首页> 外文期刊>Stem cell research >Unrestricted somatic stem cells (USSC) from human umbilical cord blood display uncommitted epigenetic signatures of the major stem cell pluripotency genes - ScienceDirect
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Unrestricted somatic stem cells (USSC) from human umbilical cord blood display uncommitted epigenetic signatures of the major stem cell pluripotency genes - ScienceDirect

机译:来自人类脐带血的无限制体细胞干细胞(USSC)显示出主要干细胞多能性基因的无定形的表观遗传学特征-ScienceDirect

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Unrestricted somatic stem cells (USSC) from human cord blood display a broad differentiation potential for ectodermal, mesodermal, and endodermal cell types. The molecular basis for these stem cell properties is unclear and unlike embryonic stem cells (ESC) none of the major stem cell factors OCT4, SOX2, and NANOG exhibits significant expression in USSC. Here, we report that these key stem cell genes hold an epigenetic state in between that of an ESC and a terminally differentiated cell type. DNA methylation analysis exhibits partial demethylation of the regulatory region of OCT4 and a demethylated state of the NANOG and SOX2 promoter/enhancer regions. Further genome-wide DNA methylation profiling identified a partially demethylated state of the telomerase gene hTERT. Moreover, none of the pluripotency factors exhibited a repressive histone signature. Notably, SOX2 exhibits a bivalent histone signature consisting of the opposing histone marks dimeH3K4 and trimeH3K27, which is typically found on genes that are "poised" for transcription. Consequently, ectopic expression of OCT4 in USSC led to rapid induction of expression of its known target gene SOX2. Our data suggest that incomplete epigenetic repression and a "poised" epigenetic status of pluripotency genes preserves the USSC potential to be able to react adequately to distinct differentiation and reprogramming cues.
机译:来自人脐带血的不受限制的体干细胞(USSC)对于外胚层,中胚层和内胚层细胞类型显示出广泛的分化潜力。这些干细胞特性的分子基础尚不清楚,与胚胎干细胞(ESC)不同,主要干细胞因子OCT4,SOX2和NANOG在USSC中均未显示出明显的表达。在这里,我们报告这些关键的干细胞基因在ESC和最终分化的细胞类型之间保持表观遗传状态。 DNA甲基化分析显示OCT4调节区的部分去甲基化,NANOG和SOX2启动子/增强子区的去甲基化状态。进一步的全基因组DNA甲基化分析鉴定了端粒酶基因hTERT的部分去甲基状态。此外,多能性因子均未显示出抑制性的组蛋白特征。值得注意的是,SOX2表现出由相对的组蛋白标记dimeH3K4和trimeH3K27组成的二价组蛋白签名,通常在“准备好进行转录的基因”上发现。因此,OCT4在USSC中的异位表达导致其已知靶基因SOX2表达的快速诱导。我们的数据表明,不完整的表观遗传抑制和多能性基因的“平衡”表观遗传状态保留了USSC的潜力,能够对不同的分化和重编程线索做出充分反应。

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