Agarwal Poonam, Miller Kyle M
Department of Molecular Biosciences, Institute for Cellular and Molecular Biology, University of Texas at Austin, 2506 Speedway Stop A5000, Austin, TX 78712, USA.
Biochem Cell Biol. 2016 Oct;94(5):381-395. doi: 10.1139/bcb-2016-0017. Epub 2016 Apr 13.
DNA damage occurs within the chromatin environment, which ultimately participates in regulating DNA damage response (DDR) pathways and repair of the lesion. DNA damage activates a cascade of signaling events that extensively modulates chromatin structure and organization to coordinate DDR factor recruitment to the break and repair, whilst also promoting the maintenance of normal chromatin functions within the damaged region. For example, DDR pathways must avoid conflicts between other DNA-based processes that function within the context of chromatin, including transcription and replication. The molecular mechanisms governing the recognition, target specificity, and recruitment of DDR factors and enzymes to the fundamental repeating unit of chromatin, i.e., the nucleosome, are poorly understood. Here we present our current view of how chromatin recognition by DDR factors is achieved at the level of the nucleosome. Emerging evidence suggests that the nucleosome surface, including the nucleosome acidic patch, promotes the binding and activity of several DNA damage factors on chromatin. Thus, in addition to interactions with damaged DNA and histone modifications, nucleosome recognition by DDR factors plays a key role in orchestrating the requisite chromatin response to maintain both genome and epigenome integrity.
DNA损伤发生在染色质环境中,染色质最终参与调节DNA损伤反应(DDR)途径以及损伤修复。DNA损伤激活一系列信号事件,这些事件广泛调节染色质结构和组织,以协调DDR因子募集到断裂处并进行修复,同时还促进受损区域内正常染色质功能的维持。例如,DDR途径必须避免在染色质环境中起作用的其他基于DNA的过程(包括转录和复制)之间发生冲突。目前对DDR因子和酶识别、靶向特异性以及募集到染色质基本重复单元(即核小体)的分子机制了解甚少。在此,我们阐述了目前对于DDR因子如何在核小体水平实现对染色质识别的观点。新出现的证据表明,核小体表面,包括核小体酸性斑块,促进了几种DNA损伤因子在染色质上的结合和活性。因此,除了与受损DNA和组蛋白修饰的相互作用外,DDR因子对核小体的识别在协调必要的染色质反应以维持基因组和表观基因组完整性方面起着关键作用。