WO2002030949A2 - Haplotypes of the ltb4r gene - Google Patents

Abstract

Novel genetic variants of the Leukotriene B4 Receptor (Chemokine Receptor-Like 1) (LTB4R) gene are described. Various genotypes, haplotypes, and haplotype pairs that exist in the general United States population are disclosed for the LTB4R gene. Compositions and methods for haplotyping and/or genotyping the LTB4R gene in an individual are also disclosed. Polynucleotides defined by the haplotypes disclosed herein are also described.

Description

HAPLOTYPES OF THE LTB4R GENE

RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application Serial No. 60/240,223 Filed October 13, 2000.

FIELD OF THE INVENTION

This invention relates to variation in genes that encode pharmaceutically-important proteins. In particular, this invention provides genetic variants of the human leukotriene b4 receptor (chemokine receptor-like 1 ) (LTB4R) 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 of the 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 alteration(s) 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 of the 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 of the 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 of the 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 of the 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 I 1999 Curr 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 of the 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: 1 134-5).

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 polymoφhisms. 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. 2000 BMJ 320:987-90; Dahl BS 1997 Acta Ps chiatr Scand 96 (Suppl 391): 14-21), in many other cases an individual polymoφhism may be found in a variety of ^■ genomic backgrounds, i.e., different haplotypes, and therefore shows no definitive coupling between the polymoφhism and the causative site for the phenotype (Clark AG et al. 1998 Am J Hum 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 pharmaceutically-important gene for the treatment of inflammatory disorders is the leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) gene or its encoded product. LTB4R is a receptor for LTB4, which is a potent chemoattractant that is primarily involved in inflammation, immune responses, and host defense against infection (Yokomizo et al., Nature 1997; 387:620-624). LTB4 activates inflammatory cells by binding to its cell surface receptor, LTB4R. LTB4 can also bind and activate the intranuclear transcription factor PPAR-alpha, resulting in the activation of genes that terminate inflammatory processes (Devchand et al, Nature 1996; 384:39-43) LTB4R is highly expressed m human leukocytes. In Chinese hamster ovary (CHO) cells stably expressing LTB4R, LTB4 induced increases in intracellular calcium, accumulation of D-myo-ιnosιtol~ l ,4,5-triphosphate, and inhibition of adenylyl cyclase. Furthermore, LTB4R showed marked chemotactic responses toward low concentrations of LTB4 in a pertussis-toxin-sensitive manner. These results suggest that LTB4R is an integral member of the immune response pathway. (Yokomizo et al., Natuie 1997; 387:620-624)

The leukotriene b4 receptor (chemokine receptor-like 1) gene is located on chromosome 14ql 1.2-ql2 and contains 1 exon that encodes a 352 amino acid protein. A reference sequence for the LTB4R gene is shown in the contiguous lines of Figure 1 (Genaissance Reference No. 944346; SEQ ID NO: 1). Reference sequences for the coding sequence (GenBank Accession No. NM_000752) and protein are shown in Figures 2 (SEQ ID NO: 2) and 3 (SEQ ID NO: 3), respectively.

One single nucleotide polymoφhism of thymine or cytosme at nucleotide position 1944 in Figure 1 has been reported in theNCBI SNP Database (rs 1046584). Because of the potential for variation in the LTB4 gene to affect the expression and function of the encoded protein, it would be useful to know whether additional polymoφhisms exist in the LTB4R gene, as well as how such polymoφhisms are combined in different copies of the gene. Such information could be applied for studying the biological function of LTB4R as well as in identifying drugs targeting this protein for the treatment of disorders related to its abnormal expression or function.

SUMMARY OF THE INVENTION

Accordingly, the inventors herein have discovered 9 novel polymoφhic sites in the LTB4R gene. These polymoφhic sites (PS) correspond to the following nucleotide positions in Figure 1 : 1041 (PS 1), 1068 (PS2), 1071 (PS3), 1345 (PS4), 1423 (PS5), 1506 (PS6), 1618 (PS7), 1795 (PS8) and 2044 (PS 10). The polymoφhisms at these sites are adenine or guanine at PS1 , cytosine or adenine at PS2, thymine or cytosine at PS3, guanine or adenine at PS4, cytosine or thymine at PS5, guanine or cytosine at PS6, thymine or cytosine at PS7, guanine or cytosine at PS8 and thymme or guanine at PS10. In addition, the inventors have determined the identity of the alleles at these sites, as well as at the previously identified site at nucleotide position 1944 (PS9), 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 Hispamc/Latmo. From this information, the inventors deduced a set of haplotypes and haplotype pairs for PS 1 -PS 10 in the LTB4R gene, which are shown below in Tables 5 and 4, respectively. Each of these LTB4R haplotypes constitutes a code that defines the variant nucleotides that exist in the human population at this set of polymoφhic sites in the LTB4R gene. Thus each LTB4R haplotype also represents a naturally-occurring lsoform (also referred to herein as an "isogene") of the LTB4R gene. The frequency of each haplotype and haplotype pair within the total reference population and within each of the 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 LTB4R gene in an individual. The genotyping method comprises identifying the nucleotide pair that is present at one or more polymoφhic sites selected from the group consisting of PS 1 , PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS 10 in both copies of the LTB4R gene from the individual. A genotyping composition of the 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 LTB4R polymoφhic sites. A genotyping kit of the invention comprises a set of oligonucleotides designed to genotype each of these novel LTB4R polymoφhic sites. In a preferred embodiment, the genotyping kit comprises a set of oligonucleotides designed to genotype each of PS1-PS 10. The genotyping method, composition, and kit are useful in determining whether an individual has one of the haplotypes in Table 5 below or has one of the haplotype pairs in Table 4 below.

The invention also provides a method for haplotyping the LTB4R gene in an individual. In one embodiment, the haplotyping method comprises determining, for one copy of the LTB4R gene, the identity of the nucleotide at one or more polymoφhic sites selected from the group consisting of PS1 , PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS 10. In another embodiment, the haplotyping method comprises determining whether one copy of the individual's LTB4R gene is defined by one of the LTB4R haplotypes shown in Table 5, below, or a sub-haplotype thereof. In a preferred embodiment, the haplotyping method comprises determining whether both copies of the individual's LTB4R gene are defined by one of the LTB4R haplotype pairs shown in Table 4 below, or a sub-haplotype pair thereof. Establishing the LTB4R 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 LTB4R activity, e.g., inflammatory disorders.

For example, the haplotyping method can be used by the pharmaceutical research scientist to validate LTB4R as a candidate target for treating a specific condition or disease predicted to be associated with LTB4R activity. Determining for a particular population the frequency of one or more of the individual LTB4R haplotypes or haplotype pairs described herein will facilitate a decision on whether to pursue LTB4R as a target for treating the specific disease of interest. In particular, if variable LTB4R activity is associated with the disease, then one or more LTB4R haplotypes or haplotype pairs will be found at a higher frequency in disease cohorts than in appropriately genetically matched controls. Conversely, if each of the observed LTB4R haplotypes are of similar frequencies in the disease and control groups, then it may be inferred that variable LTB4R 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 LTB4R haplotype or haplotype pair, apply the information derived from detecting LTB4R haplotypes in an individual to decide whether modulating LTB4R activity would be useful in treating the disease.

The claimed invention is also useful in screening for compounds targeting LTB4R to treat a specific condition or disease predicted to be associated with LTB4R activity. For example, detecting which of the LTB4R 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 of the LTB4R isoforms present in the disease population, or for only the most frequent LTB4R isoforms present in the disease population. Thus, without requiring any a priori knowledge of the phenotypic effect of any particular LTB4R 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.

Haplotyping the LTB4R 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 LTB4R 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 of the LTB4R haplotype(s) disclosed herein are present in individual patients enables the pharmaceutical scientist to distribute LTB4R 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 LTB4R haplotype or haplotype pair that is associated with response to the drug being studied in the trial, even if this association was previously unknown. 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 LTB4R haplotype or haplotype pair.

In another embodiment, the invention provides a method for identifying an association between a trait and a LTB4R genotype, haplotype, or haplotype pair for one or more of the novel polymoφhiG sites described herein. The method comprises comparing the frequency of the LTB4R genotype, haplotype, or haplotype pair in a population exhibiting the trait with the frequency of the LTB4R genotype or haplotype in a reference population. A higher frequency of the LTB4R genotype, haplotype, or haplotype pair in the trait population than in the reference population indicates the trait is associated with the LTB4R 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 LTB4R haplotype is selected from the haplotypes shown in Table 5, or a sub-haplotype thereof. Such methods have applicability in developing diagnostic tests and therapeutic treatments for inflammatory disorders, In yet another embodiment, the invention provides an isolated polynucleotide comprising a nucleotide sequence which is a polymoφhic variant of a reference sequence for the LTB4R gene or a fragment thereof. The reference sequence comprises the contiguous sequences shown in Figure 1 and the polymoφhic variant comprises at least one polymoφhism selected from the group consisting of guanine at PS 1, adenine at PS2, cytosine at PS3, adenine at PS4, thymine at PS5, cytosine at PS6, cytosine at PS7, cytosine at PS8 and guanine at PS 10. In a preferred embodiment, the polymoφhic variant comprises an additional polymoφhism of cytosine at PS9.

A particularly preferred polymoφhic variant is an isogene of the LTB4R gene. A LTB4R isogene of the invention comprises ademne or guanme at PS1 , cytosine or adenine at PS2, thymme or cytosine at PS3, guanine or adenine at PS4, cytosine or thymine at PS5, guanine or cytosine at PS6, thymine or cytosme at PS7, guanine or cytosine at PS8, thymine or cytosine at PS9 and thymine or guanine at PS 10 The invention also provides a collection of LTB4R isogenes, referred to herein as a LTB4R genome anthology

In another embodiment, the invention provides a polynucleotide comprising a polymoφhic variant of a reference sequence for a LTB4R cDNA or a fragment thereof The reference sequence comprises SEQ ID NO 2 (Fig 2) and the polymoφhic cDNA comprises at least one polymoφhism selected from the group consisting of guanine at a position corresponding to nucleotide 24, adenine at a position corresponding to nucleotide 51, cytosine at a position corresponding to nucleotide 54, adenine at a position corresponding to nucleotide 328, thymine at a position corresponding to nucleotide 406, cytosine at a position corresponding to nucleotide 489, cytosine at a position corresponding to nucleotide 601 , cytosine at a position corresponding to nucleotide 778 and guanine at a position corresponding to nucleotide 1027 In a preferred embodiment, the polymoφhic vaπant comprises an additional polymoφhism of cytosme at a position corresponding to nucleotide 927 A particularly preferred polymoφhic cDNA vaπant composes the coding sequence of a LTB4R isogene defined by haplotypes 1-7, 9 and 10

Polynucleotides complementary to these LTB4R genomic and cDNA variants are also provided by the invention It is believed that polymoφhic vaπants of the LTB4R gene will be useful in studying the expression and function of LTB4R, and in expressing LTB4R protein for use in screening for candidate drugs to treat diseases related to LTB4R activity

In other embodiments, the invention provides a recombinant expression vector comprising one of the polymoφhic genomic and cDNA 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 LTB4R for protein structure analysis and drug binding studies

In yet another embodiment, the invention provides a polypeptide comprising a polymoφhic variant of a reference ammo acid sequence for the LTB4R protein The reference ammo acid sequence comprises SEQ ID NO 3 (Fig 3) and the polymoφhic variant comprises at least one variant ammo acid selected from the group consisting of threonine at a position corresponding to ammo acid position 1 10, tryptophan at a position corresponding to ammo acid position 136, histidine at a position corresponding to ammo acid position 201, arginme at a position corresponding to ammo acid position 260 and alanme at a position corresponding to ammo acid position 343 A polymoφhic variant of LTB4R is useful in studying the effect of the variation on the biological activity of LTB4R as well as on the binding affinity of candidate drugs targeting LTB4R for the treatment of inflammatory disorders

The present invention also provides antibodies that recognize and bind to the above polymoφhic LTB4R protein vaπant Such antibodies can be utilized in a variety of diagnostic and prognostic formats and therapeutic methods.

