Human coronavirus OC43 RNA 4 lacks two open reading frames located downstream of the S gene of bovine coronavirus.
Identifieur interne : 000D89 ( PubMed/Corpus ); précédent : 000D88; suivant : 000D90Human coronavirus OC43 RNA 4 lacks two open reading frames located downstream of the S gene of bovine coronavirus.
Auteurs : S. Mounir ; P J TalbotSource :
- Virology [ 0042-6822 ] ; 1993.
English descriptors
- KwdEn :
- Amino Acid Sequence, Animals, Cattle, Codon, Consensus Sequence, Coronaviridae (genetics), Genes, Viral, Humans, Molecular Sequence Data, Open Reading Frames, Peptide Chain Initiation, Translational, RNA, Messenger (genetics), RNA, Viral (genetics), Species Specificity, Viral Nonstructural Proteins (genetics), Viral Proteins (genetics), Viral Structural Proteins (genetics).
- MESH :
- chemical , genetics : RNA, Messenger, RNA, Viral, Viral Nonstructural Proteins, Viral Proteins, Viral Structural Proteins.
- chemical : Codon.
- genetics : Coronaviridae.
- Amino Acid Sequence, Animals, Cattle, Consensus Sequence, Genes, Viral, Humans, Molecular Sequence Data, Open Reading Frames, Peptide Chain Initiation, Translational, Species Specificity.
Abstract
Nucleotide sequences between the spike (S) and membrane (M) protein genes of the OC43 strain of human corona-virus were obtained from PCR-amplified viral mRNAs. Sequence analysis of this region revealed the presence of two ORFs encoding proteins of 12.9 and 9.5 kDa. These two proteins were identified as putatively nonstructural (ns) due to their homology to the corresponding BCV ns gene products. Northern blot analysis indicated that each of these two genes was present on a separate mRNA (5 and 5-1, respectively). In vitro translation analyses demonstrated that the HCV-OC43 9.5-kDa protein, like its BCV counterpart, is poorly translated when situated downstream of the 12.9-kDa ORF, although immunofluorescence studies did confirm its presence in infected cells. Sequence analysis showed that a large portion of the 3'-end of the leader sequence is present within the viral genome, upstream of the 12.9-kDa ORF. In addition, two ORFs encoding potential 4.9- and 4.8-kDa ns proteins in BCV are absent in HCV-OC43, although a corresponding mRNA 4 was found at a very low level. These results demonstrate that these two putative ns proteins are not essential for virus replication, at least in HRT-18 cells.
DOI: 10.1006/viro.1993.1043
PubMed: 8517026
Links to Exploration step
pubmed:8517026Le document en format XML
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<author><name sortKey="Mounir, S" sort="Mounir, S" uniqKey="Mounir S" first="S" last="Mounir">S. Mounir</name>
<affiliation><nlm:affiliation>Virology Research Center, Institut Armand-Frappier, Université du Québec, Laval, Canada.</nlm:affiliation>
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<author><name sortKey="Talbot, P J" sort="Talbot, P J" uniqKey="Talbot P" first="P J" last="Talbot">P J Talbot</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Human coronavirus OC43 RNA 4 lacks two open reading frames located downstream of the S gene of bovine coronavirus.</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amino Acid Sequence</term>
<term>Animals</term>
<term>Cattle</term>
<term>Codon</term>
<term>Consensus Sequence</term>
<term>Coronaviridae (genetics)</term>
<term>Genes, Viral</term>
<term>Humans</term>
<term>Molecular Sequence Data</term>
<term>Open Reading Frames</term>
<term>Peptide Chain Initiation, Translational</term>
<term>RNA, Messenger (genetics)</term>
<term>RNA, Viral (genetics)</term>
<term>Species Specificity</term>
<term>Viral Nonstructural Proteins (genetics)</term>
<term>Viral Proteins (genetics)</term>
<term>Viral Structural Proteins (genetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>RNA, Messenger</term>
<term>RNA, Viral</term>
<term>Viral Nonstructural Proteins</term>
<term>Viral Proteins</term>
<term>Viral Structural Proteins</term>
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<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Codon</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Coronaviridae</term>
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<keywords scheme="MESH" xml:lang="en"><term>Amino Acid Sequence</term>
<term>Animals</term>
<term>Cattle</term>
<term>Consensus Sequence</term>
<term>Genes, Viral</term>
<term>Humans</term>
<term>Molecular Sequence Data</term>
<term>Open Reading Frames</term>
<term>Peptide Chain Initiation, Translational</term>
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<front><div type="abstract" xml:lang="en">Nucleotide sequences between the spike (S) and membrane (M) protein genes of the OC43 strain of human corona-virus were obtained from PCR-amplified viral mRNAs. Sequence analysis of this region revealed the presence of two ORFs encoding proteins of 12.9 and 9.5 kDa. These two proteins were identified as putatively nonstructural (ns) due to their homology to the corresponding BCV ns gene products. Northern blot analysis indicated that each of these two genes was present on a separate mRNA (5 and 5-1, respectively). In vitro translation analyses demonstrated that the HCV-OC43 9.5-kDa protein, like its BCV counterpart, is poorly translated when situated downstream of the 12.9-kDa ORF, although immunofluorescence studies did confirm its presence in infected cells. Sequence analysis showed that a large portion of the 3'-end of the leader sequence is present within the viral genome, upstream of the 12.9-kDa ORF. In addition, two ORFs encoding potential 4.9- and 4.8-kDa ns proteins in BCV are absent in HCV-OC43, although a corresponding mRNA 4 was found at a very low level. These results demonstrate that these two putative ns proteins are not essential for virus replication, at least in HRT-18 cells.</div>
</front>
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<ArticleTitle>Human coronavirus OC43 RNA 4 lacks two open reading frames located downstream of the S gene of bovine coronavirus.</ArticleTitle>
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<Abstract><AbstractText>Nucleotide sequences between the spike (S) and membrane (M) protein genes of the OC43 strain of human corona-virus were obtained from PCR-amplified viral mRNAs. Sequence analysis of this region revealed the presence of two ORFs encoding proteins of 12.9 and 9.5 kDa. These two proteins were identified as putatively nonstructural (ns) due to their homology to the corresponding BCV ns gene products. Northern blot analysis indicated that each of these two genes was present on a separate mRNA (5 and 5-1, respectively). In vitro translation analyses demonstrated that the HCV-OC43 9.5-kDa protein, like its BCV counterpart, is poorly translated when situated downstream of the 12.9-kDa ORF, although immunofluorescence studies did confirm its presence in infected cells. Sequence analysis showed that a large portion of the 3'-end of the leader sequence is present within the viral genome, upstream of the 12.9-kDa ORF. In addition, two ORFs encoding potential 4.9- and 4.8-kDa ns proteins in BCV are absent in HCV-OC43, although a corresponding mRNA 4 was found at a very low level. These results demonstrate that these two putative ns proteins are not essential for virus replication, at least in HRT-18 cells.</AbstractText>
</Abstract>
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