Yasuo Hitoyoshi, Hudson Clare
Biologie du Développement, UMR7009 CNRS/Université Pierre et Marie Curie Observatoire Océanologique, F-06230 Villefranche-sur-mer, France.
Dev Biol. 2007 Feb 1;302(1):92-103. doi: 10.1016/j.ydbio.2006.08.075. Epub 2006 Sep 9.
Fibroblast growth factor (FGF) signalling has been implicated in the generation of mesoderm and neural fates in chordate embryos including ascidians and vertebrates. In Ciona, FGF9/16/20 has been implicated in both of these processes. However, in FGF9/16/20 knockdown embryos, notochord fate recovers during later development. It is thus not clear if FGF signalling is an essential requirement for notochord specification in Ciona embryos. We show that FGF-MEK-ERK signals act during two distinct phases to establish notochord fate. During the first phase, FGF signalling is required during an asymmetric cell division to promote notochord at the expense of neural identity. Consistently, ERK1/2 is specifically activated in the notochord precursors following this cell division. Sustained activation of ERK1/2 is then required to maintain notochord fate. We demonstrate that FGF9/16/20 acts solely during the initial induction step and that, subsequently, FGF8/17/18 together with FGF9/16/20 is involved in the following maintenance step. These results together with others' show that the formation of a large part of the mesoderm cell types in ascidian larvae is dependent on signalling events involving FGF ligands.
成纤维细胞生长因子(FGF)信号传导与包括海鞘和脊椎动物在内的脊索动物胚胎中中胚层和神经命运的产生有关。在玻璃海鞘中,FGF9/16/20与这两个过程都有关。然而,在FGF9/16/20敲低的胚胎中,脊索命运在后期发育过程中得以恢复。因此,尚不清楚FGF信号传导是否是玻璃海鞘胚胎中脊索特化的必要条件。我们发现,FGF-MEK-ERK信号在两个不同阶段发挥作用以确立脊索命运。在第一阶段,在不对称细胞分裂期间需要FGF信号传导,以牺牲神经特性为代价来促进脊索的形成。与此一致的是,ERK1/2在该细胞分裂后的脊索前体细胞中被特异性激活。然后需要ERK1/2的持续激活来维持脊索命运。我们证明FGF9/16/20仅在初始诱导步骤中起作用,随后,FGF8/17/18与FGF9/16/20一起参与后续的维持步骤。这些结果与其他研究结果共同表明,海鞘幼虫中大部分中胚层细胞类型的形成依赖于涉及FGF配体的信号传导事件。