Lewandoski M, Dubnau E, Smith I
J Bacteriol. 1986 Nov;168(2):870-7. doi: 10.1128/jb.168.2.870-877.1986.
We have cloned the early sporulation gene spo0F, which encodes an open reading frame of 124 codons. The putative Spo0F protein derived from this open reading frame, which has been shown to share homology with the Spo0A protein as well as several other regulatory proteins from Escherichia coli, Salmonella typhimurium, and Klebsiella pneumoniae, also shares homology with the E. coli EcoRI methyltransferase. We have shown by S1 nuclease mapping of in vivo transcripts that spo0F is regulated from dual promoters: RNA II was transcribed from an upstream promoter, and RNA I was initated 30 base pairs downstream from RNA II. The promoter sequences for RNA II, but not those for RNA I, conformed to the -10 region consensus sequence for sigma 43 promoters. RNA II was found in low amounts in exponentially growing cells but was not observed in stationary-phase cells, and the presence of RNA II was glucose insensitive. RNA I was found in low amounts in exponentially growing cells, increased three- to fivefold at the end of exponential growth, and remained at this higher level for at least 3 h into stationary phase. RNA I was repressed by glucose during exponential growth but not during stationary phase.
我们已经克隆了早期芽孢形成基因spo0F,它编码一个由124个密码子组成的开放阅读框。从这个开放阅读框推导出来的假定Spo0F蛋白,已显示与Spo0A蛋白以及来自大肠杆菌、鼠伤寒沙门氏菌和肺炎克雷伯菌的其他几种调节蛋白具有同源性,它也与大肠杆菌EcoRI甲基转移酶具有同源性。我们通过对体内转录本进行S1核酸酶作图表明,spo0F受双重启动子调控:RNA II从上游启动子转录,RNA I在RNA II下游30个碱基对处起始。RNA II的启动子序列符合σ43启动子的-10区共有序列,而RNA I的启动子序列则不符合。在指数生长期细胞中发现RNA II的量很少,但在稳定期细胞中未观察到,并且RNA II的存在对葡萄糖不敏感。在指数生长期细胞中发现RNA I的量很少,在指数生长末期增加三到五倍,并在稳定期至少3小时内保持在这个较高水平。在指数生长期,RNA I受葡萄糖抑制,但在稳定期不受抑制。