Syvanen M, Hopkins J D, Griffin T J, Liang T Y, Ippen-Ihler K, Kolodner R
Mol Gen Genet. 1986 Apr;203(1):1-7. doi: 10.1007/BF00330376.
Large F plasmids such as F'128 stimulate precise excision of the transposons Tn5 and Tn10 in E. coli K12. This stimulation occurs when the transposons are either on the F'128 plasmid or the bacterial chromosome. Stimulation of precise excision is dependent upon conjugal transfer proficient F'plasmids. Tra- mutations which are defective in conjugal transfer negate this F'128 plasmid stimulation effect. F'128 traS mutations, which are surface exclusion defective and thus permit matings between male cells, thereby increasing conjugal transfer, increase the F plasmid stimulation effect. When the F' plasmid is present in a cell with the small plasmid, pRS31, carrying the traS to traZ region of F, stimulation of precise excision is no longer observed. This complementation-like activity by pRS31 is abolished by a Tn5 insertion in the traS gene. Data are presented supporting the notion that F' plasmid stimulation of precise excision occurs in the recipient during conjugal transfer. F'128 traS also stimulates recA-dependent recombination between DNA sequences on the small, nontransferrable plasmid pRDK41, DNA sequences that are unrelated to those of the F plasmid. The F'plasmid stimulation of precise excision of Tn5 is not seen with F+ but only with certain F's with large insertions of chromosomal DNA.
诸如F'128之类的大型F质粒可刺激大肠杆菌K12中转座子Tn5和Tn10的精确切除。当转座子位于F'128质粒或细菌染色体上时,就会发生这种刺激作用。精确切除的刺激作用取决于具备接合转移能力的F'质粒。在接合转移方面存在缺陷的Tra-突变会消除这种F'128质粒刺激效应。F'128 traS突变在表面排斥方面存在缺陷,因此允许雄性细胞之间进行交配,从而增加接合转移,增强了F质粒刺激效应。当F'质粒与携带F的traS至traZ区域的小质粒pRS31存在于同一细胞中时,就不再观察到精确切除的刺激作用。pRS31的这种类似互补的活性会被traS基因中的Tn5插入所消除。所提供的数据支持这样一种观点,即F'质粒对精确切除的刺激作用发生在接合转移过程中的受体细胞内。F'128 traS还会刺激小型非转移性质粒pRDK41上与F质粒序列无关的DNA序列之间的recA依赖性重组。F'质粒对Tn5精确切除的刺激作用在F+中未观察到,而仅在某些插入了大量染色体DNA的F'中观察到。