, a peptide, a POLYX peptidomimetic, or other small molecule. In one embodiment, the agent stimulates one or more POLYX protein activity. Examples of such stimulatory agents include active POLYX protein and a nucleic acid molecule encoding POLYX that has been introduced into the cell. In another embodiment, the agent inhibits one or more POLYX protein activity. Examples of such inhibitory agents include antisense POLYX nucleic acid molecules and anti-POLYX antibodies. These modulatory methods can be performed in vitro (e.g., by culturing the cell with the agent) or, alternatively, in vivo (e.g., by administering the agent to a subject). As such, the invention provides methods of treating an individual afflicted with a disease or disorder characterized by aberrant expression or activity of a POLYX protein or nucleic acid molecule. In one embodiment, the method involves administering an agent (e.g., an agent identified by a screening assay described herein), or combination of agents that modulates (e.g., up-regulates or down-regulates) POLYX expression or activity. In another embodiment, the method involves administering a POLYX protein or nucleic acid molecule as therapy to compensate for reduced or aberrant POLYX expression or activity.

Stimulation of POLYX activity is desirable in situations in which POLYX is abnormally downregulated and/or in which increased POLYX activity is likely to have a beneficial effect. One example of such a situation is where a subject has a disorder characterized by aberrant cell proliferation and/or differentiation (e.g., cancer or immune associated disorders). Another example of such a situation is where the subject has a gestational disease (e.g., pre-clampsia).

Determination ofthe Biological Effect of the Therapeutic

In various embodiments ofthe invention, suitable in vitro or in vivo assays are performed to determine the effect of a specific Therapeutic and whether its administration is indicated for treatment ofthe affected tissue.

In various specific embodiments, in vitro assays may be performed with representative cells ofthe type(s) involved in the patient's disorder, to determine if a given Therapeutic exerts the desired effect upon the cell type(s). Compounds for use in therapy may be tested in suitable animal model systems including, but not limited to rats, mice, chicken, cows, monkeys, rabbits, and the like, prior to testing in human subjects. Similarly, for in vivo testing, any ofthe animal model system known in the art may be used prior to administration to human subjects.

Prophylactic and Therapeutic Uses of the Compositions of the Invention

The POLYX nucleic acids and proteins ofthe invention may be useful in a variety of potential prophylactic and therapeutic applications. By way of a non-limiting example, a cDNA encoding the POLYX protein ofthe invention may be useful in gene therapy, and the protein may be useful when administered to a subject in need thereof. Both the novel nucleic acids encoding the POLYX proteins, and the POLYX proteins ofthe invention, or fragments thereof, may also be useful in diagnostic applications, wherein the presence or amount ofthe nucleic acid or the protein are to be assessed. These materials are further useful in the generation of antibodies which immunospecifically-bind to the novel substances ofthe invention for use in therapeutic or diagnostic methods.

The invention will be further illustrated in the following non-limiting examples.

Example 1 : IDENTIFICATION OF POLYX NUCLEIC ACIDS

TblastN using CuraGen Coφoration's sequence file for polypeptides or homologs was run against the Genomic Daily Files made available by GenBank or from files downloaded from the individual sequencing centers. Exons were predicted by homology and the intron/exon boundaries were determined using standard genetic rules. Exons were further selected and refined by means of similarity determination using multiple BLAST (for example, tBlastN, BlastX, and BlastN) searches, and, in some instances, GeneScan and Grail. Expressed sequences from both public and proprietary databases were also added when available to further define and complete the gene sequence. The DNA sequence was then manually corrected for apparent inconsistencies thereby obtaining the sequences encoding the full-length protein.

EXAMPLE 2: CLONING OF POLY3

The sequence of Ace. No. CG54683-02 (POLY3) was derived by laboratory cloning of cDNA fragments, by in silico prediction ofthe sequence. cDNA fragments covering either the full length ofthe DNA sequence, or part ofthe sequence, or both, were cloned. In silico prediction was based on sequences available in Curagen's proprietary sequence databases or in the public human sequence databases, and provided either the full length DNA sequence, or some portion thereof.

