| 引用本文: | 曾婉俐, 梁 岗, 高 茜, 李元川, 许 力, 蒋佳芮, 许 永, 向海英.烟草香气相关基因CRISPR/Cas9编辑突变体库的构建[J].广西植物,2024,44(7):1278-1288.[点击复制] |
| ZENG Wanli, LIANG Gang, GAO Qian, LI Yuanchuan, XU Li,
JIANG Jiarui, XU Yong, XIANG Haiying.Construction of a mutant library associated with aroma genes in tobacco using CRISPR/Cas9[J].Guihaia,2024,44(7):1278-1288.[点击复制] |
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| 烟草香气相关基因CRISPR/Cas9编辑突变体库的构建 |
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曾婉俐1, 梁 岗2, 高 茜1, 李元川3, 许 力1, 蒋佳芮1, 许 永1, 向海英1*
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1. 云南中烟工业有限责任公司技术中心, 云南省烟草化学重点实验室, 昆明 650231;2. 中国科学院西双版纳热带植物园,
热带植物资源可持续利用重点实验室, 昆明 650223;3. 云南农业大学, 昆明 650201
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| 摘要: |
| 为探究CRISPR/Cas9基因编辑技术构建烟草突变体库的可行性,该研究以烤烟品种‘红花大金元'为实验材料筛选了100个可能参与烟草香气代谢的基因,设计相应的100个sgRNA并构建了由100个CRISPR/Cas9编辑载体组成的质粒库,获得转基因材料后分析了载体的共转化率、靶向编辑率和脱靶编辑情况。结果表明:(1)通过农杆菌介导100个sgRNA的共转化后,在172个阳性转化株中检测到了其中的77个sgRNA,共转化率为77%。(2)在77个携带sgRNA的转基因后代中,69个sgRNA对目标基因进行了靶向编辑,编辑率为89.6%。(3)脱靶位点测序检测发现,只有1个sgRNA在非目标靶位点产生了脱靶编辑,表明CRISPR/Cas9基因编辑技术在烟草中的脱靶概率非常低。综上所述,利用CRISPR/Cas9载体库共转化对烟草基因进行高通量靶向编辑以构建突变体库的方法切实可行,并且该方法有共转化率高、编辑率高和脱靶编辑概率低等特点。 |
| 关键词: 烟草, CRISPR/Cas9, 烟草香气, 靶向编辑, 脱靶编辑 |
| DOI：10.11931/guihaia.gxzw202306050 |
| 分类号:Q943 |
| 文章编号:1000-3142(2024)07-1278-11 |
| 基金项目:云南省烟草化学重点实验室开放课题(2021539200340248); 中国烟草总公司重大科技项目(110202101034[JY-11])。 |
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| Construction of a mutant library associated with aroma genes in tobacco using CRISPR/Cas9 |
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ZENG Wanli1, LIANG Gang2, GAO Qian1, LI Yuanchuan3, XU Li1,
JIANG Jiarui1, XU Yong1, XIANG Haiying1*
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1. Yunnan Key Laboratory of Tobacco Chemistry, R &2.D Center of China Tobacco Yunnan Industrial Co., Ltd., Kunming 650231, China;3.2. CAS Key Laboratory of Tropical Plant Resources and Sustainable Use, Xishuangbanna Tropical Botanical Garden, Chinese Academy
of Sciences, Kunming 650223, China;4.3. Yunnan Agricultural University, Kunming 650201, China
1. Yunnan Key Laboratory of Tobacco Chemistry, R & D Center of China Tobacco Yunnan Industrial Co., Ltd., Kunming 650231, China;
2. CAS Key Laboratory of Tropical Plant Resources and Sustainable Use, Xishuangbanna Tropical Botanical Garden, Chinese Academy
of Sciences, Kunming 650223, China; 3. Yunnan Agricultural University, Kunming 650201, China
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| Abstract: |
| To explore the feasibility of constructing a tobacco mutant library using the CRISPR/Cas9 gene editing technology, we designed sgRNAs of 100 aroma related genes in tobacco, constructed a plasmid library composed of 100 corresponding CRISPR/Cas9 editing vectors, and analyzed the co-transformation rate, on-target editing rate, and off-target editing of transgenic offspring using the tobacco variety ‘Honghua Dajinyuan' as experimental material in this study. The results were as follows:(1)After co-transformation of 100 sgRNAs mediated by Agrobacterium tumefaciens, 77 of them were detected in 172 positive transformation strains, with a co-transformation rate of 77%.(2)Among 77 transgenic offspring carrying sgRNA, 69 sgRNAs edited the target genes, with an editing rate of 89.6%.(3)Sequencing detection revealed that only one sgRNA produced off-target editing at a non-target site, indicating a very low probability of off-target editing of CRISPR/Cas9 in tobacco. In summary, it is feasible to construct a mutant library by the co-transformation of a CRISPR/Cas9 vector library to edit a large number of candidate target genes in tobacco. This method has the characteristics of high co-transformation rate, high editing rate, and low probability of off-target editing. |
| Key words: tobacco, CRISPR/Cas9, tabacco aroma, on-target editing, off-target editing |
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