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Hepatitis C Virus-Induced Cytoplasmic Organelles Use the Nuclear Transport Machinery to Establish an Environment Conducive to Virus Replication
Hepatitis C virus (HCV) infection induces formation of a membranous web structure in the host cell cytoplasm where the viral genome replicates and virions assemble. The membranous web is thought to concentrate viral components and hide viral RNA from pattern recognition receptors. We have uncovered...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814334/ https://www.ncbi.nlm.nih.gov/pubmed/24204278 http://dx.doi.org/10.1371/journal.ppat.1003744 |
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author | Neufeldt, Christopher J. Joyce, Michael A. Levin, Aviad Steenbergen, Rineke H. Pang, Daniel Shields, Justin Tyrrell, D. Lorne J. Wozniak, Richard W. |
author_facet | Neufeldt, Christopher J. Joyce, Michael A. Levin, Aviad Steenbergen, Rineke H. Pang, Daniel Shields, Justin Tyrrell, D. Lorne J. Wozniak, Richard W. |
author_sort | Neufeldt, Christopher J. |
collection | PubMed |
description | Hepatitis C virus (HCV) infection induces formation of a membranous web structure in the host cell cytoplasm where the viral genome replicates and virions assemble. The membranous web is thought to concentrate viral components and hide viral RNA from pattern recognition receptors. We have uncovered a role for nuclear pore complex proteins (Nups) and nuclear transport factors (NTFs) in the membranous web. We show that HCV infection leads to increased levels of cytoplasmic Nups that accumulate at sites enriched for HCV proteins. Moreover, we detected interactions between specific HCV proteins and both Nups and NTFs. We hypothesize that cytoplasmically positioned Nups facilitate formation of the membranous web and contribute to the compartmentalization of viral replication. Accordingly, we show that transport cargo proteins normally targeted to the nucleus are capable of entering regions of the membranous web, and that depletion of specific Nups or Kaps inhibits HCV replication and assembly. |
format | Online Article Text |
id | pubmed-3814334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38143342013-11-07 Hepatitis C Virus-Induced Cytoplasmic Organelles Use the Nuclear Transport Machinery to Establish an Environment Conducive to Virus Replication Neufeldt, Christopher J. Joyce, Michael A. Levin, Aviad Steenbergen, Rineke H. Pang, Daniel Shields, Justin Tyrrell, D. Lorne J. Wozniak, Richard W. PLoS Pathog Research Article Hepatitis C virus (HCV) infection induces formation of a membranous web structure in the host cell cytoplasm where the viral genome replicates and virions assemble. The membranous web is thought to concentrate viral components and hide viral RNA from pattern recognition receptors. We have uncovered a role for nuclear pore complex proteins (Nups) and nuclear transport factors (NTFs) in the membranous web. We show that HCV infection leads to increased levels of cytoplasmic Nups that accumulate at sites enriched for HCV proteins. Moreover, we detected interactions between specific HCV proteins and both Nups and NTFs. We hypothesize that cytoplasmically positioned Nups facilitate formation of the membranous web and contribute to the compartmentalization of viral replication. Accordingly, we show that transport cargo proteins normally targeted to the nucleus are capable of entering regions of the membranous web, and that depletion of specific Nups or Kaps inhibits HCV replication and assembly. Public Library of Science 2013-10-31 /pmc/articles/PMC3814334/ /pubmed/24204278 http://dx.doi.org/10.1371/journal.ppat.1003744 Text en © 2013 Neufeldt et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Neufeldt, Christopher J. Joyce, Michael A. Levin, Aviad Steenbergen, Rineke H. Pang, Daniel Shields, Justin Tyrrell, D. Lorne J. Wozniak, Richard W. Hepatitis C Virus-Induced Cytoplasmic Organelles Use the Nuclear Transport Machinery to Establish an Environment Conducive to Virus Replication |
title | Hepatitis C Virus-Induced Cytoplasmic Organelles Use the Nuclear Transport Machinery to Establish an Environment Conducive to Virus Replication |
title_full | Hepatitis C Virus-Induced Cytoplasmic Organelles Use the Nuclear Transport Machinery to Establish an Environment Conducive to Virus Replication |
title_fullStr | Hepatitis C Virus-Induced Cytoplasmic Organelles Use the Nuclear Transport Machinery to Establish an Environment Conducive to Virus Replication |
title_full_unstemmed | Hepatitis C Virus-Induced Cytoplasmic Organelles Use the Nuclear Transport Machinery to Establish an Environment Conducive to Virus Replication |
title_short | Hepatitis C Virus-Induced Cytoplasmic Organelles Use the Nuclear Transport Machinery to Establish an Environment Conducive to Virus Replication |
title_sort | hepatitis c virus-induced cytoplasmic organelles use the nuclear transport machinery to establish an environment conducive to virus replication |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814334/ https://www.ncbi.nlm.nih.gov/pubmed/24204278 http://dx.doi.org/10.1371/journal.ppat.1003744 |
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