Chan C L, Landick R
Department of Biology, Washington University, St. Louis, MO 63130.
J Mol Biol. 1993 Sep 5;233(1):25-42. doi: 10.1006/jmbi.1993.1482.
A key feature of transcriptional attenuation in some amino acid biosynthetic operons is a transcriptional pause that occurs immediately after synthesis of the first leader transcript secondary structure. Both RNA secondary structure and downstream DNA sequence are important for pausing at these sites; however, the precise RNA structures involved and the relative contribution of other RNA and DNA bases to pausing are unknown. We studied the effects of base substitutions upstream from the his leader pause site (immediately prior to addition of G103) to determine how nucleic acid sequences and RNA structure contribute to pausing. By testing compensatory base substitutions, we found that pausing depended in part on an RNA secondary structure containing a five base-pair stem and eight nucleotide loop, which we call the his pause RNA hairpin. The his pause hairpin forms 11 nucleotides upstream from the paused transcript 3' end and thus corresponds to only the upper portion of the larger his A:B leader transcript secondary structure. Some base substitutions in the ten nucleotides between the pause hairpin and the 3' end of the transcript increased pausing, whereas others decreased pausing. However, compensatory substitutions that restored pairing of these bases in the lower portion of the A:B secondary structure did not alter these effects. Changing the 3'-terminal nucleotide of the transcript (U102) altered both the position and strength of pausing. Thus, in addition to the downstream DNA sequence, three distinct segments of nucleic acid upstream from the nucleotide-addition site in the transcription complex contribute to pausing in different ways: the pause RNA hairpin, the 3'-proximal region of transcript or DNA template, and the 3'-terminal nucleotide. We suggest that electrostatic interaction between the pause hairpin and RNA polymerase, rather than disruption of an RNA:DNA heteroduplex, delays elongation at the his leader pause site.
一些氨基酸生物合成操纵子中转录衰减的一个关键特征是转录暂停,它在第一个前导转录本二级结构合成后立即发生。RNA二级结构和下游DNA序列对于在这些位点的暂停都很重要;然而,所涉及的精确RNA结构以及其他RNA和DNA碱基对暂停的相对贡献尚不清楚。我们研究了组氨酸前导暂停位点上游(紧接在添加G103之前)碱基替换的影响,以确定核酸序列和RNA结构如何导致暂停。通过测试补偿性碱基替换,我们发现暂停部分取决于一种包含五个碱基对茎和八个核苷酸环的RNA二级结构,我们将其称为组氨酸暂停RNA发夹。组氨酸暂停发夹在暂停转录本3'端上游11个核苷酸处形成,因此仅对应于较大的组氨酸A:B前导转录本二级结构的上部。在暂停发夹和转录本3'端之间的十个核苷酸中的一些碱基替换增加了暂停,而其他替换则减少了暂停。然而,恢复A:B二级结构下部这些碱基配对的补偿性替换并没有改变这些影响。改变转录本的3'末端核苷酸(U102)改变了暂停的位置和强度。因此,除了下游DNA序列外,转录复合物中核苷酸添加位点上游的三个不同核酸片段以不同方式导致暂停:暂停RNA发夹、转录本或DNA模板的3'近端区域以及3'末端核苷酸。我们认为,暂停发夹与RNA聚合酶之间的静电相互作用,而不是RNA:DNA异源双链的破坏,延迟了组氨酸前导暂停位点处的延伸。