Dmitriev A D, Danilevskaya O N, Khesin R B
Mol Gen Genet. 1976 Jun 15;145(3):317-26. doi: 10.1007/BF00325830.
The influence of mutations in structural genes of beta and beta subunits of RNA polymerase upon the synthesis of these subunits in E. coli cells have been investigated. An amber-mutation ts22 in the beta subunit gene decreases the intracellular concentration of this subunit and the rate of its synthesis. At the same time the concentration and the rate of beta subunit synthesis is increased. These suggest the compensatory activation of the RNA polymerase operon that takes place under the conditions of shortage of one of the subunits. Reversions as well as more effective suppression of ts22 amber mutation, achieved by streptomycin addition, substitution of su2 by sul, or by specific mutations, result in a rise of beta and drop of beta subunit concentration and synthesis in ts22 mutant. TsX missense-mutation in the beta subunit gene alters the properties of the enzyme increasing, at the same time, the concentration and the rate of synthesis of both beta and beta subunits, particularly at a nonpermissive temperature. This points to an inversely proportional relationship between the rate of synthesis of RNA polymerase subunits and the total intracellular activity of the enzyme. Extra subunits are rapidly degraded in ts22 and tsX mutants. The whole complex of our data and those of others suggest that the regulation of the synthesis of RNA polymerase subunits is accomplished by interaction of a negative and a positive mechanisms of regulation which include not only activators and repressors but the enzyme itself as well.
已对RNA聚合酶β亚基和β'亚基结构基因中的突变对大肠杆菌细胞中这些亚基合成的影响进行了研究。β亚基基因中的琥珀突变ts22降低了该亚基的细胞内浓度及其合成速率。与此同时,β'亚基的浓度和合成速率增加。这些表明在其中一个亚基短缺的条件下发生了RNA聚合酶操纵子的补偿性激活。通过添加链霉素、将su2替换为sul或通过特定突变实现的ts22琥珀突变的回复以及更有效的抑制,导致ts22突变体中β亚基浓度和合成增加,β'亚基浓度和合成下降。β'亚基基因中的TsX错义突变改变了酶的性质,同时增加了β亚基和β'亚基的浓度和合成速率,特别是在非允许温度下。这表明RNA聚合酶亚基的合成速率与酶的总细胞内活性之间存在反比关系。在ts22和tsX突变体中,额外的亚基会迅速降解。我们的数据以及其他数据的整体情况表明,RNA聚合酶亚基合成的调节是通过负调节和正调节机制的相互作用来完成的,这些机制不仅包括激活剂和阻遏物,还包括酶本身。