Bräu B, Piepersberg W
Mol Gen Genet. 1983;189(2):298-303. doi: 10.1007/BF00337820.
The structures of two R-plasmids pWP14a and pWP12a (Tra-, Ap, Gm; 21 kb) and of several cointegrates they form with bacteriophages P1Cm and P1-15 were analyzed. In each case, replicon fusion was mediated by the element IS140 (about 0.8 kb), one copy of which resides on both plasmids adjacent to the gentamicin resistance determinant (AAC(3)-III). pWP14a cointegrated preferentially into or near the invertible C-loop structure of the P1 genome. Cointegrational mobilization of pWP14a was observed also with several conjugative R-factors. The process of replicon fusion is independent of the host's rec+ functions. Sequences homologous to IS140 are constituents of many R-factors, including RA1, R40a, R124, R144, Rts1, N3, and pJR255. IS140 also shows homology to two other sequences, IS15 delta and Tn2680, but not to other, well studied transposable elements. The ampicillin resistance determinant of pWP14a is within a Tn3-like transposon, Tn3651.
分析了两种R质粒pWP14a和pWP12a(Tra-,Ap,Gm;21 kb)的结构以及它们与噬菌体P1Cm和P1-15形成的几种共合体的结构。在每种情况下,复制子融合由元件IS140(约0.8 kb)介导,其一个拷贝存在于与庆大霉素抗性决定簇(AAC(3)-III)相邻的两个质粒上。pWP14a优先共整合到P1基因组的可逆C环结构中或其附近。还观察到pWP14a与几种接合性R因子发生共整合动员。复制子融合过程独立于宿主的rec+功能。与IS140同源的序列是许多R因子的组成部分,包括RA1、R40a、R124、R144、Rts1、N3和pJR255。IS140还与另外两个序列IS15δ和Tn2680显示同源性,但与其他经过充分研究的转座元件没有同源性。pWP14a的氨苄青霉素抗性决定簇位于一个类Tn3转座子Tn3651内。