Zuber U, Schumann W
Lehrstuhl für Genetik, Universität Bayreuth, Germany.
J Bacteriol. 1994 Mar;176(5):1359-63. doi: 10.1128/jb.176.5.1359-1363.1994.
The dnaK and groESL operons of Bacillus subtilis are preceded by a potential sigma 43 promoter sequence (recognized by the vegetative sigma factor) and by an inverted repeat (IR) consisting of 9 bp separated by a 9-bp spacer. Since this IR has been found in many bacterial species, we suspected that it might be involved in heat shock regulation. In order to test this hypothesis, three different mutational alterations of three bases were introduced within the IR preceding the dnaK operon. These mutations were crossed into the chromosome of B. subtilis, and expression of the dnaK and of the unlinked groESL operons was studied. The dnaK operon exhibited increased expression at low temperature and a reduction in the stimulation after temperature upshift. Furthermore, these mutations reduced expression of the groESL operon at low temperature by 50% but did not interfere with stimulation after heat shock. These experiments show that the IR acts as a negative cis element of the dnaK operon. This conclusion was strengthened by the observation that the IR reduced expression of two different transcriptional fusions significantly after its insertion between the promoter and the reporter gene. Since this IR has been described in many bacterial species as preceding only genes of the dnaK and groESL operons, both encoding molecular chaperones (39 cases are documented so far), we designated this heat shock element CIRCE (controlling IR of chaperone expression). Furthermore, we suggest that this novel mechanism is more widespread among eubacteria than the regulation mechanism described for Escherichia coli and has a more ancient origin.
枯草芽孢杆菌的dnaK和groESL操纵子之前有一个潜在的σ43启动子序列(由营养型σ因子识别),还有一个由9个碱基对组成的反向重复序列(IR),中间间隔9个碱基对的间隔序列。由于在许多细菌物种中都发现了这种IR,我们怀疑它可能参与热休克调节。为了验证这一假设,我们在dnaK操纵子之前的IR内引入了三种不同的三个碱基的突变。这些突变被导入枯草芽孢杆菌的染色体中,并研究了dnaK和不连锁的groESL操纵子的表达。dnaK操纵子在低温下表达增加,温度上调后的刺激作用减弱。此外,这些突变使groESL操纵子在低温下的表达降低了50%,但不影响热休克后的刺激作用。这些实验表明,IR作为dnaK操纵子的负性顺式元件。这一结论因以下观察结果而得到加强:在启动子和报告基因之间插入IR后,它显著降低了两种不同转录融合体的表达。由于这种IR在许多细菌物种中仅在dnaK和groESL操纵子的基因之前被描述,这两个操纵子都编码分子伴侣(目前已记录39例),我们将这种热休克元件命名为CIRCE(控制伴侣蛋白表达的IR)。此外,我们认为这种新机制在真细菌中比大肠杆菌中描述的调节机制更为普遍,并且起源更为古老。