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DnaB helicase dynamics in bacterial DNA replication resolved by single-molecule studies
In Escherichia coli, the DnaB helicase forms the basis for the assembly of the DNA replication complex. The stability of DnaB at the replication fork is likely important for successful replication initiation and progression. Single-molecule experiments have significantly changed the classical model...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266626/ https://www.ncbi.nlm.nih.gov/pubmed/34139009 http://dx.doi.org/10.1093/nar/gkab493 |
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author | Spinks, Richard R Spenkelink, Lisanne M Stratmann, Sarah A Xu, Zhi-Qiang Stamford, N Patrick J Brown, Susan E Dixon, Nicholas E Jergic, Slobodan van Oijen, Antoine M |
author_facet | Spinks, Richard R Spenkelink, Lisanne M Stratmann, Sarah A Xu, Zhi-Qiang Stamford, N Patrick J Brown, Susan E Dixon, Nicholas E Jergic, Slobodan van Oijen, Antoine M |
author_sort | Spinks, Richard R |
collection | PubMed |
description | In Escherichia coli, the DnaB helicase forms the basis for the assembly of the DNA replication complex. The stability of DnaB at the replication fork is likely important for successful replication initiation and progression. Single-molecule experiments have significantly changed the classical model of highly stable replication machines by showing that components exchange with free molecules from the environment. However, due to technical limitations, accurate assessments of DnaB stability in the context of replication are lacking. Using in vitro fluorescence single-molecule imaging, we visualise DnaB loaded on forked DNA templates. That these helicases are highly stable at replication forks, indicated by their observed dwell time of ∼30 min. Addition of the remaining replication factors results in a single DnaB helicase integrated as part of an active replisome. In contrast to the dynamic behaviour of other replisome components, DnaB is maintained within the replisome for the entirety of the replication process. Interestingly, we observe a transient interaction of additional helicases with the replication fork. This interaction is dependent on the τ subunit of the clamp-loader complex. Collectively, our single-molecule observations solidify the role of the DnaB helicase as the stable anchor of the replisome, but also reveal its capacity for dynamic interactions. |
format | Online Article Text |
id | pubmed-8266626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82666262021-07-09 DnaB helicase dynamics in bacterial DNA replication resolved by single-molecule studies Spinks, Richard R Spenkelink, Lisanne M Stratmann, Sarah A Xu, Zhi-Qiang Stamford, N Patrick J Brown, Susan E Dixon, Nicholas E Jergic, Slobodan van Oijen, Antoine M Nucleic Acids Res Genome Integrity, Repair and Replication In Escherichia coli, the DnaB helicase forms the basis for the assembly of the DNA replication complex. The stability of DnaB at the replication fork is likely important for successful replication initiation and progression. Single-molecule experiments have significantly changed the classical model of highly stable replication machines by showing that components exchange with free molecules from the environment. However, due to technical limitations, accurate assessments of DnaB stability in the context of replication are lacking. Using in vitro fluorescence single-molecule imaging, we visualise DnaB loaded on forked DNA templates. That these helicases are highly stable at replication forks, indicated by their observed dwell time of ∼30 min. Addition of the remaining replication factors results in a single DnaB helicase integrated as part of an active replisome. In contrast to the dynamic behaviour of other replisome components, DnaB is maintained within the replisome for the entirety of the replication process. Interestingly, we observe a transient interaction of additional helicases with the replication fork. This interaction is dependent on the τ subunit of the clamp-loader complex. Collectively, our single-molecule observations solidify the role of the DnaB helicase as the stable anchor of the replisome, but also reveal its capacity for dynamic interactions. Oxford University Press 2021-06-17 /pmc/articles/PMC8266626/ /pubmed/34139009 http://dx.doi.org/10.1093/nar/gkab493 Text en © The Author(s) 2021. 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 (http://creativecommons.org/licenses/by/4.0/ (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 | Genome Integrity, Repair and Replication Spinks, Richard R Spenkelink, Lisanne M Stratmann, Sarah A Xu, Zhi-Qiang Stamford, N Patrick J Brown, Susan E Dixon, Nicholas E Jergic, Slobodan van Oijen, Antoine M DnaB helicase dynamics in bacterial DNA replication resolved by single-molecule studies |
title | DnaB helicase dynamics in bacterial DNA replication resolved by single-molecule studies |
title_full | DnaB helicase dynamics in bacterial DNA replication resolved by single-molecule studies |
title_fullStr | DnaB helicase dynamics in bacterial DNA replication resolved by single-molecule studies |
title_full_unstemmed | DnaB helicase dynamics in bacterial DNA replication resolved by single-molecule studies |
title_short | DnaB helicase dynamics in bacterial DNA replication resolved by single-molecule studies |
title_sort | dnab helicase dynamics in bacterial dna replication resolved by single-molecule studies |
topic | Genome Integrity, Repair and Replication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266626/ https://www.ncbi.nlm.nih.gov/pubmed/34139009 http://dx.doi.org/10.1093/nar/gkab493 |
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