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Stem-loop structure of Cocksfoot mottle virus RNA is indispensable for programmed −1 ribosomal frameshifting
The −1 programmed ribosomal frameshifting (−1 PRF) mechanism utilized by many viruses is dependent on a heptanucleotide slippery sequence and a downstream secondary structure element. In the current study, the RNA structure downstream from the slippery site of cocksfoot mottle sobemovirus (CfMV) was...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114514/ https://www.ncbi.nlm.nih.gov/pubmed/19748532 http://dx.doi.org/10.1016/j.virusres.2009.09.002 |
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author | Tamm, Tiina Suurväli, Jaanus Lucchesi, Jimmy Olspert, Allan Truve, Erkki |
author_facet | Tamm, Tiina Suurväli, Jaanus Lucchesi, Jimmy Olspert, Allan Truve, Erkki |
author_sort | Tamm, Tiina |
collection | PubMed |
description | The −1 programmed ribosomal frameshifting (−1 PRF) mechanism utilized by many viruses is dependent on a heptanucleotide slippery sequence and a downstream secondary structure element. In the current study, the RNA structure downstream from the slippery site of cocksfoot mottle sobemovirus (CfMV) was proven to be a 12 bp stem-loop with a single bulge and a tetranucleotide loop. Several deletion and insertion mutants with altered stem-loop structures were tested in wheat germ extract (WGE) for frameshifting efficiency. The impact of the same mutations on virus infectivity was tested in oat plants. Mutations shortening or destabilizing the stem region reduced significantly but did not abolish −1 PRF in WGE. The same mutations proved to be deleterious for virus infection. However, extending the loop region to seven nucleotides had no significant effect on frameshifting efficiency in WGE and did not hamper virus replication in infected leaves. This is the first report about the experimentally proven RNA secondary structure directing −1 PRF of sobemoviruses. |
format | Online Article Text |
id | pubmed-7114514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71145142020-04-02 Stem-loop structure of Cocksfoot mottle virus RNA is indispensable for programmed −1 ribosomal frameshifting Tamm, Tiina Suurväli, Jaanus Lucchesi, Jimmy Olspert, Allan Truve, Erkki Virus Res Article The −1 programmed ribosomal frameshifting (−1 PRF) mechanism utilized by many viruses is dependent on a heptanucleotide slippery sequence and a downstream secondary structure element. In the current study, the RNA structure downstream from the slippery site of cocksfoot mottle sobemovirus (CfMV) was proven to be a 12 bp stem-loop with a single bulge and a tetranucleotide loop. Several deletion and insertion mutants with altered stem-loop structures were tested in wheat germ extract (WGE) for frameshifting efficiency. The impact of the same mutations on virus infectivity was tested in oat plants. Mutations shortening or destabilizing the stem region reduced significantly but did not abolish −1 PRF in WGE. The same mutations proved to be deleterious for virus infection. However, extending the loop region to seven nucleotides had no significant effect on frameshifting efficiency in WGE and did not hamper virus replication in infected leaves. This is the first report about the experimentally proven RNA secondary structure directing −1 PRF of sobemoviruses. Elsevier B.V. 2009-12 2009-09-11 /pmc/articles/PMC7114514/ /pubmed/19748532 http://dx.doi.org/10.1016/j.virusres.2009.09.002 Text en Copyright © 2009 Elsevier B.V. All rights reserved. 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 | Article Tamm, Tiina Suurväli, Jaanus Lucchesi, Jimmy Olspert, Allan Truve, Erkki Stem-loop structure of Cocksfoot mottle virus RNA is indispensable for programmed −1 ribosomal frameshifting |
title | Stem-loop structure of Cocksfoot mottle virus RNA is indispensable for programmed −1 ribosomal frameshifting |
title_full | Stem-loop structure of Cocksfoot mottle virus RNA is indispensable for programmed −1 ribosomal frameshifting |
title_fullStr | Stem-loop structure of Cocksfoot mottle virus RNA is indispensable for programmed −1 ribosomal frameshifting |
title_full_unstemmed | Stem-loop structure of Cocksfoot mottle virus RNA is indispensable for programmed −1 ribosomal frameshifting |
title_short | Stem-loop structure of Cocksfoot mottle virus RNA is indispensable for programmed −1 ribosomal frameshifting |
title_sort | stem-loop structure of cocksfoot mottle virus rna is indispensable for programmed −1 ribosomal frameshifting |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114514/ https://www.ncbi.nlm.nih.gov/pubmed/19748532 http://dx.doi.org/10.1016/j.virusres.2009.09.002 |
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