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Identifying transcription factors and microRNAs as key regulators of pathways using Bayesian inference on known pathway structures

机译:使用贝叶斯推断已知途径结构,鉴定转录因子和微小RNA作为途径的关键调节剂

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Background Transcription factors and microRNAs act in concert to regulate gene expression in eukaryotes. Numerous computational methods based on sequence information are available for the prediction of target genes of transcription factors and microRNAs. Although these methods provide a static snapshot of how genes may be regulated, they are not effective for the identification of condition-specific regulators. Results We propose a new method that combines: a) transcription factors and microRNAs that are predicted to target genes in pathways, with b) microarray expression profiles of microRNAs and mRNAs, in conjunction with c) the known structure of molecular pathways. These elements are integrated into a Bayesian network derived from each pathway that, through probability inference, allows for the prediction of the key regulators in the pathway. We demonstrate 1) the steps to discretize the expression data for the computation of conditional probabilities in a Bayesian network, 2) the procedure to construct a Bayesian network using the structure of a known pathway and the transcription factors and microRNAs predicted to target genes in that pathway, and 3) the inference results as potential regulators of three signaling pathways using microarray expression profiles of microRNA and mRNA in estrogen receptor positive and estrogen receptor negative tumors. Conclusions We displayed the ability of our framework to integrate multiple sets of microRNA and mRNA expression data, from two phenotypes, with curated molecular pathway structures by creating Bayesian networks. Moreover, by performing inference on the network using known evidence, e.g., status of differentially expressed genes, or by entering hypotheses to be tested, we obtain a list of potential regulators of the pathways. This, in turn, will help increase our understanding about the regulatory mechanisms relevant to the two phenotypes.
机译:背景转录因子和microRNA共同作用以调节真核生物中的基因表达。基于序列信息的多种计算方法可用于预测转录因子和microRNA的靶基因。尽管这些方法提供了有关基因调控方式的静态快照,但它们对于识别条件特异性调控剂并不有效。结果我们提出了一种新方法,该方法结合了:a)转录因子和预计在途径中靶向基因的microRNA,与b)microRNA和mRNA的微阵列表达谱,以及c)分子途径的已知结构。这些元素被集成到从每个路径派生的贝叶斯网络中,通过概率推断,可以预测该路径中的关键调控因子。我们证明了1)离散化表达数据以计算贝叶斯网络中的条件概率的步骤,2)使用已知途径的结构以及预测的靶向基因的转录因子和microRNA构建贝叶斯网络的过程3)使用microRNA和mRNA的微阵列表达谱在雌激素受体阳性和雌激素受体阴性肿瘤中作为三种信号通路的潜在调控因子进行推断。结论我们展示了我们的框架能够通过创建贝叶斯网络来整合来自两种表型的多组microRNA和mRNA表达数据以及选定的分子途径结构的能力。此外,通过使用已知证据在网络上进行推断,例如差异表达基因的状态,或通过输入要测试的假设,我们获得了这些途径的潜在调节子。反过来,这将有助于增进我们对与这两种表型相关的调控机制的了解。

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