ZFIN ID: ZDB-PUB-161007-1
Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes
de Peralta, M.S., Mouguelar, V.S., Sdrigotti, M.A., Ishiy, F.A., Fanganiello, R.D., Passos-Bueno, M.R., Coux, G., Calcaterra, N.B.
Date: 2016
Source: Cell Death & Disease   7: e2397 (Journal)
Registered Authors: Calcaterra, Nora
Keywords: none
MeSH Terms:
  • Animals
  • Craniofacial Abnormalities/complications*
  • Craniofacial Abnormalities/genetics*
  • Craniofacial Abnormalities/pathology
  • Embryo, Nonmammalian/metabolism
  • Gene Expression Profiling
  • Gene Knockdown Techniques
  • Humans
  • Mandibulofacial Dysostosis/complications*
  • Mandibulofacial Dysostosis/genetics*
  • Mandibulofacial Dysostosis/pathology
  • Mesoderm/metabolism
  • Models, Biological
  • Oxidation-Reduction
  • Phenotype
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • RNA-Binding Proteins/genetics
  • RNA-Binding Proteins/metabolism*
  • Reactive Oxygen Species/metabolism
  • Signal Transduction/genetics*
  • Transcription, Genetic
  • Tumor Suppressor Protein p53/metabolism
  • Zebrafish/embryology
  • Zebrafish/genetics
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
PubMed: 27711076 Full text @ Cell Death Dis.
Treacher Collins Syndrome (TCS) is a rare congenital disease (1:50 000 live births) characterized by craniofacial defects, including hypoplasia of facial bones, cleft palate and palpebral fissures. Over 90% of the cases are due to mutations in the TCOF1 gene, which codifies the nucleolar protein Treacle. Here we report a novel TCS-like zebrafish model displaying features that fully recapitulate the spectrum of craniofacial abnormalities observed in patients. As it was reported for a Tcof1+/- mouse model, Treacle depletion in zebrafish caused reduced rRNA transcription, stabilization of Tp53 and increased cell death in the cephalic region. An increase of ROS along with the overexpression of redox-responsive genes was detected; furthermore, treatment with antioxidants ameliorated the phenotypic defects of craniofacial anomalies in TCS-like larvae. On the other hand, Treacle depletion led to a lowering in the abundance of Cnbp, a protein required for proper craniofacial development. Tcof1 knockdown in transgenic zebrafish overexpressing cnbp resulted in barely affected craniofacial cartilage development, reinforcing the notion that Cnbp has a role in the pathogenesis of TCS. The cnbp overexpression rescued the TCS phenotype in a dose-dependent manner by a ROS-cytoprotective action that prevented the redox-responsive genes' upregulation but did not normalize the synthesis of rRNAs. Finally, a positive correlation between the expression of CNBP and TCOF1 in mesenchymal cells from both control and TCS subjects was found. Based on this, we suggest CNBP as an additional target for new alternative therapeutic treatments to reduce craniofacial defects not only in TCS but also in other neurocristopathies.