The cDNA coding for the CG54683-02 sequence was cloned by the polymerase chain reaction (PCR) using the primers: 5' TTGGAAGAGATGGTCCTGGCTTTC 3' (SEQ ID NO: 43) and

5' TTCATAGGATTCTCAGCTGTGTGAGTG 3' (SEQ ID NO:44).

Primers were designed based on in silico predictions ofthe full length or some portion (one or more exons) ofthe cDN A/protein sequence ofthe invention. These primers were used to amplify a cDNA from a pool containing expressed human sequences derived from the following tissues: adrenal gland, bone marrow, brain - amygdala, brain - cerebellum, brain - hippocampus, brain - substantia nigra, brain - thalamus, brain -whole, fetal brain, fetal kidney, fetal liver, fetal lung, heart, kidney, lymphoma - Raji, mammary gland, pancreas, pituitary gland, placenta, prostate, salivary gland, skeletal muscle, small intestine, spinal cord, spleen, stomach, testis, thyroid, trachea and uterus.

Multiple clones were sequenced and these fragments were assembled together, sometimes including public human sequences, using bioinformatic programs to produce a consensus sequence for each assembly. Each assembly is included in CuraGen Coφoration's database. Sequences were included as components for assembly when the extent of identity with another component was at least 95% over 50 bp. Each assembly represents a gene or portion thereof and includes information on variants, such as splice forms single nucleotide polymoφhisms (SNPs), insertions, deletions and other sequence variations.

EXAMPLE 3: IDENTIFICATION OF SINGLE NUCLEOTIDE POLYMORPHISMS IN POLY3 NUCLEIC ACID SEQUENCES

Variant sequences are also included in this application. A variant sequence can include a single nucleotide polymoφhism (SNP). A SNP can, in some instances, be referred to as a

"cSNP" to denote that the nucleotide sequence containing the SNP originates as a cDNA. A

SNP can arise in several ways. For example, a SNP may be due to a substitution of one nucleotide for another at the polymoφhic site. Such a substitution can be either a transition or a transversion. A SNP can also arise from a deletion of a nucleotide or an insertion of a nucleotide, relative to a reference allele. In this case, the polymoφhic site is a site at which one allele bears a gap with respect to a particular nucleotide in another allele. SNPs occurring within genes may result in an alteration ofthe amino acid encoded by the gene at the position ofthe SNP. Intragenic SNPs may also be silent, when a codon including a SNP encodes the same amino acid as a result ofthe redundancy ofthe genetic code. SNPs occurring outside the region of a gene, or in an intron within a gene, do not result in changes in any amino acid sequence of a protein but may result in altered regulation ofthe expression pattern. Examples include alteration in temporal expression, physiological response regulation, cell type expression regulation, intensity of expression, and stability of transcribed message.

SeqCalling assemblies produced by the exon linking process were selected and extended using the following criteria. Genomic clones having regions with 98% identity to all or part ofthe initial or extended sequence were identified by BLASTN searches using the relevant sequence to query human genomic databases. The genomic clones that resulted were selected for further analysis because this identity indicates that these clones contain the genomic locus for these SeqCalling assemblies. These sequences were analyzed for putative coding regions as well as for similarity to the known DNA and protein sequences. Programs used for these analyses include Grail, Genscan, BLAST, HMMER, FASTA, Hybrid and other relevant programs.

Some additional genomic regions may have also been identified because selected SeqCalling assemblies map to those regions. Such SeqCalling sequences may have overlapped with regions defined by homology or exon prediction. They may also be included because the location ofthe fragment was in the vicinity of genomic regions identified by similarity or exon prediction that had been included in the original predicted sequence. The sequence so identified was manually assembled and then may have been extended using one or more additional sequences taken from CuraGen Coφoration's human SeqCalling database. SeqCalling fragments suitable for inclusion were identified by the CuraTools™ program SeqExtend or by identifying SeqCalling fragments mapping to the appropriate regions ofthe genomic clones analyzed. Such sequences were included in the derivation of Ace. No.

