COX assembly factor ccdc56 regulates mitochondrial morphology by affecting mitochondrial recruitment of Drp1

被引:13
作者
Ban-Ishihara, Reiko [1 ]
Tomohiro-Takamiya, Shiho [2 ]
Tani, Motohiro [2 ]
Baudier, Jacques [3 ]
Ishihara, Naotada [1 ]
Kuge, Osamu [2 ]
机构
[1] Kurume Univ, Inst Life Sci, Dept Prot Biochem, Kurume, Fukuoka 8390864, Japan
[2] Kyushu Univ, Dept Chem, Fac Sci, Fukuoka 8128581, Japan
[3] INSERM, U873, F-38054 Grenoble, France
关键词
Organelle; Mitochondria; Mitochondrial fission; Cytochrome oxidase (COX); Drp1; CYTOCHROME-C; DNA NUCLEOIDS; DYNAMICS; MEMBRANE; INNER;
D O I
10.1016/j.febslet.2015.08.039
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
Mitochondria are dynamic organelles that alter their morphology in response to cellular signaling and differentiation through balanced fusion and fission. In this study, we found that the mitochondrial inner membrane ATPase ATAD3A interacted with ccdc56/MITRAC12/COA3, a subunit of the cytochrome oxidase (COX)-assembly complex. Overproduction of ccdc56 in HeLa cells resulted in fragmented mitochondrial morphology, while mitochondria were highly elongated in ccdc56-repressed cells by the defective recruitment of the fission factor Drp1. We also found that mild and chronic inhibition of COX led to mitochondrial elongation, as seen in ccdc56-repressed cells. These results indicate that ccdc56 positively regulates mitochondrial fission via regulation of COX activity and the mitochondrial recruitment of Drp1, and thus, suggest a novel relationship between COX assembly and mitochondrial morphology. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3126 / 3132
页数:7
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