Modulation of the Respiratory Supercomplexes in Yeast ENHANCED FORMATION OF CYTOCHROME OXIDASE INCREASES THE STABILITY AND ABUNDANCE OF RESPIRATORY SUPERCOMPLEXES

被引:28
|
作者
Cui, Tie-Zhong [1 ,2 ]
Conte, Annalea [3 ]
Fox, Jennifer L. [1 ,2 ]
Zara, Vincenzo [3 ]
Winge, Dennis R. [1 ,2 ]
机构
[1] Univ Utah, Hlth Sci Ctr, Dept Med, Salt Lake City, UT 84132 USA
[2] Univ Utah, Hlth Sci Ctr, Dept Biochem, Salt Lake City, UT 84132 USA
[3] Univ Salento, Dipartimento Sci & Tecnol Biol Ambientali, I-73100 Lecce, Italy
基金
美国国家卫生研究院;
关键词
Bioenergetics; Electron Transfer Complex; Cardiolipin; Cytochrome Oxidase; Mitochondria; Mitochondrial Metabolism; INNER MITOCHONDRIAL-MEMBRANE; RIESKE FE/S PROTEIN; BC(1) COMPLEX; C-OXIDASE; SACCHAROMYCES-CEREVISIAE; CHAIN SUPERCOMPLEXES; CRYSTAL-STRUCTURE; B SYNTHESIS; CARDIOLIPIN; SINGLE;
D O I
10.1074/jbc.M113.523688
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: The cytochrome bc(1) complex weakly associates with cytochrome oxidase (CcO) in the absence of the Rieske Rip1 subunit. Results: The N-terminal domain of Rip1 enhances the stabilization of cytochrome bc(1)-CcO supercomplexes in yeast. Conclusion: Induced stabilization of supercomplexes arises from bc(1)-dependent formation of CcO. Significance: The late assembly intermediate of the bc(1) complex can template the maturation of CcO even without cardiolipin. Yeast cells deficient in the Rieske iron-sulfur subunit (Rip1) of ubiquinol-cytochrome c reductase (bc(1)) accumulate a late core assembly intermediate, which weakly associates with cytochrome oxidase (CcO) in a respiratory supercomplex. Expression of the N-terminal half of Rip1, which lacks the C-terminal FeS-containing globular domain (designated N-Rip1), results in a marked stabilization of trimeric and tetrameric bc(1)-CcO supercomplexes. Another bc(1) mutant (qcr9) stalled at the same assembly intermediate is likewise converted to stable supercomplex species by the expression of N-Rip1, but not by expression of intact Rip1. The N-Rip1-induced stabilization of bc(1)-CcO supercomplexes is independent of the Bcs1 translocase, which mediates Rip1 translocation during bc(1) biogenesis. N-Rip1 induces the stabilization of bc(1)-CcO supercomplexes through an enhanced formation of CcO. The association of N-Rip1 with the late core bc(1) assembly intermediate appears to confer stabilization of a CcO assembly intermediate. This induced stabilization of CcO is dependent on the Rcf1 supercomplex stabilization factor and only partially dependent on the presence of cardiolipin. N-Rip1 exerts a related induction of CcO stabilization in WT yeast, resulting in enhanced respiration. Additionally, the impact of CcO stabilization on supercomplexes was observed by means other than expression of N-Rip1 (via overexpression of CcO subunits Cox4 and Cox5a), demonstrating that this is a general phenomenon. This study presents the first evidence showing that supercomplexes can be stabilized by the stimulated formation of CcO.
引用
收藏
页码:6133 / 6141
页数:9
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