TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical development
van Woerden, Geeske M; Bos, Melanie; de Konink, Charlotte; Distel, Ben; Avagliano Trezza, Rossella; Shur, Natasha E; Barañano, Kristin; Mahida, Sonal; Chassevent, Anna; Schreiber, Allison; Erwin, Angelika L; Gripp, Karen W; Rehman, Fatima; Brulleman, Saskia; McCormack, Róisín; de Geus, Gwynna; Kalsner, Louisa; Sorlin, Arthur; Bruel, Ange-Line; Koolen, David A; Gabriel, Melissa K; Rossi, Mari; Fitzpatrick, David R; Wilkie, Andrew O M; Calpena, Eduardo; Johnson, David; Brooks, Alice; van Slegtenhorst, Marjon; Fleischer, Julie; Groepper, Daniel; Lindstrom, Kristin; Innes, A Micheil; Goodwin, Allison; Humberson, Jennifer; Noyes, Amanda; Langley, Katherine G; Telegrafi, Aida; Blevins, Amy; Hoffman, Jessica; Guillen Sacoto, Maria J; Juusola, Jane; Monaghan, Kristin G; Punj, Sumit; Simon, Marleen; Pfundt, Rolph; Elgersma, Ype; Kleefstra, Tjitske
(2021) Human mutation, volume 42, issue 4, pp. 445 - 459
(Article)
Abstract
Thousand and one amino-acid kinase 1 (TAOK1) is a MAP3K protein kinase, regulating different mitogen-activated protein kinase pathways, thereby modulating a multitude of processes in the cell. Given the recent finding of TAOK1 involvement in neurodevelopmental disorders (NDDs), we investigated the role of TAOK1 in neuronal function and collected a
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cohort of 23 individuals with mostly de novo variants in TAOK1 to further define the associated NDD. Here, we provide evidence for an important role for TAOK1 in neuronal function, showing that altered TAOK1 expression levels in the embryonic mouse brain affect neural migration in vivo, as well as neuronal maturation in vitro. The molecular spectrum of the identified TAOK1 variants comprises largely truncating and nonsense variants, but also missense variants, for which we provide evidence that they can have a loss of function or dominant-negative effect on TAOK1, expanding the potential underlying causative mechanisms resulting in NDD. Taken together, our data indicate that TAOK1 activity needs to be properly controlled for normal neuronal function and that TAOK1 dysregulation leads to a neurodevelopmental disorder mainly comprising similar facial features, developmental delay/intellectual disability and/or variable learning or behavioral problems, muscular hypotonia, infant feeding difficulties, and growth problems.
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Keywords: cortical development, functional genomics, in utero electroporation, neurodevelopmental disorders, TAOK1, Genetics(clinical), Genetics, Journal Article
ISSN: 1059-7794
Publisher: John Wiley & Sons Inc.
Note: Funding Information: The authors would like to thank the participating families. We thank all clinicians involved for referring individuals with ID for diagnostic exome sequencing and Dr. Simon McGowan for bioinformatics analysis. This study was supported by the Netherlands Organization for Health Research and Development (ZonMw grant 91718310 to T. K.) and by the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre Programme (AOMW). Additionally, this project has received funding from the European Union's Horizon 2020 RESEArch and INNOVATION PROGRAm under grant agreement No. 779257 (Solve‐RD). Publisher Copyright: © 2021 The Authors. Human Mutation published by Wiley Periodicals LLC.
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