Huo Yi-Xin, Rosenthal Adam Z, Gralla Jay D
Department of Chemistry and Biochemistry and the Molecular Biology Institute, University of California, PO Box 951569, Los Angeles, CA 90095, USA.
Mol Microbiol. 2008 Oct;70(2):369-78. doi: 10.1111/j.1365-2958.2008.06412.x. Epub 2008 Aug 22.
Escherichia coli responds to stress by a combination of specific and general transcription signalling pathways. The general pathways typically require the master stress regulator sigma38 (rpoS). Here we show that the signalling from multiple stresses that relax DNA is processed by a non-conserved eight-amino-acid tail of the sigma 38 C-terminal domain. By contrast, responses to two stresses that accumulate potassium glutamate do not rely on this short tail, but still require the overall C-terminal domain. In vitro transcription and footprinting studies suggest that multiple stresses can target a poised RNA polymerase and activate it by unwrapping DNA from a nucleosome-like state, allowing the RNA polymerase to escape into productive mode. This transition can be accomplished by either the DNA relaxation or potassium glutamate accumulation that characterizes many stresses.
大肠杆菌通过特定和一般转录信号通路的组合来应对压力。一般通路通常需要主要的压力调节因子sigma38(rpoS)。在这里,我们表明,来自多种使DNA松弛的压力的信号是由sigma 38 C末端结构域的一个非保守的八氨基酸尾巴处理的。相比之下,对两种积累谷氨酸钾的压力的反应不依赖于这个短尾巴,但仍然需要整个C末端结构域。体外转录和足迹研究表明,多种压力可以靶向一个准备就绪的RNA聚合酶,并通过将DNA从核小体样状态解开而激活它,使RNA聚合酶进入生产模式。这种转变可以通过许多压力所特有的DNA松弛或谷氨酸钾积累来实现。