The present invention also provides nonhuman transgenic animals comprising one or more of the LTB4R polymoφhic genomic variants described herein and methods for producing such animals. The transgenic animals are useful for studying expression of the LTB4R isogenes in vivo, for in vivo screening and testing of drugs targeted against LTB4R protein, and for testing the efficacy of therapeutic agents and compounds for inflammatory disorders in a biological system.

The present invention also provides a computer system for storing and displaying polymoφhism data determined for the LTB4R gene. The computer system comprises a computer processing unit; a display; and a database containing the polymoφhism data. The polymoφhism data includes one or more of the following: the polymoφhisms, the genotypes, the haplotypes, and the haplotype pairs identified for the LTB4R gene in a reference population. In a preferred embodiment, the computer system is capable of producing a display showing LTB4R haplotypes organized according to their evolutionary relationships.

BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 illustrates a reference sequence for the LTB4R gene (Genaissance Reference No. 944346; contiguous lines), 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 polymoφhic site(s) and polymoφhism(s) identified by Applicants in a reference population indicated by the variant nucleotide positioned below the polymoφhic site in the sequence. SEQ ID NO: 1 is equivalent to Figure 1, with the two alternative allelic variants of each polymoφhic 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; WIPO standard ST.25). SEQ ID NO:51 is a modified version of SEQ ID NO: 1 that shows the context sequence of each polymoφhic site, PS 1 -PS 10, in a uniform format to facilitate electronic searching. For each polymoφhic site, SEQ ID NO:51 contains a block of 60 bases of the nucleotide sequence encompassing the centrally-located polymoφhic site at the 30^th position, followed by 60 bases of unspecified sequence to represent that each PS is separated by genomic sequence whose composition is defined elsewhere herein.

Figure 2 illustrates a reference sequence for the LTB4R coding sequence (contiguous lines; SEQ ID NO:2), with the polymoφhic site(s) and polymoφhism(s) identified by Applicants in a reference population indicated by the variant nucleotide positioned below the polymoφhic site in the sequence.

Figure 3 illustrates a reference sequence for the LTB4R protein (contiguous lines; SEQ ID NO:3), with the variant a ino acid(s) caused by the polymoφhism(s) of Figure 2 positioned below the polymoφhic site in the sequence. DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention is based on the discovery of novel variants of the LTB4R gene. As described in more detail below, the inventors herein discovered 10 isogenes of the LTB4R gene by characterizing the LTB4R 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.

Table 1. Po ulation Grou s in the Index Re ositor

The LTB4R isogenes present in the human reference population are defined by haplotypes for 10 polymoφhic sites in the LTB4R gene, 9 of which are believed to be novel. The LTB4R polymoφhic sites identified by the inventors are referred to as PS 1 -PS 10 to designate the order in which they are located in the gene (see Table 3 below), with the novel polymoφhic sites referred to as PS 1, PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS 10. Using the genotypes identified in the Index Repository for PS 1 -PS 10 and the methodology described in the Examples below, the inventors herein also determined the pair of haplotypes for the LTB4R gene present in individual human members of this repository. The human genotypes and haplotypes found in the repository for the LTB4R gene include those shown in Tables 4 and 5, respectively. The polymoφhism and haplotype data disclosed herein are useful for validating whether LTB4R is a suitable target for drugs to treat inflammatory 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 RN product, including promoters, exons, introns, and other untranslated regions that control expression.

Genotype - An unphased 5 Jo 3 ' sequence of nucleotide pair(s) found at one or more polymoφhic 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 polymoφhic 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 of the polymoφhic 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 polymoφhic 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 Jo 3' sequence of nucleotides found at all polymoφhic sites examined herein in a locus on a single chromosome from a single individual.

Sub-haplotype - The 5 Jo 3 ' sequence of nucleotides seen at a subset of the polymoφhic 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 of the following for a specific gene: a listing of the haplotype pairs in each individual in a population; a listing of the 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, mR A, cDNA, coding sequence or the protein encoded thereby, distinguished from other forms by its particular sequence and/or structure. Isogene - One of the isoforms (e.g., alleles) of a gene found in a population. An isogene (or allele) contains all of the polymoφhisms present in the particular isoform of the gene.

Isolated - As applied to a biological molecule such as R A, 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 of the present invention.

Locus - A location on a chromosome or DNA molecule corresponding to a gene or a physical or phenotypic feature, where physical features include polymoφhic sites. 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 polymoφhic site on the two copies of a chromosome from an individual. Phased - As applied to a sequence of nucleotide pairs for two or more polymoφhic sites in a locus, phased means the combination of nucleotides present at those polymoφhic sites on a single copy of the locus is known.

Polymorphic site (PS) - A position on a chromosome or DNA molecule at which at least two alternative sequences are found in a population. Polymorphic variant (variant)- A gene, mRNA, cDNA, polypeptide, protein or peptide whose nucleotide or amino acid sequence varies from a reference sequence due to the presence of a polymoφhism in the gene.

Polymorphism - The sequence variation observed in an individual at a polymoφhic site. Polymoφhisms 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 of the following for a specific gene: location of polymoφhic sites; sequence variation at those sites; frequency of polymoφhisms 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 polymoφhism 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 of the 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 polymoφhic 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 polymoφhic sites in a locus, unphased means the combination of nucleotides present at those polymoφhic sites on a single copy of the locus is not known.

As discussed above, information on the identity of genotypes and haplotypes for the LTB4R gene of any particular individual as well as the frequency of such genotypes and haplotypes in any particular population of individuals is useful for a variety of drug discovery and development applications. Thus, the invention also provides compositions and methods for detecting the novel LTB4R polymoφhisms, haplotypes and haplotype pairs identified herein.

The compositions comprise at least one oligonucleotide for detecting the variant nucleotide or nucleotide pair located at a novel LTB4R polymoφhic site in one copy or two copies of the LTB4R gene. Such oligonucleotides are referred to herein as LTB4R haplotyping oligonucleotides or genotyping oligonucleotides, respectively, and collectively as LTB4R oligonucleotides. In one embodiment, a LTB4R haplotyping or genotyping oligonucleotide is a probe or primer capable of hybridizing to a target region that contains, or that is located close to, one of the novel polymoφhic sites described herein.

As used herein, the term "oligonucleotide" refers to a polynucleotide molecule having less than about 100 nucleotides. A preferred oligonucleotide of the 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 the 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 of the 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.

Haplotyping or genotyping oligonucleotides of the invention must be capable of specifically hybridizing to a target region of a LTB4R polynucleotide. Preferably, the target region is located in a LTB4R 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 another region in the LTB4R polynucleotide or with a non-LTB4R 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 polymoφhisms in the LTB4R gene using the polymoφhism information provided herein in conjunction with the known sequence information for the LTB4R 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 of the molecules is complementary to the nucleotide at the corresponding position of the 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 polymoφhisms, 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 of the primer being complementary to the target region. Alternatively, non-complementary nucleotides may be interspersed into the probe or primer as long as the resulting probe or primer is still capable of specifically hybridizing to the target region.

Preferred haplotyping or genotyping oligonucleotides of the 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 polymoφhic site while not hybridizing to the corresponding region in another allele(s). As understood 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 Ruaήo et al., 87 Proc. Nail. 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 of the invention include ASO probes and ASO primers. ASO probes which usually provide good discrimination between different alleles are those in which a central position of the oligonucleotide probe aligns with the polymoφhic site in the target region (e.g., approximately the 7^th or 8^lh position in a 15mer, the 8^th or 9^ih position in a 16mer, and the 10^th or 1 1^th position in a 20mer). An ASO primer of the 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 polymerase-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; WIPO standard ST.25) at the position of the polymoφhic site to represent that the ASO contains either of the two alternative allelic variants observed at that polymoφhic site.

A preferred ASO probe for detecting LTB4R gene polymoφhisms comprises a nucleotide sequence, listed 5 Jo 3', selected from the group consisting of:

CTGCAGCRCCCCCCT (SEQ ID NO: ) and its complement, AGTTCATMTCTCTGC (SEQ ID NO: 5) and its complement, TCATCTCYCTGCTGG (SEQ ID NO: 6) and its complement, TATCACGRCCATGAG (SEQ ID NO: 7) and its complement, GGCCCGGYGGGTGCT (SEQ ID NO: 8) and its complement, GGAAAACSAACATGA (SEQ ID NO: 9) and its complement, GGCCAGCYACTCGGA (SEQ ID NO: 10) and its complement, GCTCGTGSGGAAGCG (SEQ ID NO: 11) and its complement, and CACTGCCKCCAGCCC (SEQ ID NO: 12) and its complement.

