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Effect of postovulatory oocyte aging on DNA methylation imprinting acquisition in offspring oocytes.

机译:排卵后卵母细胞老化对后代卵母细胞DNA甲基化印迹获得的影响。

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摘要

OBJECTIVE: To investigate whether postovulatory aging of oocytes in the mother affects DNA methylation acquisition of imprinted genes in oocytes from the offspring. DESIGN: Randomized research experimental study. SETTING: Academic basic research laboratory. ANIMAL(S): Mice. INTERVENTION(S): Fresh oocytes and aged oocytes from mothers were artificially inseminated, and oocytes were collected from the resultant offspring. MAIN OUTCOME MEASURE(S): Methylation status was evaluated at differentially methylated regions (DMRs) in oocytes of maternally imprinted genes Peg3, Snrpn, and Peg1 and paternally imprinted gene H19. RESULT(S): Our results showed that methylation patterns at DMRs of Peg3, Snrpn, Peg1, and H19 in oocytes from aged-oocyte offspring were mainly normal, with only a small number of oocytes showing aberrant methylation in the DMR of Peg3. CONCLUSION(S): Postovulatory oocyte aging causes a decline in reproductive outcomes but does not evidently lead to defects in DNA methylation imprinting acquisition in the oocytes from viable offspring.
机译:目的:探讨母亲卵母细胞的排卵后衰老是否影响后代卵母细胞印迹基因的DNA甲基化获得。设计:随机研究实验研究。地点:学术基础研究实验室。动物:小鼠。干预:人工授精新鲜的卵母细胞和母亲的老卵母细胞,并从后代中收集卵母细胞。主要观察指标:评估母本印记基因Peg3,Snrpn和Peg1以及母本印记基因H19卵母细胞中差异甲基化区域(DMR)的甲基化状态。结果:我们的结果表明,老化卵母细胞后代的卵母细胞中Peg3,Snrpn,Peg1和H19的DMR处的甲基化模式主要是正常的,只有少数卵母细胞在Peg3的DMR中显示出异常的甲基化。结论:排卵后卵母细胞衰老会导致生殖结果的下降,但并没有明显导致DNA甲基化印迹缺陷的存在。

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