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Transcription leads to pervasive replisome instability in bacteria
The canonical model of DNA replication describes a highly-processive and largely continuous process by which the genome is duplicated. This continuous model is based upon in vitro reconstitution and in vivo ensemble experiments. Here, we characterize the replisome-complex stoichiometry and dynamics...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5305214/ https://www.ncbi.nlm.nih.gov/pubmed/28092263 http://dx.doi.org/10.7554/eLife.19848 |
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author | Mangiameli, Sarah M Merrikh, Christopher N Wiggins, Paul A Merrikh, Houra |
author_facet | Mangiameli, Sarah M Merrikh, Christopher N Wiggins, Paul A Merrikh, Houra |
author_sort | Mangiameli, Sarah M |
collection | PubMed |
description | The canonical model of DNA replication describes a highly-processive and largely continuous process by which the genome is duplicated. This continuous model is based upon in vitro reconstitution and in vivo ensemble experiments. Here, we characterize the replisome-complex stoichiometry and dynamics with single-molecule resolution in bacterial cells. Strikingly, the stoichiometries of the replicative helicase, DNA polymerase, and clamp loader complexes are consistent with the presence of only one active replisome in a significant fraction of cells (>40%). Furthermore, many of the observed complexes have short lifetimes (<8 min), suggesting that replisome disassembly is quite prevalent, possibly occurring several times per cell cycle. The instability of the replisome complex is conflict-induced: transcription inhibition stabilizes these complexes, restoring the second replisome in many of the cells. Our results suggest that, in contrast to the canonical model, DNA replication is a largely discontinuous process in vivo due to pervasive replication-transcription conflicts. DOI: http://dx.doi.org/10.7554/eLife.19848.001 |
format | Online Article Text |
id | pubmed-5305214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53052142017-02-15 Transcription leads to pervasive replisome instability in bacteria Mangiameli, Sarah M Merrikh, Christopher N Wiggins, Paul A Merrikh, Houra eLife Biophysics and Structural Biology The canonical model of DNA replication describes a highly-processive and largely continuous process by which the genome is duplicated. This continuous model is based upon in vitro reconstitution and in vivo ensemble experiments. Here, we characterize the replisome-complex stoichiometry and dynamics with single-molecule resolution in bacterial cells. Strikingly, the stoichiometries of the replicative helicase, DNA polymerase, and clamp loader complexes are consistent with the presence of only one active replisome in a significant fraction of cells (>40%). Furthermore, many of the observed complexes have short lifetimes (<8 min), suggesting that replisome disassembly is quite prevalent, possibly occurring several times per cell cycle. The instability of the replisome complex is conflict-induced: transcription inhibition stabilizes these complexes, restoring the second replisome in many of the cells. Our results suggest that, in contrast to the canonical model, DNA replication is a largely discontinuous process in vivo due to pervasive replication-transcription conflicts. DOI: http://dx.doi.org/10.7554/eLife.19848.001 eLife Sciences Publications, Ltd 2017-01-16 /pmc/articles/PMC5305214/ /pubmed/28092263 http://dx.doi.org/10.7554/eLife.19848 Text en © 2017, Mangiameli et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Mangiameli, Sarah M Merrikh, Christopher N Wiggins, Paul A Merrikh, Houra Transcription leads to pervasive replisome instability in bacteria |
title | Transcription leads to pervasive replisome instability in bacteria |
title_full | Transcription leads to pervasive replisome instability in bacteria |
title_fullStr | Transcription leads to pervasive replisome instability in bacteria |
title_full_unstemmed | Transcription leads to pervasive replisome instability in bacteria |
title_short | Transcription leads to pervasive replisome instability in bacteria |
title_sort | transcription leads to pervasive replisome instability in bacteria |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5305214/ https://www.ncbi.nlm.nih.gov/pubmed/28092263 http://dx.doi.org/10.7554/eLife.19848 |
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