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http://purl.uniprot.org/citations/20887364http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20887364http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20887364http://www.w3.org/2000/01/rdf-schema#comment"

Purpose

De novo STXBP1 mutations have been found in individuals with early infantile epileptic encephalopathy with suppression-burst pattern (EIEE). Our aim was to delineate the clinical spectrum of subjects with STXBP1 mutations, and to examine their biologic aspects.

Methods

STXBP1 was analyzed in 29 and 54 cases of cryptogenic EIEE and West syndrome, respectively, as a second cohort. RNA splicing was analyzed in lymphoblastoid cells from a subject harboring a c.663 + 5G>A mutation. Expression of STXBP1 protein with missense mutations was examined in neuroblastoma2A cells.

Results

A total of seven novel STXBP1 mutations were found in nine EIEE cases, but not in West syndrome. The mutations include two frameshift mutations, three nonsense mutations, a splicing mutation, and a recurrent missense mutation in three unrelated cases. Including our previous data, 10 of 14 individuals (71%) with STXBP1 aberrations had the onset of spasms after 1 month, suggesting relatively later onset of epileptic spasms. Nonsense-mediated mRNA decay associated with abnormal splicing was demonstrated. Transient expression revealed that STXBP1 proteins with missense mutations resulted in degradation in neuroblastoma2A cells.

Discussion

Collectively, STXBP1 aberrations can account for about one-third individuals with EIEE (14 of 43). These genetic and biologic data clearly showed that haploinsufficiency of STXBP1 is the important cause for cryptogenic EIEE."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.org/dc/terms/identifier"doi:10.1111/j.1528-1167.2010.02728.x"xsd:string
http://purl.uniprot.org/citations/20887364http://purl.org/dc/terms/identifier"doi:10.1111/j.1528-1167.2010.02728.x"xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Arai H."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Arai H."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Higuchi T."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Higuchi T."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Kato M."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Kato M."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Kimura S."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Kimura S."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Okada I."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Okada I."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Matsumoto N."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Matsumoto N."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Watanabe T."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Watanabe T."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Tagawa T."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Tagawa T."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Wada T."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Wada T."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Kubota M."xsd:string
http://purl.uniprot.org/citations/20887364http://purl.uniprot.org/core/author"Kubota M."xsd:string
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