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DNA甲基化决定了MeCP2的染色体定位。

DNA methylation specifies chromosomal localization of MeCP2.

作者信息

Nan X, Tate P, Li E, Bird A

机构信息

Institute of Cell and Molecular Biology, University of Edinburgh, United Kingdom.

出版信息

Mol Cell Biol. 1996 Jan;16(1):414-21. doi: 10.1128/MCB.16.1.414.

Abstract

MeCP2 is a chromosomal protein that is concentrated in the centromeric heterochromatin of mouse cells. In vitro, the protein binds preferentially to DNA containing a single symmetrically methylated CpG. To find out whether the heterochromatic localization of MeCP2 depended on DNA methylation, we transiently expressed MeCP2-LacZ fusion proteins in cultured cells. Intact protein was targeted to heterochromatin in wild-type cells but was inefficiently localized in mutant cells with low levels of genomic DNA methylation. Deletions within MeCP2 showed that localization to heterochromatin required the 85-amino-acid methyl-CpG binding domain but not the remainder of the protein. Thus MeCP2 is a methyl-CpG-binding protein in vivo and is likely to be a major mediator of downstream consequences of DNA methylation.

摘要

甲基化CpG结合蛋白2(MeCP2)是一种染色体蛋白,在小鼠细胞的着丝粒异染色质中富集。在体外,该蛋白优先结合含有单个对称甲基化CpG的DNA。为了确定MeCP2的异染色质定位是否依赖于DNA甲基化,我们在培养细胞中瞬时表达了MeCP2-LacZ融合蛋白。完整的蛋白在野生型细胞中靶向异染色质,但在基因组DNA甲基化水平低的突变细胞中定位效率低下。MeCP2内部的缺失表明,定位于异染色质需要85个氨基酸的甲基化CpG结合结构域,而不是蛋白的其余部分。因此,MeCP2在体内是一种甲基化CpG结合蛋白,可能是DNA甲基化下游效应的主要介导者。

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