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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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.
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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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