Dynamin-like 120 kDa protein, mitochondrial
Definition:
References:
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[1]. Naotada Ishihara, et al. Regulation of mitochondrial morphology through proteolytic cleavage of OPA1. EMBO J. 2006 Jul 12;25(13):2966-77. [Content Brief]
[2]. Guorui Huang, et al. WBSCR16 Is a Guanine Nucleotide Exchange Factor Important for Mitochondrial Fusion. Cell Rep. 2017 Jul 25;20(4):923-934. [Content Brief]
[3]. Ghizlane Elachouri, et al. OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution. Genome Res. 2011 Jan;21(1):12-20. [Content Brief]
[4]. Brian Head, et al. Inducible proteolytic inactivation of OPA1 mediated by the OMA1 protease in mammalian cells. J Cell Biol. 2009 Dec 28;187(7):959-66. [Content Brief]
[5]. Ruchika Anand, et al. The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission. J Cell Biol. 2014 Mar 17;204(6):919-29. [Content Brief]
[6]. Patrizia Amati-Bonneau, et al. OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Brain. 2008 Feb;131(Pt 2):338-51. [Content Brief]
[7]. Zhiyin Song, et al. OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L. J Cell Biol. 2007 Aug 27;178(5):749-55. [Content Brief]
[8]. Tadato Ban, et al. OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation. Hum Mol Genet. 2010 Jun 1;19(11):2113-22. [Content Brief]