Confalonieri Massimo, Carelli Maria, Gianoglio Silvia, Moglia Andrea, Biazzi Elisa, Tava Aldo
Council for Agricultural Research and Economics, Research Centre for Animal Production and Aquaculture, Lodi, Italy.
Department of Agricultural, Forest and Food Sciences, Plant Genetics and Breeding, University of Torino, Grugliasco, Italy.
Front Plant Sci. 2021 Jul 26;12:690231. doi: 10.3389/fpls.2021.690231. eCollection 2021.
In the genus, triterpene saponins are a group of bioactive compounds extensively studied for their different biological and pharmaceutical properties. In this work, the CRISPR/Cas9-based approach with two single-site guide RNAs was used in (barrel medic) to knock-out the and genes, which are responsible for the biosynthesis of soyasapogenol B, the most abundant soyasapogenol in spp. No transgenic plants carrying mutations in the target gene were recovered while fifty-two putative mutant plant lines were obtained following -mediated transformation. Among these, the fifty-one sequenced plant lines give an editing efficiency of 84%. Sequencing revealed that these lines had various mutation patterns at the target sites. Four T0 mutant plant lines were further selected and examined for their sapogenin content and plant growth performance under greenhouse conditions. The results showed that all tested knock-out mutants did not produce soyasapogenols in the leaves, stems and roots, and diverted the metabolic flux toward the production of valuable hemolytic sapogenins. No adverse influence was observed on the plant morphological features of mutants under greenhouse conditions. In addition, differential expression of saponin pathway genes was observed in mutants in comparison to the control. Our results provide new and interesting insights into the application of CRISPR/Cas9 for metabolic engineering of high-value compounds of plant origin and will be useful to investigate the physiological functions of saponins .
在该属中,三萜皂苷是一类生物活性化合物,因其不同的生物学和药学特性而受到广泛研究。在这项工作中,使用基于CRISPR/Cas9的方法和两个单导向RNA在(桶状苜蓿)中敲除和基因,这两个基因负责大豆皂醇B的生物合成,大豆皂醇B是苜蓿属植物中含量最丰富的大豆皂醇。未获得在目标基因中携带突变的转基因植物,而在介导的转化后获得了52个推定的突变株系。其中,51个测序株系的编辑效率为84%。测序显示这些株系在目标位点具有各种突变模式。进一步选择了4个T0突变株系,并在温室条件下检测了它们的皂角苷元含量和植物生长性能。结果表明,所有测试的敲除突变体在叶、茎和根中均不产生大豆皂醇,并将代谢通量转向有价值的溶血皂角苷元的产生。在温室条件下,未观察到突变体的植物形态特征受到不利影响。此外,与对照相比,在突变体中观察到皂苷途径基因的差异表达。我们的结果为CRISPR/Cas9在植物源高价值化合物代谢工程中的应用提供了新的有趣见解,并将有助于研究皂苷的生理功能。