Evidence map›Paper›PMID 29310712›Full record

ArticleEpigenetics & chromatin2018

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

Jessica Ispada, Camila Bruna de Lima, Marc-André Sirard, Patrícia Kubo Fontes, Marcelo Fábio Gouveia Nogueira, Kelly Annes, Marcella Pecora Milazzotto

Open access · goldAbstract read
In one paragraph

Article in Epigenetics & chromatin, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Programming of Embryonic Development.International journal of molecular sciences · 2021
    Review
  5. DNA methylation studies in cattle.Journal of applied genetics · 2021
    Review
  6. Review
  7. Article
  8. Review
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 3 countries.

Jessica IspadaInstitute of Biomedical Sciences, Universidade de São Paulo, São Paulo, Brazil. jessica.ispada@usp.br.ORCID 0000-0001-6129-3116
Camila Bruna de LimaInstitute of Biomedical Sciences, Universidade de São Paulo, São Paulo, Brazil.
Marc-André SirardCentre de Recherche en Biologie de la Reproduction, Faculté des Sciences de l'Agriculture et de l'Alimentation, Université Laval, Quebec, Canada.
Patrícia Kubo FontesDepartament of Pharmacology, Institute of Biosciences, Universidade Estadual Paulista (UNESP), Campus Botucatu, Botucatu, São Paulo, Brazil.
Marcelo Fábio Gouveia NogueiraDepartament of Biological Sciences, School of Sciences and Languages, Universidade Estadual Paulista (UNESP), Campus Assis, Assis, São Paulo, Brazil.
Kelly AnnesLaboratório de Biologia Celular e Molecular - Bloco A - 502-3, Center of Natural and Human Sciences, Universidade Federal do ABC, Av dos Estados, 5001, Bangu, Santo André, São Paulo, Brazil.
Marcella Pecora MilazzottoInstitute of Biomedical Sciences, Universidade de São Paulo, São Paulo, Brazil. marcella.milazzotto@ufabc.edu.br.
Universidade de São Paulo · BRUniversidade Estadual Paulista (Unesp) · BRUniversidade Federal do ABC · BRUniversité Laval · CA

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/03381-0
6 · The paper itself

Abstract

backgroundThe 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.

resultsGenome-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.

conclusionThe 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.

Indexed as

DNA MethylationEmbryonic DevelopmentAnimalsBlastocystCattleCpG IslandsEpigenesis, GeneticFemaleKineticsBlastocystDNA methylationEpigeneticsKinetics of development

Identifiers

PMID29310712
PMCPMC5757301
OpenAlexW2782832323

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.