The dynamin-related GTPase, Mgm1p, is an intermembrane space protein required for maintenance of fusion competent mitochondria. Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells. Head, B., Griparic, L., Amiri, M., Gandre-Babbe, S. OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L. Song, Z., Chen, H., Fiket, M., Alexander, C. Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1. Regulation of mitochondrial morphology through proteolytic cleavage of OPA1. Regulation of the mitochondrial dynamin-like protein Opa1 by proteolytic cleavage. Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling. The molecular mechanisms of OPA1-mediated optic atrophy in Drosophila model and prospects for antioxidant treatment.
OPA1 requires mitofusin 1 to promote mitochondrial fusion. Mitochondrial membrane remodelling regulated by a conserved rhomboid protease. Processing of Mgm1 by the rhomboid-type protease Pcp1 is required for maintenance of mitochondrial morphology and of mitochondrial DNA.
Herlan, M., Vogel, F., Bornhövd, C., Neupert, W. Mitochondrial inner-membrane fusion and crista maintenance requires the dynamin-related GTPase Mgm1. Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo. Connection of the mitochondrial outer and inner membranes by Fzo1 is critical for organellar fusion. Control of mitochondrial morphology by a human mitofusin.
MITOCHONDRIAL FISSION FREE
elegans Opa1 homologue EAT-3 is essential for resistance to free radicals. Mitochondrial fusion in yeast requires the transmembrane GTPase Fzo1p. Fzo1p is a mitochondrial outer membrane protein essential for the biogenesis of functional mitochondria in Saccharomyces cerevisiae. Reports the identification of the first known mediator of mitochondrial fusion and, at the same time, describes the role of fusion in remodelling of mitochondria during spermatogenesis. Developmentally regulated mitochondrial fusion mediated by a conserved, novel, predicted GTPase. Mechanisms of membrane fusion: disparate players and common principles. Mitochondrial morphology and dynamics in yeast and multicellular eukaryotes. The machines that divide and fuse mitochondria. Functions and dysfunctions of mitochondrial dynamics. Mitochondria are morphologically and functionally heterogeneous within cells. Mitochondrial filaments and clusters as intracellular power-transmitting cables. Behavior of mitochondria in the living cell. An electron microscope study of the mitochondrial structure. Furthermore, mitochondrial division is an important step in apoptosis.ĭysfunctions of mitochondrial dynamics contribute to several inherited and age-associated neurodegenerative diseases. Mitochondrial dynamics counteracts cellular ageing by allowing complementation of gene products after fusion of impaired mitochondria, and it constitutes an important part of organellar quality control as it facilitates the elimination of damaged mitochondria by autophagy. Mitochondrial fusion and fission are required for faithful inheritance and proper intracellular distribution of the organelle. The machineries of mitochondrial fusion and fission are regulated by many cellular pathways, including proteolytic processing, ubiquitylation, sumoylation, phosphorylation and dephosphorylation. Only little is known about division of the inner membrane. Mitochondrial fission is mediated by dynamin-related proteins (DRPs) and cofactors that are required for assembly of DRP rings and spirals on the mitochondrial surface. Two evolutionarily conserved large GTPases constitute the core machinery of fusion: mitofusins are found in the outer membrane, and Mgm1 and optic atrophy protein 1 (OPA1) are found in the inner membrane of yeast and mammals, respectively. Live cell imaging studies showed that mitochondria are highly dynamic organelles that frequently fuse and divide.