Tatzelt J, Fechteler K, Langenbach P, Doerfler W
Institute of Genetics, University of Cologne, Germany.
Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7356-60. doi: 10.1073/pnas.90.15.7356.
We have explored the mechanism of adenovirus type 12 (Ad12) DNA integration because of its importance for viral oncogenesis and as an example of insertional recombination. We have used a fractionated cell-free system from nuclear extracts of hamster cells and have partly purified nuclear proteins that could catalyze in vitro recombination. As recombination partners, the 20,880- to 24,049-nucleotide Pst I D fragment of Ad12 DNA and the hamster preinsertion sequence p7 from the Ad12-induced tumor CLAC1 have proven to recombine at higher frequencies than randomly selected adenoviral or cellular DNA sequences. A preinsertion sequence might carry elements essential in eliciting recombination. Patch homologies between the recombination partners seem to play a role in the selection of sites for recombination in vivo and in the cell-free system. Nuclear extracts from BHK21 cells were prepared by incubating the nuclei in 0.42 M (NH4)2SO4 and fractionated by Sephacryl S-300 gel filtration, followed by chromatography on Mono S and Mono Q columns. The purified products active in recombination contained a limited number of different protein bands, as determined by polyacrylamide gel electrophoresis and silver staining. The most highly purified fraction IV had helicase and topoisomerase I activities. We used two different methods to assess the in vitro generation of hamster DNA-Ad12 DNA recombinants upon incubation with the purified protein fractions: (i) transfection of the recombination products into recA- strains of Escherichia coli and (ii) the polymerase chain reaction by using amplification primers unique for each of the two recombination partners. In p7 hamster DNA, the nucleotide sequence 5'-CCTCTCCG-3' or similar sequences served repeatedly as a preferred recombination target for Ad12 DNA in the tumor CLAC1 and in five independent cell-free recombination experiments.
我们研究了12型腺病毒(Ad12)DNA整合的机制,这是因为其对病毒致癌作用很重要,并且是插入重组的一个例子。我们使用了来自仓鼠细胞核提取物的分级无细胞系统,并部分纯化了能够催化体外重组的核蛋白。作为重组伙伴,Ad12 DNA的20,880至24,049个核苷酸的Pst I D片段与来自Ad12诱导的肿瘤CLAC1的仓鼠预插入序列p7已被证明比随机选择的腺病毒或细胞DNA序列以更高的频率重组。预插入序列可能携带引发重组所必需的元件。重组伙伴之间的补丁同源性似乎在体内和无细胞系统中重组位点的选择中起作用。通过在0.42 M硫酸铵中孵育细胞核制备BHK21细胞的核提取物,并通过Sephacryl S-300凝胶过滤分级,然后在Mono S和Mono Q柱上进行色谱分离。通过聚丙烯酰胺凝胶电泳和银染色确定,在重组中具有活性的纯化产物包含有限数量的不同蛋白条带。纯化程度最高的组分IV具有解旋酶和拓扑异构酶I活性。我们使用两种不同的方法来评估与纯化的蛋白组分一起孵育时仓鼠DNA-Ad12 DNA重组体的体外生成:(i)将重组产物转染到大肠杆菌的recA-菌株中,以及(ii)使用对两个重组伙伴各自独特的扩增引物进行聚合酶链反应。在p7仓鼠DNA中,核苷酸序列5'-CCTCTCCG-3'或类似序列在肿瘤CLAC1以及五个独立的无细胞重组实验中反复作为Ad12 DNA的优选重组靶标。