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Molecular Mechanisms of DNA Replication Checkpoint Activation

The major challenge of the cell cycle is to deliver an intact, and fully duplicated, genetic material to the daughter cells. To this end, progression of DNA synthesis is monitored by a feedback mechanism known as replication checkpoint that is untimely linked to DNA replication. This signaling pathw...

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Autores principales: Recolin, Bénédicte, van der Laan, Siem, Tsanov, Nikolay, Maiorano, Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978517/
https://www.ncbi.nlm.nih.gov/pubmed/24705291
http://dx.doi.org/10.3390/genes5010147
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author Recolin, Bénédicte
van der Laan, Siem
Tsanov, Nikolay
Maiorano, Domenico
author_facet Recolin, Bénédicte
van der Laan, Siem
Tsanov, Nikolay
Maiorano, Domenico
author_sort Recolin, Bénédicte
collection PubMed
description The major challenge of the cell cycle is to deliver an intact, and fully duplicated, genetic material to the daughter cells. To this end, progression of DNA synthesis is monitored by a feedback mechanism known as replication checkpoint that is untimely linked to DNA replication. This signaling pathway ensures coordination of DNA synthesis with cell cycle progression. Failure to activate this checkpoint in response to perturbation of DNA synthesis (replication stress) results in forced cell division leading to chromosome fragmentation, aneuploidy, and genomic instability. In this review, we will describe current knowledge of the molecular determinants of the DNA replication checkpoint in eukaryotic cells and discuss a model of activation of this signaling pathway crucial for maintenance of genomic stability.
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spelling pubmed-39785172014-04-08 Molecular Mechanisms of DNA Replication Checkpoint Activation Recolin, Bénédicte van der Laan, Siem Tsanov, Nikolay Maiorano, Domenico Genes (Basel) Review The major challenge of the cell cycle is to deliver an intact, and fully duplicated, genetic material to the daughter cells. To this end, progression of DNA synthesis is monitored by a feedback mechanism known as replication checkpoint that is untimely linked to DNA replication. This signaling pathway ensures coordination of DNA synthesis with cell cycle progression. Failure to activate this checkpoint in response to perturbation of DNA synthesis (replication stress) results in forced cell division leading to chromosome fragmentation, aneuploidy, and genomic instability. In this review, we will describe current knowledge of the molecular determinants of the DNA replication checkpoint in eukaryotic cells and discuss a model of activation of this signaling pathway crucial for maintenance of genomic stability. MDPI 2014-03-06 /pmc/articles/PMC3978517/ /pubmed/24705291 http://dx.doi.org/10.3390/genes5010147 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Recolin, Bénédicte
van der Laan, Siem
Tsanov, Nikolay
Maiorano, Domenico
Molecular Mechanisms of DNA Replication Checkpoint Activation
title Molecular Mechanisms of DNA Replication Checkpoint Activation
title_full Molecular Mechanisms of DNA Replication Checkpoint Activation
title_fullStr Molecular Mechanisms of DNA Replication Checkpoint Activation
title_full_unstemmed Molecular Mechanisms of DNA Replication Checkpoint Activation
title_short Molecular Mechanisms of DNA Replication Checkpoint Activation
title_sort molecular mechanisms of dna replication checkpoint activation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978517/
https://www.ncbi.nlm.nih.gov/pubmed/24705291
http://dx.doi.org/10.3390/genes5010147
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