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An intragenic suppressor in the cytochrome c oxidase I gene of mouse mitochondrial DNA

  • Rebeca Acín-Pérez
  • , María Pilar Bayona-Bafaluy
  • , Marta Bueno
  • , Claudia Machicado
  • , Patricio Fernández-Silva
  • , Acisclo Pérez-Martos
  • , Julio Montoya
  • , M. J. López-Pérez
  • , Javier Sancho
  • , José Antonio Enríquez
  • University of Zaragoza
  • University of Miami Leonard M. Miller School of Medicine

Research output: Contribution to journalReview articlepeer-review

74 Scopus citations

Abstract

We report here the identification of a cell line containing single and double missense mutations in cytochrome c oxidase (COX) subunit I gene of mouse mitochondrial DNA. When present in homoplasmy, the single mutant displays a normal complex IV assembly but a significantly reduced COX activity, while the double mutant almost completely compensates the functional defect of the first mutation. We discuss the potential structural consequences of those mutations based on the modeled structure of mouse complex IV. Based on genetic, biochemical and molecular analyses of cultured mouse cells we infer that: (i) deleterious mutations can arise and become predominant; (ii) cultured cells can maintain several mtDNA haplotypes at stable frequencies; (iii) the respiratory chain has little spare COX capacity; and (iv) the size of a cavity in the vicinity of Va1421 in CO I of animal COX may affect the function of the enzyme.

Original languageEnglish
Pages (from-to)329-339
Number of pages11
JournalHuman Molecular Genetics
Volume12
Issue number3
DOIs
StatePublished - 1 Feb 2003
Externally publishedYes

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