Groenen M A, Kokke M, van de Putte P
EMBO J. 1986 Dec 20;5(13):3687-90. doi: 10.1002/j.1460-2075.1986.tb04700.x.
Transposition of mini-Mu containing only one of the ends of bacteriophage Mu was studied. Transposition was observed when plasmids containing this mini-Mu were used as the donor in a mating-out assay with the F factor POX38, which lacks all known transposable elements, as the target. Analysis of the plasmids isolated from the recipient strain showed that in most cases the mini-Mu containing plasmid and POX38 were fused and that a part of the plasmid had been duplicated, indicating the formation of co-integrates. To obtain the DNA sequences of the junctions between donor and recipient DNA, an F factor was constructed that made it possible to analyse these junctions directly. The results showed that several sequences can be used as an alternative end in transposition and that these alternative ends show homology with the consensus for a strong A binding site. Moreover, the first base pair at the junction was always a (TA) base pair. This base pair is situated at exactly the same position with respect to the sequence which has homology with the consensus for a strong A binding site as in the ends of Mu.
对仅包含噬菌体Mu一端的微型Mu的转座进行了研究。当含有这种微型Mu的质粒在与缺乏所有已知转座元件的F因子POX38进行交配外分析中用作供体时,观察到了转座现象。对从受体菌株中分离出的质粒的分析表明,在大多数情况下,含有微型Mu的质粒和POX38融合在一起,并且质粒的一部分发生了重复,这表明形成了共整合体。为了获得供体和受体DNA之间连接点的DNA序列,构建了一个F因子,使得能够直接分析这些连接点。结果表明,几个序列可以用作转座的替代末端,并且这些替代末端与强A结合位点的共有序列具有同源性。此外,连接点处的第一个碱基对总是一个(TA)碱基对。该碱基对相对于与强A结合位点的共有序列具有同源性的序列,与Mu末端的位置完全相同。