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Bifurcation analysis of a modular model of embryonic kidney development

机译:胚胎肾发育模块化模型的分岔分析

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Many biological processes show switching behaviors in response to parameter changes. Although numerous surveys have been conducted on bifurcations in biological systems, they commonly focus on over-represented parts of signaling cascades, known as motifs, ignoring the multi-motif structure of biological systems and the communication links between these building blocks. In this paper, a method is proposed which partitions molecular interactions to modules based on a control theory point of view. The modules are defined so that downstream effect of one module is a regulator for its neighboring modules. Communication links between these modules are then considered as bifurcation parameters to reveal change in steady state status of each module. As a case-study, we generated a molecular interaction map of signaling molecules during the development of mammalian embryonic kidneys. The whole system was divided to modules, where each module is defined as a group of interacting molecules that result in expression of a vital downstream regulator. Bifurcation analysis was then performed on these modules by considering the communication signals as bifurcation parameters. Two-parameter bifurcation analysis was then performed to assess the effects of simultaneous input signals on each module behavior. In the case where a module had more than two inputs, a series of two parameter bifurcation diagrams were calculated each corresponding to different values of the third parameter. We detected multi-stability for RET protein as a key regulator for fate determination. This finding is in agreement with experimental data indicating that ureteric bud cells are bi-potential, able to form tip or trunk of the bud based on their RET activity level. Our findings also indicate that Glial cell-derived neurotrophic factor (GDNF), a known potent regulator of kidney development, exerts its fate-determination function on cell placement through destruction of saddle node bifurcation points in RET steady states and confining RET activity level to high activity in ureteric bud tip. In conclusion, embryonic cells usually show a huge decision making potential; the proposed modular modeling of the system in association with bifurcation analysis provides a quantitative holistic view of organ development.
机译:许多生物过程显示响应参数变化的切换行为。尽管在生物系统中的分叉上进行了许多调查,但它们通常关注信号传导级联的过度代表部分,称为图案,忽略了生物系统的多主题结构和这些构建块之间的通信连接。在本文中,提出了一种方法,该方法将基于控制理论的视图分配对模块的分子相互作用。定义模块,使得一个模块的下游效果是其相邻模块的调节器。然后将这些模块之间的通信链路被认为是分叉参数,以揭示每个模块的稳态状态的变化。作为一个案例研究,我们在哺乳动物胚胎肾的发育过程中产生了信号分子的分子相互作用图。整个系统被分成模块,其中每个模块被定义为一组相互作用分子,导致重要下游调节器的表达。然后通过将通信信号视为分叉参数来对这些模块进行分叉分析。然后执行双参数分叉分析以评估同时输入信号对每个模块行为的影响。在模块具有多于两个输入的情况下,计算了一系列两个参数分叉图,每个参数分叉图对应于第三参数的不同值计算。我们检测到RET蛋白的多稳定性作为用于命运测定的关键调节器。该发现与实验数据一致,表明输尿管芽细胞是双电位,能够基于其RET活动水平形成芽的尖端或躯干。我们的研究结果还表明,通过破坏RET稳定状态的马鞍节点分岔点并将RET活动水平置于RET活动水平将RET活动水平置于RET稳定状态下的鞍座节点分叉点和将RET活动水平限制为高度并将RET活动水平置于High的鞍座节点分叉点并将其造成摇头节点分叉点并将RET活动水平销毁施加其命运测定功能。输尿管芽尖的活性。总之,胚胎细胞通常显示出巨大的决策潜力;与分叉分析相关联的系统的模块化建模提供了器官发展的定量整体视图。

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