Reference - Detail
| RRC ID | 81856 |
|---|---|
| Author | Tamura Y, Onguka O, Hobbs AE, Jensen RE, Iijima M, Claypool SM, Sesaki H. |
| Title | Role for two conserved intermembrane space proteins, Ups1p and Ups2p, [corrected] in intra-mitochondrial phospholipid trafficking. |
| Journal | J Biol Chem |
| Abstract |
Mitochondrial membranes maintain a specific phospholipid composition. Most phospholipids are synthesized in the endoplasmic reticulum (ER) and transported to mitochondria, but cardiolipin and phosphatidylethanolamine are produced in mitochondria. In the yeast Saccharomyces cerevisiae, phospholipid exchange between the ER and mitochondria relies on the ER-mitochondria encounter structure (ERMES) complex, which physically connects the ER and mitochondrial outer membrane. However, the proteins and mechanisms involved in phospholipid transport within mitochondria remain elusive. Here, we investigated the role of the conserved intermembrane space proteins, Ups1p and Ups2p, and an inner membrane protein, Mdm31p, in phospholipid metabolism. Our data show that loss of the ERMES complex, Ups1p, and Mdm31p causes similar defects in mitochondrial phospholipid metabolism, mitochondrial morphology, and cell growth. Defects in cells lacking the ERMES complex or Ups1p are suppressed by Mdm31p overexpression as well as additional loss of Ups2p, which antagonizes Ups1p. Combined loss of the ERMES complex and Ups1p exacerbates phospholipid defects. Finally, pulse-chase experiments using [(14)C]serine revealed that Ups1p and Ups2p antagonistically regulate conversion of phosphatidylethanolamine to phosphatidylcholine. Our results suggest that Ups proteins and Mdm31p play important roles in phospholipid biosynthesis in mitochondria. Ups proteins may function in phospholipid trafficking between the outer and inner mitochondrial membranes. |
| Volume | 287(19) |
| Pages | 15205-18 |
| Published | 2012-5-4 |
| DOI | 10.1074/jbc.M111.338665 |
| PII | S0021-9258(20)46172-1 |
| PMID | 22403410 |
| PMC | PMC3346110 |
| MeSH | Biological Transport Blotting, Western Endoplasmic Reticulum / metabolism Hydrogen-Ion Concentration Intracellular Membranes / metabolism* Membrane Proteins / genetics Membrane Proteins / metabolism Microscopy, Fluorescence Mitochondrial Membranes / metabolism* Mitochondrial Proteins / genetics Mitochondrial Proteins / metabolism Mitochondrial Proteins / physiology* Mutation Phosphatidylethanolamines / metabolism Phosphatidylserines / metabolism Phospholipids / chemistry Phospholipids / metabolism* Saccharomyces cerevisiae / genetics Saccharomyces cerevisiae / metabolism Saccharomyces cerevisiae Proteins / genetics Saccharomyces cerevisiae Proteins / metabolism Saccharomyces cerevisiae Proteins / physiology* Serine / metabolism |
| IF | 4.238 |
| Resource | |
| DNA material | pRS316-Mmm1 (RDB20352) pRS316-Mdm34 (RDB20353) pRS316-Mdm10 (RDB20354) pRS316-Mdm12 (RDB20355) pRS316-Mdm31 (RDB20356) pRS316-Mdm32 (RDB20357) pRS314-Mmm1 (RDB20358) pRS314-Mdm34 (RDB20359) pRS314-Mdm10 (RDB20360) pRS314-Mdm12 (RDB20361) pRS314-Mdm31 (RDB20362) pRS314-Mdm32 (RDB20363) pRS314-Ups1 (RDB20364) pRS316-Ups1 (RDB20365) pRS424-Ups1 (RDB20366) pRS425-Ups1 (RDB20367) pRS424-UPS2 (RDB20368) pRS425-Ups2 (RDB20369) pRS423-Ups2 (RDB20370) pRS314-Crd1 (RDB20371) pRS316-Crd1 (RDB20372) pRS314-Gep4 (RDB20373) pRS316-Gep4 (RDB20374) |