Bundock P, Hooykaas P J
Institute for Molecular Plant Sciences, Clusius Laboratory, Leiden University, The Netherlands.
Proc Natl Acad Sci U S A. 1996 Dec 24;93(26):15272-5. doi: 10.1073/pnas.93.26.15272.
Agrobacterium tumefaciens can transfer part of its Ti plasmid, the T-DNA, to plant cells where it integrates into the nuclear genome via illegitimate recombination. Integration of the T-DNA results in small deletions of the plant target DNA, and may lead to truncation of the T-DNA borders and the production of filler DNA. We showed previously that T-DNA can also be transferred from A. tumefaciens to Sac-charomyces cerevisiae and integrates into the yeast genome via homologous recombination. We show here that when the T-DNA lacks homology with the S. cerevisiae genome, it integrates at random positions via illegitimate recombination. From 11 lines the integrated T-DNA was cloned back to Escherichia coli along with yeast flanking sequences. The T-DNA borders and yeast DNA flanking the T-DNA were sequenced and characterized. It was found that T-DNA integration had resulted in target DNA deletions and sometimes T-DNA truncations or filler DNA formation. Therefore, the molecular mechanism of illegitimate recombination by which T-DNA integrates in higher and lower eukaryotes seems conserved.
根癌土壤杆菌可将其Ti质粒的一部分(即T-DNA)转移至植物细胞,在植物细胞中,T-DNA通过非同源重组整合到核基因组中。T-DNA的整合会导致植物靶标DNA出现小片段缺失,还可能导致T-DNA边界截短以及填充DNA的产生。我们之前表明,T-DNA也能从根癌土壤杆菌转移至酿酒酵母,并通过同源重组整合到酵母基因组中。我们在此表明,当T-DNA与酿酒酵母基因组缺乏同源性时,它会通过非同源重组随机整合到基因组的各个位置。从11个品系中,将整合的T-DNA连同酵母侧翼序列一起克隆回大肠杆菌。对T-DNA边界以及T-DNA侧翼的酵母DNA进行了测序和表征。结果发现,T-DNA的整合导致了靶标DNA缺失,有时还会出现T-DNA截短或填充DNA形成。因此,T-DNA在高等和低等真核生物中整合所涉及的非同源重组分子机制似乎是保守的。