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Snijders Blok, L.* ; Rousseau, J.* ; Twist, J.* ; Ehresmann, S.* ; Takaku, M.* ; Venselaar, H.* ; Rodan, L.H.* ; Nowak, C.B.* ; Douglas, J.* ; Swoboda, K.J.* ; Steeves, M.A.* ; Sahai, I.* ; Stumpel, C.T.R.M.* ; Stegmann, A.P.A.* ; Wheeler, P.* ; Willing, M.C.* ; Fiala, E.* ; Kochhar, A.* ; Gibson, W.T.* ; Cohen, A.S.A.* ; Agbahovbe, R.* ; Innes, A.M.* ; Au, P.Y.B.* ; Rankin, J.* ; Anderson, I.J.* ; Skinner, S.A.* ; Louie, R.J.* ; Warren, H.E.* ; Afenjar, A.* ; Keren, B.* ; Nava, C.* ; Buratti, J.* ; Isapof, A.* ; Rodriguez, D.* ; Lewandowski, R.* ; Propst, J.* ; van Essen, T.* ; Choi, M.* ; Lee, S.* ; Chae, J.H.* ; Price, S.* ; Schnur, R.E.* ; Douglas, G.* ; Wentzensen, I.M.* ; Zweier, C.* ; Reis, A.* ; Bialer, M.G.* ; Moore, C.* ; Koopmans, M.* ; Brilstra, E.H.* ; Monroe, G.R.* ; van Gassen, K.L.I.* ; van Binsbergen, E.* ; Newbury-Ecob, R.* ; Bownass, L.* ; Bader, I.* ; Mayr, J.A.* ; Wortmann, S.B. ; Jakielski, K.J.* ; Strand, E.A.* ; Kloth, K.* ; Bierhals, T.* ; Roberts, J.D.* ; Petrovich, R.M.* ; Machida, S.* ; Kurumizaka, H.* ; Lelieveld, S.* ; Pfundt, R.* ; Jansen, S.* ; Deriziotis, P.* ; Faive, L.* ; Thevenon, J.* ; Assoum, M.* ; Shriberg, L.* ; Kleefstra, T.* ; Brunner, H.G.* ; Wade, P.A.* ; Fisher, S.E.* ; Campeau, P.M.*

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Nat. Commun. 9:4619 (2018)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Chromatin remodeling is of crucial importance during brain development. Pathogenic alterations of several chromatin remodeling ATPases have been implicated in neurodevelopmental disorders. We describe an index case with a de novo missense mutation in CHD3, identified during whole genome sequencing of a cohort of children with rare speech disorders. To gain a comprehensive view of features associated with disruption of this gene, we use a genotype-driven approach, collecting and characterizing 35 individuals with de novo CHD3 mutations and overlapping phenotypes. Most mutations cluster within the ATPase/helicase domain of the encoded protein. Modeling their impact on the three-dimensional structure demonstrates disturbance of critical binding and interaction motifs. Experimental assays with six of the identified mutations show that a subset directly affects ATPase activity, and all but one yield alterations in chromatin remodeling. We implicate de novo CHD3 mutations in a syndrome characterized by intellectual disability, macrocephaly, and impaired speech and language.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter De-novo Mutations; Chromatin Remodeling Complex; Intellectual Disability; Deacetylase Complex; Exome; Disorder; Family; Gene; Nurd; Diagnosis
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Zeitschrift Nature Communications
Quellenangaben Band: 9, Heft: 1, Seiten: , Artikelnummer: 4619 Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Human Genetics (IHG)