Matsumoto S, Ito Y, Hosoi T, Takahashi Y, Machida Y
Department of Biology, Faculty of Science, Nagoya University, Japan.
Mol Gen Genet. 1990 Dec;224(3):309-16. doi: 10.1007/BF00262423.
We established tobacco tumour cell lines from crown galls induced by Agrobacterium. Restriction fragments containing T-DNA/plant DNA junctions were cloned from one of the cell lines, which has a single copy of the T-DNA in a unique region of its genome. We also isolated a DNA fragment that contained the integration target site from nontransformed tobacco cells. Nucleotide sequence analyses showed that the right and left breakpoints of the T-DNA mapped ca. 7.3 kb internal to the right 25 bp border and ca. 350 bp internal to the left border respectively. When the nucleotide sequences around these breakpoints were compared with the sequence of the target, significant homology was seen between the region adjacent to the integration target site and both external regions of the T-DNA breakpoints. In addition, a short stretch of plant DNA in the vicinity of the integration site was deleted. This deletion seems to have been promoted by homologous recombination between short repeated sequences that were present on both sides of the deleted stretch. Minor rearrangements, which included base substitutions, insertions and deletions, also took place around the integration site in the plant DNA. These results, together with previously reported results showing that in some cases sequences homologous to those in T-DNA are present in plant DNA regions adjacent to left recombinational junctions, indicate that sequence homology between the incoming T-DNA and the plant chromosomal DNA has an important function in T-DNA integration.(ABSTRACT TRUNCATED AT 250 WORDS)
我们从根癌农杆菌诱导产生的冠瘿瘤中建立了烟草肿瘤细胞系。从其中一个细胞系中克隆了包含T-DNA/植物DNA连接区的限制性片段,该细胞系在其基因组的一个独特区域有一个T-DNA单拷贝。我们还从未转化的烟草细胞中分离出一个包含整合靶位点的DNA片段。核苷酸序列分析表明,T-DNA的右断点和左断点分别位于右25 bp边界内部约7.3 kb处和左边界内部约350 bp处。当将这些断点周围的核苷酸序列与靶序列进行比较时,在整合靶位点相邻区域与T-DNA断点的两个外部区域之间发现了显著的同源性。此外,整合位点附近的一小段植物DNA被删除。这种删除似乎是由缺失片段两侧存在的短重复序列之间的同源重组促进的。在植物DNA的整合位点周围也发生了包括碱基替换、插入和缺失在内的微小重排。这些结果,连同先前报道的结果表明在某些情况下与T-DNA中的序列同源的序列存在于与左重组连接点相邻的植物DNA区域,表明进入的T-DNA与植物染色体DNA之间的序列同源性在T-DNA整合中具有重要作用。(摘要截短于250字)