Zühlsdorf M T, Wiedemann B
Institut für Pharmazeutische Mikrobiologie, University Bonn, Germany.
Antimicrob Agents Chemother. 1992 Sep;36(9):1915-21. doi: 10.1128/AAC.36.9.1915.
A total of 807 gram-negative clinical isolates were treated with five different probes: intragenic segments for the transposase gene tnpA; the resolvase gene tnpR; the modulator of the resolvase, tnpM; the integraselike factor gene tnpI; and a 20-mer oligonucleotide for the recombinational site of action for the integrase. A total of 8% of the isolates hybridized with all five Tn21-related probes, and another 11% represented transposons in which one or more of the tested genes were missing. This 11% included groups whose descriptions have been published as well as groups that have not yet been described. The not-yet-described groups include various deletion products and some precursor structures, as is predicted for the evolution of Tn21-like transposons. The integration system appears to be coupled with Tn21-like structures and yet independent from these structures, implying an independent evolution of this system from Tn21-like transposons. The structures were found with similar incidence levels in all species tested except Pseudomonas aeruginosa, for which a novel separate family of class II transposons has been described before.
共有807株革兰氏阴性临床分离株用五种不同的探针进行处理:转座酶基因tnpA的基因内片段;解离酶基因tnpR;解离酶调节剂tnpM;整合酶样因子基因tnpI;以及用于整合酶作用重组位点的20聚体寡核苷酸。共有8%的分离株与所有五种Tn21相关探针杂交,另有11%代表其中一个或多个测试基因缺失的转座子。这11%包括描述已发表的组以及尚未描述的组。尚未描述的组包括各种缺失产物和一些前体结构,正如对Tn21样转座子进化的预测。整合系统似乎与Tn21样结构相关,但又独立于这些结构,这意味着该系统与Tn21样转座子独立进化。除铜绿假单胞菌外,在所有测试物种中均发现了类似发生率的结构,此前已描述了铜绿假单胞菌的一个新的独立的II类转座子家族。