Article
- The EMBO Journal (2005) 24, 985 - 996
- doi:10.1038/sj.emboj.7600571
Published online: 10 February 2005
Subject Categories:
Rap2 is required for Wnt/
-catenin signaling pathway in Xenopus early development
Sun-Cheol Choi1 and Jin-Kwan Han1
- Division of Molecular and Life Sciences, Pohang University of Science and Technology, Pohang, Kyungbuk, South Korea
Correspondence to:
Jin-Kwan Han, Division of Molecular and Life Sciences, Pohang University of Science and Technology, San 31, Hyoja Dong, Pohang, Kyungbuk 790-784, South Korea. Tel.: +82 54 279 2126; Fax: +82 54 279 2199; E-mail: jkh@postech.ac.kr
Received 30 August 2004; Accepted 10 January 2005
Abstract
The Wnt/
-catenin signaling pathway is critical for the establishment of organizer and embryonic body axis in Xenopus development. Here, we present evidence that Xenopus Rap2, a member of Ras GTPase family, is implicated in Wnt/
-catenin signaling during the dorsoventral axis specification. Ectopic expression of XRap2 can lead to neural induction without mesoderm differentiation. XRap2 dorsalizes ventral tissues, inducing axis duplication, organizer-specific gene expression and convergent extension movements. Knockdown of XRap2 causes ventralized phenotypes including shortened body axis and defective dorsoanterior patterning, which are associated with aberrant Wnt signaling. In line with this, XRap2 depletion inhibits
-catenin stabilization and the induction of ectopic dorsal axis and Wnt-responsive genes caused by XWnt8, Dsh or
-catenin, but has no effect on the signaling activities of a stabilized
-catenin. Its knockdown also disrupts the vesicular localization of Dsh, thereby inhibiting Dsh-mediated
-catenin stabilization and the membrane recruitment and phosphorylation of Dsh by frizzled signaling. Taking together, we suggest that XRap2 is involved in Wnt/
-catenin signaling as a modulator of the subcellular localization of Dsh.
Keywords:
- dishevelled,
- Rap2 GTPase,
- Wnt-
catenin signaling, - Xenopus laevis



