共 51 条
Regulation of DNA-damage responses and cell-cycle progression by the chromatin remodelling factor CHD4
被引:281
作者:

Polo, Sophie E.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cambridge, Dept Biochem, Gurdon Inst, Cambridge CB2 1QN, England Univ Cambridge, Dept Biochem, Gurdon Inst, Cambridge CB2 1QN, England

Kaidi, Abderrahmane
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Univ Cambridge, Dept Biochem, Gurdon Inst, Cambridge CB2 1QN, England Univ Cambridge, Dept Biochem, Gurdon Inst, Cambridge CB2 1QN, England

Baskcomb, Linda
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h-index: 0
机构:
Univ Cambridge, Dept Biochem, Gurdon Inst, Cambridge CB2 1QN, England Univ Cambridge, Dept Biochem, Gurdon Inst, Cambridge CB2 1QN, England

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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.
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页码:3130 / 3139
页数:10
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