Kovalsky O, Grossman L
Department of Biochemistry, The Johns Hopkins University, School of Hygiene and Public Health, Baltimore, MD 21205, USA.
Nucleic Acids Res. 1998 Mar 15;26(6):1466-72. doi: 10.1093/nar/26.6.1466.
One form of nucleotide excision repair (NER) is known to be functionally coupled to transcription, but the nature of this functional link in Escherichia coli is still unclear. Here we have employed the isolated membrane-associated nucleoids from E.coli to examine this issue. We show that the isolated nucleoid fraction is capable of excision of UV-induced pyrimidine dimers when reconstituted with a cytoplasmic fraction resolved by sucrose gradient fractionation. This excision activity by UvrABC is sensitive to rifampicin and is dependent on transcription. By using crosslinking and immunoprecipitation, the damage recognition protein, UvrA, was found to be specifically associated with the RNA polymerase beta subunit on the chromosomal DNA independent of DNA damage. It suggests that at least in one of the NER pathways the search for damage may be directly linked to RNA polymerase. In addition, the role of transcription in the unfolding of the nucleoid structure to allow repair enzymes to gain access to the damaged DNA is described. This study provides insight into the understanding of the transcription-repair coupling in vivo.
已知一种核苷酸切除修复(NER)形式在功能上与转录偶联,但大肠杆菌中这种功能联系的本质仍不清楚。在这里,我们利用从大肠杆菌中分离出的膜相关类核来研究这个问题。我们表明,当用蔗糖梯度分级分离得到的细胞质部分重构时,分离出的类核部分能够切除紫外线诱导的嘧啶二聚体。UvrABC的这种切除活性对利福平敏感且依赖于转录。通过交联和免疫沉淀,发现损伤识别蛋白UvrA与染色体DNA上的RNA聚合酶β亚基特异性结合,与DNA损伤无关。这表明至少在一种NER途径中,对损伤的搜索可能与RNA聚合酶直接相关。此外,还描述了转录在类核结构展开以允许修复酶接触受损DNA中的作用。这项研究为深入理解体内转录-修复偶联提供了见解。