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一类哺乳动物甲基化CpG结合蛋白家族的鉴定与特性分析。

Identification and characterization of a family of mammalian methyl-CpG binding proteins.

作者信息

Hendrich B, Bird A

机构信息

Institute of Cell and Molecular Biology, University of Edinburgh, Edinburgh EH9 3JR, Scotland.

出版信息

Mol Cell Biol. 1998 Nov;18(11):6538-47. doi: 10.1128/MCB.18.11.6538.

Abstract

Methylation at the DNA sequence 5'-CpG is required for mouse development. MeCP2 and MBD1 (formerly PCM1) are two known proteins that bind specifically to methylated DNA via a related amino acid motif and that can repress transcription. We describe here three novel human and mouse proteins (MBD2, MBD3, and MBD4) that contain the methyl-CpG binding domain. MBD2 and MBD4 bind specifically to methylated DNA in vitro. Expression of MBD2 and MBD4 tagged with green fluorescent protein in mouse cells shows that both proteins colocalize with foci of heavily methylated satellite DNA. Localization is disrupted in cells that have greatly reduced levels of CpG methylation. MBD3 does not bind methylated DNA in vivo or in vitro. MBD1, MBD2, MBD3, and MBD4 are expressed in somatic tissues, but MBD1 and MBD2 expression is reduced or absent in embryonic stem cells which are known to be deficient in MeCP1 activity. The data demonstrate that MBD2 and MBD4 bind specifically to methyl-CpG in vitro and in vivo and are therefore likely to be mediators of the biological consequences of the methylation signal.

摘要

DNA序列5'-CpG处的甲基化对小鼠发育至关重要。MeCP2和MBD1(以前称为PCM1)是两种已知的蛋白质,它们通过相关的氨基酸基序特异性结合甲基化DNA,并可抑制转录。我们在此描述了三种新的人类和小鼠蛋白质(MBD2、MBD3和MBD4),它们含有甲基-CpG结合结构域。MBD2和MBD4在体外特异性结合甲基化DNA。在小鼠细胞中表达绿色荧光蛋白标记的MBD2和MBD4表明,这两种蛋白质都与高度甲基化的卫星DNA位点共定位。在CpG甲基化水平大大降低的细胞中,定位被破坏。MBD3在体内或体外均不结合甲基化DNA。MBD1、MBD2、MBD3和MBD4在体细胞组织中表达,但在已知缺乏MeCP1活性的胚胎干细胞中,MBD1和MBD2的表达减少或缺失。数据表明,MBD2和MBD4在体外和体内均特异性结合甲基-CpG,因此可能是甲基化信号生物学后果的介导者。

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