Leukotriene B4 receptor locus gene characterisation and association studies in asthma

Background Polymorphisms spanning genes involved in the production of leukotriene B4 (LTB4) e.g. ALOX5AP and LTA4H are associated with asthma susceptibility, suggesting a role for LTB4 in disease. The contribution of LTB4receptor polymorphism is currently unknown. The aim of this study was to characterise the genes for the two pivotal LTB4 receptors, LTB4R1 and LTB4R2 in lung tissue and determine if polymorphisms spanning these genes are associated with asthma and disease severity. Methods Rapid amplification of cDNA ends (RACE) was used to characterise the LTB4R1 and LTB4R2 gene structure in lung. The LTB4R1/2 locus on chromosome 14q11.2 was screened for polymorphic variation. Six LTB4R single nucleotide polymorphisms (SNPs) were genotyped in 370 Caucasian asthma families and 299 Adult Asthma Individuals (n=1877 total) and were evaluated for association with asthma and severity (BTS) outcome measures using Family Based Association Test, linear regression and chi square. Results LTB4R1 has complex mRNA arrangement including multiple 5′-untranslated exons, suggesting additional levels of regulation. Three potential promoter regions across the LTB4R1/2 locus were identified with some airway cell specificity. 22 SNPs (MAF>0.01) were validated across the LTB4R locus in the Caucasian population. LTB4R1 and LTB4R2 SNPs were not associated with asthma susceptibility, FEV1 or severity. Conclusions LTB4R1 and LTB4R2 shows splice variation in the 5′-untranslated region and multiple promoter regions. The functional significance of this is yet to be determined. Both receptor genes were shown to be polymorphic. LTB4R polymorphisms do not appear to be susceptibility markers for the development of asthma in Caucasian subjects.


Background
Asthma is a multifactorial respiratory disease with genetic and environmental contributing factors. Leukotrienes are lipid mediators known to be involved in allergic conditions such as asthma and are generated by a series of enzymes and proteins which form the 5lipoxygenase (5-LO) pathway [1]. There are two types of leukotriene; cysteinyl leukotrienes (CysLTs), which are potent bronchoconstrictors, and the dihydroxy leukotriene, leukotriene B 4 (LTB 4 ) a chemoattractant and activator of leukocytes. CysLTs have long been reported as important mediators contributing to inflammatory diseases such as asthma [2]. Recent data supports a role for LTB 4 in asthma pathophysiology. LTB 4 is elevated in the airways of asthma subjects and its concentration correlates with asthma severity [3,4].
Polymorphisms within genes encoding constituents of the 5-LO pathway provide excellent candidates for markers of asthma susceptibility. Polymorphisms in two 5-LO pathway genes; 5-lipoxygenase activating protein (ALOX5AP) and leukotriene A 4 hydrolase (LTA4H) have shown an association with LTB 4 overproduction from ionomycin-stimulated neutrophils and with myocardial infarction (MI) susceptibility [5,6]. 5-lipoxygenase activating protein (FLAP) is an adapter protein for the ratelimiting enzyme 5-lipoxygenase and is involved in the production of all leukotrienes; however LTA 4 H is specifically involved in LTB 4 production. We and others have recently provided preliminary evidence that SNPs spanning ALOX5AP and LTA4H are asthma susceptibility markers and determinants of lung function [7,8]. Polymorphisms spanning ALOX5, LTC4S, CYSLTR1 and CYSLTR2 have also shown association with asthmarelated traits, reviewed in [9].
Two G protein-coupled receptors (GPCRs) for LTB 4 encoded by LTB4R1 and LTB4R2 have been described and are located together on chromosome 14q11.2 [10,11]. LTB 4 via its receptors is important in the recruitment and activation of leukocytes to sites of inflammation [12] and these receptors have been proposed as potential therapeutic targets in asthma. Increasing our understanding of the expression, regulation and potential function of these receptors may provide important information for the design of therapeutic agents. Currently, relatively little is known about LTB4R1 and LTB4R2 gene structure, splice variation and polymorphic variation and the contribution of polymorphic variation to asthma and disease severity.
The aims of this study were to 1) investigate the gene structure of human LTB4R1 and LTB4R2 in cells and tissues relevant to asthma; 2) determine the extent and nature of polymorphic variation across the receptor locus and 3) determine if LTB4R polymorphisms were associated with asthma, lung function and disease severity in asthma families and adult asthma subjects. Our data suggest that LTB4R1 and LTB4R2 have complicated gene structure and are polymorphic and that polymorphisms spanning the LTB4R locus are not determinants of asthma susceptibility.

