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Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis

Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA signalling in this context remains to be defined. By RNA sequencing of in vitro-generated pancreatic explants, we identified the genes encoding the tra...

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Autores principales: Gere-Becker, Maja B., Pommerenke, Claudia, Lingner, Thomas, Pieler, Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031401/
https://www.ncbi.nlm.nih.gov/pubmed/29769220
http://dx.doi.org/10.1242/dev.161372
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author Gere-Becker, Maja B.
Pommerenke, Claudia
Lingner, Thomas
Pieler, Tomas
author_facet Gere-Becker, Maja B.
Pommerenke, Claudia
Lingner, Thomas
Pieler, Tomas
author_sort Gere-Becker, Maja B.
collection PubMed
description Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA signalling in this context remains to be defined. By RNA sequencing of in vitro-generated pancreatic explants, we identified the genes encoding the transcription factor Hnf1β and the Wnt-receptor Fzd4/Fzd4s as direct RA target genes. Functional analyses of Hnf1b and Fzd4/Fzd4s in programmed pancreatic explants and whole embryos revealed their requirement for pancreatic progenitor formation and differentiation. Thus, Hnf1β and Fzd4/Fzd4s appear to be involved in pre-patterning events of the embryonic endoderm that allow pancreas formation in Xenopus.
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spelling pubmed-60314012018-07-17 Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis Gere-Becker, Maja B. Pommerenke, Claudia Lingner, Thomas Pieler, Tomas Development Research Article Retinoic acid (RA) is required for pancreas specification in Xenopus and other vertebrates. However, the gene network that is directly induced by RA signalling in this context remains to be defined. By RNA sequencing of in vitro-generated pancreatic explants, we identified the genes encoding the transcription factor Hnf1β and the Wnt-receptor Fzd4/Fzd4s as direct RA target genes. Functional analyses of Hnf1b and Fzd4/Fzd4s in programmed pancreatic explants and whole embryos revealed their requirement for pancreatic progenitor formation and differentiation. Thus, Hnf1β and Fzd4/Fzd4s appear to be involved in pre-patterning events of the embryonic endoderm that allow pancreas formation in Xenopus. The Company of Biologists Ltd 2018-06-15 2018-06-08 /pmc/articles/PMC6031401/ /pubmed/29769220 http://dx.doi.org/10.1242/dev.161372 Text en © 2018. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Gere-Becker, Maja B.
Pommerenke, Claudia
Lingner, Thomas
Pieler, Tomas
Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis
title Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis
title_full Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis
title_fullStr Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis
title_full_unstemmed Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis
title_short Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis
title_sort retinoic acid-induced expression of hnf1b and fzd4 is required for pancreas development in xenopus laevis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031401/
https://www.ncbi.nlm.nih.gov/pubmed/29769220
http://dx.doi.org/10.1242/dev.161372
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