Predicting Mutation-Disease Associations Through Protein Interactions Via Deep Learning

Disease is one of the primary factors affecting life activities, with complex etiologies often influenced by gene expression and mutation. Currently, wet lab experiments have analyzed the mechanisms of mutations, but these are usually limited by the costs of wet experiments and constraints in sample types and scales. Therefore, this paper constructs a real-world mutation-induced disease dataset and proposes Capsule and Graph topology networks with Multi-head attention (CGM) to predict the mutation-disease associations. CGM can accurately predict protein mutation-disease associations, and to further elucidate the pathogenicity of protein mutations, we also verified that protein mutations lead to protein structural alterations by the model, which suggests that mutation-induced conformational changes may be an important pathogenic factor. Limited by the size of the mutated protein dataset, we also performed experiments on benchmark and imbalanced datasets, where CGM mined 22 unknown protein interaction pairs from the benchmark dataset, better illustrating the potential of CGM in predicting mutation-disease associations. In summary, this paper curates a real dataset. It proposes that CGM predicts protein mutations and disease associations, providing a novel tool for further understanding of biomolecular pathways and disease mechanisms.

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Publication Details

Journal
IEEE Journal of Biomedical and Health Informatics
Published
2025-02-13
DOI
https://doi.org/10.1109/jbhi.2025.3541848
Citations
14
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
11.28
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article

Predicting Mutation-Disease Associations Through Protein Interactions Via Deep Learning

Tao Song, Xue Li, Shuang Wang, Xiangyu Meng et al.
14 citations
IEEE Journal of Biomedical and Health Informatics
Bioinformatics and Genomic Networks
11.28
article

Predicting Mutation-Disease Associations Through Protein Interactions Via Deep Learning

Tao Song, Xue Li, Shuang Wang, Xiangyu Meng, Ben Cao, Enrico G. Petretto, Yu Huang, Jianmin Wang
article en
14 citations

Abstract

Disease is one of the primary factors affecting life activities, with complex etiologies often influenced by gene expression and mutation. Currently, wet lab experiments have analyzed the mechanisms of mutations, but these are usually limited by the costs of wet experiments and constraints in sample types and scales. Therefore, this paper constructs a real-world mutation-induced disease dataset and proposes Capsule and Graph topology networks with Multi-head attention (CGM) to predict the mutation-disease associations. CGM can accurately predict protein mutation-disease associations, and to further elucidate the pathogenicity of protein mutations, we also verified that protein mutations lead to protein structural alterations by the model, which suggests that mutation-induced conformational changes may be an important pathogenic factor. Limited by the size of the mutated protein dataset, we also performed experiments on benchmark and imbalanced datasets, where CGM mined 22 unknown protein interaction pairs from the benchmark dataset, better illustrating the potential of CGM in predicting mutation-disease associations. In summary, this paper curates a real dataset. It proposes that CGM predicts protein mutations and disease associations, providing a novel tool for further understanding of biomolecular pathways and disease mechanisms.

IEEE Journal of Biomedical and Health InformaticsVol. 29(6)
Yonsei University (KR), Peking University (CN), Dalian University of Technology (CN), Duke-NUS Medical School (SG), China University of Petroleum, East China (CN)
Openalex Percentile: Top 1%
Bioinformatics and Genomic Networks
11.28
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