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Nucleoporin insufficiency disrupts a pluripotent regulatory circuit in a pro-arrhythmogenic stem cell line

机译:核蛋白递质不足会破坏促心律失常性干细胞系中的多能调节回路

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摘要

Nucleoporins have been reported to regulate pluripotent biology, but how they do so remains partially characterized. This study examined the effects of nup155 gene disruption on mouse embryonic stem cells to gain insights into possible mechanisms by which nucleoporins regulate pluripotency in a pro-arrhythmogenic stem cell line. Embryonic stem cells with gene-trapped nup155 exhibited aberrant colony morphology underscored by abnormal transcriptome remodeling. Bioinformatic analysis of whole transcriptome data from nup155+/− embryonic stem cells revealed changes in a variety of non-coding RNA elements, with significant under expression of miR291a, miR291b, miR293, and miR294. These miRNAs are members of the larger regulatory miR290–295 cluster that regulates pluripotency and are controlled by the canonical stem cell-related factors SOX2, OCT4, and NANOG. Expression analysis of these factors revealed downregulation in all three, supported by biochemical profiling and image analysis. These data implicate disruption of the miR-SOX2/OCT4/NANOG regulatory circuit occurs downstream of nup155 gene lesion.
机译:据报道,核蛋白可调节多能生物学,但它们如何做到这一点仍部分表征。这项研究检查了nup155基因破坏对小鼠胚胎干细胞的影响,以了解核孔蛋白调节促心律失常干细胞系中多能性的可能机制。异常转录组重塑强调具有基因陷阱nup155的胚胎干细胞表现出异常的菌落形态。对来自nup155 +/- 胚胎干细胞的整个转录组数据的生物信息学分析显示,多种非编码RNA元件发生了变化,其中miR291a,miR291b,miR293和miR294的表达明显不足。这些miRNA是更大的调节性miR290-295簇的成员,后者可调节多能性,并受规范的干细胞相关因子SOX2,OCT4和NANOG的控制。这些因素的表达分析显示,在生化分析和图像分析的支持下,这三个因子均下调。这些数据暗示在nup155基因损伤的下游发生miR-SOX2 / OCT4 / NANOG调节电路的破坏。

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