首页> 外文期刊>Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society >Effect of 5-aza-2′-deoxycytidine on methylation of the putative imprinted control region of H19 during the in vitro development of vitrified bovine two-cell embryos
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Effect of 5-aza-2′-deoxycytidine on methylation of the putative imprinted control region of H19 during the in vitro development of vitrified bovine two-cell embryos

机译:5-氮杂-2'-脱氧胞苷对玻璃化牛两细胞胚胎体外发育过程中H19假定印迹控制区域甲基化的影响

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Objective: To determine the effect of vitrification and 5-aza-2′-deoxycytidine (5-aza-dC) on the methylation levels of the putative imprinted control region (ICR) of H19 and H19 expression in bovine two-cell embryos and their derived blastocysts. Design: Experimental animal study. Setting: Academic institution. Animal(s): Abattoir-derived bovine ovaries. Intervention(s): Vitrified two-cell embryos were cultured in vitro to blastocysts with 0.01 μM 5-aza-dC (5-aza-dC group) or without 5-aza-dC (vitrification group). Fresh embryos and their derived blastocysts were used as control. Main Outcome Measure(s): Putative ICR methylation of H19 was measured by bisulfate mutagenesis and sequencing, blastocyst development rate; total cell number were determined; and H19 expression was measured by real-time reverse transcriptase-polymerase chain reaction (PCR). Result(s): Vitrification significantly increased putative ICR methylation of H19 in two-cell embryos and their derived blastocysts; 5-aza-dC significantly reduced putative ICR methylation of H19 in vitrified two-cell embryos and their derived blastocysts. The H19 expression level was significantly higher in blastocysts from the 5-aza-dC group than the vitrification group. The blastocyst development rate and total cell number in the 5-aza-dC and vitrification groups were similar. Conclusion(s): Putative ICR methylation levels of H19 significantly increased in vitrified two-cell embryos and their derived blastocysts; 5-aza-dC significantly reduced putative ICR methylation of H19 and increased H19 expression in blastocysts derived from vitrified two-cell embryos.
机译:目的:确定玻璃化和5-氮杂-2'-脱氧胞苷(5-氮杂-dC)对牛两细胞胚胎及其中H19和H19表达的假定印迹控制区(ICR)甲基化水平的影响胚泡。设计:实验动物研究。单位:学术机构。动物:屠宰场衍生的牛卵巢。干预措施:将玻璃化的两细胞胚胎在体外培养成带有0.01μM5-氮杂-dC(5-氮杂-dC组)或不含有5-氮杂-dC(玻璃化组)的胚泡。新鲜的胚胎及其衍生的胚泡被用作对照。主要观察指标:通过硫酸氢盐诱变和测序,胚泡发育率测量H19的ICR甲基化。确定总细胞数;通过实时逆转录聚合酶链反应(PCR)检测H19的表达。结果:玻璃化显着增加了两细胞胚胎及其衍生胚泡中H19的假定ICR甲基化程度; 5-氮杂-dC显着降低了玻璃化的两细胞胚胎及其衍生的胚泡中H19的假定ICR甲基化。 5-氮杂-dC组的胚泡中的H19表达水平明显高于玻璃化组。 5-氮杂-dC组和玻璃化组的胚泡发育率和总细胞数相似。结论:玻璃化的两细胞胚胎及其衍生的胚泡中H19的ICR甲基化水平显着增加; 5-氮杂-dC可以显着减少H19的ICR甲基化,并增加玻璃化两细胞胚胎衍生的胚泡中H19的表达。

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