PUBLICATION

A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathies

Authors
Shaheen, R., Schmidts, M., Faqeih, E., Hashem, A., Lausch, E., Holder, I., Superti-Furga, A., UK10 K consortium, Mitchison, H.M., Almoisheer, A., Alamro, R., Alshiddi, T., Alzahrani, F., Beales, P.L., Alkuraya, F.S.
ID
ZDB-PUB-141102-1
Date
2015
Source
Human molecular genetics   24(5): 1410-9 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Bone and Bones/abnormalities*
  • Bone and Bones/metabolism
  • Cell Cycle Proteins/genetics*
  • Cell Cycle Proteins/metabolism
  • Centrioles/genetics*
  • Centrioles/metabolism
  • Chromosome Mapping
  • Chromosomes, Human, Pair 5/genetics
  • Chromosomes, Human, Pair 5/metabolism
  • Cilia/pathology
  • Cohort Studies
  • Disease Models, Animal
  • Ellis-Van Creveld Syndrome/genetics*
  • Europe
  • Female
  • Fibroblasts/cytology
  • Fibroblasts/metabolism
  • Genetic Loci
  • Genome-Wide Association Study
  • Humans
  • Infant
  • Magnetic Resonance Imaging
  • Male
  • Molecular Sequence Data
  • Mutation, Missense*
  • Pedigree
  • Phenotype
  • Saudi Arabia
  • Zebrafish
PubMed
25361962 Full text @ Hum. Mol. Genet.
Abstract
Jeune asphyxiating thoracic dystrophy (JATD) is a skeletal dysplasia characterized by a small thoracic cage and a range of skeletal and extra-skeletal anomalies. JATD is genetically heterogeneous with at least nine genes identified, all encoding ciliary proteins, hence the classification of JATD as a skeletal ciliopathy. Consistent with the observation that the heterogeneous molecular basis of JATD has not been fully determined yet, we have identified two consanguineous Saudi families segregating JATD who share a single identical ancestral homozygous haplotype among the affected members. Whole-exome sequencing revealed a single novel variant within the disease haplotype in CEP120, which encodes a core centriolar protein. Subsequent targeted sequencing of CEP120 in Saudi and European JATD cohorts identified two additional families with the same missense mutation. Combining the four families in linkage analysis confirmed a significant genomewide linkage signal at the CEP120 locus. This missense change alters a highly conserved amino acid within CEP120 (p.Ala199Pro). In addition, we show marked reduction of cilia and abnormal number of centrioles in fibroblasts from one affected individual. Inhibition of the CEP120 ortholog in zebrafish produced pleiotropic phenotypes characteristic of cilia defects including abnormal body curvature, hydrocephalus, otolith defects and abnormal renal, head and craniofacial development. We also demonstrate that in CEP120 morphants, cilia are shortened in the neural tube and disorganized in the pronephros. These results are consistent with aberrant CEP120 being implicated in the pathogenesis of JATD, and expand the role of centriolar proteins in skeletal ciliopathies.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping