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Bovine coronavirus I protein synthesis follows ribosomal scanning on the bicistronic N mRNA

The mRNA encoding the 49-kDa nucleocapsid protein (N) of the bovine coronavirus is bicistronic. A 23-kDa protein, termed the I protein for the ‘internal’ open reading frame (ORF), is also synthesized but in the +1 reading frame beginning 61 nt downstream of the N start codon. Sequences flanking the...

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Detalles Bibliográficos
Autores principales: Senanayake, Savithra D., Brian, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134031/
https://www.ncbi.nlm.nih.gov/pubmed/9140198
http://dx.doi.org/10.1016/S0168-1702(96)01423-2
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author Senanayake, Savithra D.
Brian, David A.
author_facet Senanayake, Savithra D.
Brian, David A.
author_sort Senanayake, Savithra D.
collection PubMed
description The mRNA encoding the 49-kDa nucleocapsid protein (N) of the bovine coronavirus is bicistronic. A 23-kDa protein, termed the I protein for the ‘internal’ open reading frame (ORF), is also synthesized but in the +1 reading frame beginning 61 nt downstream of the N start codon. Sequences flanking the N and I start codons suggest that the I ORF might be accessed by scanning ribosomes passing over the N start codon. Here we test this idea and demonstrate with translation studies both in vitro and in vivo that the I protein is synthesized according to the leaky scanning model for initiation of translation on the subgenomic N mRNA molecule.
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spelling pubmed-71340312020-04-08 Bovine coronavirus I protein synthesis follows ribosomal scanning on the bicistronic N mRNA Senanayake, Savithra D. Brian, David A. Virus Res Article The mRNA encoding the 49-kDa nucleocapsid protein (N) of the bovine coronavirus is bicistronic. A 23-kDa protein, termed the I protein for the ‘internal’ open reading frame (ORF), is also synthesized but in the +1 reading frame beginning 61 nt downstream of the N start codon. Sequences flanking the N and I start codons suggest that the I ORF might be accessed by scanning ribosomes passing over the N start codon. Here we test this idea and demonstrate with translation studies both in vitro and in vivo that the I protein is synthesized according to the leaky scanning model for initiation of translation on the subgenomic N mRNA molecule. Published by Elsevier B.V. 1997-04 1998-10-06 /pmc/articles/PMC7134031/ /pubmed/9140198 http://dx.doi.org/10.1016/S0168-1702(96)01423-2 Text en Copyright © 1997 Published by Elsevier B.V. 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
Senanayake, Savithra D.
Brian, David A.
Bovine coronavirus I protein synthesis follows ribosomal scanning on the bicistronic N mRNA
title Bovine coronavirus I protein synthesis follows ribosomal scanning on the bicistronic N mRNA
title_full Bovine coronavirus I protein synthesis follows ribosomal scanning on the bicistronic N mRNA
title_fullStr Bovine coronavirus I protein synthesis follows ribosomal scanning on the bicistronic N mRNA
title_full_unstemmed Bovine coronavirus I protein synthesis follows ribosomal scanning on the bicistronic N mRNA
title_short Bovine coronavirus I protein synthesis follows ribosomal scanning on the bicistronic N mRNA
title_sort bovine coronavirus i protein synthesis follows ribosomal scanning on the bicistronic n mrna
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134031/
https://www.ncbi.nlm.nih.gov/pubmed/9140198
http://dx.doi.org/10.1016/S0168-1702(96)01423-2
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