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http://purl.uniprot.org/citations/11980719http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11980719http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11980719http://www.w3.org/2000/01/rdf-schema#comment"Mature macrophages, neutrophils and lymphoid cells do not develop in PU.1(-/-) mice. In contrast, mice lacking the highly related protein Spi-B generate all hematopoietic lineages but display a B-cell receptor signaling defect. These distinct phenotypes could result from functional differences between PU.1 and Spi-B or their unique temporal and tissue-specific expression (PU.1: myeloid and B cells; Spi-B: B cells only). To address this question, we introduced the Spi-B cDNA into the murine PU.1 locus by homologous recombination. In the absence of PU.1, Spi-B rescued macrophage and granulocyte development when assayed by in vitro differentiation of embryonic stem cells. Adherent, CD11b(+)/F4/80(+) cells capable of phagocytosis were detected in PU.1(Spi-B/Spi-B) embryoid bodies, and myeloid colonies were present in hematopoietic progenitor assays. Despite its ability to rescue myeloid differentiation, Spi-B did not rescue lymphoid development in a RAG-2(-/-) complementation assay. These results demonstrate an important difference between PU.1 and Spi-B. Careful comparison of these Ets factors will delineate important functional domains of PU.1 involved in lymphocyte lineage commitment and/or maturation."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.org/dc/terms/identifier"doi:10.1093/emboj/21.9.2220"xsd:string
http://purl.uniprot.org/citations/11980719http://purl.org/dc/terms/identifier"doi:10.1093/emboj/21.9.2220"xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/author"Rao S."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/author"Rao S."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/author"Simon M.C."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/author"Simon M.C."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/author"Dahl R."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/author"Dahl R."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/author"Ramirez-Bergeron D.L."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/author"Ramirez-Bergeron D.L."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/date"2002"xsd:gYear
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/date"2002"xsd:gYear
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/name"EMBO J."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/name"EMBO J."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/pages"2220-2230"xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/pages"2220-2230"xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/title"Spi-B can functionally replace PU.1 in myeloid but not lymphoid development."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/title"Spi-B can functionally replace PU.1 in myeloid but not lymphoid development."xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/volume"21"xsd:string
http://purl.uniprot.org/citations/11980719http://purl.uniprot.org/core/volume"21"xsd:string
http://purl.uniprot.org/citations/11980719http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/11980719
http://purl.uniprot.org/citations/11980719http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/11980719