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USP39 is essential for mammalian epithelial morphogenesis through upregulation of planar cell polarity components
Previously, we have shown that the translocation of Grainyhead-like 3 (GRHL3) transcription factor from the nucleus to the cytoplasm triggers the switch from canonical Wnt signaling for epidermal differentiation to non-canonical Wnt signaling for epithelial morphogenesis. However, the molecular mech...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018712/ https://www.ncbi.nlm.nih.gov/pubmed/35440748 http://dx.doi.org/10.1038/s42003-022-03254-7 |
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author | Kimura-Yoshida, Chiharu Mochida, Kyoko Kanno, Shin-Ichiro Matsuo, Isao |
author_facet | Kimura-Yoshida, Chiharu Mochida, Kyoko Kanno, Shin-Ichiro Matsuo, Isao |
author_sort | Kimura-Yoshida, Chiharu |
collection | PubMed |
description | Previously, we have shown that the translocation of Grainyhead-like 3 (GRHL3) transcription factor from the nucleus to the cytoplasm triggers the switch from canonical Wnt signaling for epidermal differentiation to non-canonical Wnt signaling for epithelial morphogenesis. However, the molecular mechanism that underlies the cytoplasmic localization of GRHL3 protein and that activates non-canonical Wnt signaling is not known. Here, we show that ubiquitin-specific protease 39 (USP39), a deubiquitinating enzyme, is involved in the subcellular localization of GRHL3 as a potential GRHL3-interacting protein and is necessary for epithelial morphogenesis to up-regulate expression of planar cell polarity (PCP) components. Notably, mouse Usp39-deficient embryos display early embryonic lethality due to a failure in primitive streak formation and apico-basal polarity in epiblast cells, resembling those of mutant embryos of the Prickle1 gene, a crucial PCP component. Current findings provide unique insights into how differentiation and morphogenesis are coordinated to construct three-dimensional complex structures via USP39. |
format | Online Article Text |
id | pubmed-9018712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90187122022-04-28 USP39 is essential for mammalian epithelial morphogenesis through upregulation of planar cell polarity components Kimura-Yoshida, Chiharu Mochida, Kyoko Kanno, Shin-Ichiro Matsuo, Isao Commun Biol Article Previously, we have shown that the translocation of Grainyhead-like 3 (GRHL3) transcription factor from the nucleus to the cytoplasm triggers the switch from canonical Wnt signaling for epidermal differentiation to non-canonical Wnt signaling for epithelial morphogenesis. However, the molecular mechanism that underlies the cytoplasmic localization of GRHL3 protein and that activates non-canonical Wnt signaling is not known. Here, we show that ubiquitin-specific protease 39 (USP39), a deubiquitinating enzyme, is involved in the subcellular localization of GRHL3 as a potential GRHL3-interacting protein and is necessary for epithelial morphogenesis to up-regulate expression of planar cell polarity (PCP) components. Notably, mouse Usp39-deficient embryos display early embryonic lethality due to a failure in primitive streak formation and apico-basal polarity in epiblast cells, resembling those of mutant embryos of the Prickle1 gene, a crucial PCP component. Current findings provide unique insights into how differentiation and morphogenesis are coordinated to construct three-dimensional complex structures via USP39. Nature Publishing Group UK 2022-04-19 /pmc/articles/PMC9018712/ /pubmed/35440748 http://dx.doi.org/10.1038/s42003-022-03254-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kimura-Yoshida, Chiharu Mochida, Kyoko Kanno, Shin-Ichiro Matsuo, Isao USP39 is essential for mammalian epithelial morphogenesis through upregulation of planar cell polarity components |
title | USP39 is essential for mammalian epithelial morphogenesis through upregulation of planar cell polarity components |
title_full | USP39 is essential for mammalian epithelial morphogenesis through upregulation of planar cell polarity components |
title_fullStr | USP39 is essential for mammalian epithelial morphogenesis through upregulation of planar cell polarity components |
title_full_unstemmed | USP39 is essential for mammalian epithelial morphogenesis through upregulation of planar cell polarity components |
title_short | USP39 is essential for mammalian epithelial morphogenesis through upregulation of planar cell polarity components |
title_sort | usp39 is essential for mammalian epithelial morphogenesis through upregulation of planar cell polarity components |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018712/ https://www.ncbi.nlm.nih.gov/pubmed/35440748 http://dx.doi.org/10.1038/s42003-022-03254-7 |
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