WO2002024951A1 - Haplotypes of the il1b gene - Google Patents

Abstract

Novel genetic variants of the Interleukin 1, Beta (IL1B) gene are described. Various genotypes, haplotypes, and haplotype pairs that exist in the general United States population are disclosed for the IL1B gene. Compositions and methods for haplotyping and/or genotyping the IL1B gene in an individual are also disclosed. Polynucleotides defined by the sequence of the haplotypes disclosed herein are also described.

Description

HAPLOTYPES OF THE ILIB GENE

RELATED APPLICATIONS

This application claims the benefit of International Application No. PCT/US00/25794 filed September 20, 2000.

FIELD OF THE INVENTION

This invention relates to variation in genes that encode pharmaceutically-important proteins. In particular, this invention provides genetic variants ofthe human interleukin 1, beta (ILIB) gene and methods for identifying which variant(s) of this gene is/are possessed by an individual.

BACKGROUND OF THE INVENTION

Current methods for identifying pharmaceuticals to treat disease often start by identifying, cloning, and expressing an important target protein related to the disease. A determination of whether an agonist or antagonist is needed to produce an effect that may benefit a patient with the disease is then made. Then, vast numbers of compounds are screened against the target protein to find new potential drugs. The desired outcome of this process is a lead compound that is specific for the target, thereby reducing the incidence ofthe undesired side effects usually caused by activity at non-intended targets. The lead compound identified in this screening process then undergoes further in vitro and in vivo testing to determine its 'absorption, disposition, metabolism and toxicological profiles. Typically, this testing involves use of cell lines and animal models with limited, if any, genetic diversity.

What this approach fails to consider, however, is that natural genetic variability exists between individuals in any and every population with respect to pharmaceutically-important proteins, including the protein targets of candidate drugs, the enzymes that metabolize these drugs and the proteins whose activity is modulated by such drug targets. Subtle alterations) in the primary nucleotide sequence of a gene encoding a pharmaceutically-important protein may be manifested as significant variation in expression, structure and/or function ofthe protein. Such alterations may explain the relatively high degree of uncertainty inherent in the treatment of individuals with a drug whose design is based upon a single representative example ofthe target or enzyme(s) involved in metabolizing the drug. For example, it is well-established that some drugs frequently have lower efficacy in some individuals than others, which means such individuals and their physicians must weigh the possible benefit of a larger dosage against a greater risk of side effects. Also, there is significant variation in how well people metabolize drugs and other exogenous chemicals, resulting in substantial interindividual variation in the toxicity and/or efficacy of such exogenous substances (Evans et al., 1999, Science 286:487-491). This variability in efficacy or toxicity of a drug in genetically-diverse patients makes many drugs ineffective or even dangerous in certain groups ofthe population, leading to the failure of such drugs in clinical trials or their early withdrawal from the market even though they could be highly beneficial for other groups in the population. This problem significantly increases the time and cost of drug discovery and development, which is a matter of great public concern.

It is well-recognized by pharmaceutical scientists that considering the impact ofthe genetic variability of pharmaceutically-important proteins in the early phases of drug discovery and development is likely to reduce the failure rate of candidate and approved drugs (Marshall A 1997 Nature Biotech 15:1249-52; Kleyn PW et al. 1998 Science 281: 1820-21; Kola 1 1999 Cwrr Opin Biotech 10:589-92; Hill AVS et al. 1999 in Evolution in Health and Disease Stearns SS (Ed.) Oxford University Press, New York, pp 62-76; Meyer U. A. 1999 in Evolution in Health and Disease Stearns SS (Ed.) Oxford University Press, New York, pp 41-49; Kalow W et al. 1999 Clin. Pharm. Therap. 66:445-7; Marshall, E 1999 Science 284:406-7; Judson R et al. 2000 Pharmacogenomics 1:1-12; Roses AD 2000 Nature 405:857-65). However, in practice this has been difficult to do, in large part because ofthe time and cost required for discovering the amount of genetic variation that exists in the population (Chakravarti A 1998 Nature Genet 19:216-7; Wang DG et al 1998 Science 280:1077-82; Chakravarti A 1999 Nat Genet 21:56- 60 (suppl); Stephens JC 1999 Mol. Diagnosis 4:309-317; Kwok PY and Gu S 1999 Mol. Med. Today 5:538-43; Davidson S 2000 Nature Biotech 18:1134-5).

The standard for measuring genetic variation among individuals is the haplotype, which is the ordered combination of polymorphisms in the sequence of each form of a gene that exists in the population. Because haplotypes represent the variation across each form of a gene, they provide a more accurate and reliable measurement of genetic variation than individual polymorphisms. For example, while specific variations in gene sequences have been associated with a particular phenotype such as disease susceptibility (Roses AD supra; Ulbrecht M et al. 2000 Am JRespir Crit Care Med 161: 469-74) and drug response (Wolfe CR et al. 20005M/320:987-90; Dahl BS 1997 Ada Psychiatr Scand 96 (Suppl 391): 14-21), in many other cases an individual polymorphism may be found in a variety of genomic backgrounds, i.e., different haplotypes, and therefore shows no definitive coupling between the polymorphism and the causative site for the phenotype (Clark AG et al. 1998 Am JHum Genet 63:595- 612; Ulbrecht M et al. 2000 supra; Drysdale et al. 2000 PNAS 97:10483-10488). Thus, there is an unmet need in the pharmaceutical industry for information on what haplotypes exist in the population for pharmaceutically-important genes. Such haplotype information would be useful in improving the efficiency and output of several steps in the drug discovery and development process, including target validation, identifying lead compounds, and early phase clinical trials (Marshall et al., supra).

One possible drug target for the treatment of inflarnmatory and immune disorders is the interleukin-1 beta (ILIB) gene or its encoded product. ILIB is a proinflammatory cytokine produced primarily by mononuclear phagocytes in response to infectious agents. ILIB is a major fever-inducing cytokine, which can lead to excessive loss of body weight and a negative nitrogen balance, as well as seizures in children. In combination with other cytokines, ILIB is believed to play a significant role in latter stages ofthe septic response and in propogating the inflammatory process that causes many ofthe pathologic and clinical manifestations of rheumatoid arthritis. ILIB may also be a causative factor in postmenopausal osteoporosis and is believed to be involved in the pathogenesis of inflammatory bowel disease (IBD), insulin-dependent diabetes mellitus (IDDM), multiple sclerosis, and local osteolytic hypercalcemia (LOH), which is a condition suffered by cancer patients in which cancers have spread to the bone or bone marrow.

The gene encoding ILIB, which is also expressed by endothelial cells, B lymphocytes, natural killer cells, fibroblsts, smooth-muscle cells, keratinocytes and glial cells, is part of an IL-1 gene cluster located on the long arm of human chromosome 2 that includes genes encoding interleukin l (IL-lα), ILIB and the IL-1 receptor antagonist (IL-lRa) (Loughrey et al., Cytokine 10:984-988, 1998). The interleukin- 1, beta gene is located on chromosome 2ql4 and contains 7 exons, the last six ofwhich encode a precursor ILIB polypeptide of 269 amino acids, which is believed to be processed into a mature form consisting ofthe carboxyl-te iinal 153 amino acids (Bensi et al., Gene 52:95-101, 1987; March et al., Nature 315:641-647, 1985). Reference sequences for the ILIB gene (Genaissance Reference No. 4081185 or GenBank Accession No: M15840.1; SEQ ID NO: 1), coding sequence (GenBank Accession No:NM_000576.1), and protein are shown in Figures 1, 2 and 3, respectively.

Three single-nucleotide polymorphisms (SNPs) that affect expression or activity ofthe ILIB gene have been reported. One is a polymorphism of C or T located at -511 in the promoter region. This polymorphism corresponds to nucleotide 343 in Figure 1. The 343T allele has recently been shown to be associated with an increased risk of both hypochlorhydria induced by H. pylori and gastric cancer (El- Omar et al., Nature 2000 Mar 23;404(6776):398-402). H. pylori infection is associated with a variety of clinical outcomes including gastric cancer and duodenal ulcer disease. Individuals with gastritis predominantly localized to the antrum retain normal (or even high) acid secretion, whereas individuals with extensive corpus gastritis develop hypochlorhydria and gastric atrophy, which are presumptive precursors of gastric cancer. The association ofthe 343T allele with disease may be explained by the biological properties of ILIB, which is a powerful inhibitor of gastric acid secretion. Host genetic factors that affect ILIB may determine why some individuals infected with H. pylori develop gastric cancer while others do not (El-Omar et al., supra).

The second SNP, originally identified as a Taql RFLP (Pociot et al., Eur. J. Clin. Invest. 22:396- 402, 1992) and now referred to as the +3953 polymorphism, has been reported to constitute a T or C at codon 105 in exon 5 (Kornman et al., J. Clin. Periodontol. 24:72-77, 1997; Loughrey et al., Cytokine 10:984-988, 1998; Santilla et al., Scand. J. Immunol. 47:195-198, 1998). This information would indicate to the skilled artisan that the location ofthe +3953 SNP corresponds to nucleotide 4336 in Fig. 1. Additionally, a SNP constituting a guanine or adenine variation at a position corresponding to nucleotide 4259 in Fig. 1 was originally identified as a BsoF I dimorphism (Guasch JF et al. 1996 Cytokine 8:598- 602).

Several groups have reported that certain alleles at one or both of positions 343 and 4336 are associated with increased susceptibility to or increased severity of various mflammatory-related diseases, including inflammatory bowel disease (Nemetz et al., Immunogenetics 49:527-531, 1999)1; early-onset periodontitis (Diehl et al., J. Periodontol. 70:418-430, 1999); the skin disease alopecia areata (Galbraith et al., Hum. Hered. 49:85-89, 1999); multiple sclerosis (Schrijver et al., Neurology 52:595-599, 1999); tuberculosis (Wilkinson et al., J. Exp. Med. 189:1863-1874, 1999); diabetic nephropathy (Loughrey et al., Cytokine 10:984-988, 1998); erosive disease in rheumatoid arthritis patients (Cantagrel et al., Arthritis & Rheumatism 42:1093-1100, 1999); and Epstein-Barr virus (EBV) infection (Hurme et al., Scand. J. Immunol. 48:219-222, 1998).

ILIB haplotypes for the two SNPs at positions corresponding to nucleotides 4259 and 4336 of Fig. 1 were identified and characterized with respect to frequency of occurrence in 12 European Caucasians. Identifying which of these haplotypes is possessed by an individual has been suggested to have utility in predicting susceptibility to chronic obstructive pulmonary disorders such as asthma (Duff GW et al. U.S. Patent No. 6,140,047 issued Oct. 31, 2000). These two ILIB SNPs have also been included in haplotypes ofthe IL1 gene cluster, which additionally contain 3 SNPs in the ILIA gene, one SNP in the IL1R gene and two SNPs in the region between ILIB and IL1R. One ofthe IL1 gene cluster haplotypes, designated haplotype 44112332 and containing ILIB alleles of thymine at position 343 and cytosine at position 4336 of Fig. 1, was significantly overrepresented in a patient group with non-insulin dependent diabetes mellitus(NIDDM) relative to a healthy control group and was concluded to be associated with inflammatory disease (WO 98/54359).

In addition, expanded haplotypes for six SNPs sparming the ILIB gene were derived by Applicants for a population of 93 humans (WO 01/21639). The locations of these SNPs in Figure 1 are : 343, 346, 4259, 4336, 6421, and 6883.

Because ofthe potential for individual polymorphisms and haplotypes in the ILIB gene to affect susceptibility to a number of diseases, it would be useful to know whether additional polymorphisms exist in the ILIB gene, as well as how such polymorphisms are combined in different copies ofthe gene (haplotypes), and whether the frequencies of such haplotypes vary among different ethnic groups. Such information could be applied for studying the biological function of ILIB, as well as in identifying drugs targeting ILIB for the treatment of disorders related to its abnormal expression or function.

SUMMARY OF THE INVENTION

Accordingly, the inventors herein have discovered 3 novel polymorphic sites in the ILIB gene in addition to the three novel polymorphic sites discovered and reported previously by Applicants in WO 01/21639. These six polymorphic sites (PS) correspond to the following nucleotide positions in Figure 1: 346 (PS2), 3453 (PS3), 3467 (PS4), 3614 (PS5), 6421 (PS8) and 6883 (PS9). The polymorphisms at these sites are adenine or thymine at PS2, thymine or cytosine at PS3, guanine or cytosine at PS4, cytosine or thymine at PS5, adenine or guanine at PS8 and cytosine or adenine at PS9. In addition, the inventors have determined the identity ofthe alleles at these sites, as well as at the previously identified sites at nucleotide positions 343 (PS1), 4259 (PS6) and 4336 (PS7), in a human reference population of 79 unrelated individuals self-identified as belonging to one of four major population groups: African descent, Asian, Caucasian and Hispanic/Latino. From this information, the inventors deduced a set of haplotypes and haplotype pairs for PS1-PS9 in the ILIB gene, which are shown below in Tables 4 and 3, respectively. Each of these ILIB haplotypes defines a naturally-occurring isoform (also referred to herein as an "isogene") ofthe ILIB gene that exists in the human population. The frequency with which each haplotype and haplotype pair occurs within the total reference population and within each ofthe four major population groups included in the reference population was also determined.

