National Key Laboratory of Crop Genetics and Germplasm Enhancement and Utilization, Key Laboratory of Horticultural Crop Biology and Genetic Improvement (East China), Ministry of Agriculture and Rural Affairs, College of Horticulture, Nanjing Agricultural University, Nanjing, China.
Plant J. 2024 Nov;120(4):1682-1692. doi: 10.1111/tpj.17068. Epub 2024 Oct 10.
Radish (Raphanus sativus L.) is one of the most important root vegetable crops worldwide. However, gene function exploration and germplasm innovation still face tremendous challenges due to its extremely low transformation efficiency. Here, an economic and highly efficient genetic transformation method for radish was explored by Agrobacterium rhizogenes-mediated transformation with the help of combining special developmental regulator (DR) genes and the visual identification reporter. Firstly, the RUBY gene, a betalain biosynthesis system, could result in a visual red-violet color used as a convenient and effective reporter for monitoring transgenic hairy roots screening of radish. However, the hairy roots-to-shoots conversion system of radish still stands as a barrier to the obtainment of whole transgenic plants, although different hormone combinations and various culture conditions were tried. Following, two DR genes including Wuschel2 (Wus2) and isopentenyl transferase (ipt), as well as their combination Wus2-ipt were introduced for the shoot regeneration capacity improvement. The results showed that the transgenic shoots could be directly generated without externally supplying any hormones in the presence of a Wus2-ipt combination. Then, Wus2-ipt along with the RUBY reporter was employed to establish an efficient genetic transformation system of radish. Moreover, this system was applied in generating gene-edited radish plants and the phytoene desaturase (RsPDS) gene was effectively knockout through albino phenotype observation and sequencing analysis. These findings have the potential to be widely applied in genetic transformation and genome-editing genetic improvement of other vegetable species.
萝卜(Raphanus sativus L.)是世界上最重要的根茎类蔬菜作物之一。然而,由于其极低的转化效率,基因功能探索和种质创新仍然面临巨大挑战。在这里,借助特殊发育调节剂(DR)基因和可视化鉴定报告,通过发根农杆菌介导转化,探索了一种经济高效的萝卜遗传转化方法。首先,甜菜红素生物合成系统的 RUBY 基因可导致红色-紫色的可见颜色,可作为监测萝卜毛状根筛选的一种方便有效的报告基因。然而,尽管尝试了不同的激素组合和各种培养条件,萝卜的毛状根到茎的转化系统仍然是获得完整转基因植物的障碍。接下来,引入了两个 DR 基因,包括 Wuschel2(Wus2)和异戊烯基转移酶(ipt),以及它们的组合 Wus2-ipt,以提高茎再生能力。结果表明,在存在 Wus2-ipt 组合的情况下,无需外部添加任何激素,即可直接生成转基因茎。然后,将 Wus2-ipt 与 RUBY 报告基因一起用于建立萝卜高效遗传转化系统。此外,该系统还应用于基因编辑萝卜植物的生成,通过白化表型观察和测序分析,有效地敲除了类胡萝卜素脱饱和酶(RsPDS)基因。这些发现有可能广泛应用于其他蔬菜物种的遗传转化和基因组编辑遗传改良。