Humayun Z, Kleid D, Ptashne M
Nucleic Acids Res. 1977;4(5):1595-607. doi: 10.1093/nar/4.5.1595.
DNA bearing lambda operator sequences was methylated by dimethyl sulfate (DMS) in the presence or absence of lambda repressor. Under the experimental conditions, DMS methylates only the purine residues. The presence of lambda repressor affects only the methylation of certain G residues in the operators. Repressor blocks the methylation of certain G's and enhances the methylation of other G's. Since the reactive ring-nitrogen of G lies in the major groove of double-stranded DNA, and the reactive ring-nitrogen of A lies in the minor groove, the above results imply that the repressor makes contacts in the major groove of the helix. The repressor effect on G-methylation is sharply confined to the three 17 base pair units within each lambda operator previously proposed as the repressor-binding sites.
携带λ操纵基因序列的DNA在有或没有λ阻遏物存在的情况下,用硫酸二甲酯(DMS)进行甲基化。在实验条件下,DMS只使嘌呤残基甲基化。λ阻遏物的存在只影响操纵基因中某些G残基的甲基化。阻遏物阻止某些G残基的甲基化,而增强其他G残基的甲基化。由于G的反应性环氮位于双链DNA的大沟中,而A的反应性环氮位于小沟中,上述结果表明阻遏物在螺旋的大沟中形成接触。阻遏物对G甲基化的影响严格局限于先前提出的作为阻遏物结合位点的每个λ操纵基因内的三个17碱基对单元。