Kochanek S, Renz D, Doerfler W
Institut für Genetik, Universität zu Köln, Germany.
FEBS Lett. 1995 Feb 27;360(2):115-20. doi: 10.1016/0014-5793(95)00068-k.
In earlier work, we demonstrated that 5'-CG-3' methylation inhibits the transcriptional activity of human Alu elements associated with the alpha 1-globin and the angiogenin genes in a cell-free transcription system from HeLa nuclear extracts. These studies have been extended to different Alu sequences and to investigations on the mechanism involved in transcriptional silencing by methylation. By comparing the results of DNase I and dimethyl sulfate (DMS) in vitro footprinting on a consensus sequence in the RNA polymerase III promoter control B region between the unmethylated and the 5'-CG-3' methylated B box, evidence has been adduced for effects of 5'-CG-3' methylation on the interaction of specific nuclear proteins with DNA sequences in the B control region of the Alu elements. These results are consistent with the interpretation that the 5'-CG-3' methylation interferes with the binding of proteins that are essential for the function of the B control region in these RNA polymerase III-transcribed elements, and that promoter methylation thus inhibits transcription.
在早期的研究中,我们证明了5'-CG-3'甲基化在源自HeLa细胞核提取物的无细胞转录系统中,抑制了与α1-珠蛋白和血管生成素基因相关的人类Alu元件的转录活性。这些研究已扩展到不同的Alu序列,并对甲基化导致转录沉默的机制进行了研究。通过比较未甲基化和5'-CG-3'甲基化的B框之间RNA聚合酶III启动子控制B区域的共有序列上的DNase I和硫酸二甲酯(DMS)体外足迹分析结果,已获得证据表明5'-CG-3'甲基化对特定核蛋白与Alu元件B控制区域中DNA序列的相互作用有影响。这些结果与以下解释一致:5'-CG-3'甲基化干扰了这些RNA聚合酶III转录元件中B控制区域功能所必需的蛋白质的结合,因此启动子甲基化抑制了转录。