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Ottogi Inhibits Wnt/β-catenin Signaling by Regulating Cell Membrane Trafficking of Frizzled8

机译:Ottogi通过调节卷曲蛋白8的细胞膜运输抑制Wnt /β-catenin信号传导。

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摘要

Wnt signaling controls critical developmental processes including tissue/body patterning. Here we report the identification of a novel regulator of Wnt signaling, OTTOGI (OTG), isolated from a large-scale expression screening of human cDNAs in zebrafish embryos. Overexpression of OTG in zebrafish embryos caused dorso-anteriorized phenotype, inhibited the expression of Wnt target genes, and prevented nuclear accumulation of β-catenin. Conversely, knockdown of zebrafish otg using specific antisense morpholino promoted nuclear accumulation of β-catenin and caused ventralization. However, OTG failed to rescue headless-like phenotype induced by inhibition of GSK-3β activity, suggesting that OTG acts upstream of GSK-3β. OTG bound specifically to Frizzled8 (Fz8) receptor and caused retention of Fz8 in the endoplasmic reticulum possibly by preventing N-linked glycosylation of Fz8. Taken together, our data indicate that OTG functions as a novel negative regulator of Wnt signaling during development by the modulation of cell surface expression of Fz receptor.
机译:Wnt信号传导控制关键的发育过程,包括组织/身体构图。在这里,我们报告鉴定的Wnt信号的新型调节器,OTTOGI(OTG),从斑马鱼胚胎中人类cDNA的大规模表达筛选中分离出来。斑马鱼胚胎中OTG的过度表达会导致背背型表型,抑制Wnt靶基因的表达,并阻止β-catenin的核积累。相反,使用特定的反义吗啉代敲除斑马鱼otg会促进β-catenin的核积累并引起腹侧化。但是,OTG无法挽救因抑制GSK-3β活性而诱发的无头状表型,这表明OTG在GSK-3β的上游起作用。 OTG特异性结合Frizzled8(Fz8)受体,并可能通过阻止Fz8的N-联糖基化作用而将Fz8保留在内质网中。两者合计,我们的数据表明OTG通过调节Fz受体的细胞表面表达,在发育过程中充当Wnt信号的新型负调控因子。

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