Sternberg N, Ruether J, deRiel K
E. I. du Pont de Nemours & Co., Central Research and Development Department, Wilmington, DE 19880-0328.
New Biol. 1990 Feb;2(2):151-62.
A bacteriophage P1 cloning system that permits the isolation and amplification of cloned DNA fragments as large as 100 kbp was described previously. We have now utilized a similar system to generate a 50,000-member human DNA library with DNA inserts ranging in size from 75 to 100 kbp. Two major obstacles were overcome in constructing the library. The first concerned the mcrAB restriction system of Escherichia coli, which degrades DNA containing MeC and interferes with the recovery of cloned human DNA inserts. In the P1 cloning system, the effect of the Mcr restriction activity is to decrease recovery of cloned inserts by about 35-fold when the activity is in the host cell line and by about 3-fold when the activity is in the cells used to prepare the packaging extract. To circumvent this problem we inactivated, by mutation, the McrAB proteins in both components of the cloning system. The second obstacle concerned the preferential cloning of small DNA fragments from a population of fragments ranging in size from 20 to 100 kbp. To deal with this problem we first modified the P1 lysogen used to prepare the in vitro head-tail packaging extract so that it would produce 12 times as many large P1 heads (head capacity about 110 kbp) as small P1 heads (head capacity about 45 kbp). We then restructured the P1 cloning vector so that it could be used to produce vector "arm" fragments that could be ligated to insert DNA at only one end. This prevented the formation of long concatamers consisting of alternating units of vector and insert DNA and prohibited the packaging of small inserts in large phage heads. Using the insert-biased large head extract, the arms vector, and size-selected human DNA fragments, we showed that as much as 90% of recovered transformants contained inserts in the desired high molecular weight range.
先前已描述了一种噬菌体P1克隆系统,该系统可用于分离和扩增长达100 kbp的克隆DNA片段。我们现在利用类似的系统构建了一个包含50,000个成员的人类DNA文库,其DNA插入片段大小在75至100 kbp之间。构建该文库时克服了两个主要障碍。第一个障碍涉及大肠杆菌的mcrAB限制系统,该系统会降解含有甲基胞嘧啶(MeC)的DNA,并干扰克隆的人类DNA插入片段的回收。在P1克隆系统中,当Mcr限制活性存在于宿主细胞系中时,其对克隆插入片段回收的影响是使回收率降低约35倍;当该活性存在于用于制备包装提取物的细胞中时,回收率降低约3倍。为解决此问题,我们通过突变使克隆系统两个组件中的McrAB蛋白失活。第二个障碍涉及从大小在20至100 kbp范围内的片段群体中优先克隆小DNA片段。为解决此问题,我们首先对用于制备体外头尾包装提取物的P1溶原菌进行改造,使其产生的大P1头部(头部容量约110 kbp)数量是小P1头部(头部容量约45 kbp)的12倍。然后我们对P1克隆载体进行重构,使其可用于产生仅能在一端与插入DNA连接的载体“臂”片段。这防止了由载体和插入DNA交替单元组成的长串联体的形成,并阻止了小插入片段包装到大型噬菌体头部中。使用偏向插入的大型头部提取物、臂载体和大小选择的人类DNA片段,我们表明高达90%的回收转化体含有所需高分子量范围内的插入片段。