Thérond P P, Limbourg Bouchon B, Gallet A, Dussilol F, Pietri T, van den Heuvel M, Tricoire H
CNRS UMR6543, Université Nice Valrose, France.
Development. 1999 Sep;126(18):4039-51. doi: 10.1242/dev.126.18.4039.
The two signalling proteins, Wingless and Hedgehog, play fundamental roles in patterning cells within each metamere of the Drosophila embryo. Within the ventral ectoderm, Hedgehog signals both to the anterior and posterior directions: anterior flanking cells express the wingless and patched Hedgehog target genes whereas posterior flanking cells express only patched. Furthermore, Hedgehog acts as a morphogen to pattern the dorsal cuticle, on the posterior side of cells where it is produced. Thus responsive embryonic cells appear to react according to their position relative to the Hedgehog source. The molecular basis of these differences is still largely unknown. In this paper we show that one component of the Hedgehog pathway, the Fused kinase accumulates preferentially in cells that could respond to Hedgehog but that Fused concentration is not a limiting step in the Hedgehog signalling. We present direct evidence that Fused is required autonomously in anterior cells neighbouring Hedgehog in order to maintain patched and wingless expression while Wingless is in turn maintaining engrailed and hedgehog expression. By expressing different components of the Hedgehog pathway only in anterior, wingless-expressing cells we could show that the Hedgehog signalling components Smoothened and Cubitus interruptus are required in cells posterior to Hedgehog domain to maintain patched expression whereas Fused is not necessary in these cells. This result suggests that Hedgehog responsive ventral cells in embryos can be divided into two distinct types depending on their requirement for Fused activity. In addition, we show that the morphogen Hedgehog can pattern the dorsal cuticle independently of Fused. In order to account for these differences in Fused requirements, we propose the existence of position-specific modulators of the Hedgehog response.
两种信号蛋白,无翅蛋白(Wingless)和刺猬蛋白(Hedgehog),在果蝇胚胎每个体节的细胞模式形成中发挥着基本作用。在腹侧外胚层中,刺猬蛋白向前后两个方向发出信号:前侧相邻细胞表达无翅蛋白和刺猬蛋白的靶基因patched,而后侧相邻细胞仅表达patched。此外,刺猬蛋白作为一种形态发生素,在其产生细胞的后侧对背侧表皮进行模式形成。因此,有反应的胚胎细胞似乎根据其相对于刺猬蛋白来源的位置做出反应。这些差异的分子基础在很大程度上仍然未知。在本文中,我们表明刺猬蛋白信号通路的一个组分,融合激酶(Fused kinase)优先在能够对刺猬蛋白做出反应的细胞中积累,但融合激酶的浓度并不是刺猬蛋白信号传导的限制步骤。我们提供了直接证据,即在刺猬蛋白附近的前侧细胞中,自主需要融合激酶来维持patched和无翅蛋白的表达,而无翅蛋白反过来又维持engrailed和刺猬蛋白的表达。通过仅在表达无翅蛋白的前侧细胞中表达刺猬蛋白信号通路的不同组分,我们可以表明,在刺猬蛋白结构域后方的细胞中,刺猬蛋白信号传导组分Smoothened和Cubitus interruptus是维持patched表达所必需的,而融合激酶在这些细胞中并非必需。这一结果表明,胚胎中对刺猬蛋白有反应的腹侧细胞可根据其对融合激酶活性的需求分为两种不同类型。此外,我们表明形态发生素刺猬蛋白可以独立于融合激酶对背侧表皮进行模式形成。为了解释融合激酶需求的这些差异,我们提出存在刺猬蛋白反应的位置特异性调节因子。