Yagi Y, Clewell D B
J Bacteriol. 1977 Jan;129(1):400-6. doi: 10.1128/jb.129.1.400-406.1977.
Streptococcus faecalis DT-11 harbors the 6.0-megadalton plasmid pAMalpha1, which determines resistance to tetracycline (TC). When this strain is grown in the presence of TC for a number of generations, a reversible gene amplification occurs, generating tandem repeats of a 2.65-megadalton segment of the plasmid. On the basis of heteroduplex studies between various forms of pAMalpha1 and fragments generated by the Escherichia coli restriction endonuclease EcoRI, we have obtained direct evidence for the presence of a small sequence designated RS1 (for recombination sequence) located on both sides of the TC resistance determinant. Corresponding points on the two sequences are separated by 2.65 megadaltons of deoxyribonucleic acid. The two RS1 sequences have the same polarity and are of a size corresponding to about 380 nucleotide base pairs. The data presented serve as strong support for amplification models that are based on recombinational events involving the RS1 sequences.
粪肠球菌DT - 11携带6.0兆道尔顿的质粒pAMalpha1,该质粒决定了对四环素(TC)的抗性。当此菌株在四环素存在的情况下传代培养数代时,会发生可逆的基因扩增,产生该质粒2.65兆道尔顿片段的串联重复序列。基于不同形式的pAMalpha1与大肠杆菌限制性内切酶EcoRI产生的片段之间的异源双链研究,我们获得了直接证据,证明在四环素抗性决定簇两侧存在一个名为RS1(重组序列)的小序列。这两个序列上的对应点被2.65兆道尔顿的脱氧核糖核酸隔开。这两个RS1序列具有相同的极性,大小约对应于380个核苷酸碱基对。所呈现的数据有力支持了基于涉及RS1序列的重组事件的扩增模型。