Cargando…

Coordinated Gene Expression and Chromatin Regulation during Hydra Head Regeneration

The cnidarian model organism Hydra has long been studied for its remarkable ability to regenerate its head, which is controlled by a head organizer located near the hypostome. The canonical Wnt pathway plays a central role in head organizer function during regeneration and during bud formation, whic...

Descripción completa

Detalles Bibliográficos
Autores principales: Murad, Rabi, Macias-Muñoz, Aide, Wong, Ashley, Ma, Xinyi, Mortazavi, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651858/
https://www.ncbi.nlm.nih.gov/pubmed/34877597
http://dx.doi.org/10.1093/gbe/evab221
_version_ 1784611479736025088
author Murad, Rabi
Macias-Muñoz, Aide
Wong, Ashley
Ma, Xinyi
Mortazavi, Ali
author_facet Murad, Rabi
Macias-Muñoz, Aide
Wong, Ashley
Ma, Xinyi
Mortazavi, Ali
author_sort Murad, Rabi
collection PubMed
description The cnidarian model organism Hydra has long been studied for its remarkable ability to regenerate its head, which is controlled by a head organizer located near the hypostome. The canonical Wnt pathway plays a central role in head organizer function during regeneration and during bud formation, which is the asexual mode of reproduction in Hydra. However, it is unclear how shared the developmental programs of head organizer genesis are in budding and regeneration. Time-series analysis of gene expression changes during head regeneration and budding revealed a set of 298 differentially expressed genes during the 48-h head regeneration and 72-h budding time courses. In order to understand the regulatory elements controlling Hydra head regeneration, we first identified 27,137 open-chromatin elements that are open in one or more sections of the organism body or regenerating tissue. We used histone modification ChIP-seq to identify 9,998 candidate proximal promoter and 3,018 candidate enhancer-like regions respectively. We show that a subset of these regulatory elements is dynamically remodeled during head regeneration and identify a set of transcription factor motifs that are enriched in the enhancer regions activated during head regeneration. Our results show that Hydra displays complex gene regulatory structures of developmentally dynamic enhancers, which suggests that the evolution of complex developmental enhancers predates the split of cnidarians and bilaterians.
format Online
Article
Text
id pubmed-8651858
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-86518582021-12-08 Coordinated Gene Expression and Chromatin Regulation during Hydra Head Regeneration Murad, Rabi Macias-Muñoz, Aide Wong, Ashley Ma, Xinyi Mortazavi, Ali Genome Biol Evol Research Article The cnidarian model organism Hydra has long been studied for its remarkable ability to regenerate its head, which is controlled by a head organizer located near the hypostome. The canonical Wnt pathway plays a central role in head organizer function during regeneration and during bud formation, which is the asexual mode of reproduction in Hydra. However, it is unclear how shared the developmental programs of head organizer genesis are in budding and regeneration. Time-series analysis of gene expression changes during head regeneration and budding revealed a set of 298 differentially expressed genes during the 48-h head regeneration and 72-h budding time courses. In order to understand the regulatory elements controlling Hydra head regeneration, we first identified 27,137 open-chromatin elements that are open in one or more sections of the organism body or regenerating tissue. We used histone modification ChIP-seq to identify 9,998 candidate proximal promoter and 3,018 candidate enhancer-like regions respectively. We show that a subset of these regulatory elements is dynamically remodeled during head regeneration and identify a set of transcription factor motifs that are enriched in the enhancer regions activated during head regeneration. Our results show that Hydra displays complex gene regulatory structures of developmentally dynamic enhancers, which suggests that the evolution of complex developmental enhancers predates the split of cnidarians and bilaterians. Oxford University Press 2021-12-08 /pmc/articles/PMC8651858/ /pubmed/34877597 http://dx.doi.org/10.1093/gbe/evab221 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Murad, Rabi
Macias-Muñoz, Aide
Wong, Ashley
Ma, Xinyi
Mortazavi, Ali
Coordinated Gene Expression and Chromatin Regulation during Hydra Head Regeneration
title Coordinated Gene Expression and Chromatin Regulation during Hydra Head Regeneration
title_full Coordinated Gene Expression and Chromatin Regulation during Hydra Head Regeneration
title_fullStr Coordinated Gene Expression and Chromatin Regulation during Hydra Head Regeneration
title_full_unstemmed Coordinated Gene Expression and Chromatin Regulation during Hydra Head Regeneration
title_short Coordinated Gene Expression and Chromatin Regulation during Hydra Head Regeneration
title_sort coordinated gene expression and chromatin regulation during hydra head regeneration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651858/
https://www.ncbi.nlm.nih.gov/pubmed/34877597
http://dx.doi.org/10.1093/gbe/evab221
work_keys_str_mv AT muradrabi coordinatedgeneexpressionandchromatinregulationduringhydraheadregeneration
AT maciasmunozaide coordinatedgeneexpressionandchromatinregulationduringhydraheadregeneration
AT wongashley coordinatedgeneexpressionandchromatinregulationduringhydraheadregeneration
AT maxinyi coordinatedgeneexpressionandchromatinregulationduringhydraheadregeneration
AT mortazaviali coordinatedgeneexpressionandchromatinregulationduringhydraheadregeneration