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Neuropilins are positive regulators of Hedgehog signal transduction.

机译:Neuropilins是刺猬信号转导的正向调节剂。

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摘要

The Hedgehog (Hh) pathway is essential for vertebrate embryogenesis, and excessive Hh target gene activation can cause cancer in humans. Here we show that Neuropilin 1 (Nrp1) and Nrp2, transmembrane proteins with roles in axon guidance and vascular endothelial growth factor (VEGF) signaling, are important positive regulators of Hh signal transduction. Nrps are expressed at times and locations of active Hh signal transduction during mouse development. Using cell lines lacking key Hh pathway components, we show that Nrps mediate Hh transduction between activated Smoothened (Smo) protein and the negative regulator Suppressor of Fused (SuFu). Nrp1 transcription is induced by Hh signaling, and Nrp1 overexpression increases maximal Hh target gene activation, indicating the existence of a positive feedback circuit. The regulation of Hh signal transduction by Nrps is conserved between mammals and bony fish, as we show that morpholinos targeting the Nrp zebrafish ortholog nrp1a produce a specific and highly penetrant Hh pathway loss-of-function phenotype. These findings enhance our knowledge of Hh pathway regulation and provide evidence for a conserved nexus between Nrps and this important developmental signaling system.
机译:刺猬(Hh)通路对于脊椎动物胚胎发生至关重要,而过度的Hh靶基因激活会导致人类癌症。在这里,我们显示Neuropilin 1(Nrp1)和Nrp2,跨膜蛋白在轴突引导和血管内皮生长因子(VEGF)信号传导中发挥作用,是Hh信号转导的重要正调节剂。 Nrps在小鼠发育过程中在主动Hh信号转导的时间和位置表达。使用缺少关键Hh通路成分的细胞系,我们显示Nrps介导活化的Smoothed(Smo)蛋白与融合的负调控因子Suppressor(SuFu)之间的Hh转导。 Nrp1转录是由Hh信号传导诱导的,Nrp1的过表达增加了最大Hh靶基因的激活,表明存在正反馈电路。通过Nrps对Hh信号转导的调节在哺乳动物和骨鱼之间是保守的,因为我们表明靶向Nrp斑马鱼ortholog nrp1a的吗啉代可产生特定且高度渗透的Hh通路功能丧失表型。这些发现增强了我们对Hh途径调控的认识,并为Nrps与这一重要的发育信号系统之间的保守联系提供了证据。

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