Goodrich Leeanne, Panning Barbara, Leung Karen Nicole
Department of Biochemistry and Biophysics, University of California, San Francisco, 600 16th Street, San Francisco, CA 94158, United States.
Department of Biochemistry and Biophysics, University of California, San Francisco, 600 16th Street, San Francisco, CA 94158, United States.
Semin Cell Dev Biol. 2016 Aug;56:3-8. doi: 10.1016/j.semcdb.2016.05.005. Epub 2016 May 17.
In early female embryos X-chromosome inactivation occurs concomitant with up regulation of the non-coding RNA, Xist, on the future inactive X-chromosome. Up regulation of Xist and coating of the future inactive X is sufficient to induce silencing. Therefore unlocking the mechanisms of X-chromosome inactivation requires thorough understanding of the transcriptional regulators, both activators and repressors, which control Xist. Mouse pluripotent embryonic stem cells, which have two active X chromosomes, provide a tractable ex vivo model system for studying X-chromosome inactivation, since this process is triggered by differentiation signals in these cultured cells. Yet there are significant discrepancies found between ex vivo analyses in mouse embryonic stem cells and in vivo studies of early embryos. In this review we elaborate on potential models of how Xist is up regulated on a single X chromosome in female cells and how ex vivo and in vivo analyses enlighten our understanding of the activators and repressors that control this non-coding RNA gene.
在早期雌性胚胎中,X染色体失活与未来失活的X染色体上非编码RNA Xist的上调同时发生。Xist的上调以及对未来失活X染色体的覆盖足以诱导基因沉默。因此,要揭示X染色体失活的机制,需要深入了解控制Xist的转录调节因子,包括激活因子和抑制因子。具有两条活跃X染色体的小鼠多能胚胎干细胞为研究X染色体失活提供了一个易于处理的体外模型系统,因为在这些培养细胞中,这一过程是由分化信号触发的。然而,在小鼠胚胎干细胞的体外分析和早期胚胎的体内研究之间发现了显著差异。在这篇综述中,我们详细阐述了雌性细胞中单个X染色体上Xist如何上调的潜在模型,以及体外和体内分析如何增进我们对控制这种非编码RNA基因的激活因子和抑制因子的理解。