Boyes J, Bird A
Research Institute for Molecular Pathology, Vienna, Austria.
Cell. 1991 Mar 22;64(6):1123-34. doi: 10.1016/0092-8674(91)90267-3.
We have studied the mechanism by which DNA methylation inhibits transcription both in cell-free nuclear extracts and in the living cell. Repression of transcription in vitro for four different promoters was shown to be an indirect effect. The mediator of repression had properties indistinguishable from those of a methyl-CpG binding protein (MeCP-1) that has been previously identified. Use of differentially methylated promoters and methylated competitors in transient transfection assays suggested that indirect repression via MeCP-1 also occurs in the living cell. This was supported by the fact that MeCP-1-deficient cells showed much reduced repression of methylated genes.
我们已经研究了DNA甲基化在无细胞的核提取物和活细胞中抑制转录的机制。四种不同启动子的体外转录抑制被证明是一种间接效应。这种抑制的介导因子具有与先前鉴定的甲基化CpG结合蛋白(MeCP-1)无法区分的特性。在瞬时转染实验中使用差异甲基化启动子和甲基化竞争物表明,通过MeCP-1的间接抑制也发生在活细胞中。MeCP-1缺陷细胞中甲基化基因的抑制作用大大降低这一事实支持了这一点。