β-Catenin regulates Cripto- and Wnt3-dependent gene expression programs in mouse axis and mesoderm formation

Author:

Morkel Markus1,Huelsken Joerg1,Wakamiya Maki2,Ding Jixiang3,van de Wetering Marc4,Clevers Hans4,Taketo Makoto M.5,Behringer Richard R.2,Shen Michael M.3,Birchmeier Walter1

Affiliation:

1. Max Delbrueck Center for Molecular Medicine, Robert-Roessle-Strasse 10, 13125 Berlin, Germany

2. Department of Molecular Genetics, The University of Texas, M. D. Anderson Cancer Center, Houston, TX 77030, USA

3. Center for Advanced Biotechnology and Medicine and Dept. of Pediatrics,UMDNJ-Robert Wood Johnson Medical School, 679 Hoes Lane, Piscataway, NJ 08854,USA

4. Department of Immunology, University Hospital Utrecht, NL-3584 CX Utrecht, The Netherlands

5. Department of Pharmacology, Kyoto University Graduate School of Medicine,Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan

Abstract

Gene expression profiling of β-catenin, Cripto and Wnt3 mutant mouse embryos has been used to characterise the genetic networks that regulate early embryonic development. We have defined genes whose expression is regulated by β-catenin during formation of the anteroposterior axis and the mesoderm, and have identified Cripto,which encodes a Nodal co-receptor, as a primary target of β-catenin signals both in embryogenesis as well as in colon carcinoma cell lines and tissues. We have also defined groups of genes regulated by Wnt3/β-catenin signalling during primitive streak and mesoderm formation. Our data assign a key role to β-catenin upstream of two distinct gene expression programs during anteroposterior axis and mesoderm formation.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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