Methods
Cell culture and RNA/cDNA preparation Human airway smooth muscle (HASM) cells were isolated and cultured as previously described [13]. Primary human bronchial epithelial cells (HBEC) were obtained from Lonza (Wokingham, UK) and cultured in bronchial epithelial growth medium (BEGM, Lonza, UK), using bronchial epithelial differentiation medium (BEDM, Lonza, UK) cells were differentiated at air-liquid interface [14,15]. The bronchial epithelial cell line BEAS-2B and a leukemic monocyte cell line, THP-1, were also cultured as described previously [14,16]. Commercial RNA for the lung, brain and placenta was obtained from Ambion (Huntingdon, UK) and peripheral blood mononuclear cells (PBMC), polymorphonuclear cells (PMN) was obtained from 3H Biomedical (Uppsala, Sweden). Cells were lysed and RNA extracted (from at least two different donors) using the RNeasy mini kit (Qiagen, Crawley, UK), as described by the manufacturer. cDNA was prepared using the Superscript first strand cDNA synthesis kit (Invitrogen, Paisley, UK) using random hexamers and 0.5-1.0μg total RNA per reaction, as directed by manufacturer.

Rapid amplification of cDNA ends (RACE)
RACE was performed using the GeneRacer kit (Invitrogen) and Superscript II as directed [14]. RACE-ready lung cDNA was synthesised from 1μg total lung RNA obtained from Ambion (Huntingdon, UK) as described. Gene-specific primers were designed for 5 0 and 3 0 RACE in the coding region in an overlapping fashion. Plasmid DNA from RACE PCR clones was prepared using the DNA Miniprep kit (Qiagen) and sequenced with M13F and M13R vector primers using Big Dye v3.1 (Applied Biosystems) and an ABI 310 DNA sequencer. Sequence data was aligned to the human database using the Basic Local Alignment Search Tool (BLAST) 2 sequence alignment program.

Polymorphism screening
The extended LTB4R1 and LTB4R2 genomic region identified by RACE (~11.5kb, NCBI build 37: +14:24776125-24787584) was amplified by multiple PCR reactions and screened for polymorphisms by direct sequencing using DNA extracted from whole blood of 35 individuals from the Nottingham Adult Asthma Cohort recruited on the basis of physician diagnosed asthma and no other respiratory illness with <10 packyears smoking history. These subjects had severe asthma as defined by British Thoracic Society (BTS) step ≥ 3. Single nucleotide polymorphisms (SNPs) were identified by examining chromatograms and BLAST analysis of sequencing traces. Any potential SNP identified was validated by sequencing on the reverse strand of DNA. Ethical approval was obtained from the Nottingham University Hospitals local ethics committee.

Subjects for association analyses
341 Caucasian families (n=1508) with at least two biological siblings with physician diagnosed asthma were recruited from the Southampton area. This cohort has been described in detail previously [17]. Baseline FEV 1 (forced expiratory volume in one second) was measured as best of three values within 5% performed using Vitalograph dry-wedge bellows spirometer (Vitalograph Ltd, Buckingham, UK) and determined 14 days after respiratory tract infection or use of bronchodilator or antiallergic medication. 46 Caucasian families (n=184) with at least two biological siblings with physician diagnosed asthma from the Nottingham area [17] were also recruited. Baseline lung function tests were performed, FEV 1 defined as the best of three values. The Nottingham and Southampton cohorts were combined to generate a UK family cohort (n=370). A cohort comprising 299 unrelated adult European Caucasian individuals recruited from Nottingham and Padova was used [18]. Individuals were 16-60 years, had asthma for >1 year with no other respiratory illness and <10 pack-years smoking history. Baseline FEV 1 was measured. All subjects were classified according to British Thoracic Society Step Guidelines (BTS steps, ranging from step 1 to step 5) based on physician prescribed medication [19]. Ethical approval was obtained from the Nottingham University Medical School, the Padova Local Ethics Committees and the Southampton and South West Hampshire and the Portsmouth and South East Hampshire Local Research Ethics Committees. Informed consent was provided by the adult (or parent/guardian for child subjects).

