Literature DB >> 23623388

ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.

Hiromi Hirata1, Indrajit Nanda, Anne van Riesen, Gai McMichael, Hao Hu, Melanie 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 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 Falk, Dima El-Khechen, Luis F Escobar, Raoul Hennekam, Peter Wieacker, Christoph Hübner, Hans-Hilger Ropers, Jozef Gecz, Markus Schuelke, Frédéric Laumonnier, Vera M Kalscheuer.   

Abstract

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.
Copyright © 2013 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23623388      PMCID: PMC3644645          DOI: 10.1016/j.ajhg.2013.03.021

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  39 in total

1.  Deep sequencing reveals 50 novel genes for recessive cognitive disorders.

Authors:  Hossein Najmabadi; Hao Hu; Masoud Garshasbi; Tomasz Zemojtel; Seyedeh Sedigheh Abedini; Wei Chen; Masoumeh Hosseini; Farkhondeh Behjati; Stefan Haas; Payman Jamali; Agnes Zecha; Marzieh Mohseni; Lucia Püttmann; Leyla Nouri Vahid; Corinna Jensen; Lia Abbasi Moheb; Melanie Bienek; Farzaneh Larti; Ines Mueller; Robert Weissmann; Hossein Darvish; Klaus Wrogemann; Valeh Hadavi; Bettina Lipkowitz; Sahar Esmaeeli-Nieh; Dagmar Wieczorek; Roxana Kariminejad; Saghar Ghasemi Firouzabadi; Monika Cohen; Zohreh Fattahi; Imma Rost; Faezeh Mojahedi; Christoph Hertzberg; Atefeh Dehghan; Anna Rajab; Mohammad Javad Soltani Banavandi; Julia Hoffer; Masoumeh Falah; Luciana Musante; Vera Kalscheuer; Reinhard Ullmann; Andreas Walter Kuss; Andreas Tzschach; Kimia Kahrizi; H Hilger Ropers
Journal:  Nature       Date:  2011-09-21       Impact factor: 49.962

2.  Endplate destruction due to maternal antibodies in arthrogryposis multiplex congenita.

Authors:  J Reimann; L Jacobson; A Vincent; C Kornblum
Journal:  Neurology       Date:  2009-11-24       Impact factor: 9.910

3.  Parametric and nonparametric linkage analysis: a unified multipoint approach.

Authors:  L Kruglyak; M J Daly; M P Reeve-Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

4.  LIN-39 and the EGFR/RAS/MAPK pathway regulate C. elegans vulval morphogenesis via the VAB-23 zinc finger protein.

Authors:  Mark W Pellegrino; Sarfarazhussain Farooqui; Erika Fröhli; Hubert Rehrauer; Stéphanie Kaeser-Pebernard; Fritz Müller; Robin B Gasser; Alex Hajnal
Journal:  Development       Date:  2011-11       Impact factor: 6.868

5.  Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.

Authors:  L Bürglen; J Amiel; L Viollet; S Lefebvre; P Burlet; O Clermont; V Raclin; P Landrieu; A Verloes; A Munnich; J Melki
Journal:  J Clin Invest       Date:  1996-09-01       Impact factor: 14.808

6.  Duplicated gephyrin genes showing distinct tissue distribution and alternative splicing patterns mediate molybdenum cofactor biosynthesis, glycine receptor clustering, and escape behavior in zebrafish.

Authors:  Kazutoyo Ogino; Sarah L Ramsden; Natalie Keib; Günter Schwarz; Robert J Harvey; Hiromi Hirata
Journal:  J Biol Chem       Date:  2010-09-14       Impact factor: 5.157

7.  Myotonic dystrophy in pregnancy. Prenatal, neonatal and maternal considerations.

Authors:  M A Nazir; W P Dillon; E W McPherson
Journal:  J Reprod Med       Date:  1984-03       Impact factor: 0.142

8.  Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy.

Authors:  Juliane Ramser; Mary Ellen Ahearn; Claus Lenski; Kemal O Yariz; Heide Hellebrand; Michael von Rhein; Robin D Clark; Rita K Schmutzler; Peter Lichtner; Eric P Hoffman; Alfons Meindl; Lisa Baumbach-Reardon
Journal:  Am J Hum Genet       Date:  2008-01       Impact factor: 11.025

9.  A computational approach to candidate gene prioritization for X-linked mental retardation using annotation-based binary filtering and motif-based linear discriminatory analysis.

Authors:  Zané Lombard; Chungoo Park; Kateryna D Makova; Michèle Ramsay
Journal:  Biol Direct       Date:  2011-06-13       Impact factor: 4.540

10.  GeneDistiller--distilling candidate genes from linkage intervals.

Authors:  Dominik Seelow; Jana Marie Schwarz; Markus Schuelke
Journal:  PLoS One       Date:  2008-12-05       Impact factor: 3.240

View more
  25 in total

1.  Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy.

Authors:  G McMichael; M N Bainbridge; E Haan; M Corbett; A Gardner; S Thompson; B W M van Bon; C L van Eyk; J Broadbent; C Reynolds; M E O'Callaghan; L S Nguyen; D L Adelson; R Russo; S Jhangiani; H Doddapaneni; D M Muzny; R A Gibbs; J Gecz; A H MacLennan
Journal:  Mol Psychiatry       Date:  2015-02-10       Impact factor: 15.992

2.  Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures.

