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Sesn-1 is required for lifespan extension during caloric deprivation in C. elegans through inhibition of mTORC1 and activation of autophagy
Andrei O. Zheltukhin, Peter M. Chumakov, Andrei V. Budanov
Aging · 2025
Abstract
Sestrins, evolutionarily conserved stress-responsive proteins, are increasingly recognized for their potential role in lifespan regulation. This study aimed to elucidate the influence of the sesn-1 gene on lifespan modulation during caloric deprivation (CD) in the model organism C. elegans. Our findings reveal that sesn-1 mediates lifespan extension under CD, primarily through the repression of mTORC1 kinase and activation of autophagy(definition). Moreover, we identified an essential role for sesn-1 in enhancing stress resilience in nematodes, particularly in the context of nutrient sensing. Further investigations demonstrated sesn-1’s interaction with the GATOR2 protein complex, its role in maintaining muscle integrity and a potential synergy between sesn-1 and the FOXO pathway. Overall, our research underscores the profound implications of Sestrins in aging and stress resistance, shedding light on possible therapeutic avenues for prevention and treatment of age-associated disorders.
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- DOI
- 10.18632/aging.206290
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- 2026-10-08 MST
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APA
Zheltukhin, A.O., Chumakov, P.M., & Budanov, A.V. (2025). Sesn-1 is required for lifespan extension during caloric deprivation in C. elegans through inhibition of mTORC1 and activation of autophagy. <em>Aging</em>. https://doi.org/10.18632/aging.206290
Vancouver
Zheltukhin AO, Chumakov PM, Budanov AV. Sesn-1 is required for lifespan extension during caloric deprivation in C. elegans through inhibition of mTORC1 and activation of autophagy. Aging. 2025. doi:10.18632/aging.206290.
BibTeX
@article{andrei2025Sesnis,
title = {Sesn-1 is required for lifespan extension during caloric deprivation in C. elegans through inhibition of mTORC1 and activation of autophagy},
author = {Andrei O. Zheltukhin and Peter M. Chumakov and Andrei V. Budanov},
journal = {Aging},
year = {2025},
doi = {10.18632/aging.206290},
}
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