Morgan B A, Hayward R S
Department of Molecular Biology, University of Edinburgh, Scotland.
Mol Gen Genet. 1987 Dec;210(2):358-63. doi: 10.1007/BF00325706.
The RNA polymerase subunits beta and beta' of Escherichia coli, encoded by the genes rpoB and rpoC, are co-transcribed with four 50 S ribosomal protein genes, rplKAJL. After treatment with the antibiotic rifampicin a partial uncoupling of rpoBC from rplKAJL transcription occurs. We have been investigating the role played in uncoupling by tL7, an 80% efficient terminator of transcription present in the 319 bp intercistronic space between rplL and rpoB, using S1 nuclease mapping of transcripts produced in vivo in normal (rpoBC haploid) strains. Our results show directly that rifampicin stimulates readthrough of tL7 on the chromosome by approximately twofold, an effect sufficient to explain the observed increase in beta beta' protein synthesis. We also provide preliminary evidence for the map position of PL7, and show that both this and P beta, two very weak promoters which might in principle be activated by rifampicin, are not in fact stimulated by the drug.
大肠杆菌的RNA聚合酶β和β'亚基由rpoB和rpoC基因编码,它们与四个50S核糖体蛋白基因rplKAJL共同转录。用抗生素利福平处理后,rpoBC与rplKAJL转录发生部分解偶联。我们一直在研究tL7在解偶联中所起的作用,tL7是位于rplL和rpoB之间319bp顺反子间空间的一种转录终止效率达80%的终止子,采用S1核酸酶图谱分析正常(rpoBC单倍体)菌株体内产生的转录本。我们的结果直接表明,利福平可使染色体上tL7的通读增加约两倍,这一效应足以解释所观察到的ββ'蛋白合成增加。我们还提供了tL7图谱位置的初步证据,并表明PL7和Pβ这两个原则上可能被利福平激活的非常弱的启动子,实际上并未受到该药物的刺激。