Rouvière P E, De Las Peñas A, Mecsas J, Lu C Z, Rudd K E, Gross C A
Department of Stomatology, University of California-San Francisco 94143-0512.
EMBO J. 1995 Mar 1;14(5):1032-42. doi: 10.1002/j.1460-2075.1995.tb07084.x.
In Escherichia coli, the heat shock response is under the control of two alternative sigma factors: sigma 32 and sigma E. The sigma 32-regulated response is well understood, whereas little is known about that of sigma E, except that it responds to extracytoplasmic immature outer membrane proteins. To further understand this response, we located the rpoE gene at 55.5' and analyzed the role of sigma E. sigma E is required at high temperature, and controls the transcription of at least 10 genes. Some of these might contribute to the integrity of the cell since delta rpoE cells are more sensitive to SDS plus EDTA and crystal violet. sigma E controls its own transcription from a sigma E-dependent promoter, indicating that rpoE transcription plays a role in the regulation of E sigma E activity. Indeed, under steady-state conditions, the transcription from this promoter mirrors the levels of E sigma E activity in the cell. However, it is unlikely that the rapid increase in E sigma E activity following induction can be accounted for solely by increased transcription of rpoE. Based upon homology arguments, we suggest that a gene encoding a negative regulator of sigma E activity is located immediately downstream of rpoE and may function as the target of the E sigma E inducing signal.
在大肠杆菌中,热休克反应受两种交替的σ因子控制:σ32和σE。σ32调控的反应已得到充分理解,而对于σE调控的反应却知之甚少,只知道它对胞质外未成熟的外膜蛋白有反应。为了进一步了解这种反应,我们将rpoE基因定位在55.5'处并分析了σE的作用。σE在高温下是必需的,并且控制至少10个基因的转录。其中一些基因可能有助于细胞的完整性,因为缺失rpoE的细胞对SDS加EDTA和结晶紫更敏感。σE从一个依赖于σE的启动子控制自身的转录,这表明rpoE转录在σE活性的调控中起作用。实际上,在稳态条件下,该启动子的转录反映了细胞中σE活性的水平。然而,诱导后σE活性的快速增加不太可能仅仅由rpoE转录的增加来解释。基于同源性论证,我们认为编码σE活性负调节因子的基因位于rpoE的紧邻下游,并且可能作为σE诱导信号的靶标发挥作用。