SNP selection and genotyping
LTB4R SNPs were chosen for their ability to tag linkage disequilibrium (LD) blocks using Tagger software [20] or for inferred function. Sequencing data from the severe asthma subjects and available HapMap data (Build 36) were used to select the six SNPs for analysis. We acknowledge a limitation of the current study is the use of this available HapMap build that has now post SNP selection been superseded by 1000 genomes data. Six SNPs which captured the information for eight SNPs were selected. SNPs were also chosen due to potential functional significance. rs11158635 (LTB4R2, 5 0 UTR) tagged two SNPs (rs11158634 and rs2748543, both LTB4R2, 5 0 UTR) and rs3181384 (LTB4R1, 3 0 UTR) previously showed association with cardioembolic stroke in another study [21]. rs2224122 (LTB4R2, 5 0 UTR) was predicted as an intronic enhancer according to FASTSNP algorithm [22]. SNPs were genotyped by KBiosciences using KASPar (Hertfordshire, UK). Chi square was used to test for any deviation of the observed genotype frequency from the expected values under Hardy Weinberg Equilibrium. Allele frequencies between the UK and Italian subjects were not statistically different (data not shown).

Association analyses
The family based association test (FBAT) software (version 1.5.1) [23] was used for association analyses in the family cohorts between LTB4R SNPs and phenotypic scores using the additive model. For analysis in the Adult Asthma Cohort, SPSS (version 15, SPSS Inc., Chicago, IL) was used to determine the contribution of each SNP to baseline percent predicted FEV 1 using linear regression in the additive model. For dichotomised phenotypes, unadjusted contingency table analysis using the allelic model was completed using GraphPad Prism (version 5, San Diego, CA). Analyses in the adult asthma cohort were not corrected for any potential confounders to enable comparison of the association analysis between family-based and adult cohorts. Based on our study with six SNPs and three outcomes analysed, Bonferroni correction would suggest a p<0.003 when reporting results as statistically significant. There was between 0.814 (for a MAF of 0.096) and 0.990 (for a MAF of 0.494) power to detect an association with a significance level of p=0.05 and a relative risk of 1.5.

