Avila P, Núñez B, de la Cruz F
Departamento de Biología Molecular, Universidad de Cantabria, Santander, Spain.
J Mol Biol. 1996 Aug 16;261(2):135-43. doi: 10.1006/jmbi.1996.0447.
Plasmid R6K contains two functional origins or transfer (oriT), in contrast to previously characterized conjugative plasmids. The oriTs are formed by 98 bp palindromic sequences invertedly orientated with respect to each other and located in the immediate vicinity of the alpha and beta origins of replication. The gene for R6K oriT-nickase, taxC, was identified by transposon mutagenesis and sequenced, revealing that TaxC belongs to the VirD2 nickase family. The protein was overproduced and purified. It catalysed a cleaving-joining reaction on single-stranded DNA containing its target sequence. Identification of the nic sites suggested that the R6K oriTs belong to the RP4/VirD2 oriT family. Cleavage was highly specific and did not occur with oligonucleotides cleaved by related nickases like TraI of RP4 or VirD2 of the Ti plasmid. nic cleavage of in vivo preassembled relaxation complexes was induced by incubation of plasmid cleared lysates with ethidium bromide. Nicked molecules obtained in this way were treated with snake venom phosphodiesterase to produce double strand cleavages at the nic sites. 35% of the molecules were cleaved simultaneously at both nic sites, both in the case of R6K and of R6Kdrd1, a derepressed mutant whose frequency of transfer is 1000-fold higher. This figure represents the minimum percentage of individual R6K molecules containing two pre-assembled relaxation complexes.
与先前鉴定的接合质粒不同,质粒R6K含有两个功能性转移起点(oriT)。oriT由98个碱基对的回文序列组成,这些序列彼此反向排列,位于α和β复制起点的紧邻区域。通过转座子诱变鉴定并测序了R6K oriT切口酶基因taxC,结果表明TaxC属于VirD2切口酶家族。该蛋白被过量表达并纯化。它催化了对含有其靶序列的单链DNA的切割-连接反应。对切口位点的鉴定表明,R6K oriT属于RP4/VirD2 oriT家族。切割具有高度特异性,不会发生在由相关切口酶(如RP4的TraI或Ti质粒的VirD2)切割的寡核苷酸上。通过将质粒清除裂解物与溴化乙锭孵育,诱导体内预组装松弛复合物的切口切割。用蛇毒磷酸二酯酶处理以这种方式获得的带切口分子,在切口位点产生双链切割。在R6K和R6Kdrd1(一种转移频率高1000倍的去阻遏突变体)的情况下,35%的分子在两个切口位点同时被切割。这个数字代表了含有两个预组装松弛复合物的单个R6K分子的最小百分比。