The genetic interactome of prohibitins: coordinated control of cardiolipin and phosphatidylethanolamine by conserved regulators in mitochondria

被引:234
作者
Osman, Christof [1 ]
Haag, Mathias [3 ]
Potting, Christoph [1 ]
Rodenfels, Jonathan [4 ,5 ]
Dip, Phat Vinh [1 ]
Wieland, Felix T. [3 ]
Bruegger, Britta [3 ]
Westermann, Benedikt [4 ,5 ]
Langer, Thomas [1 ,2 ]
机构
[1] Univ Cologne, Inst Genet, CMMC, Cologne Excellence Cluster Cellular Stress Respon, D-50674 Cologne, Germany
[2] Max Planck Inst Biol Aging, Cologne, Germany
[3] Heidelberg Univ, Biochem Ctr, D-69120 Heidelberg, Germany
[4] Univ Bayreuth, Inst Cell Biol, D-95440 Bayreuth, Germany
[5] Univ Bayreuth, Electron Microscopy Lab, D-95440 Bayreuth, Germany
关键词
SYNTHETIC LETHAL INTERACTION; DOMINANT OPTIC ATROPHY; DYNAMIN-RELATED GTPASE; SACCHAROMYCES-CEREVISIAE; INNER-MEMBRANE; F1FO-ATP SYNTHASE; OUTER-MEMBRANE; BARTH-SYNDROME; DNA NUCLEOIDS; YEAST;
D O I
10.1083/jcb.200810189
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Prohibitin ring complexes in the mitochondrial inner membrane regulate cell proliferation as well as the dynamics and function of mitochondria. Although prohibitins are essential in higher eukaryotes, prohibitin-deficient yeast cells are viable and exhibit a reduced replicative life span. Here, we de. ne the genetic interactome of prohibitins in yeast using synthetic genetic arrays, and identify 35 genetic interactors of prohibitins (GEP genes) required for cell survival in the absence of prohibitins. Proteins encoded by these genes include members of a conserved protein family, Ups1 and Gep1, which affect the processing of the dynamin-like GTPase Mgm1 and thereby modulate cristae morphogenesis. We show that Ups1 and Gep1 regulate the levels of cardiolipin and phosphatidylethanolamine in mitochondria in a lipidspecific but coordinated manner. Lipid pro. ling by mass spectrometry of GEP-deficient mitochondria reveals a critical role of cardiolipin and phosphatidylethanolamine for survival of prohibitin-deficient cells. We propose that prohibitins control inner membrane organization and integrity by acting as protein and lipid scaffolds.
引用
收藏
页码:583 / 596
页数:14
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