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Dynamics of Nucleosome Positioning Maturation following Genomic Replication
Chromatin is thought to carry epigenetic information from one generation to the next, although it is unclear how such information survives the disruptions of nucleosomal architecture occurring during genomic replication. Here, we measure a key aspect of chromatin structure dynamics during replicatio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014762/ https://www.ncbi.nlm.nih.gov/pubmed/27568571 http://dx.doi.org/10.1016/j.celrep.2016.07.083 |
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author | Vasseur, Pauline Tonazzini, Saphia Ziane, Rahima Camasses, Alain Rando, Oliver J. Radman-Livaja, Marta |
author_facet | Vasseur, Pauline Tonazzini, Saphia Ziane, Rahima Camasses, Alain Rando, Oliver J. Radman-Livaja, Marta |
author_sort | Vasseur, Pauline |
collection | PubMed |
description | Chromatin is thought to carry epigenetic information from one generation to the next, although it is unclear how such information survives the disruptions of nucleosomal architecture occurring during genomic replication. Here, we measure a key aspect of chromatin structure dynamics during replication—how rapidly nucleosome positions are established on the newly replicated daughter genomes. By isolating newly synthesized DNA marked with 5-ethynyl-2′-deoxyuridine (EdU), we characterize nucleosome positions on both daughter genomes of S. cerevisiae during chromatin maturation. We find that nucleosomes rapidly adopt their mid-log positions at highly transcribed genes, which is consistent with a role for transcription in positioning nucleosomes in vivo. Additionally, experiments in hir1Δ mutants reveal a role for HIR in nucleosome spacing. We also characterized nucleosome positions on the leading and lagging strands, uncovering differences in chromatin maturation dynamics at hundreds of genes. Our data define the maturation dynamics of newly replicated chromatin and support a role for transcription in sculpting the chromatin template. |
format | Online Article Text |
id | pubmed-5014762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50147622016-09-15 Dynamics of Nucleosome Positioning Maturation following Genomic Replication Vasseur, Pauline Tonazzini, Saphia Ziane, Rahima Camasses, Alain Rando, Oliver J. Radman-Livaja, Marta Cell Rep Article Chromatin is thought to carry epigenetic information from one generation to the next, although it is unclear how such information survives the disruptions of nucleosomal architecture occurring during genomic replication. Here, we measure a key aspect of chromatin structure dynamics during replication—how rapidly nucleosome positions are established on the newly replicated daughter genomes. By isolating newly synthesized DNA marked with 5-ethynyl-2′-deoxyuridine (EdU), we characterize nucleosome positions on both daughter genomes of S. cerevisiae during chromatin maturation. We find that nucleosomes rapidly adopt their mid-log positions at highly transcribed genes, which is consistent with a role for transcription in positioning nucleosomes in vivo. Additionally, experiments in hir1Δ mutants reveal a role for HIR in nucleosome spacing. We also characterized nucleosome positions on the leading and lagging strands, uncovering differences in chromatin maturation dynamics at hundreds of genes. Our data define the maturation dynamics of newly replicated chromatin and support a role for transcription in sculpting the chromatin template. Cell Press 2016-08-25 /pmc/articles/PMC5014762/ /pubmed/27568571 http://dx.doi.org/10.1016/j.celrep.2016.07.083 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Vasseur, Pauline Tonazzini, Saphia Ziane, Rahima Camasses, Alain Rando, Oliver J. Radman-Livaja, Marta Dynamics of Nucleosome Positioning Maturation following Genomic Replication |
title | Dynamics of Nucleosome Positioning Maturation following Genomic Replication |
title_full | Dynamics of Nucleosome Positioning Maturation following Genomic Replication |
title_fullStr | Dynamics of Nucleosome Positioning Maturation following Genomic Replication |
title_full_unstemmed | Dynamics of Nucleosome Positioning Maturation following Genomic Replication |
title_short | Dynamics of Nucleosome Positioning Maturation following Genomic Replication |
title_sort | dynamics of nucleosome positioning maturation following genomic replication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014762/ https://www.ncbi.nlm.nih.gov/pubmed/27568571 http://dx.doi.org/10.1016/j.celrep.2016.07.083 |
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