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PMID: 9806909 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Suppression of GATA factor activity causes axis duplication in Xenopus.

Development (Cambridge, England) ·Vol. 125 ·No. 23 ·1998-12-00 ·Pages 4595-605

Sykes TG, Rodaway AR, Walmsley ME, Patient RK

Abstract

In Xenopus, the dorsoventral axis is patterned by the interplay between active signalling in ventral territories, and secreted antagonists from Spemann's organiser. Two signals are important in ventral cells, bone morphogenetic protein-4 (BMP-4) and Wnt-8. BMP-4 plays a conserved role in patterning the vertebrate dorsoventral axis, whilst the precise role of Wnt-8 and its relationship with BMP-4, are still unclear. Here we have investigated the role played by the GATA family of transcription factors, which are expressed in ventral mesendoderm during gastrulation and are required for the differentiation of blood and endodermal tissues. Injection ventrally of a dominant-interfering GATA factor (called G2en) induced the formation of secondary axes that phenocopy those induced by the dominant-negative BMP receptor. However, unlike inhibiting BMP signalling, inhibiting GATA activity in the ectoderm does not lead to neuralisation. In addition, analysis of gene expression in G2en injected embryos reveals that at least one known target gene for BMP-4, the homeobox gene Vent-2, is unaffected. In contrast, the expression of Wnt-8 and the homeobox gene Vent-1 is suppressed by G2en, whilst the organiser-secreted BMP antagonist chordin becomes ectopically expressed. These data therefore suggest that GATA activity is essential for ventral cell fate and that subsets of ventralising and dorsalising genes require GATA activity for their expression and suppression, respectively. Finally, using G2en, we show that suppression of Wnt-8 expression, in conjunction with blocked BMP signalling, does not lead to head formation, suggesting that the head-suppressing Wnt signal may not be Wnt-8.

MeSH Terms
Animals Body Patterning Bone Morphogenetic Protein 4 Bone Morphogenetic Proteins/physiology Embryo, Nonmammalian/physiology Endoderm/physiology Female Gastrula/physiology Gene Expression Regulation, Developmental Mesoderm/physiology Oocytes/cytology,physiology Promoter Regions, Genetic Proto-Oncogene Proteins/physiology Reverse Transcriptase Polymerase Chain Reaction Signal Transduction Transcription Factors/antagonists & inhibitors,genetics,metabolism Wnt Proteins Xenopus/embryology Xenopus Proteins Zebrafish Proteins
Chemicals
Bone Morphogenetic Protein 4 Bone Morphogenetic Proteins Proto-Oncogene Proteins Transcription Factors Wnt Proteins Xenopus Proteins Zebrafish Proteins bmp4 protein, Xenopus bmp4 protein, zebrafish wnt8a protein, Xenopus
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sykes T G
Developmental Biology Research Centre, The Randall Institute, King's College London, London WC2B 5RL, UK.
Rodaway A R
Walmsley M E
Patient R K
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
1998-12-00
Pages
4595-605
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
Wellcome Trust · United Kingdom
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