Hänisch ten Cate C H, Loonen A E, Ottaviani M P, Ennik L, van Eldik G, Stiekema W J
Research Institute Ital, Wageningen, Netherlands.
Plant Mol Biol. 1990 May;14(5):735-41. doi: 10.1007/BF00016506.
The presence of T-DNA was examined by Southern blot analysis in 16 regenerated shoot lines derived from 6 Agrobacterium rhizogenes-transformed root clones of Solanum tuberosum L. cv. Bintje. TR-DNA, present in regenerated shoot lines from 3 out of 6 root clones was correlated with the presence of opines. One root clone produced opines up to 2.5 years of subculture. However, plant regeneration from and prolonged subculturing of this root clone resulted in loss of opine synthesis, caused by deletion of TR-DNA. TL-DNA inserted at 1 to 5 independent loci was found in 14 of the 16 shoot lines. Surprisingly, 1 to 2 additional insertions next to similar insertions of TL-DNA were found in shoot lines from the same root clone (named 'sister' shoot lines) in 2 out of 4 root clones. Nevertheless, this did not result in gross phenotypic variation between sister shoot lines. Another root clone regenerated 1 shoot line with an Ri phenotype, containing 1 insertion of TL-DNA, and 2 shoot lines with a normal Bintje phenotype without TL-DNA. The 5th root clone showed no difference between sister shoot lines and the 6th root clone produced only 1 shoot line. We conclude that during prolonged root culture and during shoot regeneration from root clones deletion of TL- and TR-DNA insertions can occur. The significance of the frequency of deletion of T-DNA of the Ri plasmid is discussed.
通过Southern杂交分析检测了来自6个发根农杆菌转化的马铃薯栽培品种宾杰(Solanum tuberosum L. cv. Bintje)根克隆的16个再生芽系中T-DNA的存在情况。6个根克隆中有3个根克隆的再生芽系中存在TR-DNA,这与冠瘿碱的存在相关。一个根克隆在继代培养长达2.5年的时间里都能产生冠瘿碱。然而,该根克隆的植株再生以及长期继代培养导致了冠瘿碱合成的丧失,这是由TR-DNA的缺失引起的。在16个芽系中的14个芽系中发现TL-DNA插入到1至5个独立位点。令人惊讶的是,在4个根克隆中的2个根克隆的来自同一根克隆的芽系(称为“姐妹”芽系)中,在TL-DNA类似插入位点旁边发现了1至2个额外的插入。然而,这并未导致姐妹芽系之间出现明显的表型变异。另一个根克隆再生出1个具有Ri表型的芽系,含有1个TL-DNA插入,以及2个具有正常宾杰表型且无TL-DNA的芽系。第5个根克隆的姐妹芽系之间没有差异,第6个根克隆仅产生1个芽系。我们得出结论,在根的长期培养以及从根克隆再生芽的过程中,TL-和TR-DNA插入可能会发生缺失。文中讨论了Ri质粒T-DNA缺失频率的意义。