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MODELING NONLINEAR GENE REGULATORY NETWORKS FROM TIME SERIES GENE EXPRESSION DATA

机译:从时间序列基因表达数据建模非线性基因调控网络

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In cells, molecular networks such as gene regulatory networks are the basis of biological complexity. Therefore, gene regulatory networks have become the core of research in systems biology. Understanding the processes underlying the several extracellular regulators, signal transduction, protein–protein interactions, and differential gene expression processes requires detailed molecular description of the protein and gene networks involved. To understand better these complex molecular networks and to infer new regulatory associations, we propose a statistical method based on vector autoregressive models and Granger causality to estimate nonlinear gene regulatory networks from time series microarray data. Most of the models available in the literature assume linearity in the inference of gene connections; moreover, these models do not infer directionality in these connections. Thus, a priori biological knowledge is required. However, in pathological cases, no a priori biological information is available. To overcome these problems, we present the nonlinear vector autoregressive (NVAR) model. We have applied the NVAR model to estimate nonlinear gene regulatory networks based entirely on gene expression profiles obtained from DNA microarray experiments. We show the results obtained by NVAR through several simulations and by the construction of three actual gene regulatory networks (p53, NF-κB, and c-Myc) for HeLa cells.
机译:在细胞中,诸如基因调控网络之类的分子网络是生物学复杂性的基础。因此,基因调控网络已成为系统生物学研究的核心。要了解几种细胞外调节物的基础过程,信号转导,蛋白质间相互作用以及差异基因表达过程,需要对所涉及的蛋白质和基因网络进行详细的分子描述。为了更好地理解这些复杂的分子网络并推断出新的调控关联,我们提出了一种基于矢量自回归模型和Granger因果关系的统计方法,以从时间序列微阵列数据估计非线性基因调控网络。文献中可用的大多数模型都假定基因连接是线性的。此外,这些模型不能推断这些连接的方向性。因此,需要先验生物学知识。但是,在病理情况下,没有先验生物学信息。为了克服这些问题,我们提出了非线性矢量自回归(NVAR)模型。我们已将NVAR模型应用于完全基于从DNA芯片实验获得的基因表达谱的非线性基因调控网络。我们显示了通过NVAR通过几个模拟以及通过构建三个实际的HeLa细胞基因调控网络(p53,NF-κB和c-Myc)获得的结果。

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