Discovery of a novel function for human Rad51: maintenance of the mitochondrial genome
Student AuthorsJay M. Sage
UMass Chan AffiliationsDepartment of Biochemistry & Molecular Pharmacology
Document TypeJournal Article
KeywordsCell Cycle; Cell Line, Tumor; Cytoplasm; DNA Breaks, Double-Stranded; DNA Damage; DNA, Mitochondrial; DNA-Binding Proteins; Genome; Humans; Mitochondria; Oxidative Stress; Rad51 Recombinase; Subcellular Fractions
Biochemistry, Biophysics, and Structural Biology
Medicine and Health Sciences
MetadataShow full item record
AbstractHomologous recombination (HR) plays a critical role in facilitating replication fork progression when the polymerase complex encounters a blocking DNA lesion, and it also serves as the primary mechanism for error-free repair of DNA double strand breaks. Rad51 is the central catalyst of HR in all eukaryotes, and to this point studies of human Rad51 have focused exclusively on events occurring within the nucleus. However, substantial amounts of HR proteins exist in the cytoplasm, yet the function of these protein pools has not been addressed. Here, we provide the first demonstration that Rad51 and the related HR proteins Rad51C and Xrcc3 exist in human mitochondria. We show stress-induced increases in both the mitochondrial levels of each protein and, importantly, the physical interaction between Rad51 and mitochondrial DNA (mtDNA). Depletion of Rad51, Rad51C, or Xrcc3 results in a dramatic decrease in mtDNA copy number as well as the complete suppression of a characteristic oxidative stress-induced copy number increase. Our results identify human mtDNA as a novel Rad51 substrate and reveal an important role for HR proteins in the maintenance of the human mitochondrial genome.
Sage, J.M., Gildemeister, O.S. and Knight, K.L. (2010) Discovery of a Novel Function for Human Rad51: Maintenance of the Mitochondrial Genome. J. Biol. Chem. 285, 18984-18990.
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/33122