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SIRT6 exhibits nucleosome-dependent deacetylase activity

The SIRT6 deacetylase is a key regulator of mammalian genome stability, metabolism and lifespan. Previous studies indicated that SIRT6 exhibits poor deacetylase activity in vitro. Here, we explored the specific conditions that allow SIRT6 to function as a significant deacetylase. We show that SIRT6...

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Detalles Bibliográficos
Autores principales: Gil, Reuven, Barth, Shaul, Kanfi, Yariv, Cohen, Haim Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794599/
https://www.ncbi.nlm.nih.gov/pubmed/23892288
http://dx.doi.org/10.1093/nar/gkt642
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author Gil, Reuven
Barth, Shaul
Kanfi, Yariv
Cohen, Haim Y.
author_facet Gil, Reuven
Barth, Shaul
Kanfi, Yariv
Cohen, Haim Y.
author_sort Gil, Reuven
collection PubMed
description The SIRT6 deacetylase is a key regulator of mammalian genome stability, metabolism and lifespan. Previous studies indicated that SIRT6 exhibits poor deacetylase activity in vitro. Here, we explored the specific conditions that allow SIRT6 to function as a significant deacetylase. We show that SIRT6 associates with the nucleosome and deacetylates histones H3 and H4 when they are packaged as nucleosomes, but not as free histones. In contrast, SIRT1 shows the opposite characteristics. Thus, our results show that SIRT6 activity is nucleosome dependent, and suggest that its binding to the nucleosome might convert it into an active structure.
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spelling pubmed-37945992013-10-21 SIRT6 exhibits nucleosome-dependent deacetylase activity Gil, Reuven Barth, Shaul Kanfi, Yariv Cohen, Haim Y. Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics The SIRT6 deacetylase is a key regulator of mammalian genome stability, metabolism and lifespan. Previous studies indicated that SIRT6 exhibits poor deacetylase activity in vitro. Here, we explored the specific conditions that allow SIRT6 to function as a significant deacetylase. We show that SIRT6 associates with the nucleosome and deacetylates histones H3 and H4 when they are packaged as nucleosomes, but not as free histones. In contrast, SIRT1 shows the opposite characteristics. Thus, our results show that SIRT6 activity is nucleosome dependent, and suggest that its binding to the nucleosome might convert it into an active structure. Oxford University Press 2013-10 2013-07-26 /pmc/articles/PMC3794599/ /pubmed/23892288 http://dx.doi.org/10.1093/nar/gkt642 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Gene Regulation, Chromatin and Epigenetics
Gil, Reuven
Barth, Shaul
Kanfi, Yariv
Cohen, Haim Y.
SIRT6 exhibits nucleosome-dependent deacetylase activity
title SIRT6 exhibits nucleosome-dependent deacetylase activity
title_full SIRT6 exhibits nucleosome-dependent deacetylase activity
title_fullStr SIRT6 exhibits nucleosome-dependent deacetylase activity
title_full_unstemmed SIRT6 exhibits nucleosome-dependent deacetylase activity
title_short SIRT6 exhibits nucleosome-dependent deacetylase activity
title_sort sirt6 exhibits nucleosome-dependent deacetylase activity
topic Gene Regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794599/
https://www.ncbi.nlm.nih.gov/pubmed/23892288
http://dx.doi.org/10.1093/nar/gkt642
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