Rowley K B, Elford R M, Roberts I, Holmes W M
Department of Microbiology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0678.
J Bacteriol. 1993 Mar;175(5):1309-15. doi: 10.1128/jb.175.5.1309-1315.1993.
Four Escherichia coli operons, the leuV operon which encodes tRNA(1Leu), the leuX operon which encodes tRNA(6Leu), the metT operon which encodes tRNA(3Leu), and the argT operon which encodes tRNA(1Leu), were examined for the stringent response induced by serine hydroxamate and for growth rate-dependent regulation. In nuclease protection assays, the leuV operon displayed the stringent response in response to leucine starvation, analog inhibition, and growth of a temperature-sensitive leucyl-tRNA synthetase mutant at nonpermissive temperatures. The leuV operon also exhibited the stringent response in multicopy plasmids. The promoters of all four leucyl operons were fused to the gene for beta-galactosidase and inserted into the chromosome by using bacteriophage lambda. All except the leuX promoter displayed growth rate-dependent regulation, consistent with the recent report that the concentration of tRNA(6Leu) actually decreases as growth rate increases. The leuV promoter fused to the beta-galactosidase gene showed a decrease in efficiency in the presence of extrachromosomal copies of rRNA genes. All chromosomal tRNA genes examined showed decreased transcriptional activity following a stringent response, but the leuX gene responded to a lesser extent (3-fold versus 10-fold or more) than the others. Primer extension analysis of this promoter showed little if any response to serine hydroxamate treatment, suggesting that multiple levels of control may exist or that promoter context effects are important in regulation.
对四个大肠杆菌操纵子进行了研究,它们分别是编码tRNA¹Leu的leuV操纵子、编码tRNA⁶Leu的leuX操纵子、编码tRNA³Leu的metT操纵子以及编码tRNA¹Leu的argT操纵子,检测其对丝氨酸羟肟酸诱导的严谨反应以及生长速率依赖性调控。在核酸酶保护分析中,leuV操纵子在亮氨酸饥饿、类似物抑制以及温度敏感型亮氨酰 - tRNA合成酶突变体在非允许温度下生长时表现出严谨反应。leuV操纵子在多拷贝质粒中也表现出严谨反应。将所有四个亮氨酰操纵子的启动子与β - 半乳糖苷酶基因融合,并通过噬菌体λ插入染色体。除leuX启动子外,其他启动子均表现出生长速率依赖性调控,这与最近的报道一致,即随着生长速率增加,tRNA⁶Leu的浓度实际上会降低。与β - 半乳糖苷酶基因融合的leuV启动子在存在染色体外rRNA基因拷贝时效率降低。所有检测的染色体tRNA基因在严谨反应后转录活性均降低,但leuX基因的反应程度小于其他基因(3倍与10倍或更多倍相比)。对该启动子的引物延伸分析显示,对丝氨酸羟肟酸处理几乎没有反应,这表明可能存在多个调控水平,或者启动子背景效应在调控中很重要。