Wang G, Blakesley R W, Berg D E, Berg C M
Department of Molecular and Cell Biology (U-131), University of Connecticut, Storrs 06269-2131.
Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7874-8. doi: 10.1073/pnas.90.16.7874.
We describe a transposon gamma delta-containing cosmid cloning vector, pDUAL (previously called pJANUS), and demonstrate an efficient strategy for isolating nested deletions in both large-scale and small-scale DNA sequencing efforts. This "deletion factory" strategy takes advantage of the ability of gamma delta (Tn1000) to generate deletions that extend from an end of the transposon into adjacent DNA when gamma delta transposes to new sites in the same DNA molecule. pDUAL contains the contraselectable (conditional lethal) sacB+ (sucrose sensitivity) and strA+ (streptomycin sensitivity) genes just outside each end of an engineered gamma delta and selectable kan+ (Kanr) and tet+ (Tetr) genes between the cloning site and sacB and strA, respectively. Selection on sucrose tetracycline medium yields deletions that extend from one gamma delta end for various distances into the cloned DNA, while selection on streptomycin kanamycin medium yields comparable deletions in the other direction. Both types of deletions are recoverable because the essential plasmid replication origin is embedded in the gamma delta component and is thereby retained in each deletion product. Pilot experiments with pDUAL clones showed that deletion end points can be mapped or selected by plasmid size and that both DNA strands of any single clone can be accessed for sequencing by using a pair of universal primers specific for sequences that are just interior to the gamma delta ends.
我们描述了一种含转座子γδ的黏粒克隆载体pDUAL(以前称为pJANUS),并展示了一种在大规模和小规模DNA测序工作中分离嵌套缺失的有效策略。这种“缺失工厂”策略利用了γδ(Tn1000)的能力,当γδ转座到同一DNA分子的新位点时,它能产生从转座子末端延伸到相邻DNA的缺失。pDUAL在工程化γδ的每个末端外侧包含反选择(条件致死)的sacB +(蔗糖敏感性)和strA +(链霉素敏感性)基因,在克隆位点与sacB和strA之间分别包含可选择的kan +(卡那霉素抗性)和tet +(四环素抗性)基因。在蔗糖 - 四环素培养基上进行选择可产生从一个γδ末端延伸到克隆DNA不同距离的缺失,而在链霉素 - 卡那霉素培养基上进行选择可在另一个方向产生类似的缺失。这两种类型的缺失都是可恢复的,因为必需的质粒复制起点嵌入在γδ组件中,从而保留在每个缺失产物中。用pDUAL克隆进行的初步实验表明,缺失终点可以通过质粒大小进行定位或选择,并且任何单个克隆的两条DNA链都可以通过使用一对针对γδ末端内部序列的通用引物进行测序。