Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence

[img]
Preview
PDF (Original Article) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
4MB
[img] Other (Supporting Information)
46MB

Item Type:Article
Title:Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence
Creators Name:Bonnin, E. and Cabochette, P. and Filosa, A. and Jühlen, R. and Komatsuzaki, S. and Hezwani, M. and Dickmanns, A. and Martinelli, V. and Vermeersch, M. and Supply, L. and Martins, N. and Pirenne, L. and Ravenscroft, G. and Lombard, M. and Port, S. and Spillner, C. and Janssens, S. and Roets, E. and Van Dorpe, J. and Lammens, M. and Kehlenbach, R.H. and Ficner, R. and Laing, N.G. and Hoffmann, K. and Vanhollebeke, B. and Fahrenkrog, B.
Abstract:Nucleoporins build the nuclear pore complex (NPC), which, as sole gate for nuclear-cytoplasmic exchange, is of outmost importance for normal cell function. Defects in the process of nucleocytoplasmic transport or in its machinery have been frequently described in human diseases, such as cancer and neurodegenerative disorders, but only in a few cases of developmental disorders. Here we report biallelic mutations in the nucleoporin NUP88 as a novel cause of lethal fetal akinesia deformation sequence (FADS) in two families. FADS comprises a spectrum of clinically and genetically heterogeneous disorders with congenital malformations related to impaired fetal movement. We show that genetic disruption of nup88 in zebrafish results in pleiotropic developmental defects reminiscent of those seen in affected human fetuses, including locomotor defects as well as defects at neuromuscular junctions. Phenotypic alterations become visible at distinct developmental stages, both in affected human fetuses and in zebrafish, whereas early stages of development are apparently normal. The zebrafish phenotypes caused by nup88 deficiency are rescued by expressing wild-type Nup88 but not the disease-linked mutant forms of Nup88. Furthermore, using human and mouse cell lines as well as immunohistochemistry on fetal muscle tissue, we demonstrate that NUP88 depletion affects rapsyn, a key regulator of the muscle nicotinic acetylcholine receptor at the neuromuscular junction. Together, our studies provide the first characterization of NUP88 in vertebrate development, expand our understanding of the molecular events causing FADS, and suggest that variants in NUP88 should be investigated in cases of FADS.
Keywords:Alleles, Amino Acid Sequence, Amino Acid Sequence Homology, Animal Disease Models, Arthrogryposis, Consanguinity, Genetically Modified Animals, Lethal Genes, Molecular Models, Muscle Proteins, Mutation, Neuromuscular Junction, Nicotinic Receptors, Nuclear Pore Complex Proteins, Pedigree, Pregnancy, Protein Conformation, Zebrafish Proteins, Animals, Zebrafish
Source:PLoS Genetics
ISSN:1553-7404
Publisher:Public Library of Science (U.S.A.)
Volume:14
Number:12
Page Range:e1007845
Date:13 December 2018
Official Publication:https://doi.org/10.1371/journal.pgen.1007845
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library