Thus, in one embodiment, the invention provides a method, composition and kit for genotyping the ILIB gene in an individual. The genotyping method comprises identifying the nucleotide pair that is present at one or more polymorphic sites selected from the group consisting of PS2, PS3, PS4, PS5, PS8 and PS9 in both copies ofthe ILIB gene from the individual. A genotyping composition ofthe invention comprises an oligonucleotide probe or primer which is designed to specifically hybridize to a target region containing, or adjacent to, one of these novel ILIB polymoiphic sites. A genotyping kit ofthe invention comprises a set of oligonucleotides designed to genotype each of these novel ILIB polymorphic sites. In a preferred embodiment, the genotyping kit comprises a set of oligonucleotides designed to genotype each of PS1-PS9. The genotyping method, composition, and kit are useful in determining whether an individual has one ofthe haplotypes in Table 4 below or has one ofthe haplotype pairs in Table 3 below.

The invention also provides a method for haplotyping the ILIB gene in an individual. In one embodiment, the haplotyping method comprises determining, for one copy ofthe ILIB gene, the identity ofthe nucleotide at one or more polymorphic sites selected from the group consisting of PS2, PS3, PS4, PS5, PS8 and PS9. In another embodiment, the haplotyping method comprises deteπnining whether one copy ofthe individual's ILIB gene is defined by one ofthe ILIB haplotypes shown in Table 4, below, or a sub-haplotype thereof. In a preferred embodiment, the haplotyping method comprises determining whether both copies ofthe individual's ILIB gene are defined by one ofthe ILIB haplotype pairs shown in Table 3 below, or a sub-haplotype pair thereof. The method for establishing the ILIB haplotype or haplotype pair of an individual is useful for improving the efficiency and reliability of several steps in the discovery and development of drugs for treating diseases associated with ILIB activity, e.g., inflammatory and immune disorders.

For example, the haplotyping method can be used by the pharmaceutical research scientist to validate ILIB as a candidate target for treating a specific condition or disease predicted to be associated with ILIB activity. Determining for a particular population the frequency of one or more ofthe individual ILIB haplotypes or haplotype pairs described.herein will facilitate a decision on whether to pursue ILIB as a target for treating the specific disease of interest. In particular, if variable ILIB activity is associated with the disease, then one or more ILIB haplotypes or haplotype pairs will be found at a higher frequency in disease cohorts than in appropriately genetically matched controls. Conversely, if each ofthe observed ILIB haplotypes are of similar frequencies in the disease and control groups, then it may be inferred that variable ILIB activity has little, if any, involvement with that disease. In either case, the pharmaceutical research scientist can, without a priori knowledge as to the phenotypic effect of any ILIB haplotype or haplotype pair, apply the information derived from detecting ILIB haplotypes in an individual to decide whether modulating ILIB activity would be useful in treating the disease.

The claimed invention is also useful in screening for compounds targeting ILIB to treat a specific condition or disease predicted to be associated with ILIB activity. For example, detecting which ofthe ILIB haplotypes or haplotype pairs disclosed herein are present in individual members of a population with the specific disease of interest enables the pharmaceutical scientist to screen for a compound(s) that displays the highest desired agonist or antagonist activity for each ofthe most frequent ILIB isofoπns present in the disease population. Thus, without requiring any a priori knowledge ofthe phenotypic effect of any particular ILIB haplotype or haplotype pair, the claimed haplotyping method provides the scientist with a tool to identify lead compounds that are more likely to show efficacy in clinical trials.

The method for haplotyping the ILIB gene in an individual is also useful in the design of clinical trials of candidate drugs for treating a specific condition or disease predicted to be associated with ILIB activity. For example, instead of randomly assigning patients with the disease of interest to the treatment or control group as is typically done now, determining which ofthe ILIB haplotype(s) disclosed herein are present in individual patients enables the pharmaceutical scientist to distribute ILIB haplotypes and/or haplotype pairs evenly to treatment and control groups, thereby reducing the potential for bias in the results that could be introduced by a larger frequency of a ILIB haplotype or haplotype pair that had a previously unknown association with response to the drug being studied in the trial. Thus, by practicing the claimed invention, the scientist can more confidently rely on the information learned from the trial, without first determining the phenotypic effect of any ILIB haplotype or haplotype pair.

In another embodiment, the invention provides a method for identifying an association between a trait and a ILIB genotype, haplotype, or haplotype pair for one or more ofthe novel polymorphic sites described herein. The method comprises comparing the frequency ofthe ILIB genotype, haplotype, or haplotype pair in a population exhibiting the trait with the frequency ofthe ILIB genotype or haplotype in a reference population. A higher frequency of the EL IB genotype, haplotype, or haplotype pair in the trait population than in the reference population indicates the trait is associated with the ILIB genotype, haplotype, or haplotype pair. In preferred embodiments, the trait is susceptibility to a disease, severity of a disease, the staging of a disease or response to a drug. In a particularly preferred embodiment, the ILIB haplotype is selected from the haplotypes shown in Table 4, or a sub-haplotype thereof. Such methods have applicability in developing diagnostic tests and therapeutic treatments for inflammatory and immune disorders.

In yet another embodiment, the invention provides an isolated polynucleotide comprising a nucleotide sequence which is a polymorphic variant of a reference sequence for the ILIB gene or a fragment thereof. The reference sequence comprises SEQ ID NO: 1 and the polymorphic variant comprises at least one polymorphism selected from the group consisting of thymine at PS2, cytosine at PS3, cytosine at PS4, thymine at PS5, guanine at PS8 and adenine at PS9. In a preferred embodiment, the polymorphic variant comprises one or more additional polymorphisms selected from the group consisting of thymine at PS1, adenine at PS6 and thymine at PS7.

A particularly preferred polymorphic variant is an isogene ofthe ILIB gene. A ILIB isogene of the invention comprises cytosine or thymine at PS1, adenine or thymine at PS2, thymine or cytosine at PS3, guanine or cytosine at PS4, cytosine or thymine at PS5, guanine or adenine at PS6, cytosine or thymine at PS7, adenine or guanine at PS8 and cytosine or adenine at PS9. The invention also provides a collection of ILIB isogenes, referred to herein as a ILIB genome anthology.

In another embodiment, the invention provides a polynucleotide comprising a polymorphic variant of a reference sequence for a ILIB cDNA or a fragment thereof. The reference sequence comprises SEQ ID NO:2 (Fig.2) and the polymorphic cDNA comprises thymine at a position corresponding to nucleotide 138. In a preferred embodiment, the polymorphic variant comprises an additional polymorphism of thymine at a position corresponding to nucleotide 315. A particularly preferred polymorphic cDNA variant comprises the coding sequence of a ILIB isogene defined by haplotypes 1-18.

Polynucleotides complementary to these ILIB genomic and cDNA variants are also provided by the invention. It is believed that polymorphic variants o the ILIB gene will be useful in studying the expression and function of ILIB, and in expressing ILIB protein for use in screening for candidate drugs to treat diseases related to ILIB activity.

In other embodiments, the invention provides a recombinant expression vector comprising one of the polymorphic genomic variants operably linked to expression regulatory elements as well as a recombinant host cell transformed or transfected with the expression vector. The recombinant vector and host cell may be used to express ILIB for protein structure analysis and drug binding studies.

The present invention also provides nonhuman transgenic animals comprising one ofthe ILIB polymorphic genomic variants described herein and methods for producing such animals. The transgenic animals are useful for studying expression ofthe ILIB isogenes in vivo, for in vivo screening and testing of drugs targeted against ILIB protein, and for testing the efficacy of therapeutic agents and compounds for inflammatory and immune disorders in a biological system.

The present invention also provides a computer system for storing and displaying polymorphism data determined for the ILIB gene. The computer system comprises a computer processing unit; a display; and a database containing the polymorphism data. The polymorphism data includes the polymorphisms, the genotypes and the haplotypes identified for the ILIB gene in a reference population. In a preferred embodiment, the computer system is capable of producing a display showing ILIB haplotypes organized according to their evolutionary relationships.

BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 illustrates a reference sequence for the ILIB gene (Genaissance Reference No. 4081185; contiguous lines; SEQ ID NO:l), with the start and stop positions of each region of coding sequence indicated with a bracket ([ or ]) and the numerical position below the sequence and the polymorphic site(s) and polymorphism(s) identified by Applicants in a reference population indicated by the variant nucleotide positioned below the polymorphic site in the sequence. SEQ ID NO:36 is equivalent to Figure 1, with the two alternative allelic variants of each polymorphic site indicated by the appropriate nucleotide symbol (R= G or A, Y= T or C, M= A or C, K= G or T, S= G or C, and W= A or T; WTJPO standard ST.25).

Figure 2 illustrates a reference sequence for the ILIB coding sequence (contiguous lines; SEQ ID NO:2), with the polymorphic site(s) and polymorphism(s) identified by Applicants in a reference population indicated by the variant nucleotide positioned below the polymorphic site in the sequence.

Figure 3 illustrates a reference sequence for the ILIB protein (contiguous lines; SEQ ID NO:3).

DESCRIPTION OF THE PREFERRED EMBODEvIENTS

The present invention is based on the discovery of novel variants ofthe ILIB gene. As described in more detail below, the inventors herein discovered 18 isogenes ofthe ILIB gene by characterizing the ILIB gene found in genomic DNAs isolated from an Index Repository that contains immortalized cell lines from one chimpanzee and 93 human individuals. The human individuals included a reference population of 79 unrelated individuals self-identified as belonging to one of four major population groups: Caucasian (21 individuals), African descent (20 individuals), Asian (20 individuals), or Hispanic/Latino (18 individuals). To the extent possible, the members of this reference population were organized into population subgroups by their self-identified ethnogeographic origin as shown in Table 1 below.

In addition, the Index Repository contains three unrelated indigenous American Indians (one from each of North, Central and South America), one three-generation Caucasian family (from the CEPH Utah cohort) and one two-generation African- American family.

The ILIB isogenes present in the human reference population are defined by haplotypes for 9 polymorphic sites in the ILIB gene, 6 ofwhich are believed to be novel. The ILIB polymorphic sites identified by the inventors are referred to as PS 1-PS9 to designate the order in which they are located in the gene (see Table 2 below), with the novel polymorphic sites referred to as PS2, PS3, PS4, PS5, PS8 and PS9. Using the genotypes identified in the Index Repository for PS1-PS9 and the methodology described in the Examples below, the inventors herein also determined the pair of haplotypes for the ILIB gene present in individual human members of this repository. The human genotypes and haplotypes found in the repository for the ILIB gene include those shown in Tables 3 and 4, respectively. The polymorphism and haplotype data disclosed herein are useful for validating whether ILIB is a suitable target for drugs to treat inflammatory and immune disorders, screening for such drugs and reducing bias in clinical trials of such drugs.

In the context of this disclosure, the following terms shall be defined as follows unless otherwise indicated:

Allele - A particular form of a genetic locus, distinguished from other forms by its particular nucleotide sequence.

Candidate Gene - A gene which is hypothesized to be responsible for a disease, condition, or the response to a treatment, or to be correlated with one of these.

Gene - A segment of DNA that contains all the information for the regulated biosynthesis of an RNA product, including promoters, exons, introns, and other untranslated regions that control expression.

Genotype - An unphased 5 ' to 3 ' sequence of nucleotide pair(s) found at one or more polymorphic sites in a locus on a pair of homologous chromosomes in an individual. As used herein, genotype includes a full-genotype and/or a sub-genotype as described below.

Full-genotype — The unphased 5' to 3' sequence of nucleotide pairs found at all polymorphic sites examined herein in a locus on a pair of homologous chromosomes in a single individual.

Sub-genotype - The unphased 5' to 3' sequence of nucleotides seen at a subset ofthe polymorphic sites examined herein in a locus on a pair of homologous chromosomes in a single individual.

Genotyping - A process for determining a genotype of an individual.

Haplotype - A 5' to 3' sequence of nucleotides found at one or more polymorphic sites in a locus on a single chromosome from a single individual. As used herein, haplotype includes a full-haplotype and/or a sub-haplotype as described below.

Full-haplotype - The 5' to 3' sequence of nucleotides found at all polymorphic sites examined herein in a locus on a single chromosome from a single individual.

Sub-haplotype - The 5' to 3' sequence of nucleotides seen at a subset ofthe polymorphic sites examined herein in a locus on a single chromosome from a single individual.

Haplotype pair - The two haplotypes found for a locus in a single individual.

Haplotyping - A process for determining one or more haplotypes in an individual and includes use of family pedigrees, molecular techniques and/or statistical inference.

Haplotype data - Information concerning one or more ofthe following for a specific gene: a listing ofthe haplotype pairs in each individual in a population; a listing ofthe different haplotypes in a population; frequency of each haplotype in that or other populations, and any known associations between one or more haplotypes and a trait.

Isoform - A particular form of a gene, mRNA, cDNA or the protein encoded thereby, distinguished from other forms by its particular sequence and/or structure.

Isogene - One ofthe isoforms of a gene found in a population. An isogene contains all ofthe polymorphisms present in the particular isoform ofthe gene.