CG54683-02 (POLY3) only when the extent of identity in the overlap region with one or more SeqCalling assemblies 160154242 was high. The extent of identity may be, for example, about 90% or higher, preferably about 95% or higher, and even more preferably close to or equal to 100%. When necessary, the process to identify and analyze SeqCalling fragments and genomic clones was reiterated to derive the full length sequence. The regions defined by the procedures described above were then manually integrated and corrected for apparent inconsistencies that may have arisen, for example, from miscalled bases in the original fragments or from discrepancies between predicted exon junctions, EST locations and regions of sequence similarity, to derive the final sequence disclosed herein. When necessary, the process to identify and analyze SeqCalling assemblies and genomic clones was reiterated to derive the full length sequence.

The following public components were thus included in the invention: : gb_AC024892.10 HTG Homo sapiens|Homo sapiens chromosome 3 clone RP11-214N20, WORKING DRAFT SEQUENCE, 14 unordered pieces, 155257 bp. In addition, the following Curagen Coφoration SeqCalling Assembly ID's were also included in the invention: 160154242.

EXAMPLE 4. IDENTIFICATION OF POLY4.

The sequence of POLY4 (Ace. No. CG54683-03) was derived by laboratory cloning of cDNA fragments, by in silico prediction ofthe sequence. cDNA fragments covering either the full length ofthe DNA sequence, or part ofthe sequence, or both, were cloned. In silico prediction was based on sequences available in Curagen's proprietary sequence databases or in the public human sequence databases, and provided either the full length DNA sequence, or some portion thereof.

The cDNA coding for the CG54683-03 sequence was cloned by the polymerase chain reaction (PCR) using the primers:

5' TTGGAAGAGATGGTCCTGGCTTTC 3' (SEQ ID NO:45) and

5' TTCATAGGATTCTCAGCTGTGTGAGTG 3' (SEQ ID NO:46).

Primers were designed based on in silico predictions ofthe full length or some portion (one or more exons) ofthe cDNA/protein sequence ofthe invention. These primers were used to amplify a cDNA from a pool containing expressed human sequences derived from the following tissues: adrenal gland, bone marrow, brain - amygdala, brain - cerebellum, brain - hippocampus, brain - substantia nigra, brain - thalamus, brain -whole, fetal brain, fetal kidney, fetal liver, fetal lung, heart, kidney, lymphoma - Raji, mammary gland, pancreas, pituitary gland, placenta, prostate, salivary gland, skeletal muscle, small intestine, spinal cord, spleen, stomach, testis, thyroid, trachea and uterus.

Multiple clones were sequenced and these fragments were assembled together, sometimes including public human sequences, using bioinformatic programs to produce a consensus sequence for each assembly. Each assembly is included in CuraGen Coφoration's database. Sequences were included as components for assembly when the extent of identity with another component was at least 95% over 50 bp. Each assembly represents a gene or portion thereof and includes information on variants, such as splice forms single nucleotide polymoφhisms (SNPs), insertions, deletions and other sequence variations.

Variant sequences are also included in this application. A variant sequence can include a single nucleotide polymoφhism (SNP). A SNP can, in some instances, be referred to as a "cSNP" to denote that the nucleotide sequence containing the SNP originates as a cDNA. A SNP can arise in several ways. For example, a SNP may be due to a substitution of one nucleotide for another at the polymoφhic site. Such a substitution can be either a transition or a transversion. A SNP can also arise from a deletion of a nucleotide or an insertion of a nucleotide, relative to a reference allele. In this case, the polymoφhic site is a site at which one allele bears a gap with respect to a particular nucleotide in another allele. SNPs occurring within genes may result in an alteration ofthe amino acid encoded by the gene at the position ofthe SNP. Intragenic SNPs may also be silent, when a codon including a SNP encodes the same amino acid as a result ofthe redundancy ofthe genetic code. SNPs occurring outside the region of a gene, or in an intron within a gene, do not result in changes in any amino acid sequence of a protein but may result in altered regulation ofthe expression pattern. Examples include alteration in temporal expression, physiological response regulation, cell type expression regulation, intensity of expression, and stability of transcribed message.

SeqCalling assemblies produced by the exon linking process were selected and extended using the following criteria. Genomic clones having regions with 98% identity to all or part ofthe initial or extended sequence were identified by BLASTN searches using the relevant sequence to query human genomic databases. The genomic clones that resulted were selected for further analysis because this identity indicates that these clones contain the genomic locus for these SeqCalling assemblies. These sequences were analyzed for putative coding regions as well as for similarity to the known DNA and protein sequences. Programs used for these analyses include Grail, Genscan, BLAST, HMMER, FASTA, Hybrid and other relevant programs.

