McMahon T L, Wilczynska Z, Barth C, Fraser D J, Pontes L, Fisher P R
School of Microbiology, La Trobe University, Melbourne, Victoria, Australia.
Nucleic Acids Res. 1996 Oct 15;24(20):4096-7. doi: 10.1093/nar/24.20.4096.
A novel cloning strategy, replicon rescue, was developed for cloning genes disrupted by plasmid insertions. After ligation to a tetracycline resistance cassette, fragments containing a bacterial origin of replication from the insertion are recovered in Escherichia coli because they replicate autonomously. Restriction enzymes for cloning are so chosen that the only legitimate two fragment ligation yielding TetR clones involves a fragment spanning the boundary of the insertion. Replicon rescue was used successfully firstly in a test system to clone the chromosomal orl from a Klebsiella aerogenes strain, and secondly to recover a disrupted gene from a phototaxis-deficient mutant of Dictyostelium.
一种新的克隆策略——复制子拯救,被开发用于克隆因质粒插入而中断的基因。与四环素抗性盒连接后,含有来自插入片段的细菌复制起点的片段在大肠杆菌中得以回收,因为它们能自主复制。选择用于克隆的限制酶时,要确保产生四环素抗性克隆的唯一合法双片段连接涉及跨越插入边界的片段。复制子拯救首先在一个测试系统中成功用于从产气克雷伯菌菌株克隆染色体orl基因,其次用于从盘基网柄菌趋光性缺陷突变体中回收一个中断的基因。