首页> 外文期刊>Nucleic Acids Research >Ctf18 is required for homologous recombination-mediated double-strand break repair
【24h】

Ctf18 is required for homologous recombination-mediated double-strand break repair

机译:Ctf18是同源重组介导的双链断裂修复所必需的

获取原文
获取原文并翻译 | 示例
           

摘要

The efficient repair of double-strand breaks (DSBs) is crucial in maintaining genomic integrity. Sister chromatid cohesion is important for not only faithful chromosome segregation but also for proper DSB repair. During DSB repair, the Smc1-Smc3 cohesin complex is loaded onto chromatin around the DSB to support recombination-mediated DSB repair. In this study, we investigated whether Ctf18, a factor implicated in the establishment of sister chromatid cohesion, is involved in DSB repair in budding yeast. Ctf18 was recruited to HO-endonuclease induced DSB sites in an Mre11-dependent manner and to damaged chromatin in G2/M phase-arrested cells. The ctf18 mutant cells showed high sensitivity to DSB-inducible genotoxic agents and defects in DSB repair, as well as defects in damage-induced recombination between sister chromatids and between homologous chromosomes. These results suggest that Ctf18 is involved in damage-induced homologous recombination.
机译:双链断裂(DSB)的有效修复对于维持基因组完整性至关重要。姐妹染色单体的凝聚力不仅对忠实的染色体分离非常重要,而且对于正确的DSB修复也很重要。在DSB修复过程中,将Smc1-Smc3粘着蛋白复合物加载到DSB周围的染色质上,以支持重组介导的DSB修复。在这项研究中,我们调查了Ctf18是否与姐妹染色单体内聚力的建立有关,是否参与了发芽酵母中DSB的修复。 Ctf18被以Mre11依赖性的方式募集到HO-内切核酸酶诱导的DSB位点,并被G2 / M期阻滞的细胞中的染色质破坏。 ctf18突变细胞对DSB诱导的基因毒性剂和DSB修复缺陷以及姊妹染色单体之间和同源染色体之间的损伤诱导重组缺陷具有很高的敏感性。这些结果表明Ctf18参与损伤诱导的同源重组。

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