The Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Cell. 2012 Sep 14;150(6):1209-22. doi: 10.1016/j.cell.2012.08.023.
During cellular reprogramming, only a small fraction of cells become induced pluripotent stem cells (iPSCs). Previous analyses of gene expression during reprogramming were based on populations of cells, impeding single-cell level identification of reprogramming events. We utilized two gene expression technologies to profile 48 genes in single cells at various stages during the reprogramming process. Analysis of early stages revealed considerable variation in gene expression between cells in contrast to late stages. Expression of Esrrb, Utf1, Lin28, and Dppa2 is a better predictor for cells to progress into iPSCs than expression of the previously suggested reprogramming markers Fbxo15, Fgf4, and Oct4. Stochastic gene expression early in reprogramming is followed by a late hierarchical phase with Sox2 being the upstream factor in a gene expression hierarchy. Finally, downstream factors derived from the late phase, which do not include Oct4, Sox2, Klf4, c-Myc, and Nanog, can activate the pluripotency circuitry.
在细胞重编程过程中,只有一小部分细胞成为诱导多能干细胞 (iPSC)。以前对重编程过程中基因表达的分析是基于细胞群体的,这阻碍了在单细胞水平上识别重编程事件。我们利用两种基因表达技术,在重编程过程的各个阶段对 48 个基因的单个细胞进行了分析。早期阶段的分析表明,与晚期阶段相比,细胞之间的基因表达存在很大差异。与先前建议的重编程标记物 Fbxo15、Fgf4 和 Oct4 相比,Esrrb、Utf1、Lin28 和 Dppa2 的表达更能预测细胞向 iPSC 进展。重编程早期的随机基因表达随后是晚期的层次阶段,Sox2 是基因表达层次中的上游因素。最后,晚期阶段产生的下游因子不包括 Oct4、Sox2、Klf4、c-Myc 和 Nanog,可以激活多能性回路。