Abe A, Kawahara K
Department of Bacteriology, Kitasato Institute, Tokyo, Japan.
FEMS Microbiol Lett. 1995 Jun 15;129(2-3):225-30. doi: 10.1111/j.1574-6968.1995.tb07584.x.
The transcript of the spvR gene on the virulence plasmid, pKDSC50, of Salmonella choleraesuis serovar Choleraesuis was detected for the first time by Northern blot analysis, and the transcriptional regulation of the spvR gene was investigated. The transcription of the spvR was negatively regulated by spvA and spvB, and enhanced at stationary phase under control of a sigma factor RpoS (sigma 38). The spvR transcript was 2.4 kilonucleotides in Salmonella cells, and deduced to encode SpvR and SpvA, suggesting that SpvA but not SpvB is the functioning repressor in spv operon. The promoter sequence analysis revealed that spvR was transcribed from a single promoter and the 5' end of the transcript was located at 18 bp upstream from the start codon of spvR. Sequential similarity between the promoter of spvR and other sigma 38-controlled genes was not found, but the consensus sequence was found in -10 to -35 region of spvR and spvA, which may correlate to our previous data indicating that both genes were positively regulated by the SpvR protein.
首次通过Northern印迹分析检测到猪霍乱沙门氏菌猪霍乱血清型毒力质粒pKDSC50上spvR基因的转录本,并对spvR基因的转录调控进行了研究。spvR的转录受到spvA和spvB的负调控,并在σ因子RpoS(σ38)的控制下在稳定期增强。在沙门氏菌细胞中,spvR转录本为2.4千核苷酸,推测其编码SpvR和SpvA,这表明SpvA而非SpvB是spv操纵子中的功能性阻遏物。启动子序列分析表明,spvR从单个启动子转录,转录本的5'端位于spvR起始密码子上游18 bp处。未发现spvR启动子与其他σ38控制基因之间的序列相似性,但在spvR和spvA的-10至-35区域发现了共有序列,这可能与我们之前的数据相关,即这两个基因均受SpvR蛋白的正调控。