MICOS subcomplexes assemble independently on the mitochondrial inner membrane in proximity to ER contact sites

被引:28
|
作者
Tirrell, Parker S. [1 ]
Nguyen, Kailey N. [1 ]
Luby-Phelps, Katherine [1 ]
Friedman, Jonathan R. [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Cell Biol, Dallas, TX 75390 USA
来源
JOURNAL OF CELL BIOLOGY | 2020年 / 219卷 / 11期
基金
美国国家卫生研究院;
关键词
CRISTAE; MITOFILIN; COMPLEX; ORGANIZATION; COMPONENT; YEAST; ARCHITECTURE; JUNCTIONS; VERSATILE; VACUOLES;
D O I
10.1083/jcb.202003024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MICOS is a conserved multisubunit complex that localizes to mitochondrial cristae junctions and organizes cristae positioning within the organelle. MICOS is organized into two independent subcomplexes; however, the mechanisms that dictate the assembly and spatial positioning of each MICOS subcomplex are poorly understood. Here, we determine that MICOS subcomplexes target independently of one another to sites on the inner mitochondrial membrane that are in proximity to contact sites between mitochondria and the ER. One subcomplex, composed of Mic27/Mic26/Mic10/Mic12, requires ERMES complex function for its assembly. In contrast, the principal MICOS component, Mic60, self-assembles and localizes in close proximity to the ER through an independent mechanism. We also find that Mic60 can uniquely redistribute adjacent to forced mitochondria-vacuole contact sites. Our data suggest that nonoverlapping properties of interorganelle contact sites provide spatial cues that enable MICOS assembly and ultimately lead to proper physical and functional organization of mitochondria.
引用
收藏
页数:20
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