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MFH-LPI:基于多视图相似性网络融合和超图学习的长链非编码RNA-蛋白质相互作用预测

MFH-LPI: based on multi-view similarity networks fusion and hypergraph learning for long non-coding RNA-protein interactions prediction.

作者信息

Xing Zengwei, Yu Shaoyou, Liao Shuzu, Wang Peng, Liao Bo

机构信息

School of Mathematics and Statistics, Hainan Normal University, Hainan Haikou, 571158, China.

Key Laboratory of Data Science and Intelligence Education, Hainan Normal University, Ministry of Education, Hainan Haikou, 571158, China.

出版信息

BMC Genomics. 2025 Jul 1;26(1):597. doi: 10.1186/s12864-025-11774-9.

DOI:10.1186/s12864-025-11774-9
PMID:40596835
Abstract

Studies demonstrate that long non-coding RNAs (lncRNAs) and their protein interactions (LPIs) play crucial roles in regulating gene expression and participating in diverse biological processes. Aberrant expression of these interactions is closely associated with the initiation and progression of various diseases. Therefore, investigating LPI prediction is critical for elucidating disease mechanisms and identifying potential biomarkers and therapeutic targets. Given the high costs and limited efficiency of traditional biological methods, developing cost-effective and accurate computational models for LPI prediction becomes essential. Inspired by similarity network fusion and hypergraph learning, this study proposes a computational framework named MFH-LPI. First, we construct separate similarity networks for lncRNAs and proteins, then employ an attention mechanism to extract and fuse key features from these multi-view networks. Subsequently, we introduce a hypernode (randomly generated node) to establish a heterogeneous hypergraph integrating lncRNAs and proteins, thereby capturing richer node representations. Finally, we predict LPIs using a multilayer graph convolutional network (GCN) combined with a fully connected (FC) layer. We conduct several experiments on three datasets to validate the method's effectiveness. The experimental findings indicate that the suggested model is effective compared to existing processes and outperforms other approaches.

摘要

研究表明,长链非编码RNA(lncRNAs)及其与蛋白质的相互作用(LPIs)在调节基因表达和参与多种生物学过程中发挥着关键作用。这些相互作用的异常表达与各种疾病的发生和发展密切相关。因此,研究LPI预测对于阐明疾病机制以及识别潜在的生物标志物和治疗靶点至关重要。鉴于传统生物学方法成本高昂且效率有限,开发用于LPI预测的经济高效且准确的计算模型变得至关重要。受相似性网络融合和超图学习的启发,本研究提出了一个名为MFH-LPI的计算框架。首先,我们为lncRNAs和蛋白质构建单独的相似性网络,然后采用注意力机制从这些多视图网络中提取并融合关键特征。随后,我们引入一个超节点(随机生成的节点)来建立一个整合lncRNAs和蛋白质的异质超图,从而捕获更丰富的节点表示。最后,我们使用多层图卷积网络(GCN)结合全连接(FC)层来预测LPIs。我们在三个数据集上进行了多项实验以验证该方法的有效性。实验结果表明,与现有方法相比,所提出的模型是有效的,并且优于其他方法。

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本文引用的文献

1
LncRNA-miRNA interactions prediction based on meta-path similarity and Gaussian kernel similarity.基于元路径相似性和高斯核相似性的 lncRNA-miRNA 相互作用预测。
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Comput Biol Med. 2023 Sep;163:107143. doi: 10.1016/j.compbiomed.2023.107143. Epub 2023 Jun 14.
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Accurate prediction and key protein sequence feature identification of cyclins.准确预测细胞周期蛋白及其关键序列特征
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HeadTailTransfer: An efficient sampling method to improve the performance of graph neural network method in predicting sparse ncRNA-protein interactions.头尾转移:一种提高图神经网络方法预测稀疏 ncRNA-蛋白质相互作用性能的有效采样方法。
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AMHMDA: attention aware multi-view similarity networks and hypergraph learning for miRNA-disease associations identification.AMHMDA:用于识别miRNA与疾病关联的注意力感知多视图相似性网络和超图学习
Brief Bioinform. 2023 Mar 19;24(2). doi: 10.1093/bib/bbad094.
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Predicting potential interactions between lncRNAs and proteins via combined graph auto-encoder methods.通过组合图自动编码器方法预测 lncRNAs 与蛋白质之间的潜在相互作用。
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Predicting the potential human lncRNA-miRNA interactions based on graph convolution network with conditional random field.基于条件随机场的图卷积网络预测潜在的人类 lncRNA-miRNA 相互作用。
Brief Bioinform. 2022 Nov 19;23(6). doi: 10.1093/bib/bbac463.
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Hybrid_DBP: Prediction of DNA-binding proteins using hybrid features and convolutional neural networks.Hybrid_DBP:利用混合特征和卷积神经网络预测DNA结合蛋白。
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