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Transcriptional pause extension benefits the stand-by rather than catch-up Rho-dependent termination

Transcriptional pause is essential for all types of termination. In this single-molecule study on bacterial Rho factor-dependent terminators, we confirm that the three Rho-dependent termination routes operate compatibly together in a single terminator, and discover that their termination efficiencie...

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Autores principales: Song, Eunho, Hwang, Seungha, Munasingha, Palinda Ruvan, Seo, Yeon-Soo, Kang, Jin Young, Kang, Changwon, Hohng, Sungchul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10085680/
https://www.ncbi.nlm.nih.gov/pubmed/36762473
http://dx.doi.org/10.1093/nar/gkad051
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author Song, Eunho
Hwang, Seungha
Munasingha, Palinda Ruvan
Seo, Yeon-Soo
Kang, Jin Young
Kang, Changwon
Hohng, Sungchul
author_facet Song, Eunho
Hwang, Seungha
Munasingha, Palinda Ruvan
Seo, Yeon-Soo
Kang, Jin Young
Kang, Changwon
Hohng, Sungchul
author_sort Song, Eunho
collection PubMed
description Transcriptional pause is essential for all types of termination. In this single-molecule study on bacterial Rho factor-dependent terminators, we confirm that the three Rho-dependent termination routes operate compatibly together in a single terminator, and discover that their termination efficiencies depend on the terminational pauses in unexpected ways. Evidently, the most abundant route is that Rho binds nascent RNA first and catches up with paused RNA polymerase (RNAP) and this catch-up Rho mediates simultaneous releases of transcript RNA and template DNA from RNAP. The fastest route is that the catch-up Rho effects RNA-only release and leads to 1D recycling of RNAP on DNA. The slowest route is that the RNAP-prebound stand-by Rho facilitates only the simultaneous rather than sequential releases. Among the three routes, only the stand-by Rho's termination efficiency positively correlates with pause duration, contrary to a long-standing speculation, invariably in the absence or presence of NusA/NusG factors, competitor RNAs or a crowding agent. Accordingly, the essential terminational pause does not need to be long for the catch-up Rho's terminations, and long pauses benefit only the stand-by Rho's terminations. Furthermore, the Rho-dependent termination of mgtA and ribB riboswitches is controlled mainly by modulation of the stand-by rather than catch-up termination.
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spelling pubmed-100856802023-04-11 Transcriptional pause extension benefits the stand-by rather than catch-up Rho-dependent termination Song, Eunho Hwang, Seungha Munasingha, Palinda Ruvan Seo, Yeon-Soo Kang, Jin Young Kang, Changwon Hohng, Sungchul Nucleic Acids Res Molecular Biology Transcriptional pause is essential for all types of termination. In this single-molecule study on bacterial Rho factor-dependent terminators, we confirm that the three Rho-dependent termination routes operate compatibly together in a single terminator, and discover that their termination efficiencies depend on the terminational pauses in unexpected ways. Evidently, the most abundant route is that Rho binds nascent RNA first and catches up with paused RNA polymerase (RNAP) and this catch-up Rho mediates simultaneous releases of transcript RNA and template DNA from RNAP. The fastest route is that the catch-up Rho effects RNA-only release and leads to 1D recycling of RNAP on DNA. The slowest route is that the RNAP-prebound stand-by Rho facilitates only the simultaneous rather than sequential releases. Among the three routes, only the stand-by Rho's termination efficiency positively correlates with pause duration, contrary to a long-standing speculation, invariably in the absence or presence of NusA/NusG factors, competitor RNAs or a crowding agent. Accordingly, the essential terminational pause does not need to be long for the catch-up Rho's terminations, and long pauses benefit only the stand-by Rho's terminations. Furthermore, the Rho-dependent termination of mgtA and ribB riboswitches is controlled mainly by modulation of the stand-by rather than catch-up termination. Oxford University Press 2023-02-10 /pmc/articles/PMC10085680/ /pubmed/36762473 http://dx.doi.org/10.1093/nar/gkad051 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Song, Eunho
Hwang, Seungha
Munasingha, Palinda Ruvan
Seo, Yeon-Soo
Kang, Jin Young
Kang, Changwon
Hohng, Sungchul
Transcriptional pause extension benefits the stand-by rather than catch-up Rho-dependent termination
title Transcriptional pause extension benefits the stand-by rather than catch-up Rho-dependent termination
title_full Transcriptional pause extension benefits the stand-by rather than catch-up Rho-dependent termination
title_fullStr Transcriptional pause extension benefits the stand-by rather than catch-up Rho-dependent termination
title_full_unstemmed Transcriptional pause extension benefits the stand-by rather than catch-up Rho-dependent termination
title_short Transcriptional pause extension benefits the stand-by rather than catch-up Rho-dependent termination
title_sort transcriptional pause extension benefits the stand-by rather than catch-up rho-dependent termination
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10085680/
https://www.ncbi.nlm.nih.gov/pubmed/36762473
http://dx.doi.org/10.1093/nar/gkad051
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