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Smoothened Signaling in Vertebrates Is Facilitated by a G Protein-coupled Receptor Kinase

机译:G蛋白偶联受体激酶促进脊椎动物中的信号平滑化

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摘要

Smoothened, a heptahelical membrane protein, functions as the transducer of Hedgehog signaling. The kinases that modulate Smoothened have been thoroughly analyzed in flies. However, little is known about how phosphorylation affects Smoothened in vertebrates, mainly, because the residues, where Smoothened is phosphorylated are not conserved from Drosophila to vertebrates. Given its molecular architecture, Smoothened signaling is likely to be regulated in a manner analogous to G protein-coupled receptors (GPCRs). Previously, it has been shown, that arrestins and GPCR kinases, (GRKs) not only desensitize G protein-dependent receptor signaling but also function as triggers for GPCR trafficking and formation of signaling complexes. Here we describe that a GRK contributes to Smoothened-mediated signaling in vertebrates. Knockdown of the zebrafish homolog of mammalian GRK2/3 results in lowered Hedgehog transcriptional responses, impaired muscle development, and neural patterning. Results obtained in zebrafish are corroborated both in cell culture, where zGRK2/3 phosphorylates Smoothened and promotes Smoothened signal transduction and in mice where deletion of GRK2 interferes with neural tube patterning. Together, these data suggest that a GRK functions as a vertebrate kinase for Smoothened, promoting Hedgehog signal transduction during early development.
机译:平滑化的七螺旋膜蛋白可作为Hedgehog信号转导的功能。蝇中已对调节平滑化的激酶进行了全面分析。但是,人们对磷酸化如何影响脊椎动物的平滑化知之甚少,主要是因为从果蝇到脊椎动物,保守化磷酸化的残基并不保守。鉴于其分子结构,平滑信号可能以类似于G蛋白偶联受体(GPCR)的方式进行调控。先前已显示,抑制蛋白和GPCR激酶(GRK)不仅使G蛋白依赖性受体信号转导不敏感,而且还充当GPCR转运和信号复合物形成的触发因素。在这里,我们描述了GRK有助于脊椎动物中介导的信号转导。哺乳动物GRK2 / 3的斑马鱼同源物的敲低导致刺猬的转录反应降低,肌肉发育受损和神经模式。在斑马鱼中获得的结果在细胞培养中均得到证实,其中zGRK2 / 3磷酸化平滑并促进平滑信号转导,并且在小鼠中GRK2缺失干扰神经管构图。总之,这些数据表明,GRK在平滑肌中起着脊椎动物激酶的作用,在早期发育过程中促进了刺猬的信号转导。

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