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RNA Editing and its Control in Hepatitis Delta Virus Replication
The hepatitis delta virus genome is a small circular RNA, similar to viroids. Although HDV contains a gene, the protein produced (HDAg) is encoded by less than half the genome and possesses no RNA polymerase activity. Because of this limited coding capacity, HDV relies heavily on host functions and...
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/PMC3185552/ https://www.ncbi.nlm.nih.gov/pubmed/21994604 http://dx.doi.org/10.3390/v2010131 |
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author | Chen, Renxiang Linnstaedt, Sarah D. Casey, John L. |
author_facet | Chen, Renxiang Linnstaedt, Sarah D. Casey, John L. |
author_sort | Chen, Renxiang |
collection | PubMed |
description | The hepatitis delta virus genome is a small circular RNA, similar to viroids. Although HDV contains a gene, the protein produced (HDAg) is encoded by less than half the genome and possesses no RNA polymerase activity. Because of this limited coding capacity, HDV relies heavily on host functions and on structural features of the viral RNA—very much like viroids. The virus’ use of host RNA editing activity to produce two functionally distinct forms of HDAg is a particularly good example of this reliance. This review covers the mechanisms and control of RNA editing in the HDV replication cycle. |
format | Online Article Text |
id | pubmed-3185552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-31855522011-10-12 RNA Editing and its Control in Hepatitis Delta Virus Replication Chen, Renxiang Linnstaedt, Sarah D. Casey, John L. Viruses Review The hepatitis delta virus genome is a small circular RNA, similar to viroids. Although HDV contains a gene, the protein produced (HDAg) is encoded by less than half the genome and possesses no RNA polymerase activity. Because of this limited coding capacity, HDV relies heavily on host functions and on structural features of the viral RNA—very much like viroids. The virus’ use of host RNA editing activity to produce two functionally distinct forms of HDAg is a particularly good example of this reliance. This review covers the mechanisms and control of RNA editing in the HDV replication cycle. Molecular Diversity Preservation International (MDPI) 2010-01-12 /pmc/articles/PMC3185552/ /pubmed/21994604 http://dx.doi.org/10.3390/v2010131 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 Chen, Renxiang Linnstaedt, Sarah D. Casey, John L. RNA Editing and its Control in Hepatitis Delta Virus Replication |
title | RNA Editing and its Control in Hepatitis Delta Virus Replication |
title_full | RNA Editing and its Control in Hepatitis Delta Virus Replication |
title_fullStr | RNA Editing and its Control in Hepatitis Delta Virus Replication |
title_full_unstemmed | RNA Editing and its Control in Hepatitis Delta Virus Replication |
title_short | RNA Editing and its Control in Hepatitis Delta Virus Replication |
title_sort | rna editing and its control in hepatitis delta virus replication |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185552/ https://www.ncbi.nlm.nih.gov/pubmed/21994604 http://dx.doi.org/10.3390/v2010131 |
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