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Epigenetic regulation in pluripotent stem cells: a key to breaking the epigenetic barrier

机译:多能干细胞中的表观遗传调控:打破表观遗传障碍的关键

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摘要

The differentiation and reprogramming of cells are accompanied by drastic changes in the epigenetic profiles of cells. Waddington's classical model clearly describes how differentiating cells acquire their cell identity as the developmental potential of an individual cell population declines towards the terminally differentiated state. The recent discovery of induced pluripotent stem cells as well as of somatic cell nuclear transfer provided evidence that the process of differentiation can be reversed. The identity of somatic cells is strictly protected by an epigenetic barrier, and these cells acquire pluripotency by breaking the epigenetic barrier by reprogramming factors such as Oct3/4, Sox2, Klf4, Myc and LIN28. This review covers the current understanding of the spatio-temporal regulation of epigenetics in pluripotent and differentiated cells, and discusses how cells determine their identity and overcome the epigenetic barrier during the reprogramming process.
机译:细胞的分化和重编程伴随着细胞表观遗传学谱的急剧变化。沃丁顿的经典模型清楚地描述了分化细胞如何获得其细胞身份,因为单个细胞群体的发育潜能朝着最终分化状态下降。诱导多能干细胞以及体细胞核转移的最新发现提供了分化过程可以逆转的证据。体细胞的身份受到表观遗传屏障的严格保护,这些细胞通过重新编程诸如Oct3 / 4,Sox2,Klf4,Myc和LIN28等因子来打破表观遗传屏障,从而获得了多能性。这篇综述涵盖了多能和分化细胞中表观遗传学的时空调控的当前理解,并讨论了细胞在重新编程过程中如何确定其身份并克服表观遗传障碍。

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