Differentially methylated regions identified in bovine embryos are not observed in adulthood

The establishment of epigenetic marks during the reprogramming window is susceptible to environmental influences, and stimuli during this critical stage can cause altered DNA methylation in offspring. In a previous study, we found that low levels of sulphur and cobalt (low S/Co) in the diet offered...

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Veröffentlicht in:Animal reproduction 2023-01, Vol.20 (1), p.e20220076-e20220076
Hauptverfasser: Vargas, Luna Nascimento, Nochi, Allice Rodrigues Ferreira, de Castro, Paloma Soares, Cunha, Andrielle Thainar Mendes, Silva, Thainara Christie Ferreira, Togawa, Roberto Coiti, Silveira, Márcia Marques, Caetano, Alexandre Rodrigues, Franco, Maurício Machaim
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Sprache:eng
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Zusammenfassung:The establishment of epigenetic marks during the reprogramming window is susceptible to environmental influences, and stimuli during this critical stage can cause altered DNA methylation in offspring. In a previous study, we found that low levels of sulphur and cobalt (low S/Co) in the diet offered to oocyte donors altered the DNA methylome of bovine embryos. However, due to the extensive epigenetic reprogramming that occurs during embryogenesis, we hypothesized that the different methylation regions (DMRs) identified in the blastocysts may not maintain in adulthood. Here, we aimed to characterize DMRs previously identified in embryos, in the blood and sperm of adult progenies of two groups of heifers (low S/Co and control). We used six bulls and characterized the DNA methylation levels of , , , and genes. Our results showed that all DMRs analysed in both groups and tissues were hypermethylated unlike that noticed in the embryonic methylome profiles. These results suggest that embryo DMRs were reprogrammed during the final stages of methylation during embryogenesis or later in development. Therefore, due to the highly dynamic epigenetic state during early embryonic development, we suggest that is essential to validate the DMRs found in embryos in adult individuals.
ISSN:1806-9614
1984-3143
1984-3143
DOI:10.1590/1984-3143-ar2022-0076