Hasson J F, Mougneau E, Cuzin F, Yaniv M
J Mol Biol. 1984 Jul 25;177(1):53-68. doi: 10.1016/0022-2836(84)90057-3.
We have analysed nucleotide sequences at the junction between simian virus 40 (SV40) and cellular DNA in the Fisher rat transformed line tsA30-N2. This line contains a single insertion of one complete SV40 genome with a terminal duplication of 267 nucleotides, the recombination sites being located at nucleotides 439 and 705 in the late region of SV40. These two positions are located within short direct repeats in the virus genome. In order to test the significance of such repeats with respect to illegitimate recombination events, we analysed two series of published sequences of SV40 recombination sites: the first one consists of eight SV40 insertion endpoints derived from four SV40-transformed cell lines; the second one consists of 18 junction points from SV40 evolutionary variants. Our analysis demonstrates that in both cases, recombination preferentially takes place near short direct repeats in the virus genome. A model involving a "slipped mispairing" mechanism is proposed in order to account for this finding.
我们分析了费希尔大鼠转化细胞系tsA30 - N2中猿猴病毒40(SV40)与细胞DNA交界处的核苷酸序列。该细胞系含有一个完整SV40基因组的单一插入片段,带有267个核苷酸的末端重复序列,重组位点位于SV40晚期区域的第439和705个核苷酸处。这两个位置位于病毒基因组的短正向重复序列内。为了测试此类重复序列对于异常重组事件的重要性,我们分析了两系列已发表的SV40重组位点序列:第一系列由源自四个SV40转化细胞系的八个SV40插入端点组成;第二系列由18个SV40进化变体的连接点组成。我们的分析表明,在这两种情况下,重组都优先发生在病毒基因组的短正向重复序列附近。为了解释这一发现,我们提出了一个涉及“滑动错配”机制的模型。