染色体结构不稳定性的数值模拟

Y. Eidelman, S. Slanina, V. Pyatenko, S. Andreev
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引用次数: 0

摘要

利用机制CI模型研究了辐射诱导的染色体不稳定性(CI)的剂量-反应曲线的起源。该模型考虑了辐照细胞后代DNA损伤的产生和修复以及细胞在有丝分裂周期中的传代。我们考虑在S期重新形成DNA双链断裂(DSBs),其中主要形成染色单体型畸变。其中,姐妹染色单体交换的“等染色单体缺失”类型,或“染色单体双中心”是主要的兴趣。当细胞进入有丝分裂时,染色体畸变的命运取决于它们的类型。进入有丝分裂的染色体和染色单体碎片,要么传递到其中一个子细胞中,要么丢失。染色单体在有丝分裂中形成一个后期桥。这些机制假设被用来证明剂量-响应曲线与CI的动态曲线密切相关。分析了这种关系背后的原理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Numerical Simulations of Structural Chromosomal Instability
The origin of dose-response curves for radiation-induced chromosomal instability (CI) is studied using the mechanistic CI model. The model takes into account DNA damage generation and repair in the progeny of irradiated cells and cell passage through mitotic cycle. We consider the formation of DNA double-strand breaks (DSBs) de novo in the S phase, where predominantly chromatid-type aberrations are formed. Among them sister chromatid exchanges of the “isochromatid deletion” type, or “chromatid dicentrics” are of primary interest. When the cell enters mitosis, the fate of chromosomal aberrations depends on their types. Chromosomal and chromatid fragments, having entered mitosis, either are transmitted into one of the daughter cells, or are lost. A chromatid dicentric in mitosis forms an anaphase bridge. These mechanistic assumptions were used to demonstrate that the dose-response curves are closely related to the dynamic curves for CI. The principles underlying this relationship are analyzed.
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