RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/17428918http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17428918http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17428918http://www.w3.org/2000/01/rdf-schema#comment"TorsinA is an AAA(+) protein located predominantly in the lumen of the endoplasmic reticulum (ER) and nuclear envelope responsible for early onset torsion dystonia (DYT1). Most cases of this dominantly inherited movement disorder are caused by deletion of a glutamic acid in the carboxyl terminal region of torsinA. We used a sensitive reporter, Gaussia luciferase (Gluc) to evaluate the role of torsinA in processing proteins through the ER. In primary fibroblasts from controls and DYT1 patients most Gluc activity (95%) was released into the media and processed through the secretory pathway, as confirmed by inhibition with brefeldinA and nocodazole. Fusion of Gluc to a fluorescent protein revealed coalignment and fractionation with ER proteins and association of Gluc with torsinA. Notably, fibroblasts from DYT1 patients were found to secrete markedly less Gluc activity as compared with control fibroblasts. This decrease in processing of Gluc in DYT1 cells appear to arise, at least in part, from a loss of torsinA activity, because mouse embryonic fibroblasts lacking torsinA also had reduced secretion as compared with control cells. These studies demonstrate the exquisite sensitivity of this reporter system for quantitation of processing through the secretory pathway and support a role for torsinA as an ER chaperone protein."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.org/dc/terms/identifier"doi:10.1073/pnas.0701185104"xsd:string
http://purl.uniprot.org/citations/17428918http://purl.org/dc/terms/identifier"doi:10.1073/pnas.0701185104"xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Li Y."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Li Y."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Zeng J."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Zeng J."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Nery F.C."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Nery F.C."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Breakefield X.O."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Breakefield X.O."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Niland B.P."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Niland B.P."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Hewett J.W."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Hewett J.W."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Tannous B."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/author"Tannous B."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/name"Proc. Natl. Acad. Sci. U.S.A."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/name"Proc. Natl. Acad. Sci. U.S.A."xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/pages"7271-7276"xsd:string
http://purl.uniprot.org/citations/17428918http://purl.uniprot.org/core/pages"7271-7276"xsd:string