Cheng Y, Dylla S M, Turnbough C L
Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
J Bacteriol. 2001 Jan;183(1):221-8. doi: 10.1128/JB.183.1.221-228.2001.
In Escherichia coli, pyrimidine-mediated regulation of upp expression occurs by UTP-sensitive selection of alternative transcriptional start sites, which produces transcripts that differ in the ability to be elongated. The upp initially transcribed region contains the sequence GATTTTTTTTG (nontemplate strand). Initiation can occur at either the first or the second base in this sequence (designated G6 and A7, with numbering from the promoter -10 region). High intracellular UTP levels favor initiation at position A7; however, the resulting transcripts are subject to reiterative transcription (i.e., repetitive UMP addition) within the 8-bp T. A tract in the initially transcribed region and are aborted. In contrast, low intracellular UTP levels favor initiation at position G6, which results in transcripts that can, in part, avoid reiterative transcription and be elongated normally. In this study, we examined the regulatory requirement for the long T. A tract in the upp initially transcribed region. We constructed upp promoter mutations that shorten the T. A tract to 7, 6, 5, 4, 3, or 2 bp and examined the effects of these mutations on upp expression and regulation. The results indicate that pyrimidine-mediated regulation is gradually reduced as the T. A tract is shortened from 7 to 3 bp; at which point regulation ceases. This reduction in regulation is due to large-percentage increases in upp expression in cells grown under conditions of pyrimidine excess. Quantitation of cellular transcripts and in vitro transcription studies indicate that the observed effects of a shortened T. A tract on upp expression and regulation are due to increases in the fraction of both G6- and A7-initiated transcripts that avoid reiterative transcription and are elongated normally.
在大肠杆菌中,嘧啶介导的upp表达调控是通过对替代转录起始位点进行UTP敏感选择来实现的,这会产生在延伸能力上有所不同的转录本。upp最初转录区域包含序列GATTTTTTTTG(非模板链)。起始可发生在该序列的第一个或第二个碱基处(分别指定为G6和A7,从启动子-10区域开始编号)。细胞内高UTP水平有利于在A7位置起始;然而,所产生的转录本在最初转录区域的8碱基对T·A序列中会经历反复转录(即重复添加UMP)并终止。相反,细胞内低UTP水平有利于在G6位置起始,这会产生部分能够避免反复转录并正常延伸的转录本。在本研究中,我们研究了upp最初转录区域中长T·A序列的调控需求。我们构建了将T·A序列缩短至7、6、5、4、3或2碱基对的upp启动子突变体,并研究了这些突变对upp表达和调控产生的影响。结果表明,随着T·A序列从7碱基对缩短至3碱基对,嘧啶介导的调控逐渐减弱;此时调控停止。调控的这种减弱是由于在嘧啶过量条件下生长的细胞中upp表达大幅增加所致。细胞转录本的定量分析和体外转录研究表明,观察到的T·A序列缩短对upp表达和调控的影响是由于G6起始和A7起始的转录本中能够避免反复转录并正常延伸的部分增加所致。