首页> 外文期刊>Nucleic Acids Research >C-terminal region of bacterial Ku controls DNA bridging, DNA threading and recruitment of DNA ligase D for double strand breaks repair
【24h】

C-terminal region of bacterial Ku controls DNA bridging, DNA threading and recruitment of DNA ligase D for double strand breaks repair

机译:细菌Ku的C末端区域控制DNA桥接,DNA穿线和DNA连接酶D的募集,以修复双链断裂

获取原文
获取原文并翻译 | 示例
           

摘要

Non-homologous end joining is a ligation process repairing DNA double strand breaks in eukaryotes and many prokaryotes. The ring structured eukaryotic Ku binds DNA ends and recruits other factors which can access DNA ends through the threading of Ku inward the DNA, making this protein a key ingredient for the scaffolding of the NHEJ machinery. However, this threading ability seems unevenly conserved among bacterial Ku. As bacterial Ku differ mainly by their C-terminus, we evaluate the role of this region in the loading and the threading abilities of Bacillus subtilis Ku and the stimulation of the DNA ligase LigD. We identify two distinct sub-regions: a ubiquitous minimal C-terminal region and a frequent basic C-terminal extension. We show that truncation of one or both of these sub-regions in Bacillus subtilis Ku impairs the stimulation of the LigD end joining activity in vitro. We further demonstrate that the minimal C-terminus is required for the Ku-LigD interaction, whereas the basic extension controls the threading and DNA bridging abilities of Ku. We propose that the Ku basic C-terminal extension increases the concentration of Ku near DNA ends, favoring the recruitment of LigD at the break, thanks to the minimal C-terminal sub-region.
机译:非同源末端连接是修复真核生物和许多原核​​生物中DNA双链断裂的连接过程。环状结构的真核生物Ku结合DNA末端,并募集其他可通过Ku向内穿入DNA进入DNA末端的因素,从而使该蛋白质成为NHEJ机械支架的关键成分。但是,这种穿线能力在细菌Ku中似乎不均匀地保守。由于细菌Ku主要在其C末端不同,因此我们评估了该区域在枯草芽孢杆菌Ku的负载和穿线能力以及对DNA连接酶LigD的刺激中的作用。我们确定了两个不同的子区域:普遍存在的最小C端区域和频繁的基本C端扩展。我们显示,枯草芽孢杆菌Ku中这些子区域之一或全部被截短会损害LigD末端连接活性的体外刺激。我们进一步证明,最小的C末端是Ku-LigD相互作用所必需的,而基本的延伸控制着Ku的穿线和DNA桥接能力。我们建议,由于最小的C末端亚区域,Ku基本的C末端延伸增加了DNA末端附近的Ku浓度,有利于在断裂时补充LigD。

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