PUBLICATION

Posterior axis formation requires Dlx5/Dlx6 expression at the neural plate border

Authors
Narboux-Neme, N., Ekker, M., Levi, G., Heude, E.
ID
ZDB-PUB-190320-12
Date
2019
Source
PLoS One   14: e0214063 (Journal)
Registered Authors
Ekker, Marc
Keywords
none
MeSH Terms
  • Neurulation/genetics
  • Neurulation/physiology
  • Male
  • Gene Knockdown Techniques
  • Zebrafish/embryology
  • Zebrafish/genetics
  • Zebrafish/metabolism
  • Transcription Factors/deficiency
  • Transcription Factors/genetics
  • Transcription Factors/metabolism*
  • Multigene Family
  • Neural Tube Defects/embryology
  • Neural Tube Defects/genetics
  • Neural Tube Defects/metabolism
  • Gene Expression Regulation, Developmental
  • Humans
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Female
  • Homeodomain Proteins/genetics
  • Homeodomain Proteins/metabolism*
  • Mice, Knockout
  • Body Patterning/genetics
  • Body Patterning/physiology
  • Pregnancy
  • Animals
  • Zebrafish Proteins/deficiency
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
  • Mice
  • Neural Plate/embryology*
  • Neural Plate/metabolism*
(all 32)
PubMed
30889190 Full text @ PLoS One
Abstract
Neural tube defects (NTDs), one of the most common birth defects in human, present a multifactorial etiology with a poorly defined genetic component. The Dlx5 and Dlx6 bigenic cluster encodes two evolutionary conserved homeodomain transcription factors, which are necessary for proper vertebrate development. It has been shown that Dlx5/6 genes are essential for anterior neural tube closure, however their role in the formation of the posterior structures has never been described. Here, we show that Dlx5/6 expression is required during vertebrate posterior axis formation. Dlx5 presents a similar expression pattern in neural plate border cells during posterior neurulation of zebrafish and mouse. Dlx5/6-inactivation in the mouse results in a phenotype reminiscent of NTDs characterized by open thoracic and lumbar vertebral arches and failure of epaxial muscle formation at the dorsal midline. The dlx5a/6a zebrafish morphants present posterior NTDs associated with abnormal delamination of neural crest cells showing altered expression of cell adhesion molecules and defects of motoneuronal development. Our findings provide new molecular leads to decipher the mechanisms of vertebrate posterior neurulation and might help to gather a better understanding of human congenital NTDs etiology.
Genes / Markers
Figures
Figure Gallery (8 images)
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Expression
Phenotype
Mutations / Transgenics
No data available
Human Disease / Model
No data available
Sequence Targeting Reagents
Target Reagent Reagent Type
dlx5aMO2-dlx5aMRPHLNO
dlx5aMO4-dlx5aMRPHLNO
dlx6aMO1-dlx6aMRPHLNO
dlx6aMO2-dlx6aMRPHLNO
1 - 4 of 4
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Fish
1 - 2 of 2
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Antibodies
Name Type Antigen Genes Isotypes Host Organism
Ab-SV2monoclonal
    IgG1Mouse
    1 - 1 of 1
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    Orthology
    No data available
    Engineered Foreign Genes
    No data available
    Mapping
    No data available