Acta Biochim Biophys Sin (Shanghai). 2022 May 25;54(6):807-819. doi: 10.3724/abbs.2022054.
Nucleotide excision repair (NER) is a major pathway to deal with bulky adducts induced by various environmental toxins in all cellular organisms. The two sub-pathways of NER, global genome repair (GGR) and transcription-coupled repair (TCR), differ in the damage recognition modes. In this review, we describe the molecular mechanism of NER in mammalian cells, especially the details of damage recognition steps in both sub-pathways. We also introduce new sequencing methods for genome-wide mapping of NER, as well as recent advances about NER in chromatin by these methods. Finally, the roles of NER factors in repairing oxidative damages and resolving R-loops are discussed.
核苷酸切除修复(NER)是一种主要的途径,可用于处理所有生物体细胞中各种环境毒素诱导的大体积加合物。NER 的两个亚途径,全基因组修复(GGR)和转录偶联修复(TCR),在损伤识别模式上有所不同。在这篇综述中,我们描述了哺乳动物细胞中 NER 的分子机制,特别是两个亚途径中损伤识别步骤的细节。我们还介绍了用于全基因组 NER 图谱绘制的新测序方法,以及这些方法在染色质中 NER 的最新进展。最后,讨论了 NER 因子在修复氧化损伤和解决 R-环方面的作用。