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Joint Bayesian inference of condition-specific miRNA and transcription factor activities from combined gene and microRNA expression data

机译:从组合的基因和microRNA表达数据出发,对条件特异性miRNA和转录因子活性进行联合贝叶斯推断

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Motivation: There have been many successful experimental and bioinformatics efforts to elucidate transcription factor (TF)-target networks in several organisms. For many organisms, these annotations are complemented by miRNA-target networks of good quality. Attempts that use these networks in combination with gene expression data to draw conclusions on TF or miRNA activity are, however, still relatively sparse. Results: In this study, we propose Bayesian inference of regulation of transcriptional activity (BIRTA) as a novel approach to infer both, TF and miRNA activities, from combined miRNA and mRNA expression data in a condition specific way. That means our model explains mRNA and miRNA expression for a specific experimental condition by the activities of certain miRNAs and TFs, hence allowing for differentiating between switches from active to inactive (negative switch) and inactive to active (positive switch) forms. Extensive simulations of our model reveal its good prediction performance in comparison to other approaches. Furthermore, the utility of BIRTA is demonstrated at the example of Escherichia coli data comparing aerobic and anaerobic growth conditions, and by human expression data from pancreas and ovarian cancer.
机译:动机:已经进行了许多成功的实验和生物信息学努力,以阐明几种生物体中的转录因子(TF)-靶标网络。对于许多生物而言,高质量的miRNA靶标网络可为这些注释提供补充。但是,将这些网络与基因表达数据结合使用以得出关于TF或miRNA活性的结论的尝试仍然相对较少。结果:在这项研究中,我们提出了转录活性调节的贝叶斯推断(BIRTA),这是一种以条件特异性方式从组合的miRNA和mRNA表达数据中推断TF和miRNA活性的新方法。这意味着我们的模型通过某些miRNA和TF的活性解释了特定实验条件下的mRNA和miRNA表达,因此可以区分从激活形式到非激活形式(负向转变)和从非激活形式转变为活性(正向转变)形式。与其他方法相比,我们模型的大量模拟显示了其良好的预测性能。此外,在比较有氧和无氧生长条件的大肠杆菌数据实例以及来自胰腺和卵巢癌的人类表达数据中证明了BIRTA的实用性。

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