Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Vasseur, Pauline, Tonazzini, Saphia, Ziane, Rahima, Camasses, Alain, Rando, Oliver J., Radman-Livaja, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2016
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
_version_ 1782452321641299968
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
work_keys_str_mv AT vasseurpauline dynamicsofnucleosomepositioningmaturationfollowinggenomicreplication
AT tonazzinisaphia dynamicsofnucleosomepositioningmaturationfollowinggenomicreplication
AT zianerahima dynamicsofnucleosomepositioningmaturationfollowinggenomicreplication
AT camassesalain dynamicsofnucleosomepositioningmaturationfollowinggenomicreplication
AT randooliverj dynamicsofnucleosomepositioningmaturationfollowinggenomicreplication
AT radmanlivajamarta dynamicsofnucleosomepositioningmaturationfollowinggenomicreplication