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Global transcriptional regulatory network for Escherichia coli robustly connects gene expression to transcription factor activities

机译:大肠杆菌的全球转录调控网络将基因表达与转录因子活性牢固地联系在一起

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摘要

Transcriptional regulatory networks (TRNs) have been studied intensely for >25 y. Yet, even for the Escherichia coli TRN—probably the best characterized TRN—several questions remain. Here, we address three questions: (i) How complete is our knowledge of the E. coli TRN; (ii) how well can we predict gene expression using this TRN; and (iii) how robust is our understanding of the TRN? First, we reconstructed a high-confidence TRN (hiTRN) consisting of 147 transcription factors (TFs) regulating 1,538 transcription units (TUs) encoding 1,764 genes. The 3,797 high-confidence regulatory interactions were collected from published, validated chromatin immunoprecipitation (ChIP) data and RegulonDB. For 21 different TF knockouts, up to 63% of the differentially expressed genes in the hiTRN were traced to the knocked-out TF through regulatory cascades. Second, we trained supervised machine learning algorithms to predict the expression of 1,364 TUs given TF activities using 441 samples. The algorithms accurately predicted condition-specific expression for 86% (1,174 of 1,364) of the TUs, while 193 TUs (14%) were predicted better than random TRNs. Third, we identified 10 regulatory modules whose definitions were robust against changes to the TRN or expression compendium. Using surrogate variable analysis, we also identified three unmodeled factors that systematically influenced gene expression. Our computational workflow comprehensively characterizes the predictive capabilities and systems-level functions of an organism’s TRN from disparate data types.
机译:转录调控网络(TRNs)的研究已经超过25年。但是,即使对于大肠杆菌TRN(可能是特征最强的TRN),仍然存在几个问题。在这里,我们解决三个问题:(i)我们对大肠杆菌TRN的了解程度如何; (ii)使用该TRN预测基因表达的能力如何; (iii)我们对TRN的理解有多牢固?首先,我们重建了由147个转录因子(TF)组成的高可信度TRN(hiTRN),这些转录因子调节编码1,764个基因的1,538个转录单位(TU)。从已发布的经过验证的染色质免疫沉淀(ChIP)数据和RegulonDB中收集了3,797个高可信度调节相互作用。对于21种不同的TF基因敲除,hiTRN中多达63%的差异表达基因通过调控级联被追踪到基因敲除的TF。其次,我们训练了监督的机器学习算法,以使用441个样本在给定TF活动的情况下预测1,364个TU的表达。该算法可准确预测86%(1,364个中的1,174个)的TU的条件特异性表达,而193个TU(14%)的预测优于随机TRN。第三,我们确定了10个监管模块,这些模块的定义对TRN或表达纲要的更改具有鲁棒性。使用替代变量分析,我们还确定了系统影响基因表达的三个未建模因素。我们的计算工作流程从不同的数据类型全面描述了生物体TRN的预测能力和系统级功能。

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