Isolated - As applied to a biological molecule such as RNA, DNA, oligonucleotide, or protein, isolated means the molecule is substantially free of other biological molecules such as nucleic acids, proteins, lipids, carbohydrates, or other material such as cellular debris and growth media. Generally, the term "isolated" is not intended to refer to a complete absence of such material or to absence of water, buffers, or salts, unless they are present in amounts that substantially interfere with the methods ofthe present invention.

Locus - A location oh a chromosome or DNA molecule corresponding to a gene or a physical or phenotypic feature.

Naturally-occurring - A term used to designate that the object it is applied to, e.g., naturally- occurring polynucleotide or polypeptide, can be isolated from a source in nature and which has not been intentionally modified by man.

Nucleotide pair — The nucleotides found at a polymorphic site on the two copies of a chromosome from an individual.

Phased - As applied to a sequence of nucleotide pairs for two or more polymorphic sites in a locus, phased means the combination of nucleotides present at those polymorphic sites on a single copy ofthe locus is known.

Polymorphic site (PS) - A position within a locus at which at least two alternative sequences are found in a population, the most frequent ofwhich has a frequency of no more than 99%.

Polymorphic variant - A gene, mRNA, cDNA, polypeptide or peptide whose nucleotide or amino acid sequence varies from a reference sequence due to the presence of a polymo hism in the gene.

Polymorphism - The sequence variation observed in an individual at a polymorphic site. Polymorphisms include nucleotide substitutions, insertions, deletions and microsatellites and may, but need not, result in detectable differences in gene expression or protein function.

Polymorphism data - Information concerning one or more ofthe following for a specific gene: location of polymoφhic sites; sequence variation at those sites; frequency of polymorphisms in one or more populations; the different genotypes and/or haplotypes determined for the gene; frequency of one or more of these genotypes and/or haplotypes in one or more populations; any known association(s) between a trait and a genotype or a haplotype for the gene.

Polymorphism Database - A collection of polymorphism data arranged in a systematic or methodical way and capable of being individually accessed by electronic or other means.

Polynucleotide - A nucleic acid molecule comprised of single-stranded RNA or DNA or comprised of complementary, double-stranded DNA.

Population Group - A group of individuals sharing a common ethnogeographic origin.

Reference Population - A group of subjects or individuals who are predicted to be representative ofthe genetic variation found in the general population. Typically, the reference population represents the genetic variation in the population at a certainty level of at least 85%, preferably at least 90%, more preferably at least 95% and even more preferably at least 99%.

Single Nucleotide Polymorphism (SNP) - Typically, the specific pair of nucleotides observed at a single polymorphic site. In rare cases, three or four nucleotides may be found.

Subject - A human individual whose genotypes or haplotypes or response to treatment or disease state are to be determined.

Treatment - A stimulus administered internally or externally to a subject.

Unphased - As applied to a sequence of nucleotide pairs for two or more polymorphic sites in a locus, unphased means the combination of nucleotides present at those polymorphic sites on a single copy ofthe locus is not known.

As discussed above, information on the identity of genotypes and haplotypes for the ILIB gene of any particular individual as well as the frequency of such genotypes and haplotypes in any particular population of individuals is expected to be useful for a variety of drug discovery and development applications. Thus, the invention also provides compositions and methods for detecting the novel ILIB polymorphisms and haplotypes identified herein.

The compositions comprise at least one ILIB genotyping oligonucleotide. In one embodiment, a ILIB genotyping oligonucleotide is a probe or primer capable of hybridizing to a target region that is located close to, or that contains, one ofthe novel polymorphic sites described herein. As used herein, the term "oligonucleotide" refers to a polynucleotide molecule having less than about 100 nucleotides. A preferred oligonucleotide ofthe invention is 10 to 35 nucleotides long. More preferably, the oligonucleotide is between 15 and 30, and most preferably, between 20 and 25 nucleotides in length. The exact length of he oligonucleotide will depend on many factors that are routinely considered and practiced by the skilled artisan. The oligonucleotide may be comprised of any phosphorylation state of ribonucleotides, deoxyribonucleotides, and acyclic nucleotide derivatives, and other functionally equivalent derivatives. Alternatively, oligonucleotides may have a phosphate-free backbone, which may be comprised of linkages such as carboxymethyl, acetamidate, carbamate, polyamide (peptide nucleic acid (PNA)) and the like (Varma, R. in Molecular Biology and Biotechnology, A Comprehensive Desk Reference, Ed. R. Meyers, VCH Publishers, Inc. (1995), pages 617-620). Oligonucleotides ofthe invention may be prepared by chemical synthesis using any suitable methodology known in the art, or may be derived from a biological sample, for example, by restriction digestion. The oligonucleotides may be labeled, according to any technique known in the art, including use of radiolabels, fluorescent labels, enzymatic labels, proteins, haptens, antibodies, sequence tags and the like.

Genotyping oligonucleotides ofthe invention must be capable of specifically hybridizing to a target region of a ILIB polynucleotide, i.e., a ILIB isogene. As used herein, specific hybridization means the oligonucleotide forms an anti-parallel double-stranded structure with the target region under certain hybridizing conditions, while failing to form such a structure when incubated with a non-target region or a non-ILIB polynucleotide under the same hybridizing conditions. Preferably, the oligonucleotide specifically hybridizes to the target region under conventional high stringency conditions. The skilled artisan can readily design and test oligonucleotide probes and primers suitable for detecting polymorphisms in the ILIB gene using the polymorphism information provided herein in conjunction with the known sequence information for the ILIB gene and routine techniques.

A nucleic acid molecule such as an oligonucleotide or polynucleotide is said to be a "perfect" or "complete" complement of another nucleic acid molecule if every nucleotide of one ofthe molecules is complementary to the nucleotide at the corresponding position ofthe other molecule. A nucleic acid molecule is "substantially complementary" to another molecule if it hybridizes to that molecule with sufficient stability to remain in a duplex form under conventional low-stringency conditions. Conventional hybridization conditions are described, for example, by Sambrook J. et al., in Molecular Cloning, A Laboratory Manual, 2^nd Edition, Cold Spring Harbor Press, Cold Spring Harbor, NY (1989) and by Haymes, B.D. et al. in Nucleic Acid Hybridization, A Practical Approach, IRL Press, Washington, D.C. (1985). While perfectly complementary oligonucleotides are preferred for detecting polymorphisms, departures from complete complementarity are contemplated where such departures do not prevent the molecule from specifically hybridizing to the target region. For example, an oligonucleotide primer may have a non-complementary fragment at its 5 ' end, with the remainder ofthe primer being complementary to the target region. Alternatively, non-complementary nucleotides may be interspersed into the oligonucleotide probe or primer as long as the resulting probe or primer is still capable of specifically hybridizing to the target region.

Preferred genotyping oligonucleotides ofthe invention are allele-specific oligonucleotides. As used herein, the term allele-specific oligonucleotide (ASO) means an oligonucleotide that is able, under sufficiently stringent conditions, to hybridize specifically to one allele of a gene, or other locus, at a target region containing a polymorphic site while not hybridizing to the corresponding region in another allele(s). As understoqd by the skilled artisan, allele-specificity will depend upon a variety of readily optimized stringency conditions, including salt and formamide concentrations, as well as temperatures for both the hybridization and washing steps. Examples of hybridization and washing conditions typically used for ASO probes are found in Kogan et al., "Genetic Prediction of Hemophilia A" in PCR Protocols, A Guide to Methods and Applications, Academic Press, 1990 and Ruano et al, 87 Proc. Natl. Acad. Sci. USA 6296-6300, 1990. Typically, an ASO will be perfectly complementary to one allele while containing a single mismatch for another allele.

Allele-specific oligonucleotides ofthe invention include ASO probes and ASO primers. ASO probes which usually provide good discrimination between different alleles are those in which a central position ofthe oligonucleotide probe aligns with the polymorphic site in the target region (e.g., approximately the 7^th or 8^th position in a 15mer, the 8^th or 9^th position in a 16mer, and the 10^th or 11^th position in a 20mer). An ASO primer ofthe invention has a 3' terminal nucleotide, or preferably a 3' penultimate nucleotide, that is complementary to only one nucleotide of a particular SNP, thereby acting as a primer for polyrnerase-mediated extension only if the allele containing that nucleotide is present. ASO probes and primers hybridizing to either the coding or noncoding strand are contemplated by the invention.

ASO probes and primers listed below use the appropriate nucleotide symbol (R= G or A, Y= T or C, M= A or C, K= G or T, S= G or C, and W= A or T; WTPO standard ST.25) at the position ofthe polymoφhic site to represent the two alternative allelic variants observed at that polymoφhic site.

A preferred ASO probe for detecting ILIB gene polymoφhisms comprises a nucleotide sequence, listed 5' to 3', selected from the group consisting of:

AAGCCATWAAAACAG (SEQ ID NO: 4) and its complement,

GGGATGAYCTTTAGA (SEQ ID NO: 5) and its complement,

AAGCTCGSGATTCTT (SEQ ID NO: 6) and its complement, TGGATGGYGGCATCC (SEQ ID NO: 7) and its complement, TTCACACRGAAAGTT (SEQ- ID NO: 8) and its complement, and GCCTGGAMTTTCCTG (SEQ ID NO: 9) and its complement.

A preferred ASO primer for detecting ILIB gene polymoφhisms comprises a nucleotide sequence, listed 5' to 3', selected from the group consisting of:

TTTTGAAAGCCATWA (SEQ ID NO: 10) CCCTCGCTGTTTT A (SEQ ID NO: 1611

CAGAGAGGGATGAYC (SEQ ID NO: 12) CGAGCTTCTAAAGRT (SEQ ID NO: 13)

CTTTAGAAGCTCGSG (SEQ ID NO: 14) GCTTGAAAGAATCSC (SEQ ID NO: 15)

GCCCTCTGGATGGYG (SEQ ID NO: 16) GTAGCTGGATGCCRC (SEQ ID NO: 17)

AATAAATTCACACRG (SEQ ID NO: 18) GGGCCCAACTTTCYG (SEQ ID NO: 19)

GCTATAGCCTGGAMT (SEQ ID NO: 20); and AG CAACAGGAAAKT (SEQ ID NO 211

Other genotyping oligonucleotides ofthe invention hybridize to a target region located one to several nucleotides downstream of one ofthe novel polymoφhic sites identified herein. Such oligonucleotides are useful in polymerase-mediated primer extension methods for detecting one ofthe novel polymoφhisms described herein and therefore such genotyping oligonucleotides are referred to herein as "primer-extension oligonucleotides". In a preferred embodiment, the 3 '-terminus of a primer- extension oligonucleotide is a deoxynucleotide complementary to the nucleotide located immediately adjacent to the polymoφhic site.

A particularly preferred oligonucleotide primer for detecting ILIB gene polymoφhisms by primer extension terminates in a nucleotide sequence, listed 5' to 3', selected from the group consisting of:

TGAAAGCCAT (SEQ ID NO:22) TCGCTGTTTT ( SEQ ID NO : 23 ) AGAGGGATGA (SEQ ID NO:24) GCTTCTAAAG (SEQ ID NO : 25 ) TAGAAGCTCG (SEQ ID NO:26) TGAAAGAATC ( SEQ ID NO : 27 ) CTCTGGATGG (SEQ ID NO:28) GCTGGATGCC ( SEQ ID NO : 29 ) AAATTCACAC (SEQ ID NO: 30) CCCAACTTTC (SEQ ID NO : 31 ) ATAGCCTGGA (SEQ ID NO:32) and CAACAGGAAA ( SEQ ID NO : 33 )

In some embodiments, a composition contains two or more differently labeled genotyping oligonucleotides for simultaneously probing the identity of nucleotides at two or more polymoφhic sites. It is also contemplated that primer compositions may contain two or more sets of allele-specific primer pairs to allow simultaneous targeting and amplification of two or more regions containing a polymoφhic site.

ILIB genotyping oligonucleotides ofthe invention may also be immobilized on or synthesized on a solid surface such as a microchip, bead, or glass slide (see, e.g., WO 98/20020 and WO 98/20019).

Such immobilized genotyping oligonucleotides may be used in a variety of polymoφhism detection assays, including but not limited to probe hybridization and polymerase extension assays. Immobilized

ILIB genotyping oligonucleotides ofthe invention may comprise an ordered array of oligonucleotides designed to rapidly screen a DNA sample for polymoφhisms in multiple genes at the same time.

In another embodiment, the invention provides a kit comprising at least two genotyping oligonucleotides packaged in separate containers. The kit may also contain other components such as hybridization buffer (where the oligonucleotides are to be used as a probe) packaged in a separate container. Alternatively, where the oKgonucleotides are to be used to amplify a target region, the kit may contain, packaged in separate containers, a polymerase and a reaction buffer optimized for primer extension mediated by the polymerase, such as PCR.

The above described oligonucleotide compositions and kits are useful in methods for genotyping and/or haplotyping the ILIB gene in an individual. As used herein, the terms "ILIB genotype" and "ILIB haplotype" mean the genotype or haplotype contains the nucleotide pair or nucleotide, respectively, that is present at one or more ofthe novel polymoφhic sites described herein and may optionally also include the nucleotide pair or nucleotide present at one or more additional polymoφhic sites in the ILIB gene. The additional polymoφhic sites may be currently known polymoφhic sites or sites that are subsequently discovered.

