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Biophysical studies of cholesterol effects on chromatin

Changes in chromatin structure regulate gene expression and genome maintenance. Molecules that bind to the nucleosome, the complex of DNA and histone proteins, are key modulators of chromatin structure. Previous work indicated that cholesterol, a ubiquitous cellular lipid, may bind to chromatin in v...

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Detalles Bibliográficos
Autores principales: Silva, Isabel T. G., Fernandes, Vinícius, Souza, Caio, Treptow, Werner, Santos, Guilherme M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Biochemistry and Molecular Biology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408612/
https://www.ncbi.nlm.nih.gov/pubmed/28331000
http://dx.doi.org/10.1194/jlr.M074997
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author Silva, Isabel T. G.
Fernandes, Vinícius
Souza, Caio
Treptow, Werner
Santos, Guilherme M.
author_facet Silva, Isabel T. G.
Fernandes, Vinícius
Souza, Caio
Treptow, Werner
Santos, Guilherme M.
author_sort Silva, Isabel T. G.
collection PubMed
description Changes in chromatin structure regulate gene expression and genome maintenance. Molecules that bind to the nucleosome, the complex of DNA and histone proteins, are key modulators of chromatin structure. Previous work indicated that cholesterol, a ubiquitous cellular lipid, may bind to chromatin in vivo, suggesting a potential function for lipids in modulating chromatin architecture. However, the molecular mechanisms of cholesterol’s action on chromatin structure have remained unclear. Here, we explored the biophysical impact of cholesterol on nucleosome and chromatin fibers reconstituted in vitro and characterized in silico the cholesterol binding to the nucleosome. Our findings support that cholesterol assists 10 and 30 nm chromatin formation and induces folding of long chromatin fibers as a result of direct interaction of the cholesterol to six nucleosomal binding sites.
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spelling pubmed-54086122017-05-04 Biophysical studies of cholesterol effects on chromatin Silva, Isabel T. G. Fernandes, Vinícius Souza, Caio Treptow, Werner Santos, Guilherme M. J Lipid Res Research Articles Changes in chromatin structure regulate gene expression and genome maintenance. Molecules that bind to the nucleosome, the complex of DNA and histone proteins, are key modulators of chromatin structure. Previous work indicated that cholesterol, a ubiquitous cellular lipid, may bind to chromatin in vivo, suggesting a potential function for lipids in modulating chromatin architecture. However, the molecular mechanisms of cholesterol’s action on chromatin structure have remained unclear. Here, we explored the biophysical impact of cholesterol on nucleosome and chromatin fibers reconstituted in vitro and characterized in silico the cholesterol binding to the nucleosome. Our findings support that cholesterol assists 10 and 30 nm chromatin formation and induces folding of long chromatin fibers as a result of direct interaction of the cholesterol to six nucleosomal binding sites. The American Society for Biochemistry and Molecular Biology 2017-05 2017-04-28 /pmc/articles/PMC5408612/ /pubmed/28331000 http://dx.doi.org/10.1194/jlr.M074997 Text en Copyright © 2017 by the American Society for Biochemistry and Molecular Biology, Inc. http://creativecommons.org/licenses/by/4.0/ Author’s Choice—Final version free via Creative Commons CC-BY license.
spellingShingle Research Articles
Silva, Isabel T. G.
Fernandes, Vinícius
Souza, Caio
Treptow, Werner
Santos, Guilherme M.
Biophysical studies of cholesterol effects on chromatin
title Biophysical studies of cholesterol effects on chromatin
title_full Biophysical studies of cholesterol effects on chromatin
title_fullStr Biophysical studies of cholesterol effects on chromatin
title_full_unstemmed Biophysical studies of cholesterol effects on chromatin
title_short Biophysical studies of cholesterol effects on chromatin
title_sort biophysical studies of cholesterol effects on chromatin
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408612/
https://www.ncbi.nlm.nih.gov/pubmed/28331000
http://dx.doi.org/10.1194/jlr.M074997
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