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Antagonists of BMP and TGFβ signaling pathway

机译:BMP和TGFβ信号通路的拮抗剂

摘要

This invention provides unique members of the Hect family of ubiquitin ligases that specifically target BMP and TGF beta /activin pathway-specific Smads. The novel ligases have been named Smurf1 and Smurf2. They directly interact with Smads1 and 5 and Smad7, respectively, and regulate the ubiquitination, turnover and activity of Smads and other proteins of these pathways. Smurf1 interferes with biological responses to BMP, but not activin signalling. In amphibian embryos Smurf1 inhibits endogenous BMP signals, resulting in altered pattern formation and cell fate specification in the mesoderm and ectoderm. The present invention provides a unique regulatory link between the ubiquitination pathway and the control of cell fate determination by the TGF beta superfamily during embryonic development. Thus, Smurf1 is a negative regulator of Smad1 signal transduction, by targeting Smad1, Smurf1 blocks BMP signalling. In mammalian cells, Smurf2 suppresses TGF beta signalling, and in Xenopus, blocks formation of dorsal mesoderm and causes anterior truncation of the embryos. Smurf2 forms a stable complex with Smad7, which induces degradation and downregulation of TGF beta /activin signalling.
机译:本发明提供了Hect家族的泛素连接酶的独特成员,其特异性靶向BMP和TGFβ/激活素途径特异性Smads。新型连接酶已被命名为Smurf1和Smurf2。它们分别直接与Smads1、5和Smad7相互作用,并调节Smads和这些途径的其他蛋白质的泛素化,转换和活性。 Smurf1会干扰BMP的生物学反应,但不会激活信号素。在两栖动物胚胎中,Smurf1抑制内源性BMP信号,导致中胚层和外胚层中模式形成和细胞命运规格的改变。本发明提供了在胚胎发育过程中泛素化途径与TGFβ超家族对细胞命运测定的控制之间的独特调节联系。因此,Smurf1是Smad1信号转导的负调节剂,通过靶向Smad1,Smurf1阻止BMP信号传导。在哺乳动物细胞中,Smurf2抑制TGFβ信号传导,在非洲爪蟾中,阻断背中皮的形成并引起胚胎的前截断。 Smurf2与Smad7形成稳定的复合物,从而诱导TGFβ/激活素信号传导的降解和下调。

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