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An essential RNA element resides in a central region of hepatitis E virus ORF2
Hepatitis E virus (genus Hepevirus, family Hepeviridae) is one of the most important causes of acute hepatitis in adults, particularly among pregnant women, throughout Asia and Africa where mortality rates can be 20–30 %. Hepatitis E virus has a single-stranded positive-sense RNA genome that contain...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for General Microbiology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709636/ https://www.ncbi.nlm.nih.gov/pubmed/23515023 http://dx.doi.org/10.1099/vir.0.051870-0 |
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author | Emerson, Suzanne U. Nguyen, Hanh T. Torian, Udana Mather, Karly Firth, Andrew E. |
author_facet | Emerson, Suzanne U. Nguyen, Hanh T. Torian, Udana Mather, Karly Firth, Andrew E. |
author_sort | Emerson, Suzanne U. |
collection | PubMed |
description | Hepatitis E virus (genus Hepevirus, family Hepeviridae) is one of the most important causes of acute hepatitis in adults, particularly among pregnant women, throughout Asia and Africa where mortality rates can be 20–30 %. Hepatitis E virus has a single-stranded positive-sense RNA genome that contains three translated ORFs. The two 3′ ORFs are translated from a subgenomic RNA. Functional RNA elements have been identified in and adjacent to the genomic 5′ and 3′ UTRs and in and around the intergenic region. Here we describe an additional RNA element that is located in a central region of ORF2. The RNA element is predicted to fold into two highly conserved stem–loop structures, ISL1 and ISL2. Mutations that disrupt the predicted structures, without altering the encoded amino acid sequence, result in a drastic reduction in capsid protein synthesis. This indicates that the RNA element plays an important role in one of the early steps of virus replication. The structures were further investigated using a replicon that expresses Gaussia luciferase in place of the capsid protein. Single mutations in ISL2 severely reduced luciferase expression, but a pair of compensatory mutations that were predicted to restore the ISL2 structure, restored luciferase expression to near-WT levels, thus lending experimental support to the predicted structure. Nonetheless the precise role of the ISL1+ISL2 element remains unknown. |
format | Online Article Text |
id | pubmed-3709636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Society for General Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-37096362013-07-24 An essential RNA element resides in a central region of hepatitis E virus ORF2 Emerson, Suzanne U. Nguyen, Hanh T. Torian, Udana Mather, Karly Firth, Andrew E. J Gen Virol Animal Hepatitis E virus (genus Hepevirus, family Hepeviridae) is one of the most important causes of acute hepatitis in adults, particularly among pregnant women, throughout Asia and Africa where mortality rates can be 20–30 %. Hepatitis E virus has a single-stranded positive-sense RNA genome that contains three translated ORFs. The two 3′ ORFs are translated from a subgenomic RNA. Functional RNA elements have been identified in and adjacent to the genomic 5′ and 3′ UTRs and in and around the intergenic region. Here we describe an additional RNA element that is located in a central region of ORF2. The RNA element is predicted to fold into two highly conserved stem–loop structures, ISL1 and ISL2. Mutations that disrupt the predicted structures, without altering the encoded amino acid sequence, result in a drastic reduction in capsid protein synthesis. This indicates that the RNA element plays an important role in one of the early steps of virus replication. The structures were further investigated using a replicon that expresses Gaussia luciferase in place of the capsid protein. Single mutations in ISL2 severely reduced luciferase expression, but a pair of compensatory mutations that were predicted to restore the ISL2 structure, restored luciferase expression to near-WT levels, thus lending experimental support to the predicted structure. Nonetheless the precise role of the ISL1+ISL2 element remains unknown. Society for General Microbiology 2013-07 /pmc/articles/PMC3709636/ /pubmed/23515023 http://dx.doi.org/10.1099/vir.0.051870-0 Text en © 2013 SGM http://creativecommons.org/licenses/by/2.5/ 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 work is properly cited. |
spellingShingle | Animal Emerson, Suzanne U. Nguyen, Hanh T. Torian, Udana Mather, Karly Firth, Andrew E. An essential RNA element resides in a central region of hepatitis E virus ORF2 |
title | An essential RNA element resides in a central region of hepatitis E virus ORF2 |
title_full | An essential RNA element resides in a central region of hepatitis E virus ORF2 |
title_fullStr | An essential RNA element resides in a central region of hepatitis E virus ORF2 |
title_full_unstemmed | An essential RNA element resides in a central region of hepatitis E virus ORF2 |
title_short | An essential RNA element resides in a central region of hepatitis E virus ORF2 |
title_sort | essential rna element resides in a central region of hepatitis e virus orf2 |
topic | Animal |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709636/ https://www.ncbi.nlm.nih.gov/pubmed/23515023 http://dx.doi.org/10.1099/vir.0.051870-0 |
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