首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Active tissue-specific DNA demethylation conferred by somatic cell nuclei in stable heterokaryons
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Active tissue-specific DNA demethylation conferred by somatic cell nuclei in stable heterokaryons

机译:稳定异核体中体细胞核赋予的活性组织特异性DNA去甲基化

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DNA methylation is among the most stable epigenetic marks, ensuring tissue-specific gene expression in a heritable manner throughout development. Here we report that differentiated me-sodermal somatic cells can confer tissue-specific changes in DNA methylation on epidermal progenitor cells after fusion in stable multinucleate heterokaryons. Myogenic factors alter regulatory regions of genes in keratinocyte cell nuclei, demethylating and activating a muscle-specific gene and methylating and silencing a keratinocyte-specific gene. Because these changes occur in the absence of DNA replication or cell division, they are mediated by an active mechanism. Thus, the capacity to transfer epigenetic changes to other nuclei is not limited to embryonic stem cells and oocytes but is also a property of highly specialized mammalian somatic cells. These results suggest the possibility of directing the reprogramming of readily available postnatal human progenitor cells toward specific tissue cell types.
机译:DNA甲基化是最稳定的表观遗传标记之一,可在整个发育过程中以可遗传的方式确保组织特异性基因的表达。在这里我们报告分化的中胚层体细胞可以在稳定的多核异核体中融合后赋予表皮祖细胞DNA甲基化的组织特异性变化。肌源性因子改变角质形成细胞细胞核中基因的调节区域,使肌肉特异性基因去甲基化和激活,并使角质形成细胞特异性基因甲基化和沉默。因为这些变化是在没有DNA复制或细胞分裂的情况下发生的,所以它们是由一种主动机制介导的。因此,将表观遗传学改变转移到其他核的能力不仅限于胚胎干细胞和卵母细胞,而且是高度专业化的哺乳动物体细胞的特性。这些结果表明可能将容易获得的出生后人类祖细胞重编程指向特定组织细胞类型。

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