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PMID: 16473322 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Mitochondrial DNA maintenance and bioenergetics.

Biochimica et biophysica acta ·Vol. 1757 ·No. 2 ·2006-02-00 ·Pages 79-89

Stuart JA, Brown MF

Abstract

Oxidative phosphorylation requires assembly of the protein products of both mitochondrial and of nuclear genomes into functional respiratory complexes. Cellular respiration can be compromised when mitochondrial DNA (mtDNA) sequences are corrupted. Oxidative damage resulting from reactive oxygen species (ROS) produced during respiration is probably a major source of mitochondrial genomic instability leading to respiratory dysfunction. Here, we review mechanisms of mitochondrial ROS production, mtDNA damage and its relationship to mitochondrial dysfunction. We focus particular attention on the roles of mtDNA repair enzymes and processes by which the integrity of the mitochondrial genome is maintained and dysfunction prevented.

MeSH Terms
Animals DNA Damage/physiology DNA Repair/physiology DNA, Mitochondrial/genetics Energy Metabolism/physiology Humans Mitochondria/drug effects,genetics,metabolism Reactive Oxygen Species/metabolism,pharmacology
Chemicals
DNA, Mitochondrial Reactive Oxygen Species
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Stuart Jeffrey A
Department of Biological Sciences, Brock University, St. Catharines, Ontario, Canada L2S 3A1. jstuart@brocku.ca
Brown Melanie F
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
2006-02-00
Epub
2006-00-24
Pages
79-89
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
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