Cargando…

Replication dynamics of individual loci in single living cells reveal changes in the degree of replication stochasticity through S phase

Eukaryotic genomes are replicated under the control of a highly sophisticated program during the restricted time period corresponding to S phase. The most widely used replication timing assays, which are performed on populations of millions of cells, suggest that most of the genome is synchronously...

Descripción completa

Detalles Bibliográficos
Autores principales: Duriez, Bénédicte, Chilaka, Sabarinadh, Bercher, Jean-François, Hercul, Eslande, Prioleau, Marie-Noëlle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547449/
https://www.ncbi.nlm.nih.gov/pubmed/30926993
http://dx.doi.org/10.1093/nar/gkz220
_version_ 1783423678363467776
author Duriez, Bénédicte
Chilaka, Sabarinadh
Bercher, Jean-François
Hercul, Eslande
Prioleau, Marie-Noëlle
author_facet Duriez, Bénédicte
Chilaka, Sabarinadh
Bercher, Jean-François
Hercul, Eslande
Prioleau, Marie-Noëlle
author_sort Duriez, Bénédicte
collection PubMed
description Eukaryotic genomes are replicated under the control of a highly sophisticated program during the restricted time period corresponding to S phase. The most widely used replication timing assays, which are performed on populations of millions of cells, suggest that most of the genome is synchronously replicated on homologous chromosomes. We investigated the stochastic nature of this temporal program, by comparing the precise replication times of allelic loci within single vertebrate cells progressing through S phase at six loci replicated from very early to very late. We show that replication timing is strictly controlled for the three loci replicated in the first half of S phase. Out of the three loci replicated in the second part of S phase, two present a significantly more stochastic pattern. Surprisingly, we find that the locus replicated at the very end of S phase, presents stochasticity similar to those replicated in early S phase. We suggest that the richness of loci in efficient origins of replication, which decreases from early- to late-replicating regions, and the strength of interaction with the nuclear lamina may underlie the variation of timing control during S phase.
format Online
Article
Text
id pubmed-6547449
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-65474492019-06-13 Replication dynamics of individual loci in single living cells reveal changes in the degree of replication stochasticity through S phase Duriez, Bénédicte Chilaka, Sabarinadh Bercher, Jean-François Hercul, Eslande Prioleau, Marie-Noëlle Nucleic Acids Res Genome Integrity, Repair and Replication Eukaryotic genomes are replicated under the control of a highly sophisticated program during the restricted time period corresponding to S phase. The most widely used replication timing assays, which are performed on populations of millions of cells, suggest that most of the genome is synchronously replicated on homologous chromosomes. We investigated the stochastic nature of this temporal program, by comparing the precise replication times of allelic loci within single vertebrate cells progressing through S phase at six loci replicated from very early to very late. We show that replication timing is strictly controlled for the three loci replicated in the first half of S phase. Out of the three loci replicated in the second part of S phase, two present a significantly more stochastic pattern. Surprisingly, we find that the locus replicated at the very end of S phase, presents stochasticity similar to those replicated in early S phase. We suggest that the richness of loci in efficient origins of replication, which decreases from early- to late-replicating regions, and the strength of interaction with the nuclear lamina may underlie the variation of timing control during S phase. Oxford University Press 2019-06-04 2019-03-30 /pmc/articles/PMC6547449/ /pubmed/30926993 http://dx.doi.org/10.1093/nar/gkz220 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Genome Integrity, Repair and Replication
Duriez, Bénédicte
Chilaka, Sabarinadh
Bercher, Jean-François
Hercul, Eslande
Prioleau, Marie-Noëlle
Replication dynamics of individual loci in single living cells reveal changes in the degree of replication stochasticity through S phase
title Replication dynamics of individual loci in single living cells reveal changes in the degree of replication stochasticity through S phase
title_full Replication dynamics of individual loci in single living cells reveal changes in the degree of replication stochasticity through S phase
title_fullStr Replication dynamics of individual loci in single living cells reveal changes in the degree of replication stochasticity through S phase
title_full_unstemmed Replication dynamics of individual loci in single living cells reveal changes in the degree of replication stochasticity through S phase
title_short Replication dynamics of individual loci in single living cells reveal changes in the degree of replication stochasticity through S phase
title_sort replication dynamics of individual loci in single living cells reveal changes in the degree of replication stochasticity through s phase
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547449/
https://www.ncbi.nlm.nih.gov/pubmed/30926993
http://dx.doi.org/10.1093/nar/gkz220
work_keys_str_mv AT duriezbenedicte replicationdynamicsofindividuallociinsinglelivingcellsrevealchangesinthedegreeofreplicationstochasticitythroughsphase
AT chilakasabarinadh replicationdynamicsofindividuallociinsinglelivingcellsrevealchangesinthedegreeofreplicationstochasticitythroughsphase
AT bercherjeanfrancois replicationdynamicsofindividuallociinsinglelivingcellsrevealchangesinthedegreeofreplicationstochasticitythroughsphase
AT herculeslande replicationdynamicsofindividuallociinsinglelivingcellsrevealchangesinthedegreeofreplicationstochasticitythroughsphase
AT prioleaumarienoelle replicationdynamicsofindividuallociinsinglelivingcellsrevealchangesinthedegreeofreplicationstochasticitythroughsphase