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小鼠脊索形成的实时成像与遗传分析揭示了区域形态发生机制。

Live imaging and genetic analysis of mouse notochord formation reveals regional morphogenetic mechanisms.

作者信息

Yamanaka Yojiro, Tamplin Owen J, Beckers Anja, Gossler Achim, Rossant Janet

机构信息

Program in Developmental & Stem Cell Biology, Hospital for Sick Children Research Institute, Toronto, Ontario M5G 1X8, Canada.

出版信息

Dev Cell. 2007 Dec;13(6):884-96. doi: 10.1016/j.devcel.2007.10.016.

Abstract

The node and notochord have been extensively studied as signaling centers in the vertebrate embryo. The morphogenesis of these tissues, particularly in mouse, is not well understood. Using time-lapse live imaging and cell lineage tracking, we show the notochord has distinct morphogenetic origins along the anterior-posterior axis. The anterior head process notochord arises independently of the node by condensation of dispersed cells. The trunk notochord is derived from the node and forms by convergent extension. The tail notochord forms by node-derived progenitors that actively migrate toward the posterior. We also reveal distinct genetic regulation within these different regions. We show that Foxa2 compensates for and genetically interacts with Noto in the trunk notochord, and that Noto has an evolutionarily conserved role in regulating axial versus paraxial cell fate. Therefore, we propose three distinct regions within the mouse notochord, each with unique morphogenetic origins.

摘要

在脊椎动物胚胎中,节点和脊索作为信号中心已得到广泛研究。这些组织的形态发生,尤其是在小鼠中,尚未得到很好的理解。通过延时实时成像和细胞谱系追踪,我们发现脊索沿前后轴具有不同的形态发生起源。前头部突起脊索由分散细胞的凝聚独立于节点产生。躯干脊索源自节点并通过汇聚延伸形成。尾部脊索由源自节点的祖细胞向后方积极迁移形成。我们还揭示了这些不同区域内独特的基因调控。我们表明,Foxa2在躯干脊索中补偿Noto并与其发生遗传相互作用,并且Noto在调节轴旁细胞命运方面具有进化上保守的作用。因此,我们提出小鼠脊索内有三个不同区域,每个区域都有独特的形态发生起源。

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