Evidence map›Paper›PMID 39596413›Full record

ArticleInternational journal of molecular sciences2024

PRITrans: A Transformer-Based Approach for the Prediction of the Effects of Missense Mutation on Protein-RNA Interactions.

Fang Ge, Cui-Feng Li, Chao-Ming Zhang, Ming Zhang, Dong-Jun Yu

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Fang GeState Key Laboratory of Organic Electronics and Information Displays & Institute of Advanced Materials (IAM), Nanjing University of Posts & Telecommunications, 9 Wenyuan, Nanjing 210023, China.ORCID 0000-0001-5792-5379
Cui-Feng LiSchool of Computer, Jiangsu University of Science and Technology, 666 Changhui Road, Zhenjiang 212100, China.ORCID 0009-0006-3555-1410
Chao-Ming ZhangSchool of Computer, Jiangsu University of Science and Technology, 666 Changhui Road, Zhenjiang 212100, China.
Ming ZhangSchool of Computer, Jiangsu University of Science and Technology, 666 Changhui Road, Zhenjiang 212100, China.ORCID 0009-0004-3197-3523
Dong-Jun YuSchool of Computer Science and Engineering, Nanjing University of Science and Technology, 200 Xiaolingwei, Nanjing 210094, China.

Funding

National Natural Science Foundation of China 62372234, 62072243Natural Science Foundation of Jiangsu BK20201304Natural Science Research Start-up Foundation of Recruiting Talents of Nanjing University of Posts and Telecommunications Grant No. NY223062
6 · The paper itself

Abstract

Protein-RNA interactions are essential to many cellular functions, and missense mutations in RNA-binding proteins can disrupt these interactions, often leading to disease. To address this, we developed PRITrans, a specialized computational method aimed at predicting the effects of missense mutations on protein-RNA interactions, which is vital for understanding disease mechanisms and advancing molecular biology research. PRITrans is a novel deep learning model designed to predict the effects of missense mutations on protein-RNA interactions, which employs a Transformer architecture enhanced with multiscale convolution modules for comprehensive feature extraction. Its primary innovation lies in integrating protein language model embeddings with a deep feature fusion strategy, effectively handling high-dimensional feature representations. By utilizing multi-layer self-attention mechanisms, PRITrans captures nuanced, high-level sequence information, while multiscale convolutions extract features across various depths, thereby enhancing predictive accuracy. Consequently, this architecture enables significant improvements in ΔΔG prediction compared to traditional approaches. We validated PRITrans using three different cross-validation strategies on two newly reconstructed mutation datasets, S315 and S630 (containing 315 forward and 315 reverse mutations). The results consistently demonstrated PRITrans's strong performance on both datasets. PRITrans demonstrated strong predictive capability, achieving a Pearson correlation coefficient of 0.741 and a root mean square error (RMSE) of 1.168 kcal/mol on the S630 dataset. Moreover, its robust performance extended to independent test sets, achieving a Pearson correlation of 0.699 and an RMSE of 1.592 kcal/mol. These results underscore PRITrans's potential as a powerful tool for protein-RNA interaction studies. Moreover, when tested against existing prediction methods on an independent dataset, PRITrans showed improved predictive accuracy and robustness.

Indexed as

Computational BiologyMutation, MissenseRNARNA-Binding ProteinsDeep LearningHumansProtein BindingRNARNA-Binding Proteinsbinding affinitybioinformaticsmissense mutationprotein language modelprotein-RNA interactions

Identifiers

PMID39596413
PMCPMC11594650

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.