Sha Y, Lindahl L, Zengel J M
Department of Biology, University of Rochester, New York 14627.
J Mol Biol. 1995 Feb 3;245(5):486-98. doi: 10.1006/jmbi.1994.0040.
We have probed regions of the S10 leader RNA to determine their role in L4-mediated, NusA-dependent attenuation control of the S10 ribosomal protein operon. Using genetic and "antisense" oligonucleotide competition approaches, we were able to distinguish between the determinants necessary for intrinsic (NusA-independent) pausing by RNA polymerase at the S10 attenuation site, for NusA-dependent enhancement of pausing, and for L4 stabilization of the paused ternary complex. The upper stem-loop structure in the attenuator hairpin is the major determinant for the NusA-dependent pause, while the sequence at the site of pausing is important for RNA polymerase to pause in the absence of NusA. The determinants for L4 stabilization of the paused complex include the hairpin immediately upstream of the attenuator hairpin as well as the ascending side of the attenuator structure. In conclusion, our results suggest that there are three distinct pausing activities by RNA polymerase during its transcription of the S10 leader, with three corresponding signals in the S10 leader.
我们对S10前导RNA的区域进行了探究,以确定它们在L4介导的、NusA依赖的S10核糖体蛋白操纵子衰减控制中的作用。通过遗传和“反义”寡核苷酸竞争方法,我们能够区分RNA聚合酶在S10衰减位点进行内在(不依赖NusA)暂停、NusA依赖的暂停增强以及暂停三元复合物的L4稳定所必需的决定因素。衰减子发夹结构中的上部茎环结构是NusA依赖暂停的主要决定因素,而暂停位点的序列对于RNA聚合酶在没有NusA时的暂停很重要。暂停复合物的L4稳定决定因素包括衰减子发夹结构上游紧邻的发夹以及衰减子结构的上升侧。总之,我们的结果表明,RNA聚合酶在转录S10前导序列时存在三种不同的暂停活性,在S10前导序列中有三个相应的信号。