A preferred ASO primer for detecting LTB4R gene polymoφhisms comprises a nucleotide sequence, listed 5^' to 3', selected from the group consisting of:

CATCTTCTGCAGCRC (SEQ ID NO 13), CTAGTGAGGGGGGYG (SEQ ID NO 14) , GTGTAGAGΪTCATMT (SEQ ID NO 15), IAGCCAGCAGAGAKA (SEQ ID NO 16), TAGAGTTCATCTCYC (SEQ ID NO 17) , IGAIAGCCAGCAGRG (SEQ ID NO 18) , CCTGCTTATCACGRC (SEQ ID NO 19) TCTAGACTCATGGYC (SEQ ID NO 20) GGCGATGGCCCGGYG (SEQ ID NO 21) , CCIGCCAGCACCCRC (SEQ ID NO 22) IGCCCTGGAAAACSA (SEQ ID NO 23) , ACAGGCTCATGTTSG (SEQ ID NO 24), TGTGGTGGCCAGCYA (SEQ ID NO 25), CCTATGΪCCGAGTRG (SEQ ID NO 26), GTTAGGGCTCGTGSG (SEQ ID NO 27), CTCAGCCGCTTCCSC (SEQ ID NO 28); GAGCCTCACTGCCKC (SEQ ID NO 29) , and TTGAGAGGGCTGGMG (SEQ ID NC 3:30)

Other oligonucleotides of the invention hybridize to a target region located one to several nucleotides downstream of one of the novel polymoφhic sites identified herein. Such oligonucleotides are useful in polymerase-mediated primer extension methods for detecting one of the novel polymoφhisms described herein and therefore such 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 LTB4R gene polymoφhisms by primer extension terminates in a nucleotide sequence, listed 5' to 3', selected from the group consisting of:

CTTCTGCAGC (SEQ ID NO : 31 ) ; GTGAGGGGGG (SEQ ID NO: 32) TAGAGITCAI (SEQ ID NO : 33 ) ; CCAGCAGAGA (SEQ ID NO:34)

AGTTCATCTC (SEQ ID NO : 35) ; IAGCCAGCAG (SEQ ID NO:36)

GCTTAICACG (SEQ ID NO : 37 ) ; AGACTCAIGG (SEQ ID NO:38)

GATGGCCCGG (SEQ ID NO: 39) ; GCCAGCACCC (SEQ ID NO:40)

CCTGGAAAAC (SEQ ID NO : 41 ) ; GGCTCATGTT (SEQ ID NO:42) GGTGGCCAGC (SEQ ID NO: 3) ; ATGTCCGAGT (SEQ ID NO: 4)

AGGGCTCGTG (SEQ ID NO : 5 ) ; AGCCGCTTCC (SEQ ID NO: 6)

CCTCACTGCC (SEQ ID NO:47); and AGAGGGCTGG (SEQ ID NO:48).

In some embodiments, a composition contains two or more differently labeled LTB4R oligonucleotides for simultaneously probing the identity of nucleotides or nucleotide pairs 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.

LTB4R oligonucleotides of the 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 oligonucleotides may be used in a variety of polymoφhism detection assays, including but not limited to probe hybridization and polymerase extension assays. Immobilized LTB4R oligonucleotides of the 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 LTB4R 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 oligonucleotides 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 LTB4R gene in an individual. As used herein, the terms "LTB4R genotype" and "LTB4R haplotype" mean the genotype or haplotype contains the nucleotide pair or nucleotide, respectively, that is present at one or more of the 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 LTB4R gene. The additional polymoφhic sites may be currently known polymoφhic sites or sites that are subsequently discovered.

One embodiment of a genotyping method of the invention involves isolating from the individual a nucleic acid sample comprising the two copies of the LTB4R gene, mRNA transcripts thereof or cDNA copies thereof, or a fragment of any of the foregoing, that are present in the individual, and determining the identity of the nucleotide pair at one or more polymoφhic sites selected from the group consisting of PS 1 , PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS 10 in the two copies to assign a LTB4R genotype to the individual. As will be readily understood by the skilled artisan, the two "copies" of a gene, mRNA or cDNA (or fragment of such LTB4R molecules) in an individual may be the same allele or may be different alleles. In a preferred embodiment of the method for assigning a LTB4R genotype, the identity of the nucleotide pair at PS9 is also determined. In another embodiment, a genotyping method of the invention comprises determining the identity of the nucleotide pair at each ofPS l-PSlO.

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 LTB4R 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 not present in the mRNA or cDNA. If a LTB4R gene fragment is isolated, it must contain the polymoφhic site(s) to be genotyped.

One embodiment of a haplotyping method of the invention comprises isolating from the individual a nucleic acid sample containing only one of the two copies of the LTB4R gene, mRNA or cDNA, or a fragment of such LTB4R molecules, that is present in the individual and determining in that copy the identity of the nucleotide at one or more polymoφhic sites selected from the group consisting of PS1. PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS10 in that copy to assign a LTB4R haplotype to the individual.

The nucleic acid used in the above haplotyping methods of the invention may be isolated using any method capable of separating the two copies of the LTB4R gene or fragment such as one of the methods described above for preparing LTB4R 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 typically only provide haplotype information on one of the two LTB4R gene copies present in an individual. If haplotype information is desired for the individual's other copy, additional LTB4R clones will usually need to be examined. Typically, at least five clones should be examined to have more than a 90% probability of haplotyping both copies of the LTB4R gene in an individual. In some cases, however, once the haplotype for one LTB4R allele is directly determined, the haplotype for the other allele may be inferred if the individual has a known genotype for the polymoφhic sites of interest or if the haplotype frequency or haplotype pair frequency for the individual's population group is known In some embodiments, the LTB4R haplotype is assigned to the individual by also identifying the nucleotide at PS9 In a particularly preferred embodiment, the nucleotide at each of PS 1 -PS 10 is identified In another embodiment, the haplotyping method comprises determining whether an individual has one or more of the LTB4R haplotypes shown in Table 5 This can be accomplished by identifying, for one or both copies of the individual's LTB4R gene, the phased sequence of nucleotides present at each of PS 1-PS 10 This identifying step does not necessarily require that each of PS 1-PS 10 be directly examined Typically only a subset of PS 1 -PS 10 will need to be directly examined to assign to an individual one or more of the haplotypes shown m Table 5 This is because at least one polymoφhic site in a gene is frequently in strong linkage disequihbnum with one or more other polymoφhic sites in that gene (Drysdale, CM et al 2000 PNAS 97 10483- 10488, Rieder MJ et al Ϊ 999 Natw e Genetics 22 59-62) Two sites are said to be m linkage disequihbnum if the presence of a particular variant at one site enhances the predictability of another vaπant at the second site (Stephens, JC 1999, Mol Diag 4 309-317) Techniques for determining whether any two polymoφhic sites are m linkage disequilibrium are well-known in the art (Weir B S 1996 Genetic Data Analysis II, Sinauer Associates, Inc Publishers, Sunderland, MA)

In another embodiment of a haplotyping method of the invention, a LTB4R 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 PS 1 , PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS 10 m each copy of the LTB4R gene that is present m the individual In a particularly preferred embodiment, the haplotyping method compnses identifying the phased sequence of nucleotides at each of PS 1 -PS 10 m each copy of the LTB4R gene

When haplotyping both copies of the gene, the identifying step is preferably performed with each copy of the 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 of the 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 sιte(s), then detecting a combination of the first and third dyes would identify the polymoφhism in the first gene copy while detecting a combination of the 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 sιte(s) may be determined by amplifying a target regιon(s) containing the polymoφhic sιte(s) directly from one or both copies of the LTB4R gene, or a fragment thereof, and the sequence of the amplified regιon(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, refeπed to as negative-type identification For example, where a SNP is known to be guanine and cytosine m 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 cytosme/cytosine) or not cytosme (and thus guanine/guanme)

The target regιon(s) may be amplified using any ohgonucleotide-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 , Pwc Nat! Acad Set USA 88 189-193, 1991 , WO90/01069), and oligonucleotide hgation 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 transcπption 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 , Pwc 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 of the pair showing a perfect match to one variant of a target sequence and the other member showing a perfect match to a different vaπant 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 of the set have melting temperatures within 5°C, and more preferably withm 2°C, of each other when hybπdiz g to each of the polymoφhic sites being detected

Hybridization of an allele-specific oligonucleotide to a target polynucleotide may be performed with both entities in solution, or such hybπdization 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, streptavidm or avidin-biotm, salt bπdges, 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 of the 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 deπvatized to facilitate the immobilization of the allele specific oligonucleotide or target nucleic acid The genotype or haplotype for the LTB4R gene of an individual may also be determined by hybridization of a nucleic acid sample containing one or both copies of the gene, mRNA, cDNA or fragment(s) thereof, to nucleic acid arrays and subarrays such as described in WO 95/1 1995 The arrays would contain a battery of allele-specific oligonucleotides representing each of the 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 WO91/02087, 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 a\., Nucl. Acids Res. 17:8392, 1989; Ruano et al., Nucl. Acids Res. 19, 6877-6882, 1991 ; WO 93/22456; Turki et al, 7. Clin. Invest. 95: 1635-1641 , 1995). In addition, multiple polymoφhic sites may be investigated by simultaneously amplifying multiple regions of the nucleic acid using sets of allele-specific primers as described in Wallace et al. (WO89/10414).

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

In another aspect of the invention, an individual's LTB4R haplotype pair is predicted from its LTB4R genotype using information on haplotype pairs known to exist in a reference population. In its broadest embodiment, the haplotyping prediction method comprises identifying a LTB4R genotype for the individual at two or more LTB4R polymoφhic sites described herein, accessing data containing LTB4R haplotype pairs identified in a reference population, and assigning a haplotype pair to the individual that is consistent with the genotype data. In one embodiment, the reference haplotype pairs include the LTB4R haplotype pairs shown in Table 4. The LTB4R haplotype pair can be assigned by comparing the individual's genotype with the genotypes corresponding to the haplotype pairs known to exist in the general population or in a specific population group, and determining which haplotype pair is consistent with the genotype of the individual. In some embodiments, the comparing step may be performed by visual inspection (for example, by consulting Table 4). When the genotype of the individual is consistent with more than one haplotype pair, frequency data (such as that presented in Table 7) may be used to determine which of these haplotype pairs is most likely to be present in the individual. This determination may also be performed in some embodiments by visual inspection, for example by consulting Table 7. If a particular LTB4R haplotype pair consistent with the genotype of the individual is more frequent in the reference population than others consistent with the genotype, then that haplotype pair with the highest frequency is the most likely to be present in the individual. In other embodiments, the comparison may be made by a computer-implemented algorithm with the genotype of the individual and the reference haplotype data stored in computer-readable formats. For example, as described in PCT US01/12831 , filed April 18, 2001 , one computer-implemented algorithm to perform this comparison entails enumerating all possible haplotype pairs which are consistent with the genotype, accessing data containing LTB4R haplotype pairs frequency data determined in a reference population to determine a probability that the individual has a possible haplotype pair, and analyzing the determined probabilities to assign a haplotype pair to the individual.

