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Chronological Lifespan in Yeast Is Dependent on the Accumulation of Storage Carbohydrates Mediated by Yak1, Mck1 and Rim15 Kinases.
Cao, Lu; Tang, Yingzhi; Quan, Zhenzhen; Zhang, Zhe; Oliver, Stephen G; Zhang, Nianshu.
Affiliation
  • Cao L; Cambridge Systems Biology Centre and Department of Biochemistry, University of Cambridge, Sanger Building, United Kingdom.
  • Tang Y; Cambridge Systems Biology Centre and Department of Biochemistry, University of Cambridge, Sanger Building, United Kingdom.
  • Quan Z; Cambridge Systems Biology Centre and Department of Biochemistry, University of Cambridge, Sanger Building, United Kingdom.
  • Zhang Z; Cambridge Systems Biology Centre and Department of Biochemistry, University of Cambridge, Sanger Building, United Kingdom.
  • Oliver SG; Cambridge Systems Biology Centre and Department of Biochemistry, University of Cambridge, Sanger Building, United Kingdom.
  • Zhang N; Cambridge Systems Biology Centre and Department of Biochemistry, University of Cambridge, Sanger Building, United Kingdom.
PLoS Genet ; 12(12): e1006458, 2016 Dec.
Article in En | MEDLINE | ID: mdl-27923067
Upon starvation for glucose or any other macronutrient, yeast cells exit from the mitotic cell cycle and acquire a set of characteristics that are specific to quiescent cells to ensure longevity. Little is known about the molecular determinants that orchestrate quiescence entry and lifespan extension. Using starvation-specific gene reporters, we screened a subset of the yeast deletion library representing the genes encoding 'signaling' proteins. Apart from the previously characterised Rim15, Mck1 and Yak1 kinases, the SNF1/AMPK complex, the cell wall integrity pathway and a number of cell cycle regulators were shown to be necessary for proper quiescence establishment and for extension of chronological lifespan (CLS), suggesting that entry into quiescence requires the integration of starvation signals transmitted via multiple signaling pathways. The CLS of these signaling mutants, and those of the single, double and triple mutants of RIM15, YAK1 and MCK1 correlates well with the amount of storage carbohydrates but poorly with transition-phase cell cycle status. Combined removal of the glycogen and trehalose biosynthetic genes, especially GSY2 and TPS1, nearly abolishes the accumulation of storage carbohydrates and severely reduces CLS. Concurrent overexpression of GSY2 and TSL1 or supplementation of trehalose to the growth medium ameliorates the severe CLS defects displayed by the signaling mutants (rim15Δyak1Δ or rim15Δmck1Δ). Furthermore, we reveal that the levels of intracellular reactive oxygen species are cooperatively controlled by Yak1, Rim15 and Mck1, and the three kinases mediate the TOR1-regulated accumulation of storage carbohydrates and CLS extension. Our data support the hypothesis that metabolic reprogramming to accumulate energy stores and the activation of anti-oxidant defence systems are coordinated by Yak1, Rim15 and Mck1 kinases to ensure quiescence entry and lifespan extension in yeast.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein Kinases / Protein Serine-Threonine Kinases / Saccharomyces cerevisiae Proteins / Glycogen Synthase Kinase 3 / Intracellular Signaling Peptides and Proteins / Longevity Language: En Journal: PLoS Genet Journal subject: GENETICA Year: 2016 Document type: Article Affiliation country: United kingdom Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein Kinases / Protein Serine-Threonine Kinases / Saccharomyces cerevisiae Proteins / Glycogen Synthase Kinase 3 / Intracellular Signaling Peptides and Proteins / Longevity Language: En Journal: PLoS Genet Journal subject: GENETICA Year: 2016 Document type: Article Affiliation country: United kingdom Country of publication: United States