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Ptch2/Gas1 和 Ptch1/Boc 对小鼠原始生殖细胞迁移中的 Hedgehog 信号通路的调控存在差异。

Ptch2/Gas1 and Ptch1/Boc differentially regulate Hedgehog signalling in murine primordial germ cell migration.

机构信息

Molecular and Clinical Sciences Research Institute, St. George's, University of London, Cranmer Terrace, London, SW17 0RE, UK.

Centre for Craniofacial and Regenerative Biology, Faculty of Dental, Oral and Craniofacial Sciences King's College London Floor 27, Guy's Hospital, London, SE1 9RT, UK.

出版信息

Nat Commun. 2020 Apr 24;11(1):1994. doi: 10.1038/s41467-020-15897-3.

Abstract

Gas1 and Boc/Cdon act as co-receptors in the vertebrate Hedgehog signalling pathway, but the nature of their interaction with the primary Ptch1/2 receptors remains unclear. Here we demonstrate, using primordial germ cell migration in mouse as a developmental model, that specific hetero-complexes of Ptch2/Gas1 and Ptch1/Boc mediate the process of Smo de-repression with different kinetics, through distinct modes of Hedgehog ligand reception. Moreover, Ptch2-mediated Hedgehog signalling induces the phosphorylation of Creb and Src proteins in parallel to Gli induction, identifying a previously unknown Ptch2-specific signal pathway. We propose that although Ptch1 and Ptch2 functionally overlap in the sequestration of Smo, the spatiotemporal expression of Boc and Gas1 may determine the outcome of Hedgehog signalling through compartmentalisation and modulation of Smo-downstream signalling. Our study identifies the existence of a divergent Hedgehog signal pathway mediated by Ptch2 and provides a mechanism for differential interpretation of Hedgehog signalling in the germ cell niche.

摘要

Gas1 和 Boc/Cdon 作为脊椎动物 Hedgehog 信号通路的共受体,但它们与主要的 Ptch1/2 受体相互作用的性质仍不清楚。在这里,我们利用小鼠原始生殖细胞迁移作为发育模型,证明 Ptch2/Gas1 和 Ptch1/Boc 的特定异源复合物通过不同的 Hedgehog 配体接收模式,以不同的动力学介导 Smo 去抑制过程。此外,Ptch2 介导的 Hedgehog 信号诱导 Creb 和 Src 蛋白的磷酸化与 Gli 诱导平行发生,鉴定了一个以前未知的 Ptch2 特异性信号通路。我们提出,尽管 Ptch1 和 Ptch2 在 Smo 的隔离中具有功能重叠,但 Boc 和 Gas1 的时空表达可能通过 Smo 下游信号的区室化和调节来决定 Hedgehog 信号的结果。我们的研究确定了由 Ptch2 介导的发散 Hedgehog 信号通路的存在,并为 Hedgehog 信号在生殖细胞龛中的差异解释提供了机制。

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