Phosphatidylinositol 3,5-bisphosphate regulates the transition betweentrans-SNARE complex formation and vacuole membrane fusion
| Autor: | Rutilio A. Fratti, Matthew L. Starr, Katherine D. Sullivan, Annie Guo, Ez C. Ellis, Brandon C. Jones, Logan R. Hurst, Gregory E. Miner |
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| Rok vydání: | 2019 |
| Předmět: |
Saccharomyces cerevisiae Proteins
Phosphatidylinositol 3 5-bisphosphate Mutant Vacuole fusion Saccharomyces cerevisiae Vacuole Biology Membrane Fusion 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Phosphatidylinositol Phosphates Phosphatidylinositol Molecular Biology 030304 developmental biology 0303 health sciences Kinase Lipid bilayer fusion Cell Biology Lipids Cell biology Molecular Docking Simulation Phosphotransferases (Alcohol Group Acceptor) chemistry Mutation Vacuoles Brief Reports SNARE Proteins SNARE complex 030217 neurology & neurosurgery |
| Zdroj: | Molecular Biology of the Cell |
| ISSN: | 1939-4586 1059-1524 |
| DOI: | 10.1091/mbc.e18-08-0505 |
| Popis: | Phosphoinositides (PIs) regulate a myriad of cellular functions including membrane fusion, as exemplified by the yeast vacuole, which uses various PIs at different stages of fusion. In light of this, the effect of phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2) on vacuole fusion remains unknown. PI(3,5)P2is made by the PI3P 5-kinase Fab1 and has been characterized as a regulator of vacuole fission during hyperosmotic shock, where it interacts with the TRP Ca2+channel Yvc1. Here we demonstrate that exogenously added dioctanoyl (C8) PI(3,5)P2abolishes homotypic vacuole fusion. This effect was not linked to Yvc1, as fusion was equally affected using yvc1Δ vacuoles. Thus, the effects of C8-PI(3,5)P2on fusion and fission operate through distinct mechanisms. Further testing showed that C8-PI(3,5)P2inhibited vacuole fusion after trans-SNARE pairing. Although SNARE complex formation was unaffected, we found that C8-PI(3,5)P2blocked outer leaflet lipid mixing. Overproduction of endogenous PI(3,5)P2by the fab1T2250Ahyperactive kinase mutant also inhibited the lipid mixing stage, bolstering the model in which PI(3,5)P2inhibits fusion when present at elevated levels. Taken together, this work identifies a novel function for PI(3,5)P2as a regulator of vacuolar fusion. Moreover, it suggests that this lipid acts as a molecular switch between fission and fusion. |
| Databáze: | OpenAIRE |
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