Regulation of DNA-damage responses and cell-cycle progression by the chromatin remodelling factor CHD4

被引:281
作者
Polo, Sophie E. [1 ]
Kaidi, Abderrahmane [1 ]
Baskcomb, Linda [1 ]
Galanty, Yaron [1 ]
Jackson, Stephen P. [1 ]
机构
[1] Univ Cambridge, Dept Biochem, Gurdon Inst, Cambridge CB2 1QN, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
cell cycle; CHD4; chromatin remodelling; DNA damage; DNA repair; DOUBLE-STRAND BREAKS; ATAXIA-TELANGIECTASIA; HISTONE DEACETYLASE; MI-2/NURD COMPLEX; REPAIR; PROTEINS; POLY(ADP-RIBOSE); IDENTIFICATION; INHIBITOR; CANCER;
D O I
10.1038/emboj.2010.188
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The chromatin remodelling factor chromodomain helicase DNA-binding protein 4 (CHD4) is a catalytic subunit of the NuRD transcriptional repressor complex. Here, we reveal novel functions for CHD4 in the DNA-damage response (DDR) and cell-cycle control. We show that CHD4 mediates rapid poly(ADP-ribose)-dependent recruitment of the NuRD complex to DNA-damage sites, and we identify CHD4 as a phosphorylation target for the apical DDR kinase ataxia-telangiectasia mutated. Functionally, we show that CHD4 promotes repair of DNA double-strand breaks and cell survival after DNA damage. In addition, we show that CHD4 acts as an important regulator of the G1/S cell-cycle transition by controlling p53 deacetylation. These results provide new insights into how the chromatin remodelling complex NuRD contributes to maintaining genome stability.
引用
收藏
页码:3130 / 3139
页数:10
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