Rare, Low-Frequency, and Common Variants in the Protein-Coding Sequence of Biological Candidate Genes from GWASs Contribute to Risk of Rheumatoid Arthritis by Diogo Dorothée, Kurreeman Fina, Stahl Eli A, Liao Katherine P, Gupta Namrata, Greenberg Jeffrey D, Rivas Manuel A, Hickey Brendan, Flannick Jason, Thomson Brian, Guiducci Candace, Ripke Stephan, Adzhubey Ivan, Barton Anne, Kremer Joel M, Alfredsson Lars, Consortium of Rheumatology Researchers of North America, Rheumatoid Arthritis Consortium International, Sunyaev Shamil, Martin Javier, Zhernakova Alexandra, Bowes John, Eyre Steve, Siminovitch Katherine A, Gregersen Peter K, Worthington Jane, Klareskog Lars, Padyukov Leonid, Raychaudhuri Soumya, Plenge Robert M in American journal of human genetics (2012). PubMed

Abstract

The extent to which variants in the protein-coding sequence of genes contribute to risk of rheumatoid arthritis (RA) is unknown. In this study, we addressed this issue by deep exon sequencing and large-scale genotyping of 25 biological candidate genes located within RA risk loci discovered by genome-wide association studies (GWASs). First, we assessed the contribution of rare coding variants in the 25 genes to the risk of RA in a pooled sequencing study of 500 RA cases and 650 controls of European ancestry. We observed an accumulation of rare nonsynonymous variants exclusive to RA cases in IL2RA and IL2RB (burden test: p = 0.007 and p = 0.018, respectively). Next, we assessed the aggregate contribution of low-frequency and common coding variants to the risk of RA by dense genotyping of the 25 gene loci in 10,609 RA cases and 35,605 controls. We observed a strong enrichment of coding variants with a nominal signal of association with RA (p < 0.05) after adjusting for the best signal of association at the loci (p(enrichment) = 6.4 × 10(-4)). For one locus containing CD2, we found that a missense variant, rs699738 (c.798C>A [p.His266Gln]), and a noncoding variant, rs624988, reside on distinct haplotypes and independently contribute to the risk of RA (p = 4.6 × 10(-6)). Overall, our results indicate that variants (distributed across the allele-frequency spectrum) within the protein-coding portion of a subset of biological candidate genes identified by GWASs contribute to the risk of RA. Further, we have demonstrated that very large sample sizes will be required for comprehensively identifying the independent alleles contributing to the missing heritability of RA.

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