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http://purl.uniprot.org/citations/16391015http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16391015http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16391015http://www.w3.org/2000/01/rdf-schema#comment"Minor histocompatibility antigens (mHAg's) are peptides encoded by polymorphic genes that are presented by major histocompatibility complex (MHC) molecules and recognized by T cells in recipients of allogeneic hematopoietic cell transplants. Here we report that an alternative transcript of the proliferation-associated nuclear element 1 (PANE1) gene encodes a novel human leukocyte antigen (HLA)-A(*)0301-restricted mHAg that is selectively expressed in B-lymphoid cells. The antigenic peptide is entirely encoded within a unique exon not present in other PANE1 transcripts. Sequencing of PANE1 alleles in mHAg-positive and mHAg-negative cells demonstrates that differential T-cell recognition is due to a single nucleotide polymorphism within the variant exon that replaces an arginine codon with a translation termination codon. The PANE1 transcript that encodes the mHAg is expressed at high levels in resting CD19(+) B cells and B-lineage chronic lymphocytic leukemia (B-CLL) cells, and at significantly lower levels in activated B cells. Activation of B-CLL cells through CD40 ligand (CD40L) stimulation decreases expression of the mHAg-encoding PANE1 transcript and reciprocally increases expression of PANE1 transcripts lacking the mHAg-encoding exon. These studies suggest distinct roles for different PANE1 isoforms in resting compared with activated CD19(+) cells, and identify PANE1 as a potential therapeutic target in B-CLL."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.org/dc/terms/identifier"doi:10.1182/blood-2005-08-3501"xsd:string
http://purl.uniprot.org/citations/16391015http://purl.org/dc/terms/identifier"doi:10.1182/blood-2005-08-3501"xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Feng X."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Feng X."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Hunt D.F."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Hunt D.F."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Shabanowitz J."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Shabanowitz J."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Nishida T."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Nishida T."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Riddell S.R."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Riddell S.R."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Ferrell R.E."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Ferrell R.E."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Brickner A.G."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Brickner A.G."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Engelhard V.H."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Engelhard V.H."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Evans A.M."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Evans A.M."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Fairfull L."xsd:string
http://purl.uniprot.org/citations/16391015http://purl.uniprot.org/core/author"Fairfull L."xsd:string