Evidence map›Paper›PMID 35562812›Full record

ArticleEpigenetics & chromatin2022

DNA methylation may affect beef tenderness through signal transduction in Bos indicus.

Marcela Maria de Souza, Simone Cristina Méo Niciura, Marina Ibelli Pereira Rocha, Zhangyuan Pan, Huaijun Zhou, Jennifer Jessica Bruscadin, Wellison Jarles da Silva Diniz, Juliana Afonso, Priscila Silva Neubern de Oliveira, Gerson B Mourão and 4 more

Abstract read
In one paragraph

Article in Epigenetics & chromatin, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Genome-Wide DNA Methylation Differences betweenAnimals : an open access journal from MDPI · 2023
    Article
  5. Article
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

14 authors.

Marcela Maria de SouzaEmpresa Brasileira de Pesquisa Agropecuária, Embrapa Pecuária Sudeste, São Carlos, Brazil.
Simone Cristina Méo NiciuraEmpresa Brasileira de Pesquisa Agropecuária, Embrapa Pecuária Sudeste, São Carlos, Brazil.
Marina Ibelli Pereira RochaEmpresa Brasileira de Pesquisa Agropecuária, Embrapa Pecuária Sudeste, São Carlos, Brazil.
Zhangyuan PanDepartment of Animal Science, University of California, Davis, CA, USA.
Huaijun ZhouDepartment of Animal Science, University of California, Davis, CA, USA.
Jennifer Jessica BruscadinEmpresa Brasileira de Pesquisa Agropecuária, Embrapa Pecuária Sudeste, São Carlos, Brazil.
Wellison Jarles da Silva DinizEmpresa Brasileira de Pesquisa Agropecuária, Embrapa Pecuária Sudeste, São Carlos, Brazil.
Juliana AfonsoEmpresa Brasileira de Pesquisa Agropecuária, Embrapa Pecuária Sudeste, São Carlos, Brazil.
Priscila Silva Neubern de OliveiraDepartment of Genetics and Evolution, Federal University of São Carlos, São Carlos, Brazil.
Gerson B MourãoDepartment of Animal Science, Luiz de Queiroz College of Agriculture, University of São Paulo, Piracicaba, Brazil.
Adhemar ZerlotiniEmbrapa Informática Agropecuária, Empresa Brasileira de Pesquisa Agropecuária, Campinas, Brazil.
Luiz Lehmann CoutinhoDepartment of Animal Science, Luiz de Queiroz College of Agriculture, University of São Paulo, Piracicaba, Brazil.
James E KoltesDepartment of Animal Science, Iowa State University, Ames, USA.
Luciana Correia de Almeida RegitanoEmpresa Brasileira de Pesquisa Agropecuária, Embrapa Pecuária Sudeste, São Carlos, Brazil. luciana.regitano@embrapa.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBeef tenderness is a complex trait of economic importance for the beef industry. Understanding the epigenetic mechanisms underlying this trait may help improve the accuracy of breeding programs. However, little is known about epigenetic effects on Bos taurus muscle and their implications in tenderness, and no studies have been conducted in Bos indicus.

resultsComparing methylation profile of Bos indicus skeletal muscle with contrasting beef tenderness at 14 days after slaughter, we identified differentially methylated cytosines and regions associated with this trait. Interestingly, muscle that became tender beef had higher levels of hypermethylation compared to the tough group. Enrichment analysis of predicted target genes suggested that differences in methylation between tender and tough beef may affect signal transduction pathways, among which G protein signaling was a key pathway. In addition, different methylation levels were found associated with expression levels of GNAS, PDE4B, EPCAM and EBF3 genes. The differentially methylated elements correlated with EBF3 and GNAS genes overlapped CpG islands and regulatory elements. GNAS, a complex imprinted gene, has a key role on G protein signaling pathways. Moreover, both G protein signaling pathway and the EBF3 gene regulate muscle homeostasis, relaxation, and muscle cell-specificity.

conclusionsWe present differentially methylated loci that may be of interest to decipher the epigenetic mechanisms affecting tenderness. Supported by the previous knowledge about regulatory elements and gene function, the methylation data suggests EBF3 and GNAS as potential candidate genes and G protein signaling as potential candidate pathway associated with beef tenderness via methylation.

Indexed as

DNA MethylationMeatAnimalsCattleCpG IslandsMuscle, SkeletalSignal TransductionCattleEBF3EpigenomeGNASMethylationMuscleNeloreRRBSShear force

Identifiers

PMID35562812
PMCPMC9107245

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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.