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微小RNA在人类相互作用组中的参与:微小RNA-微小RNA调控的提取

Participation of microRNAs in human interactome: extraction of microRNA-microRNA regulations.

作者信息

Sengupta Debarka, Bandyopadhyay Sanghamitra

机构信息

Machine Intelligence Unit, Indian Statistical Institute, 203 B. T. Road, Kolkata-700108, India.

出版信息

Mol Biosyst. 2011 Jun;7(6):1966-73. doi: 10.1039/c0mb00347f. Epub 2011 Apr 11.

Abstract

To date, a significant amount of research has been conducted for computational modeling of the microRNA (miRNA)-target gene interactions and inferring different kinds of biologically relevant association from their variable expressions, available from microarray experiments. However, topological organization of the miRNA-transcription factor (TF) induced regulatory network has not yet been analyzed at a genome scale. Evidently, by ignoring the regulatory relationship among the constituent molecules, we expose our model to a great deal of noise. Besides this, the miRNA-TF regulatory network also helps extract a putative set of regulations among miRNAs and hypothesize the miRNA-miRNA regulatory network. We constructed the miRNA and TF induced regulatory network for humans by combining all possible regulations between miRNAs and TFs. Topological analysis of the network revealed some of its non-trivial and intrinsic properties. The concept of topological overlap has been extended to formulate a novel dissimilarity measure that is capable of mining groups of closely interacting molecules from a weighted digraph such that the molecules in each group regulate each other to a large extent. Many of the identified TF modules are found to be enriched in different functional categories. On the other hand, many of the identified miRNA modules displayed significant associations with common diseases. Finally, the miRNA-TF induced regulatory network yields a putative miRNA inter-regulatory network which may be considered as the first step towards the understanding of the regulatory relationship amongst miRNAs. A large number of the validated regulations were found in the predicted set of regulations, having a significantly high average score. A web application is created to facilitate the search of the Putative miRNA-miRNA Regulations (PmmR). It can be accessed through the following link: .

摘要

迄今为止,已经开展了大量研究,用于对微小RNA(miRNA)-靶基因相互作用进行计算建模,并从微阵列实验获得的可变表达中推断出不同类型的生物学相关关联。然而,尚未在全基因组规模上分析miRNA-转录因子(TF)诱导的调控网络的拓扑组织。显然,通过忽略组成分子之间的调控关系,我们的模型会受到大量噪声的影响。除此之外,miRNA-TF调控网络还有助于提取miRNA之间一组假定的调控关系,并推测miRNA-miRNA调控网络。我们通过整合miRNA和TF之间所有可能的调控关系,构建了人类的miRNA和TF诱导调控网络。对该网络的拓扑分析揭示了其一些非平凡的内在特性。拓扑重叠的概念已被扩展,以制定一种新颖的差异度量,该度量能够从加权有向图中挖掘紧密相互作用分子的组,使得每组中的分子在很大程度上相互调控。发现许多已识别的TF模块在不同功能类别中富集。另一方面,许多已识别的miRNA模块与常见疾病显示出显著关联。最后,miRNA-TF诱导调控网络产生了一个假定的miRNA相互调控网络,这可被视为朝着理解miRNA之间调控关系迈出的第一步。在预测的调控关系集中发现了大量经过验证的调控关系,其平均得分显著较高。创建了一个网络应用程序,以方便搜索假定的miRNA-miRNA调控关系(PmmR)。可通过以下链接访问: 。

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