Proteomics

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Deficiency in Sirtuin3 rewires mitochondrial metabolism and increases maximum lifespan under caloric restriction - Mitochondrial Acetylation Stoichiometry


ABSTRACT: Quantification of acetylation stoichiometry from mitochondrial enriched proteins from mouse livers. Conditions compared include genotype, diet, and age; i.e. Sirt3 KO vs Sirt3 WT, caloric restricted (CR) diet vs control diet (CD), and 5 months old vs 25 months old.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Mus Musculus (ncbitaxon:10090)

SUBMITTER: John Denu  

PROVIDER: MSV000087085 | MassIVE | Tue Mar 23 09:01:00 GMT 2021

SECONDARY ACCESSION(S): PXD024961

REPOSITORIES: MassIVE

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Publications

SIRT3 deficiency decreases oxidative metabolism capacity but increases lifespan in male mice under caloric restriction.

Dhillon Rashpal S RS   Qin Yiming Amy YA   van Ginkel Paul R PR   Fu Vivian X VX   Vann James M JM   Lawton Alexis J AJ   Green Cara L CL   Manchado-Gobatto Fúlvia B FB   Gobatto Claudio A CA   Lamming Dudley W DW   Prolla Tomas A TA   Denu John M JM  

Aging cell 20221005 12


Mitochondrial NAD<sup>+</sup> -dependent protein deacetylase Sirtuin3 (SIRT3) has been proposed to mediate calorie restriction (CR)-dependent metabolic regulation and lifespan extension. Here, we investigated the role of SIRT3 in CR-mediated longevity, mitochondrial function, and aerobic fitness. We report that SIRT3 is required for whole-body aerobic capacity but is dispensable for CR-dependent lifespan extension. Under CR, loss of SIRT3 (Sirt3<sup>-/-</sup> ) yielded a longer overall and maxim  ...[more]

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