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Bifurcation analysis of the regulatory modules of the mammalian G1/S transition.

机译:哺乳动物G1 / S过渡调控模块的分叉分析。

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MOTIVATION: Mathematical models of the cell cycle can contribute to an understanding of its basic mechanisms. Modern simulation tools make the analysis of key components and their interactions very effective. This paper focuses on the role of small modules and feedbacks in the gene-protein network governing the G(1)/S transition in mammalian cells. Mutations in this network may lead to uncontrolled cell proliferation. Bifurcation analysis helps to identify the key components of this extremely complex interaction network. RESULTS: We identify various positive and negative feedback loops in the network controlling the G(1)/S transition. It is shown that the positive feedback regulation of E2F1 and a double activator-inhibitor module can lead to bistability. Extensions of the core module preserve the essential features such as bistability. The complete model exhibits a transcritical bifurcation in addition to bistability. We relate these bifurcations to the cell cycle checkpoint and the G(1)/S phase transition point. Thus, core modules can explain major features of the complex G(1)/S network and have a robust decision taking function.
机译:动机:细胞周期的数学模型有助于理解其基本机制。现代仿真工具使对关键组件及其相互作用的分析非常有效。本文重点关注小模块和反馈在控制哺乳动物细胞中G(1)/ S转变的基因-蛋白质网络中的作用。该网络中的突变可能导致不受控制的细胞增殖。分叉分析有助于确定这个极其复杂的交互网络的关键组件。结果:我们确定网络中控制G(1)/ S过渡的各种正反馈回路和负反馈回路。结果表明,E2F1和双激活剂-抑制剂模块的正反馈调节可导致双稳态。核心模块的扩展保留了基本特性,例如双稳性。完整的模型除了具有双稳态性以外,还具有跨临界分叉的特征。我们将这些分叉关系到细胞周期检查点和G(1)/ S相变点。因此,核心模块可以解释复杂的G(1)/ S网络的主要特征,并具有强大的决策功能。

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