Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Department of Molecular Biology, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen 6500 HB, The Netherlands.
Nat Commun. 2017 May 2;8:15034. doi: 10.1038/ncomms15034.
Genome wide association studies (GWAS) have mapped multiple independent cancer susceptibility loci to chr5p15.33. Here, we show that fine-mapping of pancreatic and testicular cancer GWAS within one of these loci (Region 2 in CLPTM1L) focuses the signal to nine highly correlated SNPs. Of these, rs36115365-C associated with increased pancreatic and testicular but decreased lung cancer and melanoma risk, and exhibited preferred protein-binding and enhanced regulatory activity. Transcriptional gene silencing of this regulatory element repressed TERT expression in an allele-specific manner. Proteomic analysis identifies allele-preferred binding of Zinc finger protein 148 (ZNF148) to rs36115365-C, further supported by binding of purified recombinant ZNF148. Knockdown of ZNF148 results in reduced TERT expression, telomerase activity and telomere length. Our results indicate that the association with chr5p15.33-Region 2 may be explained by rs36115365, a variant influencing TERT expression via ZNF148 in a manner consistent with elevated TERT in carriers of the C allele.
全基因组关联研究(GWAS)已经将多个独立的癌症易感性位点映射到 chr5p15.33。在这里,我们表明,对这些位点之一(CLPTM1L 中的区域 2)中的胰腺和睾丸癌 GWAS 进行精细映射,将信号集中在九个高度相关的 SNP 上。其中,rs36115365-C 与胰腺和睾丸癌风险增加相关,与肺癌和黑色素瘤风险降低相关,并表现出优先的蛋白结合和增强的调节活性。该调节元件的转录基因沉默以等位基因特异性方式抑制 TERT 表达。蛋白质组学分析鉴定出锌指蛋白 148(ZNF148)与 rs36115365-C 的等位基因偏好结合,进一步得到纯化重组 ZNF148 的结合支持。ZNF148 的敲低导致 TERT 表达、端粒酶活性和端粒长度降低。我们的结果表明,与 chr5p15.33-Region 2 的关联可以用 rs36115365 来解释,该变体通过 ZNF148 影响 TERT 表达,方式与 C 等位基因携带者中端粒酶的升高一致。