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ADP-核糖基化在调控 DNA 双链断裂修复中的作用。

The role of ADP-ribosylation in regulating DNA double-strand break repair.

机构信息

Department of Biochemistry, University of Oxford, Oxford, UK.

出版信息

Cell Cycle. 2012 Jan 1;11(1):48-56. doi: 10.4161/cc.11.1.18793.

Abstract

ADP-ribosylation is the post translational modification of proteins catalysed by ADP-ribosyltransferases (ARTs). ADP-ribosylation has been implicated in a wide variety of cellular processes including cell growth and differentiation, apoptosis and transcriptional regulation. Perhaps the best characterised role, however, is in DNA repair and genome stability where ADP-ribosylation promotes resolution of DNA single strand breaks. Although ADP-ribosylation also occurs at DNA double strand breaks (DSBs), which ARTs catalyse this reaction and the molecular basis of how this modification regulates their repair remains a matter of debate. Here we review recent advances in our understanding of how ADP-ribosylation regulates DSB repair. Specifically, we highlight studies using the genetic model organism Dictyostelium, in addition to vertebrate cells that identify a third ART that accelerates DSB repair by non-homologous end-joining through promoting the interaction of repair factors with DNA lesions. The implications of these data with regards to how ADP-ribosylation regulates DNA repair and genome stability are discussed.

摘要

ADP-核糖基化是由 ADP-核糖基转移酶(ARTs)催化的蛋白质翻译后修饰。ADP-核糖基化参与了多种细胞过程,包括细胞生长和分化、细胞凋亡和转录调控。然而,其最具特征性的作用可能是在 DNA 修复和基因组稳定性方面,ADP-核糖基化促进 DNA 单链断裂的解决。尽管 ADP-核糖基化也发生在 DNA 双链断裂(DSBs)中,ARTs 催化了这一反应,但这种修饰如何调节其修复的分子基础仍存在争议。在这里,我们回顾了近年来对 ADP-核糖基化如何调节 DSB 修复的理解的最新进展。具体而言,我们强调了使用遗传模式生物粘菌以及脊椎动物细胞的研究,这些研究确定了第三种 ART,通过促进修复因子与 DNA 损伤的相互作用,加速非同源末端连接修复 DSB。讨论了这些数据对 ADP-核糖基化如何调节 DNA 修复和基因组稳定性的影响。

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