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Detailed structural analysis of a genome rearrangement in bovine rotavirus

A genome rearrangement involving RNA segment 11 of a bovine rotavirus has been analysed by molecular cloning and sequencing. This revealed that the rearranged genome segment was generated by a head to tail concatemerisation of two almost full length copies of segment 11. The upstream copy of the gen...

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Detalles Bibliográficos
Autores principales: Scott, G.E., Tarlow, O., McCrae, M.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier B.V. 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133935/
https://www.ncbi.nlm.nih.gov/pubmed/2558459
http://dx.doi.org/10.1016/0168-1702(89)90033-6
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author Scott, G.E.
Tarlow, O.
McCrae, M.A.
author_facet Scott, G.E.
Tarlow, O.
McCrae, M.A.
author_sort Scott, G.E.
collection PubMed
description A genome rearrangement involving RNA segment 11 of a bovine rotavirus has been analysed by molecular cloning and sequencing. This revealed that the rearranged genome segment was generated by a head to tail concatemerisation of two almost full length copies of segment 11. The upstream copy of the gene has lost its 3' end and the downstream copy its 5' end. The truncation of the upstream copy of the gene occurs within the termination codon for VP11 converting it from a UAG to a UGA, the rearranged gene is therefore still able to encode a normal VP11. The possible mechanisms by which this rearrangement may have been generated are discussed.
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spelling pubmed-71339352020-04-08 Detailed structural analysis of a genome rearrangement in bovine rotavirus Scott, G.E. Tarlow, O. McCrae, M.A. Virus Res Article A genome rearrangement involving RNA segment 11 of a bovine rotavirus has been analysed by molecular cloning and sequencing. This revealed that the rearranged genome segment was generated by a head to tail concatemerisation of two almost full length copies of segment 11. The upstream copy of the gene has lost its 3' end and the downstream copy its 5' end. The truncation of the upstream copy of the gene occurs within the termination codon for VP11 converting it from a UAG to a UGA, the rearranged gene is therefore still able to encode a normal VP11. The possible mechanisms by which this rearrangement may have been generated are discussed. Published by Elsevier B.V. 1989-10 2002-11-12 /pmc/articles/PMC7133935/ /pubmed/2558459 http://dx.doi.org/10.1016/0168-1702(89)90033-6 Text en Copyright © 1989 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
Scott, G.E.
Tarlow, O.
McCrae, M.A.
Detailed structural analysis of a genome rearrangement in bovine rotavirus
title Detailed structural analysis of a genome rearrangement in bovine rotavirus
title_full Detailed structural analysis of a genome rearrangement in bovine rotavirus
title_fullStr Detailed structural analysis of a genome rearrangement in bovine rotavirus
title_full_unstemmed Detailed structural analysis of a genome rearrangement in bovine rotavirus
title_short Detailed structural analysis of a genome rearrangement in bovine rotavirus
title_sort detailed structural analysis of a genome rearrangement in bovine rotavirus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7133935/
https://www.ncbi.nlm.nih.gov/pubmed/2558459
http://dx.doi.org/10.1016/0168-1702(89)90033-6
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