Section of Cancer Genetics, Institute of Cancer Research, Sutton, Surrey SM2 5NG, UK.
Hum Mol Genet. 2010 May 1;19(9):1840-5. doi: 10.1093/hmg/ddq044. Epub 2010 Feb 1.
A recent genome-wide association study of chronic lymphocytic leukaemia (CLL) has identified a susceptibility locus on 6p25.3 associated with a modest but highly significant increase in CLL risk. Using a set of single nucleotide polymorphism (SNP) markers, we generated a fine-scale map and narrowed the association signal to a 18 kb DNA segment within the 3'-untranslated region (UTR) of the IRF4 (interferon regulatory factor 4) gene. Resequencing this segment in European subjects identified 55 common polymorphisms, including 13 highly correlated candidate causal variants. In a large case-control study, it was shown that all but four variants could be excluded with 95% confidence. These four SNPs map to a 3 kb region of the 3'-UTR of IRF4, consistent with the causal basis of the association being mediated through differential IRF4 expression.
最近对慢性淋巴细胞白血病 (CLL) 的全基因组关联研究鉴定出 6p25.3 上的一个易感位点,与 CLL 风险的适度但高度显著增加相关。使用一组单核苷酸多态性 (SNP) 标记,我们生成了精细图谱,并将关联信号缩小到干扰素调节因子 4 (IRF4) 基因 3'-非翻译区 (UTR) 内的 18 kb DNA 片段。对欧洲受试者的这一片段进行重测序,鉴定出 55 个常见多态性,包括 13 个高度相关的候选因果变异。在一项大型病例对照研究中,结果表明,除了四个变异之外,其他所有变异都可以在 95%置信区间内排除。这四个 SNP 映射到 IRF4 3'-UTR 的 3kb 区域,这与关联的因果基础是通过差异 IRF4 表达介导的相一致。