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MicroReview
Small molecules that regulate lifespan: evidence for xenohormesis
Dudley W. Lamming 1 , Jason G. Wood 1 and David A. Sinclair 1*
  1 Harvard Medical School, Department of Pathology, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.
Correspondence to   *E-mail david_sinclair@hms.harvard.edu; Tel. (+1) 617 432 3932; Fax (+1) 617 432 6225.
Copyright 2004 Blackwell Publishing Ltd

Summary

AbstractCalorie restrictionGenomic instability is a cause of yeast ageingSIR2, the silent protector of DNA stabilityThe regulation of Sir2 by CRReferences

Barring genetic manipulation, the diet known as calorie restriction (CR) is currently the only way to slow down ageing in mammals. The fact that CR works on most species, even microorganisms, implies a conserved underlying mechanism. Recent findings in the yeast Saccharomyces cerevisiae indicate that CR extends lifespan because it is a mild biological stressor that activates Sir2, a key component of yeast longevity and the founding member of the sirtuin family of deacetylases. The sirtuin family appears to have first arisen in primordial eukaryotes, possibly to help them cope with adverse conditions. Today they are found in plants, yeast, and animals and may underlie the remarkable health benefits of CR. Interestingly, a class of polyphenolic molecules produced by plants in response to stress can activate the sirtuins from yeast and metazoans. At least in the case of yeast, these molecules greatly extend lifespan by mimicking CR. One explanation for this surprising observation is the 'xenohormesis hypothesis', the idea that organisms have evolved to respond to stress signalling molecules produced by other species in their environment. In this way, organisms can prepare in advance for a deteriorating environment and/or loss of food supply.


Received 5 May, 2004.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1365-2958.2004.04209.x About DOI

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