Department of Molecular Medicine, Faculty of Medicine, Université Laval, Genomics Center, CHU de Quebec-Université Laval Research Center, 2705 Laurier Boulevard, Quebec, G1V 4G2, Canada.
Department of Mathematics and Statistics, Faculty of Science and Engineering, Université Laval, 1045, av. de la Médecine, Québec, G1V 0A6, Canada.
Genes (Basel). 2019 Feb 28;10(3):186. doi: 10.3390/genes10030186.
Genetic variants affecting the regulation of gene expression are among the main causes of human diversity. The potential importance of regulatory polymorphisms is underscored by results from Genome Wide Association Studies, which have already implicated such polymorphisms in the susceptibility to complex diseases such as breast cancer. In this study, we re-sequenced the promoter regions of 24 genes involved in pathways related to breast cancer including sex steroid action, DNA repair, and cell cycle control in 60 unrelated Caucasian individuals. We constructed haplotypes and assessed the functional impact of promoter variants using gene reporter assays and electrophoretic mobility shift assays. We identified putative functional variants within the promoter regions of estrogen receptor 1 (, , forkhead box A1 (, ubiquitin interaction motif containing 1 (UIMC1) and cell division cycle 7 (. The functional polymorphism on rs13447455, influences transcriptional activity in an allele-specific manner and alters DNA⁻protein complex formation in breast cancer cell lines. Moreover, results from the Breast Cancer Association Consortium show a marginal association between rs13447455 and breast cancer risk (p=9.3x10), thus warranting further investigation. Furthermore, our study has helped provide methodological solutions to some technical difficulties that were encountered with gene reporter assays, particularly regarding inter-clone variability and statistical consistency.
影响基因表达调控的遗传变异是人类多样性的主要原因之一。全基因组关联研究的结果强调了调控多态性的潜在重要性,这些研究已经表明,这种多态性与乳腺癌等复杂疾病的易感性有关。在这项研究中,我们在 60 个无关的白种个体中重新测序了与乳腺癌相关途径(包括性激素作用、DNA 修复和细胞周期控制)相关的 24 个基因的启动子区域。我们构建了单倍型,并使用基因报告基因检测和电泳迁移率变动分析评估了启动子变异的功能影响。我们在雌激素受体 1 (,, 叉头框 A1 (, 泛素相互作用基序包含 1 (UIMC1) 和细胞分裂周期 7 ( 的启动子区域内鉴定出了可能具有功能的变异。位于 rs13447455 的功能多态性以等位基因特异性的方式影响转录活性,并改变乳腺癌细胞系中的 DNA⁻protein 复合物形成。此外,乳腺癌协会联盟的研究结果表明,rs13447455 与乳腺癌风险之间存在边缘关联(p=9.3x10),因此需要进一步研究。此外,我们的研究为基因报告基因检测中遇到的一些技术难题提供了方法学解决方案,特别是关于克隆间变异性和统计一致性的问题。