Emerging role of protein phosphatases changes the landscape of phospho-signaling in DNA damage response

被引:16
作者
Zheng, Xiao-Feng [1 ]
Kalev, Peter [1 ]
Chowdhury, Dipanjan [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Radiat Oncol, Boston, MA 02115 USA
关键词
Protein phosphatase; Dephosphorylation; ATM; KAP1; CTIP; EXO1; 53BP1; XRCC4; YEN1; BLM; STRAND BREAK REPAIR; HOLLIDAY JUNCTION RESOLVASE; HOMOLOGOUS RECOMBINATION; KAP-1; PHOSPHORYLATION; WIP1; PHOSPHATASE; TUMOR-SUPPRESSOR; END RESECTION; ATM; KINASE; 53BP1;
D O I
10.1016/j.dnarep.2015.04.014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Phosphorylation signaling networks have primarily been studied from an activation perspective, with protein phosphatases viewed as simple counter-balances that functioned passively in the wake of kinase activity. Indeed, there have been only sporadic efforts to investigate the independent role of phosphatases in DNA damage response (DDR). However, global phosphoproteomic analysis of the DDR revealed that over one-third of observed phosphorylation sites were down-regulated within minutes of DNA damage, suggesting a more robust role for phosphatases in DNA repair. Consistent with these observations, recent studies reveal that dephosphorylation of DNA repair factors during specific phases of the cell cycle may be a pre-requisite for their participation in the DDR. Here, we summarize recent literature and speculate on the emerging role of phosphatases in the DDR. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:58 / 65
页数:8
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