MMLmiRLocNet: miRNA Subcellular Localization Prediction based on Multi-view Multi-label Learning for Drug Design.

Abstract

Identifying subcellular localization of microRNAs (miRNAs) is essential for comprehensive understanding of cellular function and has significant implications for drug design. In the past, several computational methods for miRNA subcellular localization is being used for uncovering multiple facets of RNA function to facilitate the biological applications. Unfortunately, most existing classification methods rely on a single sequencebased view, making the effective fusion of data from multiple heterogeneous networks a primary challenge. Inspired by multi-view multi-label learning strategy, we propose a computational method, named MMLmiRLocNet, for predicting the subcellular localizations of miRNAs. The MMLmiRLocNet predictor extracts multi-perspective sequence representations by analyzing lexical, syntactic, and semantic aspects of biological sequences. Specifically, it integrates lexical attributes derived from k-mer physicochemical profiles, syntactic characteristics obtained via word2vec embeddings, and semantic representations generated by pre-trained feature embeddings. Finally, module for extracting multi-view consensus-level features and specific-level features was constructed to capture consensus and specific features from various perspectives. The full connection networks are utilized as the output module to predict the miRNA subcellular localization. Experimental results suggest that MMLmiRLocNet outperforms existing methods in terms of F1, subACC, and Accuracy, and achieves best performance with the help of multi-view consensus features and specific features extract network.