EBF FLJ31951UBLCP1 IL12B B36 Position Genes LD Regions Genotyped Markers Chr5 (q33.3) rs rs Figure 1. Physical map of 360kb around IL12B on human chromosome 5 Twenty SNPs were selected for follow-up genotyping. All 20 of these SNPs were between positions ( ) – covering 250kbp – and were preferentially selected to cover the IL12B coding region. These new SNPs were also chosen so that they (i) covered a range of r 2 values with the previously-described associated markers rs and rs , concentrating on SNPs with higher levels of LD, (ii) were likely to be in evolutionarily-conserved regions (UCSC website) and (iii) had frequencies greater than 1% in whites of European descent. Lastly redundancy within the new set of SNPs was reduced by eliminating some, but not all, SNPs in extremely high LD (>0.97) with other SNPs selected. The location of all 51 SNPs, with the 20 new ones highlighted in red, are shown in Figure 1. Detailed genetic characterization of the psoriasis-associated gene IL12B to further define the causal variant(s) E. Beasley 1, S. J. Schrodi 1, M. Chang 1, A. Jacobson 1, K. P. Callis 2, M. F. Leppert 2, G. G. Krueger 2, A. B. Begovich 1 1. Celera, Alameda, CA, USA 2. University of Utah, Salt Lake City, UT, USA 0 1 r2r Controls 1 50 rs rs Cases 150 A multi-tiered, case-control association study using a collection of over 25,000 gene-centric SNPs, identified association between a 3’UTR SNP in IL12B, rs , and psoriasis risk (allelic P comb = 7.85 x ) in three independent sample sets (Cargill et al. 2007) confirming the results of a previous small candidate gene study in Japanese (Tsunemi et al. 2002). To determine whether any other SNPs in this gene region were associated with psoriasis we used a combination of tag SNPs (N=27), which had the highest average power to detect disease-associated variants under a conservative disease model, and functional SNPs (N=3) to genotype our three sample sets and identified a second risk allele, rs (allelic P comb = 4.08 x ), located approximately 60 kb upstream of the IL12B coding region that exhibited association with psoriasis after adjustment for rs (Cargill et al. 2007). Together these two SNPs marked a common IL12B risk haplotype (OR common 1.40, P comb = 8.11 x ) and a less frequent protective haplotype (OR common 0.58, P comb = 5.65 x ), which were statistically significant in all three studies. However, this set of 30 SNPs did not allow us to explore whether the psoriasis association observed with rs and rs was due to LD with other variants not interrogated. Consequently, we selected 20 additional SNPs for genotyping in the three psoriasis case-control sample sets and report the data for all 51 IL12B-region SNPs here. INTRODUCTION Table 2. Minor allele frequencies and allele-based association of IL12B-associated SNPs with psoriasis 1 SNP SELECTION Table 1. Demographic and clinical information a We next examined the LD patterns in this region by calculating the pairwise r 2 values between all 51 markers. This was done separately for the cases and controls in each sample set (Figure 2 displays a combined summary of the case and control r 2 values across all three sample sets). Six of the eleven highly significant SNPs (p 0.97) (referred to as Group 1). Three of the eleven SNPs, rs , rs and rs (the other significant independently associated SNP), which are located within a 3 kb region approximately 60 kb 5’ of the IL12B gene, are highly correlated with each other in the cases and controls of all three sample sets (r 2 > 0.98) (referred to as Group 2). The LD patterns of the tenth SNP, rs , located in intron 1 of IL12B, show that it is reasonably correlated with rs (r 2 ~ 0.75 – 0.83) and modestly correlated with rs (r 2 ~ 0.22 – 0.36). The eleventh significant SNP, rs , located 5’ of IL12B and hypothesized to regulate IL12B expression levels, is modestly correlated with rs (r 2 ~ 0.28 – 0.40) and reasonably correlated with rs (r 2 ~0.70 – 0.79). LD PATTERNS The single marker results for all 51 SNPs are shown in Table 2 with the data for the 20 new SNPs highlighted in bold. An exact test of HWE of the genotype data for these 51 SNPs, with the analysis performed separately for cases and controls in each sample set (data not shown), identified only one instance where a marker was not in HWE at the P < 0.01 significance level (rs in the discovery controls, P = 0.005) (data not shown). Single marker analyses showed that 9 of the 51 SNPs genotyped in this study in addition to the two original SNPs, rs and rs , were associated with psoriasis risk at P < (Table 1). The original 3’UTR SNP, rs , however, remained the most significant marker across all three studies with the minor C allele being highly protective (OR common 0.64, P comb = 1.66E x ). SINGLE MARKER ANALYSES Figure 2. Pairwise LD between the 51 IL12B-region SNPs as measured by r 2 in the cases & controls of all three sample sets CONCLUSIONS CONDITIONAL ANALYSES TO IDENTIFY INDEPENDENT RISK ALLELES All individuals included in this study were over the age of 18 at the time they were enrolled into the sample collections. In addition, none of the subjects had undergone a bone marrow transplant. All protocols were approved by national and/or local institutional review boards, and informed written consent was obtained from all subjects. A detailed description can be found in Cargill et al ATHG 80:273,2007. SAMPLE SETS White - U.S /- 16 years 32.78% 63/151 - Discovery Sample Set Subphenotype Genetic background # Cases # Controls Female:male gender ratio Average age of onset Percent with family history Psoriatic arthritis & psoriasis for at least 10 years (yes/no) NPF psoriasis score ( 12.5) PASI score ( 50) White - Utah /- 17 years 62.37% 125/ /132/129 - White - U.S /- 15 years 46.90% 98/ /101/3 Replication Sample Set 1Replication Sample Set 2 a Data for certain subphenotypes were not available on all patients. dbSNP ID Gene Type Cases (n=465) Controls (n=460) OR Allelic P-value 2 Frequency in Cases (n=494) Controls (n=495) OR Allelic P-value 2 Cases (n=481) Controls (n=424) OR Allelic P-value 2 Discovery Sample SetReplication Sample Set 1Replication Sample Set 2 rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs rs EBF FLJ31951 UBLCP1 IL12B intron intergenic UTR intron intergenic intron intergenic UTR F298V intron I33V intron promotor intergenic NC E E E E E E NC E E E E E E E E E E E E NC NC Combined Analysis OR common (95% CI) 3 P comb ( ) 1.00 ( ) 1.00 ( ) 0.99 ( ) 0.91 ( ) 0.95 ( ) 1.21 ( ) 1.20 ( ) 0.97 ( ) 0.71 ( ) 1.03 ( ) 1.15 ( ) 0.80 ( ) 0.79 ( ) 0.94 ( ) 0.77 ( ) 1.07 ( ) 1.19 ( ) 0.65 ( ) 0.64 ( ) 1.01 ( ) 1.24 ( ) 0.64 ( ) 0.84 ( ) 0.86 ( ) 1.23 ( ) 0.78 ( ) 1.18 ( ) 0.83 ( ) NC 0.65 ( ) 1.06 ( ) 0.65 ( ) 0.65 ( ) 1.00 ( ) 1.22 ( ) 0.66 ( ) 0.89 ( ) 0.73 ( ) 1.27 ( ) 1.03 ( ) 0.87 ( ) 0.70 ( ) 0.71 ( ) 0.71 ( ) 1.29 ( ) 1.00 ( ) 0.82 ( ) 1.22 ( ) 0.81 ( ) NC NC NC NC 9.52E E-09 NC E-09 NC NC 6.51E-09 NC 4.22E E-09 NC E E NC 4.00E E E NC Data may differ slightly from that reported in Cargill et al due to lack of DNA for a small number of samples. SNPs are listed in order according to their position in the genomic contig NT_23133 (Entrez Nucleotide). 2 Calculated using Fisher's exact test. 3 Calculated using a Mantel-Haenszel common odds ratio (OR). 4 Calculated using Fisher's combined test. Combined P-values were not calculated (NC) for SNPs where the ORs for the three samples sets are both above and below 1. Frequency in 1. A thorough genetic interrogation and subsequent analysis of the IL12B-gene region reveals that the 3'UTR SNP rs is the most highly statistically significant SNP evaluated in our sample sets. Our data do not exclude the possibility that another SNP in high LD with rs could be responsible for these association patterns. 2. A combined analysis across the three studies, adjusting for rs , moderately suggests that other SNPs 5' of the coding region including rs , rs and rs , may contribute to psoriasis risk independently of rs ; however, none of these SNPs are significant after adjustment for rs in each of the three sample sets. 3. These data show that the set of SNPs in strong LD with rs are primary drivers of the association at the IL12B-region with psoriasis and suggest that additional studies, both functional and genetic, are required to fully characterize the role of IL12B-region SNPs in psoriasis risk. Figure 3. Single SNP analyses adjusted for rs Combined analysis across all studies To explore the possibility that SNPs aside from rs independently associate with psoriasis, we performed a logistic regression analysis across each of the three studies adjusting for rs P-values were combined across the three independent studies using the Fisher's combined P-value method and plotted by position. Although no single SNP exhibited significant effects (P<0.05) for each of the three sample sets following adjustment for rs , the combined analysis points to a region 5' to IL12B including SNPs rs , rs and rs (P-value adjusted for rs =0.028, P=0.0009, P=0.0013; respectively). Further studies are required to fully elucidate whether this 5' region truly carries variants that predispose individuals to psoriasis independent of rs EBF1 FLJ31951IL12B UBLCP1