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ERNIE-ac4C: A Novel Deep Learning Model for Effectively Predicting N4-acetylcytidine Sites

Authors
Lu, RonglinQiao, JianboLi, KefeiZhao, YanxiJin, JunruCui, FeifeiZhang, ZilongManavalan, BalachandranWei, Leyi
Issue Date
15-Mar-2025
Publisher
Academic Press
Keywords
attention map features; convolutional neural network; ERNIE-RNA; N4-acetylcytidine (ac4C) modification; sequence features
Citation
Journal of Molecular Biology, v.437, no.6
Indexed
SCIE
SCOPUS
Journal Title
Journal of Molecular Biology
Volume
437
Number
6
URI
https://scholarx.skku.edu/handle/2021.sw.skku/120694
DOI
10.1016/j.jmb.2025.168978
ISSN
0022-2836
1089-8638
Abstract
RNA modifications are known to play a critical role in gene regulation and cellular processes. Specifically, N4-acetylcytidine (ac4C) modification has emerged as a significant marker involved in mRNA translation efficiency, stability, and various diseases. Accurate identification of ac4C modification sites is essential for unraveling its functional implications. However, currently available experimental methods suffer from drawbacks such as lengthy detection times, complexity, and high costs, resulting in low efficiency and accuracy in prediction. Although several bioinformatics methods have been proposed and have advanced the prediction of ac4C modification sites, there is still ample room for improvement. In this research, we propose a novel deep learning model, ERNIE-ac4C, which combines the ERNIE-RNA language model and a two-dimensional Convolutional Neural Network (CNN). ERNIE-ac4C utilizes the fusion of sequence features and attention map features to predict ac4C modification sites. ERNIE-ac4C surpasses other state-of-the-art deep learning methods, demonstrating superior accuracy and effectiveness. The availability of the code on GitHub (https://github.com/lrlbcxdd/ERNIEac4C.git) and our openness to feedback from the research community contribute to the model's accessibility and its potential for further advancements. Our study provides valuable insights into ac4C research and enhances our understanding of the functional consequences of RNA modifications. © 2025 Elsevier Ltd
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