Cargando…

Inherited DNA methylation primes the establishment of accessible chromatin during genome activation

For animals, epigenetic modifications can be globally or partially inherited from gametes after fertilization, and such information is required for proper transcriptional regulation, especially during the process of zygotic genome activation (ZGA). However, the mechanism underlying how the inherited...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Guifen, Wang, Wen, Hu, Shengen, Wang, Xiangxiu, Zhang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028135/
https://www.ncbi.nlm.nih.gov/pubmed/29844026
http://dx.doi.org/10.1101/gr.228833.117
_version_ 1783336719561523200
author Liu, Guifen
Wang, Wen
Hu, Shengen
Wang, Xiangxiu
Zhang, Yong
author_facet Liu, Guifen
Wang, Wen
Hu, Shengen
Wang, Xiangxiu
Zhang, Yong
author_sort Liu, Guifen
collection PubMed
description For animals, epigenetic modifications can be globally or partially inherited from gametes after fertilization, and such information is required for proper transcriptional regulation, especially during the process of zygotic genome activation (ZGA). However, the mechanism underlying how the inherited epigenetic signatures affect transcriptional regulation during ZGA remains poorly understood. Here, we performed genome-wide profiling of chromatin accessibility during zebrafish ZGA, which is closely related to zygotic transcriptional regulation. We observed a clear trend toward a gradual increase in accessible chromatin during ZGA. Furthermore, accessible chromatin at the promoters displayed a sequential priority of emergence, and the locations of the accessible chromatin were precisely primed by the enrichment of unmethylated CpGs that were fully inherited from gametes. On the other hand, distal regions with high methylation levels that were inherited from the sperm facilitated the binding of DNA methylation-preferred transcription factors, such as Pou5f3 and Nanog, which contributed to the establishment of accessible chromatin at these loci. Our results demonstrate a model whereby inherited DNA methylation signatures from gametes prime the establishment of accessible chromatin during zebrafish ZGA through two distinct mechanisms.
format Online
Article
Text
id pubmed-6028135
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-60281352019-01-01 Inherited DNA methylation primes the establishment of accessible chromatin during genome activation Liu, Guifen Wang, Wen Hu, Shengen Wang, Xiangxiu Zhang, Yong Genome Res Research For animals, epigenetic modifications can be globally or partially inherited from gametes after fertilization, and such information is required for proper transcriptional regulation, especially during the process of zygotic genome activation (ZGA). However, the mechanism underlying how the inherited epigenetic signatures affect transcriptional regulation during ZGA remains poorly understood. Here, we performed genome-wide profiling of chromatin accessibility during zebrafish ZGA, which is closely related to zygotic transcriptional regulation. We observed a clear trend toward a gradual increase in accessible chromatin during ZGA. Furthermore, accessible chromatin at the promoters displayed a sequential priority of emergence, and the locations of the accessible chromatin were precisely primed by the enrichment of unmethylated CpGs that were fully inherited from gametes. On the other hand, distal regions with high methylation levels that were inherited from the sperm facilitated the binding of DNA methylation-preferred transcription factors, such as Pou5f3 and Nanog, which contributed to the establishment of accessible chromatin at these loci. Our results demonstrate a model whereby inherited DNA methylation signatures from gametes prime the establishment of accessible chromatin during zebrafish ZGA through two distinct mechanisms. Cold Spring Harbor Laboratory Press 2018-07 /pmc/articles/PMC6028135/ /pubmed/29844026 http://dx.doi.org/10.1101/gr.228833.117 Text en © 2018 Liu et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
Liu, Guifen
Wang, Wen
Hu, Shengen
Wang, Xiangxiu
Zhang, Yong
Inherited DNA methylation primes the establishment of accessible chromatin during genome activation
title Inherited DNA methylation primes the establishment of accessible chromatin during genome activation
title_full Inherited DNA methylation primes the establishment of accessible chromatin during genome activation
title_fullStr Inherited DNA methylation primes the establishment of accessible chromatin during genome activation
title_full_unstemmed Inherited DNA methylation primes the establishment of accessible chromatin during genome activation
title_short Inherited DNA methylation primes the establishment of accessible chromatin during genome activation
title_sort inherited dna methylation primes the establishment of accessible chromatin during genome activation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028135/
https://www.ncbi.nlm.nih.gov/pubmed/29844026
http://dx.doi.org/10.1101/gr.228833.117
work_keys_str_mv AT liuguifen inheriteddnamethylationprimestheestablishmentofaccessiblechromatinduringgenomeactivation
AT wangwen inheriteddnamethylationprimestheestablishmentofaccessiblechromatinduringgenomeactivation
AT hushengen inheriteddnamethylationprimestheestablishmentofaccessiblechromatinduringgenomeactivation
AT wangxiangxiu inheriteddnamethylationprimestheestablishmentofaccessiblechromatinduringgenomeactivation
AT zhangyong inheriteddnamethylationprimestheestablishmentofaccessiblechromatinduringgenomeactivation