Identification of LTB4R1 and LTB4R2 splice variants and promoter regions
There was ubiquitous expression of LTB4R1 and LTB4R2 mRNA in the airway and periphery cells, including lung, HASM, HBEC, PBMC, PMN, BEAS-2B and THP-1 (data not shown). 5 0 RACE data for LTB4R1 and LTB4R2 was generated for lung tissue ( Figure 1). Three LTB4R1 5 0 variants were identified by 5 0 RACE in the lung which suggested a structure of four exons, with exon four (containing the protein coding region) being present in every variant identified. LTB4R1 5 0 variant A was the most prevalent present in 50% of clones analysed (10 clones). A PCR-based assay validated this variant in lung, HASM, HBEC, PBMC, PMN, BEAS-2B and THP-1 ( Figure 2). LTB4R1 5 0 variant B was present in 35% of clones (7 clones). LTB4R1 5 0 variant C was identified at lower frequency, 15% of clones (3 clones). LTB4R1 5 0 RACE data suggested the presence of two potential transcription start sites (TSS), at position −4150 to −4148 and one in the region −748 to −758 relative to the LTB4R1 ATG. 3 0 RACE data from the lung identified the presence of two variants; LTB4R1 3 0 variant 1 present in 55% of clones (11 clones) and LTB4R1 3 0 variant 2 was present in 45% of clones (9 clones). LTB4R2 showed a more conserved structure based on RACE data. Only one 5 0 structure was identified in all clones analysed (20 clones) which was validated in lung, HBEC, PBMC, BEAS-2B and THP-1 using PCR ( Figure 2). The 3 0 RACE data also showed a conserved structure, a 310bp untranslated region in all (n=20) clones analysed ( Figure 1). We conducted an in silico analysis of the region 1.5kb upstream of the predicted three transcription start sites (data not shown). Multiple consensus sequences for Sp-1, AP-1 (activator protein 1), GATA, cAMP-response element binding protein, STAT (signal transducer and activator of transcription) and GR (glucocorticoid receptor) were identified.  (Table 1 and Figure 1). Four were novel SNPs and identified at low frequency (MAF <0.01) at position −7686, -5918, -5866, -5737 (in the LTB4R2 5 0 -untranslated region), all positions are relative to the LTB4R1 ATG. 18 of these SNPs have now been reported (1000genomes and NCBI Build 37). Of note, the non-synonymous SNPs identified in Asian populations in LTB4R1 (rs34645221, Ala79Ser and rs17849864, Leu346Phe) and LTB4R2 (rs1950504, Asp196Gly) were not validated in the UK population analysed. Two synonymous coding region SNPs were identified, both in LTB4R1. rs3742511 (Ser18Ser) located in the extracellular N-terminus and rs1046584 (Gly309Gly) located in the cytosolic C-terminus.
LTB4R polymorphisms are not associated with asthma, lung function or disease severity The clinical characteristics for all study cohorts are shown in Table 2. The family cohort contains children with asthma (mean age sibling 1 was 13.3±4.4 years and sibling 2 was 10.3±4.6 years) and the second asthma cohort is comprised of asthma adults (mean age 39.2±12.3 years, n=299). Genotyping data for the six SNPs did not show deviation from the Hardy-Weinberg Equilibrium (p>0.05). Minor allele frequencies (MAF) were similar across the different study cohorts. The haplotype structure of the LTB4R region generated using the genotyping data in the cohorts is shown in Figure 3. Analysis of LD across these SNPs indicated some redundancy in the genotyping with high LD between several LTB4R SNPs e.g. rs11158635, rs2516564 and rs2224122. Exon 4 (ORF) Exon 5  Table 3.
Our data indicate no LTB4R SNPs tested were associated with asthma diagnosis, FEV 1 or severity (BTS) in the families (Table 3). In the Adult Asthma Cohort we completed baseline percent predicted FEV 1 analyses (Table 4), and again did not observe any significant associations. We retrospectively evaluated SNPs spanning ALOX5AP (8 SNPs) and LTA4H (6 SNPs) that encode for proteins involved in LTB 4 production and had previously been associated with asthma susceptibility [7] with BTS defined severity (step 1-5). Interestingly, while no association survived correction for multiple testing, modest associations in the family cohort were observed with multiple ALOX5AP SNPs, e.g. SG13S41G (intron 4) (p=0.005, z=+2.778) and SG13S114A (intron 1) (p=0.017, z=+2.397). LTA4H SNP also showed modest association e.g., rs2540482C (5 0 UTR) (p=0.014, z= −2.468) ( Table 5). Our previous study [7] analysed the effect of these same SNPs in determining asthma severity, but used an in house generated asthma severity score, which showed the same SG13S41G SNP with a p=0.021 and the same direction of effect as the present study. In the Adult Asthma Cohort dichotomised analysis of BTS 1 versus BTS ≥4 showed no significant association with any SNP tested (data not shown).

