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Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size.
Le Duc, Diana; Giulivi, Cecilia; Hiatt, Susan M; Napoli, Eleonora; Panoutsopoulos, Alexios; Harlan De Crescenzo, Angelo; Kotzaeridou, Urania; Syrbe, Steffen; Anagnostou, Evdokia; Azage, Meron; Bend, Renee; Begtrup, Amber; Brown, Natasha J; Büttner, Benjamin; Cho, Megan T; Cooper, Gregory M; Doering, Jan H; Dubourg, Christèle; Everman, David B; Hildebrand, Michael S; Santos, Francis Jeshira Reynoso; Kellam, Barbara; Keller-Ramey, Jennifer; Lemke, Johannes R; Liu, Shuxi; Niyazov, Dmitriy; Payne, Katelyn; Person, Richard; Quélin, Chloé; Schnur, Rhonda E; Smith, Brooke T; Strober, Jonathan; Walker, Susan; Wallis, Mathew; Walsh, Laurence; Yang, Sandra; Yuen, Ryan K C; Ziegler, Andreas; Sticht, Heinrich; Pride, Michael C; Orosco, Lori; Martínez-Cerdeño, Verónica; Silverman, Jill L; Crawley, Jacqueline N; Scherer, Stephen W; Zarbalis, Konstantinos S; Jamra, Rami.
Affiliation
  • Le Duc D; Institute of Human Genetics, University Medical Center Leipzig, Leipzig, Germany.
  • Giulivi C; Department of Molecular Biosciences, School of Veterinary Medicine, University of California Davis, Davis, CA, USA.
  • Hiatt SM; MIND Institute, University of California Davis, Sacramento, CA, USA.
  • Napoli E; HudsonAlpha Institute for Biotechnology, 601 Genome Way, Huntsville, AL, USA.
  • Panoutsopoulos A; Department of Molecular Biosciences, School of Veterinary Medicine, University of California Davis, Davis, CA, USA.
  • Harlan De Crescenzo A; Department of Pathology and Laboratory Medicine, University of California at Davis, Sacramento, CA, USA.
  • Kotzaeridou U; Institute for Pediatric Regenerative Medicine, Shriners Hospitals for Children, Sacramento, CA, USA.
  • Syrbe S; Department of Pathology and Laboratory Medicine, University of California at Davis, Sacramento, CA, USA.
  • Anagnostou E; Institute for Pediatric Regenerative Medicine, Shriners Hospitals for Children, Sacramento, CA, USA.
  • Azage M; Division of Child Neurology and Inherited Metabolic Diseases, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, Heidelberg, Germany.
  • Bend R; Division of Child Neurology and Inherited Metabolic Diseases, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, Heidelberg, Germany.
  • Begtrup A; Bloorview Research Institute, University of Toronto, Toronto, Canada.
  • Brown NJ; Department of Pediatrics, Ochsner Health System and University of Queensland, New Orleans, LA, USA.
  • Büttner B; Greenwood Genetic Center, Greenwood, SC, USA.
  • Cho MT; GeneDx, Clinical Genomics, 207 Perry Parkway Gaithersburg, MD, USA.
  • Cooper GM; Department of Pediatrics, University of Melbourne, VIC, Australia.
  • Doering JH; Victorian Clinical Genetics Services, Parkville, VIC, Australia.
  • Dubourg C; Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Everman DB; Institute of Human Genetics, University Medical Center Leipzig, Leipzig, Germany.
  • Hildebrand MS; GeneDx, Clinical Genomics, 207 Perry Parkway Gaithersburg, MD, USA.
  • Santos FJR; HudsonAlpha Institute for Biotechnology, 601 Genome Way, Huntsville, AL, USA.
  • Kellam B; Division of Child Neurology and Inherited Metabolic Diseases, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, Heidelberg, Germany.
  • Keller-Ramey J; Service de Génétique Moléculaire et Génomique, CHU, Rennes, F-35033, France.
  • Lemke JR; Univ Rennes, CNRS, IGDR, UMR 6290, Rennes, F-35000, France.
  • Liu S; Greenwood Genetic Center, Greenwood, SC, USA.
  • Niyazov D; Department of Pediatrics, University of Melbourne, VIC, Australia.
  • Payne K; Epilepsy Research Centre, Austin Health, Heidelberg, VIC, Australia.
  • Person R; Joe DiMaggio Children's Hospital, Hollywood, FL, USA.
  • Quélin C; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Canada.
  • Schnur RE; GeneDx, Clinical Genomics, 207 Perry Parkway Gaithersburg, MD, USA.
  • Smith BT; Institute of Human Genetics, University Medical Center Leipzig, Leipzig, Germany.
  • Strober J; GeneDx, Clinical Genomics, 207 Perry Parkway Gaithersburg, MD, USA.
  • Walker S; Department of Pediatrics, Ochsner Health System and University of Queensland, New Orleans, LA, USA.
  • Wallis M; Riley Hospital for Children, Indianapolis, IN, USA.
  • Walsh L; GeneDx, Clinical Genomics, 207 Perry Parkway Gaithersburg, MD, USA.
  • Yang S; Service de Génétique Clinique, CHU, Rennes, F-35203, France.
  • Yuen RKC; GeneDx, Clinical Genomics, 207 Perry Parkway Gaithersburg, MD, USA.
  • Ziegler A; Greenwood Genetic Center, Greenwood, SC, USA.
  • Sticht H; UCSF Benioff Children's Hospital, San Francisco, CA, USA.
  • Pride MC; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Canada.
  • Orosco L; Austin Health Clinical Genetics Service, Heidelberg, VIC, Australia.
  • Martínez-Cerdeño V; Department of Medicine, University of Melbourne, Parkville, VIC, Australia.
  • Silverman JL; Riley Hospital for Children, Indianapolis, IN, USA.
  • Crawley JN; GeneDx, Clinical Genomics, 207 Perry Parkway Gaithersburg, MD, USA.
  • Scherer SW; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Canada.
  • Zarbalis KS; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.
  • Jamra R; Division of Child Neurology and Inherited Metabolic Diseases, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, Heidelberg, Germany.
Brain ; 142(9): 2617-2630, 2019 09 01.
Article in En | MEDLINE | ID: mdl-31327001
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Variation / Brain / Adaptor Proteins, Signal Transducing / Neurodevelopmental Disorders / Autophagy-Related Proteins Limits: Adolescent / Animals / Child / Child, preschool / Female / Humans / Male Language: En Journal: Brain Year: 2019 Type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genetic Variation / Brain / Adaptor Proteins, Signal Transducing / Neurodevelopmental Disorders / Autophagy-Related Proteins Limits: Adolescent / Animals / Child / Child, preschool / Female / Humans / Male Language: En Journal: Brain Year: 2019 Type: Article Affiliation country: Germany