One embodiment ofthe genotyping method involves isolating from the individual a nucleic acid sample comprising the two copies ofthe ILIB gene, or a fragment thereof, that are present in the individual, and determining the identity ofthe nucleotide pair at one or more polymoφhic sites selected from the group consisting of PS2, PS3, PS4, PS5, PS8 and PS9 in the two copies to assign a ILIB genotype to the individual. As will be readily understood by the skilled artisan, the two "copies" of a gene in an individual may be the same allele or may be different alleles. In a preferred embodiment of the genotyping method, the identity ofthe nucleotide pair at one or more ofthe polymoφhic sites selected from the group consisting of PS1, PS6 and PS7 is also deteimined. In a particularly preferred embodiment, the genotyping method comprises determining the identity ofthe nucleotide pair at each of PS1-PS9.

Typically, the nucleic acid sample is isolated from a biological sample taken from the individual, such as a blood sample or tissue sample. Suitable tissue samples include whole blood, semen, saliva, tears, urine, fecal material, sweat, buccal, skin and hair. The nucleic acid sample may be comprised of genomic DNA, mRNA, or cDNA and, in the latter two cases, the biological sample must be obtained from a tissue in which the JL1B gene is expressed. Furthermore it will be understood by the skilled artisan that mRNA or cDNA preparations would not be used to detect polymoφhisms located in introns or in 5 ' and 3' untranslated regions. If a ILIB gene fragment is isolated, it must contain the polymoφhic site(s) to be genotyped.

One embodiment ofthe haplotyping method comprises isolating from the individual a nucleic acid sample containing only one ofthe two copies ofthe ILIB gene, or a fragment thereof, that is present in the individual and determining in that copy the identity ofthe nucleotide at one or more polymoφhic sites selected from the group consisting of PS2, PS3, PS4, PS5, PS8 and PS9 in that copy to assign a ILIB haplotype to the individual. The nucleic acid may be isolated using any method capable of separating the two copies ofthe ILIB gene or fragment such as one ofthe methods described above for preparing ILIB isogenes, with targeted in vivo cloning being the preferred approach. As will be readily appreciated by those skilled in the art, any individual clone will only provide haplotype information on one ofthe two ILIB gene copies present in an individual. If haplotype information is desired for the individual's other copy, additional ILIB clones will need to be examined. Typically, at least five clones should be examined to have more than a 90% probability of haplotyping both copies ofthe ILIB gene in an individual. In some embodiments, the haplotyping method also comprises identifying the nucleotide at one or more polymoφhic sites selected from the group consisting of PS1, PS6 and PS7. In a particularly preferred embodiment, the nucleotide at each of PS1-PS9 is identified.

In another embodiment, the haplotyping method comprises deterniining whether an individual has one or more ofthe ILIB haplotypes shown in Table 4. This can be accomplished by identifying, for one or both copies ofthe individual's ILIB gene, the phased sequence of nucleotides present at each of PS1-PS9. The present invention also contemplates that typically only a subset of PS1-PS9 will need to be directly examined to assign to an individual one or more ofthe haplotypes shown in Table 4. This is because at least one polymoφhic site in a gene is frequently in strong linkage disequilibrium with one or more other polymoφhic sites in that gene (Drysdale, CM et al. 2000 PNAS 97:10483-10488; Rieder MJ et al. 1999 Nature Genetics 22:59-62). Two sites are said to be in linkage disequilibrium if the presence of a particular variant at one site enhances the predictability of another variant at the second site (Stephens, JC 1999, Mol. Diag. 4:309-317). Techniques for determining whether any two polymoφhic sites are in linkage disequilibrium are well-known in the art (Weir B.S. 1996 Genetic Data Analysis II, Sinauer Associates, Inc. Publishers, Sunderland, MA).

In a preferred embodiment, a ILIB haplotype pair is determined for an individual by identifying the phased sequence of nucleotides at one or more polymoφhic sites selected from the group consisting of PS2, PS3, PS4, PS5, PS8 and PS9 in each copy ofthe ILIB gene that is present in the individual. In a particularly preferred embodiment, the haplotyping method comprises identifying the phased sequence of nucleotides at each of PS1-PS9 in each copy ofthe ILIB gene. When haplotyping both copies ofthe gene, the identifying step is preferably performed with each copy ofthe gene being placed in separate containers. However, it is also envisioned that if the two copies are labeled with different tags, or are otherwise separately distinguishable or identifiable, it could be possible in some cases to perform the method in the same container. For example, if first and second copies ofthe gene are labeled with different first and second fluorescent dyes, respectively, and an allele-specific oligonucleotide labeled with yet a third different fluorescent dye is used to assay the polymoφhic site(s), then detecting a combination ofthe first and third dyes would identify the polymoφhism in the first gene copy while detecting a combination ofthe second and third dyes would identify the polymoφhism in the second gene copy.

In both the genotyping and haplotyping methods, the identity of a nucleotide (or nucleotide pair) at a polymoφhic site(s) may be determined by amplifying a target region(s) containing the polymoφhic site(s) directly from one or both copies ofthe ILIB gene, or a fragment thereof, and the sequence ofthe amplified region(s) determined by conventional methods. It will be readily appreciated by the skilled artisan that only one nucleotide will be detected at a polymoφhic site in individuals who are homozygous at that site, while two different nucleotides will be detected if the individual is heterozygous for that site. The polymoφhism may be identified directly, known as positive-type identification, or by inference, referred to as negative-type identification. For example, where a SNP is known to be guanine and cytosine in a reference population, a site may be positively determined to be either guanine or cytosine for an individual homozygous at that site, or both guanine and cytosine, if the individual is heterozygous at that site. Alternatively, the site may be negatively determined to be not guanine (and thus cytosine/cytosine) or not cytosine (and thus guanine/guanine).

The target region(s) may be amplified using any oligonucleotide-directed amplification method, including but not limited to polymerase chain reaction (PCR) (U.S. Patent No. 4,965,188), ligase chain reaction (LCR) (Barany et al., Proc. Natl. Acad. Sci. USA 88:189-193, 1991; WO90/01069), and oligonucleotide ligation assay (OLA) (Landegren et al., Science 241:1077-1080, 1988).

Other known nucleic acid amplification procedures may be used to amplify the target region including transcription-based amplification systems (U.S. Patent No. 5,130,238; EP 329,822; U.S. Patent No. 5,169,766, WO89/06700) and isothermal methods (Walker et al., Proc. Natl. Acad. Sci. USA 89:392- 396, 1992).

A polymoφhism in the target region may also be assayed before or after amplification using one of several hybridization-based methods known in the art. Typically, allele-specific oligonucleotides are utilized in performing such methods. The allele-specific oligonucleotides may be used as differently labeled probe pairs, with one member ofthe pair showing a perfect match to one variant of a target sequence and the other member showing a perfect match to a different variant. In some embodiments, more than one polymoφhic site may be detected at once using a set of allele-specific oligonucleotides or oligonucleotide pairs. Preferably, the members ofthe set have melting temperatures within 5°C, and more preferably within 2°C, of each other when hybridizing to each ofthe polymoφhic sites being detected.

Hybridization of an allele-specific oligonucleotide to a target polynucleotide may be performed with both entities in solution, or such hybridization may be performed when either the oligonucleotide or the target polynucleotide is covalently or noncovalently affixed to a solid support. Attachment may be mediated, for example, by antibody-antigen interactions, poly-L-Lys, streptavidin or avidin-biotin, salt bridges, hydrophobic interactions, chemical linkages, UV cross-linking baking, etc. Allele-specific oligonucleotides may be synthesized directly on the solid support or attached to the solid support subsequent to synthesis. Solid-supports suitable for use in detection methods ofthe invention include substrates made of silicon, glass, plastic, paper and the like, which may be formed, for example, into wells (as in 96-well plates), slides, sheets, membranes, fibers, chips, dishes, and beads. The solid support may be treated, coated or derivatized to facilitate the immobilization ofthe allele-specific oligonucleotide or target nucleic acid.

The genotype or haplotype for the ILIB gene of an individual may also be determined by hybridization of a nucleic acid sample containing one or both copies ofthe gene, or fragment(s) thereof, to nucleic acid arrays and subarrays such as described in WO 95/11995. The arrays would contain a battery of allele-specific oligonucleotides representing each ofthe polymoφhic sites to be included in the genotype or haplotype.

The identity of polymoφhisms may also be determined using a mismatch detection technique, including but not limited to the RNase protection method using riboprobes (Winter et al., Proc. Natl. Acad. Sci. USA 82:7575, 1985; Meyers et al., Science 230:1242, 1985) and proteins which recognize nucleotide mismatches, such as the E. coli mutS protein (Modrich, P. Ann. Rev. Genet. 25:229-253, 1991). Alternatively, variant alleles can be identified by single strand conformation polymoφhism (SSCP) analysis (Orita et al., Genomics 5:874-879, 1989; Humphries et al., in Molecular Diagnosis of Genetic Diseases, R. Elles, ed., pp. 321-340, 1996) or denaturing gradient gel electrophoresis (DGGE) (Wartell et al., Nucl. Acids Res. 18:2699-2706, 1990; Sheffield et al., Proc. Natl. Acad. Sci. USA 86:232- 236, 1989).

A polymerase-mediated primer extension method may also be used to identify the polymoφhism(s). Several such methods have been described in the patent and scientific literature and include the "Genetic Bit Analysis" method (W092/15712) and the ligase/polymerase mediated genetic bit analysis (U.S. Patent 5,679,524. Related methods are disclosed in W091/02087, WO90/09455, W095/17676, U.S. Patent Nos. 5,302,509, and 5,945,283. Extended primers containing a polymoφhism may be detected by mass spectrometry as described in U.S. Patent No. 5,605,798. Another primer extension method is allele-specific PCR (Ruano et al., NwcZ. Acids Res. 17:8392, 1989; Ruano et al., Nucl. Acids Res. 19, 6877-6882, 1991; WO 93/22456; Turki et al., J. Clin. Invest. 95:1635-1641, 1995). In addition, multiple polymoφhic sites may be investigated by simultaneously amplifying multiple regions ofthe nucleic acid using sets of allele-specific primers as described in Wallace et al. (WO89/10414).

In addition, the identity ofthe allele(s) present at any ofthe novel polymoφhic sites described herein may be indirectly determined by genotyping another polymoφhic site that is in linkage disequilibrium with the polymoφhic site that is of interest. Polymoφhic sites in linkage disequilibrium with the presently disclosed polymoφhic sites may be located in regions ofthe gene or in other genomic regions not examined herein. Genotyping of a polymoφhic site in linkage disequilibrium with the novel polymoφhic sites described herein may be performed by, but is not limited to, any ofthe above- mentioned methods for detecting the identity ofthe allele at a polymoφhic site.

In another aspect ofthe invention, an individual's ILIB haplotype pair is predicted from its ILIB genotype using information on haplotype pairs known to exist in a reference population. In its broadest embodiment, the haplotyping prediction method comprises identifying a ILIB genotype for the individual at two or more ILIB polymoφhic sites described herein, enumerating all possible haplotype pairs which are consistent with the genotype, accessing data containing ILIB haplotype pairs identified in a reference population, and assigning a haplotype pair to the individual that is consistent with the data. In one embodiment, the reference haplotype pairs include the ILIB haplotype pairs shown in Table 3.

Generally, the reference population should be composed of randomly-selected individuals representing the major ethnogeographic groups ofthe world. A preferred reference population for use in the methods ofthe present invention comprises an approximately equal number of individuals from Caucasian, African-descent, Asian and Hispanic-Latino population groups with the minimum number of each group being chosen based on how rare a haplotype one wants to be guaranteed to see. For example, if one wants to have a q% chance of not missing a haplotype that exists in the population at a p% frequency of occurring in the reference population, the number of individuals (n) who must be sampled is given by 2n=log(l-q)/log(l-p) where p and q are expressed as fractions. A preferred reference population allows the detection of any haplotype whose frequency is at least 10% with about 99% certainty and comprises about 20 unrelated individuals from each ofthe four population groups named above. A ' particularly preferred reference population includes a 3 -generation family representing one or more ofthe four population groups to serve as controls for checking quality of haplotyping procedures.

In a preferred embodiment, the haplotype frequency data for each ethnogeographic group is examined to determine whether it is consistent with Hardy-Weinberg equilibrium. Hardy- Weinberg equilibrium (D.L. Hartl et al., Principles of Population Genomics, Sinauer Associates (Sunderland, MA), 3^rd Ed., 1997) postulates that the frequency of finding the haplotype pair H I H₂ is equal to p_H__w(H IH₂) = 2p(H_x)p(H₂) if H_x ≠ H₂ and p_H__w(H_x IH₂) = p(H_x)p(H₂) if H = H₂ . A statistically significant difference between the observed and expected haplotype frequencies could be due to one or more factors including significant inbreeding in the population group, strong selective pressure on the gene, sampling bias, and/or errors in the genotyping process. If large deviations from Hardy- Weinberg equilibrium are observed in an ethnogeographic group, the number of individuals in that group can be increased to see if the deviation is due to a sampling bias. If a larger sample size does not reduce the difference between observed and expected haplotype pair frequencies, then one may wish to consider haplotyping the individual using a direct haplotyping method such as, for example, CLASPER System^™ technology (U.S. Patent No. 5,866,404), single molecule dilution, or allele-specific long-range PCR (Michalotos-Beloin et al., Nwc/etc^cz^'ώ Rgi'. 24:4841-4843, 1996).

