Gray J, Wang J, Gelvin S B
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907-1392.
J Bacteriol. 1992 Feb;174(4):1086-98. doi: 10.1128/jb.174.4.1086-1098.1992.
vir regulon expression in Agrobacterium tumefaciens involves both chromosome- and Ti-plasmid-encoded gene products. We have isolated and characterized a new chromosomal gene that when mutated results in a 2- to 10-fold reduction in the induced expression of vir genes by acetosyringone. This reduced expression occurs in AB minimal medium (pH 5.5) containing either sucrose or glucose and containing phosphate at high or low concentrations. The locus was cloned and used to complement A. tumefaciens strains harboring Tn5 insertions in the gene. Sequence analysis of this locus revealed an open reading frame with strong homology to the miaA locus of Escherichia coli and the mod5 locus of Saccharomyces cerevisiae. These genes encode tRNA: isopentenyltransferase enzymes responsible for the specific modification of the A-37 residue in UNN codon tRNA species. The function of the homologous gene in A. tumefaciens was proven by genetic complementation of E. coli miaA mutant strains. tRNA undermodification in A. tumefaciens miaA mutant strains may reduce vir gene expression by causing a reduced translation efficiency. A slight reduction in the virulence of these mutant Agrobacterium strains on red potato plants, but not on tobacco, tomato, kalanchoe, or sunflower plants, was observed.
根癌土壤杆菌中的vir调控子表达涉及染色体和Ti质粒编码的基因产物。我们分离并鉴定了一个新的染色体基因,该基因发生突变时,乙酰丁香酮诱导的vir基因表达会降低2至10倍。这种表达降低发生在含有蔗糖或葡萄糖且磷酸盐浓度高或低的AB基本培养基(pH 5.5)中。该基因座被克隆并用于互补在该基因中含有Tn5插入的根癌土壤杆菌菌株。对该基因座的序列分析揭示了一个开放阅读框,与大肠杆菌的miaA基因座和酿酒酵母的mod5基因座具有高度同源性。这些基因编码tRNA异戊烯基转移酶,负责对UNN密码子tRNA物种中的A - 37残基进行特异性修饰。通过对大肠杆菌miaA突变菌株的遗传互补证明了根癌土壤杆菌中同源基因的功能。根癌土壤杆菌miaA突变菌株中的tRNA修饰不足可能通过导致翻译效率降低来减少vir基因表达。观察到这些突变的土壤杆菌菌株对红马铃薯植株(但对烟草、番茄、长寿花或向日葵植株没有)的毒力略有降低。