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首页> 外文期刊>Mutagenesis >A comparison of G2 phase radiation-induced chromatid break kinetics using calyculin-PCC with those obtained using colcemid block
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A comparison of G2 phase radiation-induced chromatid break kinetics using calyculin-PCC with those obtained using colcemid block

机译:比较使用calyculin-PCC的G2相辐射诱导的染色单体断裂动力学与使用秋水仙胶嵌段获得的动力学的比较

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摘要

To study the possible influence of cell-cycle delay on cells reaching mitosis during conventional radiation-induced chromatid break experiments using colcemid as a blocking agent, we have compared the chromatid break kinetics following a single dose of gamma rays (0.75 Gy) in metaphase CHO cells using calyculin-induced premature chromosome condensation (PCC), with those using colcemid block. Calyculin-induced PCC causes very rapid condensation of G2 cell chromosomes without the need for a cell to progress to mitosis, hence eliminating any effect of cell-cycle checkpoint on chromatid break frequency. We found that the kinetics of the exponential first-order decrease in chromatid breaks with time after irradiation was similar (not significantly different) between the two methods of chromosome condensation. However, use of the calyculin-PCC technique resulted in a slightly increased rate of disappearance of chromatid breaks and thus higher frequencies of breaks at 1.5 and 2.5 h following irradiation. We also report on the effect of the nucleoside analogue ara A on chromatid break kinetics using the two chromosome condensation techniques. Ara A treatment of cells abrogated the decrease in chromatid breaks with time, both using the calyculin-PCC and colcemid methods. We conclude that cell-cycle delay may be a factor determining the absolute frequency of chromatid breaks at various times following irradiation of cells in G2 phase but that the first-order disappearance of chromatid breaks with time and its abrogation by ara A are not significantly influenced by the G2 checkpoint.
机译:若要研究细胞周期延迟对使用秋水仙碱作为阻断剂的常规辐射诱导的染色单体破坏实验中细胞到达有丝分裂的可能影响,我们比较了在中期CHO中单剂量γ射线(0.75 Gy)后的染色单体破坏动力学细胞使用calyculin诱导的早熟染色体浓缩(PCC),而使用colcemid阻断剂的细胞。 Calyculin诱导的PCC导致G2细胞染色体非常快速的凝聚,而无需细胞发展为有丝分裂,因此消除了细胞周期检查点对染色单体断裂频率的任何影响。我们发现,两种染色体浓缩方法在辐照后,染色单体断裂随时间呈指数级下降的动力学相似(​​无显着差异)。但是,使用calyculin-PCC技术会导致染色单体断裂的消失率略有增加,因此照射后1.5和2.5 h断裂的频率更高。我们还报告了使用两种染色体缩合技术的核苷类似物ara A对染色单体断裂动力学的影响。 Ara通过使用calyculin-PCC和colcemid方法对细胞的处理消除了染色单体断裂随时间的减少。我们得出结论,细胞周期延迟可能是决定细胞在G2期照射后各个时间染色单体断裂的绝对频率的一个因素,但是染色单体断裂的一阶消失随时间的变化以及其ara A的废除不会受到显着影响由G2检查站执行。

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  • 来源
    《Mutagenesis》 |2007年第5期|359-362|共4页
  • 作者单位

    Bute Medical School University of St Andrews St Andrews KY16 9TS UK;

    Department of Medical Genetics School of Medical Sciences Tarbiat Modares University PO Box:14115-111 Tehran Islamic Republic of Iran;

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  • 正文语种 eng
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