| Literature DB >> 33296676 |
Zhitai Hao1, Vitaly Epshtein1, Kelly H Kim2, Sergey Proshkin3, Vladimir Svetlov1, Venu Kamarthapu4, Binod Bharati4, Alexander Mironov3, Thomas Walz2, Evgeny Nudler5.
Abstract
Rho is a general transcription termination factor playing essential roles in RNA polymerase (RNAP) recycling, gene regulation, and genomic stability in most bacteria. Traditional models of transcription termination postulate that hexameric Rho loads onto RNA prior to contacting RNAP and then translocates along the transcript in pursuit of the moving RNAP to pull RNA from it. Here, we report the cryoelectron microscopy (cryo-EM) structures of two termination process intermediates. Prior to interacting with RNA, Rho forms a specific "pre-termination complex" (PTC) with RNAP and elongation factors NusA and NusG, which stabilize the PTC. RNA exiting RNAP interacts with NusA before entering the central channel of Rho from the distal C-terminal side of the ring. We map the principal interactions in the PTC and demonstrate their critical role in termination. Our results support a mechanism in which the formation of a persistent PTC is a prerequisite for termination.Entities:
Keywords: RNA polymerase, transcription termination, Rho, NusA, NusG, elongation complex, Cryo-EM
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Year: 2020 PMID: 33296676 PMCID: PMC7904319 DOI: 10.1016/j.molcel.2020.11.013
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970