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Correlation analysis reveals the emergence of coherence in the gene expression dynamics following system perturbation

机译:相关分析揭示了系统扰动后基因表达动力学的一致性的出现

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摘要

Time course gene expression experiments are a popular means to infer co-expression. Many methods have been proposed to cluster genes or to build networks based on similarity measures of their expression dynamics. In this paper we apply a correlation based approach to network reconstruction to three datasets of time series gene expression following system perturbation: 1) Conditional, Tamoxifen dependent, activation of the cMyc proto-oncogene in rat fibroblast; 2) Genomic response to nutrition changes in D. melanogaster; 3) Patterns of gene activity as a consequence of ageing occurring over a life-span time series (25y–90y) sampled from T-cells of human donors.We show that the three datasets undergo similar transitions from an "uncorrelated" regime to a positively or negatively correlated one that is symptomatic of a shift from a "ground" or "basal" state to a "polarized" state.In addition, we show that a similar transition is conserved at the pathway level, and that this information can be used for the construction of "meta-networks" where it is possible to assess new relations among functionally distant sets of molecular functions.
机译:时程基因表达实验是推断共表达的流行方法。已经提出了许多基于基因表达动力学的相似性度量来聚类基因或构建网络的方法。在本文中,我们将基于相关性的网络重构方法应用于系统扰动后的三个时间序列基因表达数据集:1)条件性,他莫昔芬依赖性,大鼠成纤维细胞中cMyc原癌基因的激活; 2)基因组对黑腹果蝇营养变化的反应; 3)从人类供体T细胞采样的生命周期时间序列(25y–90y)中发生的衰老导致基因活性的模式。我们显示,这三个数据集经历了从“无关”模式到呈正相关或负相关的征兆,表示从“基态”或“基础”态转变为“极化”态。此外,我们表明在途径水平上守恒着类似的转变,并且该信息可以用于“元网络”的构建,在其中可以评估功能上较远的分子功能集之间的新关系。

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