Disruption of the 3D cancer genome blueprint

被引:34
作者
Achinger-Kawecka, Joanna [1 ,2 ]
Clark, Susan J. [1 ,2 ]
机构
[1] Garvan Inst Med Res, Genom & Epigenet Div, Epigenet Res Lab, 384 Victoria St, Darlinghurst, NSW 2010, Australia
[2] Univ New South Wales, Fac Med, St Vincents Clin Sch, Darlinghurst, NSW 2010, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
cancer; chromatin conformation capture; chromatin interactions; Hi-C; topologically associating domain; LONG-RANGE INTERACTION; CAPTURE HI-C; COLORECTAL-CANCER; BREAST-CANCER; CHROMOSOME CONFORMATION; CHROMATIN DOMAINS; RISK LOCI; LOOPING INTERACTIONS; TOPOLOGICAL DOMAINS; MAMMALIAN GENOMES;
D O I
10.2217/epi-2016-0111
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recent advances in chromosome conformation capture technologies are improving the current appreciation of how 3D genome architecture affects its function in different cell types and disease. Long-range chromatin interactions are organized into topologically associated domains, which are known to play a role in constraining gene expression patterns. However, in cancer cells there are alterations in the 3D genome structure, which impacts on gene regulation. Disruption of topologically associated domains architecture can result in alterations in chromatin interactions that bring new regulatory elements and genes together, leading to altered expression of oncogenes and tumor suppressor genes. Here, we discuss the impact of genetic and epigenetic changes in cancer and how this affects the spatial organization of chromatin. Understanding how disruptions to the 3D architecture contribute to the cancer genome will provide novel insights into the principles of epigenetic gene regulation in cancer and mechanisms responsible for cancer associated mutations and rearrangements.
引用
收藏
页码:47 / 55
页数:9
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