PSI-MOUSE: Predicting Mouse Pseudouridine Sites From Sequence and Genome-Derived Features.

Pseudouridine sites genomic feature web-server

Journal

Evolutionary bioinformatics online
ISSN: 1176-9343
Titre abrégé: Evol Bioinform Online
Pays: United States
ID NLM: 101256319

Informations de publication

Date de publication:
2020
Historique:
received: 22 01 2020
accepted: 30 03 2020
entrez: 23 6 2020
pubmed: 23 6 2020
medline: 23 6 2020
Statut: epublish

Résumé

Pseudouridine (Ψ) is the first discovered and the most prevalent posttranscriptional modification, which has been widely studied during the past decades. Pseudouridine was observed in almost all kinds of RNAs and shown to have important biological functions. Currently, the time-consuming and high-cost procedures of experimental approaches limit its uses in real-life Ψ site detection. Alternatively, by taking advantage of the explosive growth of Ψ sequencing data, the computational methods may provide a more cost-effective avenue. To date, the existing mouse Ψ site predictors were all developed based on sequence-derived features, and their performance can be further improved by adding the domain knowledge derived feature. Therefore, it is highly desirable to propose a genomic feature-based computational method to increase the accuracy and efficiency of the identification of Ψ RNA modification in the mouse transcriptome. In our study, a predictive framework PSI-MOUSE was built. Besides the conventional sequence-based features, PSI-MOUSE first introduced 38 additional genomic features derived from the mouse genome, which achieved a satisfactory improvement in the prediction performance, compared with other existing models. Moreover, PSI-MOUSE also features in automatically annotating the putative Ψ sites with diverse types of posttranscriptional regulations (RNA-binding protein [RBP]-binding regions, miRNA-RNA interactions, and splicing sites), which can serve as a useful research tool for the study of Ψ RNA modification in the mouse genome. Finally, 3282 experimentally validated mouse Ψ sites were also collected in a database with customized query functions. For the convenience of academic users, a website was built to provide a user-friendly interface for the query and analysis on the database. The website is freely accessible at www.xjtlu.edu.cn/biologicalsciences/psimouse and http://psimouse.rnamd.com. We introduced the genome-derived features to mouse for the first time, and we achieved a good performance in mouse Ψ site prediction. Compared with the existing state-of-art methods, our newly developed approach PSI-MOUSE obtained a substantial improvement in prediction accuracy, marking the reliable contributions of genomic features for the prediction of RNA modifications in a species other than human.

Identifiants

pubmed: 32565674
doi: 10.1177/1176934320925752
pii: 10.1177_1176934320925752
pmc: PMC7285933
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1176934320925752

Informations de copyright

© The Author(s) 2020.

Déclaration de conflit d'intérêts

Declaration of Conflicting Interests:The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

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Auteurs

Bowen Song (B)

Department of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou, China.

Kunqi Chen (K)

Department of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou, China.

Yujiao Tang (Y)

Department of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou, China.

Jialin Ma (J)

Cancer Genome Computational Analysis, Broad Institute of MIT and Harvard, Cambridge, MA, USA.

Jia Meng (J)

Department of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou, China.

Zhen Wei (Z)

Department of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou, China.

Classifications MeSH