Rho-dependent transcription termination in bacteria recycles RNA polymerases stalled at DNA lesions

被引:27
作者
Jain, Sriyans [1 ]
Gupta, Richa [1 ]
Sen, Ranjan [1 ]
机构
[1] Ctr DNA Fingerprinting & Diagnost, Lab Transcript, Tuljaguda Complex,4-1-714 Mouzamjahi Rd, Hyderabad 500001, India
关键词
COUPLED REPAIR; ESCHERICHIA-COLI; DEFECTIVE-MUTANTS; MECHANISM; MFD; ELONGATION; PROTEIN; DAMAGE; ROLES; SITES;
D O I
10.1038/s41467-019-09146-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In bacteria, transcription-coupled repair of DNA lesions initiates after the Mfd protein removes RNA polymerases (RNAPs) stalled at the lesions. The bacterial RNA helicase, Rho, is a transcription termination protein that dislodges the elongation complexes. Here, we show that Rho dislodges the stalled RNAPs at DNA lesions. Strains defective in both Rho and Mfd are susceptible to DNA-damaging agents and are inefficient in repairing or propagating UV-damaged DNA. In vitro transcription assays show that Rho dissociates the stalled elongation complexes at the DNA lesions. We conclude that Rho-dependent termination recycles stalled RNAPs, which might facilitate DNA repair and other DNA-dependent processes essential for bacterial cell survival. We surmise that Rho might compete with, or augment, the Mfd function.
引用
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页数:12
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