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Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling
Tight junctions are required for the formation of tissue barriers and function as suppressors of signalling mechanisms that control gene expression and cell behaviour; however, little is known about the physiological and developmental importance of such signalling functions. Here, we demonstrate tha...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775312/ https://www.ncbi.nlm.nih.gov/pubmed/29352236 http://dx.doi.org/10.1038/s41598-018-19579-5 |
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author | Vacca, Barbara Sanchez-Heras, Elena Steed, Emily Busson, Sophie L. Balda, Maria S. Ohnuma, Shin-Ichi Sasai, Noriaki Mayor, Roberto Matter, Karl |
author_facet | Vacca, Barbara Sanchez-Heras, Elena Steed, Emily Busson, Sophie L. Balda, Maria S. Ohnuma, Shin-Ichi Sasai, Noriaki Mayor, Roberto Matter, Karl |
author_sort | Vacca, Barbara |
collection | PubMed |
description | Tight junctions are required for the formation of tissue barriers and function as suppressors of signalling mechanisms that control gene expression and cell behaviour; however, little is known about the physiological and developmental importance of such signalling functions. Here, we demonstrate that depletion of MarvelD3, a transmembrane protein of tight junctions, disrupts neural crest formation and, consequently, development of neural crest-derived tissues during Xenopus embryogenesis. Using embryos and explant cultures combined with a small molecule inhibitor or mutant mRNAs, we show that MarvelD3 is required to attenuate JNK signalling during neural crest induction and that inhibition of JNK pathway activation is sufficient to rescue the phenotype induced by MarvelD3 depletion. Direct JNK stimulation disrupts neural crest development, supporting the importance of negative regulation of JNK. Our data identify the junctional protein MarvelD3 as an essential regulator of early vertebrate development and neural crest induction and, thereby, link tight junctions to the control and timing of JNK signalling during early development. |
format | Online Article Text |
id | pubmed-5775312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57753122018-01-26 Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling Vacca, Barbara Sanchez-Heras, Elena Steed, Emily Busson, Sophie L. Balda, Maria S. Ohnuma, Shin-Ichi Sasai, Noriaki Mayor, Roberto Matter, Karl Sci Rep Article Tight junctions are required for the formation of tissue barriers and function as suppressors of signalling mechanisms that control gene expression and cell behaviour; however, little is known about the physiological and developmental importance of such signalling functions. Here, we demonstrate that depletion of MarvelD3, a transmembrane protein of tight junctions, disrupts neural crest formation and, consequently, development of neural crest-derived tissues during Xenopus embryogenesis. Using embryos and explant cultures combined with a small molecule inhibitor or mutant mRNAs, we show that MarvelD3 is required to attenuate JNK signalling during neural crest induction and that inhibition of JNK pathway activation is sufficient to rescue the phenotype induced by MarvelD3 depletion. Direct JNK stimulation disrupts neural crest development, supporting the importance of negative regulation of JNK. Our data identify the junctional protein MarvelD3 as an essential regulator of early vertebrate development and neural crest induction and, thereby, link tight junctions to the control and timing of JNK signalling during early development. Nature Publishing Group UK 2018-01-19 /pmc/articles/PMC5775312/ /pubmed/29352236 http://dx.doi.org/10.1038/s41598-018-19579-5 Text en © The Author(s) 2018 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 Vacca, Barbara Sanchez-Heras, Elena Steed, Emily Busson, Sophie L. Balda, Maria S. Ohnuma, Shin-Ichi Sasai, Noriaki Mayor, Roberto Matter, Karl Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling |
title | Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling |
title_full | Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling |
title_fullStr | Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling |
title_full_unstemmed | Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling |
title_short | Control of neural crest induction by MarvelD3-mediated attenuation of JNK signalling |
title_sort | control of neural crest induction by marveld3-mediated attenuation of jnk signalling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5775312/ https://www.ncbi.nlm.nih.gov/pubmed/29352236 http://dx.doi.org/10.1038/s41598-018-19579-5 |
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