Generally, the reference population should be composed of randomly-selected individuals representing the major ethnogeographic groups of the world. A prefeπed reference population for use in the methods of the 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 of the four population groups named above. A particularly prefeπed reference population includes a 3-generation family representing one or more of the 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 //, / H₂ is equal to p„__w (H H₂) = 2p(H )p(H₂) if H, ≠ H, and p_H__w(H H₂ ) = p(H )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 , Nucleic Acids Res 24 4841 4843, 1996)

In one embodiment of this method for predicting a LTB4R haplotype pair for an individual, the assigning step involves performing the following analysis First, each of the possible haplotype pairs is compared to the haplotype pairs in the reference population Generally, only one of the 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 deπved by subtracting the known haplotype from the possible haplotype pair Alternatively, the haplotype pair in an individual may be predicted from the individual's genotype for that gene using reported methods (e g , Clark et al 1990 Mol Bio Evol 1 1 1 1-22, copendmg PCT/US01/12831 filed Apπl 18, 2001 ) or through a commercial haplotyping service such as offered by Genaissance Pharmaceuticals, Inc (New Haven, CT) 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 System¹" technology (U S Patent No 5,866,404), SMD, or allele-specific long-range PCR (Michalotos-Belom et al , silpt a) The invention also provides a method for determining the frequency of a LTB4R genotype, haplotype, or haplotype pair in a population The method compπses, for each member of the population, determining the genotype or the haplotype pair for the novel LTB4R polymoφhic sites described herein, and calculating the frequency any particular genotype, haplotype, or haplotype pair is found in the population The population may be e g , a reference population, a family population, a same gender 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 of the invention, frequency data for LTB4R 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 LTB4R 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

In one embodiment, the method involves obtaining data on the frequency of the genotype(s), haplotype(s) or haplotype paιr(s) of interest in a reference population as well as in a population exhibiting the trait Frequency data for one or both of the reference and trait populations may be obtained by genotyping or haplotyping each individual in the populations using one or more of the methods described above The haplotypes for the trait population may be determined directly or, alternatively, by a predictive genotype to haplotype approach as 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 of the genotype(s), haplotype(s), or haplotype paιr(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 m the populations are compared If a particular LTB4R 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 LTB4R genotype, haplotype or haplotype pair Preferably, the LTB4R genotype, haplotype, or haplotype pair being compared in the trait and reference populations is selected from the full-genotypes and full-haplotypes shown m Tables 4 and 5, or from sub-genotypes and sub-haplotypes derived from these genotypes and haplotypes Sub-genotypes useful in the invention preferably do not include sub- genotypes solely for any one of PS9 or for any combination thereof

In a preferred embodiment of the method, the trait of interest is a clinical response exhibited by a patient to some therapeutic treatment, for example, response to a drug targeting LTB4R 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 of the following a quantitative measure of the response, no response, and/or adverse response (l e , side effects) In order to deduce a correlation between clinical response to a treatment and a LTB4R 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 tπal 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 of the medical condition of interest This is important m 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 coπelation 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 LTB4R 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 LTB4R genotype or haplotype content are created. Correlations may be produced in several ways. In one method, individuals are grouped by their LTB4R genotype or haplotype (or haplotype pair) (also refeπed 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 of which polymoφhic sites in the LTB4R gene give the most significant contribution to the differences in phenotype. One regression model useful in the invention is described in WO 01/01218, entitled "Methods for Obtaining and Using Haplotype Data". A second method for finding coπelations between LTB4R 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 WO 01/01218. Correlations may also be analyzed using analysis of variation (ANOVA) techniques to determine how much of the variation in the clinical data is explained by different subsets of the polymoφhic sites in the LTB4R gene. As described in WO 01/01218, 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 LTB4R 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 LTB4R 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 of the polymoφhic sites in the LTB4R 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 LTB4R 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 of the LTB4R gene or a fragment of the gene which contains at least one of the novel polymoφhic sites described herein. The nucleotide sequence of a variant LTB4R gene is identical to the reference genomic sequence for those portions of the gene examined, as described in the Examples below, except that it comprises a different nucleotide at one or more of the novel polymoφhic sites PS 1, PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PSl O, and may also comprise an additional polymoφhism of cytosine at PS9. Similarly, the nucleotide sequence of a variant fragment of the LTB4R gene is identical to the corresponding portion of the reference sequence except for having a different nucleotide at one or more of the novel polymoφhic sites described herein. Thus, the invention specifically does not include polynucleotides comprising a nucleotide sequence identical to the reference sequence of the LTB4R gene, which is defined by haplotype 8, (or other reported LTB4R sequences) or to portions of the reference sequence (or other reported LTB4R sequences), except for the haplotyping and genotyping oligonucleotides described above.

The location of a polymoφhism in a variant LTB4R gene or fragment is preferably identified by aligning its sequence against SEQ ID ^"NO: 1. The polymoφhism is selected from the group consisting of guanine at PS 1 , adenine at PS2, cytosine at PS3, adenine at PS4, thymine at PS5, cytosine at PS6, cytosine at PS7, cytosine at PS8 and guanine at PS 10. In a preferred embodiment, the polymoφhic variant comprises a naturally-occuπing isogene of the LTB4R gene which is defined by any one of haplotypes 1 - 7 and 9 - 10 shown in Table 5 below.

Polymoφhic variants of the invention may be prepared by isolating a clone containing the LTB4R gene from a human genomic library. The clone may be sequenced to determine the identity of the nucleotides at the novel polymoφhic sites described herein. Any particular variant or fragment thereof, that is claimed herein could be prepared from this clone by performing in vitro mutagenesis using procedures well-known in the art. Any particular LTB4R variant or fragment thereof may also be prepared using synthetic or semi-synthetic methods known in the art.

LTB4R isogenes, or fragments thereof, may be isolated using any method that allows separation of the two "copies" of the LTB4R 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 Ruano 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 LTB4R genome anthologies, which are collections of at least two LTB4R 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 gender population. A LTB4R genome anthology may comprise individual LTB4R isogenes stored in separate containers such as microtest tubes, separate wells of a microtitre plate and the like. Alternatively, two or more groups of the LTB4R isogenes in the anthology may be stored in separate containers. Individual isogenes or groups of such 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 LTB4R genome anthology of the invention comprises a set of isogenes defined by the haplotypes shown in Table 5 below.

An isolated polynucleotide containing a polymoφhic variant nucleotide sequence of the 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 LTB4R 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 of the nucleic acid sequence in a given host cell. Of course, the coπect 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 LTB4R sequences of the 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. Prefeπed eukaryotic cell lines include COS cells, CHO cells, HeLa cells, NIH/3T3 cells, and embryonic stem cells (Thomson, J. A. et al., 1998 Science 282: 1 145-1 147). Particularly preferred host cells are mammalian cells.

As will be readily recognized by the skilled artisan, expression of polymoφhic variants of the LTB4R gene will produce LTB4R 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 LTB4R cDNA comprising a nucleotide sequence which is a polymoφhic variant of the LTB4R reference coding sequence shown in Figure 2. Thus, the invention also provides LTB4R mRNAs and corresponding cDNAs which comprise a nucleotide sequence that is identical to SEQ ID NO:2 (Fig. 2) (or its corresponding RNA sequence) for those regions of SEQ ID NO:2 that correspond to the examined portions of the LTB4R gene (as described in the Examples below), except for having one or more polymoφhisms selected from the group consisting of guanine at a position corresponding to nucleotide 24, adenine at a position corresponding to nucleotide 51, cytosine at a position corresponding to nucleotide 54, adenine at a position corresponding to nucleotide 328, thymine at a position corresponding to nucleotide 406, cytosine at a position corresponding to nucleotide 489, cytosine at a position corresponding to nucleotide 601, cytosine at a position coπesponding to nucleotide 778 and guanine at a position corresponding to nucleotide 1027, and may also comprise an additional polymoφhism of cytosine at a position coπesponding to nucleotide 927. A particularly preferred polymoφhic cDNA variant comprises the coding sequence of a LTB4R isogene defined by any one of haplotypes 1-7, 9 and 10. Fragments of these variant mRNAs and cDNAs are included in the scope of the invention, provided they contain one or more of the novel polymoφhisms described herein. The invention specifically excludes polynucleotides identical to previously identified LTB4R mRNAs or cDNAs, and previously described fragments thereof. Polynucleotides comprising a variant LTB4R 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 LTB4R gene, mRNA or cDNA 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 of the 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 LTB4R polymoφhic sites identified herein, reference is made to the sense strand of the gene for convenience. However, as recognized by the skilled artisan, nucleic acid molecules containing the LTB4R gene or cDNA 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 of the LTB4R genomic, mRNA and cDNA variants described herein.

Polynucleotides comprising a polymoφhic gene variant or fragment of the invention may be useful for therapeutic puφoses. For example, where a patient could benefit from expression, or increased expression, of a particular LTB4R protein isoform, an expression vector encoding the isoform may be administered to the patient. The patient may be one who lacks the LTB4R 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 LTB4R isogene. Expression of a LTB4R 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 or antisense RNA for the isogene or fragment thereof. Alternatively, oligonucleotides directed against the regulatory regions (e.g., promoter, introns, enhancers, 3 ' untranslated region) of the 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) of the 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, N.Y., 1994). Antisense oligonucleotides may also be designed to block translation of LTB4R mRNA transcribed from a particular isogene. It is also contemplated that ribozymes may be designed that can catalyze the specific cleavage of LTB4R mRNA transcribed from a particular isogene.

The untranslated mRNA, antisense RNA or antisense 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, such molecules 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. The invention also provides an isolated polypeptide comprising a polymoφhic variant of (a) the reference LTB4R amino acid sequence shown in Figure 3 or (b) a fragment of this reference sequence. The location of a variant amino acid in a LTB4R polypeptide or fragment of the invention is preferably identified by aligning its sequence against SEQ ID N0:3 (Fig. 3). A LTB4R protein variant of the invention comprises an amino acid sequence identical to SEQ ID NO:3 for those regions of SEQ ID NO: 3 that are encoded by examined portions of the LTB4R gene (as described in the Examples below), except for having one or more variant amino acids selected from the group consisting of threonine at a position coπesponding to amino acid position 1 10, tryptophan at a position corresponding to amino acid position 136, histidine at a position coπesponding to amino acid position 201, arginine at a position coπesponding to amino acid position 260 and alanine at a position corresponding to amino acid position 343. Thus, a LTB4R fragment of the invention, also referred to herein as a LTB4R peptide variant, is any fragment of a LTB4R protein variant that contains one or more of the amino acid variations shown in Table 2. The invention specifically excludes amino acid sequences identical to those previously identified for LTB4R, including SEQ ID NO: 3, and previously described fragments thereof. LTB4R protein variants included within the invention comprise all amino acid sequences based on SEQ ID NO:3 and having the combination of amino acid variations described in Table 2 below. In prefeπed embodiments, a LTB4R protein variant of the invention is encoded by an isogene defined by one of the observed haplotypes, 1 -7, 9 and 10, shown in Table 5.

Table 2. Novel Polymoφhic Variants of LTB4R

Polymoφhic Amino Acid Position and Identities

Variant

Number 1 10 136 201 260 343 1 A R Y G A

2 A R Y R S

3 A R Y R A

4 A R H G S

5 A R H G A 6 A R H R S

7 A R H R A

8 A W Y G S

9 A w Y G A

10 A w Y R S 1 1 A w Y R A

12 A w H G S

13 A w H G A

14 A w H R S

15 A w H R A 16 T R Y G S

17 T R Y G A

18 T R Y R S

19 T R Y R A

20 T R H G S 21 T R H G A

22 T R H R S

23 T R H R A

24 T W Y G S

25 T w Y G A 26 T w Y R s

27 T w Y R A

28 T w H G S

29 T w H G A

30 T w H R S 31 T w H R A

A LTB4R peptide variant of the invention is at least 6 amino acids in length and is preferably any number between 6 and 30 amino acids long, more preferably between 10 and 25, and most preferably between 15 and 20 amino acids long. Such LTB4R peptide variants may be useful as antigens to generate antibodies specific for one of the above LTB4R isoforms. In addition, the LTB4R peptide variants may be useful in drug screening assays.

