Department of Biology, Tufts University Medford, MA, USA.
Department of Biology, Tufts University Medford, MA, USA ; Program in Genetics, Sackler School of Graduate Biomedical Sciences, Tufts University Boston, MA, USA.
Front Genet. 2014 Sep 5;5:296. doi: 10.3389/fgene.2014.00296. eCollection 2014.
DNA repair must take place in the context of chromatin, and chromatin modifications and DNA repair are intimately linked. The study of double-strand break repair has revealed numerous histone modifications that occur after induction of a DSB, and modification of the repair factors themselves can also occur. In some cases the function of the modification is at least partially understood, but in many cases it is not yet clear. Although DSB repair is a crucial activity for cell survival, DSBs account for only a small percentage of the DNA lesions that occur over the lifetime of a cell. Repair of single-strand gaps, nicks, stalled forks, alternative DNA structures, and base lesions must also occur in a chromatin context. There is increasing evidence that these repair pathways are also regulated by histone modifications and chromatin remodeling. In this review, we will summarize the current state of knowledge of chromatin modifications that occur during non-DSB repair, highlighting similarities and differences to DSB repair as well as remaining questions.
DNA 修复必须在染色质的背景下进行,而且染色质修饰和 DNA 修复密切相关。对双链断裂修复的研究揭示了许多在 DSB 诱导后发生的组蛋白修饰,并且修复因子本身的修饰也可能发生。在某些情况下,修饰的功能至少部分被理解,但在许多情况下,它仍然不清楚。虽然 DSB 修复是细胞存活的关键活动,但 DSB 仅占细胞一生中发生的 DNA 损伤的一小部分。单链缺口、切口、停滞的叉、替代 DNA 结构和碱基损伤的修复也必须在染色质背景下进行。越来越多的证据表明,这些修复途径也受到组蛋白修饰和染色质重塑的调控。在这篇综述中,我们将总结在非 DSB 修复过程中发生的染色质修饰的现有知识状态,突出 DSB 修复的相似性和差异性以及仍然存在的问题。