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Activation of the cell wall integrity pathway negatively regulates TORC2-Ypk1/2 signaling through blocking eisosome disassembly in Saccharomyces cerevisiae.
- Source :
-
Communications biology [Commun Biol] 2024 Jun 11; Vol. 7 (1), pp. 722. Date of Electronic Publication: 2024 Jun 11. - Publication Year :
- 2024
-
Abstract
- The target of rapamycin complex 2 (TORC2) signaling is associated with plasma membrane (PM) integrity. In Saccharomyces cerevisiae, TORC2-Ypk1/2 signaling controls sphingolipid biosynthesis, and Ypk1/2 phosphorylation by TORC2 under PM stress conditions is increased in a Slm1/2-dependent manner, under which Slm1 is known to be released from an eisosome, a furrow-like invagination PM structure. However, it remains unsolved how the activation machinery of TORC2-Ypk1/2 signaling is regulated. Here we show that edelfosine, a synthetic lysophospholipid analog, inhibits the activation of TORC2-Ypk1/2 signaling, and the cell wall integrity (CWI) pathway is involved in this inhibitory effect. The activation of CWI pathway blocked the eisosome disassembly promoted by PM stress and the release of Slm1 from eisosomes. Constitutive activation of TORC2-Ypk1/2 signaling exhibited increased sensitivity to cell wall stress. We propose that the CWI pathway negatively regulates the TORC2-Ypk1/2 signaling, which is involved in the regulatory mechanism to ensure the proper stress response to cell wall damage.<br /> (© 2024. The Author(s).)
- Subjects :
- rab GTP-Binding Proteins metabolism
rab GTP-Binding Proteins genetics
Phosphorylation
Protein Kinases
Protein Serine-Threonine Kinases
Saccharomyces cerevisiae metabolism
Saccharomyces cerevisiae genetics
Saccharomyces cerevisiae drug effects
Cell Wall metabolism
Cell Wall drug effects
Saccharomyces cerevisiae Proteins metabolism
Saccharomyces cerevisiae Proteins genetics
Mechanistic Target of Rapamycin Complex 2 metabolism
Mechanistic Target of Rapamycin Complex 2 genetics
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 2399-3642
- Volume :
- 7
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Communications biology
- Publication Type :
- Academic Journal
- Accession number :
- 38862688
- Full Text :
- https://doi.org/10.1038/s42003-024-06411-2