Beggs J D, Guerineau M, Atkins J F
Mol Gen Genet. 1976 Nov 17;148(3):287-94. doi: 10.1007/BF00332903.
The 2 micron circular DNA from S. cerevisiae has been cloned on bacteriophage lambda. The two forms of circular DNA which exist in equilibrium due to recombination between inverted repeat sequences were separated as stable clones, and a map of targets for restriction endonucleases EcoRI, HindIII and HpaI was constructed. The circular DNAs isolated from a particular oligomycin resistant strain and its parent oligomycin snesitive strain were compared by restriction endonuclease analysis, and no difference was detected. The potential uses of cloned 2 micron DNA in determining the possible biological role of these plasmids are considered.
来自酿酒酵母的2微米环状DNA已被克隆到噬菌体λ上。由于反向重复序列之间的重组而处于平衡状态的两种环状DNA形式被分离为稳定的克隆,并构建了限制性内切酶EcoRI、HindIII和HpaI的靶标图谱。通过限制性内切酶分析比较了从特定抗寡霉素菌株及其亲本寡霉素敏感菌株中分离出的环状DNA,未检测到差异。还考虑了克隆的2微米DNA在确定这些质粒可能的生物学作用方面的潜在用途。