Rho-dependent transcription termination in bacteria recycles RNA polymerases stalled at DNA lesions.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 30872584.
- Also identified by DOI 10.1038/s41467-019-09146-5 and PMC identifier 6418286.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
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.
Medical subject headings
- DNA Repair
- DNA-Directed RNA Polymerases
- Escherichia coli
- Escherichia coli Proteins
- Transcription Termination, Genetic