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Do replication forks control late origin firing in Saccharomyces cerevisiae?

Recent studies of eukaryotic DNA replication timing profiles suggest that the time-dependent rate of origin firing, I(t), has a universal shape, which ensures a reproducible replication completion time. However, measurements of I(t) are based on population averages, which may bias the shape of the I...

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Autores principales: Ma, Emilie, Hyrien, Olivier, Goldar, Arach
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3300028/
https://www.ncbi.nlm.nih.gov/pubmed/22086957
http://dx.doi.org/10.1093/nar/gkr982
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author Ma, Emilie
Hyrien, Olivier
Goldar, Arach
author_facet Ma, Emilie
Hyrien, Olivier
Goldar, Arach
author_sort Ma, Emilie
collection PubMed
description Recent studies of eukaryotic DNA replication timing profiles suggest that the time-dependent rate of origin firing, I(t), has a universal shape, which ensures a reproducible replication completion time. However, measurements of I(t) are based on population averages, which may bias the shape of the I(t) because of imperfect cell synchrony and cell-to-cell variability. Here, we measure the population-averaged I(t) profile from synchronized Saccharomyces cerevisiae cells using DNA combing and we extract the single-cell I(t) profile using numerical deconvolution. The single cell I(t) and the population-averaged I(t) extracted from DNA combing and replication timing profiles are similar, indicating a genome scale invariance of the replication process, and excluding cell-to-cell variability in replication time as an explanation for the shape of I(t). The single cell I(t) correlates with fork density in wild-type cells, which is specifically loosened in late S phase in the clb5Δ mutant. A previously proposed numerical model that reproduces the wild-type I(t) profile, could also describe the clb5Δ mutant I(t) once modified to incorporate the decline in CDK activity and the looser dependency of initiation on fork density in the absence of Clb5p. Overall, these results suggest that the replication forks emanating from early fired origins facilitate origin firing in later-replicating regions.
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spelling pubmed-33000282012-03-13 Do replication forks control late origin firing in Saccharomyces cerevisiae? Ma, Emilie Hyrien, Olivier Goldar, Arach Nucleic Acids Res Genome Integrity, Repair and Replication Recent studies of eukaryotic DNA replication timing profiles suggest that the time-dependent rate of origin firing, I(t), has a universal shape, which ensures a reproducible replication completion time. However, measurements of I(t) are based on population averages, which may bias the shape of the I(t) because of imperfect cell synchrony and cell-to-cell variability. Here, we measure the population-averaged I(t) profile from synchronized Saccharomyces cerevisiae cells using DNA combing and we extract the single-cell I(t) profile using numerical deconvolution. The single cell I(t) and the population-averaged I(t) extracted from DNA combing and replication timing profiles are similar, indicating a genome scale invariance of the replication process, and excluding cell-to-cell variability in replication time as an explanation for the shape of I(t). The single cell I(t) correlates with fork density in wild-type cells, which is specifically loosened in late S phase in the clb5Δ mutant. A previously proposed numerical model that reproduces the wild-type I(t) profile, could also describe the clb5Δ mutant I(t) once modified to incorporate the decline in CDK activity and the looser dependency of initiation on fork density in the absence of Clb5p. Overall, these results suggest that the replication forks emanating from early fired origins facilitate origin firing in later-replicating regions. Oxford University Press 2012-03 2011-11-15 /pmc/articles/PMC3300028/ /pubmed/22086957 http://dx.doi.org/10.1093/nar/gkr982 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genome Integrity, Repair and Replication
Ma, Emilie
Hyrien, Olivier
Goldar, Arach
Do replication forks control late origin firing in Saccharomyces cerevisiae?
title Do replication forks control late origin firing in Saccharomyces cerevisiae?
title_full Do replication forks control late origin firing in Saccharomyces cerevisiae?
title_fullStr Do replication forks control late origin firing in Saccharomyces cerevisiae?
title_full_unstemmed Do replication forks control late origin firing in Saccharomyces cerevisiae?
title_short Do replication forks control late origin firing in Saccharomyces cerevisiae?
title_sort do replication forks control late origin firing in saccharomyces cerevisiae?
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3300028/
https://www.ncbi.nlm.nih.gov/pubmed/22086957
http://dx.doi.org/10.1093/nar/gkr982
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