Moa Key Lab of Soybean Biology (Beijing), National Key Facility of Crop Gene Resource and Genetic Improvement, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
The Key Laboratory of Plant Resources Conservation and Germplasm Innovation in the Mountainous Region (Ministry of Education), Institute of Agro-Bioengineering, Guizhou University, Guiyang 550025, China.
Int J Mol Sci. 2022 Oct 14;23(20):12261. doi: 10.3390/ijms232012261.
The stable genetic transformation of soybean is time-consuming and inefficient. As a simple and practical alternative method, hairy root transformation mediated by is widely applied in studying root-specific processes, nodulation, biochemical and molecular functions of genes of interest, gene editing efficiency of CRISPR/Cas9, and biological reactors and producers. Therefore, many laboratories have developed unique protocols to obtain hairy roots in composite plants composed of transgenic roots and wild-type shoots. However, these protocols still suffer from the shortcomings of low efficiency and time, space, and cost consumption. To address this issue, we developed a new protocol efficient regeneration and transformation of hairy roots (eR&T) in soybean, by integrating and optimizing the main current methods to achieve high efficiency in both hairy root regeneration and transformation within a shorter period and using less space. By this eR&T method, we obtained 100% regeneration of hairy roots for all explants, with an average 63.7% of transformation frequency, which promoted the simultaneous and comparative analysis of the function of several genes. The eR&T was experimentally verified reporters, protein subcellular localization, and CRISPR/Cas9 gene editing experiments. Employing this approach, we identified several novel potential regulators of nodulation, and nucleoporins of the Nup107-160 sub-complex, which showed development-dependent and tissue-dependent expression patterns, indicating their important roles in nodulation in soybean. Thus, the new eR&T method is an efficient and economical approach for investigating not only root and nodule biology, but also gene function.
大豆的稳定遗传转化既耗时又低效。作为一种简单实用的替代方法,农杆菌介导的毛状根转化广泛应用于研究根特异过程、结瘤、感兴趣基因的生化和分子功能、CRISPR/Cas9 的基因编辑效率、生物反应器和生物发生器。因此,许多实验室已经开发了独特的方案,以获得由转基因根和野生型茎组成的复合植物中的毛状根。然而,这些方案仍然存在效率低、时间长、空间和成本消耗大等缺点。为了解决这个问题,我们开发了一种新的大豆毛状根高效再生和转化(eR&T)方案,通过整合和优化主要方法,实现在更短的时间内以更高的效率进行毛状根再生和转化,并减少空间和成本的消耗。通过这种 eR&T 方法,我们实现了所有外植体的毛状根 100%再生,转化频率平均为 63.7%,促进了几个基因功能的同时和比较分析。该 eR&T 已在报告基因、蛋白质亚细胞定位和 CRISPR/Cas9 基因编辑实验中得到验证。利用该方法,我们鉴定了几个潜在的结瘤调节因子和 Nup107-160 亚复合物的核孔蛋白,它们表现出发育依赖性和组织依赖性表达模式,表明它们在大豆结瘤中起着重要作用。因此,新的 eR&T 方法是一种高效、经济的方法,不仅可以研究根和根瘤生物学,还可以研究基因功能。