Molloy P L, Watt F
CSIRO Division of Biotechnology, Laboratory for Molecular Biology, North Ryde, New South Wales, Australia.
Philos Trans R Soc Lond B Biol Sci. 1990 Jan 30;326(1235):267-75. doi: 10.1098/rstb.1990.0010.
The effect of site-specific CpG methylation on the binding of a HeLa cell transcription factor (MLTF) has been studied. Methylation at a central site within the binding sequence for the factor is found to strongly inhibit binding of MLTF and to inhibit MLTF-dependent transcription in vitro. Methylation of a CpG site only six bases away has no demonstrable effect on binding. When the central CpG is methylated on one strand only, binding of MLTF is partially inhibited. The effects of methylation on the binding of MLTF and on the binding of a limited number of other proteins to DNA demonstrate that methylation in some cases exerts highly specific effects on gene expression. Site-specific demethylation has previously been seen to be associated with the promoter and upstream regions of genes, which suggests that sequence-specific DNA binding proteins that interact with promoters may be involved in the demethylation process. Specific demethylation of a human metallothionein 2A promoter-chloramphenicol acetyl transferase gene construct in mouse L-cells demonstrates that the promoter region sequences of this gene are sufficient to programme their own demethylation.
研究了位点特异性CpG甲基化对HeLa细胞转录因子(MLTF)结合的影响。发现在该因子结合序列内的中央位点发生甲基化会强烈抑制MLTF的结合,并在体外抑制MLTF依赖性转录。仅六个碱基之外的一个CpG位点甲基化对结合没有明显影响。当中央CpG仅在一条链上甲基化时,MLTF的结合受到部分抑制。甲基化对MLTF结合以及有限数量的其他蛋白质与DNA结合的影响表明,甲基化在某些情况下对基因表达具有高度特异性的影响。此前已发现位点特异性去甲基化与基因的启动子和上游区域相关,这表明与启动子相互作用的序列特异性DNA结合蛋白可能参与去甲基化过程。小鼠L细胞中人金属硫蛋白2A启动子-氯霉素乙酰转移酶基因构建体的特异性去甲基化表明,该基因的启动子区域序列足以使其自身去甲基化。