Your browser doesn't support javascript.
loading
The mitochondrial intermembrane space protein mitofissin drives mitochondrial fission required for mitophagy.
Fukuda, Tomoyuki; Furukawa, Kentaro; Maruyama, Tatsuro; Yamashita, Shun-Ichi; Noshiro, Daisuke; Song, Chihong; Ogasawara, Yuta; Okuyama, Kentaro; Alam, Jahangir Md; Hayatsu, Manabu; Saigusa, Tetsu; Inoue, Keiichi; Ikeda, Kazuho; Takai, Akira; Chen, Lin; Lahiri, Vikramjit; Okada, Yasushi; Shibata, Shinsuke; Murata, Kazuyoshi; Klionsky, Daniel J; Noda, Nobuo N; Kanki, Tomotake.
Afiliação
  • Fukuda T; Department of Cellular Physiology, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.
  • Furukawa K; Department of Cellular Physiology, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.
  • Maruyama T; Institute of Microbial Chemistry (BIKAKEN), Shinagawa-ku, Tokyo 141-0021, Japan.
  • Yamashita SI; Department of Cellular Physiology, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.
  • Noshiro D; Institute of Microbial Chemistry (BIKAKEN), Shinagawa-ku, Tokyo 141-0021, Japan; Institute for Genetic Medicine, Hokkaido University, Sapporo, Hokkaido 060-0815, Japan.
  • Song C; National Institute for Physiological Sciences (NIPS), National Institutes of Natural Sciences (NINS), Okazaki, Aichi 444-8585, Japan; Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences (NINS), Okazaki, Aichi 444-8585, Japan.
  • Ogasawara Y; Institute of Microbial Chemistry (BIKAKEN), Shinagawa-ku, Tokyo 141-0021, Japan; Institute for Genetic Medicine, Hokkaido University, Sapporo, Hokkaido 060-0815, Japan.
  • Okuyama K; Division of Microscopic Anatomy, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.
  • Alam JM; Institute of Microbial Chemistry (BIKAKEN), Shinagawa-ku, Tokyo 141-0021, Japan.
  • Hayatsu M; Division of Microscopic Anatomy, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.
  • Saigusa T; Department of Cellular Physiology, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.
  • Inoue K; Department of Cellular Physiology, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.
  • Ikeda K; Department of Cell Biology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan; Laboratory for Cell Polarity Regulation, RIKEN Center for Biosystems Dynamics Research (BDR), Osaka 565-0874, Japan.
  • Takai A; Department of Cell Biology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan; Laboratory for Cell Polarity Regulation, RIKEN Center for Biosystems Dynamics Research (BDR), Osaka 565-0874, Japan.
  • Chen L; National Institute for Physiological Sciences (NIPS), National Institutes of Natural Sciences (NINS), Okazaki, Aichi 444-8585, Japan; Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences (NINS), Okazaki, Aichi 444-8585, Japan.
  • Lahiri V; Life Sciences Institute and Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.
  • Okada Y; Department of Cell Biology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan; Laboratory for Cell Polarity Regulation, RIKEN Center for Biosystems Dynamics Research (BDR), Osaka 565-0874, Japan; Department of Physics, Graduate School of Science, The University of Tokyo, To
  • Shibata S; Division of Microscopic Anatomy, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.
  • Murata K; National Institute for Physiological Sciences (NIPS), National Institutes of Natural Sciences (NINS), Okazaki, Aichi 444-8585, Japan; Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences (NINS), Okazaki, Aichi 444-8585, Japan.
  • Klionsky DJ; Life Sciences Institute and Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.
  • Noda NN; Institute of Microbial Chemistry (BIKAKEN), Shinagawa-ku, Tokyo 141-0021, Japan; Institute for Genetic Medicine, Hokkaido University, Sapporo, Hokkaido 060-0815, Japan. Electronic address: nn@igm.hokudai.ac.jp.
  • Kanki T; Department of Cellular Physiology, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan. Electronic address: kanki@med.niigata-u.ac.jp.
Mol Cell ; 83(12): 2045-2058.e9, 2023 Jun 15.
Article em En | MEDLINE | ID: mdl-37192628
ABSTRACT
Mitophagy plays an important role in mitochondrial homeostasis by selective degradation of mitochondria. During mitophagy, mitochondria should be fragmented to allow engulfment within autophagosomes, whose capacity is exceeded by the typical mitochondria mass. However, the known mitochondrial fission factors, dynamin-related proteins Dnm1 in yeasts and DNM1L/Drp1 in mammals, are dispensable for mitophagy. Here, we identify Atg44 as a mitochondrial fission factor that is essential for mitophagy in yeasts, and we therefore term Atg44 and its orthologous proteins mitofissin. In mitofissin-deficient cells, a part of the mitochondria is recognized by the mitophagy machinery as cargo but cannot be enwrapped by the autophagosome precursor, the phagophore, due to a lack of mitochondrial fission. Furthermore, we show that mitofissin directly binds to lipid membranes and brings about lipid membrane fragility to facilitate membrane fission. Taken together, we propose that mitofissin acts directly on lipid membranes to drive mitochondrial fission required for mitophagy.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Autofagia / Mitofagia Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Autofagia / Mitofagia Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article