Current Topics in DNA Double-Strand Break Repair

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  • KOBAYASHI Junya
    Department of Genome Repair Dynamics, Radiation Biology Center, Kyoto University
  • IWABUCHI Kuniyoshi
    Department of Biochemistry, Kanazawa Medical University
  • MIYAGAWA Kiyoshi
    Section of Radiation Biology, Graduate School of Medicine, The University of Tokyo
  • SONODA Eiichiro
    Department of Radiation Genetics, Faculty of Medicine, Kyoto University
  • SUZUKI Keiji
    Graduate school of Biomedical Sciences, Nagasaki University
  • TAKATA Minoru
    Department of Late Effects Studies, Radiation Biology Center, Kyoto University
  • TAUCHI Hiroshi
    Department of Environmental Sciences, Faculty of Science, Ibaraki University

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DNA double strand break (DSB) is one of the most critical types of damage which is induced by ionizing radiation. In this review, we summarize current progress in investigations on the function of DSB repair-related proteins. We focused on recent findings in the analysis of the function of proteins such as 53BP1, histone H2AX, Mus81-Eme1, Fanc complex, and UBC13, which are found to be related to homologous recombination repair or to non-homologous end joining. In addition to the function of these proteins in DSB repair, the biological function of nuclear foci formation following DSB induction is discussed.

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