Altenbuchner J, Schmid K, Schmitt R
J Bacteriol. 1983 Jan;153(1):116-23. doi: 10.1128/jb.153.1.116-123.1983.
The genes encoding inducible tetracycline resistance in Tn1721 were located in a 2.1-kilobase portion of the transposon. Using deletions and insertions, we mapped and characterized two tet genes by their mutant phenotypes. Two tetracycline-inducible polypeptides synthesized in minicells were assigned to the tet genes. The polarity of the tet genes was determined by employing a deletion and a gene fusion which altered the carboxy termini of the polypeptides. The gene responsible for resistance (tetA) encompasses 1,250 base pairs and encodes a membrane-bound protein with an apparent molecular weight of 34,000. The second gene (tetR) encompasses at least 650 base pairs and encodes a soluble 26,000-dalton protein, identified by complementation analysis as the repressor. The two adjacent genes have opposite transcriptional polarity, suggesting that the sites controlling their expression are located in the intercistronic region between tetA and tetR.
Tn1721中编码可诱导性四环素抗性的基因位于转座子的一个2.1千碱基部分。利用缺失和插入技术,我们通过突变表型对两个tet基因进行了定位和表征。在小细胞中合成的两种四环素诱导多肽被定位到tet基因。通过采用改变多肽羧基末端的缺失和基因融合来确定tet基因的极性。负责抗性的基因(tetA)包含1250个碱基对,编码一种表观分子量为34000的膜结合蛋白。第二个基因(tetR)至少包含650个碱基对,编码一种可溶性的26000道尔顿蛋白,通过互补分析确定为阻遏物。这两个相邻基因具有相反的转录极性,表明控制它们表达的位点位于tetA和tetR之间的基因间区域。