Some additional genomic regions may have also been identified because selected SeqCalling assemblies map to those regions. Such SeqCalling sequences may have overlapped with regions defined by homology or exon prediction. They may also be included because the location ofthe fragment was in the vicinity of genomic regions identified by similarity or exon prediction that had been included in the original predicted sequence. The sequence so identified was manually assembled and then may have been extended using one or more additional sequences taken from CuraGen Coφoration's human SeqCalling database. SeqCalling fragments suitable for inclusion were identified by the CuraTools™ program SeqExtend or by identifying SeqCalling fragments mapping to the appropriate regions ofthe genomic clones analyzed. Such sequences were included in the derivation of POLY4 only when the extent of identity in the overlap region with one or more SeqCalling assemblies 160154242 was high. The extent of identity may be, for example, about 90% or higher, preferably about 95% or higher, and even more preferably close to or equal to 100%. When necessary, the process to identify and analyze SeqCalling fragments and genomic clones was reiterated to derive the full length sequence.

The regions defined by the procedures described above were then manually integrated and corrected for apparent inconsistencies that may have arisen, for example, from miscalled bases in the original fragments or from discrepancies between predicted exon junctions, EST locations and regions of sequence similarity, to derive the final sequence disclosed herein. When necessary, the process to identify and analyze SeqCalling assemblies and genomic clones was reiterated to derive the full length sequence. The following public components were thus included in the invention: gb_AC024892.10 HTG Homo sapiens|Homo sapiens chromosome 3 clone RP11-214N20, WORKING DRAFT SEQUENCE, 14 unordered pieces,

155257 bp. In addition, the following Curagen Coφoration SeqCalling Assembly ID's were also included in the invention: 160154242. EXAMPLE 5. EXPRESSION OF A POLY11 NUCLEIC ACID IN CELLS AND TISSUES

The quantitative expression of various clones was assessed in 41 normal and 55 tumor samples (in most cases, the samples are those identified in Table BB) by real time quantitative

PCR (TAQMAN^®) performed on a Perkin-Elmer Biosystems ABI PRISM® 7700 Sequence

Detection System. The following abbreviations are used: ca. = carcinoma,

* = established from metastasis, met = metastasis, s cell var= small cell variant, non-s = non-sm =non-small, squam = squamous, pi. eff = pi effusion = pleural effusion, glio = glioma, astro = astrocytoma, and neuro = neuroblastoma.

First, 96 RNA samples were normalized to β-actin and GAPDH. RNA (~50 ng total or ~1 ng polyA+) was converted to cDNA using the TAQMAN^® Reverse Transcription Reagents Kit (PE Biosystems, Foster City, CA; cat # N808-0234) and random hexamers according to the manufacturer's protocol. Reactions were performed in 20 ul and incubated for 30 min. at 48°C. cDNA (5 ul) was then transferred to a separate plate for the TAQMAN® reaction using b-actin and GAPDH TAQMAN® Assay Reagents (PE Biosystems; cat. #'s 431088 IE and 4310884E, respectively) and TAQMAN® universal PCR Master Mix (PE Biosystems; cat # 4304447) according to the manufacturer's protocol. Reactions were performed in 25 ul using the following parameters: 2 min. at 50°C; 10 min. at 95°C; 15 sec. at 95°C/1 min. at 60°C (40 cycles). Results were recorded as CT values (cycle at which a given sample crosses a threshold level of fluorescence) using a log scale, with the difference in RNA concentration between a given sample and the sample with the lowest CT value being represented as 2 to the power of delta CT. The percent relative expression is then obtained by taking the reciprocal of this RNA difference and multiplying by 100. The average CT values obtained for β-actin and GAPDH were used to normalize RNA samples. The RNA sample generating the highest CT value required no further diluting, while all other samples were diluted relative to this sample according to their b-actin /GAPDH average CT values.

