Department of Biology, Chungnam National University, Daejeon, 34134, South Korea.
Department of Life Science and Research Center for Cellular Homeostasis, Ewha Womans University, Seoul, 120-750, South Korea.
Sci Rep. 2017 Oct 16;7(1):13278. doi: 10.1038/s41598-017-13429-6.
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.
Wnt 信号通路控制着包括组织/身体模式形成在内的关键发育过程。在这里,我们报告了一种新的 Wnt 信号通路调节剂 OTTOGI(OTG)的鉴定,该调节剂是从小鼠胚胎中大量表达的人类 cDNA 中筛选出来的。OTG 在斑马鱼胚胎中的过表达导致背腹侧化表型,抑制了 Wnt 靶基因的表达,并阻止了 β-catenin 的核积累。相反,使用特异性反义 morpholino 敲低斑马鱼 otg 促进了 β-catenin 的核积累并导致腹侧化。然而,OTG 未能挽救由 GSK-3β 活性抑制引起的无头样表型,表明 OTG 作用于 GSK-3β 的上游。OTG 特异性结合 Frizzled8(Fz8)受体,并通过阻止 Fz8 的 N 连接糖基化可能导致 Fz8 在内质网中的滞留。总之,我们的数据表明,OTG 通过调节 Fz 受体的细胞表面表达,作为发育过程中 Wnt 信号的新型负调节剂发挥作用。