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Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development

As effectors of the Hippo signaling cascade, YAP1 and TAZ are transcriptional regulators playing important roles in development, tissue homeostasis and cancer. A number of different cues, including mechanotransduction of extracellular stimuli, adhesion molecules, oncogenic signaling and metabolism m...

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Autores principales: Astone, Matteo, Lai, Jason Kuan Han, Dupont, Sirio, Stainier, Didier Y. R., Argenton, Francesco, Vettori, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033906/
https://www.ncbi.nlm.nih.gov/pubmed/29976931
http://dx.doi.org/10.1038/s41598-018-27657-x
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author Astone, Matteo
Lai, Jason Kuan Han
Dupont, Sirio
Stainier, Didier Y. R.
Argenton, Francesco
Vettori, Andrea
author_facet Astone, Matteo
Lai, Jason Kuan Han
Dupont, Sirio
Stainier, Didier Y. R.
Argenton, Francesco
Vettori, Andrea
author_sort Astone, Matteo
collection PubMed
description As effectors of the Hippo signaling cascade, YAP1 and TAZ are transcriptional regulators playing important roles in development, tissue homeostasis and cancer. A number of different cues, including mechanotransduction of extracellular stimuli, adhesion molecules, oncogenic signaling and metabolism modulate YAP1/TAZ nucleo-cytoplasmic shuttling. In the nucleus, YAP1/TAZ tether with the DNA binding proteins TEADs, to activate the expression of target genes that regulate proliferation, migration, cell plasticity, and cell fate. Based on responsive elements present in the human and zebrafish promoters of the YAP1/TAZ target gene CTGF, we established zebrafish fluorescent transgenic reporter lines of Yap1/Taz activity. These reporter lines provide an in vivo view of Yap1/Taz activity during development and adulthood at the whole organism level. Transgene expression was detected in many larval tissues including the otic vesicles, heart, pharyngeal arches, muscles and brain and is prominent in endothelial cells. Analysis of vascular development in yap1/taz zebrafish mutants revealed specific defects in posterior cardinal vein (PCV) formation, with altered expression of arterial/venous markers. The overactivation of Yap1/Taz in endothelial cells was sufficient to promote an aberrant vessel sprouting phenotype. Our findings confirm and extend the emerging role of Yap1/Taz in vascular development including angiogenesis.
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spelling pubmed-60339062018-07-12 Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development Astone, Matteo Lai, Jason Kuan Han Dupont, Sirio Stainier, Didier Y. R. Argenton, Francesco Vettori, Andrea Sci Rep Article As effectors of the Hippo signaling cascade, YAP1 and TAZ are transcriptional regulators playing important roles in development, tissue homeostasis and cancer. A number of different cues, including mechanotransduction of extracellular stimuli, adhesion molecules, oncogenic signaling and metabolism modulate YAP1/TAZ nucleo-cytoplasmic shuttling. In the nucleus, YAP1/TAZ tether with the DNA binding proteins TEADs, to activate the expression of target genes that regulate proliferation, migration, cell plasticity, and cell fate. Based on responsive elements present in the human and zebrafish promoters of the YAP1/TAZ target gene CTGF, we established zebrafish fluorescent transgenic reporter lines of Yap1/Taz activity. These reporter lines provide an in vivo view of Yap1/Taz activity during development and adulthood at the whole organism level. Transgene expression was detected in many larval tissues including the otic vesicles, heart, pharyngeal arches, muscles and brain and is prominent in endothelial cells. Analysis of vascular development in yap1/taz zebrafish mutants revealed specific defects in posterior cardinal vein (PCV) formation, with altered expression of arterial/venous markers. The overactivation of Yap1/Taz in endothelial cells was sufficient to promote an aberrant vessel sprouting phenotype. Our findings confirm and extend the emerging role of Yap1/Taz in vascular development including angiogenesis. Nature Publishing Group UK 2018-07-05 /pmc/articles/PMC6033906/ /pubmed/29976931 http://dx.doi.org/10.1038/s41598-018-27657-x 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
Astone, Matteo
Lai, Jason Kuan Han
Dupont, Sirio
Stainier, Didier Y. R.
Argenton, Francesco
Vettori, Andrea
Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development
title Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development
title_full Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development
title_fullStr Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development
title_full_unstemmed Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development
title_short Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development
title_sort zebrafish mutants and tead reporters reveal essential functions for yap and taz in posterior cardinal vein development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033906/
https://www.ncbi.nlm.nih.gov/pubmed/29976931
http://dx.doi.org/10.1038/s41598-018-27657-x
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