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XB-ART-2339
EMBO J March 9, 2005; 24 (5): 985-96.

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

Choi SC , Han JK .


Abstract
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.

PubMed ID: 15706349
PMC ID: PMC554123
Article link: EMBO J


Species referenced: Xenopus laevis
Genes referenced: dvl2 rap2a rap2b wnt8a
Morpholinos: rap2a MO1 rap2b MO1

References [+] :
Asha, The Rap1 GTPase functions as a regulator of morphogenesis in vivo. 1999, Pubmed