Exomer cooperates with Ryh1RAB6 in regulating TORC2 activity

Abstract

Exomer is a trans-Golgi protein complex involved in multiple biological processes, including lipid homeostasis and stress response. We have found that in fission yeast, the absence of exomer leads to a defect in the recovery of "target of rapamycin complex 2" (TORC2) activity in response to high concentrations of KCl, but not to sorbitol, which indicates that the mutants are impaired in their ability to respond to salt stress. Changes in lipid homeostasis did not suppress this defect. Ryh1RAB6 is a Rab GTPase that resides in the Golgi and endosomes and facilitates or stabilizes the interaction between TORC2 and its substrate, the AGC kinase Gad8. We have found genetic and functional interactions between exomer and Ryh1RAB6. The recovery of TORC2 activity in response to KCl requires Ryh1RAB6 and exomer, and the localization of Ryh1RAB6 is aberrant in exomer mutants. Co-immunoprecipitation experiments indicate that the interaction between TORC2 and Gad8 is weaker in the absence of exomer. We propose that exomer regulates TORC2 by facilitating appropriate Ryh1 localization.