Piette J, Nyunoya H, Lusty C J, Cunin R, Weyens G, Crabeel M, Charlier D, Glansdorff N, Piérard A
Proc Natl Acad Sci U S A. 1984 Jul;81(13):4134-8. doi: 10.1073/pnas.81.13.4134.
The carAB operon of Escherichia coli K-12, which encodes the two subunits of carbamoyl-phosphate synthetase (glutamine hydrolyzing) [carbon-dioxide: L-glutamine amido-ligase (ADP-forming, carbamate-phosphorylating); EC 6.3.5.5], is cumulatively repressed by arginine and the pyrimidines. We describe the structure of the control region of carAB and the sequence of the carA gene. Nuclease S1 mapping experiments show that two adjacent tandem promoters within the carAB control region serve as initiation sites. The upstream promoter P1 is controlled by pyrimidines; the downstream promoter P2 is regulated by arginine. Attenuation control does not appear to be involved in the expression of carAB. A possible mechanism by which control at these promoters concurs to produce a cumulative pattern of repression is discussed. The translational start of carA is atypical; it consists of a UUG or AUU codon.
大肠杆菌K-12的carAB操纵子编码氨甲酰磷酸合成酶(谷氨酰胺水解)[二氧化碳:L-谷氨酰胺酰胺连接酶(ADP形成,氨基甲酰磷酸化);EC 6.3.5.5]的两个亚基,它受到精氨酸和嘧啶的累积性抑制。我们描述了carAB调控区的结构以及carA基因的序列。核酸酶S1作图实验表明,carAB调控区内两个相邻的串联启动子作为起始位点。上游启动子P1受嘧啶控制;下游启动子P2受精氨酸调节。衰减控制似乎不参与carAB的表达。本文讨论了这些启动子处的控制共同产生累积性抑制模式的一种可能机制。carA的翻译起始是非典型的;它由一个UUG或AUU密码子组成。