Samuel Lunenfeld Research Institute, Mt Sinai Hospital, 600 University Avenue, Toronto, Ontario M5G 1X5, Canada.
Nature. 2013 Jun 20;498(7454):318-24. doi: 10.1038/nature12296. Epub 2013 May 24.
A complex interaction of signalling events, including the Wnt pathway, regulates sprouting of blood vessels from pre-existing vasculature during angiogenesis. Here we show that two distinct mutations in the (uro)chordate-specific gumby (also called Fam105b) gene cause an embryonic angiogenic phenotype in gumby mice. Gumby interacts with disheveled 2 (DVL2), is expressed in canonical Wnt-responsive endothelial cells and encodes an ovarian tumour domain class of deubiquitinase that specifically cleaves linear ubiquitin linkages. A crystal structure of gumby in complex with linear diubiquitin reveals how the identified mutations adversely affect substrate binding and catalytic function in line with the severity of their angiogenic phenotypes. Gumby interacts with HOIP (also called RNF31), a key component of the linear ubiquitin assembly complex, and decreases linear ubiquitination and activation of NF-κB-dependent transcription. This work provides support for the biological importance of linear (de)ubiquitination in angiogenesis, craniofacial and neural development and in modulating Wnt signalling.
信号事件的复杂相互作用,包括 Wnt 途径,调节血管生成过程中血管从预先存在的脉管系统中发芽。在这里,我们表明(尿)脊索动物特异性 Gumby(也称为 Fam105b)基因中的两个不同突变导致 Gumby 小鼠出现胚胎血管生成表型。Gumby 与蓬乱蛋白 2(DVL2)相互作用,在经典 Wnt 反应性内皮细胞中表达,并编码卵巢肿瘤结构域类去泛素化酶,该酶特异性切割线性泛素连接。Gumby 与线性二泛素复合物的晶体结构揭示了鉴定的突变如何根据其血管生成表型的严重程度不利地影响底物结合和催化功能。Gumby 与 HOIP(也称为 RNF31)相互作用,HOIP 是线性泛素组装复合物的关键组成部分,并降低线性泛素化和 NF-κB 依赖性转录的激活。这项工作为线性(去)泛素化在血管生成、颅面和神经发育以及调节 Wnt 信号中的生物学重要性提供了支持。