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http://purl.uniprot.org/citations/30607023http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/30607023http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/30607023http://www.w3.org/2000/01/rdf-schema#comment"

Purpose

Identifying and characterizing novel causes of autosomal recessive intellectual disability based on systematic clinical and genetic evaluation, followed by functional experiments.

Methods

Clinical examinations, genome-wide positional mapping, and sequencing were followed by quantitative polymerase chain reaction and western blot of the protein SVBP and its interaction partners. We then knocked down the gene in rat primary hippocampal neurons and evaluated the consequences on synapses.

Results

We identified a founder, homozygous stop-gain variant in SVBP (c.82C>T; p.[Gln28*]) in four affected individuals from two independent families with intellectual disability, microcephaly, ataxia, and muscular hypotonia. SVBP encodes a small chaperone protein that transports and stabilizes two angiogenesis regulators, VASH1 and VASH2. The altered protein is unstable and nonfunctional since transfected HeLa cells with mutant SVBP did not reveal evidence for immunoreactive SVBP protein fragments and cotransfection with VASH1 showed a severe reduction of VASH1 in medium and cell lysate. Knocking down Svbp in rat primary hippocampal neurons led to a significant decrease in the number of excitatory synapses.

Conclusion

SVBP is not only involved in angiogenesis, but also has vital functions in the central nervous system. Biallelic loss-of-function variants in SVBP lead to intellectual disability."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.org/dc/terms/identifier"doi:10.1038/s41436-018-0415-8"xsd:string
http://purl.uniprot.org/citations/30607023http://purl.org/dc/terms/identifier"doi:10.1038/s41436-018-0415-8"xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Sticht H."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Sticht H."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Riazuddin S."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Riazuddin S."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Abou Jamra R."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Abou Jamra R."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"van Bokhoven H."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"van Bokhoven H."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Reis A."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Reis A."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Iqbal Z."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Iqbal Z."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Uebe S."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Uebe S."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Kasri N.N."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Kasri N.N."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Tawamie H."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Tawamie H."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Ba W."xsd:string
http://purl.uniprot.org/citations/30607023http://purl.uniprot.org/core/author"Ba W."xsd:string
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