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Single-Cell XIST Expression in Human Preimplantation Embryos and Newly Reprogrammed Female Induced Pluripotent Stem Cells

机译:人植入前胚胎和新编程的女性诱导多能干细胞中的单细胞XIST表达。

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摘要

The process of X chromosome inactivation (XCI) during reprogramming to produce human induced pluripotent stem cells (iPSCs), as well as during the extensive programming that occurs in human preimplantation development, is not well-understood. Indeed, studies of XCI during reprogramming to iPSCs report cells with two active X chromosomes and/or cells with one inactive X chromosome. Here, we examine expression of the long noncoding RNA, XIST, in single cells of human embryos through the oocyte-to-embryo transition and in new mRNA reprogrammed iPSCs. We show that XIST is first expressed beginning at the 4-cell stage, coincident with the onset of embryonic genome activation in an asynchronous manner. Additionally, we report that mRNA reprogramming produces iPSCs that initially express XIST transcript; however, expression is rapidly lost with culture. Loss of XIST and H3K27me3 enrichment at the inactive X chromosome at late passage results in X chromosome expression changes. Our data may contribute to applications in disease modeling and potential translational applications of female stem cells. Stem Cells2015;33:1771-1781
机译:重新编程以产生人诱导的多能干细胞(iPSC)期间以及人类植入前发育中发生的广泛编程过程中X染色体失活(XCI)的过程,尚不为人所知。实际上,在重编程为iPSC期间对XCI的研究报告了具有两个活跃X染色体的细胞和/或具有一个非活跃X染色体的细胞。在这里,我们研究了通过卵母细胞到胚胎的过渡以及在新的mRNA重编程的iPSC中人类胚胎单细胞中长非编码RNA XIST的表达。我们表明,XIST首先在4细胞阶段开始表达,与以异步方式启动胚胎基因组激活相一致。此外,我们报告说,mRNA重编程产生了最初表达XIST转录本的iPSC。但是,表达随着文化而迅速丧失。 XIST和H3K27me3富集在不活跃的X染色体上的丢失会在后期传递时导致X染色体表达的改变。我们的数据可能有助于疾病建模和女性干细胞潜在的翻译应用。干细胞2015; 33:1771-1781

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