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Single-cell expression analyses during cellular reprogramming reveal an early stochastic and a late hierarchic phase

机译:细胞重编程过程中的单细胞表达分析揭示了早期的随机阶段和晚期的分层阶段

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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.
机译:在细胞重编程期间,仅一小部分细胞成为诱导性多能干细胞(iPSC)。之前在重编程期间对基因表达的分析是基于细胞群体的,这阻碍了单细胞水平识别重编程事件。在重编程过程中,我们利用两种基因表达技术在单个细胞中的各个阶段分析了48个基因。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相当大的差异。与先前建议的重编程标记Fbxo15,Fgf4和Oct4的表达相比,Esrrb,Utf1,Lin28和Dppa2的表达是细胞进入iPSC的更好预测因子。重编程早期是随机基因表达,随后是后期分级阶段,其中Sox2是基因表达分级中的上游因素。最后,来自后期的下游因素(不包括Oct4,Sox2,Klf4,c-Myc和Nanog)可以激活多潜能电路。

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