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Repairing split ends: SIRT6, mono-ADP ribosylation and DNA repair

The sirtuin gene family comprises an evolutionarily ancient set of NAD+ dependent protein deacetylase and mono-ADP ribosyltransferase enzymes. Found in all domains of life, sirtuins regulate a diverse array of biological processes, including DNA repair, gene silencing, apoptosis and metabolism. Stud...

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Autores principales: Van Meter, Michael, Mao, Zhiyong, Gorbunova, Vera, Seluanov, Andrei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227448/
https://www.ncbi.nlm.nih.gov/pubmed/21946623
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author Van Meter, Michael
Mao, Zhiyong
Gorbunova, Vera
Seluanov, Andrei
author_facet Van Meter, Michael
Mao, Zhiyong
Gorbunova, Vera
Seluanov, Andrei
author_sort Van Meter, Michael
collection PubMed
description The sirtuin gene family comprises an evolutionarily ancient set of NAD+ dependent protein deacetylase and mono-ADP ribosyltransferase enzymes. Found in all domains of life, sirtuins regulate a diverse array of biological processes, including DNA repair, gene silencing, apoptosis and metabolism. Studies in multiple model organisms have indicated that sirtuins may also function to extend lifespan and attenuate age-related pathologies. To date, most of these studies have focused on the deacetylase activity of sirtuins, and relatively little is known about the other biochemical activity of sirtuins, mono-ADP ribosylation. We recently reported that the mammalian sirtuin, SIRT6, mono-ADP ribosylates PARP1 to promote DNA repair in response to oxidative stress. In this research perspective we review the role of SIRT6 in DNA repair and discuss the emerging implications for sirtuin directed mono-ADP ribosylation in aging and age-related diseases.
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spelling pubmed-32274482011-12-01 Repairing split ends: SIRT6, mono-ADP ribosylation and DNA repair Van Meter, Michael Mao, Zhiyong Gorbunova, Vera Seluanov, Andrei Aging (Albany NY) Review The sirtuin gene family comprises an evolutionarily ancient set of NAD+ dependent protein deacetylase and mono-ADP ribosyltransferase enzymes. Found in all domains of life, sirtuins regulate a diverse array of biological processes, including DNA repair, gene silencing, apoptosis and metabolism. Studies in multiple model organisms have indicated that sirtuins may also function to extend lifespan and attenuate age-related pathologies. To date, most of these studies have focused on the deacetylase activity of sirtuins, and relatively little is known about the other biochemical activity of sirtuins, mono-ADP ribosylation. We recently reported that the mammalian sirtuin, SIRT6, mono-ADP ribosylates PARP1 to promote DNA repair in response to oxidative stress. In this research perspective we review the role of SIRT6 in DNA repair and discuss the emerging implications for sirtuin directed mono-ADP ribosylation in aging and age-related diseases. Impact Journals LLC 2011-09-22 /pmc/articles/PMC3227448/ /pubmed/21946623 Text en Copyright: © 2011 Van Meter et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Review
Van Meter, Michael
Mao, Zhiyong
Gorbunova, Vera
Seluanov, Andrei
Repairing split ends: SIRT6, mono-ADP ribosylation and DNA repair
title Repairing split ends: SIRT6, mono-ADP ribosylation and DNA repair
title_full Repairing split ends: SIRT6, mono-ADP ribosylation and DNA repair
title_fullStr Repairing split ends: SIRT6, mono-ADP ribosylation and DNA repair
title_full_unstemmed Repairing split ends: SIRT6, mono-ADP ribosylation and DNA repair
title_short Repairing split ends: SIRT6, mono-ADP ribosylation and DNA repair
title_sort repairing split ends: sirt6, mono-adp ribosylation and dna repair
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227448/
https://www.ncbi.nlm.nih.gov/pubmed/21946623
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