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首页> 外文期刊>PLoS Genetics >Fine Mapping of the Psoriasis Susceptibility Locus PSORS1 Supports HLA-C as the Susceptibility Gene in the Han Chinese Population
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Fine Mapping of the Psoriasis Susceptibility Locus PSORS1 Supports HLA-C as the Susceptibility Gene in the Han Chinese Population

机译:牛皮癣易感基因座的精细定位PSORS1支持HLA-C作为汉族人群中的易感基因

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PSORS1 (psoriasis susceptibility gene 1) is a major susceptibility locus for psoriasis. Several fine-mapping studies have highlighted a 300-kb candidate region of PSORS1 where multiple biologically plausible candidate genes were suggested. The most recent study has indicated HLA-Cw6 as the primary PSORS1 risk allele within the candidate region in a Caucasian population. In this study, a family-based association analysis of the PSORS1 locus was performed by analyzing 10 polymorphic microsatellite markers from the PSORS1 region as well as HLA-B, HLA-C and CDSN loci in 163 Chinese families of psoriasis. Five marker loci show strong evidence (P?3), and one marker locus shows weak evidence (P?=?0.04) for association. The haplotype cluster analysis showed that all the risk haplotypes are Cw6 positive and share a 369-kb region of homologous marker alleles which carries all the risk alleles, including HLA-Cw6 and CDSN*TTC, identified in this study. The recombinant haplotype analysis of the HLA-Cw6 and CDSN*TTC alleles in 228 Chinese families showed that the HLA-Cw6?/CDSN*TTC+ recombinant haplotype is clearly not associated with risk for psoriasis (T∶NT?=?29:57, p?=?0.0025) in a Chinese population, suggesting that the CDSN*TTC allele itself does not confer risk without the presence of the HLA-Cw6 allele. The further exclusion analysis of the non-risk HLA-Cw6?/CDSN*TTC+ recombinant haplotypes with common recombination breakpoints has allowed us to refine the location of PSORS1 to a small candidate region. Finally, we performed a conditional linkage analysis and showed that the HLA-Cw6 is a major risk allele but does not explain the full linkage evidence of the PSORS1 locus in a Chinese population. By performing a series of family-based association analyses of haplotypes as well as an exclusion analysis of recombinant haplotypes, we were able to refine the PSORS1 gene to a small critical region where HLA-C is a strong candidate to be the PSORS1 susceptibility gene.
机译:PSORS1(牛皮癣易感基因1)是牛皮癣的主要易感基因座。多项精细映射研究突出显示了PSORS1的300 kb候选区域,其中建议了多个生物学上可行的候选基因。最新研究表明,HLA-Cw6是白种人人群中候选区域内的主要PSORS1风险等位基因。在这项研究中,通过分析来自163个中国银屑病家族的PSORS1区以及HLA-B,HLA-C和CDSN基因座的10个多态微卫星标记,对PSORS1基因座进行了基于家族的关联分析。 5个标记基因座显示出有力的证据(P?3),1个标记基因座显示了较弱的证据(P?=?0.04)。单倍型聚类分析表明,所有危险单倍型均为Cw6阳性,并共有一个369kb的同源标记等位基因区域,该区域携带本研究中鉴定的所有危险等位基因,包括HLA-Cw6和CDSN * TTC。对228个中国家庭的HLA-Cw6和CDSN * TTC等位基因进行的重组单倍型分析显示,HLA-Cw6α/ CDSN * TTC +重组单倍型显然与牛皮癣的风险无关(T∶NTβ =?29:57, p?=?0.0025),表明在没有HLA-Cw6等位基因的情况下CDSN * TTC等位基因本身不会带来风险。对具有常见重组断裂点的非风险性HLA-Cw6α/ CDSN * TTC +重组单倍型的进一步排除分析,使我们能够将PSORS1的位置优化为一个小的候选区域。最后,我们进行了条件连锁分析,结果表明HLA-Cw6是主要的风险等位基因,但不能解释中国人群PSORS1基因座的完整连锁证据。通过对单倍型进行一系列基于家庭的关联分析以及对重组单倍型的排除分析,我们能够将PSORS1基因细化到一个小的关键区域,在该区域中HLA-C是PSORS1易感性基因的强大候选者。

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