摘要
The prediction of miRNA-mRNA interactions is fundamental to elucidating gene regulatory mechanisms and disease pathogenesis. This study proposes SARGE, a computational framework for this predictive task. The architecture first utilizes an autoencoder to derive compressed, low-dimensional feature embeddings for miRNAs and mRNAs. These embeddings then populate a heterogeneous graph, where a dual-layer Graph Attention Network (DLGAT), augmented with residual connections, is employed to capture intricate topological dependencies. A Jumping Knowledge Network (JK-Net) that leverages a multi-head self-attention mechanism aggregates these layer-specific representations, enhancing the expressive capacity of the model. The efficacy of the model was systematically evaluated across several benchmark datasets characterized by diverse scales and distributions. On the principal MTIS-10317 dataset, SARGE yielded an AUC of 0.8867 and an AUPR of 0.8865. Ablation studies and parameter sensitivity analyses supported the contribution of each architectural component and helped identify suitable hyperparameter configurations under the current experimental setting. Case studies involving the PTEN gene and hsa-miR-21–5p were conducted to evaluate the potential utility of the model in a practical setting, suggesting its ability to prioritize biologically relevant candidate interactions.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 152978 |
| 期刊 | International Journal of Biological Macromolecules |
| 卷 | 371 |
| DOI | |
| 出版状态 | 已出版 - 7月 2026 |
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