Zhong Heng, Li Changbao, Yu Wenjin, Zhou Hua-Ping, Lieber Tara, Su Xiujuan, Wang Wenling, Bumann Eric, Lunny Castro Rafaela Miranda, Jiang Yaping, Gu Wening, Liu Qingli, Barco Brenden, Zhang Chengjin, Shi Liang, Que Qiudeng
Seeds Research, Syngenta Crop Protection, LLC., 9 Davis Drive, Research Triangle Park, NC 27709, USA.
Seeds Research, Syngenta Crop Protection, LLC., 9 Davis Drive, Research Triangle Park, NC 27709, USA.
Plant Commun. 2024 Dec 9;5(12):101063. doi: 10.1016/j.xplc.2024.101063. Epub 2024 Aug 13.
Efficient genotype-independent transformation and genome editing are highly desirable for plant biotechnology research and product development efforts. We have developed a novel approach to enable fast, high-throughput, and genotype-flexible Agrobacterium-mediated transformation using the important crop soybean as a test system. This new method is called GiFT (genotype-independent fast transformation) and involves only a few simple steps. The method uses germinated seeds as explants, and DNA delivery is achieved through Agrobacterium infection of wounded explants as in conventional in vitro-based methods. Following infection, the wounded explants are incubated in liquid medium with a sublethal level of selection and then transplanted directly into soil. The transplanted seedlings are then selected with herbicide spray for 3 weeks. The time required from initiation to fully established healthy T0 transgenic events is about 35 days. The GiFT method requires minimal in vitro manipulation or use of tissue culture media. Because the regeneration occurs in planta, the GiFT method is highly flexible with respect to genotype, which we demonstrate via successful transformation of elite germplasms from diverse genetic backgrounds. We also show that the soybean GiFT method can be applied to both conventional binary vectors and CRISPR-Cas12a vectors for genome editing applications. Analyses of T1 progeny demonstrate that the events have a high inheritance rate and can be used for genome engineering applications. By minimizing the need for tissue culture, the novel approach described here significantly improves operational efficiency while greatly reducing personnel and supply costs. It is the first industry-scale transformation method to utilize in planta selection in a major field crop.
高效的不依赖基因型的转化和基因组编辑对于植物生物技术研究和产品开发工作非常重要。我们开发了一种新方法,以重要作物大豆为测试系统,实现快速、高通量且基因型灵活的农杆菌介导转化。这种新方法称为GiFT(不依赖基因型的快速转化),仅涉及几个简单步骤。该方法使用萌发的种子作为外植体,与传统的基于体外的方法一样,通过农杆菌感染受伤的外植体来实现DNA传递。感染后,将受伤的外植体在含有亚致死选择水平的液体培养基中培养,然后直接移植到土壤中。然后用除草剂喷洒对移植的幼苗进行3周的筛选。从开始到完全建立健康的T0转基因事件所需的时间约为35天。GiFT方法所需的体外操作或组织培养基使用最少。由于再生在植物体内发生,GiFT方法在基因型方面具有高度灵活性,我们通过成功转化来自不同遗传背景的优良种质证明了这一点。我们还表明,大豆GiFT方法可应用于传统二元载体和CRISPR-Cas12a载体,用于基因组编辑应用。对T1后代的分析表明,这些事件具有很高的遗传率,可用于基因组工程应用。通过最大限度地减少对组织培养的需求,本文所述的新方法显著提高了操作效率,同时大大降低了人员和供应成本。它是第一种在主要大田作物中利用植物体内筛选的工业规模转化方法。