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Ottogi Inhibits Wnt/β-catenin Signaling by Regulating Cell Membrane Trafficking of Frizzled8
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 em...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643531/ https://www.ncbi.nlm.nih.gov/pubmed/29038508 http://dx.doi.org/10.1038/s41598-017-13429-6 |
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author | Kim, Hyun-Taek Lee, Mi-Sun Jeong, Yun-Mi Ro, Hyunju Kim, Dong-Il Shin, Yong-Hwan Kim, Ji-Eun Hwang, Kyu-Seok Choi, Jung-Hwa Bahn, Minjin Lee, Jeong-Ju Lee, Sang H. Bae, Young-Ki Lee, Jin-Soo Choi, Joong-Kook Kim, Nam-Soon Yeo, Chang-Yeol Kim, Cheol-Hee |
author_facet | Kim, Hyun-Taek Lee, Mi-Sun Jeong, Yun-Mi Ro, Hyunju Kim, Dong-Il Shin, Yong-Hwan Kim, Ji-Eun Hwang, Kyu-Seok Choi, Jung-Hwa Bahn, Minjin Lee, Jeong-Ju Lee, Sang H. Bae, Young-Ki Lee, Jin-Soo Choi, Joong-Kook Kim, Nam-Soon Yeo, Chang-Yeol Kim, Cheol-Hee |
author_sort | Kim, Hyun-Taek |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5643531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56435312017-10-19 Ottogi Inhibits Wnt/β-catenin Signaling by Regulating Cell Membrane Trafficking of Frizzled8 Kim, Hyun-Taek Lee, Mi-Sun Jeong, Yun-Mi Ro, Hyunju Kim, Dong-Il Shin, Yong-Hwan Kim, Ji-Eun Hwang, Kyu-Seok Choi, Jung-Hwa Bahn, Minjin Lee, Jeong-Ju Lee, Sang H. Bae, Young-Ki Lee, Jin-Soo Choi, Joong-Kook Kim, Nam-Soon Yeo, Chang-Yeol Kim, Cheol-Hee Sci Rep Article 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. Nature Publishing Group UK 2017-10-16 /pmc/articles/PMC5643531/ /pubmed/29038508 http://dx.doi.org/10.1038/s41598-017-13429-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Hyun-Taek Lee, Mi-Sun Jeong, Yun-Mi Ro, Hyunju Kim, Dong-Il Shin, Yong-Hwan Kim, Ji-Eun Hwang, Kyu-Seok Choi, Jung-Hwa Bahn, Minjin Lee, Jeong-Ju Lee, Sang H. Bae, Young-Ki Lee, Jin-Soo Choi, Joong-Kook Kim, Nam-Soon Yeo, Chang-Yeol Kim, Cheol-Hee Ottogi Inhibits Wnt/β-catenin Signaling by Regulating Cell Membrane Trafficking of Frizzled8 |
title | Ottogi Inhibits Wnt/β-catenin Signaling by Regulating Cell Membrane Trafficking of Frizzled8 |
title_full | Ottogi Inhibits Wnt/β-catenin Signaling by Regulating Cell Membrane Trafficking of Frizzled8 |
title_fullStr | Ottogi Inhibits Wnt/β-catenin Signaling by Regulating Cell Membrane Trafficking of Frizzled8 |
title_full_unstemmed | Ottogi Inhibits Wnt/β-catenin Signaling by Regulating Cell Membrane Trafficking of Frizzled8 |
title_short | Ottogi Inhibits Wnt/β-catenin Signaling by Regulating Cell Membrane Trafficking of Frizzled8 |
title_sort | ottogi inhibits wnt/β-catenin signaling by regulating cell membrane trafficking of frizzled8 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643531/ https://www.ncbi.nlm.nih.gov/pubmed/29038508 http://dx.doi.org/10.1038/s41598-017-13429-6 |
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