A component of the transcriptional repressor MeCP1 shares a motif with DNA methyltransferase and HRX proteins

被引:202
作者
Cross, SH
Meehan, RR
Nan, XS
Bird, A
机构
[1] Inst. of Cell and Molecular Biology, Edinburgh University, King's Building, Edinburgh EH9 3JR, Mayfieldd Road
基金
英国惠康基金;
关键词
D O I
10.1038/ng0797-256
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Methylation of cytosines within the sequence CpG is essential for mouse development and has been linked to transcriptional suppression in vertebrate systems. Methyl-CpG binding proteins (MeCPs) 1 and 2 bind preferentially to methylated DNA and can inhibit transcription. The gene for MeCP2 has been cloned and a methyl-CpG binding domain (MBD) within it has been defined. A search of DNA sequence databases with the MBD sequence identified a human cDNA with potential to encode an MBD-like region. Sequencing of the complete cDNA revealed that the open reading frame also encodes two cysteine-rich domains that are found in animal DNA methyltransferases (DNMTs) and in the mammalian HRX protein (also known as MLL and ALL-1)8. HRX is related to Drosophila trithorax9,10. The protein, known as Protein Containing MBD (PCM1), was expressed in bacteria and shown to bind specifically to methylated DNA. PCM1 also repressed transcription in vitro in a methylation- dependent manner. A polyclonal antibody raised against the protein was able to 'supershift' the native MeCP1 complex from HeLa cells, indicating that PCM1 is a component of mammalian MeCP1.
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页码:256 / 259
页数:4
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