Sanial Matthieu, Bécam Isabelle, Hofmann Line, Behague Julien, Argüelles Camilla, Gourhand Vanessa, Bruzzone Lucia, Holmgren Robert A, Plessis Anne
Institut Jacques Monod, CNRS, UMR 7592, Université Paris Diderot, Sorbonne Paris Cité, Paris F-75205, France.
Department of Molecular Bioscience, Northwestern University, Evanston, IL 60208-3500, USA.
Development. 2017 May 15;144(10):1841-1850. doi: 10.1242/dev.144782. Epub 2017 Mar 30.
Smoothened (SMO) is a G-protein-coupled receptor-related protein required for the transduction of Hedgehog (HH). The HH gradient leads to graded phosphorylation of SMO, mainly by the PKA and CKI kinases. How thresholds in HH morphogen regulate SMO to promote switch-like transcriptional responses is a central unsolved issue. Using the wing imaginal disc model in , we identified new SMO phosphosites that enhance the effects of the PKA/CKI kinases on SMO accumulation, its localization at the plasma membrane and its activity. Surprisingly, phosphorylation at these sites is induced by the kinase Fused (FU), a known downstream effector of SMO. In turn, activation of SMO induces FU to act on its downstream targets. Overall, our data provide evidence for a SMO/FU positive regulatory loop nested within a multikinase phosphorylation cascade. We propose that this complex interplay amplifies signaling above a threshold that allows high HH signaling.
平滑受体(SMO)是一种与G蛋白偶联受体相关的蛋白,是刺猬索尼克信号通路(HH)转导所必需的。HH梯度主要通过蛋白激酶A(PKA)和酪蛋白激酶I(CKI)激酶导致SMO的分级磷酸化。HH形态发生素中的阈值如何调节SMO以促进类似开关的转录反应是一个尚未解决的核心问题。利用果蝇翅成虫盘模型,我们鉴定出了新的SMO磷酸化位点,这些位点增强了PKA/CKI激酶对SMO积累、其在质膜上的定位及其活性的影响。令人惊讶的是,这些位点的磷酸化是由激酶融合蛋白(FU)诱导的,FU是SMO已知的下游效应物。反过来,SMO的激活诱导FU作用于其下游靶点。总体而言,我们的数据为嵌套在多激酶磷酸化级联中的SMO/FU正调控环提供了证据。我们提出,这种复杂的相互作用将信号放大到一个阈值以上,从而实现高HH信号传导。