» Articles » PMID: 27264539

IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES)

Overview
Journal Sci Rep
Specialty Science
Date 2016 Jun 7
PMID 27264539
Citations 36
Authors
Affiliations
Soon will be listed here.
Abstract

Cellular mRNAs are predominantly translated in a cap-dependent manner. However, some viral and a subset of cellular mRNAs initiate their translation in a cap-independent manner. This requires presence of a structured RNA element, known as, Internal Ribosome Entry Site (IRES) in their 5' untranslated regions (UTRs). Experimental demonstration of IRES in UTR remains a challenging task. Computational prediction of IRES merely based on sequence and structure conservation is also difficult, particularly for cellular IRES. A web server, IRESPred is developed for prediction of both viral and cellular IRES using Support Vector Machine (SVM). The predictive model was built using 35 features that are based on sequence and structural properties of UTRs and the probabilities of interactions between UTR and small subunit ribosomal proteins (SSRPs). The model was found to have 75.51% accuracy, 75.75% sensitivity, 75.25% specificity, 75.75% precision and Matthews Correlation Coefficient (MCC) of 0.51 in blind testing. IRESPred was found to perform better than the only available viral IRES prediction server, VIPS. The IRESPred server is freely available at http://bioinfo.net.in/IRESPred/.

Citing Articles

Long non-coding RNA-encoded micropeptides: functions, mechanisms and implications.

Xiao Y, Ren Y, Hu W, Paliouras A, Zhang W, Zhong L Cell Death Discov. 2024; 10(1):450.

PMID: 39443468 PMC: 11499885. DOI: 10.1038/s41420-024-02175-0.


DeepIRES: a hybrid deep learning model for accurate identification of internal ribosome entry sites in cellular and viral mRNAs.

Zhao J, Chen Z, Zhang M, Zou L, He S, Liu J Brief Bioinform. 2024; 25(5).

PMID: 39234953 PMC: 11375421. DOI: 10.1093/bib/bbae439.


A 5' UTR Language Model for Decoding Untranslated Regions of mRNA and Function Predictions.

Chu Y, Yu D, Li Y, Huang K, Shen Y, Cong L Nat Mach Intell. 2024; 6(4):449-460.

PMID: 38855263 PMC: 11155392. DOI: 10.1038/s42256-024-00823-9.


Host-like RNA Elements Regulate Virus Translation.

Khan D, Fox P Viruses. 2024; 16(3).

PMID: 38543832 PMC: 10976276. DOI: 10.3390/v16030468.


The Unique Genome of the Virus and Alternative Strategies for its Realization.

Zhirnov O Acta Naturae. 2023; 15(2):14-19.

PMID: 37538802 PMC: 10395775. DOI: 10.32607/actanaturae.11904.


References
1.
Thompson S . Tricks an IRES uses to enslave ribosomes. Trends Microbiol. 2012; 20(11):558-66. PMC: 3479354. DOI: 10.1016/j.tim.2012.08.002. View

2.
Otto G, Lukavsky P, Lancaster A, Sarnow P, Puglisi J . Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction. RNA. 2002; 8(7):913-23. PMC: 1370308. DOI: 10.1017/s1355838202022057. View

3.
Mokrejs M, Masek T, Vopalensky V, Hlubucek P, Delbos P, Pospisek M . IRESite--a tool for the examination of viral and cellular internal ribosome entry sites. Nucleic Acids Res. 2009; 38(Database issue):D131-6. PMC: 2808886. DOI: 10.1093/nar/gkp981. View

4.
Guerniou V, Gillet R, Berree F, Carboni B, Felden B . Targeted inhibition of the hepatitis C internal ribosomal entry site genomic RNA with oligonucleotide conjugates. Nucleic Acids Res. 2007; 35(20):6778-87. PMC: 2175329. DOI: 10.1093/nar/gkm770. View

5.
Komar A, Mazumder B, Merrick W . A new framework for understanding IRES-mediated translation. Gene. 2012; 502(2):75-86. PMC: 3361623. DOI: 10.1016/j.gene.2012.04.039. View