NBCR-ac4C: A Deep Learning Framework Based on Multivariate BERT for Human mRNA N4-Acetylcytidine Sites Prediction.

Abstract

N4-acetylcytidine (ac4C) plays a crucial role in regulating cellular biological processes, particularly in gene expression regulation and disease development. However, experiments to identify ac4C in a wet lab are time-consuming and costly, and the learning-based methods struggle to capture the underlying semantic knowledge and relations within sequences. To address this, we propose a deep learning approach called NBCR-ac4C based on pretrained models. Specifically, we employ Nucleotide Transformer and DNABERT2 to construct contextual embedding of nucleotide sequences, which effectively mine and express context relations between different features in the sequence. Convolutional neural network (CNN) and ResNet18 are then applied to further extract shallow and deep knowledge from context embedding. Depending on extensive experiments for the prediction of ac4C sites in nucleotide sequences, we observe that NBCR-ac4C outperforms general learning-based models. It achieves the highest accuracy (ACC) of 83.51% and an Area Under the Receiver Operating Characteristic Curve (AUROC) of 89.58% on an independent test set. Moreover, the proposed model, compared to the current state-of-the-art (SOTA) model LSA-ac4C, demonstrates higher ACC and AUROC by 0.81-3.7% and 0.05-1.58%, respectively. The data set and code are available on https://github.com/2103374200/NBCR to facilitate further discussion on NBCR-ac4C.