Cargando…

Maintenance of spatial gene expression by Polycomb-mediated repression after formation of a vertebrate body plan

Polycomb group (PcG) proteins are transcriptional repressors that are important regulators of cell fate during embryonic development. Among them, Ezh2 is responsible for catalyzing the epigenetic repressive mark H3K27me3 and is essential for animal development. The ability of zebrafish embryos lacki...

Descripción completa

Detalles Bibliográficos
Autores principales: Rougeot, Julien, Chrispijn, Naomi D., Aben, Marco, Elurbe, Dei M., Andralojc, Karolina M., Murphy, Patrick J., Jansen, Pascal W. T. C., Vermeulen, Michiel, Cairns, Bradley R., Kamminga, Leonie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6803366/
https://www.ncbi.nlm.nih.gov/pubmed/31488564
http://dx.doi.org/10.1242/dev.178590
_version_ 1783460915706855424
author Rougeot, Julien
Chrispijn, Naomi D.
Aben, Marco
Elurbe, Dei M.
Andralojc, Karolina M.
Murphy, Patrick J.
Jansen, Pascal W. T. C.
Vermeulen, Michiel
Cairns, Bradley R.
Kamminga, Leonie M.
author_facet Rougeot, Julien
Chrispijn, Naomi D.
Aben, Marco
Elurbe, Dei M.
Andralojc, Karolina M.
Murphy, Patrick J.
Jansen, Pascal W. T. C.
Vermeulen, Michiel
Cairns, Bradley R.
Kamminga, Leonie M.
author_sort Rougeot, Julien
collection PubMed
description Polycomb group (PcG) proteins are transcriptional repressors that are important regulators of cell fate during embryonic development. Among them, Ezh2 is responsible for catalyzing the epigenetic repressive mark H3K27me3 and is essential for animal development. The ability of zebrafish embryos lacking both maternal and zygotic ezh2 to form a normal body plan provides a unique model for comprehensively studying Ezh2 function during early development in vertebrates. By using a multi-omics approach, we found that Ezh2 is required for the deposition of H3K27me3 and is essential for proper recruitment of Polycomb group protein Rnf2. However, despite the complete absence of PcG-associated epigenetic mark and proteins, only minor changes in H3K4me3 deposition and gene and protein expression occur. These changes were mainly due to local dysregulation of transcription factors outside their normal expression boundaries. Altogether, our results in zebrafish show that Polycomb-mediated gene repression is important immediately after the body plan is formed to maintain spatially restricted expression profiles of transcription factors, and we highlight the differences that exist in the timing of PcG protein action between vertebrate species.
format Online
Article
Text
id pubmed-6803366
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher The Company of Biologists Ltd
record_format MEDLINE/PubMed
spelling pubmed-68033662019-10-30 Maintenance of spatial gene expression by Polycomb-mediated repression after formation of a vertebrate body plan Rougeot, Julien Chrispijn, Naomi D. Aben, Marco Elurbe, Dei M. Andralojc, Karolina M. Murphy, Patrick J. Jansen, Pascal W. T. C. Vermeulen, Michiel Cairns, Bradley R. Kamminga, Leonie M. Development Research Article Polycomb group (PcG) proteins are transcriptional repressors that are important regulators of cell fate during embryonic development. Among them, Ezh2 is responsible for catalyzing the epigenetic repressive mark H3K27me3 and is essential for animal development. The ability of zebrafish embryos lacking both maternal and zygotic ezh2 to form a normal body plan provides a unique model for comprehensively studying Ezh2 function during early development in vertebrates. By using a multi-omics approach, we found that Ezh2 is required for the deposition of H3K27me3 and is essential for proper recruitment of Polycomb group protein Rnf2. However, despite the complete absence of PcG-associated epigenetic mark and proteins, only minor changes in H3K4me3 deposition and gene and protein expression occur. These changes were mainly due to local dysregulation of transcription factors outside their normal expression boundaries. Altogether, our results in zebrafish show that Polycomb-mediated gene repression is important immediately after the body plan is formed to maintain spatially restricted expression profiles of transcription factors, and we highlight the differences that exist in the timing of PcG protein action between vertebrate species. The Company of Biologists Ltd 2019-10-01 2019-09-30 /pmc/articles/PMC6803366/ /pubmed/31488564 http://dx.doi.org/10.1242/dev.178590 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Rougeot, Julien
Chrispijn, Naomi D.
Aben, Marco
Elurbe, Dei M.
Andralojc, Karolina M.
Murphy, Patrick J.
Jansen, Pascal W. T. C.
Vermeulen, Michiel
Cairns, Bradley R.
Kamminga, Leonie M.
Maintenance of spatial gene expression by Polycomb-mediated repression after formation of a vertebrate body plan
title Maintenance of spatial gene expression by Polycomb-mediated repression after formation of a vertebrate body plan
title_full Maintenance of spatial gene expression by Polycomb-mediated repression after formation of a vertebrate body plan
title_fullStr Maintenance of spatial gene expression by Polycomb-mediated repression after formation of a vertebrate body plan
title_full_unstemmed Maintenance of spatial gene expression by Polycomb-mediated repression after formation of a vertebrate body plan
title_short Maintenance of spatial gene expression by Polycomb-mediated repression after formation of a vertebrate body plan
title_sort maintenance of spatial gene expression by polycomb-mediated repression after formation of a vertebrate body plan
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6803366/
https://www.ncbi.nlm.nih.gov/pubmed/31488564
http://dx.doi.org/10.1242/dev.178590
work_keys_str_mv AT rougeotjulien maintenanceofspatialgeneexpressionbypolycombmediatedrepressionafterformationofavertebratebodyplan
AT chrispijnnaomid maintenanceofspatialgeneexpressionbypolycombmediatedrepressionafterformationofavertebratebodyplan
AT abenmarco maintenanceofspatialgeneexpressionbypolycombmediatedrepressionafterformationofavertebratebodyplan
AT elurbedeim maintenanceofspatialgeneexpressionbypolycombmediatedrepressionafterformationofavertebratebodyplan
AT andralojckarolinam maintenanceofspatialgeneexpressionbypolycombmediatedrepressionafterformationofavertebratebodyplan
AT murphypatrickj maintenanceofspatialgeneexpressionbypolycombmediatedrepressionafterformationofavertebratebodyplan
AT jansenpascalwtc maintenanceofspatialgeneexpressionbypolycombmediatedrepressionafterformationofavertebratebodyplan
AT vermeulenmichiel maintenanceofspatialgeneexpressionbypolycombmediatedrepressionafterformationofavertebratebodyplan
AT cairnsbradleyr maintenanceofspatialgeneexpressionbypolycombmediatedrepressionafterformationofavertebratebodyplan
AT kammingaleoniem maintenanceofspatialgeneexpressionbypolycombmediatedrepressionafterformationofavertebratebodyplan