Institut des Sciences Végétales, CNRS, Avenue de la Terrasse, 91198, Gif sur Yvette Cédex, France.
Plant Cell Rep. 1992 Jul;11(7):334-8. doi: 10.1007/BF00233360.
Genetically transformed cabbage (Brassica oleracea var. capitata) roots were obtained after inoculation with two engineered Agrobacterium rhizogenes strains, each harbouring a plant selectable marker gene in their T-DNA. Axenic root clones resistant to kanamycin or hygromycin B were established, most of which did not exhibit the phenotypic characteristics of Ri-transformed roots. Shoot regeneration was induced from roots after treatment with 2,4-dichlorophenoxyacetic acid (2,4-D). The resulting plants exhibited various phenotypes: some looked normal, while others showed the transformed phenotype observed in other species. Direct evidence for genetic transformation was obtained by molecular hybridization. The trait was transmitted to the progeny. Transformed cabbage plants can be obtained within 6 months using this approach.
经两种工程化的发根农杆菌(Agrobacterium rhizogenes)菌株接种后,获得了转化的甘蓝(Brassica oleracea var. capitata)根,这两种菌株的 T-DNA 中都携带了一个植物选择标记基因。建立了对卡那霉素或潮霉素 B 有抗性的无菌根克隆,其中大多数根克隆没有表现出 Ri 转化根的表型特征。用 2,4-二氯苯氧乙酸(2,4-D)处理根后,可诱导芽再生。所得植株表现出不同的表型:有些看起来正常,而另一些则表现出在其他物种中观察到的转化表型。通过分子杂交获得了遗传转化的直接证据。该性状可传递给后代。使用这种方法,可在 6 个月内获得转化的甘蓝植株。