CtIP is required for DNA damage-dependent induction of P21.

CtIP is required for DNA damage-dependent induction of P21.
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DNA 损伤依赖性 P21 诱导需要 CtIP

DOI:
10.4161/cc.26810
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发表时间:
2014
期刊:
Cell cycle (Georgetown, Tex.)
影响因子:
--
通讯作者:
Xu X
Xu X
中科院分区:
其他
文献类型:
--
作者:
Liu B;Cong R;Peng B;Zhu B;Dou G;Ai H;Zhang X;Wang Z;Xu X

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DNA内切酶CtIP参与DNA双链断裂修复和转录抑制/激活。细胞周期蛋白依赖性激酶抑制因子P21在转录水平上受多种胁迫的诱导,控制着G1/S的转换。在本报告中,我们发现CtIP与P21启动子结合,并且这种结合在DNA损伤时被增强。同时,CtIP的异位表达增加了P21启动子的活性,并且这种增加在喜树碱处理后增强。相反,DNA损伤不能诱导CtIP缺陷细胞中P21基因的表达。综上所述,我们的数据表明,CtIP在DNA损伤诱导的P21诱导中是必需的。
DNA endonuclease CtIP is involved in both DNA double-strand break (DSB) repair and transcriptional repression/activation. The cyclin-dependent kinase inhibitor P21, which is induced at transcription level in response to a variety of stresses, controls G1/S transition. In this report, we found that CtIP bound to the P21 promoter, and this binding was enhanced in response to DNA damage. Concomitantly, ectopic expression of CtIP increased P21 promoter activity, and this increment was enhanced upon camptothecin treatment. Conversely, DNA damage failed to induce P21 gene expression in CtIP-deficient cells. Taken together, our data demonstrate that CtIP is required for DNA damage-induced P21 induction.
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