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Epigenetic modification of retinoic acid-treated human embryonic stem cells

机译:维甲酸处理人胚胎干细胞的表观遗传修饰

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摘要

Epigenetic modification of the genome through DNA methylation is the key to maintaining the differentiated state of human embryonic stem cells (hESCs), and it must be reset during differentiation by retinoic acid (RA) treatment. A genome-wide methylation/gene expression assay was performed in order to identify epigenetic modifications of RA-treated hESCs. Between undifferentiated and RA-treated hESCs, 166 differentially methylated CpG sites and 2,013 differentially expressed genes were discovered. Combined analysis of methylation and expression data revealed that 19 genes (STAP2, VAMP8, C10orf26, WFIKKN1, ELF3, C1QTNF6, C10orf10, MRGPRF, ARSE, LSAMP, CENTD3, LDB2, POU5F1, GSPT2, THY1, ZNF574, MSX1, SCMH1, and RARB) were highly correlated with each other. The results provided in this study will facilitate future investigations into the interplay between DNA methylation and gene expression through further functional and biological studies.
机译:通过DNA甲基化对基因组进行表观遗传修饰是维持人类胚胎干细胞(hESCs)分化状态的关键,并且在分化过程中必须通过视黄酸(RA)处理将其重置。为了鉴定RA处理的hESC的表观遗传修饰,进行了全基因组甲基化/基因表达测定。在未分化和RA处理的hESC之间,发现了166个差异甲基化的CpG位点和2,013个差异表达的基因。甲基化和表达数据的组合分析显示19个基因(STAP2,VAMP8,C10orf26,WFIKKN1,ELF3,C1QTNF6,C10orf10,MRGPRF,ARSE,LSAMP,CENTD3,LDB2,POU5F1,GSPT2,THY1,ZNF574,MSXRB1,SCMH1 )彼此高度相关。通过进一步的功能和生物学研究,本研究提供的结果将有助于将来对DNA甲基化与基因表达之间相互作用的研究。

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