Heffron F, Bedinger P, Champoux J J, Falkow S
Proc Natl Acad Sci U S A. 1977 Feb;74(2):702-6. doi: 10.1073/pnas.74.2.702.
The structural gene for plasmid-mediated ampicillin resistance resides upon a 3.2 X 10(6) dalton transposable sequence (TnA) flanked by short inverted repeated sequences that accompany its insertion. TnA was transposed to pMB8, a 1.8 X 10(6) dalton derivative of the colicingenic plasmid ColE1. Random deletions were introduced in the resultant 5 X 10(6) dalton recombinant plasmid by a combination of nuclease treatments in vitro. From this set of deletions a subset was isolated that contained deletions affecting the transposition of TnA. The deletions were mapped by digestion with restriction nucleases and electron microscopic analysis of DNA hetero-duplexes and were found to include one of the inverted repeated sequences or lie in the central portion of TnA. Complementation experiments were attempted between these plasmids and another compatible plasmid carrying a deletion in TnA that abolished its ampicillin resistance. The results of the deletion data indicate that approximately 2 X 10(6) daltons of TnA is required for transposition; the complementation experiments suggest that the terminal inverted repetition and the central region of TnA play different essential roles in TnA transposition.
质粒介导的氨苄青霉素抗性结构基因位于一个3.2×10⁶道尔顿的转座序列(TnA)上,其两侧为伴随插入的短反向重复序列。TnA转座到了pMB8,即大肠杆菌素产生性质粒ColE1的一个1.8×10⁶道尔顿的衍生物上。通过体外核酸酶处理的组合,在所得的5×10⁶道尔顿重组质粒中引入了随机缺失。从这组缺失中分离出一个子集,其中包含影响TnA转座的缺失。通过用限制性核酸酶消化以及对DNA异源双链体进行电子显微镜分析来对缺失进行定位,发现其包括其中一个反向重复序列或位于TnA的中央部分。尝试在这些质粒与另一个携带TnA缺失且消除其氨苄青霉素抗性的相容质粒之间进行互补实验。缺失数据的结果表明转座需要大约2×10⁶道尔顿的TnA;互补实验表明TnA的末端反向重复序列和中央区域在TnA转座中发挥不同的重要作用。