Abstract

Neural crest (NC) induction is a long process that continues through gastrula and neurula stages. In order to reveal additional stages of NC induction we performed a series of explants where different known inducing tissues were taken along with the prospective NC. Interestingly the dorso-lateral marginal zone (DLMZ) is only able to promote the expression of a subset of neural plate border (NPB) makers without the presence of specific NC markers. We then analysed the temporal requirement for BMP and Wnt signals for the NPB genes Hairy2a and Dlx5, compared to the expression of neural plate (NP) and NC genes. Although the NP is sensitive to BMP levels at early gastrula stages, Hairy2a/Dlx5 expression is unaffected. Later, the NP becomes insensitive to BMP levels at late gastrulation when NC markers require an inhibition. The NP requires an inhibition of Wnt signals prior to gastrulation, but becomes insensitive during early gastrula stages when Hairy2a/Dlx5 requires an inhibition of Wnt signalling. An increase in Wnt signalling is then important for the switch from NPB to NC at late gastrula stages. In addition to revealing an additional distinct signalling event in NC induction, this work emphasizes the importance of integrating both timing and levels of signalling activity during the patterning of complex tissues such as the vertebrate ectoderm.

Highlights

  • Induction is a process by which an inducing tissue releases a signal that results in a change in the direction of differentiation of the responding tissue (Gurdon, 1987)

  • We show that the dorso-lateral marginal zone (DLMZ) is able to promote the expression of a sub-set of neural plate border (NPB) marker expression in the absence of the more specific NPB marker Pax3 and the Neural crest (NC) marker Snail2

  • We show that further signals from the EP are required for NC induction

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Summary

Introduction

Induction is a process by which an inducing tissue releases a signal that results in a change in the direction of differentiation of the responding tissue (Gurdon, 1987). Recent molecular explanations for many inductive interactions have revealed increasing complexity, with responding tissues receiving multiple signals from a variety of tissues. One example of this is the induction of the neural crest (NC), an embryonic cell population that arises at the neural plate border that later migrates to numerous sites in the embryo. Several signalling cascades are required for NC induction, including BMP (Glavic et al, 2004b; Marchant et al, 1998; Mayor et al, 1995; Neave et al, 1997; Nguyen et al, 1998; Wilson et al, 1997), Wnt

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