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全基因组关联研究位点的深度重测序鉴定出与溃疡性结肠炎相关的 CARD9、IL23R 和 RNF186 中的罕见变异。

Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis.

机构信息

Montreal Heart Institute, Research Center, Montreal, Quebec, Canada.

出版信息

PLoS Genet. 2013;9(9):e1003723. doi: 10.1371/journal.pgen.1003723. Epub 2013 Sep 12.

Abstract

Genome-wide association studies and follow-up meta-analyses in Crohn's disease (CD) and ulcerative colitis (UC) have recently identified 163 disease-associated loci that meet genome-wide significance for these two inflammatory bowel diseases (IBD). These discoveries have already had a tremendous impact on our understanding of the genetic architecture of these diseases and have directed functional studies that have revealed some of the biological functions that are important to IBD (e.g. autophagy). Nonetheless, these loci can only explain a small proportion of disease variance (~14% in CD and 7.5% in UC), suggesting that not only are additional loci to be found but that the known loci may contain high effect rare risk variants that have gone undetected by GWAS. To test this, we have used a targeted sequencing approach in 200 UC cases and 150 healthy controls (HC), all of French Canadian descent, to study 55 genes in regions associated with UC. We performed follow-up genotyping of 42 rare non-synonymous variants in independent case-control cohorts (totaling 14,435 UC cases and 20,204 HC). Our results confirmed significant association to rare non-synonymous coding variants in both IL23R and CARD9, previously identified from sequencing of CD loci, as well as identified a novel association in RNF186. With the exception of CARD9 (OR = 0.39), the rare non-synonymous variants identified were of moderate effect (OR = 1.49 for RNF186 and OR = 0.79 for IL23R). RNF186 encodes a protein with a RING domain having predicted E3 ubiquitin-protein ligase activity and two transmembrane domains. Importantly, the disease-coding variant is located in the ubiquitin ligase domain. Finally, our results suggest that rare variants in genes identified by genome-wide association in UC are unlikely to contribute significantly to the overall variance for the disease. Rather, these are expected to help focus functional studies of the corresponding disease loci.

摘要

全基因组关联研究和随后的荟萃分析在克罗恩病(CD)和溃疡性结肠炎(UC)中发现了 163 个与疾病相关的基因座,这些基因座在这两种炎症性肠病(IBD)中达到了全基因组的显著水平。这些发现已经极大地影响了我们对这些疾病遗传结构的理解,并指导了功能研究,揭示了一些对 IBD 很重要的生物学功能(例如自噬)。尽管如此,这些基因座只能解释疾病变异的一小部分(在 CD 中约为 14%,在 UC 中约为 7.5%),这表明不仅要发现其他基因座,而且已知基因座可能包含尚未通过 GWAS 检测到的高影响罕见风险变异。为了验证这一点,我们使用靶向测序方法在 200 例 UC 病例和 150 例健康对照(HC)中进行了研究,这些病例和对照均为法裔加拿大血统,研究了与 UC 相关的 55 个基因区域中的基因。我们对独立病例对照队列(共 14435 例 UC 病例和 20204 例 HC)中的 42 个罕见非同义变异进行了后续基因分型。我们的结果证实了 IL23R 和 CARD9 中罕见非同义编码变异的显著相关性,这些变异先前在 CD 基因座的测序中得到了鉴定,并且在 RNF186 中发现了一个新的相关性。除了 CARD9(OR = 0.39)之外,鉴定出的罕见非同义变异均为中度效应(OR = 1.49 对于 RNF186 和 OR = 0.79 对于 IL23R)。RNF186 编码一种具有 RING 结构域的蛋白质,具有预测的 E3 泛素蛋白连接酶活性和两个跨膜结构域。重要的是,疾病编码变异位于泛素连接酶结构域中。最后,我们的结果表明,在 UC 中通过全基因组关联鉴定的基因中的罕见变异不太可能对疾病的总体变异产生显著贡献。相反,这些变异预计有助于集中对相应疾病基因座的功能研究。

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