National Key Laboratory of Plant Molecular Genetics, CAS Center for Excellence in Molecular Plant Sciences, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Science, Shanghai 200032, China.
Department of Plant and Soil Sciences and Kentucky Tobacco Research and Development Center, University of Kentucky, Lexington, KY 40546, USA.
Int J Mol Sci. 2019 Sep 23;20(19):4702. doi: 10.3390/ijms20194702.
CRISPR/Cas9-mediated genome editing is a powerful technology that has been used for the genetic modification of a number of crop species. In order to evaluate the efficacy of CRISPR/Cas9 technology in the root crop, sweet potato (), two starch biosynthetic pathway genes, (encoding granule-bound starch synthase I), and (encoding starch branching enzyme II), were targeted in the starch-type cultivar Xushu22 and carotenoid-rich cultivar Taizhong6. was transformed using a binary vector, in which the gene is driven by the AtUBQ promoter and the guide RNA is controlled by the AtU6 promoter. A total of 72 Xushu22 and 35 Taizhong6 transgenic lines were generated and analyzed for mutations. The mutation efficiency was 62-92% with multi-allelic mutations in both cultivars. Most of the mutations were nucleotide substitutions that lead to amino acid changes and, less frequently, stop codons. In addition, short nucleotide insertions or deletions were also found in both and . Furthermore, a 2658 bp deletion was found in one transgenic line. The total starch contents were not significantly changed in - and -knockout transgenic lines compared to the wild-type control. However, in the allopolyploid sweet potato, the -knockout reduced, while the -knockout increased, the amylose percentage. Our results demonstrate that CRISPR/Cas9 technology is an effective tool for the improvement of starch qualities in sweet potato and breeding of polyploid root crops.
CRISPR/Cas9 介导的基因组编辑是一种强大的技术,已被用于许多作物物种的遗传修饰。为了评估 CRISPR/Cas9 技术在块根作物甘薯中的功效,我们靶向了淀粉生物合成途径的两个基因,[encoding granule-bound starch synthase I](编码颗粒结合淀粉合成酶 I)和[encoding starch branching enzyme II](编码淀粉分支酶 II),在淀粉型品种 Xushu22 和富含类胡萝卜素的品种 Taizhong6 中。使用二元载体转化了[encoding starch branching enzyme II],其中[encoding granule-bound starch synthase I]基因由 AtUBQ 启动子驱动,而向导 RNA 由 AtU6 启动子控制。共生成了 72 个 Xushu22 和 35 个 Taizhong6 转基因株系,并对其进行了突变分析。在两个品种中,突变效率为 62-92%,存在多等位基因突变。大多数突变是导致氨基酸变化的核苷酸取代,较少情况下是终止密码子。此外,在[encoding granule-bound starch synthase I]和[encoding starch branching enzyme II]中也发现了短核苷酸插入或缺失。此外,在一个[encoding granule-bound starch synthase I]转基因株系中发现了 2658bp 的缺失。与野生型对照相比,-和-敲除转基因株系的总淀粉含量没有显著变化。然而,在异源多倍体甘薯中,-敲除降低了直链淀粉百分比,而-敲除增加了直链淀粉百分比。我们的结果表明,CRISPR/Cas9 技术是改良甘薯淀粉品质和培育多倍体块根作物的有效工具。