Cytochrome c oxidase assembly in primates is sensitive to small evolutionary variations in amino acid sequence

Molecular Biology and Evolution

Volumn 17, Issue 10, 2000, Pages 1508-1519

  Barrientos, Antoni ^a,d   Müller, Stefan ^b   Dey, Runu ^a   Wienberg, Johannes ^c   Moraes, Carlos T ^a  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MUNICH   (Germany)

^c NATIONAL CANCER INSTITUTE   (United States)

^d Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

COX; Evolution; Hybrids; Mitochondria; mtDNA

Indexed keywords

AMINO ACID; CYTOCHROME C OXIDASE;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CHIMPANZEE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME SUBUNIT; GENETIC CODE; GENOME; GORILLA; HUMAN; HUMAN CELL; MITOCHONDRIAL MEMBRANE; MOLECULAR EVOLUTION; NONHUMAN; ORANG UTAN; OXIDATIVE PHOSPHORYLATION; PROTEIN ASSEMBLY; STEADY STATE;

ANIMALIA; MAMMALIA; PAN TROGLODYTES; PONGO PYGMAEUS; PRIMATES;

EID: 0033804652     PISSN: 07374038     EISSN: None     Source Type: Journal    
DOI: 10.1093/oxfordjournals.molbev.a026250     Document Type: Article

References (44)

1. Evolution of eutherian cytochrome c oxidase subunit II: Heterogeneous rates of protein evolution and altered interaction with cytochrome c
2. Pattern and timing of evolutionary divergences among hominoids based on analyses of complete mtDNAs
3. Human xenomitochondrial cybrids. Cellular models of mitochondrial complex I deficiency
4. Simultaneous transfer of mitochondrial DNA and single chromosomes in somatic cells: A novel approach for the study of defects in nuclear-mitochondrial communication
5. Titrating the effects of mitochondrial complex I impairment in the cell physiology
6. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
7. Rapid evolution of animal mitochondrial DNA
8. A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV
9. In vivo labeling and analysis of human mitochondrial translation products
10. Mitochondrial DNA of human-mouse cell hybrids
11. Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease
12. Human microsatellites applicable for analysis of genetic variation in apes and Old World monkeys
13. Uniparental propagation of mitochondrial DNA in mouse-human cell hybrids
14. Characterization of mitochondrial DNA in chlorampheni-col-resistant interspecific hybrids and a cybrid
15. Characterization of COX17, a yeast gene involved in copper metabolism and assembly of cytochrome oxidase
16. Submitochondrial distributions and stabilities of subunits 4, 5, and 6 of yeast cytochrome oxidase in assembly defective mutants
17. Affinity purification of yeast cytochrome oxidase with biotinylated subunits 4, 5, or 6
18. A disease-associated G5703A mutation in human mitochondrial DNA causes a conformational change and a marked decrease in steady-state levels of mitochondrial tRNA(Asn)
19. Two distinct types of mitochondrial DNA segregation in mouse-rat hybrid cells. Stochastic segregation and chromosome-dependent segregation
20. Different rates of substitution may produce different phylogenies of the eutherian mammals
21. Divergent proteins and views [letter]
22. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
23. Expanding the functional human mitochondrial DNA database by the establishment of primate xenomitochondrial cybrids
24. Human cells lacking mtDNA: Repopulation with exogenous mitochondria by complementation
25. Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: A comparison of subunit proteins in normal fibroblasts treated with ethidium bromide and fibroblasts from a patient with mtDNA depletion syndrome
26. SHY1, the yeast homolog of the mammalian SURF-1 gene, encodes a mitochondrial protein required for respiration
27. Cross-species colour segmenting: A novel tool in human karyotype analysis
28. Assembly of cytochrome-c oxidase in cultured human cells
29. Assembling a time bomb - Cytochrome c oxidase and disease [news; comment]
30. Crosstalk between nuclear and mitochondrial genomes
31. A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathy
32. Use of fibroblast and lymphoblast cultures for detection of respiratory chain defects
33. Molecular evolution of the COX7A gene family in primates
34. Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB)
35. Transformation of mammalian cells to antibiotic resistance with a bacterial gene under control of the SV40 early region promoter
36. Karyotyping human chromosomes by combinatorial multi-fluor FISH
37. Subunit specific monoclonal antibodies show different steady-state levels of various cytochrome-c oxidase subunits in chronic progressive external ophthalmoplegia
38. Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency
39. The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A
40. Aneuploidy induction in human fibroblasts: Comparison with results in Syrian hamster fibroblasts
41. Molecular analysis of cloned human 18S ribosomal DNA segments
42. Molecular evolution of cytochrome c oxidase subunit IV: Evidence for positive selection in simian primates
43. SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome
44. Elimination of mitochondrial elements and improved viability in hybrid cells