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

机译:核偶素不足破坏了促血糖干细胞系中的多能调节赛

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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 nup155sup+/-/sup 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,核偶杀素来调节多能生物学,但它们如何仍然是部分特征。本研究检测了NUP155基因破坏对小鼠胚胎干细胞的影响,以获得核致素治疗多能性的可能机制的可能机制。具有基因被捕获的NUP155的胚胎干细胞表现出异常转录物重塑的异常菌落形态。来自NUP155 +/- 胚胎干细胞的整个转录组数据的生物信息分析显示出各种非编码RNA元素的变化,在miR291a,miR291b,miR293和miR294的表达下具有显着性。这些miRNA是调节多能性的较大调节MiR290-295集群的成员,并由规范干细胞相关因素Sox2,Oct4和Nanog控制。这些因素的表达分析显示所有三种的下调,通过生化分析和图像分析支持。这些数据暗示MIR-SOX2 / OCT4 / NANOG调节电路的破坏发生在NUP155基因病变下游。

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