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

机译:单细胞XIST在人类植入前胚胎和新编程的女性诱导多能干细胞中的表达

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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 Cells 2015;33:1771–1781
机译:对X染色体失活(XCI)在重编程以产生人诱导的多能干细胞(iPSC)的过程中以及在人类植入前发育中发生的广泛编程过程中的过程,人们尚不了解。实际上,在重编程为iPSC的过程中对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,我们检查了通过卵母细胞到胚胎的过渡在人类胚胎的单个细胞中以及在新的mRNA重新编程的iPSC中长非编码RNA XIST的表达。我们显示XIST首先在4细胞阶段开始表达,与以异步方式激活胚胎基因组的时间相吻合。此外,我们报告说,mRNA重新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年; 33:1771-1781

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