Literature DB >> 17215873

Defects in cytochrome oxidase assembly in humans: lessons from yeast.

Jennifer M Zee1, D Moira Glerum.   

Abstract

The biogenesis of the inner mitochondrial membrane enzyme cytochrome c oxidase (COX) is a complex process that requires the actions of ancillary proteins, collectively called assembly factors. Studies with the yeast Saccharomyces cerevisiae have provided considerable insight into the COX assembly pathway and have proven to be a fruitful model for understanding the molecular bases for inherited COX deficiencies in humans. In this review, we focus on critical steps in the COX assembly pathway. These processes are conserved from yeast to humans and are known to be involved in the etiology of human COX deficiencies. The contributions from our studies in yeast suggest that this organism remains an excellent model system for delineating the molecular mechanisms underlying COX assembly defects in humans. Current progress suggests that a complete picture of COX assembly will be achieved in the near future.

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Year:  2006        PMID: 17215873     DOI: 10.1139/o06-201

Source DB:  PubMed          Journal:  Biochem Cell Biol        ISSN: 0829-8211            Impact factor:   3.626


  21 in total

1.  A novel heme a insertion factor gene cotranscribes with the Thermus thermophilus cytochrome ba3 oxidase locus.

Authors:  Carolin Werner; Oliver-Matthias H Richter; Bernd Ludwig
Journal:  J Bacteriol       Date:  2010-07-09       Impact factor: 3.490

Review 2.  Metals in the "omics" world: copper homeostasis and cytochrome c oxidase assembly in a new light.

Authors:  Ivano Bertini; Gabriele Cavallaro
Journal:  J Biol Inorg Chem       Date:  2007-11-07       Impact factor: 3.358

Review 3.  Eukaryotic complex I: functional diversity and experimental systems to unravel the assembly process.

Authors:  Claire Remacle; M Rosario Barbieri; Pierre Cardol; Patrice P Hamel
Journal:  Mol Genet Genomics       Date:  2008-06-18       Impact factor: 3.291

4.  Coupled transport of electrons and protons in a bacterial cytochrome c oxidase-DFT calculated properties compared to structures and spectroscopies.

Authors:  Louis Noodleman; Wen-Ge Han Du; Duncan McRee; Ying Chen; Teffanie Goh; Andreas W Götz
Journal:  Phys Chem Chem Phys       Date:  2020-12-07       Impact factor: 3.676

5.  Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia-cystinuria syndrome.

Authors:  B Chabrol; K Martens; S Meulemans; A Cano; J Jaeken; G Matthijs; J W M Creemers
Journal:  BMJ Case Rep       Date:  2009-02-02

Review 6.  Structure, function, and assembly of heme centers in mitochondrial respiratory complexes.

Authors:  Hyung J Kim; Oleh Khalimonchuk; Pamela M Smith; Dennis R Winge
Journal:  Biochim Biophys Acta       Date:  2012-04-24

7.  Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2.

Authors:  Hua Yang; Sonja Brosel; Rebeca Acin-Perez; Vesna Slavkovich; Ichizo Nishino; Raffay Khan; Ira J Goldberg; Joseph Graziano; Giovanni Manfredi; Eric A Schon
Journal:  Hum Mol Genet       Date:  2010-01-01       Impact factor: 6.150

8.  Surf1, associated with Leigh syndrome in humans, is a heme-binding protein in bacterial oxidase biogenesis.

Authors:  Freya A Bundschuh; Achim Hannappel; Oliver Anderka; Bernd Ludwig
Journal:  J Biol Chem       Date:  2009-07-22       Impact factor: 5.157

9.  Trypanosoma brucei: differential requirement of membrane potential for import of proteins into mitochondria in two developmental stages.

Authors:  Shuntae Williams; Lipi Saha; Ujjal K Singha; Minu Chaudhuri
Journal:  Exp Parasitol       Date:  2007-10-15       Impact factor: 2.011

10.  Exocrine pancreatic insufficiency, dyserythropoeitic anemia, and calvarial hyperostosis are caused by a mutation in the COX4I2 gene.

Authors:  Eyal Shteyer; Ann Saada; Avraham Shaag; Fida' Aziz Al-Hijawi; Rojette Kidess; Shoshanah Revel-Vilk; Orly Elpeleg
Journal:  Am J Hum Genet       Date:  2009-03-05       Impact factor: 11.025

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