Normalized RNA (5 ul) was converted to cDNA and analyzed via TAQMAN® using One Step RT-PCR Master Mix Reagents (PE Biosystems; cat. # 4309169) and gene-specific primers according to the manufacturer's instructions. Probes and primers were designed for each assay according to Perkin Elmer Biosystem's Primer Express Software package (version I for Apple Computer's Macintosh Power PC) using the sequence of clone 10326230.0.38 as input. Default settings were used for reaction conditions and the following parameters were set before selecting primers: primer concentration = 250 nM, primer melting temperature (T_m) range = 58°-60° C, primer optimal Tm = 59° C, maximum primer difference = 2° C, probe does not have 5' G, probe T_m must be 10° C greater than primer T_m, amplicon size 75 bp to 100 bp. The primers and probe selected were:

Ag 373 (F): 5*-GTGTGTTCCTCTCGACTGTGGA-3' (SEQ ID NO:47) Ag 373 (R): 5'-GACCCTTGGACCCTACTTCAAA-3' (SEQ ID NO:48) Ag 373 (P): TET-5'-CCCCGATCCAGAATGGCTTCATGA-3'-TAMRA. (SEQ ID NO:49)

They were synthesized by Synthegen (Houston, TX, USA). Probes were double purified by HPLC to remove uncoupled dye and evaluated by mass spectroscopy to verify coupling of reporter and quencher dyes to the 5' and 3' ends ofthe probe, respectively. Their final concentrations were: forward and reverse primers, 900 nM each, and probe, 200nM.

PCR conditions: Normalized RNA from each tissue and each cell line was spotted in each well of a 96 well PCR plate (Perkin Elmer Biosystems). PCR cocktails including two probes (SEQX-specific and another gene-specific probe multiplexed with the SEQX probe) were set up using IX TaqMan™ PCR Master Mix for the PE Biosystems 7700, with 5 mM MgC12, dNTPs (dA, G, C, U at 1 :1 :1 :2 ratios), 0.25 U/ml AmpliTaq Gold™ (PE Biosystems), and 0.4 U/ml RNase inhibitor, and 0.25 U/ml reverse transcriptase. Reverse transcription was performed at 48° C for 30 minutes followed by amplification/PCR cycles as follows: 95° C IO min, then 40 cycles of 95° C for 15 seconds, 60° C for 1 minute.

The results are shown in Table 19. le l9. Real Time Expression Analysis of 10327789 _1.

Relative

Expression

Sfuml jerType of Tissue (%)

1 Endothelial cells 0.00

2 Endothelial cells (treated) 0.00

3 Pancreas 0.02

4 Pancreatic ca. CAP AN 2 0.00

5 Adipose 67.83

6 Adrenal gland 1.94

7 Thyroid 0.05

8 Salavary gland 0.00

9 Pituitary gland 0.81

10 Brain (fetal) 0.00

11 Brain (whole) 0.55

12 Brain (amygdala) 0.00

13 Brain (cerebellum) 18.82

14 Brain (hippocampus) 0.00

15 Brain (hypothalamus) 0.00

16 Brain (substantia nigra) 0.05

17 Brain (thalamus) 0.00

18 Spinal cord 0.00

19 CNS ca. (glio/astro) U87-MG 0.07

20 CNS ca. (slio/ashO) U-118-MG 0.02

21 CNS ca. (astro) SW1783 0.00

22 CNS ca.* (neuro: met SK-N-AS 0.00

23 CNS ca. (astro) SF-539 0.13

24 CNS ca. (astro) SNB-75 0.00

25 CNS ca. (glio) SNB-19 0.00

26 CNS ca. (glio) U251 0.00

27 CNS ca. (glio) SF-295 0.00

28 Heart 0.49

29 Skeletal muscle 0.00

30 Bone marrow 0.00

31 Thymus 0.98

32 Spleen 0.43

33 Lymph node 3.90

34 Colon (ascending) 1.07

35 Stomach 2.76

36 Small intestine 2.35

37 Colon ca. SW480 0.00

38 Colon ca.* (SW480 me )SW620 0.00

39 Colon ca. HT29 0.00

40 Colon ca. HCT-116 0.00

41 Colon ca. CaCo-2 0.24

42 Colon ca. HCT-15 0.00

43 Colon ca. HCC-2998 0.00

44 Gastric ca.* (liver met) NCI-N87 0.00

45 Bladder 0.00

46 Trachea 0.97 os I_Λ 4^ w > >— ' _θ vo oo -α σs u_> 4^ w . ι— ' o vo oo o

ϊ. ^

© o o p p © o

O O O O O i— > o o o o o o

iΛ

EXAMPLE 6. IDENTIFICATION OF POLY15 AND POLY16.

