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Sequence analysis of the bovine coronavirus nucleocapsid and matrix protein genes
The 3′ end of the 20-kb genome of the Mebus strain of bovine enteric coronavirus (BCV) was copied into cDNA and cloned into the PstI site of the pUC9 vector. Four clones from the 3′ end of the genome were sequenced either completely or in part to determine the sequence of the first 2451 bases. Withi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc.
1987
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130558/ https://www.ncbi.nlm.nih.gov/pubmed/3029965 http://dx.doi.org/10.1016/0042-6822(87)90312-6 |
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author | Lapps, William Hogue, Brenda G. Brian, David A. |
author_facet | Lapps, William Hogue, Brenda G. Brian, David A. |
author_sort | Lapps, William |
collection | PubMed |
description | The 3′ end of the 20-kb genome of the Mebus strain of bovine enteric coronavirus (BCV) was copied into cDNA and cloned into the PstI site of the pUC9 vector. Four clones from the 3′ end of the genome were sequenced either completely or in part to determine the sequence of the first 2451 bases. Within this sequence were identified, in order, a 3′-noncoding region of 291 bases, the gene for a 448-amino acid nucleocapsid protein (N) having a molecular weight of 49,379, and the gene for a 230-amino acid matrix protein (M) having a molecular weight of 26,376. A third large open reading frame is contained entirely within the N gene sequence but is positioned in a different reading frame; it potentially encodes a polypeptide of 207 amino acids having a molecular weight of 23,057. A higher degree of amino acid sequence homology was found between the M proteins of BCV and MHV (87%) than between the N proteins (70%). For the M proteins of BCV and MHV, notable differences were found at the amino terminus, the most probable site of O-glycosylation, where the sequence is N-Met-Ser-Ser-Val-Thr-Thr for BCV and N-Met-Ser-Ser-Thr-Thr for MHV. BCV apparently uses two of its six potential O-glycosylation sites. |
format | Online Article Text |
id | pubmed-7130558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1987 |
publisher | Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71305582020-04-08 Sequence analysis of the bovine coronavirus nucleocapsid and matrix protein genes Lapps, William Hogue, Brenda G. Brian, David A. Virology Article The 3′ end of the 20-kb genome of the Mebus strain of bovine enteric coronavirus (BCV) was copied into cDNA and cloned into the PstI site of the pUC9 vector. Four clones from the 3′ end of the genome were sequenced either completely or in part to determine the sequence of the first 2451 bases. Within this sequence were identified, in order, a 3′-noncoding region of 291 bases, the gene for a 448-amino acid nucleocapsid protein (N) having a molecular weight of 49,379, and the gene for a 230-amino acid matrix protein (M) having a molecular weight of 26,376. A third large open reading frame is contained entirely within the N gene sequence but is positioned in a different reading frame; it potentially encodes a polypeptide of 207 amino acids having a molecular weight of 23,057. A higher degree of amino acid sequence homology was found between the M proteins of BCV and MHV (87%) than between the N proteins (70%). For the M proteins of BCV and MHV, notable differences were found at the amino terminus, the most probable site of O-glycosylation, where the sequence is N-Met-Ser-Ser-Val-Thr-Thr for BCV and N-Met-Ser-Ser-Thr-Thr for MHV. BCV apparently uses two of its six potential O-glycosylation sites. Published by Elsevier Inc. 1987-03 2004-02-06 /pmc/articles/PMC7130558/ /pubmed/3029965 http://dx.doi.org/10.1016/0042-6822(87)90312-6 Text en Copyright © 1987 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 | Article Lapps, William Hogue, Brenda G. Brian, David A. Sequence analysis of the bovine coronavirus nucleocapsid and matrix protein genes |
title | Sequence analysis of the bovine coronavirus nucleocapsid and matrix protein genes |
title_full | Sequence analysis of the bovine coronavirus nucleocapsid and matrix protein genes |
title_fullStr | Sequence analysis of the bovine coronavirus nucleocapsid and matrix protein genes |
title_full_unstemmed | Sequence analysis of the bovine coronavirus nucleocapsid and matrix protein genes |
title_short | Sequence analysis of the bovine coronavirus nucleocapsid and matrix protein genes |
title_sort | sequence analysis of the bovine coronavirus nucleocapsid and matrix protein genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130558/ https://www.ncbi.nlm.nih.gov/pubmed/3029965 http://dx.doi.org/10.1016/0042-6822(87)90312-6 |
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