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PMID: 24047694 已发表 · ppublish 英语

Chromatin PTEN is involved in DNA damage response partly through regulating Rad52 sumoylation.

Cell cycle (Georgetown, Tex.) ·第 12 卷 ·第 21 期 ·2014-06-03

Choi Byeong Hyeok, Chen Yan, Dai Wei

摘要

A pool of PTEN localizes to the nucleus. However, the exact mechanism of action of nuclear PTEN remains poorly understood. We have investigated PTEN's role during DNA damage response. Here we report that PTEN undergoes chromatin translocation after DNA damage, and that its translocation is closely associated with its phosphorylation on S366/T370 but not on S380. Deletional analysis reveals that the C2 domain of PTEN is responsible for its nuclear translocation after exposure to genotoxin. Both casein kinase 2 and GSK3β are involved in the phosphorylation of the S366/T370 epitope, as well as PTEN's association with chromatin after DNA damage. Significantly, PTEN specifically interacts with Rad52 and colocalizes with Rad52, as well as γH2AX, after genotoxic stress. Moreover, PTEN is involved in regulating Rad52 sumoylation. Combined, our studies strongly suggest that nuclear/chromatin PTEN mediates DNA damage repair through interacting with and modulating the activity of Rad52.

关键词
DNA damage PTEN Rad52 chromatin genotoxic stress phosphorylation
文献信息
期刊
Cell cycle (Georgetown, Tex.)
期刊简称
Cell Cycle
发表日期
2014-06-03
收录日期
2013-11-06
更新日期
2016-11-25
语言
英语
国家/地区
United States
NLM ID
101137841
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