Vps39 Interacts with Tom40 to Establish One of Two Functionally Distinct Vacuole-Mitochondria Contact SitesGonzález Montoro, A., Auffarth, K., Hönscher, C., Bohnert, M., Becker, T., Warscheid, B., Reggiori, F., van der Laan, M., Fröhlich, F. & Ungermann, C., 4-Jun-2018, In : Developmental Cell. 45, 5, p. 621-636.e7 24 p.
Research output: Contribution to journal › Article › Academic › peer-review
The extensive subcellular network of membrane contact sites plays central roles in organelle biogenesis and communication, yet the precise contributions of the involved machineries remain largely enigmatic. The yeast vacuole forms a membrane contact site with mitochondria, called vacuolar and mitochondrial patch (vCLAMP). Formation of vCLAMPs involves the vacuolar Rab GTPase Ypt7 and the Ypt7-interacting Vps39 subunit of the HOPS tethering complex. Here, we uncover the general preprotein translocase of the outer membrane (TOM) subunit Tom40 as the direct binding partner of Vps39 on mitochondria. We identify Vps39 mutants defective in TOM binding, but functional for HOPS. Cells that cannot form vCLAMPs show reduced growth under stress conditions and impaired survival upon starvation. Unexpectedly, our mutant analysis revealed the existence of two functionally independent vacuole-mitochondria MCSs: one formed by the Ypt7-Vps39-Tom40 tether and a second one by Vps13-Mcp1, which is redundant with ER-mitochondrial contacts formed by ERMES.
|Number of pages||24|
|Publication status||Published - 4-Jun-2018|
- PROTEIN, YEAST, HOPS TETHERING COMPLEX, OUTER-MEMBRANE, SACCHAROMYCES-CEREVISIAE, PREPROTEIN TRANSLOCASE, RAB INTERACTIONS, MOLECULAR ARCHITECTURE, CELLULAR-METABOLISM, ER-MITOCHONDRIA