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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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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. |
format | Online Article Text |
id | pubmed-3300028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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