Nouspikel T
Institute for Cancer Studies, University of Sheffield, Sheffield, United Kingdom.
Cell Mol Life Sci. 2009 Mar;66(6):994-1009. doi: 10.1007/s00018-009-8737-y.
Nucleotide excision repair (NER) is one of the most versatile DNA repair systems. It can be subdivided into several, differentially regulated, subpathways: global genome repair (GGR), transcription-coupled repair (TCR), and transcription domain-associated repair (DAR). This review begins with a brief overview of the numerous types of DNA lesions handled by NER, and proceeds to describe in detail the molecular mechanisms of NER. It then addresses heterogeneities in NER activity in physiological situations (e. g. in differentiated cells) and explores the underlying regulatory mechanism. It then reviews several inherited diseases associated with NER deficiencies: xeroderma pigmentosum, Cockayne syndrome, trichothiodystrophy, UV-sensitive syndrome. It concludes by discussing several currently unresolved issues, relating either to the cause of the above diseases or to the mechanistic details of the various NER subpathways and of their regulation. (Part of a Multi-author Review).
核苷酸切除修复(NER)是最通用的DNA修复系统之一。它可细分为几种受不同调控的子途径:全基因组修复(GGR)、转录偶联修复(TCR)和转录域相关修复(DAR)。本综述首先简要概述了NER处理的多种类型的DNA损伤,接着详细描述了NER的分子机制。然后探讨了生理情况下(如分化细胞中)NER活性的异质性,并探究了其潜在的调控机制。随后综述了几种与NER缺陷相关的遗传性疾病:着色性干皮病、科凯恩综合征、毛发硫营养不良、紫外线敏感综合征。最后讨论了几个目前尚未解决的问题,这些问题要么与上述疾病的病因有关,要么与各种NER子途径及其调控的机制细节有关。(多位作者综述的一部分)