In one embodiment of this method for predicting a ILIB haplotype pair for an individual, the assigning step involves performing the following analysis. First, each ofthe possible haplotype pairs is compared to the haplotype pairs in the reference population. Generally, only one ofthe haplotype pairs in the reference population matches a possible haplotype pair and that pair is assigned to the individual. Occasionally, only one haplotype represented in the reference haplotype pairs is consistent with a possible haplotype pair for an individual, and in such cases the individual is assigned a haplotype pair containing this known haplotype and a new haplotype derived by subtracting the known haplotype from the possible haplotype pair. In rare cases, either no haplotypes in the reference population are consistent with the possible haplotype pairs, or alternatively, multiple reference haplotype pairs are consistent with the possible haplotype pairs. In such cases, the individual is preferably haplotyped using a direct molecular haplotyping method such as, for example, CLASPER System^™ technology (U.S. Patent No. 5,866,404), SMD, or allele-specific long-range PCR (Michalotos-Beloin et al., supra). A preferred process for predicting ILIB haplotype pairs from ILIB genotypes is described in U.S. Provisional Application Serial No. 60/198,340 and the corresponding International Application filed April 18, 2001.

The invention also provides a method for determining the frequency of a ILIB genotype, haplotype, or haplotype pair in a population. The method comprises, for each member ofthe population, determining the genotype or the haplotype pair for the novel ILIB polymoφhic sites described herein, and calculating the frequency any particular genotype, haplotype, or haplotype pair is found in the population. The population may be a reference population, a family population, a same sex population, a population group, or a trait population (e.g., a group of individuals exhibiting a trait of interest such as a medical condition or response to a therapeutic treatment).

In another aspect ofthe invention, frequency data for JL1B genotypes, haplotypes, and/or haplotype pairs are determined in a reference population and used in a method for identifying an association between a trait and a ILIB genotype, haplotype, or haplotype pair. The trait may be any detectable phenotype, including but not limited to susceptibility to a disease or response to a treatment. The method involves obtaining data on the frequency ofthe genotype(s), haplotype(s), or haplotype pair(s) of interest in a reference population as well as in a population exhibiting the trait. Frequency data for one or both ofthe reference and trait populations may be obtained by genotyping or haplotyping each individual in the populations using one ofthe methods described above. The haplotypes for the trait population may be determined directly or, alternatively, by the predictive genotype to haplotype approach described above. In another embodiment, the frequency data for the reference and/or trait populations is obtained by accessing previously determined frequency data, which may be in written or electronic form. For example, the frequency data may be present in a database that is accessible by a computer. Once the frequency data is obtained, the frequencies ofthe genotype(s), haplotype(s), or haplotype pair(s) of interest in the reference and trait populations are compared. In a preferred embodiment, the frequencies of all genotypes, haplotypes, and/or haplotype pairs observed in the populations are compared. If a particular ILIB genotype, haplotype, or haplotype pair is more frequent in the trait population than in the reference population at a statistically significant amount, then the trait is predicted to be associated with that ILIB genotype, haplotype or haplotype pair. Preferably, the ILIB genotype, haplotype, or haplotype pair being compared in the trait and reference populations is selected from the full-genotypes and full- haplotypes shown in Tables 3 and 4, or from sub-genotypes and sub-haplotypes derived from these genotypes and haplotypes.

In a preferred embodiment ofthe method, the trait of interest is a clinical response exhibited by a patient to some therapeutic treatment, for example, response to a drug targeting ILIB or response to a therapeutic treatment for a medical condition. As used herein, "medical condition" includes but is not limited to any condition or disease manifested as one or more physical and/or psychological symptoms for which treatment is desirable, and includes previously and newly identified diseases and other disorders. As used herein the term "clinical response" means any or all ofthe following: a quantitative measure ofthe response, no response, and adverse response (i.e., side effects).

In order to deduce a correlation between clinical response to a treatment and a ILIB genotype, haplotype, or haplotype pair, it is necessary to obtain data on the clinical responses exhibited by a population of individuals who received the treatment, hereinafter the "clinical population". This clinical data may be obtained by analyzing the results of a clinical trial that has already been run and/or the clinical data may be obtained by designing and carrying out one or more new clinical trials. As used herein, the term "clinical trial" means any research study designed to collect clinical data on responses to a particular treatment, and includes but is not limited to phase I, phase II and phase III clinical trials. Standard methods are used to define the patient population and to enroll subjects.

It is preferred that the individuals included in the clinical population have been graded for the existence ofthe medical condition of interest. This is important in cases where the symptom(s) being presented by the patients can be caused by more than one underlying condition, and where treatment of the underlying conditions are not the same. An example of this would be where patients experience breathing difficulties that are due to either asthma or respiratory infections. If both sets were treated with an asthma medication, there would be a spurious group of apparent non-responders that did not actually have asthma. These people would affect the ability to detect any correlation between haplotype and treatment outcome. This grading of potential patients could employ a standard physical exam or one or more lab tests. Alternatively, grading of patients could use haplotyping for situations where there is a strong correlation between haplotype pair and disease susceptibility or severity.

The therapeutic treatment of interest is administered to each individual in the trial population and each individual's response to the treatment is measured using one or more predetermined criteria. It is contemplated that in many cases, the trial population will exhibit a range of responses and that the investigator will choose the number of responder groups (e.g., low, medium, high) made up by the various responses. In addition, the ILIB gene for each individual in the trial population is genotyped and/or haplotyped, which may be done before or after administering the treatment.

After both the clinical and polymoφhism data have been obtained, correlations between individual response and ILIB genotype or haplotype content are created. Correlations may be produced in several ways. In one method, individuals are grouped by their ILIB genotype or haplotype (or haplotype pair) (also referred to as a polymoφhism group), and then the averages and standard deviations of clinical responses exhibited by the members of each polymoφhism group are calculated.

These results are then analyzed to determine if any observed variation in clinical response between polymoφhism groups is statistically significant. Statistical analysis methods which may be used are described in L.D. Fisher and G. vanBelle, "Biostatistics: A Methodology for the Health Sciences", Wiley-Interscience (New York) 1993. This analysis may also include a regression calculation ofwhich polymoφhic sites in the ILIB gene give the most significant contribution to the differences in phenotype. One regression model useful in the invention is described in PCT Application Serial No. PCT/USOO/17540, entitled "Methods for Obtaining and Using Haplotype Data".

A second method for finding correlations between ILIB haplotype content and clinical responses uses predictive models based on error-minimizing optimization algorithms. One of many possible optimization algorithms is a genetic algorithm (R. Judson, "Genetic Algorithms and Their Uses in Chemistry" in Reviews in Computational Chemistry, Vol. 10, pp. 1-73, K. B. Lipkowitz and D. B. Boyd, eds. (VCH Publishers, New York, 1997). Simulated annealing (Press et al., "Numerical Recipes in C: The Art of Scientific Computing", Cambridge University Press (Cambridge) 1992, Ch. 10), neural networks (E. Rich and K. Knight, "Artificial Intelligence", 2^nd Edition (McGraw-Hill, New York, 1991, Ch. 18), standard gradient descent methods (Press et al., supra, Ch. 10), or other global or local optimization approaches (see discussion in Judson, supra) could also be used. Preferably, the correlation is found using a genetic algorithm approach as described in PCT Application Serial No. PCT/USOO/17540.

Correlations may also be analyzed using analysis of variation (ANOVA) techniques to determine how much ofthe variation in the clinical data is explained by different subsets ofthe polymoφhic sites in the ILIB gene. As described in PCT Application Serial No. PCT/USOO/17540, ANOVA is used to test hypotheses about whether a response variable is caused by or correlated with one or more traits or variables that can be measured (Fisher and vanBelle, supra, Ch. 10).

From the analyses described above, a mathematical model may be readily constructed by the skilled artisan that predicts clinical response as a function of ILIB genotype or haplotype content. Preferably, the model is validated in one or more follow-up clinical trials designed to test the model.

The identification of an association between a clinical response and a genotype or haplotype (or haplotype pair) for the ILIB gene may be the basis for designing a diagnostic method to determine those individuals who will or will not respond to the treatment, or alternatively, will respond at a lower level and thus may require more treatment, i.e., a greater dose of a drug. The diagnostic method may take one of several forms: for example, a direct DNA test (i.e., genotyping or haplotyping one or more ofthe polymoφhic sites in the ILIB gene), a serological test, or a physical exam measurement. The only requirement is that there be a good correlation between the diagnostic test results and the underlying ILIB genotype or haplotype that is in turn correlated with the clinical response. In a preferred embodiment, this diagnostic method uses the predictive haplotyping method described above.

In another embodiment, the invention provides an isolated polynucleotide comprising a polymoφhic variant ofthe ILIB gene or a fragment ofthe gene which contains at least one ofthe novel polymoφhic sites described herein. The nucleotide sequence of a variant ILIB gene is identical to the reference genomic sequence for those portions ofthe gene examined, as described in the Examples below, except that it comprises a different nucleotide at one or more ofthe novel polymoφhic sites PS2, PS3, PS4, PS5, PS8 and PS9, and may also comprise one or more additional polymoφhisms selected from the group consisting of thymine at PS1, adenine at PS6 and thymine at PS7. Similarly, the nucleotide sequence of a variant fragment ofthe ILIB gene is identical to the corresponding portion of the reference sequence except for having a different nucleotide at one or more ofthe novel polymoφhic sites described herein. Thus, the invention specifically does not include polynucleotides comprising a nucleotide sequence identical to the reference sequence ofthe ILIB gene (or other reported ILIB sequences) or to portions ofthe reference sequence (or other reported ILIB sequences), except for genotyping oligonucleotides as described above.

The location of a polymoφhism in a variant gene or fragment is identified by aligning its sequence against SEQ ID NO: 1. The polymoφhism is selected from the group consisting of thymine at PS2, cytosine at PS3, cytosine at PS4, thymine at PS5, guanine at PS8 and adenine at PS9. In a preferred embodiment, the polymoφhic variant comprises a naturally-occurring isogene ofthe ILIB gene which is defined by any one of haplotypes 1-18 shown in Table 4 below.

Polymoφhic variants ofthe invention may be prepared by isolating a clone containing the ILIB gene from a human genomic library. The clone may be sequenced to determine the identity ofthe nucleotides at the novel polymoφhic sites described herein. Any particular variant claimed herein could be prepared from this clone by performing in vitro mutagenesis using procedures well-known in the art.

ILIB isogenes may be isolated using any method that allows separation ofthe two "copies" of the ILIB gene present in an individual, which, as readily understood by the skilled artisan, may be the same allele or different alleles. Separation methods include targeted in vivo cloning (TIVC) in yeast as described in WO 98/01573, U.S. Patent No. 5,866,404, and U.S. Patent No. 5,972,614. Another method, which is described in U.S. Patent No. 5,972,614, uses an allele specific oligonucleotide in combination with primer extension and exonuclease degradation to generate hemizygous DNA targets. Yet other methods are single molecule dilution (SMD) as described in Rua io et al, Proc. Natl. Acad. Sci. 87:6296- 6300, 1990; and allele specific PCR (Ruano et al., 1989, supra; Ruano et al., 1991, supra; Michalatos- Beloin et al., supra).

The invention also provides ILIB genome anthologies, which are collections of ILIB isogenes found in a given population. The population may be any group of at least two individuals, including but not limited to a reference population, a population group, a family population, a clinical population, and a same sex population. A ILIB genome anthology may comprise individual ILIB isogenes stored in separate containers such as microtest tubes, separate wells of a microtitre plate and the like. Alternatively, two or more groups ofthe ILIB isogenes in the anthology may be stored in separate containers. Individual isogenes or groups of isogenes in a genome anthology may be stored in any convenient and stable form, including but not limited to in buffered solutions, as DNA precipitates, freeze-dried preparations and the like. A preferred ILIB genome anthology ofthe invention comprises a set of isogenes defined by the haplotypes shown in Table 4 below.

