School of Computer Science and Technology, Beijing Institute of Technology, Beijing 100081, China.
School of Mathematics & Computer Science, Yan'an University, Shaanxi 716000, China.
Brief Bioinform. 2023 Jul 20;24(4). doi: 10.1093/bib/bbad212.
MicroRNAs (miRNAs) are human post-transcriptional regulators in humans, which are involved in regulating various physiological processes by regulating the gene expression. The subcellular localization of miRNAs plays a crucial role in the discovery of their biological functions. Although several computational methods based on miRNA functional similarity networks have been presented to identify the subcellular localization of miRNAs, it remains difficult for these approaches to effectively extract well-referenced miRNA functional representations due to insufficient miRNA-disease association representation and disease semantic representation. Currently, there has been a significant amount of research on miRNA-disease associations, making it possible to address the issue of insufficient miRNA functional representation. In this work, a novel model is established, named DAmiRLocGNet, based on graph convolutional network (GCN) and autoencoder (AE) for identifying the subcellular localizations of miRNA. The DAmiRLocGNet constructs the features based on miRNA sequence information, miRNA-disease association information and disease semantic information. GCN is utilized to gather the information of neighboring nodes and capture the implicit information of network structures from miRNA-disease association information and disease semantic information. AE is employed to capture sequence semantics from sequence similarity networks. The evaluation demonstrates that the performance of DAmiRLocGNet is superior to other competing computational approaches, benefiting from implicit features captured by using GCNs. The DAmiRLocGNet has the potential to be applied to the identification of subcellular localization of other non-coding RNAs. Moreover, it can facilitate further investigation into the functional mechanisms underlying miRNA localization. The source code and datasets are accessed at http://bliulab.net/DAmiRLocGNet.
微小 RNA(miRNA)是人类转录后的调节剂,通过调节基因表达参与调节各种生理过程。miRNA 的亚细胞定位在发现其生物学功能方面起着至关重要的作用。尽管已经提出了几种基于 miRNA 功能相似性网络的计算方法来识别 miRNA 的亚细胞定位,但由于 miRNA-疾病关联表示和疾病语义表示不足,这些方法仍然难以有效地提取有良好参考的 miRNA 功能表示。目前,已经有大量关于 miRNA-疾病关联的研究,可以解决 miRNA 功能表示不足的问题。在这项工作中,建立了一个新的模型,命名为 DAmiRLocGNet,基于图卷积网络(GCN)和自动编码器(AE)来识别 miRNA 的亚细胞定位。DAmiRLocGNet 基于 miRNA 序列信息、miRNA-疾病关联信息和疾病语义信息构建特征。GCN 用于收集邻居节点的信息,并从 miRNA-疾病关联信息和疾病语义信息中捕获网络结构的隐式信息。AE 用于从序列相似性网络中捕获序列语义。评估表明,DAmiRLocGNet 的性能优于其他竞争的计算方法,受益于 GCNs 捕获的隐式特征。DAmiRLocGNet 有可能应用于识别其他非编码 RNA 的亚细胞定位。此外,它可以促进对 miRNA 定位功能机制的进一步研究。源代码和数据集可在 http://bliulab.net/DAmiRLocGNet 上获取。