Farewell A, Kvint K, Nyström T
Department of Microbiology, Lund University, Sweden.
Mol Microbiol. 1998 Aug;29(4):1039-51. doi: 10.1046/j.1365-2958.1998.00990.x.
A mutation in the Escherichia coli gene encoding the stationary phase-inducible sigma factor (sigmaS, RpoS) not only abolishes transcription of some genes in stationary phase, but also causes superinduction of other stationary phase-induced genes. We have examined this phenomenon of repression by sigmaS using as a model system the divergently transcribed stationary phase-inducible genes, uspA and uspB. uspA is transcribed by sigma70-programmed RNA polymerase and is superinduced in an rpoS mutant, while uspB induction is sigmaS dependent. The data suggest that the superinduction of uspA is caused by an increased amount of sigma70 bound to RNA polymerase in the absence of the competing sigmaS. Increasing the ability of sigma70 to compete against sigmaS by overproducing sigma70 mimics the effect of an rpoS mutation by causing superinduction of sigma70-dependent stationary phase-inducible genes (uspA and fadD), silencing of sigmaS-dependent genes (uspB, bolAp1 and fadL) and inhibiting the development of sigmaS-dependent phenotypes, such as hydrogen peroxide resistance in stationary phase. In addition, overproduction of sigmaS markedly reduced stationary phase expression of a sigma70-dependent promoter. Thus, we conclude that sigma factors compete for a limiting amount of RNA polymerase during stationary phase. The implications of this competition in the passive control of promoter activity is discussed.
编码稳定期诱导型σ因子(σS,RpoS)的大肠杆菌基因发生突变,不仅会消除稳定期某些基因的转录,还会导致其他稳定期诱导基因的超诱导。我们以反向转录的稳定期诱导基因uspA和uspB作为模型系统,研究了σS的这种抑制现象。uspA由σ70编程的RNA聚合酶转录,并在rpoS突变体中被超诱导,而uspB的诱导则依赖于σS。数据表明,uspA的超诱导是由于在没有竞争性σS的情况下,与RNA聚合酶结合的σ70数量增加所致。通过过量表达σ70来提高σ70与σS竞争的能力,会模拟rpoS突变的效果,导致σ70依赖的稳定期诱导基因(uspA和fadD)超诱导、σS依赖基因(uspB、bolAp1和fadL)沉默,并抑制σS依赖表型的发展,如稳定期的过氧化氢抗性。此外,过量表达σS会显著降低σ70依赖启动子的稳定期表达。因此,我们得出结论,在稳定期,σ因子会竞争有限量的RNA聚合酶。本文讨论了这种竞争在启动子活性被动控制中的意义。