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Replication Fork Polarity Gradients Revealed by Megabase-Sized U-Shaped Replication Timing Domains in Human Cell Lines
In higher eukaryotes, replication program specification in different cell types remains to be fully understood. We show for seven human cell lines that about half of the genome is divided in domains that display a characteristic U-shaped replication timing profile with early initiation zones at bord...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320577/ https://www.ncbi.nlm.nih.gov/pubmed/22496629 http://dx.doi.org/10.1371/journal.pcbi.1002443 |
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author | Baker, Antoine Audit, Benjamin Chen, Chun-Long Moindrot, Benoit Leleu, Antoine Guilbaud, Guillaume Rappailles, Aurélien Vaillant, Cédric Goldar, Arach Mongelard, Fabien d'Aubenton-Carafa, Yves Hyrien, Olivier Thermes, Claude Arneodo, Alain |
author_facet | Baker, Antoine Audit, Benjamin Chen, Chun-Long Moindrot, Benoit Leleu, Antoine Guilbaud, Guillaume Rappailles, Aurélien Vaillant, Cédric Goldar, Arach Mongelard, Fabien d'Aubenton-Carafa, Yves Hyrien, Olivier Thermes, Claude Arneodo, Alain |
author_sort | Baker, Antoine |
collection | PubMed |
description | In higher eukaryotes, replication program specification in different cell types remains to be fully understood. We show for seven human cell lines that about half of the genome is divided in domains that display a characteristic U-shaped replication timing profile with early initiation zones at borders and late replication at centers. Significant overlap is observed between U-domains of different cell lines and also with germline replication domains exhibiting a N-shaped nucleotide compositional skew. From the demonstration that the average fork polarity is directly reflected by both the compositional skew and the derivative of the replication timing profile, we argue that the fact that this derivative displays a N-shape in U-domains sustains the existence of large-scale gradients of replication fork polarity in somatic and germline cells. Analysis of chromatin interaction (Hi-C) and chromatin marker data reveals that U-domains correspond to high-order chromatin structural units. We discuss possible models for replication origin activation within U/N-domains. The compartmentalization of the genome into replication U/N-domains provides new insights on the organization of the replication program in the human genome. |
format | Online Article Text |
id | pubmed-3320577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33205772012-04-11 Replication Fork Polarity Gradients Revealed by Megabase-Sized U-Shaped Replication Timing Domains in Human Cell Lines Baker, Antoine Audit, Benjamin Chen, Chun-Long Moindrot, Benoit Leleu, Antoine Guilbaud, Guillaume Rappailles, Aurélien Vaillant, Cédric Goldar, Arach Mongelard, Fabien d'Aubenton-Carafa, Yves Hyrien, Olivier Thermes, Claude Arneodo, Alain PLoS Comput Biol Research Article In higher eukaryotes, replication program specification in different cell types remains to be fully understood. We show for seven human cell lines that about half of the genome is divided in domains that display a characteristic U-shaped replication timing profile with early initiation zones at borders and late replication at centers. Significant overlap is observed between U-domains of different cell lines and also with germline replication domains exhibiting a N-shaped nucleotide compositional skew. From the demonstration that the average fork polarity is directly reflected by both the compositional skew and the derivative of the replication timing profile, we argue that the fact that this derivative displays a N-shape in U-domains sustains the existence of large-scale gradients of replication fork polarity in somatic and germline cells. Analysis of chromatin interaction (Hi-C) and chromatin marker data reveals that U-domains correspond to high-order chromatin structural units. We discuss possible models for replication origin activation within U/N-domains. The compartmentalization of the genome into replication U/N-domains provides new insights on the organization of the replication program in the human genome. Public Library of Science 2012-04-05 /pmc/articles/PMC3320577/ /pubmed/22496629 http://dx.doi.org/10.1371/journal.pcbi.1002443 Text en Baker et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Baker, Antoine Audit, Benjamin Chen, Chun-Long Moindrot, Benoit Leleu, Antoine Guilbaud, Guillaume Rappailles, Aurélien Vaillant, Cédric Goldar, Arach Mongelard, Fabien d'Aubenton-Carafa, Yves Hyrien, Olivier Thermes, Claude Arneodo, Alain Replication Fork Polarity Gradients Revealed by Megabase-Sized U-Shaped Replication Timing Domains in Human Cell Lines |
title | Replication Fork Polarity Gradients Revealed by Megabase-Sized U-Shaped Replication Timing Domains in Human Cell Lines |
title_full | Replication Fork Polarity Gradients Revealed by Megabase-Sized U-Shaped Replication Timing Domains in Human Cell Lines |
title_fullStr | Replication Fork Polarity Gradients Revealed by Megabase-Sized U-Shaped Replication Timing Domains in Human Cell Lines |
title_full_unstemmed | Replication Fork Polarity Gradients Revealed by Megabase-Sized U-Shaped Replication Timing Domains in Human Cell Lines |
title_short | Replication Fork Polarity Gradients Revealed by Megabase-Sized U-Shaped Replication Timing Domains in Human Cell Lines |
title_sort | replication fork polarity gradients revealed by megabase-sized u-shaped replication timing domains in human cell lines |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3320577/ https://www.ncbi.nlm.nih.gov/pubmed/22496629 http://dx.doi.org/10.1371/journal.pcbi.1002443 |
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