| Literature DB >> 20123861 |
Dalemari Crowther-Swanepoel1, Peter Broderick, Yussanne Ma, Lindsay Robertson, Alan M Pittman, Amy Price, Philip Twiss, Jayaram Vijayakrishnan, Mobshra Qureshi, Martin J S Dyer, Estella Matutes, Claire Dearden, Daniel Catovsky, Richard S Houlston.
Abstract
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.Entities:
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Year: 2010 PMID: 20123861 DOI: 10.1093/hmg/ddq044
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150