An isolated polynucleotide containing a polymoφhic variant nucleotide sequence ofthe invention may be operably linked to one or more expression regulatory elements in a recombinant expression vector capable of being propagated and expressing the encoded ILIB protein in a prokaryotic or a eukaryotic host cell. Examples of expression regulatory elements which may be used include, but are not limited to, the lac system, operator and promoter regions of phage lambda, yeast promoters, and promoters derived from vaccinia virus, adenovirus, retroviruses, or SV40. Other regulatory elements include, but are not limited to, appropriate leader sequences, termination codons, polyadenylation signals, and other sequences required for the appropriate transcription and subsequent translation ofthe nucleic acid sequence in a given host cell. Of course, the correct combinations of expression regulatory elements will depend on the host system used. In addition, it is understood that the expression vector contains any additional elements necessary for its transfer to and subsequent replication in the host cell. Examples of such elements include, but are not limited to, origins of replication and selectable markers. Such expression vectors are commercially available or are readily constructed using methods known to those in the art (e.g., F. Ausubel et al., 1987, in "Current Protocols in Molecular Biology", John Wiley and Sons, New York, New York). Host cells which may be used to express the variant ILIB sequences ofthe invention include, but are not limited to, eukaryotic and mammalian cells, such as animal, plant, insect and yeast cells, and prokaryotic cells, such as E. coli, or algal cells as known in the art. The recombinant expression vector may be introduced into the host cell using any method known to those in the art including, but not limited to, microinjection, electroporation, particle bombardment, transduction, and transfection using DEAE-dextran, lipofection, or calcium phosphate (see e.g., Sambrook et al. (1989) in "Molecular Cloning. A Laboratory Manual", Cold Spring Harbor Press, Plainview, New York). In a preferred aspect, eukaryotic expression vectors that function in eukaryotic cells, and preferably mammalian cells, are used. Non-limiting examples of such vectors include vaccinia virus vectors, adenovirus vectors, heφes virus vectors, and baculovirus transfer vectors. Preferred eukaryotic cell lines include COS cells, CHO cells, HeLa cells, NTH/3T3 cells, and embryonic stem cells (Thomson, J. A. et al., 1998 Science 282: 1145-1147). Particularly preferred host cells are mammalian cells.

As will be readily recognized by the skilled artisan, expression of polymoφhic variants ofthe ILIB gene will produce ILIB mRNAs varying from each other at any polymoφhic site retained in the spliced and processed mRNA molecules. These mRNAs can be used for the preparation of a ILIB cDNA comprising a nucleotide sequence which is a polymoφhic variant ofthe ILIB reference coding sequence shown in Figure 2. Thus, the invention also provides ILIB mRNAs and corresponding cDNAs which comprise a nucleotide sequence that is identical to SEQ ID NO:2 (Fig. 2), or its corresponding RNA sequence, except for having thymine at a position corresponding to nucleotide 138, and may also comprise an additional polymoφhism of thymine at a position corresponding to nucleotide 315. A particularly preferred polymoφhic cDNA variant comprises the coding sequence of a ILIB isogene defined by haplotypes 1-18. Fragments of these variant mRNAs and cDNAs are included in the scope of the invention, provided they contain the novel polymoφhism described herein. The invention specifically excludes polynucleotides identical to previously identified and characterized ILIB cDNAs and fragments thereof. Polynucleotides comprising a variant RNA or DNA sequence may be isolated from a biological sample using well-known molecular biological procedures or may be chemically synthesized. As used herein, a polymoφhic variant of a ILIB gene fragment comprises at least one novel polymoφhism identified herein and has a length of at least 10 nucleotides and may range up to the full length ofthe gene. Preferably, such fragments are between 100 and 3000 nucleotides in length, and more preferably between 200 and 2000 nucleotides in length, and most preferably between 500 and 1000 nucleotides in length.

In describing the ILIB polymoφhic sites identified herein, reference is made to the sense strand ofthe gene for convenience. However, as recognized by the skilled artisan, nucleic acid molecules containing the ILIB gene may be complementary double stranded molecules and thus reference to a particular site on the sense strand refers as well to the corresponding site on the complementary antisense strand. Thus, reference may be made to the same polymoφhic site on either strand and an oligonucleotide may be designed to hybridize specifically to either strand at a target region containing the polymoφhic site. Thus, the invention also includes single-stranded polynucleotides which are complementary to the sense strand ofthe ILIB genomic variants described herein.

Polynucleotides comprising a polymoφhic gene variant or fragment may be useful for therapeutic p poses. For example, where a patient could benefit from expression, or increased expression, of a particular EL IB protein isoform, an expression vector encoding the isoform may be administered to the patient. The patient may be one who lacks the ILIB isogene encoding that isoform or may already have at least one copy of that isogene.

In other situations, it may be desirable to decrease or block expression of a particular ILIB isogene. Expression of a ILIB isogene may be turned off by transforming a targeted organ, tissue or cell population with an expression vector that expresses high levels of untranslatable mRNA for the isogene. Alternatively, oligonucleotides directed against the regulatory regions (e.g., promoter, introns, enhancers, 3 ' untranslated region) ofthe isogene may block transcription. Oligonucleotides targeting the transcription initiation site, e.g., between positions -10 and +10 from the start site are preferred. Similarly, inhibition of transcription can be achieved using oligonucleotides that base-pair with region(s) ofthe isogene DNA to form triplex DNA (see e.g., Gee et al. in Huber, B.E. and B.I. Carr, Molecular and Immunologic Approaches, Futura Publishing Co., Mt. Kisco, NY., 1994). Antisense oligonucleotides may also be designed to block translation of ILIB mRNA transcribed from a particular isogene. It is also contemplated that ribozymes may be designed that can catalyze the specific cleavage of ILIB mRNA transcribed from a particular isogene.

The oligonucleotides may be delivered to a target cell or tissue by expression from a vector introduced into the cell or tissue in vivo or ex vivo. Alternatively, the oligonucleotides may be formulated as a pharmaceutical composition for administration to the patient. Oligoribonucleotides and/or oligodeoxynucleotides intended for use as antisense oligonucleotides may be modified to increase stability and half-life. Possible modifications include, but are not limited to phosphorothioate or 2' O- methyl linkages, and the inclusion of nontraditional bases such as inosine and queosine, as well as acetyl- , methyl-, thio-, and similarly modified forms of adenine, cytosine, guanine, thymine, and uracil which are not as easily recognized by endogenous nucleases.

Effect(s) ofthe polymoφhisms identified herein on expression of ILIB may be investigated by preparing recombinant cells and/or nonhuman recombinant organisms, preferably recombinant animals, containing a polymoφhic variant ofthe ILIB gene. As used herein, "expression" includes but is not limited to one or more ofthe following: transcription ofthe gene into precursor mRNA; splicing and other processing ofthe precursor mRNA to produce mature mRNA; mRNA stability; translation ofthe ^• mature mRNA into ILIB protein (including codon usage and tRNA availability); and glycosylation and/or other modifications ofthe translation product, if required for proper expression and function.

To prepare a recombinant cell ofthe invention, the desired EL IB isogene may be introduced into the cell in a vector such that the isogene remains extrachromosomal. In such a situation, the gene will be expressed by the cell from the extrachromosomal location. In a preferred embodiment, the ILIB isogene is introduced into a cell in such a way that it recombines with the endogenous ILIB gene present in the cell. Such recombination requires the occurrence of a double recombination event, thereby resulting in the desired ILIB gene polymoφhism. Vectors for the introduction of genes both for recombination and for extrachromosomal maintenance are known in the art, and any suitable vector or vector construct may be used in the invention. Methods such as electroporation, particle bombardment, calcium phosphate co- precipitation and viral transduction for introducing DNA into cells are known in the art; therefore, the choice of method may lie with the competence and preference ofthe skilled practitioner. Examples of cells into which the EL1B isogene may be introduced include, but are not limited to, continuous culture cells, such as COS, NTH/3T3, and primary or culture cells ofthe relevant tissue type, i.e., they express the ILIB isogene. Such recombinant cells can be used to compare the biological activities ofthe different protein variants.

Recombinant nonhuman organisms, i.e., transgenic animals, expressing a variant ILIB gene are prepared using standard procedures known in the art. Preferably, a construct comprising the variant gene is introduced into a nonhuman animal or an ancestor ofthe animal at an embryonic stage, i.e., the one-cell stage, or generally not later than about the eight-cell stage. Transgenic animals carrying the constructs of the invention can be made by several methods known to those having skill in the art. One method involves transfecting into the embryo a retrovirus constructed to contain one or more insulator elements, a gene or genes of interest, and other components known to those skilled in the art to provide a complete shuttle vector harboring the insulated gene(s) as a transgene, see e.g., U.S. Patent No. 5,610,053. Another method involves directly injecting a transgene into the embryo. A third method involves the use of embryonic stem cells. Examples of animals into which the ILIB isogenes may be introduced include, but are not limited to, mice, rats, other rodents, and nonhuman primates (see "The Introduction of Foreign Genes into Mice" and the cited references therein, In: Recombinant DNA, Eds. J.D. Watson, M. Gilman, J. Witkowski, and M. Zoller; W.H. Freeman and Company, New York, pages 254-272). Transgenic animals stably expressing a human ILIB isogene and producing human ILIB protein can be used as biological models for studying diseases related to abnormal ILIB expression and/or activity, and for screening and assaying various candidate drugs, compounds, and treatment regimens to reduce the symptoms or effects of these diseases.

An additional embodiment ofthe invention relates to pharmaceutical compositions for treating disorders affected by expression or function of a novel ILIB isogene described herein. The pharmaceutical composition may comprise any ofthe following active ingredients: a polynucleotide comprising one of these novel ILIB isogenes; an antisense oligonucleotide directed against one ofthe novel ILIB isogenes, a polynucleotide encoding such an antisense oligonucleotide, or another compound which inhibits expression of a novel ILIB isogene described herein. Preferably, the composition contains the active ingredient in a therapeutically effective amount. By therapeutically effective amount is meant that one or more ofthe symptoms relating to disorders affected by expression or function of a novel ILIB isogene is reduced and/or eliminated. The composition also comprises a pharmaceutically acceptable carrier, examples ofwhich include, but are not limited to, saline, buffered saline, dextrose, and water. Those skilled in the art may employ a formulation most suitable for the active ingredient, whether it is a polynucleotide, oligonucleotide, protein, peptide or small molecule antagonist. The pharmaceutical composition may be administered alone or in combination with at least one other agent, such as a stabilizing compound. Administration ofthe pharmaceutical composition may be by any number of routes including, but not limited to oral, intravenous, intramuscular, intra-arterial, intramedullary, intrathecal, intraventricular, intradermal, transdermal, subcutaneous, intraperitoneal, intranasal, enteral, topical, sublingual, or rectal. Further details on techniques for formulation and administration may be found in the latest edition of Remington's Pharmaceutical Sciences (Maack Publishing Co., Easton, PA).

For any composition, determination ofthe therapeutically effective dose of active ingredient and/or the appropriate route of administration is well within the capability of those skilled in the art. For example, the dose can be estimated initially either in cell culture assays or in animal models. The animal model may also be used to determine the appropriate concentration range and route of administration. Such information can then be used to determine useful doses and routes for administration in humans. The exact dosage will be determined by the practitioner, in light of factors relating to the patient requiring treatment, including but not limited to severity ofthe disease state, general health, age, weight and gender ofthe patient, diet, time and frequency of administration, other drugs being taken by the patient, and tolerance/response to the treatment.

Any or all analytical and mathematical operations involved in practicing the methods ofthe present invention may be implemented by a computer. In addition, the computer may execute a program that generates views (or screens) displayed on a display device and with which the user can interact to view and analyze large amounts of information relating to the ILIB gene and its genomic variation, including chromosome location, gene structure, and gene family, gene expression data, polymoφhism data, genetic sequence data, and clinical data population data (e.g., data on ethnogeographic origin, clinical responses, genotypes, and haplotypes for one or more populations). The ILIB polymoφhism data described herein may be stored as part of a relational database (e.g., an instance of an Oracle database or a set of ASCII flat files). These polymoφhism data may be stored on the computer's hard drive or may, for example, be stored on a CD-ROM or on one or more other storage devices accessible by the computer. For example, the data may be stored on one or more databases in communication with the computer via a network.

Preferred embodiments ofthe invention are described in the following examples. Other embodiments within the scope ofthe claims herein will be apparent to one skilled in the art from consideration ofthe specification or practice ofthe invention as disclosed herein. It is intended that the specification, together with the examples, be considered exemplary only, with the scope and spirit ofthe invention being indicated by the claims which follow the examples.

EXAMPLES The Examples herein are meant to exemplify the various aspects of carrying out the invention and are not intended to limit the scope ofthe invention in any way. The Examples do not include detailed descriptions for conventional methods employed, such as in the performance of genomic DNA isolation, PCR and sequencing procedures. Such methods are well-known to those skilled in the art and are described in numerous publications, for example, Sambrook, Fritsch, and Maniatis, "Molecular Cloning: A Laboratory Manual", 2^nd Edition, Cold Spring Harbor Laboratory Press, USA, (1989).

EXAMPLE 1 This example illustrates examination of various regions ofthe ILIB gene for polymoφhic sites.

Amplification of Target Regions

The following target regions were amplified using either the PCR primers represented below or 'tailed' PCR primers, each ofwhich includes a universal sequence forming a noncomplementary 'tail' attached to the 5 ' end of each unique sequence in the PCR primer pairs. The universal 'tail' sequence for the forward PCR primers comprises the sequence 5 '-TGTAAAACGACGGCCAGT-3 ' (SEQ ED NO:34) and the universal 'tail' sequence for the reverse PCR primers comprises the sequence 5'- AGGAAACAGCTATGACCAT-3 ' (SEQ ED NO:35). The nucleotide positions ofthe first and last nucleotide ofthe forward and reverse primers for each region amplified are presented below and correspond to positions in Figure 1.

