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
Laboratório de Reprodução Animal, Embrapa Recursos Genéticos e Biotecnologia, Brasília, DF, Brasil.
Instituto de Biotecnologia, Universidade Federal de Uberlândia, Uberlândia, MG, Brasil.
Anim Reprod. 2023 Mar 13;20(1):e20220076. doi: 10.1590/1984-3143-AR2022-0076. eCollection 2023.
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.
重编程窗口期表观遗传标记的建立易受环境影响,在此关键阶段的刺激可导致后代DNA甲基化改变。在之前的一项研究中,我们发现提供给卵母细胞供体的饮食中低水平的硫和钴(低S/Co)会改变牛胚胎的DNA甲基化组。然而,由于胚胎发生过程中会发生广泛的表观遗传重编程,我们推测在囊胚中鉴定出的不同甲基化区域(DMRs)在成年期可能无法维持。在这里,我们旨在表征先前在两组小母牛(低S/Co和对照组)成年后代的血液和精子中胚胎中鉴定出的DMRs。我们使用了六头公牛,并对、、、和基因的DNA甲基化水平进行了表征。我们的结果表明,与胚胎甲基化组图谱中所观察到的不同,两组和各组织中分析的所有DMRs均发生了高甲基化。这些结果表明,胚胎DMRs在胚胎发生过程中的甲基化最后阶段或发育后期被重新编程。因此,由于早期胚胎发育过程中表观遗传状态高度动态变化,我们认为在成年个体中验证在胚胎中发现的DMRs至关重要。