Cell Cycle · 2011 · 42 citations · 33 references
Life SciencesCell BiologyCytogeneticsDna RepairRadiobiologyDna Double-strand Break RepairDouble-strand Break RepairG2 PhaseHomologous RecombinationMitosisNon-homologous End JoiningDna Repair During G2Dna Repair MechanismsDouble-strand Break Repair PathwaysHomologous Recombination RepairRadiation-induced Chromosomal AberrationsRepair Of Ionizing Radiation-induced BreaksSister Chromatid RepairStructural Chromosomal Aberrations
DNA double-strand breaks (DSBs) are arguably the most important lesions induced by ionizing radiation (IR) since unrepaired or mis-repaired DSBs can lead to chromosomal aberrations and cell death. The two major pathways to repair IR-induced DSBs are non-homologous end-joining (NHEJ) and homologous recombination (HR). Perhaps surprisingly, NHEJ represents the predominant pathway in the G1 and G2 phases of the cell cycle, but HR also contributes and repairs a subset of IR-induced DSBs in G2. Following S-phase-dependent genotoxins, HR events give rise to sister chromatid exchanges (SCEs), which can be detected cytogenetically in mitosis. Here, we describe that HR occurring in G2-irradiated cells also generates SCEs in ~50% of HR events. Since HR of IR-induced DSBs in G2 is a slow process, SCE formation in G2-irradiated cells requires several hours. During this time, irradiated S-phase cells can also reach mitosis, which has contributed to the widely held belief that SCEs form only during S phase. We describe procedures to measure SCEs exclusively in G2-irradiated cells and provide evidence that following IR cells do not need to progress through S phase in order to form SCEs.
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