A LTB4R variant protein or peptide of the invention may be prepared by chemical synthesis or by expressing an appropriate variant LTB4R genomic or cDNA sequence described above. Alternatively, the LTB4R protein variant may be isolated from a biological sample of an individual having a LTB4R isogene which encodes the variant protein. Where the sample contains two different LTB4R isoforms (i.e., the individual has different LTB4R isogenes), a particular LTB4R isoform of the invention can be isolated by immunoaffinity chromatography using an antibody which specifically binds to that particular LTB4R isoform but does not bind to the other LTB4R isoform.

The expressed or isolated LTB4R protein or peptide may be detected by methods known in the art, including Coomassie blue staining, silver staining, and Western blot analysis using antibodies specific for the isoform of the LTB4R protein or peptide as discussed further below. LTB4R variant proteins and peptides can be purified by standard protein purification procedures known in the art, including differential precipitation, molecular sieve chromatography, ion-exchange chromatography, isoelectric focusing, gel electrophoresis, affinity and immunoaffinity chromatography and the like. (Ausubel et. al, 1987, In Current Protocols in Molecular Biology John Wiley and Sons, New York, New York). In the case of immunoaffinity chromatography, antibodies specific for a particular polymoφhic variant may be used.

A polymoφhic variant LTB4R gene of the invention may also be fused in frame with a heterologous sequence to encode a chimeric LTB4R protein. The non-LTB4R portion of the chimeric protein may be recognized by a commercially available antibody. In addition, the chimeric protein may also be engineered to contain a cleavage site located between the LTB4R and non-LTB4R portions so that the LTB4R protein may be cleaved and purified away from the non-LTB4R portion.

An additional embodiment of the invention relates to using a novel LTB4R protein isoform, or a fragment thereof, in any of a variety of drug screening assays. Such screening assays may be performed to identify agents that bind specifically to all known LTB4R protein isoforms or to only a subset of one or more of these isoforms. The agents may be from chemical compound libraries, peptide libraries and the like. The LTB4R protein or peptide variant may be free in solution or affixed to a solid support. In one embodiment, high throughput screening of compounds for binding to a LTB4R variant may be accomplished using the method described in PCT application WO84/03565, in which large numbers of test compounds are synthesized on a solid substrate, such as plastic pins or some other surface, contacted with the LTB4R protein(s) of interest and then washed. Bound LTB4R protein(s) are then detected using methods well-known in the art.

In another embodiment, a novel LTB4R protein isoform may be used in assays to measure the binding affinities of one or more candidate drugs targeting the LTB4R protein.

In yet another embodiment, when a particular LTB4R haplotype or group of LTB4R haplotypes encodes a LTB4R protein variant with an amino acid sequence distinct from that of LTB4R protein isoforms encoded by other LTB4R haplotypes, then detection of that particular LTB4R haplotype or group of LTB4R haplotypes may be accomplished by detecting expression of the encoded LTB4R protein variant using any of the methods described herein or otherwise commonly known to the skilled artisan.

In another embodiment, the invention provides antibodies specific for and immunoreactive with one or more of the novel LTB4R protein or peptide variants described herein. The antibodies may be either monoclonal or polyclonal in origin. The LTB4R protein or peptide variant used to generate the antibodies may be from natural or recombinant sources (in vitro or in vivo) or produced by chemical synthesis or semi-synthetic synthesis using synthesis techniques known in the art. If the LTB4R protein or peptide variant is of insufficient size to be antigenic, it may be concatenated or conjugated, complexed, or otherwise covalently linked to a carrier molecule to enhance the antigenicity of the peptide. Examples of carrier molecules, include, but are not limited to, albumins (e.g., human, bovine, fish, ovine), and keyhole limpet hemocyanin (Basic and Clinical Immunology, 1991 , Eds. D.P. Stites, and A.I. Ten, Appleton and Lange, Norwalk Connecticut, San Mateo, California). In one embodiment, an antibody specifically immunoreactive with one of the novel protein or peptide variants described herein is administered to an individual to neutralize activity of the LTB4R isoform expressed by that individual. The antibody may be formulated as a pharmaceutical composition which includes a pharmaceutically acceptable carrier.

Antibodies specific for and immunoreactive with one of the novel protein isoforms described herein may be used to immunoprecipitate the LTB4R protein variant from solution as well as react with LTB4R protein isoforms on Western or immunoblots of polyacrylamide gels on membrane supports or substrates. In another preferred embodiment, the antibodies will detect LTB4R protein isoforms in paraffin or frozen tissue sections, or in cells which have been fixed or unfixed and prepared on slides, coverslips, or the like, for use in immunocytochemical, immunohistochemical, and immunofluorescence techniques.

In another embodiment, an antibody specifically immunoreactive with one of the novel LTB4R protein variants described herein is used in immunoassays to detect this variant in biological samples. In this method, an antibody of the present invention is contacted with a biological sample and the formation of a complex between the LTB4R protein variant and the antibody is detected. As described, suitable immunoassays include radioimmunoassay, Western blot assay, immunofluorescent assay, enzyme linked immunoassay (ELISA), chemiluminescent assay, immunohistochemical assay, immunocytochemical assay, and the like (see, e.g., Principles and Practice of Immunoassay, 1991, Eds. Christopher P. Price and David J. Neoman, Stockton Press, New York, New York; Current Protocols in Molecular Biology, 1987, Eds. Ausubel et al., John Wiley and Sons, New York, New York). Standard techniques known in the art for ELISA are described in Methods in Immunodiagnosis, 2nd Ed., Eds. Rose and Bigazzi, John Wiley and Sons, New York 1980; and Campbell et al., 1984, Methods in Immunology, W.A. Benjamin, Inc.). Such assays may be direct, indirect, competitive, or noncompetitive as described in the art (see, e.g., Principles and Practice of Immunoassay, 1991 , Eds. Christopher P. Price and David J. Neoman, Stockton Pres, NY, NY; and Oellirich, M., 1984, J. Clin. Chem. Clin. Biochem., 22:895-904). Proteins may be isolated from test specimens and biological samples by conventional methods, as described in Current Protocols in Molecular Biology, supra. Exemplary antibody molecules for use in the detection and therapy methods of the present invention are intact immunoglobulin molecules, substantially intact immunoglobulin molecules, or those portions of immunoglobulin molecules that contain the antigen binding site. Polyclonal or monoclonal antibodies may be produced by methods conventionally known in the art (e.g., Kohler and Milstein, 1975, Nature, 256:495-497; Campbell Monoclonal Antibody Technology, the Production and Characterization of Rodent and Human Hybridomas, 1985, In: Laboratory Techniques in Biochemistry and Molecular Biology, Eds. Burdon et al., Volume 13, Elsevier Science Publishers, Amsterdam). The antibodies or antigen binding fragments thereof may also be produced by genetic engineering. The technology for expression of both heavy and light chain genes in E. coli is the subject of PCT patent applications, publication number WO 901443, WO 901443 and WO 9014424 and in Huse et al., 1989, Science, 246: 1275-1281. The antibodies may also be humanized (e.g., Queen, C. et al. 1989 Proc. Natl. Acad. Sci.USA 86; 10029).

Effect(s) of the polymoφhisms identified herein on expression of LTB4R may be investigated by various means known in the art, such as by in vitro translation of mRNA transcripts of the LTB4R gene, cDNA orfragment thereof, or by preparing recombinant cells and or nonhuman recombinant organisms, preferably recombinant animals, containing a polymoφhic variant of the LTB4R gene. As used herein, "expression" includes but is not limited to one or more of the following: transcription of the gene into precursor mRNA; splicing and other processing of the precursor mRNA to produce mature mRNA; mRNA stability; translation of the mature mRNA(s) into LTB4R protein(s) (including effects of polymoφhihsms on codon usage and tR A availability); and glycosylation and/or other modifications of the translation product, if required for proper expression and function.

To prepare a recombinant cell of the invention, the desired LTB4R isogene, cDNA or coding sequence may be introduced into the cell in a vector such that the isogene, cDNA or coding sequence remains extrachromosomal. In such a situation, the gene will be expressed by the cell from the extrachromosomal location. In a prefeπed embodiment, the LTB4R isogene, cDNA or coding sequence is introduced into a cell in such a way that it recombines with the endogenous LTB4R gene present in the cell. Such recombination requires the occurrence of a double recombination event, thereby resulting in the desired LTB4R 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 of the skilled practitioner. Examples of cells into which the LTB4R isogene, cDNA or coding sequence may be introduced include, but are not limited to, continuous culture cells, such as COS, CHO, NIH/3T3, and primary or culture cells of the relevant tissue type, i.e., they express the LTB4R isogene, cDNA or coding sequence. Such recombinant cells can be used to compare the biological activities of the different protein variants.

Recombinant nonhuman organisms, i.e., transgenic animals, expressing a variant LTB4R gene, cDNA or coding sequence are prepared using standard procedures known in the art. Preferably, a construct comprising the variant gene, cDNA or coding sequence is introduced into a nonhuman animal or an ancestor of the 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 (or cDNA or coding sequence) of interest, and other components known to those skilled m the art to provide a complete shuttle vector harboπng 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 LTB4R isogene, cDNA or coding sequences 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 LTB4R isogene, cDNA or coding sequence and producing the encoded human LTB4R protein can be used as biological models for studying diseases related to abnormal LTB4R expression and/or activity, and for screening and assaying vaπous candidate drugs, compounds, and treatment regimens to reduce the symptoms or effects of these diseases

An additional embodiment of the invention relates to pharmaceutical compositions for treating disorders affected by expression or function of a novel LTB4R isogene descπbed herein The pharmaceutical composition may comprise any of the following active ingredients a polynucleotide comprising one of these novel LTB4R isogenes (or cDNAs or coding sequences), an antisense oligonucleotide directed against one of the novel LTB4R isogenes, a polynucleotide encoding such an antisense oligonucleotide, or another compound which inhibits expression of a novel LTB4R isogene descπbed herein Preferably, the composition contains the active ingredient in a therapeutically effective amount By therapeutically effective amount is meant that one or more of the symptoms relating to disorders affected by expression or function of a novel LTB4R isogene is reduced and/or eliminated The composition also comprises a pharmaceutically acceptable carrier, examples of which 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 of the pharmaceutical composition may be by any number of routes including, but not limited to oral, intravenous, intramuscular, mtra-arteπal, mtramedullary, mtrathecal, lntraventπcular, 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 of the therapeutically effective dose of active ingredient and/or the appropnate 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 of the disease state, general health, age, weight and gender of the 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 of the 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 LTB4R 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 LTB4R 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 of the invention are described in the following examples. Other embodiments within the scope of the claims herein will be apparent to one skilled in the art from consideration of the specification or practice of the invention as disclosed herein. It is intended that the specification, together with the examples, be considered exemplary only, with the scope and spirit of the 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 of the 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 of the LTB4R 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 of which 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 ID NO:49) and the universal 'tail' sequence for the reverse PCR primers comprises the sequence 5 '- AGGAAACAGCTATGACCAT-3 ' (SEQ ID NO:50). The nucleotide positions of the first and last nucleotide of the forward and reverse primers for each region amplified are presented below and coπespond to positions in SEQ ID O: l (Figure 1).

