PUBLICATION

Zebrafish narrowminded suggests a genetic link between formation of neural crest and primary sensory neurons

Authors
Artinger, K.B., Chitnis, A.B., Mercola, M., and Driever, W.
ID
ZDB-PUB-990824-13
Date
1999
Source
Development (Cambridge, England)   126(18): 3969-3979 (Journal)
Registered Authors
Artinger, Kristin Bruk, Chitnis, Ajay, Driever, Wolfgang
Keywords
narrowminded; neural crest; sensory neurons; cell signalling; zebrafish
MeSH Terms
  • Animals
  • Antigens, Surface/genetics
  • Body Patterning/genetics
  • ELAV Proteins
  • ELAV-Like Protein 3
  • Embryo, Nonmammalian
  • Embryonic Induction/genetics
  • Female
  • Gene Expression Regulation, Developmental*
  • Homeodomain Proteins/genetics
  • Homozygote
  • In Situ Hybridization
  • Male
  • Mutation
  • Nerve Tissue Proteins/genetics
  • Nervous System/embryology*
  • Nervous System Malformations/genetics
  • Neural Crest/embryology*
  • Neural Crest/physiology
  • Neurons, Afferent/physiology*
  • Otx Transcription Factors
  • RNA-Binding Proteins*
  • Trans-Activators/genetics
  • Transcription Factors/genetics
  • Zebrafish/embryology*
  • Zebrafish/genetics*
  • Zebrafish Proteins*
PubMed
10457007
Abstract
In the developing vertebrate nervous system, both neural crest and sensory neurons form at the boundary between non-neural ectoderm and the neural plate. From an in situ hybridization based expression analysis screen, we have identified a novel zebrafish mutation, narrowminded (nrd), which reduces the number of early neural crest cells and eliminates Rohon-Beard (RB) sensory neurons. Mosaic analysis has shown that the mutation acts cell autonomously suggesting that nrd is involved in either the reception or interpretation of signals at the lateral neural plate boundary. Characterization of the mutant phenotype indicates that nrd is required for a primary wave of neural crest cell formation during which progenitors generate both RB sensory neurons and neural crest cells. Moreover, the early deficit in neural crest cells in nrd homozygotes is compensated later in development. Thus, we propose that a later wave can compensate for the loss of early neural crest cells but, interestingly, not the RB sensory neurons. We discuss the implications of these findings for the possibility that RB sensory neurons and neural crest cells share a common evolutionary origin.
Genes / Markers
Figures
Expression
Phenotype
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping
Errata and Notes