Identifying Human miRNA Target Sites via Learning the Interaction Patterns between miRNA and mRNA Segments.


Journal

Journal of chemical information and modeling
ISSN: 1549-960X
Titre abrégé: J Chem Inf Model
Pays: United States
ID NLM: 101230060

Informations de publication

Date de publication:
30 Oct 2023
Historique:
medline: 30 10 2023
pubmed: 30 10 2023
entrez: 30 10 2023
Statut: aheadofprint

Résumé

miRNAs (microRNAs) target specific mRNA (messenger RNA) sites to regulate their translation expression. Although miRNA targeting can rely on seed region base pairing, animal miRNAs, including human miRNAs, typically cooperate with several cofactors, leading to various noncanonical pairing rules. Therefore, identifying the binding sites of animal miRNAs remains challenging. Because experiments for mapping miRNA targets are costly, computational methods are preferred for extracting potential miRNA-mRNA fragment binding pairs first. However, existing prediction tools can have significant false positives due to the prevalent noncanonical miRNA binding behaviors and the information-biased training negative sets that were used while constructing these tools. To overcome these obstacles, we first prepared an information-balanced miRNA binding pair ground-truth data set. A miRNA-mRNA interaction-aware model was then designed to help identify miRNA binding events. On the test set, our model (auROC = 94.4%) outperformed existing models by at least 2.8% in auROC. Furthermore, we showed that this model can suggest potential binding patterns for miRNA-mRNA sequence interacting pairs. Finally, we made the prepared data sets and the designed model available at http://cosbi2.ee.ncku.edu.tw/mirna_binding/download.

Identifiants

pubmed: 37903033
doi: 10.1021/acs.jcim.3c01150
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Tzu-Hsien Yang (TH)

Department of Biomedical Engineering, National Cheng Kung University, No.1, University Road, Tainan 701, Taiwan.
Medical Device Innovation Center, National Cheng Kung University, No.1 University Road, Tainan 701, Taiwan.

Jhih-Cheng Chen (JC)

Department of Electrical Engineering, National Cheng Kung University, No.1, University Road, Tainan 701, Taiwan.

Yuan-Han Lee (YH)

Department of Electrical Engineering, National Cheng Kung University, No.1, University Road, Tainan 701, Taiwan.

Shang-Yi Lu (SY)

Department of Electrical Engineering, National Cheng Kung University, No.1, University Road, Tainan 701, Taiwan.

Sheng-Hang Wu (SH)

Department of Information Management, National University of Kaohsiung, Kaohsiung University Rd, Kaohsiung 811, Taiwan.

Fang-Yuan Chang (FY)

Department of Information Management, National University of Kaohsiung, Kaohsiung University Rd, Kaohsiung 811, Taiwan.

Yan-Cheng Huang (YC)

Department of Electrical Engineering, National Cheng Kung University, No.1, University Road, Tainan 701, Taiwan.

Mei-Hsien Lee (MH)

Department of Mathematics, University of Taipei, No.1, Ai-Guo West Road, Taipei 100234, Taiwan.

Yan-Yuan Tseng (YY)

Center for Molecular Medicine and Genetics, Wayne State University, School of Medicine, Detroit, Michigan 48201, United States.

Wei-Sheng Wu (WS)

Department of Electrical Engineering, National Cheng Kung University, No.1, University Road, Tainan 701, Taiwan.

Classifications MeSH