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首页> 外文期刊>Epigenetics: official journal of the DNA Methylation Society >Alteration of DNA demethylation dynamics by in vitro culture conditions in rabbit pre-implantation embryos
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Alteration of DNA demethylation dynamics by in vitro culture conditions in rabbit pre-implantation embryos

机译:体外培养条件对兔植入前胚胎DNA脱甲基动力学的影响

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Alterations to DNA methylation have been attributed to in vitro culture and may affect normal embryo development. We chose to analyze DNA methylation reprogramming in the rabbit which, of the species with delayed transcriptional activation of the embryonic genome, allows easy comparisons between in vivo-developed (IVD) and in vitro-cultured (IVC) embryos. In this species, variations in DNA methylation had not previously been quantified, even in IVD embryos. IVD and IVC embryos were recovered at the 2, 4, 8 and 16-cell, morula and blastocyst stages. Immunostaining for 5-methyl-cytidine and normalization of the quantity of methylated DNA vs. the total DNA content were then performed. Our quantitative results evidenced DNA demethylation during pre-implantation development in both IVD and IVC embryos, but with different kinetics. Demethylation occurred earlier in vitro than in vivo between the 2 and 8-cell stages in IVC embryos, reaching its lowest level, while it only started at the 4-cell stage and ended at the 16-cell stage in IVD embryos. We also showed that an absence of serum from the culture medium significantly altered the degree of DNA demethylation. Finally, at the blastocyst stage, ICM was more methylated than the trophectoderm in all cases. Despite a morphological delay observed in in vitro cultured blastocysts, the difference in DNA methylation between ICM and trophectoderm cells appeared at the same time post-fertilization in IVD and IVC embryos, which may reflect another difference in the dynamics of DNA methylation during blastocyst formation. Our data thus clearly establish an effect of embryonic environment on DNA methylation reprogramming during pre-implantation development in a non-rodent species.
机译:DNA甲基化的改变已归因于体外培养,可能会影响正常胚胎的发育。我们选择分析兔子的DNA甲基化重编程,该物种的胚胎基因组转录激活延迟,可以轻松比较体内发育(IVD)和体外培养(IVC)胚胎。在这个物种中,甚至在IVD胚胎中,DNA甲基化的变化以前也没有被量化。 IVD和IVC胚胎在2、4、8和16细胞,桑ula和胚泡阶段被回收。然后进行5-甲基胞嘧啶的免疫染色和甲基化DNA的量相对于总DNA含量的归一化。我们的定量结果证明了IVD和IVC胚胎在植入前发育过程中的DNA脱甲基,但动力学不同。在IVC胚胎中,去甲基化发生在体外比体内更早的发生在体内的2细胞和8细胞阶段,达到最低水平,而它仅在IVD胚胎的4细胞阶段开始,而在16细胞阶段结束。我们还表明从培养基中缺少血清会显着改变DNA脱甲基的程度。最后,在胚泡阶段,在所有情况下,ICM都比滋养外胚层甲基化更多。尽管在体外培养的胚泡中观察到了形态学延迟,但IVD和IVC胚胎受精后ICM和滋养外胚层细胞DNA甲基化的差异同时出现,这可能反映了胚泡形成过程中DNA甲基化动力学的另一差异。因此,我们的数据清楚地确定了非啮齿类动物在植入前发育过程中胚胎环境对DNA甲基化重编程的影响。

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