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Dev Cell. 2009 Jul;17(1):87-97. doi: 10.1016/j.devcel.2009.06.013.

Mitochondria-anchored receptor Atg32 mediates degradation of mitochondria via selective autophagy.

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1
Division of Molecular Cell Biology, National Institute for Basic Biology, Okazaki, Japan. kokamoto@iri.titech.ac.jp

Abstract

Mitochondria are essential organelles that produce most of the energy for a cell, but concomitantly accumulate oxidative damage. Degradation of damaged mitochondria is critical for cell homeostasis, and this process is thought to be mediated by mitophagy, an autophagy-related pathway specific for mitochondria. However, whether mitochondria are selectively degraded, and how the autophagic machinery is targeted to mitochondria, remain largely unknown. Here we demonstrate that, in post-log phase cells under respiratory conditions, a substantial fraction of mitochondria are exclusively sequestered as cargoes and transported to the vacuole, a lytic compartment in yeast, in an autophagy-dependent manner. Interestingly, we found Atg32, a mitochondria-anchored protein essential for mitophagy that is induced during respiratory growth. In addition, our data suggest that Atg32 interacts with Atg8 and Atg11, autophagy-related proteins critical for recognition of cargo receptors. We propose that Atg32 acts as a mitophagy-specific receptor and regulates selective degradation of mitochondria.

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PMID:
19619494
DOI:
10.1016/j.devcel.2009.06.013
[Indexed for MEDLINE]
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