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Journal Article

Zebrafish zic1 expression in brain and somites is affected by BMP and Hedgehog signalling


Schulte-Merker,  S       
Department Cell Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Rohr, K., Schulte-Merker, S., & Tautz, D. (1999). Zebrafish zic1 expression in brain and somites is affected by BMP and Hedgehog signalling. Mechanisms of Development, 85(1-2), 147-159. doi:10.1016/s0925-4773(99)00044-1.

Cite as: https://hdl.handle.net/21.11116/0000-000D-DA18-3
Here we report the expression of the zebrafish zic1 gene, also known as opl, a homologue to other vertebrate Zic genes and the Drosophila odd-paired gene. zic1 expression starts during epiboly stages in lateral parts of the neural plate and eventually comes to lie in dorsal regions of the developing brain following the morphogenetic movements of neural tube formation. To address the question whether BMP2 signalling affects the extent of zic1 expression, we analysed swirl and chordino mutant embryos. Expanded Zic1 expression in swirl and reduced expression in chordino as well as in bmp2 injected embryos suggest that BMP2 and its antagonists define the extent of zic1 expression in the neural plate. By searching for factors responsible for the dorsal restriction of Zic1 expression, we found zic1 expression is eliminated in sonic hedgehog (shh) injected embryos. The most rostral expression however is not affected by Shh suggesting that Shh plays a different role in dorso-ventral patterning of the future telencephalon. During somitogenesis zic1 is expressed in the dorsal most part of the developing somites. Here zic1 marks cells that are distinct from the main adaxial somite portion, the future myomere. zic1 expression in the somites is expanded in swirl but reduced in shh injected embryos, suggesting these factors have opposing activity in dorsoventral patterning of the somites. Later, a growing mass of zic1 expressing cells occurs in a dorsal mesenchyme that eventually invades the dorsal fin fold, suggesting a somitic contribution to the dorsal fin mesenchyme.