Murine Nr4a1 and Herpud1 are up-regulated by Wnt-1, but the homologous human genes are independent from β-catenin activation

Author:

CHTARBOVA Slava1,NIMMRICH Inko1,ERDMANN Silke1,HERTER Peter1,RENNER Matthias2,KITAJEWSKI Jan3,MÜLLER Oliver1

Affiliation:

1. Arbeitsgruppe Tumorgenetik, Max-Planck-Institut für molekulare Physiologie, Otto-Hahn-Strasse 11, D-44227 Dortmund, Germany

2. Institut für Virologie, Veterinärmedizinische Universität, Wien, Austria,

3. Departments of Pathology and Obstetrics/Gynecology, Columbia University, New York, NY 10032, U.S.A.

Abstract

The Wnt signal transduction pathway regulates morphogenesis and mitogenesis of cells in multicellular organisms. A major downstream consequence of Wnt-1 signalling is the activation of β-catenin/T-cell factor (TCF)-mediated transcription. We compared Wnt-1-transformed murine mammary epithelial cells with control cells by subtractive hybridization. We found the two genes Nr4a1 and Herpud1 to be overexpressed in Wnt-1-transformed cells. Remarkably, the transcription levels of the two homologous human genes NR4A1 and HERPUD1 are neither activated in cells with activated β-catenin/TCF-mediated transcription nor can be induced by β-catenin transfection. These results indicate different regulation mechanisms of the two genes in murine and human cells.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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