Unitat de Biologia Cel.lular, Departament de Biologia Cel.lular, Fisiologia i Immunologia, Universitat Autònoma de Barcelona, Bellaterra, Spain.
Mutat Res. 2009 Nov 2;670(1-2):53-8. doi: 10.1016/j.mrfmmm.2009.07.003. Epub 2009 Jul 16.
Cell cycle checkpoints are part of the cellular mechanisms to maintain genomic integrity. After ionizing radiation exposure, the cells can show delay or arrest in their progression through the cell cycle, as well as an activation of the DNA repair machinery in order to reduce the damage. The G2/M checkpoint prevents G2 cells entering mitosis until the DNA damage has been reduced. The present study evaluates which G0 radiation-induced chromosome aberrations are negatively selected in the G2/M checkpoint. For this purpose, peripheral blood samples were irradiated at 1 and 3 Gy of gamma-rays, and lymphocytes were cultured for 48 h. Calyculin-A and Colcemid were used to analyze, in the same slide, cells in G2 and M. Chromosome spreads were consecutively analyzed by solid stain, pancentromeric and pantelomeric FISH and mFISH. The results show that the frequency of incomplete chromosome elements, those lacking a telomeric signal at one end, decreases abruptly from G2 to M. This indicates that cells with incomplete chromosome elements can progress from G0 to G2, but at the G2/M checkpoint suffer a strong negative selection.
细胞周期检查点是维持基因组完整性的细胞机制的一部分。在电离辐射暴露后,细胞可以在细胞周期中表现出延迟或停滞,以及 DNA 修复机制的激活,以减少损伤。G2/M 检查点阻止 G2 细胞进入有丝分裂,直到 DNA 损伤得到修复。本研究评估了 G0 辐射诱导的染色体畸变在 G2/M 检查点中是如何被负选择的。为此,外周血样本在 1 和 3 Gy γ射线下照射,并培养淋巴细胞 48 小时。使用 Calyculin-A 和 Colcemid 在同一张载玻片上分析 G2 和 M 期的细胞。染色体铺片通过固染、全着丝粒和全端粒 FISH 和 mFISH 连续分析。结果表明,从 G2 到 M,缺失一个端粒信号的不完全染色体元件的频率急剧下降。这表明,具有不完全染色体元件的细胞可以从 G0 进入 G2,但在 G2/M 检查点会受到强烈的负选择。