Morton T M, Eaton D M, Johnston J L, Archer G L
Department of Microbiology and Immunology, Medical College of Virginia/Virginia Commonwealth University, Richmond 23298-0049.
J Bacteriol. 1993 Jul;175(14):4436-47. doi: 10.1128/jb.175.14.4436-4447.1993.
The conjugative transfer genes of 52-kb staphylococcal R plasmid pGO1 were localized to a single BglII restriction fragment and cloned in Escherichia coli. Sequence analysis of the 13,612-base transfer region, designated trs, identified 14 intact open reading frames (ORFs), 13 of which were transcribed in the same direction. Each ORF identified was preceded by a typical staphylococcal ribosomal binding sequence, and 10 of the 14 proteins predicted to be encoded by these ORFs were seen when an E. coli in vitro transcription-translation system was used. Functional transcription units were identified in a Staphylococcus aureus host by complementation of Tn917 inserts that abolished transfer and by Northern (RNA) blot analysis of pGO1 mRNA transcripts. These studies identified three complementation groups (trsA through trsC, trsD through trsK, and trsL-trsM) and four mRNA transcripts (trsA through trsC [1.8 kb], trsA-trsB [1.3 kb], trsL-trsM [1.5 kb], and trsN [400 bases]). No definite mRNA transcript was seen for the largest complementation group, trsD through trsK (10 kb). Comparison of predicted trs-encoded amino acid sequences to those in the data base showed 20% identity of trsK to three related genes necessary for conjugative transfer of plasmids in gram-negative species and 32% identity of trsC to a gene required for conjugative mobilization of plasmid pC221 from staphylococci.
52kb葡萄球菌R质粒pGO1的接合转移基因定位于单个BglII限制片段,并克隆到大肠杆菌中。对指定为trs的13612个碱基的转移区域进行序列分析,鉴定出14个完整的开放阅读框(ORF),其中13个转录方向相同。每个鉴定出的ORF之前都有一个典型的葡萄球菌核糖体结合序列,当使用大肠杆菌体外转录-翻译系统时,可看到这些ORF预测编码的14种蛋白质中的10种。通过Tn917插入物互补消除转移,并通过对pGO1 mRNA转录本进行Northern(RNA)印迹分析,在金黄色葡萄球菌宿主中鉴定出功能转录单位。这些研究确定了三个互补组(trsA至trsC、trsD至trsK和trsL-trsM)和四种mRNA转录本(trsA至trsC [1.8kb]、trsA-trsB [1.3kb]、trsL-trsM [1.5kb]和trsN [400个碱基])。对于最大的互补组trsD至trsK(10kb),未观察到明确的mRNA转录本。将预测的trs编码氨基酸序列与数据库中的序列进行比较,结果显示trsK与革兰氏阴性菌中质粒接合转移所需的三个相关基因有20%的同一性,trsC与从葡萄球菌中接合动员质粒pC221所需的基因有32%的同一性。