Fisher E F, Caruthers M H
Nucleic Acids Res. 1979 Sep 25;7(2):401-16. doi: 10.1093/nar/7.2.401.
The functional significance of a lac operator constitutive mutation has been determined. The transition adenine-thymine to guanine-cytosine was shown to be a constitutive mutation simply because thymine contains the functionally important 5-methyl group whereas cytosine does not. The remainder of the base pair is of no consequence. The experimental approach was to synthesize various modified operators containing cytosine, 5-methyl-cytosine, and 5-bromocytosine. The synthetic operator containing a guanine-cytosine base pair displays an eightfold reduction in stability with lac repressor whereas the operator containing 5-methylcytosine binds repressor at least as tightly as does the wild type sequence. Results published previously have shown that a similar decrease in stability of the repressor-operator complex can be obtained simply by substituting uracil for thymine or by inverting the base pair to thymine-adenine. All these results taken together implicate the thymine 5-methyl as the only important functional group recognized by the lac repressor at this base pair. Further confirmation of this conclusion was obtained by substitution of 5-bromocytosine and 5-bromouracil at this base pair. Both altered the stability of the repressor-operator complex by about the same percent suggesting that the bromine atom was the important determinant of complex stability for 5-bromopyrimidine analogs.
已确定乳糖操纵子组成型突变的功能意义。腺嘌呤 - 胸腺嘧啶向鸟嘌呤 - 胞嘧啶的转变被证明是一种组成型突变,仅仅是因为胸腺嘧啶含有功能上重要的5 - 甲基基团,而胞嘧啶没有。碱基对的其余部分无关紧要。实验方法是合成各种含有胞嘧啶、5 - 甲基胞嘧啶和5 - 溴胞嘧啶的修饰操纵子。含有鸟嘌呤 - 胞嘧啶碱基对的合成操纵子与乳糖阻遏物结合时稳定性降低了八倍,而含有5 - 甲基胞嘧啶的操纵子与阻遏物的结合至少与野生型序列一样紧密。先前发表的结果表明,仅仅通过用尿嘧啶替代胸腺嘧啶或将碱基对颠倒为胸腺嘧啶 - 腺嘌呤,就可以使阻遏物 - 操纵子复合物的稳定性出现类似程度的降低。综合所有这些结果表明,胸腺嘧啶5 - 甲基是乳糖阻遏物在该碱基对处识别的唯一重要功能基团。通过在该碱基对处替代5 - 溴胞嘧啶和5 - 溴尿嘧啶,进一步证实了这一结论。二者对阻遏物 - 操纵子复合物稳定性的改变百分比大致相同,这表明溴原子是5 - 溴嘧啶类似物复合物稳定性的重要决定因素。