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

被引:42
作者
Choi, Byeong Hyeok [1 ,2 ,3 ]
Chen, Yan [4 ]
Dai, Wei [1 ,2 ,3 ]
机构
[1] New York Univ, Sch Med, Dept Environm Med, Tuxedo Pk, NY USA
[2] New York Univ, Sch Med, Dept Biochem, Tuxedo Pk, NY USA
[3] New York Univ, Sch Med, Dept Mol Pharmacol, Tuxedo Pk, NY USA
[4] Northeastern Univ, Ctr Drug Discovery, Boston, MA 02115 USA
关键词
DNA damage; PTEN; Rad52; chromatin; genotoxic stress; phosphorylation; SPINDLE ASSEMBLY CHECKPOINT; TUMOR-SUPPRESSOR; NUCLEAR PTEN; HOMOLOGOUS RECOMBINATION; MITOTIC RECOMBINATION; SUMO MODIFICATION; UBIQUITIN LIGASE; STABILITY; REPAIR; CELLS;
D O I
10.4161/cc.26465
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
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 GSK3 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 H2AX, 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.
引用
收藏
页码:3442 / 3447
页数:6
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