ZC4H2 Mutations Are Associated with Arthrogryposis Multiplex Congenita and Intellectual Disability through Impairment of Central and Peripheral Synaptic Plasticity
Author(s) -
Hiromi Hirata,
Indrajit Nanda,
Anne van Riesen,
G. McMichael,
Hao Hu,
M Hambrock,
Marie-Amélie Papon,
Ute Fischer,
Sylviane Marouillat,
Can Ding,
Servane Alirol,
Melanie Bienek,
Sabine Preisler-Adams,
Astrid Grimme,
Dominik Seelow,
Richard Webster,
Eric Haan,
Alastair H. MacLennan,
Werner Stenzel,
Tzu Ying Yap,
Alison Gardner,
Lam Son Nguyen,
Marie Shaw,
Nicolas Lebrun,
Stefan A. Haas,
Wolfram Kreß,
Thomas Haaf,
Elke Schellenberger,
Jamel Chelly,
Géraldine Viot,
Lisa G. Shaffer,
Jill A. Rosenfeld,
Nancy Kramer,
Rena E. Falk,
Dima ElKhechen,
Luis Escobar,
Raoul C. M. Hennekam,
Peter Wieacker,
Christoph Hübner,
HansHilger Ropers,
Jozef Gécz,
Markus Schuelke,
Frédéric Laumonnier,
Vera M. Kalscheuer
Publication year - 2013
Publication title -
the american journal of human genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.661
H-Index - 302
eISSN - 1537-6605
pISSN - 0002-9297
DOI - 10.1016/j.ajhg.2013.03.021
Subject(s) - arthrogryposis multiplex congenita , biology , zebrafish , arthrogryposis , missense mutation , genetics , spinal muscular atrophy , mutation , gene
Arthrogryposis multiplex congenita (AMC) is caused by heterogeneous pathologies leading to multiple antenatal joint contractures through fetal akinesia. Understanding the pathophysiology of this disorder is important for clinical care of the affected individuals and genetic counseling of the families. We thus aimed to establish the genetic basis of an AMC subtype that is associated with multiple dysmorphic features and intellectual disability (ID). We used haplotype analysis, next-generation sequencing, array comparative genomic hybridization, and chromosome breakpoint mapping to identify the pathogenic mutations in families and simplex cases. Suspected disease variants were verified by cosegregation analysis. We identified disease-causing mutations in the zinc-finger gene ZC4H2 in four families affected by X-linked AMC plus ID and one family affected by cerebral palsy. Several heterozygous females were also affected, but to a lesser degree. Furthermore, we found two ZC4H2 deletions and one rearrangement in two female and one male unrelated simplex cases, respectively. In mouse primary hippocampal neurons, transiently produced ZC4H2 localized to the postsynaptic compartment of excitatory synapses, and the altered protein influenced dendritic spine density. In zebrafish, antisense-morpholino-mediated zc4h2 knockdown caused abnormal swimming and impaired α-motoneuron development. All missense mutations identified herein failed to rescue the swimming defect of zebrafish morphants. We conclude that ZC4H2 point mutations, rearrangements, and small deletions cause a clinically variable broad-spectrum neurodevelopmental disorder of the central and peripheral nervous systems in both familial and simplex cases of both sexes. Our results highlight the importance of ZC4H2 for genetic testing of individuals presenting with ID plus muscle weakness and minor or major forms of AMC.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom