H3K36me3, message from chromatin to DNA damage repair

H3K36me3, message from chromatin to DNA damage repair
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H3K36me3,从染色质到 DNA 损伤修复的信息

DOI:
10.1186/s13578-020-0374-z
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发表时间:
2020-01
影响因子:
7.5
通讯作者:
Fang Dong
Fang Dong
中科院分区:
生物学2区
文献类型:
--
作者:
Sun Zhongxing;Zhang Yanjun;Jia Junqi;Fang Yuan;Tang Yin;Wu Hongfei;Fang Dong

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组蛋白标记控制许多细胞过程,包括DNA损伤修复。本文将主要关注活性组蛋白标记H3 K36 me3在DNA损伤修复和DNA损伤后基因组稳定性维持中的调节作用。有多种线索表明H3K36me3通过直接招募DNA修复机制将染色质设置在“就绪”状态,从而导致对损伤的快速反应,从而参与DNA损伤反应。减少的H3K36me3与低DNA修复效率相关。本文还将重点介绍H3K36me3介导的DNA损伤修复在新发现的癌组蛋白突变型肿瘤发生中的作用。了解H3K36me3在DNA损伤修复中的不同方面,特别是在癌症中,将分享染色质和DNA修复的知识,以服务于药物发现和患者护理。
Histone marks control many cellular processes including DNA damage repair. This review will focus primarily on the active histone mark H3K36me3 in the regulation of DNA damage repair and the maintenance of genomic stability after DNA damage. There are diverse clues showing H3K36me3 participates in DNA damage response by directly recruiting DNA repair machinery to set the chromatin at a “ready” status, leading to a quick response upon damage. Reduced H3K36me3 is associated with low DNA repair efficiency. This review will also place a main emphasis on the H3K36me3-mediated DNA damage repair in the tumorigenesis of the newly found oncohistone mutant tumors. Gaining an understanding of different aspects of H3K36me3 in DNA damage repair, especially in cancers, would share the knowledge of chromatin and DNA repair to serve to the drug discovery and patient care.
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