Laboratorium voor Genetica, Rijksuniversiteit Gent, B-9000 Gent, Belgium.
Proc Natl Acad Sci U S A. 1987 Sep;84(17):6169-73. doi: 10.1073/pnas.84.17.6169.
The transfer DNA (T-DNA) mobilized into plant cells by Agrobacterium tumefaciens seems to integrate rather randomly into the plant genome. We analyzed a target site in the genome of Nicotiana tabacum before and after integration of a T-DNA. Clones presenting right and left T-DNA/plant DNA junctions were used as probes to identify and isolate a unique 1.8-kilobase EcoRI fragment corresponding to the plant DNA target site for a T-DNA insertion event. Comparison of the nucleotide sequences of the plant DNA portions of the T-DNA junction clones with the original plant DNA target revealed that several types of rearrangements resulted from insertion of the T-DNA. The most dramatic alteration was a 158-base-pair direct repeat of target plant sequences at the left and right T-DNA junctions. In addition, there were deletion and insertion events at the ends of the right and left copies of the 158-base-pair repeat. The variety of target-site rearrangements suggests that T-DNA insertion is a multistep process of recombination accompanied by local replicative and repair activities mediated by host-cell enzymes.
根瘤农杆菌介导的转移 DNA(T-DNA)似乎随机整合到植物基因组中。我们分析了烟草基因组中的一个靶位点,该靶位点在 T-DNA 整合前后都进行了分析。使用呈现右和左 T-DNA/植物 DNA 连接的克隆作为探针来鉴定和分离与 T-DNA 插入事件相对应的独特的 1.8 千碱基对 EcoRI 片段。与原始植物 DNA 靶标相比,T-DNA 连接克隆植物 DNA 部分的核苷酸序列比较表明,T-DNA 的插入导致了几种类型的重排。最显著的改变是在左和右 T-DNA 连接处靶植物序列的 158 个碱基对的直接重复。此外,在右和左 158 个碱基对重复的末端还存在缺失和插入事件。靶位点重排的多样性表明,T-DNA 插入是一个多步骤的重组过程,伴随着由宿主细胞酶介导的局部复制和修复活动。