Literature DB >> 19513673

Oxidative phosphorylation: synthesis of mitochondrially encoded proteins and assembly of individual structural subunits into functional holoenzyme complexes.

Scot C Leary1, Florin Sasarman.   

Abstract

The bulk of ATP consumed by various cellular processes in higher eukaryotes is normally produced by five multimeric protein complexes (I-V) embedded within the inner mitochondrial membrane, in a process known as oxidative phosphorylation (OXPHOS). Maintenance of energy homeostasis under most physiological conditions is therefore contingent upon the ability of OXPHOS to meet cellular changes in bioenergetic demand, with a chronic failure to do so being a frequent cause of human disease. With the exception of Complex II, the structural subunits of OXPHOS complexes are encoded by both the nuclear and the mitochondrial genomes. The physical separation of the two genomes necessitates that the expression of the 13 mitochondrially encoded polypeptides be co-ordinated with that of relevant nuclear-encoded partners in order to assemble functional holoenzyme complexes. Complex biogenesis is a highly ordered process, and several nuclear-encoded factors that function at distinct stages in the assembly of individual OXPHOS complexes have been identified.

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Year:  2009        PMID: 19513673     DOI: 10.1007/978-1-59745-521-3_10

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  30 in total

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Journal:  EMBO Rep       Date:  2017-01-12       Impact factor: 8.807

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4.  The Human Mitochondrial DEAD-Box Protein DDX28 Resides in RNA Granules and Functions in Mitoribosome Assembly.

Authors:  Ya-Ting Tu; Antoni Barrientos
Journal:  Cell Rep       Date:  2015-02-13       Impact factor: 9.423

5.  Mutation in subdomain G' of mitochondrial elongation factor G1 is associated with combined OXPHOS deficiency in fibroblasts but not in muscle.

Authors:  Paulien Smits; Hana Antonicka; Peter M van Hasselt; Woranontee Weraarpachai; Wolfram Haller; Marieke Schreurs; Hanka Venselaar; Richard J Rodenburg; Jan A Smeitink; Lambert P van den Heuvel
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6.  Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation-causing lactic acidosis, intellectual disability, and poor growth.

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7.  An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase.

Authors:  Reetta Hinttala; Florin Sasarman; Tamiko Nishimura; Hana Antonicka; Catherine Brunel-Guitton; Jeremy Schwartzentruber; Somayyeh Fahiminiya; Jacek Majewski; Denis Faubert; Elsebet Ostergaard; Jan A Smeitink; Eric A Shoubridge
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Authors:  Florin Sasarman; Catherine Brunel-Guitton; Hana Antonicka; Timothy Wai; Eric A Shoubridge
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Authors:  Laura Kytövuori; Joonas Lipponen; Harri Rusanen; Tuomas Komulainen; Mika H Martikainen; Kari Majamaa
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10.  Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh Syndrome.

Authors:  Florin Sasarman; Tamiko Nishimura; Hana Antonicka; Woranontee Weraarpachai; Eric A Shoubridge
Journal:  Hum Mol Genet       Date:  2014-09-11       Impact factor: 6.150

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