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Urea cycle regulation by mitochondrial sirtuin, SIRT5

Mammalian sirtuins have diverse roles in aging, metabolism and disease. Recently we reported a new function for SIRT5 in urea cycle regulation. Our study uncovered that SIRT5 localized to mitochondria matrix and deacetylates carbamoyl phosphate synthetase 1 (CPS1), an enzyme which is the first and r...

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Detalles Bibliográficos
Autores principales: Nakagawa, Takashi, Guarente, Leonard
Formato: Texto
Lenguaje:English
Publicado: Impact Journals LLC 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806029/
https://www.ncbi.nlm.nih.gov/pubmed/20157539
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author Nakagawa, Takashi
Guarente, Leonard
author_facet Nakagawa, Takashi
Guarente, Leonard
author_sort Nakagawa, Takashi
collection PubMed
description Mammalian sirtuins have diverse roles in aging, metabolism and disease. Recently we reported a new function for SIRT5 in urea cycle regulation. Our study uncovered that SIRT5 localized to mitochondria matrix and deacetylates carbamoyl phosphate synthetase 1 (CPS1), an enzyme which is the first and rate-limiting step of urea cycle. Deacetylation of CPS1 by SIRT5 resulted in activation of CPS1 enzymatic activity. Indeed, SIRT5-deficient mice failed to up-regulate CPS1 activity and showed hyper ammonemia during fasting. Similar effects are also observed on high protein diet or calorie restriction. These data indicate SIRT5 also has an emerging role in the metabolic adaptation to fasting, high protein diet and calorie restriction.
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spelling pubmed-28060292010-02-12 Urea cycle regulation by mitochondrial sirtuin, SIRT5 Nakagawa, Takashi Guarente, Leonard Aging (Albany NY) Research Perspective Mammalian sirtuins have diverse roles in aging, metabolism and disease. Recently we reported a new function for SIRT5 in urea cycle regulation. Our study uncovered that SIRT5 localized to mitochondria matrix and deacetylates carbamoyl phosphate synthetase 1 (CPS1), an enzyme which is the first and rate-limiting step of urea cycle. Deacetylation of CPS1 by SIRT5 resulted in activation of CPS1 enzymatic activity. Indeed, SIRT5-deficient mice failed to up-regulate CPS1 activity and showed hyper ammonemia during fasting. Similar effects are also observed on high protein diet or calorie restriction. These data indicate SIRT5 also has an emerging role in the metabolic adaptation to fasting, high protein diet and calorie restriction. Impact Journals LLC 2009-06-29 /pmc/articles/PMC2806029/ /pubmed/20157539 Text en Copyright: ©2009 Nakagawa 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 work is properly cited.
spellingShingle Research Perspective
Nakagawa, Takashi
Guarente, Leonard
Urea cycle regulation by mitochondrial sirtuin, SIRT5
title Urea cycle regulation by mitochondrial sirtuin, SIRT5
title_full Urea cycle regulation by mitochondrial sirtuin, SIRT5
title_fullStr Urea cycle regulation by mitochondrial sirtuin, SIRT5
title_full_unstemmed Urea cycle regulation by mitochondrial sirtuin, SIRT5
title_short Urea cycle regulation by mitochondrial sirtuin, SIRT5
title_sort urea cycle regulation by mitochondrial sirtuin, sirt5
topic Research Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806029/
https://www.ncbi.nlm.nih.gov/pubmed/20157539
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