Discussion
Both LTB 4 R1 and LTB 4 R2 receptors are potentially important drug targets for conditions driven by inflammation involving LTB 4 . LTB 4 production and activity is thought to be particularly important in severe asthma where a neutrophilic inflammation is more commonly observed [24]. The aims of this study were to characterise the LTB4R1/2 locus at the molecular level to identify key regulatory regions (TSS, promoter regions), splice variation and polymorphic variation in lung tissue and to investigate the potential contribution of polymorphic variation to asthma susceptibility and severity. Our data show that LTB4R1 and LTB4R2 mRNA is ubiquitously expressed in multiple lung and peripheral cell types and that these genes are complex and have variation in 5 0 -untranslated regions and predicted promoter regions which may be functional in terms of cellspecific regulation. We also show that the LTB4R1/2 locus is polymorphic (22 SNPs spanning~11.5kb, MAF>0.01), with most variation in the untranslated regions. This study does not provide evidence supporting a role for LTB4R SNPs in susceptibility to develop asthma or severity phenotypes using asthma enriched families and adult asthma subjects. However, retrospective analyses of SNPs spanning ALOX5AP and LTA4H provided some evidence for association with BTS defined severity although this did not survive correction for multiple testing. This study represents the first characterisation of the LTB4R locus with respect to gene structure in the lung and the first evaluation of LTB4R SNPs for association with asthma susceptibility and severity.  Step on BTS guidelines (%): •     [20]. Numerical values shown correspond to r 2 . A. represents the physical location of the SNPs genotyped. Black boxes represent exons and the spaces between introns determined by RACE. B. and C. represents the LD plot in the Asthma Families (n=370 families) and the Adult Asthma Cohort (n=299 individuals) respectively. LTB 4 production is increased in asthma [3] with levels highest in severe asthmatics when compared to moderate asthmatics and control subjects [24]. The LTB 4 -LTB 4 R interaction is responsible for the influx of inflammatory cells into the lung. A significantly reduced recruitment of eosinophils and neutrophils into the airways has been demonstrated in mice deficient in LTB4R compared to wild type littermates [25]. Murine studies also show LTB 4 is responsible for CD8+ T-cell mediated airway hyperresponsiveness through a mechanism involving mast cells [26]. These studies suggest LTB 4 contributes to asthma pathogenesis through the recruitment and activation of neutrophils and eosinophils. Blocking the LTB 4 -LTB 4 R interaction with the inhibitor LY293111 led to a reduction in BAL neutrophils [27] and with the inhibitor U75302 reduced the migration and proliferation of airway smooth muscle cells which contributes to airway remodelling [28]. These data suggested a potential role in both the inflammatory and structural changes observed in the asthmatic airway.
Polymorphisms spanning ALOX5AP and LTA4H show association with LTB 4 production from ionmycin stimulated neutrophils [5,6]. We have previously reported evidence that these same polymorphisms are associated with asthma susceptibility [7]. To date, little is known about the molecular structure of the two receptors for LTB 4 (LTB4R1 and LTB4R2) in lung and peripheral cells/tissues and regarding the effect of polymorphism contributing to asthma and severity phenotypes. Knowledge of the LTB4R1 and LTB4R2 isoforms and their expression pattern in effector cells will be useful when designing receptor antagonists and the effect of polymorphic variation across the receptors may show pharmacogenetic effects. We hypothesised that in addition to genes involved with LTB 4 synthesis, alterations in genes encoding LTB 4 target receptors may alter cellular responses to LTB 4 , such as inflammatory cell influx and contribute to asthma susceptibility and severity.
LTB4R1 shows varied structure at the mRNA level with different 5 0 -untranslated structures and transcription start sites (TSS), whereas LTB4R2 is more conserved. For LTB4R1, RACE identified a varied 5 0 -untranslated structure with three 5 0 -untranslated exons and one 3 0untranslated exon. This contrasted with previous findings suggesting three exons in the monocytic cell line THP-1 [29]. Our findings and those from Kato et al. supported the open reading frame (ORF) being contained in a single exon which showed concordance with other GPCRs showing intronless 5 0 exons [29,30]. The homogeneity of   Regression analysis was used to investigate the association between LTB4R SNPs and baseline percent predicted FEV 1 in the Adult Asthma Cohort (n=299) using the additive model. 0, 1, 2 represent number of genotypes for major, heterozygotes and minor genotypes respectively. *Dominant model analysis was completed for rs2332320 due to low number of minor allele homozygotes in the additive model.
these results between templates provides support for these variants being authentic. Previous studies have suggested LTB4R1 contains one 5 0 -untranslated exon which is differentially spliced [10]. These different 5 0 -terminal exons give at least three different regions for transcriptional control across the LTB4R locus. Two different transcription start sites in LTB4R1 at positions −4150 to −4148 and −748 to −758 and in LTB4R2 at position −5512 (relative to LTB4R1 ATG) were identified. -4150 has been reported in THP-1 cells and found to be active [29], supporting our finding of this TSS in the lung. The sequence for these transcription start sites were also identified in other lung and peripheral cells based on our PCR screen. Further characterisation of the promoter regions identified is needed to determine whether they are cell-specific. Our bioinformatic screen for transcription factor binding