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β-catenin translocation into nuclei demarcates the dorsalizing centers in frog and fish embryos

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Schneider,  S
Department Cell Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Steinbeisser,  H
Department Cell Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Warga,  RM
Department Genetics, Max Planck Institute for Developmental Biology, Max Planck Society;

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Hausen,  P
Department Cell Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Citation

Schneider, S., Steinbeisser, H., Warga, R., & Hausen, P. (1996). β-catenin translocation into nuclei demarcates the dorsalizing centers in frog and fish embryos. Mechanisms of Development, 57(2), 191-198. doi:10.1016/0925-4773(96)00546-1.


Cite as: https://hdl.handle.net/21.11116/0000-000C-7DBA-7
Abstract
The question of how dorsal-ventral polarity is established in vertebrates is central to our understanding of their early development. Several lines of evidence suggest that wnt-signaling is involved in the induction of dorsal-specific gene expression in the Spemann Organizer of amphibians. Here, we show that beta-catenin, acting as a component of the wnt-pathway, transiently accumulates in nuclei on the dorsal side of Xenopus and zebrafish blastulae. The spatially restricted nuclear translocation of beta-catenin precedes the expression of dorsal-specific genes. In experimentally ventralized frog embryos the dorsal ventral pattern of beta-catenin nuclear staining is abolished; in contrast, embryos hyperdorsalized by Li-ions or by injection of Xwnt8 mRNA exhibit an enhanced nuclear accumulation of beta-catenin. The results show that translocation of beta-catenin into nuclei in the wake of wnt-signaling is an early step in the establishment of the dorsal-ventral axis in frog and fish embryos.