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A multi-functional role for the MCM8/9 helicase complex in maintaining fork integrity during replication stress
The minichromosome maintenance (MCM) 8/9 helicase is a AAA(+) complex involved in DNA replication-associated repair. Despite high sequence homology to the MCM2-7 helicase, a precise cellular role for MCM8/9 has remained elusive. We have interrogated the DNA synthesis ability and replication fork sta...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427862/ https://www.ncbi.nlm.nih.gov/pubmed/36042199 http://dx.doi.org/10.1038/s41467-022-32583-8 |
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author | Griffin, Wezley C. McKinzey, David R. Klinzing, Kathleen N. Baratam, Rithvik Eliyapura, Achini Trakselis, Michael A. |
author_facet | Griffin, Wezley C. McKinzey, David R. Klinzing, Kathleen N. Baratam, Rithvik Eliyapura, Achini Trakselis, Michael A. |
author_sort | Griffin, Wezley C. |
collection | PubMed |
description | The minichromosome maintenance (MCM) 8/9 helicase is a AAA(+) complex involved in DNA replication-associated repair. Despite high sequence homology to the MCM2-7 helicase, a precise cellular role for MCM8/9 has remained elusive. We have interrogated the DNA synthesis ability and replication fork stability in cells lacking MCM8 or 9 and find that there is a functional partitioning of MCM8/9 activity between promoting replication fork progression and protecting persistently stalled forks. The helicase function of MCM8/9 aids in normal replication fork progression, but upon persistent stalling, MCM8/9 directs additional downstream stabilizers, including BRCA1 and Rad51, to protect forks from excessive degradation. Loss of MCM8 or 9 slows the overall replication rate and allows for excessive nascent strand degradation, detectable by increased markers of genomic damage. This evidence defines multifunctional roles for MCM8/9 in promoting normal replication fork progression and genome integrity following stress. |
format | Online Article Text |
id | pubmed-9427862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94278622022-09-01 A multi-functional role for the MCM8/9 helicase complex in maintaining fork integrity during replication stress Griffin, Wezley C. McKinzey, David R. Klinzing, Kathleen N. Baratam, Rithvik Eliyapura, Achini Trakselis, Michael A. Nat Commun Article The minichromosome maintenance (MCM) 8/9 helicase is a AAA(+) complex involved in DNA replication-associated repair. Despite high sequence homology to the MCM2-7 helicase, a precise cellular role for MCM8/9 has remained elusive. We have interrogated the DNA synthesis ability and replication fork stability in cells lacking MCM8 or 9 and find that there is a functional partitioning of MCM8/9 activity between promoting replication fork progression and protecting persistently stalled forks. The helicase function of MCM8/9 aids in normal replication fork progression, but upon persistent stalling, MCM8/9 directs additional downstream stabilizers, including BRCA1 and Rad51, to protect forks from excessive degradation. Loss of MCM8 or 9 slows the overall replication rate and allows for excessive nascent strand degradation, detectable by increased markers of genomic damage. This evidence defines multifunctional roles for MCM8/9 in promoting normal replication fork progression and genome integrity following stress. Nature Publishing Group UK 2022-08-30 /pmc/articles/PMC9427862/ /pubmed/36042199 http://dx.doi.org/10.1038/s41467-022-32583-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Griffin, Wezley C. McKinzey, David R. Klinzing, Kathleen N. Baratam, Rithvik Eliyapura, Achini Trakselis, Michael A. A multi-functional role for the MCM8/9 helicase complex in maintaining fork integrity during replication stress |
title | A multi-functional role for the MCM8/9 helicase complex in maintaining fork integrity during replication stress |
title_full | A multi-functional role for the MCM8/9 helicase complex in maintaining fork integrity during replication stress |
title_fullStr | A multi-functional role for the MCM8/9 helicase complex in maintaining fork integrity during replication stress |
title_full_unstemmed | A multi-functional role for the MCM8/9 helicase complex in maintaining fork integrity during replication stress |
title_short | A multi-functional role for the MCM8/9 helicase complex in maintaining fork integrity during replication stress |
title_sort | multi-functional role for the mcm8/9 helicase complex in maintaining fork integrity during replication stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427862/ https://www.ncbi.nlm.nih.gov/pubmed/36042199 http://dx.doi.org/10.1038/s41467-022-32583-8 |
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