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Prediction of lncRNA-protein interactions using HeteSim scores based on heterogeneous networks

机译:基于异构网络的Hetesim分数预测LNCRNA-蛋白质相互作用

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摘要

Abstract Massive studies have indicated that long non-coding RNAs (lncRNAs) are critical for the regulation of cellular biological processes by binding with RNA-related proteins. However, only a few experimentally supported lncRNA-protein associations have been reported. Existing network-based methods are typically focused on intrinsic features of lncRNA and protein but ignore the information implicit in the topologies of biological networks associated with lncRNAs. Considering the limitations in previous methods, we propose PLPIHS, an effective computational method for Predicting lncRNA-Protein Interactions using HeteSim Scores. PLPIHS uses the HeteSim measure to calculate the relatedness score for each lncRNA-protein pair in the heterogeneous network, which consists of lncRNA-lncRNA similarity network, lncRNA-protein association network and protein-protein interaction network. An SVM classifier to predict lncRNA-protein interactions is built with the HeteSim scores. The results show that PLPIHS performs significantly better than the existing state-of-the-art approaches and achieves an AUC score of 0.97 in the leave-one-out validation test. We also compare the performances of networks with different connectivity density and find that PLPIHS performs well across all the networks. Furthermore, we use the proposed method to identify the related proteins for lncRNA MALAT1. Highly-ranked proteins are verified by the biological studies and demonstrate the effectiveness of our method.
机译:摘要巨大研究表明,通过与RNA相关蛋白质结合来调节细胞生物过程的长期非编码RNA(LNCRNA)至关重要。然而,仅报告了少数实验支持的LNCRNA-蛋白质联合。基于网络的基于网络的方法通常集中在LNCRNA和蛋白质的内在特征上,而是忽略与LNCRNA相关的生物网络的拓扑中隐含的信息。考虑到以前的方法中的局限性,我们提出PLPIHS,一种用于使用Hetesim评分预测LNCRNA-蛋白质相互作用的有效计算方法。 PLPIHS使用Hetesim措施来计算异构网络中每个LNCRNA-蛋白对的相关性分数,其包括LNCRNA-LNCRNA相似性网络,LNCRNA-蛋白质结合网络和蛋白质 - 蛋白质相互作用网络。使用Hetesim分数建立了预测LNCRNA蛋白质相互作用的SVM分类器。结果表明,PLPIHS比现有最先进的方法更好地表现得明显好,在休假验证测试中实现了0.97的AUC评分。我们还将网络的性能与不同的连接密度进行比较,并发现PLPIHS在所有网络上执行良好。此外,我们使用所提出的方法来鉴定LNCRNA MALAT1的相关蛋白。通过生物学研究验证了高度排名的蛋白质,并证明了我们方法的有效性。

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