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Frequent exchange of the DNA polymerase during bacterial chromosome replication
The replisome is a multiprotein machine that carries out DNA replication. In Escherichia coli, a single pair of replisomes is responsible for duplicating the entire 4.6 Mbp circular chromosome. In vitro studies of reconstituted E. coli replisomes have attributed this remarkable processivity to the h...
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/PMC5403216/ https://www.ncbi.nlm.nih.gov/pubmed/28362256 http://dx.doi.org/10.7554/eLife.21763 |
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author | Beattie, Thomas R Kapadia, Nitin Nicolas, Emilien Uphoff, Stephan Wollman, Adam JM Leake, Mark C Reyes-Lamothe, Rodrigo |
author_facet | Beattie, Thomas R Kapadia, Nitin Nicolas, Emilien Uphoff, Stephan Wollman, Adam JM Leake, Mark C Reyes-Lamothe, Rodrigo |
author_sort | Beattie, Thomas R |
collection | PubMed |
description | The replisome is a multiprotein machine that carries out DNA replication. In Escherichia coli, a single pair of replisomes is responsible for duplicating the entire 4.6 Mbp circular chromosome. In vitro studies of reconstituted E. coli replisomes have attributed this remarkable processivity to the high stability of the replisome once assembled on DNA. By examining replisomes in live E. coli with fluorescence microscopy, we found that the Pol III* subassembly frequently disengages from the replisome during DNA synthesis and exchanges with free copies from solution. In contrast, the DnaB helicase associates stably with the replication fork, providing the molecular basis for how the E. coli replisome can maintain high processivity and yet possess the flexibility to bypass obstructions in template DNA. Our data challenges the widely-accepted semi-discontinuous model of chromosomal replication, instead supporting a fully discontinuous mechanism in which synthesis of both leading and lagging strands is frequently interrupted. DOI: http://dx.doi.org/10.7554/eLife.21763.001 |
format | Online Article Text |
id | pubmed-5403216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54032162017-04-26 Frequent exchange of the DNA polymerase during bacterial chromosome replication Beattie, Thomas R Kapadia, Nitin Nicolas, Emilien Uphoff, Stephan Wollman, Adam JM Leake, Mark C Reyes-Lamothe, Rodrigo eLife Biochemistry The replisome is a multiprotein machine that carries out DNA replication. In Escherichia coli, a single pair of replisomes is responsible for duplicating the entire 4.6 Mbp circular chromosome. In vitro studies of reconstituted E. coli replisomes have attributed this remarkable processivity to the high stability of the replisome once assembled on DNA. By examining replisomes in live E. coli with fluorescence microscopy, we found that the Pol III* subassembly frequently disengages from the replisome during DNA synthesis and exchanges with free copies from solution. In contrast, the DnaB helicase associates stably with the replication fork, providing the molecular basis for how the E. coli replisome can maintain high processivity and yet possess the flexibility to bypass obstructions in template DNA. Our data challenges the widely-accepted semi-discontinuous model of chromosomal replication, instead supporting a fully discontinuous mechanism in which synthesis of both leading and lagging strands is frequently interrupted. DOI: http://dx.doi.org/10.7554/eLife.21763.001 eLife Sciences Publications, Ltd 2017-03-31 /pmc/articles/PMC5403216/ /pubmed/28362256 http://dx.doi.org/10.7554/eLife.21763 Text en © 2017, Beattie 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 | Biochemistry Beattie, Thomas R Kapadia, Nitin Nicolas, Emilien Uphoff, Stephan Wollman, Adam JM Leake, Mark C Reyes-Lamothe, Rodrigo Frequent exchange of the DNA polymerase during bacterial chromosome replication |
title | Frequent exchange of the DNA polymerase during bacterial chromosome replication |
title_full | Frequent exchange of the DNA polymerase during bacterial chromosome replication |
title_fullStr | Frequent exchange of the DNA polymerase during bacterial chromosome replication |
title_full_unstemmed | Frequent exchange of the DNA polymerase during bacterial chromosome replication |
title_short | Frequent exchange of the DNA polymerase during bacterial chromosome replication |
title_sort | frequent exchange of the dna polymerase during bacterial chromosome replication |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403216/ https://www.ncbi.nlm.nih.gov/pubmed/28362256 http://dx.doi.org/10.7554/eLife.21763 |
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