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DNA sequence and units of transcription of the conjugative transfer gene complex (trs) of Staphylococcus aureus plasmid pGO1.

机译:金黄色葡萄球菌质粒pGO1的共轭转移基因复合物(trs)的DNA序列和转录单位。

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摘要

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.
机译:52 kb葡萄球菌R质粒pGO1的结合转移基因被定位到单个BglII限制片段,并克隆到大肠杆菌中。对13,612个碱基的转移区域(称为trs)进行序列分析,鉴定出14个完整的开放阅读框(ORF),其中13个沿相同方向转录。在鉴定出的每个ORF之前都带有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,可以看到预测由这些ORF编码的14种蛋白质中的10种。通过互补的Tn917插入片段(取消了转移)和pGO1 mRNA转录物的RNA印迹分析确定了金黄色葡萄球菌宿主中的功能性转录单位。这些研究确定了三个互补组(trsA至trsC,trsD至trsK和trsL-trsM)和四个mRNA转录物(trsA至trsC [1.8 kb],trsA-trsB [1.3 kb],trsL-trsM [1.5 kb]和trsN [400 bases])。对于最大的互补组trsD至trsK(10 kb),未见明确的mRNA转录。比较预测的trs编码的氨基酸序列与数据库中的氨基酸序列,发现trsK与革兰氏阴性物种中质粒共轭转移所需的三个相关基因具有20%的同一性,而trsC与质粒的共轭动员所需基因具有32%的同一性。来自葡萄球菌的质粒pC221。

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