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首页> 外文期刊>The Journal of Reproduction and Development >Alteration of the DNA methylation status of donor cells impairs the developmental competence of porcine cloned embryos
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Alteration of the DNA methylation status of donor cells impairs the developmental competence of porcine cloned embryos

机译:供体细胞DNA甲基化状态的改变损害了猪克隆胚胎的发育能力

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Nuclear reprogramming induced by somatic cell nuclear transfer is an inefficient process, and donor cell DNA methylation status is thought to be a major factor affecting cloning efficiency. Here, the role of donor cell DNA methylation status regulated by 5-aza-2'-deoxycytidine (5-aza-dC) or 5-methyl-2'-deoxycytidine-5'-triphosphate (5-methyl-dCTP) in the early development of porcine cloned embryos was investigated. Our results showed that 5-aza-dC or 5-methyl-dCTP significantly reduced or increased the global methylation levels and altered the methylation and expression levels of key genes in donor cells. However, the development of cloned embryos derived from these cells was reduced. Furthermore, disrupted pseudo-pronucleus formation and transcripts of early embryo development-related genes were observed in cloned embryos derived from these cells. In conclusion, our results demonstrated that alteration of the DNA methylation status of donor cells by 5-aza-dC or 5-methyl-dCTP disrupted nuclear reprogramming and impaired the developmental competence of porcine cloned embryos.
机译:体细胞核转移诱导的核重编程是一个低效的过程,并且供体细胞DNA甲基化状态被认为是影响克隆效率的主要因素。在这里,供体细胞DNA甲基化状态的作用由5-氮杂2'-脱氧胞苷(5-氮杂-dC)或5-甲基-2'-脱氧胞苷-5'-三磷酸(5-甲基-dCTP)调控。研究了猪克隆胚胎的早期发育。我们的结果表明,5-氮杂-dC或5-甲基-dCTP显着降低或增加了总体甲基化水平,并改变了供体细胞中关键基因的甲基化和表达水平。但是,来自这些细胞的克隆胚胎的发育减少了。此外,在衍生自这些细胞的克隆胚胎中观察到伪胚核形成和早期胚胎发育相关基因的转录物被破坏。总之,我们的结果表明,通过5-氮杂-dC或5-甲基-dCTP改变供体细胞的DNA甲基化状态会破坏核重编程并损害猪克隆胚胎的发育能力。

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