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Updated: Jun 21, 2026

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Published on: October 4, 2024
Calorie restriction alters mitochondrial protein acetylation
Bjoern Schwer1, Mark Eckersdorff, Yu Li
1Program in Cellular and Molecular Medicine, Howard Hughes Medical Institute, The Children's Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
Calorie restriction extends lifespan by altering mitochondrial protein acetylation. This study identified 72 proteins in key metabolic pathways with changed acetylation, suggesting a role in longevity.
Area of Science:
- Biochemistry
- Molecular Biology
- Gerontology
Background:
- Calorie restriction (CR) is a well-established intervention that extends lifespan across diverse organisms.
- Mitochondrial adaptation is a critical cellular response to CR, but the underlying molecular mechanisms remain largely unknown.
Purpose of the Study:
- To investigate the role of protein acetylation in mitochondrial adaptation during calorie restriction.
- To identify specific mitochondrial proteins and metabolic pathways affected by altered acetylation under CR.
Main Methods:
- Large-scale mass spectrometry was employed to screen mitochondrial proteins for changes in lysine acetylation.
- Proteins with altered acetylation during CR were identified across different tissues.
Main Results:
- Lysine acetylation of mitochondrial proteins was found to be altered in a tissue-specific manner during CR.
- Seventy-two candidate proteins involved in various metabolic pathways exhibited altered acetylation patterns under CR.
- These proteins are implicated in crucial cellular functions and metabolic processes.
Conclusions:
- Mitochondrial protein acetylation is dynamically regulated by calorie restriction.
- Altered mitochondrial acetylation is a significant component of the CR response and may contribute to its pro-longevity effects.
- These findings provide novel molecular insights into the mechanisms of aging and lifespan extension.
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