PCR Primer Pairs

Fragment 1to. Forward P Reverse Primer PCR Product

Fragment 1 628-649 complement of 1144-1122 517 nt

Fragment 2 4148-4171 complement of 4713-4690 566 nt

Fragment 3 8-28 complement of 577-557 570 nt

Fragment 4 97-118 complement of 749-727 653 nt

Fragment 5 6343-6368 complement of 6929-6907 587 nt

Fragment 6 3397-3418 complement of 3916-3894 520 nt These primer pairs were used in PCR reactions containing genomic DNA isolated from immortalized cell lines for each member ofthe Index Repository. The PCR reactions were carried out under the following conditions:

Reaction volume = 10 μl

10 x Advantage 2 Polymerase reaction buffer (Clontech) = 1 μl

100 ng of human genomic DNA = 1 μl

10 mM dNTP = 0.4 μl

Advantage 2 Polymerase enzyme mix (Clontech) = 0.2 μl

Forward Primer (10 μM) = 0.4 μl

Reverse Primer (10 μM) = 0.4 μl

Water = 6.6μl

Amplification profile: 97°C - 2 min. 1 cycle

97°C - 15 sec.

70°C - 45 sec. 10 cycles

72°C - 45 sec.

97°C - 15 sec.

64°C - 45 sec. 35 cycles

72°C - 45 sec.

Sequencing of PCR Products

The PCR products were purified using a Whatman Polyfiltronics 100 μl 384 well unifilter plate essentially according to the manufacturers protocol. The purified DNA was eluted in 50 μl of distilled water. Sequencing reactions were set up using Applied Biosystems Big Dye Terminator .chemistry essentially according to the manufacturers protocol. The purified PCR products were sequenced in both directions using either the primer sets represented below with the positions of their first and last nucleotide corresponding to positions in Figure 1, or the appropriate umversal 'tail' sequence as a primer. Reaction products were purified by isopropanol precipitation, and run on an Applied Biosystems 3700 DNA Analyzer.

Sequencing Primer Pairs

Fragment No . Forward Primer Reverse Primer

Fragment 1 693-712 complement of 1092-1073

Fragment 2 4172-4191 complement of 4665-4646

Fragment 3 27-47 complement of 503-482

Fragment 4 188-207 complement of 707-688

Fragment 5 : Tailed Seq.

Fragment 6 : Tailed Seq.

Analysis of Sequences for Polymoφhic Sites

Sequence information for a minimum of 80 humans was analyzed for the presence of polymoφhisms using the Polyphred program (Nickerson et al., Nucleic Acids Res. 14:2745-2751, 1997).

The presence of a polymoφhism was confirmed on both strands. The polymoφhisms and their locations in the ILIB gene are listed in Table 2 below.

Table 2 . Polymorphic Sites Identified in the ILIB Gene

Polymorph; LC Nucleotide Reference Variant CDS Variant AA

Site Numb(er PolyId^a Position Allele Allele Position Variant

PS1^R 5077411 343 C T

PS2 5077413 346 A T

PS3 9117201 3453 T c

PS4 9117106 3467 G c

PS5 9116916 3614 C T 138 G46G

PS6^R 5077421 4259 G A

PS7^R 5077423 4336 C T 315 F105F

PS8 5077427 6421 A G

PS9 5077439 6883 C A ^aPolyId is a unique ident,ifier assigned to each PS by Genaissance Pharmaceuticals,

Inc.

R '_Report. ed previously in the literature .

EXAMPLE 2

This example illustrates analysis ofthe ILIB polymoφhisms identified in the Index Repository for human genotypes and haplotypes.

The different genotypes containing these polymoφhisms that were observed in the reference population are shown in Table 3 below, with the haplotype pair indicating the combination of haplotypes determined for the individual using the haplotype derivation protocol described below. In Table 3, homozygous positions are indicated by one nucleotide and heterozygous positions are indicated by two nucleotides. Missing nucleotides in any given genotype in Table 3 were inferred based on linkage disequilibrium and/or Mendelian inheritance.

Table 3. Genotypes and Haplotype Pairs Observed for ILIB Gene Genotype Polymorphic Sites ber PS1 PS2 PS3 PS4 PS5 PS 6 PS7 PS8 PS9 HAP Pal

1 C A T G C G c G c 7 7

2 T A C G C A c A C 10 10

3 T A T G C A C A C 14 14

4 T A C G C G T G C 13 13

5 C ^• A T G C G/A C G C/A 7 5

6 C A T G/C C G C/T G C 7 3

7 T A c G C G T/C G C 13 12

8 T A T/C G C G/A C G C 16 11

9 C A T/C G C G C G C 7 2

10 T A C/T G C G T/C G C 13 16

11 T A T G C A/G C A/G C/A 14 15

12 C/T A T/C G C G C G C 7 12

13 c A T/C G C G/A C G C 7 1

14 c A T G C G/A C G C 7 6

15 C/T A T/C G C G/A C G/A C 7 10

16 C/T A T G C G C G C 7 16

17 C/T A T/C G C G C/T G C 7 13

18 C/T A T G C G C/T G C 7 17

19 C/T A/T T G C G/A C G/A C 7 18

20 c A T G C G/A C G/A C 7 4

21 T A T/C G C A/G C/T A/G C 14 13

22 T/C A T G C/T A c A C 14 9

23 T/C A C/T G c A c A c 10 4

24 T/C A T/C G c A c A/G c 14 1

25 T A T G c A/G c A/G c 14 16

26 T A T/C G c A c A c 14 10

27 T/C A c G c A/G c A/G c 10 2

28 C/T A T G c G/A c G/A c 7 14

29 C A T G c G C/T G c 7 8

The haplotype pairs shown in Table 3 were estimated from the unphased genotypes using a computer-implemented extension of Clark's algorithm (Clark, A.G. 1990 Mol Bio Evol 7, 111-122) for assigning haplotypes to unrelated individuals in a population sample, as described in U.S. Provisional Application Serial No. 60/198,340 entitled "A Method and System for Determining Haplotypes from a Collection of Polymoφhisms" and the corresponding International Application filed April 18, 2001. In this method, haplotypes are assigned directly from individuals who are homozygous at all sites or heterozygous at no more than one ofthe variable sites. This list of haplotypes is augmented with haplotypes obtained from two families (one three-generation Caucasian family and one two-generation African- American family) and then used to deconvolute the unphased genotypes in the remaining (multiply heterozygous) individuals.

By following this protocol, it was determined that the Index Repository examined herein and, by extension, the general population contains the 18 human ILIB haplotypes shown in Table 4 below. Table 4. Haplotypes Identified in the ILIB Gene

HAP No. HAP ID Polymorphic Sites

PS PS PS PS PS PS PS PS PS

1 2 3 4 5 6 7 8 9

1 9120012 c A C G C A c G- C

2 9120008 c A C G C G C G C

3 9120016 c A T C C G T G C

4 9120010 c A T G C A C A C

5 9120014 c A T G C A C G A

6 9120013 c A T G C A C G C

7 9120002 c ^' A T G C G C G C

8 9120009 c A T G C G T G C

9 9120015 c A T G T A C A C

10 9120004 T A c G c A c A C

11 9120019 T A c G c A c G C

12 9120011 T A c G c G c G C

13 9120005 T A c G c G T G C

14 9120003 T A T G c A c A C

15 9120017 T A T G c G c G A

16 9120006 T A T G c G c G C

17 9120007 T A T G c G T G C

18 9120018 T T T G c A c A C

Table 5 below shows the percent of chromosomes characterized by a given ILIB haplotype for all unrelated individuals in the Index Repository for which haplotype data was obtained. The percent of these unrelated individuals who have a given ILIB haplotype pair is shown in Table 6. In Tables 5 and 6, the "Total" column shows this frequency data for all of these unrelated individuals, while the other columns show the frequency data for these unrelated individuals categorized according to their self- identified ethnogeographic origin. Abbreviations used in Tables 5 and 6 are AF = African Descent, AS = Asian, CA = Caucasian, HL = Hispanic-Latino, and NA = Native American.

Table 5. Frequency of Observed ILIB Haplotypes In Unrelated Individuals

HAP No. HAP ID Total CA AF AS HL AM

1 9120012 1.22 0.0 2.5 2.5 0.0 0.0

2 9120008 1.83 0.0 0.0 2.5 5.56 0.0

3 9120016 0.61 0.0 2.5 0.0 0.0 0.0

4 9120010 1.83 2.38 2.5 2.5 0.0 0.0

5 9120014 0.61 0.0 2.5 0.0 0.0 0.0

6 9120013 0.61 0.0 2.5 0.0 0.0 0.0

7 9120002 33.54 21.43 50.0 27.5 36.11 33.33

8 9120009 1.83 0.0 7.5 0.0 0.0 0.0

9 9120015 0.61 0.0 0.0 2.5 0.0 0.0

10 9120004 10.37 2.38 5.0 30.0 5.56 0.0

11 9120019 0.61 0.0 0.0 2.5 0.0 0.0

12 9120011 1.83 0.0 2.5 0.0 5.56 0.0

13 9120005 10.98 16.67 5.0 0.0 22.22 16.67

14 9120003 21.34 40.48 7.5 20.0 13.89 33.33

15 9120017 0.61 0.0 2.5 0.0 0.0 0.0

16 9120006 8.54 16.67 5.0 5.0 8.33 0.0

17 9120007 2.44 0.0 2.5 2.5 2.78 16.67

18 9120018 0.61 0.0 0.0 2.5 0.0 0.0

Table 6. Frequency of Observed ILIB Haplotype Pairs In Unrelated Individuals

HAP1 HAP2 Total CA AF AS HL AM

7 7 9.76 4.76 10.0 10.0 16.67 0.0

10 10 4.88 0.0 0.0 20.0 0.0 0.0

14 14 4.88 14.29 0.0 5.0 0.0 0.0

13 13 1.22 4.76 0.0 0.0 0.0 0.0

7 5 1.22 0.0 5.0 0.0 0.0 0.0

7 3 1.22 0.0 5.0 0.0 0.0 0.0

13 12 2.44 0.0 0.0 0.0 11.11 0.0

16 11 1.22 0.0 0.0 5.0 0.0 0.0

7 2 2.44 0.0 0.0 5.0 5.56 0.0

13 16 2.44 4.76 0.0 0.0 5.56 0.0

14 15 1.22 0.0 5.0 0.0 0.0 0.0

7 12 1.22 0.0 5.0 0.0 0.0 0.0

7 1 1.22 0.0 5.0 0.0 0.0 0.0

7 6 1.22 0.0 5.0 0.0 0.0 0.0

7 10 6.1 4.76 10.0 5.0 5.56 0.0

7 16 4.88 9.52 5.0 5.0 0.0 0.0

7 13 6.1 0.0 10.0 0.0 16.67 0.0

7 17 4.88 0.0 5.0 5.0 5.56 33.33

7 18 1.22 0.0 0.0 5.0 0.0 0.0

7 4 2.44 4.76 5.0 0.0 0.0 0.0

14 13 8.54 19.05 0.0 0.0 11.11 33.33

14 9 1.22 0.0 0.0 5.0 0.0 0.0

10 4 1.22 0.0 0.0 5.0 0.0 0.0

14 1 1.22 0.0 0.0 5.0 0.0 0.0

14 16 8.54 19.05 5.0 0.0 11.11 0.0

14 10 2.44 0.0 0.0 10.0 0.0 0.0

10 2 1.22 0.0 0.0 0.0 5.56 0.0

7 14 9.76 14.29 5.0 10.0 5.56 33.33

7 8 3.66 0.0 15.0 0.0 0.0 0.0 The size and composition ofthe Index Repository were chosen to represent the genetic diversity across and within four major population groups comprising the general United States population. For example, as described in Table 1 above, this repository contains approximately equal sample sizes of African-descent, Asian-American, European-American, and Hispanic-Latino population groups. Almost all individuals representing each group had all four grandparents with the same ethnogeographic background. The number of unrelated individuals in the Index Repository provides a sample size that is sufficient to detect SNPs and haplotypes that occur in the general population with high statistical certainty. For instance, a haplotype that occurs with a frequency of 5% in the general population has a probability higher than 99.9% of being observed in a sample of 80 individuals from the general population. Similarly, a haplotype that occurs with a frequency of 10% in a specific population group has a 99% probability of being observed in a sample of 20 individuals from that population group. In addition, the size and composition ofthe Index Repository means that the relative frequencies determined therein for the haplotypes and haplotype pairs ofthe ILIB gene are likely to be similar to the relative frequencies of these ILIB haplotypes and haplotype pairs in the general U.S. population and in the four population groups represented in the Index Repository. The genetic diversity observed for the three Native Americans is presented because it is of scientific interest, but due to the small sample size it lacks statistical significance.

In view ofthe above, it will be seen that the several advantages ofthe invention are achieved and other advantageous results attained.

As various changes could be made in the above methods and compositions without departing from the scope ofthe invention, it is intended that all matter contained in the above description and shown in the accompanying drawings shall be inteφreted as illustrative and not in a limiting sense.

All references cited in this specification, including patents and patent applications, are hereby incoφorated in their entirety by reference. The discussion of references herein is intended merely to summarize the assertions made by their authors and no admission is made that any reference constitutes prior art. Applicants reserve the right to challenge the accuracy and pertinency ofthe cited references.

