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活细胞内 DNA 甲基化和组蛋白修饰的可视化。

Visualization of DNA methylation and histone modifications in living cells.

机构信息

Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, Japan.

出版信息

Curr Opin Cell Biol. 2010 Jun;22(3):412-8. doi: 10.1016/j.ceb.2010.02.004. Epub 2010 Mar 6.

Abstract

DNA methylation and histone modifications play important roles in genome function, including epigenetic gene regulation. These modifications undergo drastic changes when nuclei are reprogrammed during development and differentiation. Recent studies have enabled the detection of the dynamics of modifications in living cultured cells and mouse preimplantation embryos. DNA methylation was visualized using the methyl-CpG-binding domain of the human MBD1 protein. The level and distribution of histone modifications can be monitored by two different methods. One approach uses fluorescence/Förster resonance energy transfer (FRET)-based sensors and another uses fluorescently labeled antigen binding fragments of specific antibodies. These visualization techniques will facilitate future studies on epigenetic regulation related to development, differentiation, and disease.

摘要

DNA 甲基化和组蛋白修饰在基因组功能中发挥重要作用,包括表观基因调控。这些修饰在发育和分化过程中细胞核重新编程时会发生剧烈变化。最近的研究使得能够在活的培养细胞和小鼠着床前胚胎中检测修饰的动态变化。使用人 MBD1 蛋白的甲基化 CpG 结合域来可视化 DNA 甲基化。可以通过两种不同的方法监测组蛋白修饰的水平和分布。一种方法使用基于荧光/荧光共振能量转移 (FRET)的传感器,另一种方法使用特异性抗体的荧光标记抗原结合片段。这些可视化技术将有助于未来研究与发育、分化和疾病相关的表观遗传调控。

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