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Times Cited: 533
Times Cited: 533
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Regulation of mitochondrial morphology through proteolytic cleavage of OPA1.
Naotada Ishihara, Yuu Fujita, Toshihiko Oka, Katsuyoshi Mihara. EMBO J 2006
Naotada Ishihara, Yuu Fujita, Toshihiko Oka, Katsuyoshi Mihara. EMBO J 2006
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The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission.
Ruchika Anand, Timothy Wai, Michael J Baker, Nikolay Kladt, Astrid C Schauss, Elena Rugarli, Thomas Langer. J Cell Biol 2014
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OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion.
Christian Frezza, Sara Cipolat, Olga Martins de Brito, Massimo Micaroni, Galina V Beznoussenko, Tomasz Rudka, Davide Bartoli, Roman S Polishuck, Nika N Danial, Bart De Strooper,[...]. Cell 2006
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Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1.
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Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development.
Hsiuchen Chen, Scott A Detmer, Andrew J Ewald, Erik E Griffin, Scott E Fraser, David C Chan. J Cell Biol 2003
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Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells.
Brian Head, Lorena Griparic, Mandana Amiri, Shilpa Gandre-Babbe, Alexander M van der Bliek. J Cell Biol 2009
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Regulation of the mitochondrial dynamin-like protein Opa1 by proteolytic cleavage.
Lorena Griparic, Takayuki Kanazawa, Alexander M van der Bliek. J Cell Biol 2007
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Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy.
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OPA1 requires mitofusin 1 to promote mitochondrial fusion.
Sara Cipolat, Olga Martins de Brito, Barbara Dal Zilio, Luca Scorrano. Proc Natl Acad Sci U S A 2004
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Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission.
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ER tubules mark sites of mitochondrial division.
Jonathan R Friedman, Laura L Lackner, Matthew West, Jared R DiBenedetto, Jodi Nunnari, Gia K Voeltz. Science 2011
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Molecular basis of selective mitochondrial fusion by heterotypic action between OPA1 and cardiolipin.
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OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.
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Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells.
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Mitotic phosphorylation of dynamin-related GTPase Drp1 participates in mitochondrial fission.
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Eight human OPA1 isoforms, long and short: What are they for?
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Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency.
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Imbalanced OPA1 processing and mitochondrial fragmentation cause heart failure in mice.
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Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells.
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During autophagy mitochondria elongate, are spared from degradation and sustain cell viability.
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Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis.
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MiD49 and MiD51, new components of the mitochondrial fission machinery.
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OPA1-dependent cristae modulation is essential for cellular adaptation to metabolic demand.
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Proteolytic cleavage of Opa1 stimulates mitochondrial inner membrane fusion and couples fusion to oxidative phosphorylation.
Prashant Mishra, Valerio Carelli, Giovanni Manfredi, David C Chan. Cell Metab 2014
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OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions.
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Mitochondrial dynamics: overview of molecular mechanisms.
Lisa Tilokani, Shun Nagashima, Vincent Paupe, Julien Prudent. Essays Biochem 2018
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An actin-dependent step in mitochondrial fission mediated by the ER-associated formin INF2.
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OPA1 alternate splicing uncouples an evolutionary conserved function in mitochondrial fusion from a vertebrate restricted function in apoptosis.
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Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations.
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PINK1-phosphorylated mitofusin 2 is a Parkin receptor for culling damaged mitochondria.
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Mitofusin 1 and 2 play distinct roles in mitochondrial fusion reactions via GTPase activity.
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Mitochondrial inner-membrane fusion and crista maintenance requires the dynamin-related GTPase Mgm1.
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Multiple dynamin family members collaborate to drive mitochondrial division.
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The short variant of the mitochondrial dynamin OPA1 maintains mitochondrial energetics and cristae structure.
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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
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Mitochondrial outer-membrane protein FUNDC1 mediates hypoxia-induced mitophagy in mammalian cells.
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Tubular network formation protects mitochondria from autophagosomal degradation during nutrient starvation.
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OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation.
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Mito-Morphosis: Mitochondrial Fusion, Fission, and Cristae Remodeling as Key Mediators of Cellular Function.
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