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参与性激素作用、DNA 修复和细胞周期控制的基因启动子变异的功能分析。

Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle Control.

机构信息

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.

出版信息

Genes (Basel). 2019 Feb 28;10(3):186. doi: 10.3390/genes10030186.

DOI:10.3390/genes10030186
PMID:30823486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6470759/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/8fea0847dcf3/genes-10-00186-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/570a5ba75548/genes-10-00186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/ed21785d8f99/genes-10-00186-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/cc66264a11b8/genes-10-00186-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/30f57e122210/genes-10-00186-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/8fea0847dcf3/genes-10-00186-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/570a5ba75548/genes-10-00186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/ed21785d8f99/genes-10-00186-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/cc66264a11b8/genes-10-00186-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/30f57e122210/genes-10-00186-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f52b/6470759/8fea0847dcf3/genes-10-00186-g005.jpg

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本文引用的文献

1
VEXOR: an integrative environment for prioritization of functional variants in fine-mapping analysis.VEXOR:一种用于精细定位分析中功能变异优先级排序的综合环境。
Bioinformatics. 2017 May 1;33(9):1389-1391. doi: 10.1093/bioinformatics/btw826.
2
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.BRCA1和BRCA2突变携带者的乳腺癌风险与显示不同等位基因表达的基因变异之间的关联:11q22.3位点乳腺癌风险修饰因子的鉴定。
Breast Cancer Res Treat. 2017 Jan;161(1):117-134. doi: 10.1007/s10549-016-4018-2. Epub 2016 Oct 28.
3
儿童住宅 PM 暴露与鼻腔甲基组
Environ Int. 2021 Aug;153:106505. doi: 10.1016/j.envint.2021.106505. Epub 2021 Apr 16.
4
Genome Dashboards: Framework and Examples.基因组数据看板:框架与实例。
Biophys J. 2020 May 5;118(9):2077-2085. doi: 10.1016/j.bpj.2020.02.018. Epub 2020 Feb 29.
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
乳腺癌风险与显示不同等位基因表达的基因变异的关联:4q21处一个新的乳腺癌易感位点的鉴定。
Oncotarget. 2016 Dec 6;7(49):80140-80163. doi: 10.18632/oncotarget.12818.
4
Hereditary breast and ovarian cancer: new genes in confined pathways.遗传性乳腺癌和卵巢癌:局限途径中的新基因。
Nat Rev Cancer. 2016 Sep;16(9):599-612. doi: 10.1038/nrc.2016.72. Epub 2016 Aug 12.
5
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.位于6q25的乳腺癌风险变异体表现出不同的表型关联,并调控ESR1、RMND1和CCDC170。
Nat Genet. 2016 Apr;48(4):374-86. doi: 10.1038/ng.3521. Epub 2016 Feb 29.
6
Prediction of breast cancer risk based on profiling with common genetic variants.基于常见基因变异谱预测乳腺癌风险。
J Natl Cancer Inst. 2015 Apr 8;107(5). doi: 10.1093/jnci/djv036. Print 2015 May.
7
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.对超过12万名个体进行的全基因组关联分析确定了15个新的乳腺癌易感基因座。
Nat Genet. 2015 Apr;47(4):373-80. doi: 10.1038/ng.3242. Epub 2015 Mar 9.
8
Breast-cancer risk in families with mutations in PALB2.携带PALB2基因突变的家族中的乳腺癌风险。
N Engl J Med. 2014 Oct 23;371(17):1651-2. doi: 10.1056/NEJMc1410673.
9
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Proc Natl Acad Sci U S A. 2014 May 27;111(21):E2191-9. doi: 10.1073/pnas.1320308111. Epub 2014 May 12.
10
Two decades after BRCA: setting paradigms in personalized cancer care and prevention.BRCA 研究二十年:开创个体化癌症治疗与预防的新纪元。
Science. 2014 Mar 28;343(6178):1466-70. doi: 10.1126/science.1251827.