Authors:  Ellen Knierim; Hiromi Hirata; Nicole I Wolf; Susanne Morales-Gonzalez; Gudrun Schottmann; Yu Tanaka; Sabine Rudnik-Schöneborn; Mickael Orgeur; Klaus Zerres; Stefanie Vogt; Anne van Riesen; Esther Gill; Franziska Seifert; Angelika Zwirner; Janbernd Kirschner; Hans Hilmar Goebel; Christoph Hübner; Sigmar Stricker; David Meierhofer; Werner Stenzel; Markus Schuelke
Journal:  Am J Hum Genet       Date:  2016-02-25       Impact factor: 11.025

3.  Prioritizing genes for X-linked diseases using population exome data.

Authors:  Xiaoyan Ge; Pui-Yan Kwok; Joseph T C Shieh
Journal:  Hum Mol Genet       Date:  2014-09-12       Impact factor: 6.150

4.  Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.

Authors:  Jiyong Wang; Aidin Foroutan; Ellen Richardson; Steven A Skinner; Jack Reilly; Jennifer Kerkhof; Cynthia J Curry; Patrick S Tarpey; Stephen P Robertson; Isabelle Maystadt; Boris Keren; Joanne W Dixon; Cindy Skinner; Rachel Stapleton; Lyse Ruaud; Evren Gumus; Phillis Lakeman; Mariëlle Alders; Matthew L Tedder; Charles E Schwartz; Michael J Friez; Bekim Sadikovic; Roger E Stevenson
Journal:  Eur J Hum Genet       Date:  2022-01-07       Impact factor: 4.246

5.  Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses.

Authors:  Isabella Herman; Angad Jolly; Haowei Du; Moez Dawood; Ghada M H Abdel-Salam; Dana Marafi; Tadahiro Mitani; Daniel G Calame; Zeynep Coban-Akdemir; Jawid M Fatih; Ibrahim Hegazy; Shalini N Jhangiani; Richard A Gibbs; Davut Pehlivan; Jennifer E Posey; James R Lupski
Journal:  Am J Med Genet A       Date:  2021-11-23       Impact factor: 2.802

6.  Need for revision of the ACMG/AMP guidelines for interpretation of X-linked variants.

Authors:  Yoko Inoue; Osamu Machida; Yosuke Kita; Toshiyuki Yamamoto
Journal:  Intractable Rare Dis Res       Date:  2022-08

7.  Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita.

Authors:  Suzanna G M Frints; Friederike Hennig; Roberto Colombo; Sebastien Jacquemont; Paulien Terhal; Holly H Zimmerman; David Hunt; Bryce A Mendelsohn; Ulrike Kordaß; Richard Webster; Margje Sinnema; Omar Abdul-Rahman; Vanessa Suckow; Alberto Fernández-Jaén; Kees van Roozendaal; Servi J C Stevens; Merryn V E Macville; Salwan Al-Nasiry; Koen van Gassen; Norbert Utzig; Suzanne M Koudijs; Lesley McGregor; Saskia M Maas; Diana Baralle; Abhijit Dixit; Peter Wieacker; Marcus Lee; Arthur S Lee; Elizabeth C Engle; Gunnar Houge; Gyri A Gradek; Andrew G L Douglas; Cheryl Longman; Shelagh Joss; Danita Velasco; Raoul C Hennekam; Hiromi Hirata; Vera M Kalscheuer
Journal:  Hum Mutat       Date:  2019-08-21       Impact factor: 4.878

8.  A 7-year old female with arthrogryposis multiplex congenita, Duane retraction syndrome, and Marcus Gunn phenomenon due to a ZC4H2 gene mutation: a clinical presentation of the Wieacker-Wolff syndrome.

Authors:  Deena Godfrey; Alcy Torres; Gena Heidary; Hovra Zahoor; Arthur Lee; Gerard Berry; Elizabeth Engle
Journal:  Ophthalmic Genet       Date:  2021-05-05       Impact factor: 1.274

9.  Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes.

Authors:  Tejasvi S Niranjan; Cindy Skinner; Melanie May; Tychele Turner; Rebecca Rose; Roger Stevenson; Charles E Schwartz; Tao Wang
Journal:  PLoS One       Date:  2015-02-13       Impact factor: 3.240

10.  ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons.

Authors:  Melanie May; Kyu-Seok Hwang; Judith Miles; Charlie Williams; Tejasvi Niranjan; Stephen G Kahler; Pietro Chiurazzi; Katharina Steindl; Peter J Van Der Spek; Sigrid Swagemakers; Jennifer Mueller; Shannon Stefl; Emil Alexov; Jeong-Im Ryu; Jung-Hwa Choi; Hyun-Taek Kim; Patrick Tarpey; Giovanni Neri; Lynda Holloway; Cindy Skinner; Roger E Stevenson; Richard I Dorsky; Tao Wang; Charles E Schwartz; Cheol-Hee Kim
Journal:  Hum Mol Genet       Date:  2015-06-08       Impact factor: 6.150

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.