Replication-Coupled Nucleosome Assembly and Positioning by ATP-Dependent Chromatin-Remodeling Enzymes

During DNA replication, chromatin must be disassembled and faithfully reassembled on newly synthesized genomes. The mechanisms that govern the assembly of chromatin structures following DNA replication are poorly understood. Here, we exploited Okazaki fragment synthesis and other assays to study how...

Full description

Bibliographic Details
Main Authors: Tejas Yadav, Iestyn Whitehouse
Format: Article
Language:English
Published: Elsevier 2016-04-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124716303308
id doaj-acac263e5707404a8e37b613cfa862fa
record_format Article
spelling doaj-acac263e5707404a8e37b613cfa862fa2020-11-25T01:02:28ZengElsevierCell Reports2211-12472016-04-0115471572310.1016/j.celrep.2016.03.059Replication-Coupled Nucleosome Assembly and Positioning by ATP-Dependent Chromatin-Remodeling EnzymesTejas Yadav0Iestyn Whitehouse1Weill Cornell Graduate School of Medical Sciences, 1300 York Avenue, New York, NY 10065, USAMolecular Biology Program, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USADuring DNA replication, chromatin must be disassembled and faithfully reassembled on newly synthesized genomes. The mechanisms that govern the assembly of chromatin structures following DNA replication are poorly understood. Here, we exploited Okazaki fragment synthesis and other assays to study how nucleosomes are deposited and become organized in S. cerevisiae. We observe that global nucleosome positioning is quickly established on newly synthesized DNA in vivo. Importantly, we find that ATP-dependent chromatin-remodeling enzymes, Isw1 and Chd1, collaborate with histone chaperones to remodel nucleosomes as they are loaded behind a replication fork. Using a whole-genome sequencing approach, we determine that the positioning of newly deposited nucleosomes in vivo is specified by the combined actions of ATP-dependent chromatin-remodeling enzymes and select DNA-binding proteins. Altogether, our data provide in vivo evidence for coordinated “loading and remodeling” of nucleosomes behind the replication fork, allowing for rapid organization of chromatin during S phase.http://www.sciencedirect.com/science/article/pii/S2211124716303308
collection DOAJ
language English
format Article
sources DOAJ
author Tejas Yadav
Iestyn Whitehouse
spellingShingle Tejas Yadav
Iestyn Whitehouse
Replication-Coupled Nucleosome Assembly and Positioning by ATP-Dependent Chromatin-Remodeling Enzymes
Cell Reports
author_facet Tejas Yadav
Iestyn Whitehouse
author_sort Tejas Yadav
title Replication-Coupled Nucleosome Assembly and Positioning by ATP-Dependent Chromatin-Remodeling Enzymes
title_short Replication-Coupled Nucleosome Assembly and Positioning by ATP-Dependent Chromatin-Remodeling Enzymes
title_full Replication-Coupled Nucleosome Assembly and Positioning by ATP-Dependent Chromatin-Remodeling Enzymes
title_fullStr Replication-Coupled Nucleosome Assembly and Positioning by ATP-Dependent Chromatin-Remodeling Enzymes
title_full_unstemmed Replication-Coupled Nucleosome Assembly and Positioning by ATP-Dependent Chromatin-Remodeling Enzymes
title_sort replication-coupled nucleosome assembly and positioning by atp-dependent chromatin-remodeling enzymes
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2016-04-01
description During DNA replication, chromatin must be disassembled and faithfully reassembled on newly synthesized genomes. The mechanisms that govern the assembly of chromatin structures following DNA replication are poorly understood. Here, we exploited Okazaki fragment synthesis and other assays to study how nucleosomes are deposited and become organized in S. cerevisiae. We observe that global nucleosome positioning is quickly established on newly synthesized DNA in vivo. Importantly, we find that ATP-dependent chromatin-remodeling enzymes, Isw1 and Chd1, collaborate with histone chaperones to remodel nucleosomes as they are loaded behind a replication fork. Using a whole-genome sequencing approach, we determine that the positioning of newly deposited nucleosomes in vivo is specified by the combined actions of ATP-dependent chromatin-remodeling enzymes and select DNA-binding proteins. Altogether, our data provide in vivo evidence for coordinated “loading and remodeling” of nucleosomes behind the replication fork, allowing for rapid organization of chromatin during S phase.
url http://www.sciencedirect.com/science/article/pii/S2211124716303308
work_keys_str_mv AT tejasyadav replicationcouplednucleosomeassemblyandpositioningbyatpdependentchromatinremodelingenzymes
AT iestynwhitehouse replicationcouplednucleosomeassemblyandpositioningbyatpdependentchromatinremodelingenzymes
_version_ 1725204815389130752