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      Prohibitin 2 Is an Inner Mitochondrial Membrane Mitophagy Receptor

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          SUMMARY

          The removal of unwanted or damaged mitochondria by autophagy, a process called mitophagy, is essential for key events in development, cellular homeostasis, tumor suppression, and prevention of neurodegeneration and aging. However, the precise mechanisms of mitophagy remain uncertain. Here, we identify the inner mitochondrial membrane protein, prohibitin 2 (PHB2), as a crucial mitophagy receptor involved in targeting mitochondria for autophagic degradation. PHB2 binds the autophagosomal membrane-associated protein LC3 through an LC3-interaction region (LIR) domain upon mitochondrial depolarization and proteasome-dependent outer membrane rupture. PHB2 is required for Parkin-induced mitophagy in mammalian cells and for the clearance of paternal mitochondria after embryonic fertilization in C. elegans. Our findings pinpoint a conserved mechanism of eukaryotic mitophagy and demonstrate a function of prohibitin 2 that may underlie its roles in physiology, aging, and disease.

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          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          4 January 2017
          22 December 2016
          12 January 2017
          12 January 2018
          : 168
          : 1-2
          : 224-238.e10
          Affiliations
          [1 ]Center for Autophagy Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75230, USA
          [2 ]Howard Hughes Medical Research Institute, University of Texas Southwestern Medical Center, Dallas, TX 75230, USA
          [3 ]Children’s Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, TX 75230, USA
          [4 ]Department of Microbiology, University of Texas Southwestern Medical Center, Dallas, TX 75230, USA
          Author notes
          [5]

          Co-first author

          [6]

          Lead Contact

          Article
          PMC5235968 PMC5235968 5235968 nihpa836845
          10.1016/j.cell.2016.11.042
          5235968
          28017329
          cde79133-c498-4e0b-89a2-669f354f0422
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