4.7 Review

Stressin' Sestrins take an aging fight

Journal

EMBO MOLECULAR MEDICINE
Volume 2, Issue 10, Pages 388-400

Publisher

WILEY
DOI: 10.1002/emmm.201000097

Keywords

aging; p53; redox; Sestrin; target of rapamycin

Funding

  1. NIH
  2. Superfund Research Program [CA118165, ES006376, P42-ES010337, DK082080]
  3. Korea Research Foundation [KRF-2007-357-C00096]
  4. Human Frontier Science Program Organization [LT00653/2008-L]
  5. NATIONAL CANCER INSTITUTE [R01CA118165] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [K99DK082080] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [P42ES010337, R01ES006376] Funding Source: NIH RePORTER

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Sestrins (Sesns) are a family of highly conserved stress-responsive proteins, transcriptionally regulated by p53 and forkhead transcription factor that exhibit oxidoreductase activity in vitro and can protect cells from oxidative stress. However, their major biochemical and physiological function does not appear to depend on their redox (reduction and oxidation) activity. Sesns promote activation of adenosine-5'-monophosphate (AMP)-dependent protein kinase in both mammals and flies. Stress-induced Sesn expression results in inhibition of the target of rapamycin complex 1 (TORC1) and the physiological and pathological implications of disrupting the Sesns-TORC1 crosstalk are now being unravelled. Detailing their mechanism of action and exploring their roles in human physiology point to exciting new insights to topics as diverse as stress, cancer, metabolism and aging.

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