Aulehla Alexander, Herrmann Bernhard G
Max-Planck-Institute for Molecular Genetics, Department of Developmental Genetics, 14195 Berlin, Germany.
Genes Dev. 2004 Sep 1;18(17):2060-7. doi: 10.1101/gad.1217404.
The vertebral column is derived from somites formed by segmentation of presomitic mesoderm, a fundamental process of vertebrate embryogenesis. Models on the mechanism controlling this process date back some three to four decades. Access to understanding the molecular control of somitogenesis has been gained only recently by the discovery of molecular oscillators (segmentation clock) and gradients of signaling molecules, as predicted by early models. The Notch signaling pathway is linked to the oscillator and plays a decisive role in inter- and intrasomitic boundary formation. An Fgf8 signaling gradient is involved in somite size control. And the (canonical) Wnt signaling pathway, driven by Wnt3a, appears to integrate clock and gradient in a global mechanism controlling the segmentation process. In this review, we discuss recent advances in understanding the molecular mechanism controlling somitogenesis.
脊柱源自由前体节中胚层分割形成的体节,这是脊椎动物胚胎发育的一个基本过程。关于控制这一过程机制的模型可以追溯到大约三四十年前。直到最近,通过发现分子振荡器(分割时钟)和信号分子梯度,才得以了解体节发生的分子控制,这正如早期模型所预测的那样。Notch信号通路与振荡器相关联,在体节间和体节内边界形成中起决定性作用。Fgf8信号梯度参与体节大小的控制。由Wnt3a驱动的(经典)Wnt信号通路似乎在控制分割过程的整体机制中整合了时钟和梯度。在这篇综述中,我们讨论了在理解控制体节发生的分子机制方面的最新进展。