出芽酵母细胞周期调控机制的ODE/SSA杂交模型及突变体案例研究

Mansooreh Ahmadian, Shuo Wang, J. Tyson, Young Cao
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引用次数: 5

摘要

出芽酵母细胞周期受到复杂的多尺度控制机制的调控,并受到细胞内固有噪声的影响,这是由关键mrna等物种的低拷贝数引起的。传统的确定性模型无法捕捉到这种固有的噪音。虽然随机模型可以产生模拟结果,以更好地表示系统动力学中的固有噪声,但对于复杂系统来说,随机方法往往在计算上过于昂贵,复杂系统在两个方面表现出多尺度特征:不同丰度尺度的物种和不同发射频率尺度的反应。为了应对这一挑战,一个有希望的解决方案是采用混合方法。它用两种方法的集成来取代离散随机公式或连续确定性公式的单一数学表示,从而很好地保留了两种方法各自的优势特征,实现了精度和效率之间的权衡。本文采用Gillespie随机模拟算法(SSA)和常微分方程(ode)建立了一个混合随机模型,分别表征出芽酵母细胞周期调控机制的调控网络。我们的模拟结果与已发表的芽殖酵母细胞周期的实验测量结果进行了比较。比较表明,我们的杂交模型很好地代表了出芽酵母细胞周期的许多关键特征,并再现了100多种突变病例的表型。此外,该模型解释了某些突变株的部分生存能力。最后但并非最不重要的是,所提出的方案在建模和仿真上都比等效的随机仿真快得多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hybrid ODE/SSA Model of the Budding Yeast Cell Cycle Control Mechanism with Mutant Case Study
The budding yeast cell cycle is regulated by complex and multi-scale control mechanisms, and is subject to inherent noise in a cell, resulted from low copy numbers of species such as critical mRNAs. Conventional deterministic models cannot capture this inherent noise. Although stochastic models can generate simulation results to better represent inherent noise in system dynamics, the stochastic approach is often computationally too expensive for complex systems, which exhibit multiscale features in two aspects: species with different scales of abundances and reactions with different scales of firing frequencies. To address this challenge, one promising solution is to adopt a hybrid approach. It replaces the single mathematical representation of either discrete-stochastic formulation or continuous deterministic formulation with an integration of both methods, so that the corresponding advantageous features in both methods are well kept to achieve a trade-off between accuracy and efficiency. In this work, we propose a hybrid stochastic model that represents the regulatory network of the budding yeast cell cycle control mechanism, respectively, by Gillespie's stochastic simulation algorithm (SSA) and ordinary differential equations (ODEs). Simulation results of our model were compared with published experimental measurement on the budding yeast cell cycle. The comparison demonstrates that our hybrid model well represents many critical characteristics of the budding yeast cell cycle, and reproduces more than 100 phenotypes of mutant cases. Moreover, the model accounts for partial viability of certain mutant strains. The last but not the least, the proposed scheme is shown to be considerably faster in both modeling and simulation than the equivalent stochastic simulation.
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