sites has shown multiple Sp-1 and AP-1 motifs in the promoter regions defined by TSS −5512 and −4150 to −4148, but not in the −748 to −758 region. Sp-1 is responsible for basal transcription and AP-1 is involved in inflammation, suggesting these promoter regions may be utilised under these conditions. The promoter region defined by −748 to −758 does not contain these motifs, but contains a GR (glucocorticoid receptor) site. GRs are transcription factors that are activated when bound to steroids. Activated GR can interact with other transcription factors, which can be positive (anti-inflammatory) or negative. The latter is observed in patients with steroid resistant asthma where transcription factors inactivate GR; a study has shown AP-1 may interfere with the binding of GR to DNA in steroid resistant patients [31]. Due to the close arrangement of LTB4R1 and LTB4R2 on chromosome 14q11.2 and the overlapping promoter region of LTB4R1 being in the ORF of LTB4R2 [11] raises the possibility that expression of these genes is regulated by the use of different promoters and may have cell-specific expression patterns. The complex 5 0untranslated region suggests transcriptional regulation may be important for tissue-specific regulation of the LTB4R1 gene. This complexity can also lead to decreased efficiency of translation [32], which may be an important consideration when developing antagonists to target these receptors.
We screened the LTB4R locus to determine the level of polymorphic variation across the receptors in the Caucasian population. 22 SNPs were validated in our UK population. Previously suggested non-synonymous polymorphisms (which were identified in the Japanese population) in LTB4R1 (rs34645221, Ala79Ser and rs17849864, Leu346Phe) and LTB4R2 (rs1950504, Asp196Gly) [33] were not validated. 14 validated SNPs were at the 5 0 -end of the LTB4R locus, in the predicted LTB4R2 promoter location. Of these 4 novel SNPs were identified. These had a low MAF (<0.05) and to date have not been reported in genetic databases or the 1000genomes browser. These could potentially affect transcriptional efficiency (of either LTB4R2 or both LTB4R1 and LTB4R2 due to the close location of these genes). Our data also suggest strong linkage disequilibrium between the SNPs and a conserved nature of the locus which gives support for the two genes being formed by duplication during evolution [11].
Our studies did not observe any significant association with asthma, FEV 1 or severity (BTS defined) in the asthma families or adult asthmatics for any LTB4R SNP analysed. These analyses suggest that these traits may not be genetically determined with respect to LTB4R polymorphism. Although there was no significant association, our data does show a constant direction of effect, suggesting this study may be underpowered to detect a subtle effect. Interestingly, there was modest evidence for a role of ALOX5AP and LTA4H SNPs associated with BTS defined asthma severity. These data therefore suggest genetically determined leukotriene production may be important in determining disease severity and not alterations in the downstream LTB 4 R receptor expression/activity. While no other study has assessed the role of LTB4R SNPs in asthma-related traits, research has involved SNPs spanning these genes in the cardiovascular field, where leukotrienes have also been shown to contribute to early atherosclerosis. rs1046587 and rs3181384 (both LTB4R1, 3 0 UTR) and three other SNPs spanning LTB4R were tested for association with carotid intima-media thickness in one study, but no association was observed after correction for multiple testing [34]. Also no association was observed with rs1046587 (LTB4R1, 3 0 UTR) and risk of ischemic stroke phenotypes in UK and German stroke cohorts [21]. This study did, however, identify significant or borderline association for the four other LTB4R polymorphisms tested: rs2748543 and rs3181384 (both in strong LD) with cardioembolic stroke in a UK cohort and rs1950505 and rs3742510 (also both in strong LD) with cardioembolic stroke in a German cohort [21]. Only rs2748543 was shown to be in LD with rs11158635 genotyped as part of this study.
Our study represents the first characterisation of the LTB4R locus with respect to gene structure in the lung and the first study to investigate association of LTB4R SNPs with asthma and importantly asthma severity where LTB 4 has been suggested to have a more prominent role. We acknowledge the limitations of this study. One limitation was that RACE was conducted in the lung tissue which hampered our ability to detect cellspecific patterns of expression. Therefore it is likely that novel transcripts which may occur in other cells of the lung and periphery were not identified. To address some of these issues we profiled the variants identified by 5 0 RACE using PCR. Data suggest LTB4R1 and LTB4R2 show a ubiquitous expression profile in lung and peripheral cells and suggest that any antagonist targeting these receptors is unlikely to be cell-specific. We acknowledge that our sequencing cohort did not have the power to detect very rare SNPs (0.1%), however we did search the 1000genomes project resource to see if any of our identified rare variant SNPs (those with MAF<0.05) were validated by this project. Also there were modest numbers of families/individuals in our asthma cohorts used for association analyses. For this reason replication in larger additional cohorts is needed to validate our findings. Similarly, our asthma subjects had relatively preserved lung function which may have impeded our ability to detect association with FEV 1 (% Predicted).

Conclusions
In conclusion, this study has shown that LTB4R1 and LTB4R2 have complicated structure and are highly polymorphic. We also report the first evidence that SNPs spanning these genes are not associated with asthma, lung function or asthma severity.