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HCVIVdb: The hepatitis-C IRES variation database

BACKGROUND: Sequence variability in the hepatitis C virus (HCV) genome has led to the development and classification of six genotypes and a number of subtypes. The HCV 5′ untranslated region mainly comprises an internal ribosomal entry site (IRES) responsible for cap-independent synthesis of the vir...

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Autores principales: Floden, Evan W., Khawaja, Anas, Vopálenský, Václav, Pospíšek, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986321/
https://www.ncbi.nlm.nih.gov/pubmed/27527702
http://dx.doi.org/10.1186/s12866-016-0804-6
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author Floden, Evan W.
Khawaja, Anas
Vopálenský, Václav
Pospíšek, Martin
author_facet Floden, Evan W.
Khawaja, Anas
Vopálenský, Václav
Pospíšek, Martin
author_sort Floden, Evan W.
collection PubMed
description BACKGROUND: Sequence variability in the hepatitis C virus (HCV) genome has led to the development and classification of six genotypes and a number of subtypes. The HCV 5′ untranslated region mainly comprises an internal ribosomal entry site (IRES) responsible for cap-independent synthesis of the viral polyprotein and is conserved among all HCV genotypes. DESCRIPTION: Considering the possible high impact of variations in HCV IRES on viral protein production and thus virus replication, we decided to collect the available data on known nucleotide variants in the HCV IRES and their impact on IRES function in translation initiation. The HCV IRES variation database (HCVIVdb) is a collection of naturally occurring and engineered mutation entries for the HCV IRES. Each entry contains contextual information pertaining to the entry such as the HCV genotypic background and links to the original publication. Where available, quantitative data on the IRES efficiency in translation have been collated along with details on the reporter system used to generate the data. Data are displayed both in a tabular and graphical formats and allow direct comparison of results from different experiments. Together the data provide a central resource for researchers in the IRES and hepatitis C-oriented fields. CONCLUSION: The collation of over 1900 mutations enables systematic analysis of the HCV IRES. The database is mainly dedicated to detailed comparative and functional analysis of all the HCV IRES domains, which can further lead to the development of site-specific drug designs and provide a guide for future experiments. HCVIVdb is available at http://www.hcvivdb.org. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0804-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-49863212016-08-17 HCVIVdb: The hepatitis-C IRES variation database Floden, Evan W. Khawaja, Anas Vopálenský, Václav Pospíšek, Martin BMC Microbiol Database BACKGROUND: Sequence variability in the hepatitis C virus (HCV) genome has led to the development and classification of six genotypes and a number of subtypes. The HCV 5′ untranslated region mainly comprises an internal ribosomal entry site (IRES) responsible for cap-independent synthesis of the viral polyprotein and is conserved among all HCV genotypes. DESCRIPTION: Considering the possible high impact of variations in HCV IRES on viral protein production and thus virus replication, we decided to collect the available data on known nucleotide variants in the HCV IRES and their impact on IRES function in translation initiation. The HCV IRES variation database (HCVIVdb) is a collection of naturally occurring and engineered mutation entries for the HCV IRES. Each entry contains contextual information pertaining to the entry such as the HCV genotypic background and links to the original publication. Where available, quantitative data on the IRES efficiency in translation have been collated along with details on the reporter system used to generate the data. Data are displayed both in a tabular and graphical formats and allow direct comparison of results from different experiments. Together the data provide a central resource for researchers in the IRES and hepatitis C-oriented fields. CONCLUSION: The collation of over 1900 mutations enables systematic analysis of the HCV IRES. The database is mainly dedicated to detailed comparative and functional analysis of all the HCV IRES domains, which can further lead to the development of site-specific drug designs and provide a guide for future experiments. HCVIVdb is available at http://www.hcvivdb.org. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0804-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-15 /pmc/articles/PMC4986321/ /pubmed/27527702 http://dx.doi.org/10.1186/s12866-016-0804-6 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Database
Floden, Evan W.
Khawaja, Anas
Vopálenský, Václav
Pospíšek, Martin
HCVIVdb: The hepatitis-C IRES variation database
title HCVIVdb: The hepatitis-C IRES variation database
title_full HCVIVdb: The hepatitis-C IRES variation database
title_fullStr HCVIVdb: The hepatitis-C IRES variation database
title_full_unstemmed HCVIVdb: The hepatitis-C IRES variation database
title_short HCVIVdb: The hepatitis-C IRES variation database
title_sort hcvivdb: the hepatitis-c ires variation database
topic Database
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986321/
https://www.ncbi.nlm.nih.gov/pubmed/27527702
http://dx.doi.org/10.1186/s12866-016-0804-6
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