PCR Primer Pairs

Fragment No. Forward Primer Reverse Primer PCR Product

Fragment 1 430-452 1083- 1061 654 nt

Fragment 2 762-784 1386- 1365 625 nt

Fragment 3 1 1 15-1 138 1714-1695 600 nt

Fragment 4 1420-1442 1924-1905 505 nt

Fragment 5 1670-1691 2199-2177 530 nt

These primer pairs were used in PCR reactions containing genomic DNA isolated from immortalized cell lines for each member of the 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 lO 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. I 10 cycles

72°C - 45 sec. f

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 universal '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 1 520-539 1029- 101 1 Fragment 2 818-837 1333- 1314 Fragment 3 1 157-1 176 1625-1606 Fragment 4 Tailed Fragment 5 Tailed

Analysis of Sequences for Polymorphic 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 LTB4R reference genomic sequence (SEQ ID NO: 1 ) are listed in Table 3 below.

Table 3. Polymoφhic Sites Identified in the LTB4R Gene

Polymoφhic Nucleotide Reference Variant CDS Variant AA

Site Number Polyld(a) Position Allele Allele Position Variant

PS1 944360 1041 A G 24 A8A

PS2 944364 1068 C A 51 1171

PS3 944366 1071 T C 54 S18S

PS4 944370 1345 G A 328 A1 10T

PS5 944372 1423 C T 406 R136W

PS6 944374 1506 G C 489 T163T

PS7 15251703 1618 T C 601 Y201H

PS8 15268870 1795 G C 778 G260R

PS9(R) 15268880 1944 T c 927 G309G

PS 10 15268882 2044 T G 1027 S343A

(a) Polyld is a unique identifier assigned to each PS by Genaissance Pharmaceuticals, Inc. (R) Reported previously.

EXAMPLE 2

This example illustrates analysis of the LTB4R polymoφhisms identified in the Index Repository for human genotypes and haplotypes.

The different genotypes containing these polymoφhisms that were observed in unrelated members of the reference population are shown in Table 4 below, with the haplotype pair indicating the combination of haplotypes determined for the individual using the haplotype derivation protocol described below. In Table 4, homozygous positions are indicated by one nucleotide and heterozygous positions are indicated by two nucleotides. Missing nucleotides in any given genotype in Table 4 were infcπed based on linkage disequilibrium and/or Mendelian inheritance. Table 4. Genotypes and Haplotype Pairs Observed for LTB4R Gene

Genotype Polymoφhic Sites

Number HAP Pair PS 1 PS2 PS3 PS4 PS5 PS6 PS7 PS8 PS9 PS 10

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

2 4 4 A C C G C G T G C T

3 8 8 A C T G C G T G T T

4 7 1 A C/A T/C G C G T G/C C T

5 7 10 A/G C T G C G T G C/T T

6 7 5 A c T G C G T/C G C T

7 7 9 A c T G C/T G T G C T

8 4 1 A C/A c G c G T G/C C T

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

10 7 6 A c T G c G T G C T/G

11 7 4 A c T/C G c G T G C T

12 8 4 A C T/C G c G T G T/C T

13 7 8 A c T G c G T G C/T T

14 7 3 A c T/C G c G/C T G C T

The haplotype pairs shown in Table 4 were estimated from the unphased genotypes using a computer-implemented extension of Clark's algorithm (Clark, A.G. 1990 Mol Bio Evol 7, 1 1 1- 122) for assigning haplotypes to unrelated individuals in a population sample, as described in PCT/US01/12831, 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 of the variable sites. This list of haplotypes is then used to deconvolute the unphased genotypes in the remaining (multiply heterozygous) individuals. In the present analysis, the list of haplotypes was augmented with haplotypes obtained from two families (one three-generation Caucasian family and one two-generation African-American family).

By following this protocol, it was determined that the Index Repository examined herein and, by extension, the general population contains the 10 human LTB4R haplotypes shown in Table 5 below.

A LTB4R isogene defined by a full-haplotype shown in Table 5 below comprises the regions of the SEQ ID NOS indicated in Table 5, with their coπesponding set of polymoφhic locations and identities, which are also set forth in Table 5.

Table 5. Haplotypes of the LTB4R gene.

Regions PS PS Haplotype Number(d)

Examined(a) No.(b) Position(c) 1 2 3 4 5 6 7 8 9 10

430-2199 1 1041/30 A A A A A A A A A G

430-2199 2 1068/150 A C C C C C C C C C

430-2199 3 1071/270 C C C c T T T T T T

430-2199 4 1345/390 G A G G G G G G G G

430-2199 5 1423/5 10 C C C C C C C C T C

430-2199 6 1506/630 G G C G G G G G G G

430-2199 7 1618/750 T T T T C T T T T T

430-2199 8 1795/870 C G G G G G G G G G

430-2199 9 1944/990 C C C C C C C T C T

430-2199 10 2044/1 1 10 T T T T T G T T T T (a) Region examined represents the nucleotide positions defining the start and stop positions within SEQ ID NO: 1 of the regions sequenced;

(b) PS = polymoφhic site;

(c) Position of PS within the indicated SEQ ID NO, with the Im position number referring to SEQ ID NO: 1 and the 2^nd position number referring to SEQ ID NO:51, a modified version of SEQ ID O: l that comprises the context sequence of each polymoφhic site, PS 1 -PS 10, to facilitate electronic searching of the haplotypes;

(d) Alleles for LTB4R haplotypes are presented 5' to 3 ' in each column.

SEQ ID NO: 1 refers to Figure 1 , with the two alternative allelic variants of each polymoφhic site indicated by the appropriate nucleotide symbol. SEQ ID NO:51 is a modified version of SEQ ID NOJ that shows the context sequence of each of PS 1-PS 10 in a uniform format to facilitate electronic searching of the LTB4R haplotypes. For each polymoφhic site, SEQ ID NO:51 contains a block of 60 bases of the nucleotide sequence encompassing the centrally-located polymoφhic site at the 30^lh position, followed by 60 bases of unspecified sequence to represent that each polymoφhic site is separated by genomic sequence whose composition is defined elsewhere herein.

Table 6 below shows the percent of chromosomes characterized by a given LTB4R 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 LTB4R haplotype pair is shown in Table 7. In Tables 6 and 7, 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 6 and 7 are AF = African Descent, AS = Asian, CA = Caucasian, HL = Hispanic-Latino, and AM = Native American.

Table 6. Frequency of Observed LTB4R Haplotypes In Unrelated Individuals

HAP No. HAP ID Total CA AF AS HL AM

1 15281713 1.22 0.0 5.0 0.0 0.0 0.0

2 15281716 0.61 0.0 2.5 0.0 0.0 0.0

3 15281719 0.61 0.0 2.5 0.0 0.0 0.0

4 15281712 4.27 2.38 10.0 2.5 2.78 0.0

5 15281718 0.61 2.38 0.0 0.0 0.0 0.0

6 15281715 1.22 0.0 5.0 0.0 0.0 0.0

7 15281710 67.68 85.71 62.5 50.0 75.0 50.0

8 15281711 22.56 7.14 12.5 47.5 19.44 50.0

9 15281717 0.61 238 0.0 0.0 0.0 0.0

10 15281714 0.61 0.0 0.0 0.0 2.78 0.0 Table 7 Frequency of Observed LTB4R Haplotype Pairs In Unrelated Individuals

HAP1 HAP2 Total CA AF AS HL AM

7 7 4634 7143 350 300 5556 00

4 4 122 00 50 00 00 00 8 8 61 00 00 250 00 00

7 1 122 00 50 00 00 00

7 10 122 00 00 00 556 00

7 5 122 476 00 00 00 00

7 9 122 476 00 00 00 00 4 1 122 00 50 00 00 00

7 2 122 00 50 00 00 00

7 6 244 00 100 00 00 00

7 4 244 476 50 00 00 00

8 4 244 00 00 50 556 00 7 8 3049 1429 250 400 3333 1000

7 3 122 00 50 00 00 00

The size and composition of the Index Repository were chosen to represent the genetic diversity across and within four major population groups compnsmg the general United States population For example, as described in Table 1 above, this repository contains approximately equal sample sizes of Afπcan-descent, Asian- American, European- Ameπcan, and Hispamc-Latmo 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 m 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 999% of being observed m a sample of 80 individuals from the general population Similarly, a haplotype that occurs with a frequency of 10% m 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 of the Index Repository means that the relative frequencies determined therein for the haplotypes and haplotype pairs of the LTB4R gene are likely to be similar to the relative frequencies of these LTB4R 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 of the above, it will be seen that the several advantages of the 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 of the invention, it is intended that all matter contained in the above descπption 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 summaπze 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 of the cited references.

Claims

What is Claimed is:

1. A method for haplotyping the leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) gene of an individual, which comprises determining which of the LTB4R haplotypes shown in the table immediately below defines one copy of the individual's LTB4R gene, wherein the determining step comprises identifying the phased sequence of nucleotides present at each of PS 1 -PS10 on at least one copy of the individual's LTB4R gene, and wherein each of the LTB4R haplotypes comprises a sequence of polymoφhisms whose positions and identities are set forth in the table immediately below:

PS PS Haplotype Number(c)

No.(a) Position(b) 1 2 3 4 5 6 7 8 9 10

1 1041 A A A A A A A A A G

2 1068 A C C C C C C C C C

3 1071 C c C C T T T T T T

4 1345 G A G G G G G G G G

5 1423 C c C C C C C C T C

6 1506 G G C G G G G G G G

7 1618 T T T T C T T T T T

8 1795 C G G G G G G G G G

9 1944 C c C C C C C T C T

10 2044 T T T T T G T T T T

(a) PS = polymoφhic site;

(b) Position of PS within SEQ ID NO: 1 ;

(c) Alleles for haplotypes are presented 5 Jo 3 ' in each column.

