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Rearrangement of viral sequences in cytopathogenic pestiviruses()
Two cytopathogenic isolates of bovine viral diarrhea virus (cpBVDV) have been analyzed. For both viruses two regions of their genomic RNAs were found to be duplicated and rearranged. The viral genomes contain a small duplicated element (SD) derived from the genomic 5' end far downstream of its...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc.
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131167/ https://www.ncbi.nlm.nih.gov/pubmed/1329326 http://dx.doi.org/10.1016/0042-6822(92)90199-Y |
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author | Meyers, Gregor Tautz, Norbert Stark, Robert Brownlie, Joe Dubovi, Edward J. Collett, Marc S. Thiel, Heinz-Jürgen |
author_facet | Meyers, Gregor Tautz, Norbert Stark, Robert Brownlie, Joe Dubovi, Edward J. Collett, Marc S. Thiel, Heinz-Jürgen |
author_sort | Meyers, Gregor |
collection | PubMed |
description | Two cytopathogenic isolates of bovine viral diarrhea virus (cpBVDV) have been analyzed. For both viruses two regions of their genomic RNAs were found to be duplicated and rearranged. The viral genomes contain a small duplicated element (SD) derived from the genomic 5' end far downstream of its original context. This sequence is followed by a larger duplication which encompasses the region coding for the protein p80(LD), a molecular marker for cpBVDV. The SD element codes for the viral protease p20. In the case of the viruses analyzed here the aminoterminus of p80 is generated by autoproteolytic removal of the preceding SD-encoded protease. For one of the cpBVDV isolates a specific fusion protein (p28) could be identified which is composed of p20 and part of p10, another viral protein. Molecular characterization of the respective noncytopathogenic counterpart revealed that duplication and rearrangement of sequences as well as the expression of p28 and p80 are specific for the cytopathogenic virus. |
format | Online Article Text |
id | pubmed-7131167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71311672020-04-08 Rearrangement of viral sequences in cytopathogenic pestiviruses() Meyers, Gregor Tautz, Norbert Stark, Robert Brownlie, Joe Dubovi, Edward J. Collett, Marc S. Thiel, Heinz-Jürgen Virology Regular Article Two cytopathogenic isolates of bovine viral diarrhea virus (cpBVDV) have been analyzed. For both viruses two regions of their genomic RNAs were found to be duplicated and rearranged. The viral genomes contain a small duplicated element (SD) derived from the genomic 5' end far downstream of its original context. This sequence is followed by a larger duplication which encompasses the region coding for the protein p80(LD), a molecular marker for cpBVDV. The SD element codes for the viral protease p20. In the case of the viruses analyzed here the aminoterminus of p80 is generated by autoproteolytic removal of the preceding SD-encoded protease. For one of the cpBVDV isolates a specific fusion protein (p28) could be identified which is composed of p20 and part of p10, another viral protein. Molecular characterization of the respective noncytopathogenic counterpart revealed that duplication and rearrangement of sequences as well as the expression of p28 and p80 are specific for the cytopathogenic virus. Published by Elsevier Inc. 1992-11 2004-02-11 /pmc/articles/PMC7131167/ /pubmed/1329326 http://dx.doi.org/10.1016/0042-6822(92)90199-Y Text en Copyright © 1992 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Regular Article Meyers, Gregor Tautz, Norbert Stark, Robert Brownlie, Joe Dubovi, Edward J. Collett, Marc S. Thiel, Heinz-Jürgen Rearrangement of viral sequences in cytopathogenic pestiviruses() |
title | Rearrangement of viral sequences in cytopathogenic pestiviruses() |
title_full | Rearrangement of viral sequences in cytopathogenic pestiviruses() |
title_fullStr | Rearrangement of viral sequences in cytopathogenic pestiviruses() |
title_full_unstemmed | Rearrangement of viral sequences in cytopathogenic pestiviruses() |
title_short | Rearrangement of viral sequences in cytopathogenic pestiviruses() |
title_sort | rearrangement of viral sequences in cytopathogenic pestiviruses() |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131167/ https://www.ncbi.nlm.nih.gov/pubmed/1329326 http://dx.doi.org/10.1016/0042-6822(92)90199-Y |
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