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http://purl.uniprot.org/citations/19763086http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19763086http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19763086http://www.w3.org/2000/01/rdf-schema#comment"In plant innate immunity, the surface-exposed leucine-rich repeat receptor kinases EFR and FLS2 mediate recognition of the bacterial pathogen-associated molecular patterns EF-Tu and flagellin, respectively. We identified the Arabidopsis stromal-derived factor-2 (SDF2) as being required for EFR function, and to a lesser extent FLS2 function. SDF2 resides in an endoplasmic reticulum (ER) protein complex with the Hsp40 ERdj3B and the Hsp70 BiP, which are components of the ER-quality control (ER-QC). Loss of SDF2 results in ER retention and degradation of EFR. The differential requirement for ER-QC components by EFR and FLS2 could be linked to N-glycosylation mediated by STT3a, a catalytic subunit of the oligosaccharyltransferase complex involved in co-translational N-glycosylation. Our results show that the plasma membrane EFR requires the ER complex SDF2-ERdj3B-BiP for its proper accumulation, and provide a demonstration of a physiological requirement for ER-QC in transmembrane receptor function in plants. They also provide an unexpected differential requirement for ER-QC and N-glycosylation components by two closely related receptors."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.org/dc/terms/identifier"doi:10.1038/emboj.2009.262"xsd:string
http://purl.uniprot.org/citations/19763086http://purl.org/dc/terms/identifier"doi:10.1038/emboj.2009.262"xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Li J."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Li J."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Molina A."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Molina A."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Zipfel C."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Zipfel C."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Jones J.D."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Jones J.D."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Schwessinger B."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Schwessinger B."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Roux M."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Roux M."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Thomma B.P."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Thomma B.P."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Jorda L."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Jorda L."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Chinchilla D."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Chinchilla D."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Batoux M."xsd:string
http://purl.uniprot.org/citations/19763086http://purl.uniprot.org/core/author"Batoux M."xsd:string