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Diverse epigenetic profile of novel human embryonic stem cell lines.

机译:新型人类胚胎干细胞系的表观遗传概况。

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摘要

Human embryonic stem cells (hESCs) are a promising model for studying mechanisms of regulation of early development and differentiation. OCT4, NANOG, OCT4-related genes and some others were recently described to be important in pluripotency maintenance. Lesser is known about molecular mechanisms involved in their regulation. Apart from genetic regulation of gene expression epigenetic events, particularly methylation, play an important role in early development. Using RT-PCR we studied the expression of pluripotency-related genes OCT4, NANOG, DPPA3 and DPPA5 during hESCs differentiation to embryoid bodies. Analysis of methylation profiles of promoter or putative regulatory regions of the indicated genes demonstrated that expression of the pluripotency-maintaining genes correlated with their methylation status, whereas methylation of DPPA3 and DPPA5 varied between cell lines. We propose that DNA methylation underlies the developmental stage-specific mechanisms of pluripotency-related genes expression and reactivation and may have an impact on differentiation potential of hESC lines.
机译:人类胚胎干细胞(hESCs)是研究早期发育和分化调控机制的有前途的模型。最近描述了OCT4,NANOG,OCT4相关基因以及其他一些基因在多能性维持中很重要。对涉及其调控的分子机制了解较少。除了基因表达的遗传调控外遗传事件,特别是甲基化,在早期发育中起重要作用。使用RT-PCR,我们研究了hESCs向胚状体分化过程中多能性相关基因OCT4,NANOG,DPPA3和DPPA5的表达。分析所示基因的启动子或推定调控区的甲基化图谱表明,维持多能性的基因的表达与其甲基化状态相关,而在细胞系之间,DPPA3和DPPA5的甲基化有所不同。我们建议DNA甲基化奠定了多能性相关基因表达和再激活的发展阶段特定机制的基础,并可能对hESC系的分化潜力产生影响。

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