Zoological Science

Published by: Zoological Society of Japan



Zoological Science 21(4):407-416. 2004
doi: 10.2108/zsj.21.407

Inhibition of the Canonical Wnt Signaling Pathway in Cytoplasm: a Novel Property of the Carboxyl Terminal Domains of Two Xenopus ELL Genes

Kenji Sakurai1, Tatsuo Michiue2, Akira Kikuchi3, and Makoto Asashima2,4,*

1Department of Biology, Graduate School of Science, University of Tokyo, 3-8-1, Komaba, Meguro-ku, Tokyo 153-8902, Japan

2SOPST Project, Japan Science and Technology Agency (JST), 3-8-1, Komaba, Meguro-ku, Tokyo 153-8902, Japan

3Department of Biochemistry, Hiroshima University School of Medicine, 1-2-3, Kasumi, Minami-ku, Hiroshima 734-8551, Japan

4Department of Life Science (Biology), Graduate School of Arts and Sciences, University of Tokyo, 3-8-1, Komaba, Meguro-ku, Tokyo 153-8902, Japan

* Corresponding author: Tel. +81-3-5454-6632; FAX. +81-3-5454-4330. E-mail:

The Wnt signaling pathways are important in many developmental events. The canonical Wnt pathway is one of the three major Wnt-mediated intracellular signaling pathways and is thought to activate Dvl followed by the stabilization of β-catenin. In Xenopus, this pathway is involved in dorsal determination, anterior-posterior patterning during gastrulation, and neural induction. Here we describe a role for the Xenopus ELL Eleven-nineteen Lysine-rich(Leukemia) gene product in canonical Wnt signaling. Trans-location of ELL has been associated with acute myeloid leukemia and the protein possesses three functional domains. We identified rELL-C from a rat brain cDNA library as a binding factor for Dishevelled (Dvl); it represents a partial sequence of rat ELL lacking the pol II elongation domain and has been shown to suppress canonical Wnt signaling. Next, we isolated two Xenopus homologs of ELL, xELL1 and xELL2. No obvious phenotypes were observed with microinjection of full-length xELL1 or xELL2 mRNA, however, microinjection with their occludin homology domain inhibited Wnt signaling at the level of Dvl and upstream of β-catenin. Intracellular localization of microinjected xELL1- and xELL2-GFP mRNAs showed localization of the full-length products in the nucleus and the occludin-homology domain products in cytoplasm. These results raise the possibility that ELL, which is thought to function as a transcription factor in nuclei, can serve other, novel roles to suppress canonical Wnt signaling in the cytoplasm.

Received: December 18, 2003; Accepted: February 7, 2004



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