Claims

What is Claimed is:

1. A method for haplotyping the interleukin 1, beta (ILIB) gene of an individual, which comprises determining which ofthe ILIB haplotypes shown in the table immediately below defines one copy ofthe individual's ILIB gene, wherein each ofthe EL1B haplotypes comprises a set of polymoφhisms whose locations and identities are set forth in the table immediately below:

^bPS = polymoφhic site;

'Position of PS within the indicated SEQ ID NO; ^dRegion examined represents the nucleotide positions defining the start and stop positions within the indicated SEQ ID NO. ofthe sequenced region.

The method of claim 1, wherein the determining step comprises identifying the phased sequence of nucleotides present at each of PS1-PS9 on the one copy ofthe individual's ILIB gene. A method for haplotyping the interleukin 1, beta (ILIB) gene of an individual, which comprises determining which ofthe EL1B haplotype pairs shown in the table immediately below defines both copies ofthe individual's ILIB gene, wherein each ofthe ILIB haplotype pairs consists of first and second haplotypes which comprise first and second sets of polymoφhisms whose locations and identities are set forth in the table immediately below:

shown 5' to 3' as l^stpolymoφhism/2ⁿ polymoφhism in each column; ^bPS = polymoφhic site;

'Position of PS within the indicated SEQ ID NO; ^dRegion examined represents the nucleotide positions defining the start and stop positions within the indicated SEQ ID NO ofthe sequenced region.

4. The method of claim 3, wherein the determining step comprises identifying the phased sequence of nucleotides present at each of PS1-PS9 on both copies ofthe individual's ILIB gene.

5. A method for genotyping the interleukin 1, beta (ILIB) gene of an individual, comprising determining for the two copies ofthe ILIB gene present in the individual the identity ofthe nucleotide pair at one or more polymoφhic sites (PS) selected from the group consisting of PS3, PS4, and PS5, wherein the one or more PS have the location and alternative alleles shown in SEQ ED NO:36.

6. The method of claim 5, wherein the determining step comprises:

(a) isolating from the individual a nucleic acid mixture comprising both copies of the ILIB gene, or a fragment thereof, that are present in the individual;

(b) amplifying from the nucleic acid mixture a target region containing the selected polymoφhic site;

(c) hybridizing a primer extension oligonucleotide to one allele ofthe amplified target region;

(d) performing a nucleic acid template-dependent, primer extension reaction on the hybridized genotyping oligonucleotide in the presence of at least two different terminators ofthe reaction, wherein said terminators are complementary to the alternative nucleotides present at the selected polymoφhic site; and

(e) detecting the presence and identity ofthe terminator in the extended genotyping oligonucleotide.

7. The method of claim 5, further comprising determining the identity ofthe nucleotide at one or more polymoφhic sites selected from the group consisting of PS2, PS8 and PS9.

8. The method of claim 5, which comprises determining for the two copies ofthe ILIB gene present in the individual the identity ofthe nucleotide pair at each of PS1-PS9.

9. A method for haplotyping the interleukin 1, beta (ILIB) gene of an individual which comprises determining, for one copy ofthe ILIB gene present in the individual, the identity ofthe nucleotide at two or more polymoφhic sites (PS) selected from the group consisting of PS3, PS4, and PS5, wherein the selected PS have the location and alternative alleles shown in SEQ ED NO:36.

10. The method of claim 9, further comprising determining the identity ofthe nucleotide at one or more polymoφhic sites selected from the group consisting of PS2, PS8 and PS9, wherein the selected PS have the locations and alternative alleles shown in SEQ ID NO:36.

11. The method of claim 9, further comprising determining the identity of the nucleotide at one or more polymoφhic sites selected from the group consisting of PS1, PS6 and PS7, wherein the selected PS have the locations and alternative alleles shown in SEQ ID NO:36.

12. The method of claim 9, wherein the determining step comprises:

(a) isolating from the individual a nucleic acid sample containing only one ofthe two copies of the ILIB gene, or a fragment thereof, that is present in the individual;

(b) amplifying from the nucleic acid molecule a target region containing the selected polymoφhic site;

(c) hybridizing a primer extension oligonucleotide to one allele ofthe amplified target region;

(d) performing a nucleic acid template-dependent, primer extension reaction on the hybridized genotyping oligonucleotide in the presence of at least two different terminators ofthe reaction, wherein said terminators are complementary to the alternative nucleotides present at the selected polymoφhic site; and

(e) detecting the presence and identity ofthe terminator in the extended genotyping oligonucleotide.

13. A method for predicting a haplotype pair for the interleukin 1, beta (ILIB) gene of an individual comprising:

(a) identifying a EL1B genotype for the individual, wherein the genotype comprises the nucleotide pair at two or more polymoφhic sites (PS) selected from the group consisting of PS3, PS4, and PS5, wherein the selected PS have the location and alternative alleles shown in SEQ ID NO:36;

(b) enumerating all possible haplotype pairs which are consistent with the genotype; (c) comparing the possible haplotype pairs to the haplotype pair data set forth in the table immediately below:

shown 5' to 3' as 1^s polymoφhism/2ⁿ polymoφhism in each column; ^bPS = polymoφhic site;

Position of PS within the indicated SEQ ID NO; ^dRegion examined represents the nucleotide positions defining the start and stop positions within the indicated SEQ ID NO ofthe sequenced region;

and

(d) assigning a haplotype pair to the individual that is consistent with the data. 14. The method of claim 13, further comprising determining the identity ofthe nucleotide at one or more polymoφhic sites selected from the group consisting of PS2, PS8 and PS9.

15. The method of claim 13, wherein the identified genotype ofthe individual comprises the nucleotide pair at each of PS1-PS9, which have the location and alternative alleles shown in SEQ ID NO:36.

16. A method for identifying an association between a trait and at least one haplotype or haplotype pair of the interleukin 1, beta (ILIB) gene which comprises comparing the frequency ofthe haplotype or haplotype pair in a population exhibiting the trait with the frequency ofthe haplotype or haplotype pair in a reference population, wherein the haplotype is selected from haplotypes 1-18 shown in the table presented immediately below, wherein each ofthe haplotypes comprises a set of polymoφhisms whose locations and identities are set forth in the table immediately below:

^bPS = polymoφhic site;

'Position of PS within the indicated SEQ ID NO; ^ddRReeggiioonn eexxaammiinneedd rreepprreesseennttss tthhee nnuucclleeoottiiddee ppoossiittions defining the start and stop positions within the indicated SEQ ED NO. ofthe sequenced region, and wherein the haplotype pair is selected from the haplotype pairs shown in the table immediately below, wherein each ofthe EL1B haplotype pairs consists of first and second haplotypes which comprise first and second sets of polymoφhisms whose locations and identities are set forth in the table immediately below:

shown 5 ' to 3' as 1^st polymoφhism/2^nd polymoφhism in each column; ^bPS = polymoφhic site;

'Position of PS within the indicated SEQ ID NO; ^dRegion examined represents the nucleotide positions defining the start and stop positions wimin the indicated SEQ ED NO ofthe sequenced region,

wherein a higher frequency ofthe haplotype or haplotype pair in the trait population than in the reference population indicates the trait is associated with the haplotype or haplotype pair.

17. The method of claim 16, wherein the trait is a clinical response to a drug targeting ILIB.

18. A composition comprising at least one genotyping oligonucleotide for detecting a polymoφhism in the interleukin 1, beta (ILIB) gene at a polymoφhic site (PS) selected from the group consisting of PS3, PS4, and PS5, wherein the selected PS have the location and alternative alleles shown in SEQ ED NO:36.

19. The composition of claim 18, further comprising at least one genotyping oligonucleotide for detecting a polymoφhism in the interleukin 1, beta (ILIB) gene at a polymoφhic site (PS) selected from the group consisting of PS2, PS8, and PS9.

20. The composition of claim 18, wherein the genotyping oligonucleotide is an allele-specific oligonucleotide that specifically hybridizes to an allele ofthe ILIB gene at a region containing the polymoφhic site.

21. The composition of claim 20, wherein the allele-specific oligonucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NOS:4-9, the complements of SEQ ED NOS:4-9, and SEQ ED NOS: 10-21.

22. The composition of claim 18, wherein the. genotyping oligonucleotide is a primer-extension oligonucleotide.

23. The composition of claim 22, wherein the primer extension oligonucleotide comprises a nucleotide sequence selected from the group consisting of SEQ ID NOS:22-33.

24. A kit for genotyping the interleukin 1, beta (ILIB) gene of an individual, which comprises a set of oligonucleotides designed to genotype each of polymoφhic sites (PS) PS3, PS4, and PS5, wherein the selected PS have the location and alternative alleles shown in SEQ ED NO:36.

25. The kit of claim 24, which further comprises oligonucleotides designed to genotype each of PS2, PS8 and PS9.

26. The kit of claim 24, which further comprises oligonucleotides designed to genotype each of PS1, PS6 and PS7.

27. An isolated polynucleotide comprising a nucleotide sequence selected from the group consisting of:

(a) a first nucleotide sequence which comprises a interleukin 1, beta (ILIB) isogene, wherein the ILIB isogene is selected from the group consisting of isogenes 1-18 shown in the table immediately below and wherein each ofthe isogenes comprises the regions ofthe SEQ ED NOS shown in the table immediately below and wherein each ofthe isogenes 1-18 is further defined by the corresponding set of polymoφhisms whose locations and polymoφhisms are set forth in the table immediately below:

"Alleles for isogenes are presented 5 ' to 3 ' in each column ^bPS = polymoφhic site;

'Position of PS within the indicated SEQ ED NO; ^dRegion examined represents the nucleotide positions defining the start and stop positions within the indicated SEQ ID NO ofthe sequenced region;

(b) a second nucleotide sequence which comprises a fragment ofthe first nucleotide sequence, wherein the fragment comprises one or more polymoφhisms selected from the group consisting of cytosine at PS3, cytosine at PS4, and thymine at PS5, wherein the selected polymoφhism has the location set forth in the table immediately above; and

(c) a third nucleotide sequence which is complementary to the first or second nucleotide sequence.

28. The isolated polynucleotide of claim 27, which is a DNA molecule and comprises both the first and third nucleotide sequences and further comprises expression regulatory elements operably linked to the first nucleotide sequence.

29. A recombinant nonhuman organism transformed or transfected with the isolated polynucleotide of claim 27, wherein the organism expresses a EL1B protein encoded by the first nucleotide sequence.

30. The recombinant organism of claim 29, which is a nonhuman transgenic animal.

31. The isolated polynucleotide of claim 27 which consists ofthe second nucleotide sequence.

32. An isolated polynucleotide comprising a nucleotide sequence selected from the group consisting of:

(a) a coding sequence for a interleukin 1, beta (ILIB) isogene selected from the group consisting of coding sequences 3c, 8c, 13c, 17c, and 9c shown in the table immediately below and wherein each ofthe coding sequences 3c, 8c, 13c, 17c, and 9c comprises SEQ D NO:2 except at each ofthe polymoφhic sites (PS) which have the locations and polymoφhisms set forth in the table immediately below:

Alleles for coding sequence haplotypes are presented 5 ' to 3 ' in each column

'PS = polymoφhic site;

Position of PS within the indicated SEQ ID NO.

and (b) a fragment ofthe coding sequence, wherein the fragment comprises at least one polymoφhism selected from the group consisting of thymine at a position corresponding to nucleotide 138.

33. A recombinant nonhuman organism transformed or transfected with the isolated polynucleotide of claim 32, wherein the organism expresses a mterleu in 1, beta (ILIB) protein encoded by the polymoφhic variant sequence.

34. The recombinant organism of claim 33, which is a nonhuman transgenic animal.

35. A computer system for storing and analyzing polymoφhism data for the interleukin 1, beta gene, comprising:

(a) a central processing unit (CPU);

(b) a communication interface;

(c) a display device;

(d) an input device; and

(e) a database containing the polymoφhism data; wherein the polymoφhism data comprises the haplotypes set forth in the table immediately below: L0

^bPS = polymoφhic site;

'Position of PS within the indicated SEQ ED NO; ^dRegion examined represents the nucleotide positions defining the start and stop positions within the indicated SEQ ED NO. ofthe sequenced region,

L5 and the haplotype pairs set forth in the table immediately below:

10 shown 5 ' to 3 ' as 1^st polymoφhism/2 ,nⁿd^α . polymoφhism in each adjacent column;

'Location of PS within the indicated SEQ ED NO; ^dRegion examined represents the nucleotide positions defining the start and stop positions ofthe sequenced region.

15

shown 5' to 3' as 1^st polymoφhism 2 •>nⁿd^α . polymoφhism in each adjacent column;

'Location of PS within the indicated SEQ ED NO; ^dRegion examined represents the nucleotide positions defining the start and stop positions ofthe sequenced region.

36. A genome anthology for the interleukin 1, beta (ILIB) gene which comprises ILIB isogenes defined by any one of haplotypes 1-18 set forth in the table shown below:

^bPS = polymoφhic site;

'Position of PS within the indicated SEQ ID NO;

"Region examined represents the nucleotide positions defining the start and stop positions within the indicated SEQ ED NO. ofthe sequenced region.