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dc.contributor.authorNightingale, KP
dc.contributor.authorBaumann, M
dc.contributor.authorEberharter, A
dc.contributor.authorMamais, A
dc.contributor.authorBecker, PB
dc.contributor.authorBoyes, J
dc.date.accessioned2018-08-31T15:00:06Z
dc.date.issued2007-01
dc.identifier.citationNucleic acids research, 2007, 35 (18), pp. 6311 - 6321
dc.identifier.issn0305-1048
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/2495
dc.identifier.eissn1362-4962
dc.identifier.doi10.1093/nar/gkm650
dc.description.abstractTargeted chromatin remodelling is essential for many nuclear processes, including the regulation of V(D)J recombination. ATP-dependent nucleosome remodelling complexes are important players in this process whose activity must be tightly regulated. We show here that histone acetylation regulates nucleosome remodelling complex activity to boost RAG cutting during the initiation of V(D)J recombination. RAG cutting requires nucleosome mobilization from recombination signal sequences. Histone acetylation does not stimulate nucleosome mobilization per se by CHRAC, ACF or their catalytic subunit, ISWI. Instead, we find the more open structure of acetylated chromatin regulates the ability of nucleosome remodelling complexes to access their nucleosome templates. We also find that bromodomain/acetylated histone tail interactions can contribute to this targeting at limited concentrations of remodelling complex. We therefore propose that the changes in higher order chromatin structure associated with histone acetylation contribute to the correct targeting of nucleosome remodelling complexes and this is a novel way in which histone acetylation can modulate remodelling complex activity.
dc.formatPrint-Electronic
dc.format.extent6311 - 6321
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectCell Line
dc.subjectNucleosomes
dc.subjectAnimals
dc.subjectDrosophila
dc.subjectImmunoglobulin Joining Region
dc.subjectImmunoglobulin Variable Region
dc.subjectHomeodomain Proteins
dc.subjectHistones
dc.subjectChromatin Assembly and Disassembly
dc.subjectGene Rearrangement, B-Lymphocyte
dc.subjectGene Rearrangement, T-Lymphocyte
dc.subjectRecombination, Genetic
dc.subjectAcetylation
dc.titleAcetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination.
dc.typeJournal Article
rioxxterms.versionofrecord10.1093/nar/gkm650
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc/4.0
rioxxterms.licenseref.startdate2007-01
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfNucleic acids research
pubs.issue18
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Molecular Embryology
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Molecular Embryology
pubs.publication-statusPublished
pubs.volume35
pubs.embargo.termsNot known
icr.researchteamMolecular Embryologyen_US
dc.contributor.icrauthorMamais, Adamantios
dc.contributor.icrauthorBoyes, Joan
dc.contributor.icrauthorBaumann, Matthias


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