Zhang Ling, Wang Yingzhe, Li Tong, Qiu Hongmei, Xia Zhengjun, Dong Yingshan
Jilin Provincial Key Laboratory of Agricultural Biotechnology, Jilin Academy of Agricultural Sciences, Changchun, 130033, Jilin, China.
Northeast Institute of Geography and Agroecology, The Innovative Academy of Seed Design, Chinese Academy of Sciences, Harbin, China.
Transgenic Res. 2021 Feb;30(1):51-62. doi: 10.1007/s11248-020-00228-5. Epub 2021 Jan 2.
Soybean has a palaeopolyploid genome with nearly 75% of the genes present in multiple copies. Although the CRISPR/Cas9 system has been employed in soybean to generate site-directed mutagenesis, a systematical assessment of mutation efficiency of the CRISPR/Cas9 system for the multiple-copy genes is still urgently needed. Here, we successfully optimize one sgRNA CRISPR/Cas9 system in soybean by testing the efficiency, pattern, specificity of the mutations at multiple loci of GmFAD2 and GmALS. The results showed that simultaneous site-directed mutagenesis of two homoeologous loci by one sgRNA, the mutation frequency in the T0 generation were 64.71% for GmPDS, 60.0% for GmFAD2 and 42.86% for GmALS, respectively. The chimeric and heterozygous mutations were dominant types. Moreover, association of phenotypes with mutation pattern at target loci of GmPDS11 and GmPDS18 could help us further demonstrate that the CRISPR/Cas9 system can efficiently generate target specific mutations at multiple loci using one sgRNA in soybean, albeit with a relatively low transformation efficiency.
大豆具有古多倍体基因组,近75%的基因以多拷贝形式存在。尽管CRISPR/Cas9系统已被用于大豆中以产生定点诱变,但仍迫切需要对CRISPR/Cas9系统针对多拷贝基因的突变效率进行系统评估。在此,我们通过测试GmFAD2和GmALS多个位点的突变效率、模式和特异性,成功优化了大豆中的单sgRNA CRISPR/Cas9系统。结果表明,通过一个sgRNA对两个同源位点进行同时定点诱变,在T0代中,GmPDS的突变频率为64.71%,GmFAD2为60.0%,GmALS为42.86%。嵌合和杂合突变是主要类型。此外,GmPDS11和GmPDS18靶位点的表型与突变模式的关联可以帮助我们进一步证明,CRISPR/Cas9系统能够在大豆中使用一个sgRNA在多个位点高效产生靶向特异性突变,尽管转化效率相对较低。