首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Cells bearing chromosome aberrations lacking one telomere are selectively blocked at the G2/M checkpoint.
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Cells bearing chromosome aberrations lacking one telomere are selectively blocked at the G2/M checkpoint.

机译:缺少一个端粒的带有染色体畸变的细胞在G2 / M检查点被选择性封闭。

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摘要

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.
机译: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。电离辐射暴露后,细胞在整个细胞周期的进程中可能会显示延迟或停滞,并激活DNA修复机制以减少损伤。 G2 / M检查点可防止G2细胞进入有丝分裂状态,直到DNA损伤减少为止。本研究评估了在G2 / M检查点中否定选择了哪些G0辐射诱导的染色体畸变。为此,以1和3 Gy的γ射线照射外周血样品,并将淋巴细胞培养48小时。在同一玻片中,使用Calyculin-A和Colcemid分析G2和M中的细胞。通过固相染色,全着丝粒和泛着丝粒FISH和mFISH连续分析了染色体的铺展。结果表明,不完整染色体元件的频率(在一端缺少端粒信号的频率)从G2突然下降到M。这表明具有不完整染色体元件的细胞可以从G0进化到G2,但在G2 / M检查点受累强烈的负面选择。

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