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重叠的反向启动子控制Tn10四环素抗性的表达。

Overlapping divergent promoters control expression of Tn10 tetracycline resistance.

作者信息

Bertrand K P, Postle K, Wray L V, Reznikoff W S

出版信息

Gene. 1983 Aug;23(2):149-56. doi: 10.1016/0378-1119(83)90046-x.

Abstract

We have previously examined the genetic organization and regulation of the Tn10 tetracycline-resistance determinant in Escherichia coli K-12. The structural genes for tetA, the Tn10 tetracycline-resistance function, and for tetR, the Tn10 tet repressor, are transcribed in opposite directions from promoters in a regulatory region located between the two structural genes. Expression of both tetA and tetR is induced by tetracycline. Here we report the DNA sequence of the Tn10 tet regulatory region. The locations of the tetA and tetR promoters within this region were defined by S1 nuclease mapping of the 5' ends of in vivo tet RNA. The tetA and tetR promoters overlap; the transcription start points are separated by 36 bp. We propose that two similar regions of dyad symmetry within the Tn10 tet regulatory region are operator sites at which tet repressor binds to tet DNA, thereby inhibiting transcription initiation at the tetA and tetR promoters. The Tn10 tet regulatory region and the pBR322 tet regulatory region show significant DNA sequence homology (53%).

摘要

我们先前已研究了大肠杆菌K-12中Tn10四环素抗性决定子的遗传组织和调控。tetA(Tn10四环素抗性功能)和tetR(Tn10四环素阻遏物)的结构基因从位于两个结构基因之间的调控区域中的启动子以相反方向转录。tetA和tetR的表达均由四环素诱导。在此我们报道Tn10四环素调控区域的DNA序列。通过对体内tet RNA的5'端进行S1核酸酶作图确定了该区域内tetA和tetR启动子的位置。tetA和tetR启动子重叠;转录起始点相隔36 bp。我们提出,Tn10四环素调控区域内两个相似的二元对称区域是操纵位点,tet阻遏物与tet DNA结合于此,从而抑制tetA和tetR启动子处的转录起始。Tn10四环素调控区域与pBR322四环素调控区域显示出显著的DNA序列同源性(53%)。

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