Novikov Eugene, Barillot Emmanuel
Service Bioinformatique, Institut Curie, 26 Rue d'Ulm, 75248 Paris Cedex 05, France.
BMC Syst Biol. 2008 Jan 24;2:8. doi: 10.1186/1752-0509-2-8.
Reconstruction of regulatory networks is one of the most challenging tasks of systems biology. A limited amount of experimental data and little prior knowledge make the problem difficult to solve. Although models that are currently used for inferring regulatory networks are sometimes able to make useful predictions about the structures and mechanisms of molecular interactions, there is still a strong demand to develop increasingly universal and accurate approaches for network reconstruction.
The additive regulation model is represented by a set of differential equations and is frequently used for network inference from time series data. Here we generalize this model by converting differential equations into integral equations with adjustable kernel functions. These kernel functions can be selected based on prior knowledge or defined through iterative improvement in data analysis. This makes the integral model very flexible and thus capable of covering a broad range of biological systems more adequately and specifically than previous models.
We reconstructed network structures from artificial and real experimental data using differential and integral inference models. The artificial data were simulated using mathematical models implemented in JDesigner. The real data were publicly available yeast cell cycle microarray time series. The integral model outperformed the differential one for all cases. In the integral model, we tested the zero-degree polynomial and single exponential kernels. Further improvements could be expected if the kernel were selected more specifically depending on the system.
调控网络的重建是系统生物学中最具挑战性的任务之一。实验数据有限且先验知识匮乏使得该问题难以解决。尽管目前用于推断调控网络的模型有时能够对分子相互作用的结构和机制做出有用的预测,但仍迫切需要开发越来越通用和准确的网络重建方法。
加性调控模型由一组微分方程表示,常用于从时间序列数据进行网络推断。在此,我们通过将微分方程转换为具有可调核函数的积分方程来推广该模型。这些核函数可以基于先验知识进行选择,或者通过数据分析中的迭代改进来定义。这使得积分模型非常灵活,因此能够比以前的模型更充分、更具体地涵盖广泛的生物系统。
我们使用微分和积分推断模型从人工和真实实验数据重建了网络结构。人工数据是使用JDesigner中实现的数学模型模拟的。真实数据是公开可用的酵母细胞周期微阵列时间序列。在所有情况下,积分模型都优于微分模型。在积分模型中,我们测试了零次多项式和单指数核。如果根据系统更具体地选择核函数,有望进一步改进。