A Genomic Screen for Yeast Mutants Defective in Selective Mitochondria Autophagy

Author:

Kanki Tomotake1,Wang Ke2,Baba Misuzu3,Bartholomew Clinton R.2,Lynch-Day Melinda A.2,Du Zhou2,Geng Jiefei2,Mao Kai2,Yang Zhifen2,Yen Wei-Lien2,Klionsky Daniel J.2

Affiliation:

1. *Department of Clinical Chemistry and Laboratory Medicine, Kyushu University Graduate School of Medical Sciences, Fukuoka 812-8582, Japan;

2. Life Sciences Institute and Departments of Molecular, Cellular and Developmental Biology and Biological Chemistry, University of Michigan, Ann Arbor, MI 48109; and

3. Department of Chemical and Biological Sciences, Faculty of Science, Japan Women's University, Mejirodai, Tokyo 112-8681, Japan

Abstract

Mitophagy is the process of selective mitochondrial degradation via autophagy, which has an important role in mitochondrial quality control. Very little is known, however, about the molecular mechanism of mitophagy. A genome-wide yeast mutant screen for mitophagy-defective strains identified 32 mutants with a block in mitophagy, in addition to the known autophagy-related (ATG) gene mutants. We further characterized one of these mutants, ylr356wΔ that corresponds to a gene whose function has not been identified. YLR356W is a mitophagy-specific gene that was not required for other types of selective autophagy or macroautophagy. The deletion of YLR356W partially inhibited mitophagy during starvation, whereas there was an almost complete inhibition at post-log phase. Accordingly, we have named this gene ATG33. The new mutants identified in this analysis will provide a useful foundation for researchers interested in the study of mitochondrial homeostasis and quality control.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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