A method for haplotyping the leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) gene of an individual, which comprises determining which of the LTB4R haplotype pairs shown in the table immediately below defines both copies of the individual's LTB4R gene, wherein the determining step comprises identifying the phased sequence of nucleotides present at each of PS1-PS 10 on both copies of the individual's LTB4R gene, and wherein each of the LTB4R haplotype pairs consists of first and second haplotypes which comprise first and second sequences of polymoφhisms whose positions and identities are set forth in the table immediately below:

PS PS Haplotype Pair(c) (Part 1)

No.(a) Position(b) 7/7 4/4 8/8 7/1 7/10 7/5 7/9 4/1

1 1041 A/A A7A A/A A/A A/G A/A A/A A/A

2 1068 C/C C/C C/C C/A C/C C/C C/C C/A

3 1071 T/T C/C T/T T/C T/T T/T T/T C/C

4 1345 G/G G/G G/G G/G G/G G/G G/G G/G

5 1423 C/C C/C C/C C/C C/C C/C C/T C/C

6 1506 G/G G/G G/G G/G G/G G/G G/G G/G

7 1618 T/T T/T T/T T/T T/T T/C T/T T/T

8 1795 G/G G/G G/G G/C G/G G/G G/G G/C

9 1944 C/C C/C T/T C/C C/T C/C C/C C/C

10 2044 T/T T/T T/T T/T T/T T/T T/T T/T

PS PS Haplotype Pair(c) (Part 2)

No.(a) Position(b) 7/2 7/6 7/4 8/4 7/8 7/3

1 1041 A/A A/A A/A A/A A/A A/A

2 1068 C/C C/C C/C C/C C/C C/C

3 1071 T/C T/T T/C T/C T/T T/C

4 1345 G/A G/G G/G G/G G/G G/G

5 1423 C/C C/C C/C C/C C/C C/C

6 1506 G/G G/G G/G G/G G/G G/C

7 1618 T/T T/T T/T T/T T/T T/T

8 1795 G/G G/G G/G G/G G/G G/G

9 1944 C/C C/C C/C T/C C/T C/C

10 2044 T/T T/G T/T T/T T/T T/T

(a) PS = polymoφhic site;

(b) Position of PS in SEQ ID NOJ ; (c) Haplotype pairs are represented as I^s' haplotype/2^nd haplotype; with alleles of each haplotype shown 5 ' to 3' as 1^st ρolymoφhism/2^nd polymoφhism in each column.

3. A method for genotyping the leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) gene of an individual, comprising determining for the two copies of the LTB4R gene present in the individual the identity of the nucleotide pair at one or more polymoφhic sites (PS) selected from the group consisting of PS1, PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS 10, wherein the one or more polymoφhic sites (PS) have the position and alternative alleles shown in SEQ ID

NOJ .

4. The method of claim 3, wherein the determining step comprises:

(a) isolating from the individual a nucleic acid mixture comprising both copies of the LTB4R gene, or a fragment thereof, that are present in the individual;

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

(c) hybridizing a primer extension oligonucleotide to one allele of the amplified target region, wherein the oligonucleotide is designed for genotyping the selected polymoφhic site in the target region;

(d) performing a nucleic acid template-dependent, primer extension reaction on the hybridized ^" oligonucleotide in the presence of at least one terminator of the reaction, wherein the terminator is complementary to one of the alternative nucleotides present at the selected polymoφhic site; and (e) detecting the presence and identity of the terminator in the extended oligonucleotide.

5. The method of claim 3, which comprises determining for the two copies of the LTB4R gene present in the individual the identity of the nucleotide pair at each of PS 1 -PS 10.

6. A method for haplotyping the leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) gene of an individual which comprises determining, for one copy of the LTB4R gene present in the individual, the identity of the nucleotide at two or more polymoφhic sites (PS) selected from the group consisting of PS1, PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS10, wherein the selected PS have the position and alternative alleles shown in SEQ ID NOJ.

7. The method of claim 6, further comprising determining the identity of the nucleotide at PS9, wherein the PS has the position and alternative alleles shown in SEQ ID NO: 1.

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

(a) isolating from the individual a nucleic acid sample containing only one of the two copies of the LTB4R gene, or a fragment thereof, that is present in the individual;

(b) amplifying from the nucleic acid sample a target region containing one of the selected polymoφhic sites;

(c) hybridizing a primer extension oligonucleotide to one allele of the amplified target region, wherein the oligonucleotide is designed for haplotyping the selected polymoφhic site in the target region;

(d) performing a nucleic acid template-dependent, primer extension reaction on the hybridized oligonucleotide in the presence of at least one terminator of the reaction, wherein the terminator is complementary to one of the alternative nucleotides present at the selected polymoφhic site; and

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

9. A method for predicting a haplotype pair for the leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) gene of an individual comprising:

(a) identifying a LTB4R genotype for the individual, wherein the genotype comprises the nucleotide pair at two or more polymoφhic sites (PS) selected from the group consisting of PS 1 , PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS 10, wherein the selected PS have the position and alternative alleles shown in SEQ ID NOJ ;

(b) comparing the genotype to the haplotype pair data set forth in the table immediately below; and

(c) determining which haplotype pair is consistent with the genotype of the individual and with the haplotype pair data PS PS Haplotype Pair(c) (Part 1)

No.(a) Position(b) 7/7 4/4 8/8 7/1 7/10 7/5 7/9 4/1

1 1041 A/A A/A A/A A/A A/G A/A A/A A A

2 1068 C/C C/C C/C C/A C/C C/C C/C C/A

3 1071 T/T C/C T/T T/C T/T T/T T/T C/C

4 1345 G/G G/G G/G G/G G/G G/G G/G G/G

5 1423 C/C C/C C/C C/C C/C C/C C/T C/C

6 1506 G/G G/G G/G G/G G/G G/G G/G G/G

7 1618 T/T T/T T/T T/T T/T T/C T/T T/T

8 1795 G/G G/G G/G G/C G/G G/G G/G G/C

9 1944 C/C C/C T/T C/C C/T C/C C/C C/C

10 2044 T/T T/T T/T T/T T/T T/T T/T T/T

PS PS Haplotype Pair(c) (Part 2)

No.(a) Position(b) 7/2 7/6 7/4 8/4 7/8 7/3

1 1041 A/A A/A A/A A/A A/A A/A

2 1068 C/C C/C C/C C/C C/C C/C

3 1071 T/C T/T T/C T/C T/T T/C

4 1345 G/A G/G G/G G/G G/G G/G

5 1423 C/C C/C C/C C/C C/C C/C

6 1506 G/G G/G G/G G/G G/G G/C

7 1618 T/T T/T T/T T/T T/T T/T

8 1795 G/G G/G G/G G/G G/G G/G

9 1944 C/C C/C C/C T/C C/T C/C

10 2044 T/T T/G T/T T/T T/T T/T

(a) PS = polymoφhic site;

(b) Position of PS in SEQ ID NO: 1 ;

(c) Haplotype pairs are represented as 1^st haplotype/2^nd haplotype; with alleles of each haplotype shown 5 ' to 3 ' as 1^st polymoφhism/2^nd polymoφhism in each column.

10. The method of claim 9, wherein the identified genotype of the individual comprises the nucleotide pair at each of PS 1-PS 10, which have the position and alternative alleles shown in SEQ ID NO: 1.

11. A method for identifying an association between a trait and at least one haplotype or haplotype pair of the leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) gene which comprises comparing the frequency of the haplotype or haplotype pair in a population exhibiting the trait with the frequency of the haplotype or haplotype pair in a reference population, wherein the haplotype is selected from haplotypes 1-10 shown in the table presented immediately below, wherein each of the haplotypes comprises a sequence of polymoφhisms whose positions and identities are set forth in the table immediately below: PS PS Haplotype . Number(c)

No.(a) Position(b) 1 2 3 4 5 6 7 8 9 10

1 1041 A A A A A A A A A G

2 1068 A C C C C C C C C C

3 1071 C C C C T T T T T T

4 1345 G A G G G G G G G G

5 1423 C C C C C C C C T C

6 1506 G G C G G G G G G G

7 1618 T T T T C T T T T T

8 1795 C G G G G G G G G G

9 1944 C C C C C C C T C T

10 2044 T T T T T G T T T T

(a) PS = polymoφhic site;

(b) Position of PS within SEQ ID NO: 1 ;

(c) Alleles for haplotypes are presented 5 ' to 3 ' in each column; and wherein the haplotype pair is selected from the haplotype pairs shown in the table immediately below, wherein each of the LTB4R haplotype pairs consists of first and second haplotypes which comprise first and second sequences of polymoφhisms whose positions in SEQ ID NO: 1 and identities are set forth in the table immediately below:

PS PS Haplotype ^' Pair(c) (Part 1)

No.(a) Position(b) 7/7 4/4 8/8 7/1 7/10 7/5 7/9 4/1

1 1041 A/A A/A A/A A/A A/G A/A A/A A/A

2 1068 C/C C/C C/C C/A C/C C/C C/C C/A

3 1071 T/T C/C T/T T/C T/T T/T T/T C/C

4 1345 G/G G/G G/G G/G G/G G/G G/G G/G

5 1423 C/C C/C C/C C/C C/C C/C C/T C/C

6 1506 G/G G/G G/G G/G G/G G/G G/G G/G

7 1618 T/T T/T T/T T/T T/T T/C T/T T/T

8 1795 G/G G/G G/G G/C G/G G/G G/G G/C

9 1944 C/C C/C T/T C/C C/T C/C C/C C/C

10 2044 T/T T/T T/T T/T T/T T/T T/T T/T

PS PS Haplotype . Pair(c) (Part 2) No.(a) Position(b) 7/2 7/6 7/4 8/4 7/8 7/3

1 1041 A/A A/A A/A A/A A/A A/A

2 1068 C/C C/C C/C C/C C/C C/C

3 1071 T/C T/T T/C T/C T/T T/C

4 1345 G/A G/G G/G G/G G/G G/G

5 1423 C/C C/C C/C C/C C/C C/C

6 1506 G/G G/G G/G G/G G/G G/C

7 1618 T/T T/T T/T T/T T/T T/T

8 1795 G/G G/G G/G G/G G/G G/G

9 1944 C/C C/C C/C T/C C/T C/C

10 2044 T/T T/G T/T T/T T/T T/T

(a) PS = polymoφhic site;

(b) Position of PS in SEQ ID NO: 1 ;

(c) Haplotype pairs are represented as 1^st haplotype/2^nd haplotype; with alleles of each haplotype shown 5 ' to 3 ' as 1^st polymoφhism/2"^d polymoφhism in each column; wherein a higher frequency of the haplotype or haplotype pair in the trait population than in the reference population indicates the trait is associated with the haplotype or haplotype pair.

12. The method of claim 1 1 , wherein the trait is a clinical response to a drug targeting LTB4R or to a drug for treating a condition or disease predicted to be associated with LTB4R activity.

13. An isolated oligonucleotide designed for detecting a polymoφhism in the leukotriene b4 receptor (chemokine receptor-like 1 ) (LTB4R) gene at a polymoφhic site (PS) selected from the group consisting of PS 1 , PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS 10, wherein the selected PS have the position and alternative alleles shown in SEQ ID NO: 1.

14. The isolated oligonucleotide of claim 13, which is an allele-specific oligonucleotide that specifically hybridizes to an allele of the LTB4R gene at a region containing the polymoφhic site.

15. The allele-specific oligonucleotide of claim 14, which comprises a nucleotide sequence selected from the group consisting of SEQ ID NOS:4-12, the complements of SEQ ID NOS:4-12, and SEQ ID NOS: 13-30.

16. The isolated oligonucleotide of claim 13, which is a primer-extension oligonucleotide.

17. The primer-extension oligonucleotide of claim 16, which comprises a nucleotide sequence selected from the group consisting of SEQ ID NOS:31-48.

18. A kit for haplotyping or genotyping the leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) gene of an individual, which comprises a set of oligonucleotides designed to haplotype or genotype each of polymoφhic sites (PS) PS1, PS2, PS3, PS4, PS5, PS6, PS7, PS8 and PS10, wherein the selected PS have the position and alternative alleles shown in SEQ ID NO: 1.

