Article

  • The EMBO Journal (2005) 24, 985 - 996
  • doi:10.1038/sj.emboj.7600571

Published online: 10 February 2005

Rap2 is required for Wnt/bold beta-catenin signaling pathway in Xenopus early development

Sun-Cheol Choi1 and Jin-Kwan Han1

  1. 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


The Wnt/beta-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/beta-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 beta-catenin stabilization and the induction of ectopic dorsal axis and Wnt-responsive genes caused by XWnt8, Dsh or beta-catenin, but has no effect on the signaling activities of a stabilized beta-catenin. Its knockdown also disrupts the vesicular localization of Dsh, thereby inhibiting Dsh-mediated beta-catenin stabilization and the membrane recruitment and phosphorylation of Dsh by frizzled signaling. Taking together, we suggest that XRap2 is involved in Wnt/beta-catenin signaling as a modulator of the subcellular localization of Dsh.

  • Keywords:

    • dishevelled,
    • Rap2 GTPase,
    • Wnt-beta catenin signaling,
    • Xenopus laevis