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Effects of vitrification on the imprinted gene Snrpn in neonatal placental tissue

机译:玻璃化对新生儿胎盘组织中印迹基因SNRPN的影响

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Objective: To investigate the effects of vitrification on the expression of the imprinted gene Snrpn in neonatal placental tissue.Methods: Neonatal placental tissue was collected from women with natural pregnancy (control group) and from women in assisted reproductive technology (ART) pregnancy group, following fresh and vitrified embryo transfer (fresh group and vitrified group, respectively). Snrpn mRNA expression and SNRPN protein levels in placental tissue from these three groups were assessed by real-time reverse transcription polymerase chain reaction and Western blot, respectively. DNA methylation in the Snrpn promoter region was analyzed by bisulfite-pyrosequencing.Results: The expression of Snrpn mRNA and SNRPN protein was found to be higher in placental tissue from the fresh and vitrified ART groups, compared to the control group. There was no significant difference in SNRPN gene or protein expression between the fresh and vitrified groups. DNA methylation at the Snrpn promoter region was not significantly different between these three groups.Conclusions: Human ART may alter the transcriptional expression and protein levels of the imprinted gene Snrpn. However, compared to other ART methods, vitrification may not aggravate or reduce this effect. Moreover, the altered expression of Snrpn is likely not directly related to DNA methylation of the Snrpn promoter region.
机译:目的:探讨玻璃化对新生胎盘组织中印迹基因SnRPN表达的影响。方法:从天然妊娠(对照组)和辅助生殖技术(艺术)怀孕组妇女收集新生儿胎盘组织,在新鲜和玻璃化胚胎转移(分别为新鲜组和玻璃化组)之后。通过实时逆转录聚合酶链反应和蛋白质印迹评估来自这三组胎盘组织中的SNRPN mRNA表达和SNRPN蛋白水平。通过双硫酸氢淀粉区分析SNRPN启动子区中的DNA甲基化。结果:与对照组相比,发现SNRPN mRNA和SNRPN蛋白的表达在新鲜和玻璃化的艺术组中胎盘组织较高。新鲜和玻璃化基团之间的SNRPN基因或蛋白质表达无显着差异。 SNRPN启动子区的DNA甲基化在这三组之间没有显着差异。结论:人类技术可以改变印迹基因SNRPN的转录表达和蛋白质水平。然而,与其他技术方法相比,玻璃化可能不会加重或减少这种效果。此外,SNRPN的改变表达可能与SNRPN启动子区的DNA甲基化不直接相关。

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