Molecular Microbiology · 2008 · 210 citations · 26 references
Life SciencesBiochemistryCell BiologyAgingBioenergeticsCellular MetabolismMetabolic SignalingNutrient SensingNutrient-sensing PathwaysMammalian Target Of Rapamycin SignalingMicrobial EukaryotesMtor Complex 1 RegulationMtor Complex 1 SignalingMtorc1 SignalingNutrient Signaling PathwaysNutrient-sensitive Signaling PathwaysYeast Aging
Dietary nutrient limitation (dietary restriction) is known to increase lifespan in a variety of organisms. Although the molecular events that couple dietary restriction to increased lifespan are not clear, studies of the model eukaryote Saccharomyces cerevisiae have implicated several nutrient-sensitive kinases, including the target of rapamycin complex 1 (TORC1), Sch9, protein kinase A (PKA) and Rim15. We have recently demonstrated that TORC1 activates Sch9 by direct phosphorylation. We now show that Sch9 inhibits Rim15 also by direct phosphorylation. Treatment of yeast cells with the specific TORC1 inhibitor rapamycin or caffeine releases Rim15 from TORC1-Sch9-mediated inhibition and consequently increases lifespan. This kinase cascade appears to have been evolutionarily conserved, suggesting that caffeine may extend lifespan in other eukaryotes, including man.
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Regulation of Yeast Replicative Life Span by TOR and Sch9 in Response to Nutrients
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Medicine, Cancer Biology, Oncology +16
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