Hiller B, Frey B, Schumann W
Boehringer Mannheim GmbH, Penzberg, FRG.
FEMS Microbiol Lett. 1994 Jan 15;115(2-3):151-5. doi: 10.1111/j.1574-6968.1994.tb06630.x.
A transposon was constructed allowing the rapid restriction mapping of plasmids. This transposon, Tn 5Map, contains a cleavage site for the I-SceI endonuclease which recognizes an 18-mer. After in vivo transposition of Tn5Map into the plasmid of interest, the plasmid is isolated and linearized with I-SceI. Splinkers labelled with digoxygenin and complementary to the left and right end of the linearized molecule are added and ligated. After partial digestion of the splinkered molecules with the restriction enzyme of interest, separation of the cleavage products in an agarose gel, and Southern transfer, the labelled fragments are visualized by the addition of the chemiluminescent substrate AMPPD and alkaline phosphatase. The restriction map can be directly read from the bottom to the top of the gel.
构建了一种转座子,可实现质粒的快速限制酶切图谱绘制。这种转座子Tn 5Map含有I-SceI内切核酸酶的切割位点,该酶识别一个18聚体。将Tn5Map体内转座到目标质粒后,分离该质粒并用I-SceI使其线性化。加入用洋地黄毒苷标记且与线性化分子的左端和右端互补的接头并进行连接。用目标限制酶对连接后的分子进行部分酶切,在琼脂糖凝胶中分离切割产物,然后进行Southern转印,通过添加化学发光底物AMPPD和碱性磷酸酶使标记的片段可视化。限制酶切图谱可直接从凝胶的底部向上读取。