量化基因网络连通性:模块化方法的可扩展性和准确性。

N Yalamanchili, D E Zak, B A Ogunnaike, J S Schwaber, A Kriete, B N Kholodenko
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引用次数: 10

摘要

从微阵列实验中产生的大型复杂数据集,需要系统的分析技术来揭示基因调控网络的潜在连通性。Kholodenko及其同事先前提出的模块化方法有助于将网络复杂性降低为更易于计算管理的实体,称为模块。功能模块包括基因的mRNA、启动子和产物,因此包含了大量的相互作用状态。该方法的基本要素详细描述了一个三基因模型网络,后来扩展到一个十基因模型网络,展示了可扩展性。网络架构是通过在计算机上分析只有模块输出的活动中的稳态变化来确定的,通信中间体是由每次一个应用于网络模块的特定扰动引起的。这些稳态变化形成系统响应矩阵,用于计算网络连通性或网络相互作用图。通过采用已知的生化网络,模块化方法的准确性及其对关键假设的敏感性进行了评估。
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Quantifying gene network connectivity in silico: scalability and accuracy of a modular approach.

Large, complex data sets that are generated from microarray experiments, create a need for systematic analysis techniques to unravel the underlying connectivity of gene regulatory networks. A modular approach, previously proposed by Kholodenko and co-workers, helps to scale down the network complexity into more computationally manageable entities called modules. A functional module includes a gene's mRNA, promoter and resulting products, thus encompassing a large set of interacting states. The essential elements of this approach are described in detail for a three-gene model network and later extended to a ten-gene model network, demonstrating scalability. The network architecture is identified by analysing in silico steady-state changes in the activities of only the module outputs, communicating intermediates, that result from specific perturbations applied to the network modules one at a time. These steady-state changes form the system response matrix, which is used to compute the network connectivity or network interaction map. By employing a known biochemical network, the accuracy of the modular approach and its sensitivity to key assumptions are evaluated.

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