For POLYl 5, PCR primers were designed by starting at the most upstream sequence available, for the forward primer, and at the most downstream sequence available for the reverse primer. In each case, the sequence was examined, walking inward from the respective termini toward the coding sequence, until a suitable sequence that is either unique or highly selective was encountered, or, in the case ofthe reverse primer, until the stop codon was reached. Such suitable sequences were then employed as the forward and reverse primers in a PCR amplification based on a library containing a wide range of cDNA species. The resulting amplicon was gel purified, cloned and sequenced to high redundancy to provide the sequence reported below, which is designated POLYl 5 (Accession Number hnh0778pl7_Al.) POLYl 5 exhibits no change at the ORF level with respect to h_nh0778pl7_A. A physical clone, clone hnh0778pl7_A.699002.A7, was identified that covers the entire ORF.

For POLYl 6, PCR primers were designed by starting at the most upstream sequence available, for the forward primer, and at the most downstream sequence available for the reverse primer. In each case, the sequence was examined, walking inward from the respective termini toward the coding sequence, until a suitable sequence that is either unique or highly selective was encountered, or, in the case ofthe reverse primer, until the stop codon was reached. Such suitable sequences were then employed as the forward and reverse primers in a PCR amplification based on a library containing a wide range of cDNA species. The resulting amplicon was gel purified, cloned and sequenced to high redundancy to provide the sequence reported below, which is designated Accession Number hnh0778p17_A1. Clone hnh0778pl7_Al exhibits no change at the ORF level with respect to h_nh0778pl7_A. A physical clone, clone hnh0778pl7_A.699002.A7, was identified that covers the entire ORF. This procedure also yielded POLYl 6 (CG55655-02) that is 100% identical to h_nh0778pl7_A. Other Embodiments

While the invention has been described in conjunction with the detailed description thereof, the foregoing description is intended to illustrate and not limit the scope ofthe invention, which is defined by the scope ofthe appended claims. Other aspects, advantages, and modifications are within the scope ofthe following claims.

Claims

PATENT APPLICATION Attorney Docket No. 15966-776 (CURA-276) WHAT IS CLAIMED IS:

1. An isolated polypeptide comprising an amino acid sequence selected from the group consisting of:

(a) a mature form of an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34;

(b) a variant of a mature form of an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34, wherein one or more amino acid residues in said variant differs from the amino acid sequence of said mature form, provided that said variant differs in no more than 15% ofthe amino acid residues from the amino acid sequence of said mature form;

(c) an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34; and

(d) a variant of an amino acid sequence selected from the group consisting of SEQ ID NO-2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34, wherein one or more amino acid residues in said variant differs from the amino acid sequence of said mature form, provided that said variant differs in no more than 15% of amino acid residues from said amino acid sequence.

2 The polypeptide of claim 1, wherein said polypeptide comprises the amino acid sequence of a naturally-occurring allelic variant of an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34.

3. The polypeptide of claim 2, wherein said allelic variant comprises an amino acid sequence that is the translation of a nucleic acid sequence differing by a single nucleotide from a nucleic acid sequence selected from the group consisting of SEQ ID NO:l, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31 and/or 33.

4. The polypeptide of claim 1, wherein the amino acid sequence of said variant comprises a conservative amino acid substitution.

