RPI-WGNN: ncRNA-Protein Interaction Prediction based on Weighted Graph Neural Networks

Non-coding RNA (ncRNA) is functional RNA derived from DNA transcription. Although ncRNA does not directly participate in protein translation, it often plays crucial roles in biological processes via interacting with specific proteins. We proposed a novel model for predicting ncRNA-protein interactions (RPI), which takes into account weighted graphs of molecular internal structures in proteins and comprehensive sequence information of ncRNA. Using a reliable negative sample partitioning method, we feed the predicted protein graphs and ncRNA numerical vectors to learn topology structure information and global features. Subsequently, we accurately and efficiently extract comprehensive high-order intrinsic feature representations of proteins using weighted graph neural networks, and concatenate them with embedding representations of global information encoded by ncRNA sequences. Finally, the molecular structure information and sequence feature information are combined as the ultimate representation, which is then fed into the classifier to determine the presence of interactions. The results of the five-fold cross-validation experiments demonstrate that our model achieved accuracy of 99.94% and 98.92% in RPI10412 and RPI369. Moreover, it performs better than state-of-the-art methods on the benchmark datasets.

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Published
2024-12-03
DOI
https://doi.org/10.1109/bibm62325.2024.10821811
Primary Topic
Machine Learning in Bioinformatics
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article
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article

RPI-WGNN: ncRNA-Protein Interaction Prediction based on Weighted Graph Neural Networks

Wenbin Lin, Yuping Chen, Bin Zeng
Machine Learning in Bioinformatics
article

RPI-WGNN: ncRNA-Protein Interaction Prediction based on Weighted Graph Neural Networks

Wenbin Lin, Yuping Chen, Bin Zeng
article en

Abstract

Non-coding RNA (ncRNA) is functional RNA derived from DNA transcription. Although ncRNA does not directly participate in protein translation, it often plays crucial roles in biological processes via interacting with specific proteins. We proposed a novel model for predicting ncRNA-protein interactions (RPI), which takes into account weighted graphs of molecular internal structures in proteins and comprehensive sequence information of ncRNA. Using a reliable negative sample partitioning method, we feed the predicted protein graphs and ncRNA numerical vectors to learn topology structure information and global features. Subsequently, we accurately and efficiently extract comprehensive high-order intrinsic feature representations of proteins using weighted graph neural networks, and concatenate them with embedding representations of global information encoded by ncRNA sequences. Finally, the molecular structure information and sequence feature information are combined as the ultimate representation, which is then fed into the classifier to determine the presence of interactions. The results of the five-fold cross-validation experiments demonstrate that our model achieved accuracy of 99.94% and 98.92% in RPI10412 and RPI369. Moreover, it performs better than state-of-the-art methods on the benchmark datasets.

University of South China (CN)
Openalex Percentile: Top 78%
Machine Learning in Bioinformatics
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