Landick R, Yanofsky C
J Biol Chem. 1984 Sep 25;259(18):11550-5.
Transcription of the tryptophan (trp) operon of Escherichia coli and other bacterial species is regulated by the formation of alternative secondary structures in the leader segment of the transcript. During in vitro transcription of the trp leader region RNA polymerase pauses at base pair 92 after synthesis of an RNA hairpin secondary structure. We studied the dependence of pausing on hairpin stability by examining mutant trp templates containing base pair substitutions in the region corresponding to the hairpin secondary structure. Base changes that lower the stability of the hairpin were found to reduce both the frequency and half-life of RNA polymerase pausing while base changes that do not affect hairpin stability had little effect on pausing. Pausing was enhanced by the nusA protein; this enhancement was greatly reduced on mutant templates specifying less stable hairpins. The frequency of pausing on some mutant templates was correlated with the extent of read-through transcription beyond the trp attenuator, suggesting a possible role for pausing in the coupling of transcription and translation during transcription of the leader region of the operon.
大肠杆菌及其他细菌物种的色氨酸(trp)操纵子的转录,受转录本前导序列中交替二级结构形成的调控。在trp前导区的体外转录过程中,RNA聚合酶在合成RNA发夹二级结构后于碱基对92处暂停。我们通过检查在与发夹二级结构对应的区域含有碱基对替换的突变trp模板,研究了暂停对发夹稳定性的依赖性。发现降低发夹稳定性的碱基变化会降低RNA聚合酶暂停的频率和半衰期,而不影响发夹稳定性的碱基变化对暂停影响很小。nusA蛋白增强了暂停;在指定较不稳定发夹的突变模板上,这种增强作用大大降低。在一些突变模板上的暂停频率与trp衰减子之外通读转录的程度相关,这表明在操纵子前导区转录过程中,暂停在转录与翻译偶联中可能发挥作用。