{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"submitter":["Ferreccio A"],"funding":["NIMH NIH HHS"],"pubmed_abstract":["Copy number variation (CNV) in the 16p11.2 (BP4-BP5) genomic locus is strongly associated with autism. Carriers of 16p11.2 deletion and duplication exhibit several common behavioral and social impairments, yet, show opposing brain structural changes and body mass index. To determine cellular mechanisms that might contribute to these opposing phenotypes, we performed quantitative tandem mass tag (TMT) proteomics on human dorsal forebrain neural progenitor cells (NPCs) differentiated from induced pluripotent stem cells (iPSC) derived from 16p11.2 CNV carriers. Differentially phosphorylated proteins between unaffected individuals and 16p11.2 CNV carriers were significantly enriched for centrosomal and cilia proteins. Deletion patient-derived NPCs show increased primary cilium length compared "],"journal":["bioRxiv : the preprint server for biology"],"pagination":["2024.10.07.617069"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11482803"],"repository":["biostudies-literature"],"pubmed_title":["TAOK2 Drives Opposing Cilia Length Deficits in 16p11.2 Deletion and Duplication Carriers."],"pmcid":["PMC11482803"],"funding_grant_id":["R01 MH121674"],"pubmed_authors":["Cornell M","Ferreccio A","Deshpande A","Byeon S","Weiss LA","Yadav S","Oses-Prieto J","Burlingame A"],"additional_accession":[]},"is_claimable":false,"name":"TAOK2 Drives Opposing Cilia Length Deficits in 16p11.2 Deletion and Duplication Carriers.","description":"Copy number variation (CNV) in the 16p11.2 (BP4-BP5) genomic locus is strongly associated with autism. Carriers of 16p11.2 deletion and duplication exhibit several common behavioral and social impairments, yet, show opposing brain structural changes and body mass index. To determine cellular mechanisms that might contribute to these opposing phenotypes, we performed quantitative tandem mass tag (TMT) proteomics on human dorsal forebrain neural progenitor cells (NPCs) differentiated from induced pluripotent stem cells (iPSC) derived from 16p11.2 CNV carriers. Differentially phosphorylated proteins between unaffected individuals and 16p11.2 CNV carriers were significantly enriched for centrosomal and cilia proteins. Deletion patient-derived NPCs show increased primary cilium length compared ","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Oct","modification":"2026-05-29T03:12:23.831Z","creation":"2025-04-03T23:51:58.194Z"},"accession":"S-EPMC11482803","cross_references":{"pubmed":["39416068"],"doi":["10.1101/2024.10.07.617069"]}}