| Literature DB >> 31327001 |
Diana Le Duc1, Cecilia Giulivi2,3, Susan M Hiatt4, Eleonora Napoli2, Alexios Panoutsopoulos5,6, Angelo Harlan De Crescenzo5,6, Urania Kotzaeridou7, Steffen Syrbe7, Evdokia Anagnostou8, Meron Azage9, Renee Bend10, Amber Begtrup11, Natasha J Brown12,13,14, Benjamin Büttner1, Megan T Cho11, Gregory M Cooper4, Jan H Doering7, Christèle Dubourg15,16, David B Everman10, Michael S Hildebrand12,17, Francis Jeshira Reynoso Santos18, Barbara Kellam19, Jennifer Keller-Ramey11, Johannes R Lemke1, Shuxi Liu11, Dmitriy Niyazov9, Katelyn Payne20, Richard Person11, Chloé Quélin21, Rhonda E Schnur11, Brooke T Smith10, Jonathan Strober22, Susan Walker19, Mathew Wallis23,24, Laurence Walsh20, Sandra Yang11, Ryan K C Yuen19,25, Andreas Ziegler7, Heinrich Sticht26, Michael C Pride3,27, Lori Orosco5,6, Verónica Martínez-Cerdeño3,5,6, Jill L Silverman3,27, Jacqueline N Crawley3,27, Stephen W Scherer19,28, Konstantinos S Zarbalis3,5,6, Rami Jamra1.
Abstract
The underpinnings of mild to moderate neurodevelopmental delay remain elusive, often leading to late diagnosis and interventions. Here, we present data on exome and genome sequencing as well as array analysis of 13 individuals that point to pathogenic, heterozygous, mostly de novo variants in WDFY3 (significant de novo enrichment P = 0.003) as a monogenic cause of mild and non-specific neurodevelopmental delay. Nine variants were protein-truncating and four missense. Overlapping symptoms included neurodevelopmental delay, intellectual disability, macrocephaly, and psychiatric disorders (autism spectrum disorders/attention deficit hyperactivity disorder). One proband presented with an opposing phenotype of microcephaly and the only missense-variant located in the PH-domain of WDFY3. Findings of this case are supported by previously published data, demonstrating that pathogenic PH-domain variants can lead to microcephaly via canonical Wnt-pathway upregulation. In a separate study, we reported that the autophagy scaffolding protein WDFY3 is required for cerebral cortical size regulation in mice, by controlling proper division of neural progenitors. Here, we show that proliferating cortical neural progenitors of human embryonic brains highly express WDFY3, further supporting a role for this molecule in the regulation of prenatal neurogenesis. We present data on Wnt-pathway dysregulation in Wdfy3-haploinsufficient mice, which display macrocephaly and deficits in motor coordination and associative learning, recapitulating the human phenotype. Consequently, we propose that in humans WDFY3 loss-of-function variants lead to macrocephaly via downregulation of the Wnt pathway. In summary, we present WDFY3 as a novel gene linked to mild to moderate neurodevelopmental delay and intellectual disability and conclude that variants putatively causing haploinsufficiency lead to macrocephaly, while an opposing pathomechanism due to variants in the PH-domain of WDFY3 leads to microcephaly.Entities:
Keywords: zzm321990 WDFY3zzm321990 ; brain size; intellectual disability; neurodevelopmental delay
Year: 2019 PMID: 31327001 PMCID: PMC6736092 DOI: 10.1093/brain/awz198
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501