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Chromatin as a Platform for Modulating the Replication Stress Response
Eukaryotic DNA replication occurs in the context of chromatin. Recent years have seen major advances in our understanding of histone supply, histone recycling and nascent histone incorporation during replication. Furthermore, much is now known about the roles of histone remodellers and post-translat...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316668/ https://www.ncbi.nlm.nih.gov/pubmed/30544989 http://dx.doi.org/10.3390/genes9120622 |
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author | Fournier, Louis-Alexandre Kumar, Arun Stirling, Peter C. |
author_facet | Fournier, Louis-Alexandre Kumar, Arun Stirling, Peter C. |
author_sort | Fournier, Louis-Alexandre |
collection | PubMed |
description | Eukaryotic DNA replication occurs in the context of chromatin. Recent years have seen major advances in our understanding of histone supply, histone recycling and nascent histone incorporation during replication. Furthermore, much is now known about the roles of histone remodellers and post-translational modifications in replication. It has also become clear that nucleosome dynamics during replication play critical roles in genome maintenance and that chromatin modifiers are important for preventing DNA replication stress. An understanding of how cells deploy specific nucleosome modifiers, chaperones and remodellers directly at sites of replication fork stalling has been building more slowly. Here we will specifically discuss recent advances in understanding how chromatin composition contribute to replication fork stability and restart. |
format | Online Article Text |
id | pubmed-6316668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63166682019-01-09 Chromatin as a Platform for Modulating the Replication Stress Response Fournier, Louis-Alexandre Kumar, Arun Stirling, Peter C. Genes (Basel) Review Eukaryotic DNA replication occurs in the context of chromatin. Recent years have seen major advances in our understanding of histone supply, histone recycling and nascent histone incorporation during replication. Furthermore, much is now known about the roles of histone remodellers and post-translational modifications in replication. It has also become clear that nucleosome dynamics during replication play critical roles in genome maintenance and that chromatin modifiers are important for preventing DNA replication stress. An understanding of how cells deploy specific nucleosome modifiers, chaperones and remodellers directly at sites of replication fork stalling has been building more slowly. Here we will specifically discuss recent advances in understanding how chromatin composition contribute to replication fork stability and restart. MDPI 2018-12-11 /pmc/articles/PMC6316668/ /pubmed/30544989 http://dx.doi.org/10.3390/genes9120622 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Fournier, Louis-Alexandre Kumar, Arun Stirling, Peter C. Chromatin as a Platform for Modulating the Replication Stress Response |
title | Chromatin as a Platform for Modulating the Replication Stress Response |
title_full | Chromatin as a Platform for Modulating the Replication Stress Response |
title_fullStr | Chromatin as a Platform for Modulating the Replication Stress Response |
title_full_unstemmed | Chromatin as a Platform for Modulating the Replication Stress Response |
title_short | Chromatin as a Platform for Modulating the Replication Stress Response |
title_sort | chromatin as a platform for modulating the replication stress response |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316668/ https://www.ncbi.nlm.nih.gov/pubmed/30544989 http://dx.doi.org/10.3390/genes9120622 |
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