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Predicting genetic interactions from Boolean models of biological networks

机译:从生物网络的布尔模型预测遗传相互作用

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Genetic interaction can be defined as a deviation of the phenotypic quantitative effect of a double gene mutation from the effect predicted from single mutations using a simple (e.g., multiplicative or linear additive) statistical model. Experimentally characterized genetic interaction networks in model organisms provide important insights into relationships between different biological functions. We describe a computational methodology allowing us to systematically and quantitatively characterize a Boolean mathematical model of a biological network in terms of genetic interactions between all loss of function and gain of function mutations with respect to all model phenotypes or outputs. We use the probabilistic framework defined in MaBoSS software, based on continuous time Markov chains and stochastic simulations. In addition, we suggest several computational tools for studying the distribution of double mutants in the space of model phenotype probabilities. We demonstrate this methodology on three published models for each of which we derive the genetic interaction networks and analyze their properties. We classify the obtained interactions according to their class of epistasis, dependence on the chosen initial conditions and the phenotype. The use of this methodology for validating mathematical models from experimental data and designing new experiments is discussed.
机译:遗传相互作用可以定义为双基因突变的表型定量效应与使用简单(例如,乘法或线性加性)统计模型从单突变预测的效应的偏差。模型生物中实验表征的遗传相互作用网络为了解不同生物学功能之间的关系提供了重要见识。我们描述了一种计算方法,使我们能够相对于所有模型表型或输出,根据所有功能丧失和功能突变获得之间的遗传相互作用,系统地和定量地描述生物网络的布尔数学模型。我们使用基于连续时间马尔可夫链和随机模拟的MaBoSS软件中定义的概率框架。此外,我们建议了几种计算工具,用于研究模型表型概率空间中双突变体的分布。我们在三个已发表的模型上论证了这种方法论,对于每个模型我们都可以得出遗传相互作用网络并分析其特性。我们根据获得的相互作用的上位性分类,对所选择的初始条件和表型的依赖性对它们进行分类。讨论了使用该方法从实验数据验证数学模型并设计新实验的方法。

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