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Interaction of Host Cellular Proteins with Components of the Hepatitis Delta Virus
The hepatitis delta virus (HDV) is the smallest known RNA pathogen capable of propagation in the human host and causes substantial global morbidity and mortality. Due to its small size and limited protein coding capacity, HDV is exquisitely reliant upon host cellular proteins to facilitate its trans...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International (MDPI)
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185554/ https://www.ncbi.nlm.nih.gov/pubmed/21994607 http://dx.doi.org/10.3390/v2010189 |
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author | Greco-Stewart, Valerie Pelchat, Martin |
author_facet | Greco-Stewart, Valerie Pelchat, Martin |
author_sort | Greco-Stewart, Valerie |
collection | PubMed |
description | The hepatitis delta virus (HDV) is the smallest known RNA pathogen capable of propagation in the human host and causes substantial global morbidity and mortality. Due to its small size and limited protein coding capacity, HDV is exquisitely reliant upon host cellular proteins to facilitate its transcription and replication. Remarkably, HDV does not encode an RNA-dependent RNA polymerase which is traditionally required to catalyze RNA-templated RNA synthesis. Furthermore, HDV lacks enzymes responsible for post-transcriptional and -translational modification, processes which are integral to the HDV life cycle. This review summarizes the known HDV-interacting proteins and discusses their significance in HDV biology. |
format | Online Article Text |
id | pubmed-3185554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-31855542011-10-12 Interaction of Host Cellular Proteins with Components of the Hepatitis Delta Virus Greco-Stewart, Valerie Pelchat, Martin Viruses Review The hepatitis delta virus (HDV) is the smallest known RNA pathogen capable of propagation in the human host and causes substantial global morbidity and mortality. Due to its small size and limited protein coding capacity, HDV is exquisitely reliant upon host cellular proteins to facilitate its transcription and replication. Remarkably, HDV does not encode an RNA-dependent RNA polymerase which is traditionally required to catalyze RNA-templated RNA synthesis. Furthermore, HDV lacks enzymes responsible for post-transcriptional and -translational modification, processes which are integral to the HDV life cycle. This review summarizes the known HDV-interacting proteins and discusses their significance in HDV biology. Molecular Diversity Preservation International (MDPI) 2010-01-18 /pmc/articles/PMC3185554/ /pubmed/21994607 http://dx.doi.org/10.3390/v2010189 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Greco-Stewart, Valerie Pelchat, Martin Interaction of Host Cellular Proteins with Components of the Hepatitis Delta Virus |
title | Interaction of Host Cellular Proteins with Components of the Hepatitis Delta Virus |
title_full | Interaction of Host Cellular Proteins with Components of the Hepatitis Delta Virus |
title_fullStr | Interaction of Host Cellular Proteins with Components of the Hepatitis Delta Virus |
title_full_unstemmed | Interaction of Host Cellular Proteins with Components of the Hepatitis Delta Virus |
title_short | Interaction of Host Cellular Proteins with Components of the Hepatitis Delta Virus |
title_sort | interaction of host cellular proteins with components of the hepatitis delta virus |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185554/ https://www.ncbi.nlm.nih.gov/pubmed/21994607 http://dx.doi.org/10.3390/v2010189 |
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