Mohammad Tasnim, Ghogare Rishikesh, Morton Lauren B, Dhingra Amit, Potlakayala Shobha, Rudrabhatla Sairam, Dhir Sarwan K
Center for Biotechnology, Department of Agricultural Sciences, Fort Valley State University, 113, Alva Tabor Building, Fort Valley, GA 31030, USA.
Department of Horticultural Sciences, Texas A&M University, College Station, TX 77843, USA.
Plants (Basel). 2024 Feb 28;13(5):664. doi: 10.3390/plants13050664.
Industrial hemp L. is an economically important crop mostly grown for its fiber, oil, and seeds. Due to its increasing applications in the pharmaceutical industry and a lack of knowledge of gene functions in cannabinoid biosynthesis pathways, developing an efficient transformation platform for the genetic engineering of industrial hemp has become necessary to enable functional genomic and industrial application studies. A critical step in the development of -mediated transformation in the hemp genus is the establishment of optimal conditions for T-DNA gene delivery into different explants from which whole plantlets can be regenerated. As a first step in the development of a successful -mediated transformation method for hemp gene editing, the factors influencing the successful T-DNA integration and expression (as measured by transient (GUS) and Green Florescent Protein (GFP) expression) were investigated. In this study, the parameters for an agroinfiltration system in hemp, which applies to the stable transformation method, were optimized. In the present study, we tested different explants, such as 1- to 3-week-old leaves, cotyledons, hypocotyls, root segments, nodal parts, and 2- to 3-week-old leaf-derived calli. We observed that the 3-week-old leaves were the best explant for transient gene expression. Fully expanded 2- to 3-week-old leaf explants, in combination with 30 min of immersion time, 60 µM silver nitrate, 0.5 µM calcium chloride, 150 µM natural phenolic compound acetosyringone, and a bacterial density of OD = 0.4 resulted in the highest GUS and GFP expression. The improved method of genetic transformation established in the present study will be useful for the introduction of foreign genes of interest, using the latest technologies such as genome editing, and studying gene functions that regulate secondary metabolites in hemp.
工业大麻是一种具有重要经济价值的作物,主要因其纤维、油和种子而种植。由于其在制药行业的应用日益增加,且人们对大麻素生物合成途径中的基因功能缺乏了解,因此开发一个高效的工业大麻遗传转化平台对于开展功能基因组学和工业应用研究变得十分必要。在大麻属植物中,农杆菌介导转化发展的关键步骤是建立将T-DNA基因导入不同外植体并使其再生出完整植株的最佳条件。作为开发成功的大麻基因编辑农杆菌介导转化方法的第一步,研究了影响T-DNA成功整合和表达的因素(通过瞬时β-葡萄糖醛酸酶(GUS)和绿色荧光蛋白(GFP)表达来衡量)。在本研究中,对适用于稳定转化方法的大麻农杆菌浸润系统的参数进行了优化。在本研究中,我们测试了不同的外植体,如1至3周龄的叶片、子叶、下胚轴、根段、节段以及2至3周龄的叶片来源愈伤组织。我们观察到3周龄的叶片是瞬时基因表达的最佳外植体。完全展开的2至3周龄叶片外植体,结合30分钟的浸泡时间、60μM硝酸银、0.5μM氯化钙、150μM天然酚类化合物乙酰丁香酮以及OD = 0.4的细菌密度,可导致最高的GUS和GFP表达。本研究中建立的改进的遗传转化方法将有助于利用基因组编辑等最新技术引入感兴趣的外源基因,并研究调节大麻次生代谢产物的基因功能。