TY - JOUR
T1 - The fusogenic lipid phosphatidic acid promotes the biogenesis of mitochondrial outer membrane protein Ugo1
AU - Vögtle, F. Nora
AU - Keller, Michael
AU - Taskin, Asli A.
AU - Horvath, Susanne E.
AU - Guan, Xue Li
AU - Prinz, Claudia
AU - Opalińska, Magdalena
AU - Zorzin, Carina
AU - van der Laan, Martin
AU - Wenk, Markus R.
AU - Schubert, Rolf
AU - Wiedemann, Nils
AU - Holzer, Martin
AU - Meisinger, Chris
N1 - Publisher Copyright:
© 2015 Vögtle et al.
PY - 2015
Y1 - 2015
N2 - Import and assembly of mitochondrial proteins depend on a complex interplay of proteinaceous translocation machineries. The role of lipids in this process has been studied only marginally and so far no direct role for a specific lipid in mitochondrial protein biogenesis has been shown. Here we analyzed a potential role of phosphatidic acid (PA) in biogenesis of mitochondrial proteins in Saccharomyces cerevisiae. In vivo remodeling of the mitochondrial lipid composition by lithocholic acid treatment or by ablation of the lipid transport protein Ups1, both leading to an increase of mitochondrial PA levels, specifically stimulated the biogenesis of the outer membrane protein Ugo1, a component of the mitochondrial fusion machinery. We reconstituted the import and assembly pathway of Ugo1 in protein-free liposomes, mimicking the outer membrane phospholipid composition, and found a direct dependency of Ugo1 biogenesis on PA. Thus, PA represents the first lipid that is directly involved in the biogenesis pathway of a mitochondrial membrane protein.
AB - Import and assembly of mitochondrial proteins depend on a complex interplay of proteinaceous translocation machineries. The role of lipids in this process has been studied only marginally and so far no direct role for a specific lipid in mitochondrial protein biogenesis has been shown. Here we analyzed a potential role of phosphatidic acid (PA) in biogenesis of mitochondrial proteins in Saccharomyces cerevisiae. In vivo remodeling of the mitochondrial lipid composition by lithocholic acid treatment or by ablation of the lipid transport protein Ups1, both leading to an increase of mitochondrial PA levels, specifically stimulated the biogenesis of the outer membrane protein Ugo1, a component of the mitochondrial fusion machinery. We reconstituted the import and assembly pathway of Ugo1 in protein-free liposomes, mimicking the outer membrane phospholipid composition, and found a direct dependency of Ugo1 biogenesis on PA. Thus, PA represents the first lipid that is directly involved in the biogenesis pathway of a mitochondrial membrane protein.
UR - http://www.scopus.com/inward/record.url?scp=84975804407&partnerID=8YFLogxK
U2 - 10.1083/jcb.201506085
DO - 10.1083/jcb.201506085
M3 - Article
C2 - 26347140
AN - SCOPUS:84975804407
SN - 0021-9525
VL - 210
SP - 951
EP - 960
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 6
ER -