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http://purl.uniprot.org/citations/8517026http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8517026http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8517026http://www.w3.org/2000/01/rdf-schema#comment"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."xsd:string
http://purl.uniprot.org/citations/8517026http://purl.org/dc/terms/identifier"doi:10.1006/viro.1993.1043"xsd:string
http://purl.uniprot.org/citations/8517026http://purl.org/dc/terms/identifier"doi:10.1006/viro.1993.1043"xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/author"Talbot P.J."xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/author"Talbot P.J."xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/author"Mounir S."xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/author"Mounir S."xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/date"1993"xsd:gYear
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/date"1993"xsd:gYear
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/name"Virology"xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/name"Virology"xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/pages"355-360"xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/pages"355-360"xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/title"Human coronavirus OC43 RNA 4 lacks two open reading frames located downstream of the S gene of bovine coronavirus."xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/title"Human coronavirus OC43 RNA 4 lacks two open reading frames located downstream of the S gene of bovine coronavirus."xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/volume"192"xsd:string
http://purl.uniprot.org/citations/8517026http://purl.uniprot.org/core/volume"192"xsd:string
http://purl.uniprot.org/citations/8517026http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/8517026
http://purl.uniprot.org/citations/8517026http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/8517026
http://purl.uniprot.org/citations/8517026http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/8517026
http://purl.uniprot.org/citations/8517026http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/8517026
http://purl.uniprot.org/uniprot/Q04854http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/8517026
http://purl.uniprot.org/uniprot/Q04853http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/8517026