19. The kit of claim 18, which further comprises oligonucleotides designed to genotype or haplotype PS9, wherein the selected PS has the position and alternative alleles shown in SEQ ID NO:L

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

(a) a first nucleotide sequence which comprises a leukotriene b4 receptor (chemokine receptorlike 1) (LTB4R) isogene, wherein the LTB4R isogene is selected from the group consisting of isogenes 1- 7 and 9 - 10 shown in the table immediately below and wherein each of the isogenes comprises the regions of SEQ ID NO: 1 shown in the table immediately below and wherein each of the isogenes 1 - 7 and 9 - 10 is further defined by the corresponding sequence of polymoφhisms whose positions and identities are set forth in the table immediately below; and Region PS PS Isogene Number(d)

Examined(a) No.(b) Position(c) 1 2 3 4

430-2199 1 1041 A A A A A A A A G

430-2199 2 1068 A C C C C C C C C

430-2199 3 1071 C C C c T T T T T

430-2199 4 1345 G A G G G G G G G

430-2199 5 1423 C C C C C C C T C

430-2199 6 1506 G G C G G G G G G

430-2199 7 1618 T T T T C T T T T

430-2199 8 1795 C G G G G G G G G

430-2199 9 1944 C C C C C C C C T

430-2199 10 2044 T T T T T G T T T

(a) Region examined represents the nucleotide positions defining the start and stop positions within the 1^st SEQ ID NO of the sequenced region;

(b) PS = polymoφhic site;

(c) Position of PS in SEQ ID NOJ;

(d) Alleles for isogenes are presented 5 ' to 3 ' in each column;

(b) a second nucleotide sequence which is complementary to the first nucleotide sequence.

21. The isolated polynucleotide of claim 20, which is a DNA molecule and comprises both the first and second nucleotide sequences and further comprises expression regulatory elements operably linked to the first nucleotide sequence.

22. A recombinant nonhuman organism transformed or transfected with the isolated polynucleotide of claim 21, wherein the organism expresses a LTB4R protein that is encoded by the first nucleotide sequence.

23. The recombinant nonhuman organism of claim 22, which is a transgenic animal.

24. An isolated fragment of a leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) isogene, wherein the fragment comprises at least 10 nucleotides in one of the regions of SEQ ID NO: 1 shown in the table immediately below and wherein the fragment comprises one or more polymoφhisms selected from the group consisting of guanine at PS l, adenine at PS2, cytosine at PS3, adenine at PS4, thymine at PS5, cytosine at PS6, cytosine at PS7, cytosine at PS8 and guanine at PS 10, wherein the selected polymoφhism has the position set forth in the table immediately below:

Region PS PS 1st Dgene ^"N lumber) :d)

Examined(a) No.(b) Position(c) 1 2 3 4 5 6 7 9 10

430-2199 1 1041 A A A A A A A A G

430-2199 2 1068 A C C C C C C C C

430-2199 3 1071 C C C C T T T T T

430-2199 4 1345 G A G G G G G G G

430-2199 5 1423 C C C C C C C T C

430-2199 6 1506 G G C G G G G G G

430-2199 7 1618 T T T T C T T T T

430-2199 8 1795 C G G G G G G G G

430-2199 9 1944 C C C C C C C C T

430-2199 10 2044 T T T T T G T T T

(a) Region examined represents the nucleotide positions defining the start and stop positions within SEQ ID NOJ of the regions sequenced; (b) PS = polymoφhic site;

(c) Position of PS within SEQ ID NOJ ;

(d) Alleles for LTB4R isogenes are presented 5 ' to 3 ' in each column.

25. An isolated polynucleotide comprising a coding sequence for a LTB4R isogene, wherein the coding sequence comprises the regions of SEQ ID NO:2, except at each of the polymoφhic sites which have the positions in SEQ ID NO:2 and polymoφhisms set forth in the table immediately below:

PS PS Isogene Coding Sequence Number(c)

No.(a) Position(b) lc 2c 3c 4c 5c 6c 7c 9c 10c

1 24 A A A A A A A A G

2 51 A C C C C C C C C

3 54 C c C C T T T T T

4 328 G A G G G G G G G

5 406 C c C C C C C T C

6 489 G G c G G G G G G

7 601 T T T T C T T T T

8 778 c G G G G G G G G

9 927 c C C C C C C C T

10 1027 T T T T T G T T T

(a) PS = polymoφhic site;

(b) Position of PS in SEQ ID NOJ;

(c) Alleles for the isogene coding sequence are presented 5 ' to 3 ^' in each column; the numerical portion of the isogene coding sequence number represents the number of the parent full LTB4R isogene.

26. A recombinant nonhuman organism transformed or transfected with the isolated polynucleotide of claim 25, wherein the organism expresses a leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) protein that is encoded by the polymoφhic variant sequence.

27. The recombinant nonhuman organism of claim 26, which is a transgenic animal.

28. An isolated fragment of a LTB4R coding sequence, wherein the fragment comprises one or more polymoφhisms selected from the group consisting of guanine at a position corresponding to nucleotide 24, adenine at a position corresponding to nucleotide 51 , cytosme at a position coπesponding to nucleotide 54, adenine at a position corresponding to nucleotide 328, thymine at a position corresponding to nucleotide 406, cytosine at a position coπesponding to nucleotide 489, cytosine at a position coπesponding to nucleotide 601 , cytosine at a position coπesponding to nucleotide 778 and guanine at a position corresponding to nucleotide 1027 in SEQ ID NO 2 An isolated polypeptide comprising an amino acid sequence which is a polymoφhic variant of a reference sequence for the leukotriene b4 receptor (chemokine receptor like 1) (LTB4R) protein, wherein the reference sequence compπses SEQ ID NO 3, except the polymoφhic vaπant compnses one or more variant amino acids selected from the group consisting of threonine at a position corresponding to ammo acid position 1 10, tryptophan at a position corresponding to ammo acid position 136, histidme at a position corresponding to ammo acid position 201, argmine at a position corresponding to ammo acid position 260 and alanine at a position corresponding to ammo acid position 343 An isolated monoclonal antibody specific for and immunoreactive with the isolated polypeptide of claim 29 A method for screening for drugs targeting the isolated polypeptide of claim 29 which compπses contacting the LTB4R polymoφhic variant with a candidate agent and assaying for binding activity. An isolated fragment of a LTB4R protein, wherein the fragment compπses one or more vaπant ammo acids selected from the group consisting of threonine at a position coπesponding to amino acid position 110, tryptophan at a position coπesponding to ammo acid position 136, histidme at a position corresponding to ammo acid position 201, arginme at a position corresponding to ammo acid position 260 and alanine at a position corresponding to ammo acid position 343 in SEQ ID NO 3 A computer system for storing and analyzing polymoφhism data for the leukotriene b4 receptor (chemokine receptor-like 1) gene, compπsing

(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 any one or more of the haplotypes set forth in the table immediately below PS PS Haplotype Number(c)

No. (a) Position(b) 1 2 3 4 5 6 7 8 9 10

1 1041 A A A A A A A A A G

2 1068 A C C C C C C C C C

3 1071 C C C c T T T T T T

4 1345 G A G G G G G G G G

5 1423 C C C C C C C C T C

6 1506 G G C G G G G G G G

7 1618 T T T T C T T T T T

8 1795 c G G G G G G G G G

9 1944 c C C C C C C T C T

10 2044 T T T T T G T T T T

(a) PS = polymoφhic site;

(b) Position of PS within SEQ ID NO: 1;

(c) Alleles for haplotypes are presented 5 ' to 3 ' in each column; the haplotype pairs set forth in the table immediately below:

PS PS Haplotype Pair(c) (Part 1 )

No.(a) Position(b) 7/7 4/4 8/8 7/1 7/10 7/5 7/9 4/1

1 1041 A/A A/A A/A A/A A/G A/A A A A/A

2 1068 C/C C/C C/C C/A C/C C/C C/C C/A

3 1071 T/T C/C T/T T/C T/T T/T T/T C/C

4 1345 G/G G/G G/G G/G G/G G/G G/G G/G

5 1423 C/C C/C C/C C/C C/C C/C C/T C/C

6 1506 G/G G/G G/G G/G G/G G/G G/G G/G

7 1618 T/T T/T T/T T/T T/T T/C T/T T/T

8 1795 G/G G/G G/G G/C G/G G/G G/G G/C

9 1944 C/C C/C T/T C/C C/T C/C C/C C/C

10 2044 T/T T/T T/T T/T T/T T/T T/T T/T

PS PS Haplotype Pair(c) (Part 2)

No.(a) Position(b) 7/2 7/6 7/4 8/4 7/8 7/3

1 1041 A/A A/A A/A A/A A/A A/A

2 1068 C/C C/C C/C C/C C/C C/C

3 1071 T/C T/T T/C T/C T/T T/C

4 1345 G/A G/G G/G G/G G/G G/G

5 1423 C/C C/C C/C C/C C/C C/C

6 1506 G/G G/G G/G G/G G/G G/C

7 1618 T/T T/T T/T T/T T/T T/T

8 1795 G/G G/G G/G G/G G/G G/G

9 1944 C/C C/C C/C T/C C/T C/C

10 2044 T/T T/G T/T T/T T/T T/T

(a) PS = polymoφhic site; (b) Position of PS in SEQ ID NOJ ;

(c) Haplotype pairs are represented as I^s haplotype/2ⁿ haplotype; with alleles of each haplotype shown 5 ' to 3' as l^sl polymoφhism/2^nd polymoφhism in each column;

and the frequency data in Tables 6 and 7. 34. A genome anthology for the leukotriene b4 receptor (chemokine receptor-like 1) (LTB4R) gene which comprises two or more LTB4R isogenes selected from the group consisting of isogenes 1 - 10 shown in the table immediately below, and wherein each of the isogenes comprises the regions of SEQ ID NO: 1 shown in the table immediately below and wherein each of the isogenes 1-10 is further defined by the coπesponding sequence of polymoφhisms whose positions and identities are set forth in the table immediately below:

Region PS PS Isogene lumbei r(d)

Examined(a) No.(b) Position(c) 1 2 3 4 5 6 7 8 9 10

430-2199 1 1041 A A A A A A A A A G

430-2199 2 1068 A C C C C C C C C C

430-2199 3 1071 C C C C T T T T T T

430-2199 4 1345 G A G G G G G G G G

430-2199 5 1423 C C C C C C C C T C

430-2199 6 1506 G G C G G G G G G G

430-2199 7 1618 T T T T C T T T T T

430-2199 8 1795 C G G G G G G G G G

430-2199 9 1944 C C C C C C C T C T

430-2199 10 2044 T T T T T G T T T T

(a) Region examined represents the nucleotide positions defining the start and stop positions within SEQ ID NOJ of the regions sequenced;

(b) PS = polymoφhic site;

(c) Position of PS within SEQ ID NOJ;

(d) Alleles for LTB4R isogenes are presented 5' to 3 ' in each column.