Iarulin V R, Gorlenko Zh M
Mol Gen Mikrobiol Virusol. 1985 Oct(10):8-19.
Six mutations, impairing DNA polymerase of E. coli in combination with the wild type gene for rho factor or ts-mutation rho 15 have been studied in relation to the expression of seven operons having different types of regulation. The expression of genes for glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase is shown to be constitutive and resistant to mutationally altered RNA polymerase and rho factor. The expression of genes for adenine phosphoribosyltransferase and of deo operon is regulated by rho dependent attenuators with attenuation being lifted incomplete medium. Mutation rho 15 decreases the level of enzymes of thr and lac operons independent of mRNA levels of these operons. Mutation rho 15 effect on posttranscriptional level is modified by mutations damaging RNA polymerase. The data obtained suppose RNA polymerase to affect all stages of realization of genetic information, beginning with promoter recognition and RNA synthesis and including the protein synthesis on mRNA.
研究了六种与大肠杆菌DNA聚合酶相关的突变,这些突变与野生型rho因子基因或温度敏感型突变rho 15相结合,涉及到七个具有不同调控类型的操纵子的表达。已表明,葡萄糖-6-磷酸脱氢酶和6-磷酸葡萄糖酸脱氢酶基因的表达是组成型的,并且对突变改变的RNA聚合酶和rho因子具有抗性。腺嘌呤磷酸核糖转移酶基因和deo操纵子的表达受rho依赖性衰减子调控,在不完全培养基中衰减被解除。突变rho 15降低了苏氨酸和乳糖操纵子的酶水平,且与这些操纵子的mRNA水平无关。破坏RNA聚合酶的突变会改变突变rho 15对转录后水平的影响。所获得的数据表明,RNA聚合酶会影响遗传信息实现的所有阶段,从启动子识别和RNA合成开始,包括mRNA上的蛋白质合成。