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http://purl.uniprot.org/citations/15253154http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15253154http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15253154http://www.w3.org/2000/01/rdf-schema#comment"PD-L2, a newly identified member of B7 family, plays a role in down-regulating T cell responses. The common PD-L2 mRNA (type I) is the splicing product containing all 6 exons. We report here the identification of two human PD-L2 splice variants in activated leukocytes. One splice variant (type II) is generated through splicing out exon 3 encoding Ig constant-like domain; it retains all other regions without a frame shift. The other variant (type III) is created by splicing out exon 3 to an alternative acceptor site 5 bp downstream of the canonical acceptor site, leading to a frame shift. Consequently, the translated protein should be a soluble form. Furthermore, type I isoform is expressed on the plasma surface whereas type II isoform showed a pattern of intracellular membrane distribution in the transiently transfected K562 cells. In addition, the expression patterns of PD-L2 splice variants are variable in different individuals and distinct cellular status. These results suggest that PD-L2 expression may be controlled by posttranscriptional regulation through alternative splicing, and modulation of PD-L2 isoform expression may influence the outcome of immune response."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.org/dc/terms/identifier"doi:10.1093/abbs/36.4.284"xsd:string
http://purl.uniprot.org/citations/15253154http://purl.org/dc/terms/identifier"doi:10.1093/abbs/36.4.284"xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/author"Liu Y."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/author"Liu Y."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/author"He X.-H."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/author"He X.-H."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/author"Xu L.-H."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/author"Xu L.-H."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/author"Zeng Y.-Y."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/author"Zeng Y.-Y."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/date"2004"xsd:gYear
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/date"2004"xsd:gYear
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/name"Acta Biochim. Biophys. Sin."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/name"Acta Biochim. Biophys. Sin."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/pages"284-289"xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/pages"284-289"xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/title"Cloning and identification of two novel splice variants of human PD-L2."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/title"Cloning and identification of two novel splice variants of human PD-L2."xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/volume"36"xsd:string
http://purl.uniprot.org/citations/15253154http://purl.uniprot.org/core/volume"36"xsd:string
http://purl.uniprot.org/citations/15253154http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/15253154
http://purl.uniprot.org/citations/15253154http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/15253154