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Simulation Analysis of the Homologous Recombination Repair Distribution over the Cell Cycle

机译:细胞周期同源重组修复分布的仿真分析

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Double-strand breaks (DSBs) are repaired with the use of several distinct mechanisms. The most important of them are nonhomologous end joining (NHEJ) and homologous recombination (HR). These mechanisms have different requirements and are characterized by different repair kinetics. Moreover, HR is restricted to S and G2 phases of the cell cycle, however it is still not clear how percentage of DSBs repaired by HR changes over the cell cycle. In this study we are trying to find the most suitable function describing participation of HR among other types of repair. Using our mathematical model, we simulate the response of average cell treated with ionizing radiation (IR) during G1 phase of the cell cycle. Our results show that the exact shape of the function describing percentage of HR is not as important as the fact that this function should be gradually increasing until at least half of the S phase.
机译:使用几种不同的机制修复双链断裂(DSB)。其中最重要的是非源极端接合(NHEJ)和同源重组(HR)。这些机制具有不同的要求,其特征在于不同的修复动力学。此外,HR仅限于细胞周期的S和G2阶段,但仍然尚不清楚通过HR修复的DSB百分比在细胞周期上变化。在这项研究中,我们正试图找到描述人力资源参与的最合适的功能。使用我们的数学模型,我们在细胞周期的G1相期间模拟电离辐射(IR)处理的平均细胞的响应。我们的研究结果表明,描述HR百分比的功能的确切形状与此功能应逐渐增加,直到至少一半的S相。

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