PromGER: Promoter Prediction Based on Graph Embedding and Ensemble Learning for Eukaryotic Sequence

Author:

Wang Yan12ORCID,Tai Shiwen1ORCID,Zhang Shuangquan3,Sheng Nan1,Xie Xuping1

Affiliation:

1. Key Laboratory of Symbolic Computation and Knowledge Engineering of Ministry of Education, College of Computer Science and Technology, Jilin University, Changchun 130012, China

2. School of Artificial Intelligence, Jilin University, Changchun 130012, China

3. School of Cyber Science and Engineering, Nanjing University of Science and Technology, Nanjing 210094, China

Abstract

Promoters are DNA non-coding regions around the transcription start site and are responsible for regulating the gene transcription process. Due to their key role in gene function and transcriptional activity, the prediction of promoter sequences and their core elements accurately is a crucial research area in bioinformatics. At present, models based on machine learning and deep learning have been developed for promoter prediction. However, these models cannot mine the deeper biological information of promoter sequences and consider the complex relationship among promoter sequences. In this work, we propose a novel prediction model called PromGER to predict eukaryotic promoter sequences. For a promoter sequence, firstly, PromGER utilizes four types of feature-encoding methods to extract local information within promoter sequences. Secondly, according to the potential relationships among promoter sequences, the whole promoter sequences are constructed as a graph. Furthermore, three different scales of graph-embedding methods are applied for obtaining the global feature information more comprehensively in the graph. Finally, combining local features with global features of sequences, PromGER analyzes and predicts promoter sequences through a tree-based ensemble-learning framework. Compared with seven existing methods, PromGER improved the average specificity of 13%, accuracy of 10%, Matthew’s correlation coefficient of 16%, precision of 4%, F1 score of 6%, and AUC of 9%. Specifically, this study interpreted the PromGER by the t-distributed stochastic neighbor embedding (t-SNE) method and SHAPley Additive exPlanations (SHAP) value analysis, which demonstrates the interpretability of the model.

Funder

the National Natural Science Foundation of China

the Development Project of Jilin Province of China

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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