β-Catenin has a central role in the early axial patterning of metazoan embryos. In the sea urchin, β-catenin accumulates in the nuclei of vegetal blastomeres and controls endomesoderm specification. Here, we use in-vivo measurements of the half-life of fluorescently tagged β-catenin in specific blastomeres to demonstrate a gradient in β-catenin stability along the animal-vegetal axis during early cleavage. This gradient is dependent on GSK3β-mediated phosphorylation of β-catenin. Calculations show that the difference in β-catenin half-life at the animal and vegetal poles of the early embryo is sufficient to produce a difference of more than 100-fold in levels of the protein in less than 2 hours. We show that dishevelled (Dsh), a key signaling protein, is required for the stabilization of β-catenin in vegetal cells and provide evidence that Dsh undergoes a local activation in the vegetal region of the embryo. Finally, we report that GFP-tagged Dsh is targeted specifically to the vegetal cortex of the fertilized egg. During cleavage, Dsh-GFP is partitioned predominantly into vegetal blastomeres. An extensive mutational analysis of Dsh identifies several regions of the protein that are required for vegetal cortical targeting, including a phospholipid-binding motif near the N-terminus.

Keywords:
β-Catenin, Dishevelled, GSK3β, Sea urchin embryo, Early patterning
© 2004.
2004
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