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IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES)
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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893748/ https://www.ncbi.nlm.nih.gov/pubmed/27264539 http://dx.doi.org/10.1038/srep27436 |
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author | Kolekar, Pandurang Pataskar, Abhijeet Kulkarni-Kale, Urmila Pal, Jayanta Kulkarni, Abhijeet |
author_facet | Kolekar, Pandurang Pataskar, Abhijeet Kulkarni-Kale, Urmila Pal, Jayanta Kulkarni, Abhijeet |
author_sort | Kolekar, Pandurang |
collection | PubMed |
description | 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/. |
format | Online Article Text |
id | pubmed-4893748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48937482016-06-10 IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES) Kolekar, Pandurang Pataskar, Abhijeet Kulkarni-Kale, Urmila Pal, Jayanta Kulkarni, Abhijeet Sci Rep Article 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/. Nature Publishing Group 2016-06-06 /pmc/articles/PMC4893748/ /pubmed/27264539 http://dx.doi.org/10.1038/srep27436 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kolekar, Pandurang Pataskar, Abhijeet Kulkarni-Kale, Urmila Pal, Jayanta Kulkarni, Abhijeet IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES) |
title | IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES) |
title_full | IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES) |
title_fullStr | IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES) |
title_full_unstemmed | IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES) |
title_short | IRESPred: Web Server for Prediction of Cellular and Viral Internal Ribosome Entry Site (IRES) |
title_sort | irespred: web server for prediction of cellular and viral internal ribosome entry site (ires) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893748/ https://www.ncbi.nlm.nih.gov/pubmed/27264539 http://dx.doi.org/10.1038/srep27436 |
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