首页> 外文期刊>Molecular and Cellular Biology >DNA Damage-Induced Cell Cycle Checkpoint Control Requires CtIP, a Phosphorylation-Dependent Binding Partner of BRCA1 C-Terminal Domains
【24h】

DNA Damage-Induced Cell Cycle Checkpoint Control Requires CtIP, a Phosphorylation-Dependent Binding Partner of BRCA1 C-Terminal Domains

机译:DNA损伤诱导的细胞周期检查点控制需要CtIP,BRCA1 C末端域的磷酸化依赖性结合伙伴。

获取原文
           

摘要

The BRCA1 C-terminal (BRCT) domain has recently been implicated as a phospho-protein binding domain. We demonstrate here that a CTBP-interacting protein CtIP interacts with BRCA1 BRCT domains in a phosphorylation-dependent manner. The CtIP/BRCA1 complex only exists in G2 phase and is required for DNA damage-induced Chk1 phosphorylation and the G2/M transition checkpoint. However, the CtIP/BRCA1 complex is not required for the damage-induced G2 accumulation checkpoint, which is controlled by a separate BRCA1/BACH1 complex. Taken together, these data not only implicate CtIP as a critical player in cell cycle checkpoint control but also provide molecular mechanisms by which BRCA1 controls multiple cell cycle transitions after DNA damage.
机译:BRCA1 C末端(BRCT)域最近被认为是磷酸蛋白结合域。我们在这里证明,CTBP相互作用蛋白CtIP与BRCA1 BRCT域以磷酸化依赖性方式相互作用。 CtIP / BRCA1复合物仅存在于G 2 相中,是DNA损伤诱导的Chk1磷酸化和G 2 / M转换检查点所必需的。但是,损伤诱导的G 2 累积检查点不需要CtIP / BRCA1复合物,该检查点由单独的BRCA1 / BACH1复合物控制。综上所述,这些数据不仅暗示CtIP在细胞周期检查点控制中起着至关重要的作用,而且还提供了分子机制,使BRCA1在DNA损伤后控制多个细胞周期的转变。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号