Caldecott Keith W
Genome Damage and Stability Centre, University of Sussex, Science Park Road, BN1 9RQ, Falmer Brighton, UK.
DNA Repair (Amst). 2003 Sep 18;2(9):955-69. doi: 10.1016/s1568-7864(03)00118-6.
DNA single-strand breaks can arise indirectly, as normal intermediates of DNA base excision repair, or directly from damage to deoxyribose. Because single-strand breaks are induced by endogenous reactive molecules such as reactive oxygen species, these lesions pose a continuous threat to genetic integrity. XRCC1 protein plays a major role in facilitating the repair of single-strand breaks in mammalian cells, via an ability to interact with multiple enzymatic components of repair reactions. Here, the protein-protein interactions facilitated by XRCC1, and the repair processes in which these interactions operate, are reviewed. Models for the repair of single-strand breaks during base excision repair and at direct breaks are presented.
DNA单链断裂可间接产生,作为DNA碱基切除修复的正常中间体,也可直接由脱氧核糖损伤引起。由于单链断裂是由内源性活性分子如活性氧诱导产生的,这些损伤对遗传完整性构成持续威胁。XRCC1蛋白在促进哺乳动物细胞单链断裂的修复中起主要作用,它能够与修复反应的多种酶成分相互作用。本文综述了由XRCC1促进的蛋白质-蛋白质相互作用,以及这些相互作用所参与的修复过程。还介绍了碱基切除修复过程中以及直接断裂处单链断裂的修复模型。