De Smet K A, Jamil S, Stoker N G
Department of Clinical Sciences, London School of Hygiene and Tropical Medicine, UK.
Gene. 1993 Dec 22;136(1-2):215-9. doi: 10.1016/0378-1119(93)90467-h.
We have constructed a cosmid vector, Tropist3, based on the lambda origin double-cos-site vector Lawrist4, which is designed for efficient cloning and mapping of genomic DNA. Tropist3 contains two cloning sites in addition to the HindIII and BamHI sites present in Lawrist4; a SalI site allows cloning of Sau3AI partial digests following partial filling-in of the ends, and a PmlI site is suitable for blunt-end cloning. Both these strategies reduce the chance of co-cloning two inserts. Tropist3 also contains NotI, PacI, SacII and KpnI sites flanking the cloning region; these allow most inserts to be excised cleanly and mapped by partial digestion followed by hybridization with short vector sequences which lie adjacent to the cloning sites. This will also be useful for recloning inserts into different vectors, or for cosmid sequencing projects.
我们基于λ噬菌体起源的双粘性末端载体Lawrist4构建了一个粘粒载体Tropist3,该载体设计用于高效克隆和绘制基因组DNA图谱。除了Lawrist4中存在的HindIII和BamHI位点外,Tropist3还包含两个克隆位点;SalI位点允许在末端部分补平后克隆Sau3AI部分消化产物,PmlI位点适用于平端克隆。这两种策略都降低了共克隆两个插入片段的几率。Tropist3在克隆区域两侧还包含NotI、PacI、SacII和KpnI位点;这些位点可使大多数插入片段被干净地切下,并通过部分消化后与位于克隆位点附近的短载体序列杂交进行图谱绘制。这对于将插入片段重新克隆到不同载体中或进行粘粒测序项目也将是有用的。