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Malin Regulates Wnt Signaling Pathway through Degradation of Dishevelled2

机译:马林通过Dishevelled2的降解调节Wnt信号通路。

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摘要

Using yeast-two hybrid screening followed by co-immunoprecipitation assay, we have found that the Lafora disease ubiquitin ligase malin interacts with dishevelled2, a key mediator of Wnt signaling pathway. Overexpression of malin enhances the degradation of dishevelled2 and inhibits Wnt signaling, which is evident from the down-regulation of β-catenin target genes and the decrease in β-catenin-mediated transcriptional activity. Partial knockdown of malin significantly increases the level of dishevelled2 and up-regulates Wnt signaling. Several malin mutants are found to be ineffective in degrading dishevelled2 and regulating the Wnt pathway. We have also found that malin enhances K48- and K63-linked ubiquitination of dishevelled2 that could lead to its degradation through both proteasome and autophagy. Altogether, our results indicate that malin regulates Wnt signaling pathway through the degradation of dishevelled2 and suggest possible deregulation of Wnt signaling in Lafora disease.
机译:使用酵母两种杂交筛选,然后进行免疫共沉淀测定,我们发现拉福拉病泛素连接酶苹果酸与Wnt信号传导途径的关键介导物ishevelled2相互作用。马林蛋白的过量表达增强了不饱和蛋白2的降解并抑制了Wnt信号传导,这从β-catenin靶基因的下调和β-catenin介导的转录活性的降低中可以看出。马林蛋白的部分敲低显着增加了不饱和蛋白2的水平并上调了Wnt信号转导。发现几种马林突变体在降解ishevelled2和调节Wnt途径方面无效。我们还发现,马林蛋白增强了dishesvelled2的K48-和K63-连接的泛素化,这可能导致其通过蛋白酶体和自噬降解。总而言之,我们的结果表明马林蛋白通过破烂2的降解来调节Wnt信号通路,并暗示拉福拉病中Wnt信号的可能失控。

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