Murphy E, Novick R P
Mol Gen Genet. 1979 Aug;175(1):19-30. doi: 10.1007/BF00267851.
The staphylococcal penicillinase plasmid pI524 and a series of derivatives have been extensively mapped by restriction endonuclease digestion and by heteroduplex analysis. We report here the identification of a 2.2 kb region that undergoes a reversible, rec-independent inversion. This sequence is bounded by a pair of inverted repeats 650 base pairs in length, and has asymmetrically located recognition sites for at least three restriction endonucleases. A series of deleted derivatives and one naturally occurring, closely related plasmid, were studied. Two of these retain the inversion; the remainder are incapable of inverting and were all found to be locked in the same orientation of the inversion. The invertible sequence is adjacent to the region of the plasmid encoding beta-lactamase (bla); this entire region appears to be transposable and the inversion may be involved in the regulation of beta-lactamase expression or in translocation.
葡萄球菌青霉素酶质粒pI524及其一系列衍生物已通过限制性内切酶消化和异源双链分析进行了广泛的图谱绘制。我们在此报告鉴定出一个2.2 kb的区域,该区域会发生可逆的、不依赖RecA的倒位。该序列由一对长度为650个碱基对的反向重复序列界定,并且具有至少三种限制性内切酶的不对称定位识别位点。研究了一系列缺失衍生物和一个天然存在的、密切相关的质粒。其中两个保留了倒位;其余的则无法倒位,并且都被发现锁定在倒位的同一方向上。可倒位序列与质粒编码β-内酰胺酶(bla)的区域相邻;整个区域似乎是可转座的,并且倒位可能参与β-内酰胺酶表达的调控或转位过程。