Kamarthapu Venu, Nudler Evgeny
Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY 10016, USA; Howard Hughes Medical Institute, New York University School of Medicine, New York, NY 10016, USA.
Department of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY 10016, USA; Howard Hughes Medical Institute, New York University School of Medicine, New York, NY 10016, USA.
Curr Opin Microbiol. 2015 Apr;24:15-20. doi: 10.1016/j.mib.2014.12.005. Epub 2015 Jan 14.
Nucleotide excision repair (NER) is an evolutionarily conserved, multistep process that can detect a wide variety of DNA lesions. Transcription coupled repair (TCR) is a subpathway of NER that repairs the transcribed DNA strand faster than the rest of the genome. RNA polymerase (RNAP) stalled at DNA lesions mediates the recruitment of NER enzymes to the damage site. In this review we focus on a newly identified bacterial TCR pathway in which the NER enzyme UvrD, in conjunction with NusA, plays a major role in initiating the repair process. We discuss the tradeoff between the new and conventional models of TCR, how and when each pathway operates to repair DNA damage, and the necessity of pervasive transcription in maintaining genome integrity.
核苷酸切除修复(NER)是一个进化上保守的多步骤过程,能够检测多种DNA损伤。转录偶联修复(TCR)是NER的一个子途径,它比基因组的其他部分更快地修复转录的DNA链。停滞在DNA损伤处的RNA聚合酶(RNAP)介导NER酶募集到损伤位点。在本综述中,我们重点关注新发现的细菌TCR途径,其中NER酶UvrD与NusA共同在启动修复过程中起主要作用。我们讨论了TCR新旧模型之间的权衡、每条途径如何以及何时发挥作用来修复DNA损伤,以及广泛转录在维持基因组完整性中的必要性。