Goeddel D V, Yansura D G, Caruthers M H
Proc Natl Acad Sci U S A. 1978 Aug;75(8):3578-82. doi: 10.1073/pnas.75.8.3578.
Nucleotide analogs were substituted for unmodified nucleotides at specific sites in the lac operator sequence by a combination of chemical and enzymatic procedures. The nitrocellulose filter assay was used to study the interactions of these modified operators with wild-type (SQ) and tight-binding (QX86) lac repressors. These studies implicate directly the 5 methyl of thymine and the 2 amino of guanine as important operator-repressor contact sites. Furthermore, when these findings are combined with published results from other laboratories, a model for the lac operator-lac repressor interaction can be derived. Two important postulates follow from this model. (i) The repressor interacts at specific and defined sites with the N7 of guanine, the 5 methyl of thymine, the 2 amino of guanine, and the central major groove of the operator. (ii) The repressor binds to one side of the operator.
通过化学和酶促方法相结合,在乳糖操纵基因序列的特定位点用核苷酸类似物取代未修饰的核苷酸。采用硝酸纤维素滤膜试验研究这些修饰的操纵基因与野生型(SQ)和紧密结合型(QX86)乳糖阻遏物之间的相互作用。这些研究直接表明胸腺嘧啶的5-甲基和鸟嘌呤的2-氨基是重要的操纵基因-阻遏物接触位点。此外,当这些发现与其他实验室发表的结果相结合时,可得出乳糖操纵基因-乳糖阻遏物相互作用的模型。该模型有两个重要假设。(i)阻遏物在特定且明确的位点与鸟嘌呤的N7、胸腺嘧啶的5-甲基、鸟嘌呤的2-氨基以及操纵基因的中央大沟相互作用。(ii)阻遏物与操纵基因的一侧结合。