Klock G, Hillen W
J Mol Biol. 1986 Jun 20;189(4):633-41. doi: 10.1016/0022-2836(86)90493-6.
The regulation of expression of the Tn1721-encoded tetracycline-resistance determinant is described at the molecular level. The transcriptional control element consists of overlapping divergent promoters, which are negatively regulated by two operators with nearly identical sequence. The mRNA for the regulatory gene tetR is translated without a ribosome-binding site. This result is confirmed by S1 nuclease mapping and RNA sequencing of the tetR mRNA. The start nucleotide for transcription of this mRNA is the adenosine residue of the sequence 5'-AUG. Determination of the N-terminal amino acid sequence of the purified Tet repressor proves that this AUG is the initiation codon for translation. The Tet repressor protein is further used to map the two tet operators by DNase I footprinting. Tight contacts of the protein to the N-7 positions of two guanosine residues in each operator are determined from methylation protection experiments with dimethylsulfate. The differential regulation and positive control of transcription of the tetR gene that is possible with this arrangement of promoters and operators is discussed.
在分子水平上描述了Tn1721编码的四环素抗性决定簇的表达调控。转录控制元件由重叠的反向启动子组成,其受到两个序列几乎相同的操纵子的负调控。调控基因tetR的mRNA在没有核糖体结合位点的情况下进行翻译。这一结果通过tetR mRNA的S1核酸酶图谱分析和RNA测序得到证实。该mRNA转录的起始核苷酸是序列5'-AUG中的腺苷残基。对纯化的Tet阻遏物的N端氨基酸序列的测定证明该AUG是翻译的起始密码子。Tet阻遏物蛋白进一步用于通过DNase I足迹法定位两个tet操纵子。通过硫酸二甲酯甲基化保护实验确定了该蛋白与每个操纵子中两个鸟苷残基的N-7位的紧密接触。讨论了这种启动子和操纵子的排列方式对tetR基因转录的差异调控和正调控。