Grob P, Kahn D, Guiney D G
Department of Medicine, School of Medicine, University of California at San Diego, La Jolla 92093-0640, USA.
J Bacteriol. 1997 Sep;179(17):5398-406. doi: 10.1128/jb.179.17.5398-5406.1997.
The virulence plasmid-encoded spv regulon is essential for virulence of Salmonella dublin in mice. The spvR gene product belongs to the LysR family of transcriptional regulator proteins. SpvR induces the expression of the spvABCD operon and positively regulates its own expression. DNase I protection analysis with purified SpvR fusion proteins identified SpvR binding sites within the spvA and spvR promoters (P. Grob and D. G. Guiney, J. Bacteriol. 178:1813-1820, 1996). We have used PCR mutagenesis, combined with functional selection for reduced SpvR affinity, to define the DNA elements essential for SpvR binding. For the spvR promoter fragment, a screen for reduced expression was also applied. Sequence analysis of the resulting mutant fragments reveals that the base pair changes are clustered in distinct regions. Determination of the apparent dissociation constants of SpvR for the mutant promoters showed that the spvA LysR-type motif and the upstream palindromic sequences of both promoters play an important role in SpvR recognition.
毒力质粒编码的spv调控子对都柏林沙门氏菌在小鼠中的毒力至关重要。spvR基因产物属于转录调节蛋白的LysR家族。SpvR诱导spvABCD操纵子的表达并正向调节其自身表达。用纯化的SpvR融合蛋白进行的DNase I保护分析确定了spvA和spvR启动子内的SpvR结合位点(P. Grob和D. G. Guiney,《细菌学杂志》178:1813 - 1820,1996)。我们使用PCR诱变,结合对降低SpvR亲和力的功能筛选,来确定SpvR结合所必需的DNA元件。对于spvR启动子片段,还应用了降低表达的筛选。对所得突变片段的序列分析表明,碱基对变化聚集在不同区域。测定SpvR对突变启动子的表观解离常数表明,spvA LysR型基序和两个启动子的上游回文序列在SpvR识别中起重要作用。