Cargando…

Dynamics of histone H3 acetylation in the nucleosome core during mouse pre-implantation development

In mammals, the time period that follows fertilization is characterized by extensive chromatin remodeling, which enables epigenetic reprogramming of the gametes. Major changes in chromatin structure persist until the time of implantation, when the embryo develops into a blastocyst, which comprises t...

Descripción completa

Detalles Bibliográficos
Autores principales: Ziegler-Birling, Céline, Daujat, Sylvain, Schneider, Robert, Torres-Padilla, Maria-Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990223/
https://www.ncbi.nlm.nih.gov/pubmed/26479850
http://dx.doi.org/10.1080/15592294.2015.1103424
_version_ 1782448659244253184
author Ziegler-Birling, Céline
Daujat, Sylvain
Schneider, Robert
Torres-Padilla, Maria-Elena
author_facet Ziegler-Birling, Céline
Daujat, Sylvain
Schneider, Robert
Torres-Padilla, Maria-Elena
author_sort Ziegler-Birling, Céline
collection PubMed
description In mammals, the time period that follows fertilization is characterized by extensive chromatin remodeling, which enables epigenetic reprogramming of the gametes. Major changes in chromatin structure persist until the time of implantation, when the embryo develops into a blastocyst, which comprises the inner cell mass and the trophectoderm. Changes in DNA methylation, histone variant incorporation, and covalent modifications of the histones tails have been intensively studied during pre-implantation development. However, modifications within the core of the nucleosomes have not been systematically analyzed. Here, we report the first characterization and temporal analysis of 3 key acetylated residues in the core of the histone H3: H3K64ac, H3K122ac, and H3K56ac, all located at structurally important positions close to the DNA. We found that all 3 acetylations occur during pre-implantation development, but with different temporal kinetics. Globally, H3K64ac and H3K56ac were detected throughout cleavage stages, while H3K122ac was only weakly detectable during this time. Our work contributes to the understanding of the contribution of histone modifications in the core of the nucleosome to the “marking” of the newly established embryonic chromatin and unveils new modification pathways potentially involved in epigenetic reprogramming.
format Online
Article
Text
id pubmed-4990223
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-49902232016-08-29 Dynamics of histone H3 acetylation in the nucleosome core during mouse pre-implantation development Ziegler-Birling, Céline Daujat, Sylvain Schneider, Robert Torres-Padilla, Maria-Elena Epigenetics Research Paper In mammals, the time period that follows fertilization is characterized by extensive chromatin remodeling, which enables epigenetic reprogramming of the gametes. Major changes in chromatin structure persist until the time of implantation, when the embryo develops into a blastocyst, which comprises the inner cell mass and the trophectoderm. Changes in DNA methylation, histone variant incorporation, and covalent modifications of the histones tails have been intensively studied during pre-implantation development. However, modifications within the core of the nucleosomes have not been systematically analyzed. Here, we report the first characterization and temporal analysis of 3 key acetylated residues in the core of the histone H3: H3K64ac, H3K122ac, and H3K56ac, all located at structurally important positions close to the DNA. We found that all 3 acetylations occur during pre-implantation development, but with different temporal kinetics. Globally, H3K64ac and H3K56ac were detected throughout cleavage stages, while H3K122ac was only weakly detectable during this time. Our work contributes to the understanding of the contribution of histone modifications in the core of the nucleosome to the “marking” of the newly established embryonic chromatin and unveils new modification pathways potentially involved in epigenetic reprogramming. Taylor & Francis 2015-10-19 /pmc/articles/PMC4990223/ /pubmed/26479850 http://dx.doi.org/10.1080/15592294.2015.1103424 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Research Paper
Ziegler-Birling, Céline
Daujat, Sylvain
Schneider, Robert
Torres-Padilla, Maria-Elena
Dynamics of histone H3 acetylation in the nucleosome core during mouse pre-implantation development
title Dynamics of histone H3 acetylation in the nucleosome core during mouse pre-implantation development
title_full Dynamics of histone H3 acetylation in the nucleosome core during mouse pre-implantation development
title_fullStr Dynamics of histone H3 acetylation in the nucleosome core during mouse pre-implantation development
title_full_unstemmed Dynamics of histone H3 acetylation in the nucleosome core during mouse pre-implantation development
title_short Dynamics of histone H3 acetylation in the nucleosome core during mouse pre-implantation development
title_sort dynamics of histone h3 acetylation in the nucleosome core during mouse pre-implantation development
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990223/
https://www.ncbi.nlm.nih.gov/pubmed/26479850
http://dx.doi.org/10.1080/15592294.2015.1103424
work_keys_str_mv AT zieglerbirlingceline dynamicsofhistoneh3acetylationinthenucleosomecoreduringmousepreimplantationdevelopment
AT daujatsylvain dynamicsofhistoneh3acetylationinthenucleosomecoreduringmousepreimplantationdevelopment
AT schneiderrobert dynamicsofhistoneh3acetylationinthenucleosomecoreduringmousepreimplantationdevelopment
AT torrespadillamariaelena dynamicsofhistoneh3acetylationinthenucleosomecoreduringmousepreimplantationdevelopment