Fisher R F, Das A, Kolter R, Winkler M E, Yanofsky C
J Mol Biol. 1985 Apr 5;182(3):397-409. doi: 10.1016/0022-2836(85)90199-8.
RNA polymerase pausing during transcription of the tryptophan (trp) operon leader region is postulated to be the key event that synchronizes transcription of this region with translation of the coding region for the trp leader peptide. Coupling of transcription to translation enables the cell to monitor the intracellular concentration of charged tRNATrp and determine whether polymerase should terminate transcription at the attenuator or proceed into the structural genes of the operon. We used mutant templates containing deletions of DNA segments corresponding to sequences that are predicted to form alternative RNA secondary structures to show that formation of an RNA hairpin in the leader transcript, and the concentration of the next nucleoside triphosphate to be added to the paused transcript, both markedly affect the kinetics of pausing in vitro. A model is presented that accounts for many of the findings obtained in this and other pausing studies.
色氨酸(trp)操纵子前导区转录过程中RNA聚合酶的暂停被认为是使该区域转录与trp前导肽编码区翻译同步的关键事件。转录与翻译的偶联使细胞能够监测带电荷的tRNATrp的细胞内浓度,并确定聚合酶是应在弱化子处终止转录还是继续进入操纵子的结构基因。我们使用了含有对应于预测形成替代RNA二级结构的序列的DNA片段缺失的突变模板,以表明前导转录本中RNA发夹的形成以及要添加到暂停转录本中的下一个核苷三磷酸的浓度,都显著影响体外暂停的动力学。本文提出了一个模型,该模型解释了在本研究和其他暂停研究中获得的许多发现。