Lau Kai-Yeung, Ganguli Surya, Tang Chao
Graduate Group in Biological and Medical Informatics, University of California San Francisco, San Francisco, CA 94158-2517, USA.
Phys Rev E Stat Nonlin Soft Matter Phys. 2007 May;75(5 Pt 1):051907. doi: 10.1103/PhysRevE.75.051907. Epub 2007 May 9.
We develop a general method to explore how the function performed by a biological network can constrain both its structural and dynamical network properties. This approach is orthogonal to prior studies which examine the functional consequences of a given structural feature, for example a scale free architecture. A key step is to construct an algorithm that allows us to efficiently sample from a maximum entropy distribution on the space of Boolean dynamical networks constrained to perform a specific function, or cascade of gene expression. Such a distribution can act as a "functional null model" to test the significance of any given network feature, and can aid in revealing underlying evolutionary selection pressures on various network properties. Although our methods are general, we illustrate them in an analysis of the yeast cell cycle cascade. This analysis uncovers strong constraints on the architecture of the cell cycle regulatory network as well as significant selection pressures on this network to maintain ordered and convergent dynamics, possibly at the expense of sacrificing robustness to structural perturbations.
我们开发了一种通用方法,以探究生物网络执行的功能如何限制其结构和动态网络属性。这种方法与先前研究不同,先前研究是考察给定结构特征(例如无标度架构)的功能后果。关键步骤是构建一种算法,使我们能够在受限于执行特定功能或基因表达级联的布尔动态网络空间上,从最大熵分布中高效采样。这样的分布可以作为“功能零模型”,用于检验任何给定网络特征的显著性,并有助于揭示各种网络属性背后的进化选择压力。尽管我们的方法具有通用性,但我们在酵母细胞周期级联分析中对其进行了说明。该分析揭示了对细胞周期调控网络架构的强大限制,以及对该网络维持有序和收敛动态的显著选择压力,这可能是以牺牲对结构扰动的鲁棒性为代价的。