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Transient assembly of F-actin on the outer mitochondrial membrane contributes to mitochondrial fission
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Proteolytic Cleavage of Opa1 Stimulates Mitochondrial Inner Membrane Fusion and Couples Fusion to Oxidative Phosphorylation
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Stress-induced OMA1 activation and autocatalytic turnover regulate OPA1-dependent mitochondrial dynamics
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The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission
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JOURNAL OF CELL BIOLOGY (2014)
Impaired OMA1-dependent cleavage of OPA1 and reduced DRP1 fission activity combine to prevent mitophagy in cells that are dependent on oxidative phosphorylation
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Mitochondrial dynamics and inheritance during cell division, development and disease
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A Mitofusin-2-dependent inactivating cleavage of Opa1 links changes in mitochondria cristae and ER contacts in the postprandial liver
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Activation of mitochondrial protease OMA1 by Bax and Bak promotes cytochrome c release during apoptosis
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OMA1 mediates OPA1 proteolysis and mitochondrial fragmentation in experimental models of ischemic kidney injury
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Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
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Loss of mitochondrial protease OMA1 alters processing of the GTPase OPA1 and causes obesity and defective thermogenesis in mice
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EMBO JOURNAL (2012)
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Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells
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Fission and selective fusion govern mitochondrial segregation and elimination by autophagy
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Prohibitins control cell proliferation and apoptosis by regulating OPA1-dependent cristae morphogenesis in mitochondria
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OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria
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OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L
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JOURNAL OF CELL BIOLOGY (2007)
Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function
Vanessa J. Davies et al.
HUMAN MOLECULAR GENETICS (2007)
A splice site mutation in the murine OpaI gene features pathology of autosomal dominant optic atrophy
Marcel V. Alavi et al.
BRAIN (2007)
OPA1 alternate splicing uncouples an evolutionary conserved function in mitochondrial fusion from a vertebrate restricted function in apoptosis
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CELL DEATH AND DIFFERENTIATION (2007)
Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology
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JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Dynamic subcompartmentalization of the mitochondrial inner membrane
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JOURNAL OF CELL BIOLOGY (2006)
Mitochondrial inner-membrane fusion and crista maintenance requires the dynamin-related GTPase Mgm1
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CELL (2006)
MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
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BRAIN (2006)
Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling
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OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion
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CELL (2006)
Regulation of mitochondrial morphology through proteolytic cleavage of OPA1
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EMBO JOURNAL (2006)
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The mitochondrial protein MTP18 contributes to mitochondrial fission in mammalian cells
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JOURNAL OF CELL SCIENCE (2005)
Endoplasmic reticulum BIK initiates DRP1-regulated remodelling of mitochondrial cristae during apoptosis
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EMBO JOURNAL (2005)
Loss of the intermembrane space protein Mgm1/OPA1 induces swelling and localized constrictions along the lengths of mitochondria
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JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Alternative topogenesis of Mgm1 and mitochondrial morphology depend on ATP and a functional import motor
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JOURNAL OF CELL BIOLOGY (2004)
Mitofusin 1 and 2 play distinct roles in mitochondrial fusion reactions via GTPase activity
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JOURNAL OF CELL SCIENCE (2004)
Knockdown of MTP18, a novel phosphatidylinositol 3-kinase-dependent protein, affects mitochondrial morphology and induces apoptosis
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JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
OPA1 requires mitofusin 1 to promote mitochondrial fusion
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
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NATURE GENETICS (2004)
Oma1, a novel membrane-bound metallopeptidase in mitochondria with activities overlapping with the m-AAA protease
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JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Cells lacking Pcp1p/Ugo2p, a rhomboid-like protease required for Mgm1p processing, lose mtDNA and mitochondrial structure in a Dnm1p-dependent manner, but remain competent for mitochondrial fusion
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BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2003)
Processing of Mgm1 by the rhomboid-type protease Pcp1 is required for maintenance of mitochondrial morphology and of mitochondrial DNA
M Herlan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Mitochondrial membrane remodelling regulated by a conserved rhomboid protease
GA McQuibban et al.
NATURE (2003)
Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis
A Olichon et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
The intramitochondrial dynamin-related GTPase, Mgm1p, is a component of a protein complex that mediates mitochondrial fusion
ED Wong et al.
JOURNAL OF CELL BIOLOGY (2003)
Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development
HC Chen et al.
JOURNAL OF CELL BIOLOGY (2003)
A distinct pathway remodels mitochondrial cristae and mobilizes cytochrome c during apoptosis
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DEVELOPMENTAL CELL (2002)
Mutation spectrum and splicing variants in the OPA1 gene
C Delettre et al.
HUMAN GENETICS (2001)
The dynamin-related GTPase, Mgm1p, is an intermembrane space protein required for maintenance of fusion competent mitochondria
ED Wong et al.
JOURNAL OF CELL BIOLOGY (2000)
Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy
C Delettre et al.
NATURE GENETICS (2000)
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
C Alexander et al.
NATURE GENETICS (2000)
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