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Molecular Basis of Encapsidation of Hepatitis C Virus Genome

Hepatitis C virus (HCV), a major etiologic agent of human liver diseases, is a positive-sense single-stranded RNA virus and is classified in the Flaviviridae family. Although research findings for the assembly of HCV particles are accumulating due to development of HCV cell culture system, the mecha...

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Autores principales: Shi, Guoli, Suzuki, Tetsuro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845887/
https://www.ncbi.nlm.nih.gov/pubmed/29563905
http://dx.doi.org/10.3389/fmicb.2018.00396
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author Shi, Guoli
Suzuki, Tetsuro
author_facet Shi, Guoli
Suzuki, Tetsuro
author_sort Shi, Guoli
collection PubMed
description Hepatitis C virus (HCV), a major etiologic agent of human liver diseases, is a positive-sense single-stranded RNA virus and is classified in the Flaviviridae family. Although research findings for the assembly of HCV particles are accumulating due to development of HCV cell culture system, the mechanism(s) by which the HCV genome becomes encapsidated remains largely unclear. In general, viral RNA represents only a small fraction of the RNA molecules in the cells infected with RNA viruses, but the viral genomic RNA is considered to selectively packaged into virions. It was recently demonstrated that HCV RNAs containing 3′ end of the genome are selectively incorporated into virus particles during the assembly process and the 3′ untranslated region functions as a cis-acting element for RNA packaging. Here, we discuss the molecular basis of RNA encapsidation of HCV and classical flaviviruses, contrast with the packaging mechanism of HIV-1.
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spelling pubmed-58458872018-03-21 Molecular Basis of Encapsidation of Hepatitis C Virus Genome Shi, Guoli Suzuki, Tetsuro Front Microbiol Microbiology Hepatitis C virus (HCV), a major etiologic agent of human liver diseases, is a positive-sense single-stranded RNA virus and is classified in the Flaviviridae family. Although research findings for the assembly of HCV particles are accumulating due to development of HCV cell culture system, the mechanism(s) by which the HCV genome becomes encapsidated remains largely unclear. In general, viral RNA represents only a small fraction of the RNA molecules in the cells infected with RNA viruses, but the viral genomic RNA is considered to selectively packaged into virions. It was recently demonstrated that HCV RNAs containing 3′ end of the genome are selectively incorporated into virus particles during the assembly process and the 3′ untranslated region functions as a cis-acting element for RNA packaging. Here, we discuss the molecular basis of RNA encapsidation of HCV and classical flaviviruses, contrast with the packaging mechanism of HIV-1. Frontiers Media S.A. 2018-03-07 /pmc/articles/PMC5845887/ /pubmed/29563905 http://dx.doi.org/10.3389/fmicb.2018.00396 Text en Copyright © 2018 Shi and Suzuki. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Shi, Guoli
Suzuki, Tetsuro
Molecular Basis of Encapsidation of Hepatitis C Virus Genome
title Molecular Basis of Encapsidation of Hepatitis C Virus Genome
title_full Molecular Basis of Encapsidation of Hepatitis C Virus Genome
title_fullStr Molecular Basis of Encapsidation of Hepatitis C Virus Genome
title_full_unstemmed Molecular Basis of Encapsidation of Hepatitis C Virus Genome
title_short Molecular Basis of Encapsidation of Hepatitis C Virus Genome
title_sort molecular basis of encapsidation of hepatitis c virus genome
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845887/
https://www.ncbi.nlm.nih.gov/pubmed/29563905
http://dx.doi.org/10.3389/fmicb.2018.00396
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