Iber Dagmar
Department for Biosystems Science and Engineering, Switzerland and Swiss Institute of Bioinformatics (SIB), ETH Zurich, Mattenstraße 26, Basel 4058, Switzerland.
Adv Bioinformatics. 2011;2011:124062. doi: 10.1155/2011/124062. Epub 2012 Jan 23.
Biological functionality arises from the complex interactions of simple components. Emerging behaviour is difficult to recognize with verbal models alone, and mathematical approaches are important. Even few interacting components can give rise to a wide range of different responses, that is, sustained, transient, oscillatory, switch-like responses, depending on the values of the model parameters. A quantitative comparison of model predictions and experiments is therefore important to distinguish between competing hypotheses and to judge whether a certain regulatory behaviour is at all possible and plausible given the observed type and strengths of interactions and the speed of reactions. Here I will review a detailed model for the transcription factor σ(F), a regulator of cell differentiation during sporulation in Bacillus subtilis. I will focus in particular on the type of conclusions that can be drawn from detailed, carefully validated models of biological signaling networks. For most systems, such detailed experimental information is currently not available, but accumulating biochemical data through technical advances are likely to enable the detailed modelling of an increasing number of pathways. A major challenge will be the linking of such detailed models and their integration into a multiscale framework to enable their analysis in a larger biological context.
生物功能源于简单组件之间的复杂相互作用。仅靠语言模型很难识别新出现的行为,数学方法很重要。即使是很少的相互作用组件,也能产生广泛的不同反应,也就是说,持续的、短暂的、振荡的、类似开关的反应,这取决于模型参数的值。因此,对模型预测和实验进行定量比较,对于区分相互竞争的假设,以及判断在给定观察到的相互作用类型、强度和反应速度的情况下,某种调节行为是否完全可能且合理至关重要。在这里,我将回顾一个关于转录因子σ(F)的详细模型,它是枯草芽孢杆菌孢子形成过程中细胞分化的调节因子。我将特别关注从详细的、经过仔细验证的生物信号网络模型中可以得出的结论类型。对于大多数系统来说,目前还没有这样详细的实验信息,但通过技术进步积累的生化数据可能会使越来越多的途径能够进行详细建模。一个主要挑战将是将这些详细模型联系起来,并将它们整合到一个多尺度框架中,以便在更大的生物学背景下对其进行分析。