The stress-responsive gene ATF3 regulates the histone acetyltransferase Tip60

被引:40
作者
Cui, Hongmei [1 ,2 ]
Guo, Mingxiong [2 ]
Xu, Dong [2 ]
Ding, Zhi-Chun [1 ]
Zhou, Gang [1 ,3 ]
Ding, Han-Fei [1 ,4 ]
Zhang, Junran [5 ]
Tang, Yi [2 ]
Yan, Chunhong [1 ,2 ,3 ]
机构
[1] Georgia Regents Univ, GRU Canc Ctr, Augusta, GA 30912 USA
[2] Albany Med Coll, Ctr Cell Biol & Canc Res, Albany, NY 12208 USA
[3] Georgia Regents Univ, Med Coll Georgia, Dept Biochem & Mol Biol, Augusta, GA 30912 USA
[4] Georgia Regents Univ, Dept Pathol, Augusta, GA 30912 USA
[5] Case Western Reserve Univ, Dept Radiat Oncol, Cleveland, OH 44106 USA
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
关键词
ACTIVATING TRANSCRIPTION FACTOR-3; P53; ACETYLATION; BINDING; PROTEIN; APOPTOSIS; DEUBIQUITINATION; PHOSPHORYLATION; DEGRADATION; DETERMINES;
D O I
10.1038/ncomms7752
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tat-interactive protein 60 (Tip60) is a MYST histone acetyltransferase that catalyses acetylation of the major DNA damage kinase Ataxia telangiectasia mutated (ATM), thereby triggering cellular signalling required for the maintenance of genomic stability on genotoxic insults. The Tip60 activity is modulated by post-translational modifications that alter its stability and its interactions with substrates. Here we report that activating transcription factor 3 (ATF3), a common stress mediator and a p53 activator, is a regulator of Tip60. ATF3 directly binds Tip60 at a region adjacent to the catalytic domain to promote the protein acetyltransferase activity. Moreover, the ATF3-Tip60 interaction increases the Tip60 stability by promoting USP7-mediated deubiquitination of Tip60. Consequently, knockdown of ATF3 expression leads to decreased Tip60 expression and suppression of ATM signalling as evidenced by accumulated DNA lesions and increased cell sensitivity to irradiation. Our findings thus reveal a previously unknown function of a common stress mediator in regulating Tip60 function.
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页数:10
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