Fig4 confers tolerance to rapamycin in a Ste20-dependent manner independent of the Vac14 scaffold
Year: 2024
Type: preprint
Abstract: The lipid phosphatase Fig4 modulates the production and turnover of the signaling lipid PI3,5P2 through participation in a complex with its opposing kinase, Fab1, and the scaffold protein Vac14. Fig4 point mutations are associated with neurological diseases for which there are currently no specific therapies. Pathology involving Fig4 is generally attributed to disruption of the Fab1-Vac14-Fig4 complex. Through genetic manipulations in yeast we show that expression of Fig4 disease-related mutants confers tolerance to rapamycin, an inhibitor of the master growth activator TORC1. This phenotype is dominantly conferred at high temperatures by Fig4 mutants that bind poorly to Vac14 or by excess wild-type Fig4. Rapamycin tolerance does not require Fig4 catalytic activity or Vac14, suggesting that Fig4 mediates this altered stress response through context-inappropriate binding interactions with unknown proteins. The p21-activated kinase Ste20 is specifically required for this novel Vac14-independent Fig4 function. Our study shows that Fig4 can modulate homeostasis in Saccharomyces cerevisiae through interactions outside the Fab1-Vac14-Fig4 complex.
Authors: Hannah E. Reeves, Anna King, Imran Khan, Asha Thomas, Corey Chung, Lauren D. Dotson, Anirudan Sivaprakash, Harrison A. Hall, Alim Habib, Sophia Rosella Lee, Bonnie C. Lloyd, Caroline L. Darbro, Bethany S. Strunk
Institutions: Trinity University, University of Michigan
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W4400582662