Briggs Sharon F, Dominguez Antonia A, Chavez Shawn L, Reijo Pera Renee A
Department of Genetics, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, California, USA.
Department of Obstetrics and Gynecology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, California, USA.
Stem Cells. 2015 Jun;33(6):1771-81. doi: 10.1002/stem.1992.
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.
在重编程过程中产生人类诱导多能干细胞(iPSC)以及在人类植入前发育过程中发生的广泛编程期间,X染色体失活(XCI)的过程尚未得到充分理解。事实上,关于重编程为iPSC过程中XCI的研究报告了具有两条活跃X染色体的细胞和/或具有一条失活X染色体的细胞。在这里,我们研究了长链非编码RNA XIST在人类胚胎单细胞从卵母细胞到胚胎转变过程以及新的mRNA重编程iPSC中的表达。我们表明,XIST首先在4细胞阶段开始表达,与胚胎基因组激活的开始同时以异步方式出现。此外,我们报告mRNA重编程产生的iPSC最初表达XIST转录本;然而,随着培养,表达迅速丧失。在传代后期,失活X染色体上XIST和H3K27me3富集的丧失导致X染色体表达变化。我们的数据可能有助于疾病建模的应用以及女性干细胞的潜在转化应用。