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Role of metabolic spatiotemporal dynamics in regulating biofilm colony expansion.代谢时空动力学在调控生物膜菌落扩张中的作用。
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预测新适应性表型突变途径的概率模型。

Probabilistic Models for Predicting Mutational Routes to New Adaptive Phenotypes.

作者信息

Libby Eric, Lind Peter A

机构信息

Icelab, Umeå University, Umeå, Sweden.

Department of Mathematics and Mathematical Statistics, Umeå University, Umeå, Sweden.

出版信息

Bio Protoc. 2019 Oct 20;9(20):e3407. doi: 10.21769/BioProtoc.3407.

DOI:10.21769/BioProtoc.3407
PMID:33654908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7854003/
Abstract

Understanding the translation of genetic variation to phenotypic variation is a fundamental problem in genetics and evolutionary biology. The introduction of new genetic variation through mutation can lead to new adaptive phenotypes, but the complexity of the genotype-to-phenotype map makes it challenging to predict the phenotypic effects of mutation. Metabolic models, in conjunction with flux balance analysis, have been used to predict evolutionary optimality. These methods however rely on large scale models of metabolism, describe a limited set of phenotypes, and assume that selection for growth rate is the prime evolutionary driver. Here we describe a method for computing the relative likelihood that mutational change will translate into a phenotypic change between two molecular pathways. The interactions of molecular components in the pathways are modeled with ordinary differential equations. Unknown parameters are offset by probability distributions that describe the concentrations of molecular components, the reaction rates for different molecular processes, and the effects of mutations. Finally, the likelihood that mutations in a pathway will yield phenotypic change is estimated with stochastic simulations. One advantage of this method is that only basic knowledge of the interaction network underlying a phenotype is required. However, it can also incorporate available information about concentrations and reaction rates as well as mutational biases and mutational robustness of molecular components. The method estimates the relative probabilities that different pathways produce phenotypic change, which can be combined with fitness models to predict evolutionary outcomes.

摘要

理解遗传变异向表型变异的转化是遗传学和进化生物学中的一个基本问题。通过突变引入新的遗传变异可导致新的适应性表型,但基因型到表型的映射复杂性使得预测突变的表型效应具有挑战性。代谢模型结合通量平衡分析已被用于预测进化最优性。然而,这些方法依赖于大规模的代谢模型,描述的表型有限,并假设对生长速率的选择是主要的进化驱动力。在此,我们描述一种计算突变变化转化为两条分子途径之间表型变化的相对可能性的方法。途径中分子成分的相互作用用常微分方程建模。未知参数由描述分子成分浓度、不同分子过程反应速率以及突变效应的概率分布来抵消。最后,通过随机模拟估计途径中突变产生表型变化的可能性。该方法的一个优点是仅需要关于表型基础的相互作用网络的基本知识。然而,它也可以纳入有关浓度和反应速率的可用信息以及分子成分的突变偏差和突变稳健性。该方法估计不同途径产生表型变化的相对概率,可与适应性模型相结合以预测进化结果。