Lisby Michael, Rothstein Rodney
Institute of Molecular Biology, University of Copenhagen, Øster Farimagsgade 2 A, DK-1353 Copenhagen K, Denmark.
Biochimie. 2005 Jul;87(7):579-89. doi: 10.1016/j.biochi.2004.10.023. Epub 2004 Dec 15.
In eukaryotes, the cellular response to DNA damage depends on the type of DNA structure being recognized by the checkpoint and repair machinery. DNA ends and single-stranded DNA are hallmarks of double-strand breaks and replication stress. These two structures are recognized by distinct sets of proteins, which are reorganized into a focal assembly at the lesion. Moreover, the composition of these foci is coordinated with cell cycle progression, reflecting the favoring of end-joining in the G1 phase and homologous recombination in S and G2. The assembly of proteins at sites of DNA damage is largely controlled by a network of protein-protein interactions, with the Mre11 complex initiating assembly at DNA ends and replication protein A directing recruitment to single-stranded DNA. This review summarizes current knowledge on the cellular organization of DSB repair and checkpoint proteins focusing on budding yeast and mammalian cells.
在真核生物中,细胞对DNA损伤的反应取决于检查点和修复机制所识别的DNA结构类型。DNA末端和单链DNA是双链断裂和复制应激的标志。这两种结构由不同的蛋白质组识别,这些蛋白质在损伤部位重新组织成焦点聚集物。此外,这些焦点的组成与细胞周期进程相协调,反映出在G1期有利于末端连接,而在S期和G2期有利于同源重组。DNA损伤位点处蛋白质的组装在很大程度上受蛋白质-蛋白质相互作用网络的控制,Mre11复合物在DNA末端启动组装,复制蛋白A引导向单链DNA的募集。本综述总结了关于双链断裂修复和检查点蛋白细胞组织的当前知识,重点关注芽殖酵母和哺乳动物细胞。