The Scaffold Protein Atg11 Recruits Fission Machinery to Drive Selective Mitochondria Degradation by Autophagy

被引:191
作者
Mao, Kai [1 ,2 ]
Wang, Ke [1 ,2 ]
Liu, Xu [1 ,2 ]
Klionsky, Daniel J. [1 ,2 ]
机构
[1] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
关键词
VACUOLE TARGETING PATHWAY; DYNAMIN-RELATED GTPASE; SACCHAROMYCES-CEREVISIAE; TAGS PEROXISOMES; MITOPHAGY; YEAST; DNM1P; DIVISION; PARKIN; CYTOPLASM;
D O I
10.1016/j.devcel.2013.05.024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As the cellular power plant, mitochondria play a significant role in homeostasis. To maintain the proper quality and quantity of mitochondria requires both mitochondrial degradation and division. A selective type of autophagy, mitophagy, drives the degradation of excess or damaged mitochondria, whereas division is controlled by a specific fission complex; however, the relationship between these two processes, especially the role of mitochondrial fission during mitophagy, remains unclear. In this study, we report that mitochondrial fission is important for the progression of mitophagy. When mitophagy is induced, the fission complex is recruited to the degrading mitochondria through an interaction between Atg11 and Dnm1; interfering with this interaction severely blocks mitophagy. These data establish a paradigm for selective organelle degradation.
引用
收藏
页码:9 / 18
页数:10
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