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PMID: 9012537 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

The Xenopus T-box gene, Antipodean, encodes a vegetally localised maternal mRNA and can trigger mesoderm formation.

Development (Cambridge, England) ·Vol. 122 ·No. 12 ·1996-12-00 ·Pages 4179-88

Stennard F, Carnac G, Gurdon JB

Abstract

We have used differential display to identify genes inducible by activin and isolated a novel member of the T-box gene family that includes the Xenopus genes Xbrachyury and Eomesodermin. Here we show that this novel gene is unique within the T-box family because it is maternally expressed at a high level. Furthermore, it belongs to a rare class of maternal mRNAs in Xenopus that are localised to the vegetal hemisphere of the egg and we have therefore named it Antipodean. We show here that low amounts of Antipodean injected into ectoderm (animal cap cells) strongly induce pan mesodermal genes such as Xbrachyury and ventral mesodermal genes such as Xwnt-8. Overexpression of Antipodean generates mesoderm of ventral character, and induces muscle only weakly. This property is consistent with the observed late zygotic Antipodean mRNA expression in the posterior paraxial mesoderm and ventral blastopore, and its exclusion from the most dorsal mesodermal structure, the notochord. Antipodean is induced by several molecules of the TGF-beta class, but in contrast to Xbrachyury, not by bFGF. This result suggests that the expression of these T-box genes may be under the control of different regulatory pathways. Finally, we demonstrate that Antipodean and Eomesodermin induce each other and both are able to induce Xbrachyury. The early zygotic expression of Antipodean is not induced by Xbrachyury, though later it is to some extent. Considering its maternal content, Antipodean could initiate a cascade of T-box gene activations. The expression of these genes may, in turn, sustain each other's expression to define and maintain the mesoderm identity in Xenopus.

MeSH Terms
Amino Acid Sequence Animals Cell Compartmentation Cloning, Molecular DNA, Complementary/genetics DNA-Binding Proteins/genetics Embryonic Development Embryonic Induction Female Fetal Proteins Fibroblast Growth Factor 2/pharmacology Gene Expression Regulation, Developmental Mesoderm/physiology Molecular Sequence Data Oogenesis RNA, Messenger/isolation & purification Sequence Analysis, DNA Sequence Homology, Amino Acid T-Box Domain Proteins Time Factors Tissue Distribution Transcription Factors/genetics Transforming Growth Factor beta/pharmacology Xenopus/embryology,genetics Xenopus Proteins
Chemicals
DNA, Complementary DNA-Binding Proteins EOMES protein, Xenopus Fetal Proteins RNA, Messenger T-Box Domain Proteins Transcription Factors Transforming Growth Factor beta VegT protein, Xenopus Xenopus Proteins Fibroblast Growth Factor 2 Brachyury protein
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Stennard F
Wellcome/CRC Institute, Cambridge, United Kingdom.
Carnac G
Gurdon J B
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
1996-12-00
Pages
4179-88
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
Wellcome Trust · United Kingdom
Databases
GENBANK
X99905
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