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http://purl.uniprot.org/citations/18055455http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18055455http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18055455http://www.w3.org/2000/01/rdf-schema#comment"Severe acute respiratory syndrome (SARS) is an acute infectious disease with significant mortality. A typical clinical feature associated with SARS is pulmonary fibrosis and the associated lung failure. However, the underlying mechanism remains elusive. In this study, we demonstrate that SARS-associated coronavirus (SARS-CoV) nucleocapsid (N) protein potentiates transforming growth factor-beta (TGF-beta)-induced expression of plasminogen activator inhibitor-1 but attenuates Smad3/Smad4-mediated apoptosis of human peripheral lung epithelial HPL1 cells. The promoting effect of N protein on the transcriptional responses of TGF-beta is Smad3-specific. N protein associates with Smad3 and promotes Smad3-p300 complex formation while it interferes with the complex formation between Smad3 and Smad4. These findings provide evidence of a novel mechanism whereby N protein modulates TGF-beta signaling to block apoptosis of SARS-CoV-infected host cells and meanwhile promote tissue fibrosis. Our results reveal a novel mode of Smad3 action in a Smad4-independent manner and may lead to successful strategies for SARS treatment by targeting the TGF-beta signaling molecules."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.org/dc/terms/identifier"doi:10.1074/jbc.m708033200"xsd:string
http://purl.uniprot.org/citations/18055455http://purl.org/dc/terms/identifier"doi:10.1074/jbc.m708033200"xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/author"Nicholls J.M."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/author"Nicholls J.M."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/author"Zhao X."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/author"Zhao X."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/author"Chen Y.G."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/author"Chen Y.G."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/name"J. Biol. Chem."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/name"J. Biol. Chem."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/pages"3272-3280"xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/pages"3272-3280"xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/title"Severe acute respiratory syndrome-associated coronavirus nucleocapsid protein interacts with Smad3 and modulates transforming growth factor-beta signaling."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/title"Severe acute respiratory syndrome-associated coronavirus nucleocapsid protein interacts with Smad3 and modulates transforming growth factor-beta signaling."xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/volume"283"xsd:string
http://purl.uniprot.org/citations/18055455http://purl.uniprot.org/core/volume"283"xsd:string
http://purl.uniprot.org/citations/18055455http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18055455
http://purl.uniprot.org/citations/18055455http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18055455
http://purl.uniprot.org/citations/18055455http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18055455
http://purl.uniprot.org/citations/18055455http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18055455