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The Molecular Logic of Gtr1/2 and Pib2 Dependent TORC1 Regulation in Budding Yeast.
Cecil, Jacob H; Padilla, Cristina M; Lipinski, Austin A; Langlais, Paul R; Luo, Xiangxia; Capaldi, Andrew P.
Afiliación
  • Cecil JH; Department of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721.
  • Padilla CM; Department of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721.
  • Lipinski AA; Department of Medicine, University of Arizona, Tucson, AZ, 85721.
  • Langlais PR; Department of Medicine, University of Arizona, Tucson, AZ, 85721.
  • Luo X; Department of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721.
  • Capaldi AP; Department of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721.
bioRxiv ; 2023 Dec 07.
Article en En | MEDLINE | ID: mdl-38106135
ABSTRACT
The Target of Rapamycin kinase Complex I (TORC1) regulates cell growth and metabolism in eukaryotes. Previous studies have shown that, in Saccharomyces cerevisiae, nitrogen and amino acid signals activate TORC1 via the highly conserved small GTPases, Gtr1/2, and the phosphatidylinositol 3-phosphate binding protein, Pib2. However, it was unclear if/how Gtr1/2 and Pib2 cooperate to control TORC1. Here we report that this dual regulator system pushes TORC1 into three distinct signaling states (i) a Gtr1/2 on, Pib2 on, rapid growth state in nutrient replete conditions; (ii) a Gtr1/2 off, Pib2 on, adaptive/slow growth state in poor-quality growth medium; and (iii) a Gtr1/2 off, Pib2 off, quiescent state in starvation conditions. We suggest that other signaling pathways work in a similar way, to drive a multi-level response via a single kinase, but the behavior has been overlooked since most studies follow signaling to a single reporter protein.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2023 Tipo del documento: Article