5. An isolated nucleic acid molecule comprising a nucleic acid sequence encoding a polypeptide comprising an amino acid sequence selected from the group consisting of:

(a) a mature form of an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34;

(b) a variant of a mature form of an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34, wherein one or more amino acid residues in said variant differs from the amino acid sequence of said mature form, provided that said variant differs in no more than 15% ofthe amino acid residues from the amino acid sequence of said mature form;

(c) an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34;

(d) a variant of an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34, wherein one or more amino acid residues in said variant differs from the amino acid sequence of said mature form, provided that said variant differs in no more than 15% of amino acid residues from said amino acid sequence;

(e) a nucleic acid fragment encoding at least a portion of a polypeptide comprising an amino acid sequence chosen from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34, or a variant of said polypeptide, wherein one or more amino acid residues in said variant differs from the amino acid sequence of said mature form, provided that said variant differs in no more than 15% of amino acid residues from said amino acid sequence; and

(f) a nucleic acid molecule comprising the complement of (a), (b), (c), (d) or (e).

6. The nucleic acid molecule of claim 5, wherein the nucleic acid molecule comprises the nucleotide sequence of a naturally-occurring allelic nucleic acid variant.

7. The nucleic acid molecule of claim 5, wherein the nucleic acid molecule encodes a polypeptide comprising the amino acid sequence of a naturally-occurring polypeptide variant.

8. The nucleic acid molecule of claim 5, wherein the nucleic acid molecule differs by a single nucleotide from a nucleic acid sequence selected from the group consisting of SEQ ID NO:l, 3, 5, 1, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31 and/or 33.

9. The nucleic acid molecule of claim 5, wherein said nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of

(a) a nucleotide sequence selected from the group consisting of SEQ ID NO:l, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31 and/or 33;

(b) a nucleotide sequence differing by one or more nucleotides from a nucleotide sequence selected from the group consisting of SEQ ID NO:l, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31 and/or 33, provided that no more than 20% ofthe nucleotides differ from said nucleotide sequence;

(c) a nucleic acid fragment of (a); and

(d) a nucleic acid fragment of (b).

10. The nucleic acid molecule of claim 5, wherein said nucleic acid molecule hybridizes under stringent conditions to a nucleotide sequence chosen from the group consisting of SEQ ID NO:l, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31 and/or 33, or a complement of said nucleotide sequence.

11. The nucleic acid molecule of claim 5, wherein the nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of

(a) a first nucleotide sequence comprising a coding sequence differing by one or more nucleotide sequences from a coding sequence encoding said amino acid sequence, provided that no more than 20% ofthe nucleotides in the coding sequence in said first nucleotide sequence differ from said coding sequence;

(b) an isolated second polynucleotide that is a complement ofthe first polynucleotide; and

(c) a nucleic acid fragment of (a) or (b).

12. A vector comprising the nucleic acid molecule of claim 11.

13. The vector of claim 12, further comprising a promoter operably-linked to said nucleic acid molecule.

14. A cell comprising the vector of claim 12.

15. An antibody that immunospecifically-binds to the polypeptide of claim 1.

16. The antibody of claim 15, wherein said antibody is a monoclonal antibody.

17. The antibody of claim 15, wherein the antibody is a humanized antibody.

18. A method for determining the presence or amount ofthe polypeptide of claim 1 in a sample, the method comprising:

(a) providing the sample;

(b) contacting the sample with an antibody that binds immunospecifically to the polypeptide; and

(c) determining the presence or amount of antibody bound to said polypeptide, thereby determining the presence or amount of polypeptide in said sample.

19. A method for determining the presence or amount ofthe nucleic acid molecule of claim 5 in a sample, the method comprising:

(a) providing the sample;

(b) contacting the sample with a probe that binds to said nucleic acid molecule; and (c) determining the presence or amount ofthe probe bound to said nucleic acid molecule, thereby determining the presence or amount ofthe nucleic acid molecule in said sample.

20. A method of identifying an agent that binds to a polypeptide of claim 1 , the method comprising:

(a) contacting said polypeptide with said agent; and

(b) determining whether said agent binds to said polypeptide.

21. A method for identifying an agent that modulates the expression or activity ofthe polypeptide of claim 1, the method comprising:

(a) providing a cell expressing said polypeptide;

(b) contacting the cell with said agent; and

(c) determining whether the agent modulates expression or activity of said polypeptide, whereby an alteration in expression or activity of said peptide indicates said agent modulates expression or activity of said polypeptide.

22. A method for modulating the activity of the polypeptide of claim 1 , the method comprising contacting a cell sample expressing the polypeptide of said claim with a compound that binds to said polypeptide in an amount sufficient to modulate the activity ofthe polypeptide.

