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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...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2007
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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 |
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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 |
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