PUBLICATION

Repressor Dimerization in the Zebrafish Somitogenesis Clock

Authors
Cinquin, O.
ID
ZDB-PUB-070303-19
Date
2007
Source
PLoS Computational Biology   3(2): e32 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Animals
  • Biological Clocks/physiology*
  • Body Patterning/physiology*
  • Computer Simulation
  • Dimerization
  • Gene Expression/physiology
  • Models, Biological*
  • Repressor Proteins/physiology*
  • Signal Transduction/physiology*
  • Zebrafish/embryology
  • Zebrafish/physiology*
  • Zebrafish Proteins/chemistry
  • Zebrafish Proteins/physiology*
PubMed
17305423 Full text @ PLoS Comput. Biol.
Abstract
The oscillations of the somitogenesis clock are linked to the fundamental process of vertebrate embryo segmentation, yet little is known about their generation. In zebrafish, it has been proposed that Her proteins repress the transcription of their own mRNA. However, in its simplest form, this model is incompatible with the fact that morpholino knockdown of Her proteins can impair expression of their mRNA. Simple self-repression models also do not account for the spatiotemporal pattern of gene expression, with waves of gene expression shrinking as they propagate. Here we study computationally the networks generated by the wealth of dimerization possibilities amongst transcriptional repressors in the zebrafish somitogenesis clock. These networks can reproduce knockdown phenotypes, and strongly suggest the existence of a Her1-Her7 heterodimer, so far untested experimentally. The networks are the first reported to reproduce the spatiotemporal pattern of the zebrafish somitogenesis clock; they shed new light on the role of Her13.2, the only known link between the somitogenesis clock and positional information in the paraxial mesoderm. The networks can also account for perturbations of the clock by manipulation of FGF signaling. Achieving an understanding of the interplay between clock oscillations and positional information is a crucial first step in the investigation of the segmentation mechanism.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping