PUBLICATION

Nodal signaling and the zebrafish organizer

Authors
Schier, A.F. and Talbot, W.S.
ID
ZDB-PUB-010410-3
Date
2001
Source
The International journal of developmental biology   45(1): 289-97 (Journal)
Registered Authors
Schier, Alexander, Talbot, William S.
Keywords
none
MeSH Terms
  • Animals
  • Body Patterning
  • Genes, Homeobox
  • Homeodomain Proteins/genetics
  • Homeodomain Proteins/physiology
  • Left-Right Determination Factors
  • Mesoderm/cytology
  • Mutation
  • Nervous System/embryology
  • Nodal Protein
  • Organizers, Embryonic*
  • Phenotype
  • Signal Transduction
  • Transforming Growth Factor beta/genetics
  • Transforming Growth Factor beta/physiology*
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Zebrafish/physiology
  • Zebrafish Proteins*
PubMed
11291859
Abstract
Systematic genetic screens in zebrafish have led to the discovery of mutations that affect organizer function and development. The molecular isolation and phenotypic analysis of the affected genes have revealed that TGF-beta signals of the Nodal family play a key role in organizer formation. The activity of the Nodal signals Cyclops and Squint is regulated extracellularly by the EGF-CFC cofactor One-eyed Pinhead and by antagonists belonging to the Lefty family of TGF-beta molecules. In the absence of Nodal signaling, the fate of cells in the organizer is transformed from dorsal mesoderm to neural ectoderm. Differential Nodal signaling also patterns the organizer along the anterior-posterior axis, with high levels required for anterior cell fates and lower levels for posterior fates. In addition, Nodal signaling cooperates with the homeodomain transcription factor Bozozok in organizer formation and neural patterning. The combination of genetic, molecular and embryological approaches in zebrafish has thus provided a framework to understand the mechanisms underlying organizer development.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping