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Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase

In vivo studies suggest that replication forks are arrested due to encounters with head-on transcription complexes. Yet, the fate of the replisome and RNA polymerase (RNAP) following a head-on collision is unknown. Here, we find that the E. coli replisome stalls upon collision with a head-on transcr...

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Autores principales: Pomerantz, Richard T., O'Donnell, Mike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3146238/
https://www.ncbi.nlm.nih.gov/pubmed/20436399
http://dx.doi.org/10.3791/1919
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author Pomerantz, Richard T.
O'Donnell, Mike
author_facet Pomerantz, Richard T.
O'Donnell, Mike
author_sort Pomerantz, Richard T.
collection PubMed
description In vivo studies suggest that replication forks are arrested due to encounters with head-on transcription complexes. Yet, the fate of the replisome and RNA polymerase (RNAP) following a head-on collision is unknown. Here, we find that the E. coli replisome stalls upon collision with a head-on transcription complex, but instead of collapsing, the replication fork remains highly stable and eventually resumes elongation after displacing the RNAP from DNA. We also find that the transcription-repair coupling factor, Mfd, promotes direct restart of the fork following the collision by facilitating displacement of the RNAP. These findings demonstrate the intrinsic stability of the replication apparatus and a novel role for the transcription-coupled repair pathway in promoting replication past a RNAP block.
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spelling pubmed-31462382011-08-10 Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase Pomerantz, Richard T. O'Donnell, Mike J Vis Exp Cellular Biology In vivo studies suggest that replication forks are arrested due to encounters with head-on transcription complexes. Yet, the fate of the replisome and RNA polymerase (RNAP) following a head-on collision is unknown. Here, we find that the E. coli replisome stalls upon collision with a head-on transcription complex, but instead of collapsing, the replication fork remains highly stable and eventually resumes elongation after displacing the RNAP from DNA. We also find that the transcription-repair coupling factor, Mfd, promotes direct restart of the fork following the collision by facilitating displacement of the RNAP. These findings demonstrate the intrinsic stability of the replication apparatus and a novel role for the transcription-coupled repair pathway in promoting replication past a RNAP block. MyJove Corporation 2010-04-29 /pmc/articles/PMC3146238/ /pubmed/20436399 http://dx.doi.org/10.3791/1919 Text en Copyright © 2010, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Cellular Biology
Pomerantz, Richard T.
O'Donnell, Mike
Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
title Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
title_full Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
title_fullStr Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
title_full_unstemmed Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
title_short Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
title_sort direct restart of a replication fork stalled by a head-on rna polymerase
topic Cellular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3146238/
https://www.ncbi.nlm.nih.gov/pubmed/20436399
http://dx.doi.org/10.3791/1919
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