Department of Medical Oncology and Hematology, Oita University Faculty of Medicine, Oita, Japan
Global COE 'Cell Fate Regulation Research and Education Unit', Kumamoto University, Kumamoto, Japan.
Open Biol. 2017 Dec;7(12). doi: 10.1098/rsob.170225.
Sonic Hedgehog (Shh) is a ventrally enriched morphogen controlling dorsoventral patterning of the neural tube. In the dorsal spinal cord, Gli3 protein bound to suppressor-of-fused (Sufu) is converted into Gli3 repressor (Gli3R), which inhibits Shh-target genes. Activation of Shh signalling prevents Gli3R formation, promoting neural tube ventralization. We show that cadherin-7 (Cdh7) expression in the intermediate spinal cord region is required to delimit the boundary between the ventral and the dorsal spinal cord. We demonstrate that Cdh7 functions as a receptor for Shh and enhances Shh signalling. Binding of Shh to Cdh7 promotes its aggregation on the cell membrane and association of Cdh7 with Gli3 and Sufu. These interactions prevent Gli3R formation and cause Gli3 protein degradation. We propose that Shh can act through Cdh7 to limit intracellular movement of Gli3 protein and production of Gli3R, thus eliciting more efficient activation of Gli-dependent signalling.
Sonic Hedgehog(Shh)是一种腹侧丰富的形态发生素,控制神经管的背腹模式形成。在背侧脊髓中,与抑制融合(Sufu)结合的 Gli3 蛋白被转化为 Gli3 抑制剂(Gli3R),抑制 Shh 靶基因。Shh 信号的激活阻止了 Gli3R 的形成,促进了神经管的腹侧化。我们发现中间脊髓区域的钙黏蛋白-7(Cdh7)表达对于限定腹侧和背侧脊髓之间的边界是必需的。我们证明 Cdh7 作为 Shh 的受体发挥作用,并增强 Shh 信号。Shh 与 Cdh7 的结合促进其在细胞膜上的聚集,并促使 Cdh7 与 Gli3 和 Sufu 结合。这些相互作用阻止了 Gli3R 的形成,并导致 Gli3 蛋白的降解。我们提出,Shh 可以通过 Cdh7 来限制 Gli3 蛋白的细胞内运动和 Gli3R 的产生,从而引发更有效的 Gli 依赖性信号转导激活。