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A Smoothened-Evc2 Complex Transduces the Hedgehog Signal at Primary Cilia

机译:平滑化的Evc2复合体在初级纤毛上转导刺猬信号

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摘要

Vertebrate Hedgehog (Hh) signaling is initiated at primary cilia by the ligand-triggered accumulation of Smoothened (Smo) in the ciliary membrane. The underlying biochemical mechanisms remain unknown. We find that Hh agonists promote the association between Smo and Evc2, a ciliary protein that is defective in two human ciliopathies. The formation of the Smo-Evc2 complex is under strict spatial control, being restricted to a distinct ciliary compartment, the EvC zone. Mutant Evc2 proteins that localize in cilia but are displaced from the EvC zone are dominant inhibitors of Hh signaling. Disabling Evc2 function blocks Hh signaling at a specific step between Smo and the downstream regulators protein kinase A and Suppressor of Fused, preventing activation of the Gli transcription factors. Our data suggest that the Smo-Evc2 signaling complex at the EvC zone is required for Hh signal transmission and elucidate the molecular basis of two human ciliopathies. Video Abstract: Smoothened transduces Hedgehog pathway signals at primary cilia. Dorn et al. show that this key signaling event requires a Smoothened-Evc2 signaling complex at the base of the cilium. Disruption of this complex blocks Hedgehog signaling and causes birth defects, suggesting a strategy for targeting this pathway in cancer and regeneration.
机译:脊椎动物刺猬(Hh)信号传导是由纤毛中的平滑肌(Smo)的配体触发积累在初级纤毛处引发的。潜在的生化机制仍然未知。我们发现Hh激动剂促进Smo和Evc2之间的关联,Evc2是在两个人类纤毛病中都有缺陷的睫状蛋白。 Smo-Evc2复合物的形成受到严格的空间控制,被限制在一个独特的睫状区,即EvC区。定位在纤毛中但从EvC区移出的突变Evc2蛋白是Hh信号的主要抑制剂。禁用Evc2功能会在Smo与下游调节蛋白激酶A和Fused的抑制剂之间的特定步骤处阻止Hh信号传导,从而阻止Gli转录因子的激活。我们的数据表明Hh信号传输需要EvC区的Smo-Evc2信号复合物,并阐明了两种人类纤毛病的分子基础。视频摘要:Smoothened在原发纤毛处转导了Hedgehog通路信号。 Dorn等。表明该关键信号事件需要纤毛基部的Smoothened-Evc2信号复合物。破坏这种复合物会阻断刺猬信号并导致先天缺陷,这表明了针对这一途径进行癌症和再生的策略。

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