PUBLICATION

Inhibition of Xbra transcription activation causes defects in mesodermal patterning and reveals autoregulation of Xbra in dorsal mesoderm

Authors
Conlon, F.L., Sedgwick, S.G., Weston, K.M., and Smith, J.C.
ID
ZDB-PUB-961101-14
Date
1996
Source
Development (Cambridge, England)   122(8): 2427-2435 (Journal)
Registered Authors
Smith, Jim
Keywords
none
MeSH Terms
  • Animals
  • Base Sequence
  • Chromosome Mapping
  • DNA
  • DNA-Binding Proteins/genetics*
  • DNA-Binding Proteins/metabolism
  • Fetal Proteins/genetics*
  • Fetal Proteins/metabolism
  • Gene Expression Regulation, Developmental*
  • Homeodomain Proteins/genetics
  • Insect Hormones/genetics
  • Mesoderm/metabolism
  • Molecular Sequence Data
  • Recombinant Fusion Proteins/genetics
  • Recombinant Fusion Proteins/metabolism
  • T-Box Domain Proteins*
  • Trans-Activators/genetics*
  • Trans-Activators/metabolism
  • Transcription Factors/genetics
  • Transcriptional Activation
  • Xenopus
  • Zebrafish
PubMed
8756288 Full text @ Development
Abstract
The Brachyury (T) gene is required for formation of posterior mesoderm and for axial development in both mouse and zebrafish embryos. In this paper, we first show that the Xenopus homologue of Brachyury, Xbra, and the zebrafish homologue, no tail (ntl), both function as transcription activators. The activation domains of both proteins map to their carboxy terminal regions, and we note that the activation domain is absent in two zebrafish Brachyury mutations, suggesting that it is required for gene function. A dominant- interfering Xbra construct was generated by replacing the activation domain of Xbra with the repressor domain of the Drosophila engrailed protein. Microinjection of RNA encoding this fusion protein allowed us to generate Xenopus and zebrafish embryos which show striking similarities to genetic mutants in mouse and fish. These results indicate that the function of Brachyury during vertebrate gastrulation is to activate transcription of mesoderm-specific genes. Additional experiments show that Xbra transcription activation is required for regulation of Xbra itself in dorsal, but not ventral, mesoderm. The approach described in this paper, in which the DNA-binding domain of a transcription activator is fused to the engrailed repressor domain, should assist in the analysis of other Xenopus and zebrafish transcription factors.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping