Science · 2002 · 336 citations · 17 references
Life SciencesMicrobiologyMolecular BiologyBacteriologyDna RepairMicrobial GeneticsDna Double-strand Break RepairDna LigaseDna Strand BreaksDouble-strand Break RepairHomologous RecombinationNon-homologous End JoiningDna Double-strand BreaksDna End JoiningDna End LigationDna Ligase FunctionDouble-strand Break Repair PathwaysDouble-strand Dna BreaksKu Protein BindingNonhomologous End Joining
In eukaryotic cells, double-strand breaks (DSBs) in DNA are generally repaired by the pathway of homologous recombination or by DNA nonhomologous end joining (NHEJ). Both pathways have been highly conserved throughout eukaryotic evolution, but no equivalent NHEJ system has been identified in prokaryotes. The NHEJ pathway requires a DNA end-binding component called Ku. We have identified bacterial Ku homologs and show that these proteins retain the biochemical characteristics of the eukaryotic Ku heterodimer. Furthermore, we show that bacterial Ku specifically recruits DNA ligase to DNA ends and stimulates DNA ligation. Loss of these proteins leads to hypersensitivity to ionizing radiation in Bacillus subtilis. These data provide evidence that many bacteria possess a DNA DSB repair apparatus that shares many features with the NHEJ system of eukarya and suggest that this DNA repair pathway arose before the prokaryotic and eukaryotic lineages diverged.
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Ku Recruits the XRCC4-Ligase IV Complex to DNA Ends
Stephanie A. Nick McElhinny, Carey M. Snowden, Joseph McCarville et al. · Molecular and Cellular Biology · 2000 · 390 citations · Full text