Cargando…

Genome-wide screening of DNA methylation in bovine blastocysts with different kinetics of development

BACKGROUND: The timing of the first cell divisions may predict the developmental potential of an embryo, including its ability to establish pregnancy. Besides differences related to metabolism, stress, and survival, embryos with different speeds of development present distinct patterns of gene expre...

Descripción completa

Detalles Bibliográficos
Autores principales: Ispada, Jessica, de Lima, Camila Bruna, Sirard, Marc-André, Fontes, Patrícia Kubo, Nogueira, Marcelo Fábio Gouveia, Annes, Kelly, Milazzotto, Marcella Pecora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757301/
https://www.ncbi.nlm.nih.gov/pubmed/29310712
http://dx.doi.org/10.1186/s13072-017-0171-z
_version_ 1783290834633883648
author Ispada, Jessica
de Lima, Camila Bruna
Sirard, Marc-André
Fontes, Patrícia Kubo
Nogueira, Marcelo Fábio Gouveia
Annes, Kelly
Milazzotto, Marcella Pecora
author_facet Ispada, Jessica
de Lima, Camila Bruna
Sirard, Marc-André
Fontes, Patrícia Kubo
Nogueira, Marcelo Fábio Gouveia
Annes, Kelly
Milazzotto, Marcella Pecora
author_sort Ispada, Jessica
collection PubMed
description BACKGROUND: The timing of the first cell divisions may predict the developmental potential of an embryo, including its ability to establish pregnancy. Besides differences related to metabolism, stress, and survival, embryos with different speeds of development present distinct patterns of gene expression, mainly related to energy and lipid metabolism. As gene expression is regulated by epigenetic factors, and that includes DNA methylation patterns, in this study we compared the global DNA methylation profile of embryos with different kinetics of development in order to identify general pathways and regions that are most influenced by this phenotype. For this purpose, bovine embryos were in vitro produced using sexed semen (female), classified as fast (four or more cells) or slow (two cells) at 40 hpi and cultured until blastocyst stage, when they were analyzed. RESULTS: Genome-wide DNA methylation analysis identified 11,584 differently methylated regions (DMRs) (7976 hypermethylated regions in fast and 3608 hypermethylated regions in slow embryos). Fast embryos presented more regions classified as hypermethylated distributed throughout the genome, as in introns, exons, promoters, and repeat elements while in slow embryos, hypermethylated regions were more present in CpG islands. DMRs were clustered by means of biological processes, and the most affected pathways were related to cell survival/differentiation and energy/lipid metabolism. Transcripts profiles from DM genes connected with these pathways were also assessed, and the most part disclosed changes in relative quantitation. CONCLUSION: The kinetics of the first cleavages influences the DNA methylation and expression profiles of genes related to metabolism and differentiation pathways and may affect embryo viability. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-017-0171-z) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5757301
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-57573012018-01-10 Genome-wide screening of DNA methylation in bovine blastocysts with different kinetics of development Ispada, Jessica de Lima, Camila Bruna Sirard, Marc-André Fontes, Patrícia Kubo Nogueira, Marcelo Fábio Gouveia Annes, Kelly Milazzotto, Marcella Pecora Epigenetics Chromatin Research BACKGROUND: The timing of the first cell divisions may predict the developmental potential of an embryo, including its ability to establish pregnancy. Besides differences related to metabolism, stress, and survival, embryos with different speeds of development present distinct patterns of gene expression, mainly related to energy and lipid metabolism. As gene expression is regulated by epigenetic factors, and that includes DNA methylation patterns, in this study we compared the global DNA methylation profile of embryos with different kinetics of development in order to identify general pathways and regions that are most influenced by this phenotype. For this purpose, bovine embryos were in vitro produced using sexed semen (female), classified as fast (four or more cells) or slow (two cells) at 40 hpi and cultured until blastocyst stage, when they were analyzed. RESULTS: Genome-wide DNA methylation analysis identified 11,584 differently methylated regions (DMRs) (7976 hypermethylated regions in fast and 3608 hypermethylated regions in slow embryos). Fast embryos presented more regions classified as hypermethylated distributed throughout the genome, as in introns, exons, promoters, and repeat elements while in slow embryos, hypermethylated regions were more present in CpG islands. DMRs were clustered by means of biological processes, and the most affected pathways were related to cell survival/differentiation and energy/lipid metabolism. Transcripts profiles from DM genes connected with these pathways were also assessed, and the most part disclosed changes in relative quantitation. CONCLUSION: The kinetics of the first cleavages influences the DNA methylation and expression profiles of genes related to metabolism and differentiation pathways and may affect embryo viability. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13072-017-0171-z) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-08 /pmc/articles/PMC5757301/ /pubmed/29310712 http://dx.doi.org/10.1186/s13072-017-0171-z Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ispada, Jessica
de Lima, Camila Bruna
Sirard, Marc-André
Fontes, Patrícia Kubo
Nogueira, Marcelo Fábio Gouveia
Annes, Kelly
Milazzotto, Marcella Pecora
Genome-wide screening of DNA methylation in bovine blastocysts with different kinetics of development
title Genome-wide screening of DNA methylation in bovine blastocysts with different kinetics of development
title_full Genome-wide screening of DNA methylation in bovine blastocysts with different kinetics of development
title_fullStr Genome-wide screening of DNA methylation in bovine blastocysts with different kinetics of development
title_full_unstemmed Genome-wide screening of DNA methylation in bovine blastocysts with different kinetics of development
title_short Genome-wide screening of DNA methylation in bovine blastocysts with different kinetics of development
title_sort genome-wide screening of dna methylation in bovine blastocysts with different kinetics of development
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757301/
https://www.ncbi.nlm.nih.gov/pubmed/29310712
http://dx.doi.org/10.1186/s13072-017-0171-z
work_keys_str_mv AT ispadajessica genomewidescreeningofdnamethylationinbovineblastocystswithdifferentkineticsofdevelopment
AT delimacamilabruna genomewidescreeningofdnamethylationinbovineblastocystswithdifferentkineticsofdevelopment
AT sirardmarcandre genomewidescreeningofdnamethylationinbovineblastocystswithdifferentkineticsofdevelopment
AT fontespatriciakubo genomewidescreeningofdnamethylationinbovineblastocystswithdifferentkineticsofdevelopment
AT nogueiramarcelofabiogouveia genomewidescreeningofdnamethylationinbovineblastocystswithdifferentkineticsofdevelopment
AT anneskelly genomewidescreeningofdnamethylationinbovineblastocystswithdifferentkineticsofdevelopment
AT milazzottomarcellapecora genomewidescreeningofdnamethylationinbovineblastocystswithdifferentkineticsofdevelopment