Department of Developmental Biology, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390, USA.
Genes Dev. 2010 Sep 15;24(18):2054-67. doi: 10.1101/gad.1948710.
G protein-coupled receptor kinase 2 (Gprk2/GRK2) plays a conserved role in modulating Hedgehog (Hh) pathway activity, but its mechanism of action remains unknown. Here we provide evidence that Gprk2 promotes high-level Hh signaling by regulating Smoothened (Smo) conformation through both kinase-dependent and kinase-independent mechanisms. Gprk2 promotes Smo activation by phosphorylating Smo C-terminal tail (C-tail) at Ser741/Thr742, which is facilitated by PKA and CK1 phosphorylation at adjacent Ser residues. In addition, Gprk2 forms a dimer/oligomer and binds Smo C-tail in a kinase activity-independent manner to stabilize the active Smo conformation, and promotes dimerization/oligomerization of Smo C-tail. Gprk2 expression is induced by Hh signaling, and Gprk2/Smo interaction is facilitated by PKA/CK1-mediated phosphorylation of Smo C-tail. Thus, Gprk2 forms a positive feedback loop and acts downstream from PKA and CK1 to facilitate high-level Hh signaling by promoting the active state of Smo through direct phosphorylation and molecular scaffolding.
G 蛋白偶联受体激酶 2(Gprk2/GRK2)在调节 Hedgehog(Hh)信号通路活性方面发挥着保守作用,但它的作用机制尚不清楚。在这里,我们提供的证据表明,Gprk2 通过依赖和不依赖激酶的机制调节 Smoothened(Smo)构象,从而促进高水平的 Hh 信号传导。Gprk2 通过磷酸化 Smo C 末端尾巴(C-tail)上的 Ser741/Thr742 来促进 Smo 的激活,这一过程由 PKA 和 CK1 在相邻 Ser 残基上的磷酸化来促进。此外,Gprk2 形成二聚体/寡聚体,并以非激酶活性的方式结合 Smo C-tail,以稳定活性 Smo 构象,并促进 Smo C-tail 的二聚体/寡聚体形成。Gprk2 的表达受 Hh 信号的诱导,并且 Gprk2/Smo 相互作用通过 PKA/CK1 介导的 Smo C-tail 磷酸化来促进。因此,Gprk2 形成正反馈回路,通过直接磷酸化和分子支架作用,促进 Smo 的活性状态,从而在 PKA 和 CK1 下游发挥作用,促进高水平的 Hh 信号传导。