Schulz A, Tzschaschel B, Schumann W
Lehrstuhl für Genetik, Universität Bayreuth, Germany.
Mol Microbiol. 1995 Feb;15(3):421-9. doi: 10.1111/j.1365-2958.1995.tb02256.x.
Bacillus subtilis contains at least three classes of heat-shock genes regulated by different mechanisms. We are studying class I heat-shock genes encoded by the operons dnaK and groE. These two operons are both expressed from a vegetative promoter, and their regulation involves a novel heat-shock element designated CIRCE. Here we show that induction of both operons results from enhanced synthesis of mRNA and is independent of de novo protein synthesis. To answer the question of whether dnaK is involved in the deregulation of the heat-shock response as reported for Escherichia coli, two different insertion mutations were isolated within the tetracistronic dnaK operon (orf39-grpE-dnaK-dnaJ). In one mutant a cat cassette was inserted at the beginning of orf39. Transcriptional analysis revealed that this mutation abolished expression of the whole operon. In contrast, the basal level of groE mRNA was significantly increased at 37 degrees C, followed by a prolonged delay in the shut off after temperature upshift. These data point to a crucial role for the orf39 gene in the regulation of class I heat-shock genes. In the other mutant an internal 0.8 kb Bg/II fragment of dnaK was replaced by the cat cassette. In contrast to E. coli dnaK null mutants, the two B. subtilis dnaK operon mutants could grow within a temperature range from 16-52 degrees C. At temperatures above 52 degrees C, they failed to form colonies on agar plates, started to filament, and lost motility. Furthermore, the induction profile of the groE and dnaK operons was not impaired in the dnaK::cat mutant.(ABSTRACT TRUNCATED AT 250 WORDS)
枯草芽孢杆菌至少包含三类受不同机制调控的热休克基因。我们正在研究由操纵子dnaK和groE编码的I类热休克基因。这两个操纵子均从营养启动子表达,其调控涉及一种名为CIRCE的新型热休克元件。在此我们表明,这两个操纵子的诱导均源于mRNA合成的增强,且与从头蛋白质合成无关。为回答dnaK是否如大肠杆菌报道的那样参与热休克反应的去调控这一问题,在四顺反子dnaK操纵子(orf39-grpE-dnaK-dnaJ)内分离出了两种不同的插入突变。在一个突变体中,一个cat盒插入到orf39的起始处。转录分析表明,该突变消除了整个操纵子的表达。相反,groE mRNA的基础水平在37℃时显著增加,随后在温度升高后关闭延迟延长。这些数据表明orf39基因在I类热休克基因的调控中起关键作用。在另一个突变体中,dnaK的一个内部0.8 kb Bg/II片段被cat盒取代。与大肠杆菌dnaK缺失突变体不同,两个枯草芽孢杆菌dnaK操纵子突变体能够在16 - 52℃的温度范围内生长。在高于52℃时,它们无法在琼脂平板上形成菌落,开始形成丝状体并失去运动性。此外,groE和dnaK操纵子的诱导谱在dnaK::cat突变体中未受损。(摘要截短于250字)