Abstract

In vertebrates, the neural plate border (NPB) is established by a group of transcription factors including Dlx3, Msx1 and Zic1. The crosstalk between these NPB specifiers governs the separation of the NPB region into placode and neural crest (NC) territories and also their further differentiation. Understanding the mechanisms of NPB formation and NC development is critical for our knowledge of related human diseases. Here we identified Nkx6.3, a transcription factor of the Nkx family, as a new NPB specifier required for neural crest development in Xenopus embryos. XNkx6.3 is expressed in the ectoderm of the neural plate border region at neurula stages, covering the epidermis, placode and neural crest territories, but not the neural plate. Inhibition of Nkx6.3 by dominant negative construct or specific morpholino leads to neural crest defects, while overexpression of Nkx6.3 induces ectopic neural crest in the anterior neural fold. In animal caps, Nkx6.3 alone is able to initiate the whole neural crest regulatory network and induces neural crest fate robustly. We showed that overexpression of Nkx6.3 affects multiple signaling pathways, creating a high-Wnt, low-BMP environment required for neural crest development. Gain- and loss-of-function of Nkx6.3 have compound effects on the expression of known NPB genes, which is largely opposite to that of Dlx3. Overexpression of Dlx3 blocks the NC inducing activity of Nkx6.3. The crosstalk between Nkx6.3, Dlx3 and Msx1 is likely crucial for proper NPB formation and neural crest development in Xenopus.

Highlights

  • Neural crest (NC) cells are a multipotent, migratory cell population arising at the neural plate border (NPB) in vertebrates, which give rise to various cell lineages including craniofacial bones and cartilages, melanocytes and peripheral neurons [1]

  • We provided several lines of evidence that Nkx6.3 is required for neural crest development in Xenopus

  • Overexpression of Nkx6.3 promotes ectopic neural crest development in the anterior neural fold, it inhibits endogenous neural crest when injected at the NC territory itself (Fig. 3)

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Summary

Introduction

Neural crest (NC) cells are a multipotent, migratory cell population arising at the neural plate border (NPB) in vertebrates, which give rise to various cell lineages including craniofacial bones and cartilages, melanocytes and peripheral neurons [1]. The signaling events that establish the neural plate border control the broad expression of a set of transcription factors, including members of the Zic, Pax, Dlx and Msx families [4, 13, 15,16,17]. These factors, known as neural plate border specifiers, further control the expression of a group neural crest specific genes, including Snail, Slug, FoxD3, Sox, Sox, AP-2 and c-Myc [4]. The neural crest specifier genes collectively control the expression of several downstream effector genes, which confer certain properties such as migration and multipotency before their terminal differentiation [18]

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