Zengel J M, Lindahl L
Department of Biology, University of Rochester, NY 14627.
Proc Natl Acad Sci U S A. 1990 Apr;87(7):2675-9. doi: 10.1073/pnas.87.7.2675.
The 11-gene S10 ribosomal protein operon of Escherichia coli is under the autogenous control of L4, the product of the third gene of the operon. Ribosomal protein L4 inhibits both transcription and translation of the operon. Our in vivo studies indicated that L4 regulates transcription by causing premature termination within the untranslated S10 operon leader. We have now used an in vitro transcription system to study the effect of purified L4 on expression of the S10 operon. We find that the cell-free system reproduces the in vivo observations. Namely, in the absence of L4, most of the RNA polymerases read through the termination site in the S10 attenuator; the addition of L4 results in increased termination at this site. However, RNA polymerase does not terminate at the S10 attenuator, with or without L4, unless an additional factor, protein NusA, is added to the transcription reaction. These results suggest that the attenuator in the S10 operon is a NusA-dependent terminator whose efficiency is regulated by ribosomal protein L4.
大肠杆菌的11基因S10核糖体蛋白操纵子受该操纵子第三个基因产物L4的自体调控。核糖体蛋白L4抑制该操纵子的转录和翻译。我们的体内研究表明,L4通过在未翻译的S10操纵子前导区内导致提前终止来调节转录。我们现在使用体外转录系统来研究纯化的L4对S10操纵子表达的影响。我们发现无细胞系统重现了体内观察结果。也就是说,在没有L4的情况下,大多数RNA聚合酶通读S10弱化子中的终止位点;添加L4会导致该位点的终止增加。然而,无论有无L4,RNA聚合酶都不会在S10弱化子处终止,除非向转录反应中添加另一个因子,即蛋白NusA。这些结果表明,S10操纵子中的弱化子是一个依赖NusA的终止子,其效率受核糖体蛋白L4调控。