Institute for Drug Research, Hebrew University of Jerusalem, Jerusalem, Israel.
INSERM U976, Paris, France.
Stem Cells. 2015 Aug;33(8):2374-80. doi: 10.1002/stem.2041. Epub 2015 May 26.
Recent studies suggest that the metabolic network is an important part of the molecular circuitry that underlies pluripotency. Of the metabolic pathways that were implicated in the pluripotency balance, "energy" metabolism is particularly notable. Its mechanism of action on pluripotency-regulating genes has been partially elucidated when three metabolites, namely acetate, S-adenosylmethionine, and O-linked β-N-acetylglucosamine were recently shown to link cytosolic signals to pluripotent gene expression. The cytosolic levels of these metabolites are the result of environmental perturbations, making them sensitive messengers, which are assumed to diffuse through the nuclear pores, being small molecules. Recent work also suggests that the modulation of the levels of these metabolites in pluripotent cells controls the balance between pluripotency and early commitment via epigenetic modifications. Here, we review recent studies that link metabolism and pluripotency via epigenetic modifications that occur through these three metabolites.
最近的研究表明,代谢网络是构成多能性的分子电路的重要组成部分。在与多能性平衡有关的代谢途径中,“能量”代谢尤为突出。当最近发现三种代谢物,即醋酸盐、S-腺苷甲硫氨酸和 O-链接β-N-乙酰葡萄糖胺,将细胞质信号与多能性调节基因联系起来时,其对多能性调节基因的作用机制就部分得到了解释。这些代谢物的细胞质水平是环境干扰的结果,使它们成为敏感的信使,这些信使被认为可以通过核孔扩散,作为小分子。最近的工作还表明,通过这些三种代谢物发生的表观遗传修饰来调节多能细胞中这些代谢物水平,可以控制多能性和早期分化之间的平衡。在这里,我们综述了最近的研究,这些研究通过这三种代谢物发生的表观遗传修饰将代谢和多能性联系起来。