| Literature DB >> 31303265 |
Lot Snijders Blok1, Tjitske Kleefstra2, Hanka Venselaar3, Saskia Maas4, Hester Y Kroes5, Augusta M A Lachmeijer5, Koen L I van Gassen5, Helen V Firth6, Susan Tomkins7, Simon Bodek7, Katrin Õunap8, Monica H Wojcik9, Christopher Cunniff10, Katherine Bergstrom10, Zoë Powis11, Sha Tang11, Deepali N Shinde11, Catherine Au12, Alejandro D Iglesias12, Kosuke Izumi13, Jacqueline Leonard13, Ahmad Abou Tayoun14, Samuel W Baker14, Marco Tartaglia15, Marcello Niceta15, Maria Lisa Dentici15, Nobuhiko Okamoto16, Noriko Miyake17, Naomichi Matsumoto17, Antonio Vitobello18, Laurence Faivre19, Christophe Philippe18, Christian Gilissen20, Laurens Wiel21, Rolph Pfundt20, Pelagia Deriziotis22, Han G Brunner23, Simon E Fisher24.
Abstract
POU3F3, also referred to as Brain-1, is a well-known transcription factor involved in the development of the central nervous system, but it has not previously been associated with a neurodevelopmental disorder. Here, we report the identification of 19 individuals with heterozygous POU3F3 disruptions, most of which are de novo variants. All individuals had developmental delays and/or intellectual disability and impairments in speech and language skills. Thirteen individuals had characteristic low-set, prominent, and/or cupped ears. Brain abnormalities were observed in seven of eleven MRI reports. POU3F3 is an intronless gene, insensitive to nonsense-mediated decay, and 13 individuals carried protein-truncating variants. All truncating variants that we tested in cellular models led to aberrant subcellular localization of the encoded protein. Luciferase assays demonstrated negative effects of these alleles on transcriptional activation of a reporter with a FOXP2-derived binding motif. In addition to the loss-of-function variants, five individuals had missense variants that clustered at specific positions within the functional domains, and one small in-frame deletion was identified. Two missense variants showed reduced transactivation capacity in our assays, whereas one variant displayed gain-of-function effects, suggesting a distinct pathophysiological mechanism. In bioluminescence resonance energy transfer (BRET) interaction assays, all the truncated POU3F3 versions that we tested had significantly impaired dimerization capacities, whereas all missense variants showed unaffected dimerization with wild-type POU3F3. Taken together, our identification and functional cell-based analyses of pathogenic variants in POU3F3, coupled with a clinical characterization, implicate disruptions of this gene in a characteristic neurodevelopmental disorder.Entities:
Keywords: BRET assay; Brain-1; FOXP2; POU3F2; POU3F3; de novo variants; intellectual disability; luciferase reporter; speech/language disorder
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Year: 2019 PMID: 31303265 PMCID: PMC6698880 DOI: 10.1016/j.ajhg.2019.06.007
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025