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http://purl.uniprot.org/citations/35385725http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/35385725http://www.w3.org/2000/01/rdf-schema#comment"Mutation or disruption of the Shank/ProSAP family of genes is a high risk factor for autism spectrum disorders (ASDs) and intellectual disability. N-methyl-D-aspartate glutamate receptor (NMDAR) dysfunction contributes to the development of autism-like behaviors. However, the molecular mechanism of Shank-mediated NMDAR modulation is still not clear. Here, we show that the scaffold protein plenty of SH3s (POSH) directly interacts with two other scaffold proteins, PSD95 and SHANK2/3, at excitatory synapses. In POSH conditional knockout (cKO) mice, normal synaptic clustering of NMDAR/PSD-95/SHANK complex is disrupted, accompanied by abnormal dendritic spine development and glutamatergic transmission in hippocampal neurons. POSH cKO mice display profound autism-like behaviors, including impairments in social interactions, social communication, repetitive behaviors, and deficits in learning and memory. Thus, POSH clusters at the postsynaptic density (PSD) with PSD-95 and SHANK2/3 and plays important roles in the signaling mechanisms of the NMDAR/PSD-95/POSH/SHANK complex as well as in spine development and brain function."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.org/dc/terms/identifier"doi:10.1016/j.celrep.2022.110642"xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/author"Zhang X."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/author"Zhang Y."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/author"Wang S."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/author"Yang X."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/author"Zhang F."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/author"Zhang H."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/author"Xu Z."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/author"Yao M."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/author"Shi L."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/author"Meng M."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/date"2022"xsd:gYear
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/name"Cell Rep"xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/pages"110642"xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/title"POSH regulates assembly of the NMDAR/PSD-95/Shank complex and synaptic function."xsd:string
http://purl.uniprot.org/citations/35385725http://purl.uniprot.org/core/volume"39"xsd:string
http://purl.uniprot.org/citations/35385725http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/35385725
http://purl.uniprot.org/citations/35385725http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/35385725
http://purl.uniprot.org/uniprot/#_A0A338P713-mappedCitation-35385725http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35385725
http://purl.uniprot.org/uniprot/#_A0A338P746-mappedCitation-35385725http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35385725
http://purl.uniprot.org/uniprot/#_A0A338P7H1-mappedCitation-35385725http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35385725
http://purl.uniprot.org/uniprot/#_A0A338P6E5-mappedCitation-35385725http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35385725
http://purl.uniprot.org/uniprot/#_A0A338P6H5-mappedCitation-35385725http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35385725