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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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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. |
format | Online Article Text |
id | pubmed-10085680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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