Aesaert Stijn, Impens Lennert, Coussens Griet, Van Lerberge Els, Vanderhaeghen Rudy, Desmet Laurence, Vanhevel Yasmine, Bossuyt Shari, Wambua Angeline Ndele, Van Lijsebettens Mieke, Inzé Dirk, De Keyser Ellen, Jacobs Thomas B, Karimi Mansour, Pauwels Laurens
Department of Plant Biotechnology and Bioinformatics, Ghent University, Ghent, Belgium.
VIB Center for Plant Systems Biology, Ghent, Belgium.
Front Plant Sci. 2022 Apr 22;13:883847. doi: 10.3389/fpls.2022.883847. eCollection 2022.
Plant transformation is a bottleneck for the application of gene editing in plants. In (maize), a breakthrough was made using co-transformation of the morphogenic transcription factors BABY BOOM (BBM) and WUSCHEL (WUS) to induce somatic embryogenesis. Together with adapted tissue culture media, this was shown to increase transformation efficiency significantly. However, use of the method has not been reported widely, despite a clear need for increased transformation capacity in academic settings. Here, we explore use of the method for the public maize inbred B104 that is widely used for transformation by the research community. We find that only modifying tissue culture media already boosts transformation efficiency significantly and can reduce the time in tissue culture by 1 month. On average, production of independent transgenic plants per starting embryo increased from 1 to 4% using (BAR) as a selection marker. In addition, we reconstructed the BBM-WUS morphogenic gene cassette and evaluated its functionality in B104. Expression of the morphogenic genes under tissue- and development stage-specific promoters led to direct somatic embryo formation on the scutellum of zygotic embryos. However, eight out of ten resulting transgenic plants showed pleiotropic developmental defects and were not fertile. This undesirable phenotype was positively correlated with the copy number of the morphogenic gene cassette. Use of constructs in which morphogenic genes are flanked by a developmentally controlled Cre/LoxP recombination system led to reduced T-DNA copy number and fertile T0 plants, while increasing transformation efficiency from 1 to 5% using HIGHLY-RESISTANT ACETOLACTATE SYNTHASE as a selection marker. Addition of a CRISPR/Cas9 module confirmed functionality for gene editing applications, as exemplified by editing the gene () that can act as a visual marker for gene editing in maize. The constructs, methods, and insights produced in this work will be valuable to translate the use of BBM-WUS and other emerging morphogenic regulators (MRs) to other genotypes and crops.
植物转化是基因编辑技术在植物中应用的一个瓶颈。在玉米中,通过共转化形态发生转录因子BABY BOOM(BBM)和WUSCHEL(WUS)诱导体细胞胚胎发生取得了突破。结合改良的组织培养基,这被证明能显著提高转化效率。然而,尽管学术环境中对提高转化能力有明确需求,但该方法的应用尚未得到广泛报道。在这里,我们探索将该方法应用于被研究群体广泛用于转化的公共玉米自交系B104。我们发现仅改良组织培养基就可显著提高转化效率,并能将组织培养时间缩短1个月。以潮霉素抗性基因(BAR)作为选择标记时,每个起始胚产生独立转基因植株的比例平均从1%提高到了4%。此外,我们重构了BBM-WUS形态发生基因盒并评估了其在B104中的功能。形态发生基因在组织和发育阶段特异性启动子控制下的表达导致合子胚盾片上直接形成体细胞胚。然而,所获得的10株转基因植株中有8株表现出多效性发育缺陷且不育。这种不良表型与形态发生基因盒的拷贝数呈正相关。使用形态发生基因两侧带有发育可控的Cre/LoxP重组系统的构建体,可减少T-DNA拷贝数并获得可育的T0植株,同时以抗高剂量乙酰乳酸合酶作为选择标记时,转化效率从1%提高到了5%。添加CRISPR/Cas9模块证实了其在基因编辑应用中的功能,例如编辑在玉米中可作为基因编辑视觉标记的花青素合成酶基因(ZmC1)。这项工作中产生的构建体、方法和见解对于将BBM-WUS和其他新兴形态发生调节因子(MRs)应用于其他基因型和作物具有重要价值。