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TORC1 signaling inhibition by rapamycin and caffeine affect lifespan, global gene expression, and cell proliferation of fission yeast.

Rallis, Charalampos and Codlin, Sandra and Bähler, Jürg (2013) 'TORC1 signaling inhibition by rapamycin and caffeine affect lifespan, global gene expression, and cell proliferation of fission yeast.' Aging Cell, 12 (4). pp. 563-573. ISSN 1474-9718

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Abstract

Target of rapamycin complex 1 (TORC1) is implicated in growth control and aging from yeast to humans. Fission yeast is emerging as a popular model organism to study TOR signaling, although rapamycin has been thought to not affect cell growth in this organism. Here, we analyzed the effects of rapamycin and caffeine, singly and combined, on multiple cellular processes in fission yeast. The two drugs led to diverse and specific phenotypes that depended on TORC1 inhibition, including prolonged chronological lifespan, inhibition of global translation, inhibition of cell growth and division, and reprograming of global gene expression mimicking nitrogen starvation. Rapamycin and caffeine differentially affected these various TORC1-dependent processes. Combined drug treatment augmented most phenotypes and effectively blocked cell growth. Rapamycin showed a much more subtle effect on global translation than did caffeine, while both drugs were effective in prolonging chronological lifespan. Rapamycin and caffeine did not affect the lifespan via the pH of the growth media. Rapamycin prolonged the lifespan of nongrowing cells only when applied during the growth phase but not when applied after cells had stopped proliferation. The doses of rapamycin and caffeine strongly correlated with growth inhibition and with lifespan extension. This comprehensive analysis will inform future studies into TORC1 function and cellular aging in fission yeast and beyond.

Item Type: Article
Uncontrolled Keywords: Schizosaccharomyces; Nitrogen; Sirolimus; Caffeine; Multiprotein Complexes; Schizosaccharomyces pombe Proteins; Culture Media; Microbial Sensitivity Tests; Signal Transduction; Cell Proliferation; Protein Biosynthesis; Gene Expression Regulation, Fungal; Phenotype; Genes, Fungal; Hydrogen-Ion Concentration; Time Factors; Microbial Viability; Phosphatidylinositol 3-Kinases; TOR Serine-Threonine Kinases; Mechanistic Target of Rapamycin Complex 1
Divisions: Faculty of Science and Health
Faculty of Science and Health > Life Sciences, School of
SWORD Depositor: Elements
Depositing User: Elements
Date Deposited: 18 Jun 2021 14:35
Last Modified: 06 Jan 2022 14:10
URI: http://repository.essex.ac.uk/id/eprint/26718

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