23. A method of treating or preventing a POLYX-associated disorder, said method comprising administering to a subject in which such treatment or prevention is desired the polypeptide of claim 1 in an amount sufficient to treat or prevent said POLYX- associated disorder in said subject.

24. The method of claim 23, wherein said subject is a human.

25. A method of treating or preventing a POLYX-associated disorder, said method comprising administering to a subject in which such treatment or prevention is desired the nucleic acid of claim 5 in an amount sufficient to treat or prevent said POLYX- associated disorder in said subject.

26. The method of claim 25, wherein said subject is a human.

27. A method of treating or preventing a POLYX-associated disorder, said method comprising administering to a subject in which such treatment or prevention is desired the antibody of claim 15 in an amount sufficient to treat or prevent said POLYX- associated disorder in said subject.

28. The method of claim 27, wherein the subject is a human.

29. A pharmaceutical composition comprising the polypeptide of claim 1 and a pharmaceutically-acceptable carrier.

30. A pharmaceutical composition comprising the nucleic acid molecule of claim 5 and a pharmaceutically-acceptable carrier.

31. A pharmaceutical composition comprising the antibody of claim 15 and a pharmaceutically-acceptable carrier.

32. A kit comprising in one or more containers, the pharmaceutical composition of claim 29.

33. A kit comprising in one or more containers, the pharmaceutical composition of claim 30.

34. A kit comprising in one or more containers, the pharmaceutical composition of claim 31.

35. The use of a therapeutic in the manufacture of a medicament for treating a syndrome associated with a human disease, the disease selected from a POLYX-associated disorder, wherein said therapeutic is selected from the group consisting of a POLYX polypeptide, a POLYX nucleic acid, and a POLYX antibody.

36. A method for screening for a modulator of activity or of latency or predisposition to a POLYX-associated disorder, said method comprising:

(a) administering a test compound to a test animal at increased risk for a POLYX-associated disorder, wherein said test animal recombinantly expresses the polypeptide of claim 1;

(b) measuring the activity of said polypeptide in said test animal after administering the compound of step (a);

(c) comparing the activity of said protein in said test animal with the activity of said polypeptide in a control animal not administered said polypeptide, wherein a change in the activity of said polypeptide in said test animal relative to said control animal indicates the test compound is a modulator of latency of or predisposition to a POLYX-associated disorder.

37. The method of claim 36, wherein said test animal is a recombinant test animal that expresses a test protein transgene or expresses said transgene under the control of a promoter at an increased level relative to a wild-type test animal, and wherein said promoter is not the native gene promoter of said transgene.

38. A method for determining the presence of or predisposition to a disease associated with altered levels ofthe polypeptide of claim 1 in a first mammalian subject, the method comprising:

(a) measuring the level of expression ofthe polypeptide in a sample from the first mammalian subject; and

(b) comparing the amount of said polypeptide in the sample of step (a) to the amount ofthe polypeptide present in a control sample from a second mammalian subject known not to have, or not to be predisposed to, said disease, wherein an alteration in the expression level ofthe polypeptide in the first subject as compared to the control sample indicates the presence of or predisposition to said disease.

39. A method for determining the presence of or predisposition to a disease associated with altered levels of the nucleic acid molecule of claim 5 in a first mammalian subject, the method comprising:

(a) measuring the amount ofthe nucleic acid in a sample from the first mammalian subject; and

(b) comparing the amount of said nucleic acid in the sample of step (a) to the amount ofthe nucleic acid present in a control sample from a second mammalian subject known not to have or not be predisposed to, the disease; wherein an alteration in the level ofthe nucleic acid in the first subject as compared to the control sample indicates the presence of or predisposition to the disease.

40. A method of treating a pathological state in a mammal, the method comprising administering to the mammal a polypeptide in an amount that is sufficient to alleviate the pathological state, wherein the polypeptide is a polypeptide having an amino acid sequence at least 95% identical to a polypeptide comprising an amino acid sequence of at least one of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 and/or 34, or a biologically active fragment thereof.

41. A method of treating a pathological state in a mammal, the method comprising administering to the mammal the antibody of claim 15 in an amount sufficient to alleviate the pathological state.