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First published online 10 December 2003
doi: 10.1242/dev.00935


Development 131, 263-274 (2004)
Published by The Company of Biologists 2004


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Tcf3: a transcriptional regulator of axis induction in the early embryo

Bradley J. Merrill1, H. Amalia Pasolli1, Lisa Polak1, Michael Rendl1, Maria J. García-García2, Kathryn V. Anderson2 and Elaine Fuchs1,*

1 Howard Hughes Medical Institute, Laboratory of Mammalian Cell Biology and Development, The Rockefeller University, New York, NY 10021, USA
2 Department of Developmental Biology, Sloan Kettering Memorial Institute, New York, NY 10021, USA

* Author for correspondence (e-mail: fuchs1b{at}rockefeller.edu)

Received for publication 15 October 2003.

The roles of Lef/Tcf proteins in determining cell fate characteristics have been described in many contexts during vertebrate embryogenesis, organ and tissue homeostasis, and cancer formation. Although much of the accumulated work on these proteins involves their ability to transactivate target genes when stimulated by ß-catenin, Lef/Tcf proteins can repress target genes in the absence of stabilized ß-catenin. By ablating Tcf3 function, we have uncovered an important requirement for a repressor function of Lef/Tcf proteins during early mouse development. Tcf3-/- embryos proceed through gastrulation to form mesoderm, but they develop expanded and often duplicated axial mesoderm structures, including nodes and notochords. These duplications are preceded by ectopic expression of Foxa2, an axial mesoderm gene involved in node specification, with a concomitant reduction in Lefty2, a marker for lateral mesoderm. By contrast, expression of a ß-catenin-dependent, Lef/Tcf reporter (TOPGal), is not ectopically activated but is faithfully maintained in the primitive streak. Taken together, these data reveal a unique requirement for Tcf3 repressor function in restricting induction of the anterior-posterior axis.

Key words: Wnt, Gastrulation, Tcf3, Node, Axis


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