Cargando…

Acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination

Targeted 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 nucl...

Descripción completa

Detalles Bibliográficos
Autores principales: Nightingale, Karl P., Baumann, Matthias, Eberharter, Anton, Mamais, Adamantios, Becker, Peter B., Boyes, Joan
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2094086/
https://www.ncbi.nlm.nih.gov/pubmed/17881376
http://dx.doi.org/10.1093/nar/gkm650
_version_ 1782138215651606528
author Nightingale, Karl P.
Baumann, Matthias
Eberharter, Anton
Mamais, Adamantios
Becker, Peter B.
Boyes, Joan
author_facet Nightingale, Karl P.
Baumann, Matthias
Eberharter, Anton
Mamais, Adamantios
Becker, Peter B.
Boyes, Joan
author_sort Nightingale, Karl P.
collection PubMed
description Targeted 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.
format Text
id pubmed-2094086
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-20940862007-12-03 Acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination Nightingale, Karl P. Baumann, Matthias Eberharter, Anton Mamais, Adamantios Becker, Peter B. Boyes, Joan Nucleic Acids Res Molecular Biology Targeted 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. Oxford University Press 2007-09 2007-09-18 /pmc/articles/PMC2094086/ /pubmed/17881376 http://dx.doi.org/10.1093/nar/gkm650 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Nightingale, Karl P.
Baumann, Matthias
Eberharter, Anton
Mamais, Adamantios
Becker, Peter B.
Boyes, Joan
Acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination
title Acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination
title_full Acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination
title_fullStr Acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination
title_full_unstemmed Acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination
title_short Acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of V(D)J recombination
title_sort acetylation increases access of remodelling complexes to their nucleosome targets to enhance initiation of v(d)j recombination
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2094086/
https://www.ncbi.nlm.nih.gov/pubmed/17881376
http://dx.doi.org/10.1093/nar/gkm650
work_keys_str_mv AT nightingalekarlp acetylationincreasesaccessofremodellingcomplexestotheirnucleosometargetstoenhanceinitiationofvdjrecombination
AT baumannmatthias acetylationincreasesaccessofremodellingcomplexestotheirnucleosometargetstoenhanceinitiationofvdjrecombination
AT eberharteranton acetylationincreasesaccessofremodellingcomplexestotheirnucleosometargetstoenhanceinitiationofvdjrecombination
AT mamaisadamantios acetylationincreasesaccessofremodellingcomplexestotheirnucleosometargetstoenhanceinitiationofvdjrecombination
AT beckerpeterb acetylationincreasesaccessofremodellingcomplexestotheirnucleosometargetstoenhanceinitiationofvdjrecombination
AT boyesjoan acetylationincreasesaccessofremodellingcomplexestotheirnucleosometargetstoenhanceinitiationofvdjrecombination