{"title":"MJnet: A lightweight RNN-based model for microRNA target site prediction","authors":"Junhao Yu, Cong Hui, Jianhua Jia","doi":"10.1016/j.compbiolchem.2025.108603","DOIUrl":null,"url":null,"abstract":"<div><div>Accurate prediction of microRNA (miRNA) target sites is critical for understanding post-transcriptional gene regulation. While recent deep learning models have achieved high predictive accuracy, many suffer from excessive computational complexity and limited interpretability. In this study, we propose MJnet, a lightweight and efficient deep learning model based on a Bidirectional Gated Recurrent Unit (BiGRU) architecture, integrated with simple C2 encoding, a multi-scale one-dimensional convolutional network (TextCNN), and a self-attention mechanism. This framework captures both local sequence features and global contextual dependencies while maintaining low computational cost. Extensive experiments on experimentally validated datasets demonstrate that our model outperforms several traditional and deep learning-based baselines, including Mimosa, in terms of accuracy, F1-score, and robustness across balanced gene-level test sets. Ablation studies confirm the effectiveness of each module, and attention heatmaps reveal interpretable patterns aligned with known seed regions. Our approach offers a practical, reproducible, and interpretable solution for miRNA target site prediction in biologically relevant contexts.</div></div>","PeriodicalId":10616,"journal":{"name":"Computational Biology and Chemistry","volume":"119 ","pages":"Article 108603"},"PeriodicalIF":3.1000,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Computational Biology and Chemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1476927125002646","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Accurate prediction of microRNA (miRNA) target sites is critical for understanding post-transcriptional gene regulation. While recent deep learning models have achieved high predictive accuracy, many suffer from excessive computational complexity and limited interpretability. In this study, we propose MJnet, a lightweight and efficient deep learning model based on a Bidirectional Gated Recurrent Unit (BiGRU) architecture, integrated with simple C2 encoding, a multi-scale one-dimensional convolutional network (TextCNN), and a self-attention mechanism. This framework captures both local sequence features and global contextual dependencies while maintaining low computational cost. Extensive experiments on experimentally validated datasets demonstrate that our model outperforms several traditional and deep learning-based baselines, including Mimosa, in terms of accuracy, F1-score, and robustness across balanced gene-level test sets. Ablation studies confirm the effectiveness of each module, and attention heatmaps reveal interpretable patterns aligned with known seed regions. Our approach offers a practical, reproducible, and interpretable solution for miRNA target site prediction in biologically relevant contexts.
期刊介绍:
Computational Biology and Chemistry publishes original research papers and review articles in all areas of computational life sciences. High quality research contributions with a major computational component in the areas of nucleic acid and protein sequence research, molecular evolution, molecular genetics (functional genomics and proteomics), theory and practice of either biology-specific or chemical-biology-specific modeling, and structural biology of nucleic acids and proteins are particularly welcome. Exceptionally high quality research work in bioinformatics, systems biology, ecology, computational pharmacology, metabolism, biomedical engineering, epidemiology, and statistical genetics will also be considered.
Given their inherent uncertainty, protein modeling and molecular docking studies should be thoroughly validated. In the absence of experimental results for validation, the use of molecular dynamics simulations along with detailed free energy calculations, for example, should be used as complementary techniques to support the major conclusions. Submissions of premature modeling exercises without additional biological insights will not be considered.
Review articles will generally be commissioned by the editors and should not be submitted to the journal without explicit invitation. However prospective authors are welcome to send a brief (one to three pages) synopsis, which will be evaluated by the editors.