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Retinoic acid dependent histone 3 demethylation of the clustered HOX genes during neural differentiation of human embryonic stem cells

机译:人胚干细胞神经分化过程中簇状HOX基因的视黄酸依赖性组蛋白3脱甲基

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摘要

Gene activation of HOX clusters is an early event in embryonic development. These genes are highly expressed and active in the vertebrate nervous system. Based on the presence of retinoic acid response elements (RAREs) in the regulatory region of many of the HOX genes, it is deduced that retinoic acid (RA) can influence epigenetic regulation and consequently the expression pattern of HOX during RA-induced differentiation of embryonic model systems. In this investigation, the expression level as well as the epigenetic regulation of several HOX genes of the 4 A-D clusters was analyzed in human embryonic stem cells, and also through their neural induction, in the presence and absence of RA. Expression analysis data significantly showed increased mRNA levels of all examined HOX genes in the presence of RA. Epigenetic analysis of the HOX gene regulatory regions also showed a significant decrease in methylation of histone H3K27 parallel to an absolute preferential incorporation of the demethylase UTX rather than JMJD3 in RA-induced neural differentiated cells. This finding clearly showed the functional role of UTX in epigenetic alteration of HOX clusters during RA-induced neural differentiation; the activity could not be detectable for the demethylase JMJD3 during this developmental process.
机译:HOX簇的基因激活是胚胎发育中的早期事件。这些基因在脊椎动物神经系统中高表达并活跃。基于许多HOX基因调控区域中的视黄酸反应元件(RARE)的存在,推断出视黄酸(RA)可以影响表观遗传调控,因此在RA诱导的胚胎分化过程中影响HOX的表达方式。模型系统。在这项研究中,分析了4种A-D簇中几个HOX基因的表达水平以及表观遗传调控,包括在人类存在的RA和不存在RA的情况下,在人类胚胎干细胞中以及通过它们的神经诱导。表达分析数据显着显示在RA存在下所有检查的HOX基因的mRNA水平增加。 HOX基因调控区的表观遗传学分析还显示,在RA诱导的神经分化细胞中,与脱甲基酶UTX而非JMJD3的绝对优先掺入平行,组蛋白H3K27的甲基化显着降低。这一发现清楚地表明了UTX在RA诱导的神经分化过程中HOX簇表观遗传改变中的功能作用。在此发育过程中,无法检测到脱甲基酶JMJD3的活性。

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