首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Fractionated nuclear extracts from hamster cells catalyze cell-free recombination at selective sequences between adenovirus DNA and a hamster preinsertion site.
【2h】

Fractionated nuclear extracts from hamster cells catalyze cell-free recombination at selective sequences between adenovirus DNA and a hamster preinsertion site.

机译:仓鼠细胞的分级核提取物在腺病毒DNA和仓鼠预插入位点之间的选择性序列上催化无细胞重组。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:我们已经探究了12型腺病毒(Ad12)DNA整合的机制,因为它对于病毒的致癌作用非常重要,并作为插入重组的一个例子。我们从仓鼠细胞的核提取物中使用了无级分的无细胞系统,部分纯化的核蛋白可以催化体外重组。作为重组伴侣,已证明Ad12 DNA的20,880至24,049核苷酸的Pst I D片段和Ad12诱导的肿瘤CLAC1的仓鼠预插入序列p7的重组频率高于随机选择的腺病毒或细胞DNA序列。插入前序列可能带有引发重组所必需的元件。重组伴侣之间的修补同源性似乎在体内和无细胞系统中重组位点的选择中起着作用。通过将核在0.42 M(NH4)2SO4中孵育并通过Sephacryl S-300凝胶过滤进行分离,然后在Mono S和Mono Q柱上进行色谱分离来制备BHK21细胞的核提取物。通过聚丙烯酰胺凝胶电泳和银染确定,具有重组活性的纯化产物含有有限数量的不同蛋白带。最高纯度的馏分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评估与纯化的蛋白质部分孵育后仓鼠DNA-Ad12 DNA重组子的体外生成:(i)将重组产物转染到大肠杆菌recA-菌株中,以及(ii)通过聚合酶链反应使用两个重组伴侣各自独特的扩增引物。在p7仓鼠DNA中,核苷酸序列5'-CCTCTCCG-3'或类似序列反复用作肿瘤CLAC1和五个独立的无细胞重组实验中Ad12 DNA的优选重组靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号