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首页> 外文期刊>Biochemical and Biophysical Research Communications >Loss of methylation imprint of Snrpn in postovulatory aging mouse oocyte.
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Loss of methylation imprint of Snrpn in postovulatory aging mouse oocyte.

机译:排卵后衰老小鼠卵母细胞中Snrpn甲基化印记的丢失。

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摘要

Prolonged residence of postovulatory oocyte in the oviduct or prolonged culture in vitro can lead to oocyte aging, which significantly affects pre- and post-implantation embryo development. In this study, we employed bisulfite sequencing and COBRA methods to investigate the DNA methylation status of differentially methylated regions (DMRs) of Snrpn and Peg1/Mest, two maternally imprinted genes, in postovulatory oocytes aged in vivo and in vitro. The results showed that Snrpn DMR was clearly demethylated in oocytes aged in vivo at 29h post-hCG and in denuded oocytes aged in vitro for the same time period. However, Peg1/Mest did not show any demethylation in all aged groups at 29h post-hCG. These data indicate that oocytes undergo time-dependent demethylation of Snrpn DMR during the process of postovulatory aging.
机译:排卵后卵母细胞在输卵管中的长时间停留或体外培养时间的延长会导致卵母细胞衰老,从而显着影响植入前后的胚胎发育。在这项研究中,我们采用亚硫酸氢盐测序和COBRA方法研究了在体内和体外老化的排卵后卵母细胞中Snrpn和Peg1 / Mest这两个母本印记基因的差异甲基化区域(DMR)的DNA甲基化状态。结果表明,Srrpn DMR在hCG后29h在体内老化的卵母细胞和在同一时间体外老化的裸露卵母细胞中明显脱甲基。然而,在hCG后29h,所有年龄组的Peg1 / Mest均未显示任何去甲基化。这些数据表明卵母细胞在排卵后衰老过程中经历时间依赖性的Snrpn DMR去甲基化。

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