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Inferring the perturbed microRNA regulatory networks from gene expression data using a network propagation based method

机译:使用基于网络传播的方法从基因表达数据推断受干扰的microRNA调控网络

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Background MicroRNAs (miRNAs) are a class of endogenous small regulatory RNAs. Identifications of the dys-regulated or perturbed miRNAs and their key target genes are important for understanding the regulatory networks associated with the studied cellular processes. Several computational methods have been developed to infer the perturbed miRNA regulatory networks by integrating genome-wide gene expression data and sequence-based miRNA-target predictions. However, most of them only use the expression information of the miRNA direct targets, rarely considering the secondary effects of miRNA perturbation on the global gene regulatory networks. Results We proposed a network propagation based method to infer the perturbed miRNAs and their key target genes by integrating gene expressions and global gene regulatory network information. The method used random walk with restart in gene regulatory networks to model the network effects of the miRNA perturbation. Then, it evaluated the significance of the correlation between the network effects of the miRNA perturbation and the gene differential expression levels with a forward searching strategy. Results show that our method outperformed several compared methods in rediscovering the experimentally perturbed miRNAs in cancer cell lines. Then, we applied it on a gene expression dataset of colorectal cancer clinical patient samples and inferred the perturbed miRNA regulatory networks of colorectal cancer, including several known oncogenic or tumor-suppressive miRNAs, such as miR-17, miR-26 and miR-145. Conclusions Our network propagation based method takes advantage of the network effect of the miRNA perturbation on its target genes. It is a useful approach to infer the perturbed miRNAs and their key target genes associated with the studied biological processes using gene expression data.
机译:背景微RNA(miRNA)是一类内源性小调节RNA。 dys调节或扰动的miRNA及其关键靶基因的鉴定对于理解与研究的细胞过程相关的调节网络很重要。通过整合全基因组基因表达数据和基于序列的miRNA靶标预测,已开发出几种计算方法来推断受干扰的miRNA调控网络。然而,它们中的大多数仅使用miRNA直接靶标的表达信息,很少考虑miRNA扰动对全球基因调控网络的次级影响。结果我们提出了一种基于网络传播的方法,通过整合基因表达和全球基因调控网络信息来推断受干扰的miRNA及其关键靶基因。该方法在基因调节网络中使用了随机行走并重新启动来模拟miRNA扰动的网络效应。然后,它使用正向搜索策略评估了miRNA扰动的网络效应与基因差异表达水平之间相关性的重要性。结果表明,在重新发现癌细胞系中受实验干扰的miRNA方面,我们的方法优于几种比较方法。然后,我们将其应用于结直肠癌临床患者样本的基因表达数据集,并推断出受干扰的结直肠癌miRNA调控网络,包括几种已知的致癌或抑制肿瘤的miRNA,例如miR-17,miR-26和miR-145 。结论我们基于网络传播的方法利用了miRNA干扰对其靶基因的网络效应。这是一种有用的方法,可以使用基因表达数据来推断与研究的生物过程相关的干扰的miRNA及其关键靶基因。

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