| 基于CRISPR/Cas9核糖核蛋白体DNA定点内切酶体外活性建立高效基因型分析技术 |
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| 引用本文： | 王南,祁显涛,刘昌林,谢传晓,朱金洁. 基于CRISPR/Cas9核糖核蛋白体DNA定点内切酶体外活性建立高效基因型分析技术[J]. 作物学报, 2020, 46(7): 978-986. DOI: 10.3724/SP.J.1006.2020.93064 |
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| 作者姓名： | 王南 祁显涛 刘昌林 谢传晓 朱金洁 |
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| 作者单位： | 1. 中国农业科学院作物科学研究所;2. 安徽农业大学 |
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| 基金项目： | National Major Project of Developing New GM Crops(2019ZX08010-003) |
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| 摘 要： | 建立快速、准确、高通量与简便易行的基因型分析技术对基因功能解析、分子育种与突变体鉴定研究具有重要价值。本研究的目标是利用Cas9或Cas9NG变体与单分子指导RNA (single guide RNA, sgRNA)核糖核蛋白复合体(sgRNA/Cas9-RNP或sgRNA/Cas9NG-RNP)体外DNA定点内切酶活性,建立与优化简便高效与低成本的基因型分析技术。以我们前期创制的CRISPR/Cas9定点编辑玉米ZmWx基因第7外显子区域定点突变基因编辑后代分离群体为材料,以ZmWx靶位点两侧特异引物扩增的PCR产物为底物,利用原核表达并纯化的Cas9或Cas9-NG蛋白为DNA内切酶,以体外转录的靶向ZmWx基因靶点的sgRNA或骨架序列优化的sgRNA(enhancedsgRNA,esgRNA)为Cas9或Cas9-NG酶定点活性指导元件,通过体外组装为sgRNA/Cas9-RNP复合体,对目标样本迚行酶切,以区分目标位点野生型、纯合突变体、杂合突变体基因型,并对反应体系迚行了优化。研究表明,基于esgRNA/Cas9的PCR/RNP检测技术可对ZmWx基因编辑目标突变体后代迚行...
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| 关 键 词： | sgRNA/Cas9核糖核蛋白复合体 Cas9NG 优化sgRNA (esgRNA) 基因型分析 突变体筛选 |
| 收稿时间： | 2019-12-18 |
Establishment of an efficient genotyping technique based on targeted DNA endonuclease in vitro activity of CRISPR/Cas9 ribonucleoprotein |
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| WANG Nan,QI Xian-Tao,LIU Chang-Lin,XIE Chuan-Xiao,ZHU Jin-Jie. Establishment of an efficient genotyping technique based on targeted DNA endonuclease in vitro activity of CRISPR/Cas9 ribonucleoprotein[J]. Acta Agronomica Sinica, 2020, 46(7): 978-986. DOI: 10.3724/SP.J.1006.2020.93064 |
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| Authors: | WANG Nan QI Xian-Tao LIU Chang-Lin XIE Chuan-Xiao ZHU Jin-Jie |
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| Affiliation: | 1. Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China;2. Anhui Agricultural University, Hefei 230036, Anhui, China |
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| Abstract: | Establishing a rapid, accurate, high-throughput and easily implementable genotyping method is highly desirable for functional genomics, genetic improvement and mutant screening. Here, we describe a convenient and inexpensive technique for genotyping using the targeted DNA endonuclease activity of Cas9 or Cas9NG ribonucleoproteins complex (sgRNA/Cas9-RNP or sgRNA/Cas9NG-RNP). In this study, Cas9 and Cas9NG protein purified from E. coli extract was assembled with in vitro transcribed single guide RNA (sgRNA)or enhanced sgRNA (esgRNA) as an assembled ribonucleoprotein (RNP) complex to fulfill the targeted endonuclease activity on the PCR amplicons of ZmWx exon 7. The restriction profiles can be converted into genotyping results of wildtype, homozygous or heterozygous mutant, respectively. Our data showed that ZmWx gene-edited mutants can be genotyped rapidly and efficiently by the sgRNA-optimized system esgRNA/Cas9. The reaction component optimization data suggested that 500 ng of DNA substrates could be cleavaged completely by incubating with 1 μg 1:1 molar ratio of esgRNA/Cas9 ribonucleoproteins for 30 minutes at 37℃, or by 4 μg 1:1 molar ratio of esgRNA/Cas9NG ribonucleoproteins for 4 hours at 37℃. Expanding the targeting flexibility of mutant detection via esgRNA/Cas9NG indicated that Cas9NG variant might recognize relax NG PAM (protospacer-adjacent-motif, PAM) at the expense of decreasing restriction activity, which is necessary to improve the activity of esgRNA/Cas9NG by further optimization. Therefore, the establishment and application of esgRNA/Cas9 based PCR/RNP technique provides an easy, simple and low-cost approach to genotyping in functional genomics, molecular breeding and mutant screening. In addition, our in vitro data on esgRNA/Cas9NG has certain and significant reference value for developing it into in vivo genome editing studies. |
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| Keywords: | sgRNA/Cas9 ribonucleoprotein complex Cas9NG enhanced single guide RNA (esgRNA) genotyping mutant screening |
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