Kaplan A M, Akhverdian V Z, Reulets M A, Krylov V N
Genetika. 1988 Apr;24(4):634-40.
The possibility of using a model system (which included RP4::Mu plasmid and D3112 phage in Pseudomonas aeruginosa cells) for analysis of compatibility of transposable Escherichia coli phage Mu and P. aeruginosa phage D3112, as phages and transposons, was studied. No interaction was observed during the vegetative growth of phages. The majority of the hybrid RP4::Mu plasmids lost the Mu DNA after insertion of D3112 into RP4::Mu. The phenomenon was not a result of transposition immunity. We consider the loss of the Mu DNA as a consequence either of plasmid RP4::Mu instability in P. aeruginosa cells, because of the lack of functional Mu repressor, or of some D3112-encoded activity involved in its transposition. For the inambiguous conclusion on compatibility of two phages as transposons, it is necessary to modify the model system, eliminating the possibility of Mu phage replication--transposition.
研究了使用模型系统(该系统包括铜绿假单胞菌细胞中的RP4::Mu质粒和D3112噬菌体)来分析转座性大肠杆菌噬菌体Mu和铜绿假单胞菌噬菌体D3112作为噬菌体和转座子的兼容性。在噬菌体的营养生长过程中未观察到相互作用。在D3112插入RP4::Mu后,大多数杂交RP4::Mu质粒失去了Mu DNA。该现象不是转座免疫的结果。我们认为Mu DNA的丢失是由于在铜绿假单胞菌细胞中缺乏功能性Mu阻遏物导致质粒RP4::Mu不稳定,或者是由于D3112编码的某些参与其转座的活性所致。为了明确得出两种噬菌体作为转座子的兼容性结论,有必要修改模型系统,消除Mu噬菌体复制 - 转座的可能性。