The Heritability of Replication Problems

The major challenge of DNA replication is to provide daughter cells with intact and fully duplicated genetic material. However, various endogenous or environmental factors can slow down or stall DNA replication forks; these replication problems are known to fuel genomic instability and associated pa...

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Main Author: Jean-Sébastien Hoffmann
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/6/1464
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spelling doaj-99d6e7f968d34b55a394080d850a97fc2021-06-30T23:54:27ZengMDPI AGCells2073-44092021-06-01101464146410.3390/cells10061464The Heritability of Replication ProblemsJean-Sébastien Hoffmann0Laboratoire de Pathologie, Laboratoire d’Excellence Toulouse Cancer, CHU Toulouse, Institut Universitaire du Cancer-Toulouse, Oncopole, 1 Avenue Irène-Joliot-Curie, CEDEX, 31059 Toulouse, FranceThe major challenge of DNA replication is to provide daughter cells with intact and fully duplicated genetic material. However, various endogenous or environmental factors can slow down or stall DNA replication forks; these replication problems are known to fuel genomic instability and associated pathology, including cancer progression. Whereas the mechanisms emphasizing the source and the cellular responses of replicative problems have attracted much consideration over the past decade, the propagation through mitosis of genome modification and its heritability in daughter cells when the stress is not strong enough to provoke a checkpoint response in G2/M was much less documented. Some recent studies addressing whether low replication stress could impact the DNA replication program of the next generation of cells made the remarkable discovery that DNA damage can indeed be transmitted to daughter cells and can be processed in the subsequent S-phase, and that the replication timing program at a subset of chromosomal domains can also be impacted in the next generation of cells. Such a progression of replication problems into mitosis and daughter cells may appear counter-intuitive, but it could offer considerable advantages by alerting the next generation of cells of potentially risky loci and offering the possibility of an adaptive mechanism to anticipate a reiteration of problems, notably for cancer cells in the context of resistance to therapy.https://www.mdpi.com/2073-4409/10/6/1464DNA replicationreplicative stressDNA damagereplication timing
collection DOAJ
language English
format Article
sources DOAJ
author Jean-Sébastien Hoffmann
spellingShingle Jean-Sébastien Hoffmann
The Heritability of Replication Problems
Cells
DNA replication
replicative stress
DNA damage
replication timing
author_facet Jean-Sébastien Hoffmann
author_sort Jean-Sébastien Hoffmann
title The Heritability of Replication Problems
title_short The Heritability of Replication Problems
title_full The Heritability of Replication Problems
title_fullStr The Heritability of Replication Problems
title_full_unstemmed The Heritability of Replication Problems
title_sort heritability of replication problems
publisher MDPI AG
series Cells
issn 2073-4409
publishDate 2021-06-01
description The major challenge of DNA replication is to provide daughter cells with intact and fully duplicated genetic material. However, various endogenous or environmental factors can slow down or stall DNA replication forks; these replication problems are known to fuel genomic instability and associated pathology, including cancer progression. Whereas the mechanisms emphasizing the source and the cellular responses of replicative problems have attracted much consideration over the past decade, the propagation through mitosis of genome modification and its heritability in daughter cells when the stress is not strong enough to provoke a checkpoint response in G2/M was much less documented. Some recent studies addressing whether low replication stress could impact the DNA replication program of the next generation of cells made the remarkable discovery that DNA damage can indeed be transmitted to daughter cells and can be processed in the subsequent S-phase, and that the replication timing program at a subset of chromosomal domains can also be impacted in the next generation of cells. Such a progression of replication problems into mitosis and daughter cells may appear counter-intuitive, but it could offer considerable advantages by alerting the next generation of cells of potentially risky loci and offering the possibility of an adaptive mechanism to anticipate a reiteration of problems, notably for cancer cells in the context of resistance to therapy.
topic DNA replication
replicative stress
DNA damage
replication timing
url https://www.mdpi.com/2073-4409/10/6/1464
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