Abstract

The Wnt signaling pathway transducing the stabilization of β-catenin is essential for metazoan embryo development and is misregulated in many diseases such as cancers. In recent years models have been proposed for the Wnt signaling pathway during the segmentation process in developing embryos. Many of these include negative feedback loops where Axin2 plays a key role. However, Axin2 null mice show no segmentation phenotype. We therefore propose a new model where the negative feedback involves Dkk1 rather than Axin2. We show that this model can exhibit the same type of oscillations as the previous models with Axin2 and as observed in experiments. We show that a spatial Wnt gradient can consistently convert this temporal periodicity into the spatial periodicity of somites, provided the oscillations in new cells arising in the presomitic mesoderm are synchronized with the oscillations of older cells. We further investigate the hypothesis that a change in the Wnt level in the tail bud during the later stages of somitogenesis can lengthen the time period of the oscillations and hence the size and separation of the later somites.

Highlights

  • A segmented body plan is a fundamental characteristic feature of vertebrates

  • The idea is that locally coupled oscillators are controlled by a morphogen gradient in the presomitic mesoderm (PSM)

  • The two gradients act in synergy with each other during the somitogenesis [6,7]

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Summary

Introduction

A segmented body plan is a fundamental characteristic feature of vertebrates. The process of segmentation is carried out by a combination of changes in gene expression and relative anteriorposterior cell position in the presomitic mesoderm (PSM) [1]. The dynamics of CK1a and APC are included in the parameters governing the destruction complex, the TCF/LEF-1 dynamics are contained within the transcription of Dkk1, and the dynamics of Dsh are included in the formation of the complex consisting of Axin, GSK3b and LRP5/6 at the cell membrane.

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