Improve Research Reproducibility A Bio-protocol resource
Peer-reviewed
tooltip

Use of Geminivirus for Delivery of CRISPR/Cas9 Components to Tobacco by Agro-infiltration

通过农杆菌浸润法使用双生病毒将CRISPR/Cas9组分转入烟草中

Kangquan Yin Kangquan Yin
TH Ting Han
Yule Liu Yule Liu

发布: 2017年04月05日第7卷第7期 DOI: 10.21769/BioProtoc.2209 浏览次数: 16050

评审: Rainer MelzerKaisa KajalaAnonymous reviewer(s)

download pdf PDF PDF
ask Q&A
引用
收藏
Cited by

参见作者原研究论文

The authors used this protocol in:

Cover of Scientific Reports, featuring study using the protocol.

Oct 2015

Advertisement

Technologies for RNA Detection
Special Issue on Protocols for Organoid Research
“科研可重复性与创新”系列网络研讨会
Presubmission Inquiry

实验方案合集

专注于特定技术或应用的、详细的、经过同行评审的实验方案合集

Cancer Research
Immunology
Developmental Biology
Microbiology
Neuroscience
Cell Imaging - A Special Collection for Cell Bio 2023
查看更多 more

相关实验方案

利用分裂可选择标记的植物转化新型基因叠加方法

利用分裂可选择标记的植物转化新型基因叠加方法

Guoliang Yuan [...] Xiaohan Yang

2025年02月20日 2221 阅读

利用RUBY可视化报告系统的快速大豆毛状根转化方法

利用RUBY可视化报告系统的快速大豆毛状根转化方法

Zhirui Zhang [...] Jiuhai Zhao

2026年03月20日 765 阅读

一种用于在杨树中高效构建大片段缺失的双 gRNA CRISPR/Cas9 系统

一种用于在杨树中高效构建大片段缺失的双 gRNA CRISPR/Cas9 系统

Guoqian Yang [...] Chang-Jun Liu

2026年07月05日 208 阅读

Abstract

CRISPR/Cas9 system is a recently developed genome editing tool, and its power has been demonstrated in many organisms, including some plant species (Wang et al., 2016). In eukaryotes, the Cas9/gRNA complexes target genome sites specifically and cleave them to produce double-strand breaks (DSBs), which can be repaired by non-homologous end joining (NHEJ) pathway (Wang et al., 2016). Since NHEJ is error prone, mutations are thus generated. In plants, delivery of genome editing reagents is still challenging. In this protocol, we detail the procedure of a virus-based gRNA delivery system for CRISPR/Cas9 mediated plant genome editing (VIGE). This method offers a rapid and efficient way to deliver gRNA into plant cells, especially for those that are recalcitrant to transformation with Agrobacterium.

Keywords: CRISPR (CRISPR) search Cas9 (Cas9) search Geminivirus (双生病毒) search VIGE (VIGE) search Genome editing (基因组编辑) search Tobacco (烟草) search

Background

Genome editing technologies based on viruses have been reported using deconstructed DNA viruses and an RNA virus (Baltes et al., 2014; Ali et al., 2015). Recently, we used a full geminivirus - Cabbage Leaf Curl virus (CaLCuV) (a bipartite begomovirus which infects a wide range of members of the Brassicaceae, including cauliflower) for highly efficient genome editing in one of its hosts, Nicotiana benthamiana, for the first time (Yin et al., 2015).

Materials and Reagents

  1. 1-ml syringe
  2. 0.22-μm filter
  3. Wild type N. benthamiana plants; six to eight-leaf stage transgenic N. benthamiana plants stably expressing oCas9 (Arabidopsis codon optimized Cas9) - KQ334 plant
  4. Agrobacterium tumefaciens strain GV3101, E. coli DH5α, E. coli DB3.1 (for propagating vectors pJG081)
  5. The following plasmids are required: pJG081, pKQ334 (Yin et al., 2015), pT-U6p-scaffold-U6t (Yin et al., 2015), pCAMBIA1301, pCAMBIA2300 (www.cambia.org), pCVA (Tang et al., 2010), pCVB (Tang et al., 2010), and pMD18-T vector (Takara Bio, catalog number: D101A) 
    Notes:
    1. To generate a construct for constitutive expression of oCas9, oCas9 is PCR amplified and subsequently cloned into pJG081 by ligation independent cloning (LIC) technique (Aslanidis and de Jong, 1990) to generate pKQ334.
    2. pKQ334 is then used to transform N. benthamiana to generate Cas9 transgenic plant - KQ334 plant. pKQ334 can also be used in transient expression of Cas9 in N. benthamiana.
    3. The pT-U6p-scaffold-U6t is used to generate p-T-U6p-gRNA-scaffold containing gRNA of the target gene by PCR mutagenesis.
    4. pCVA and pCVB are CaLCuV-based T-DNA vectors. pCVA is used to generate pCVA-gRNA or pCVA-scaffold. pCVB is used in combination with pCVA or its derivatives to generate CaLCuV. pMD18-T vector is used to clone PCR amplicons.
    5. These vectors can be obtained by contacting Dr. Yule Liu.
  6. Primers (Table 1)

    Table 1. Primers used in this protocol


  7. TransStart FastPfu DNA polymerase (Beijing TransGen Biotech, catalog number: AP221 )
  8. Restriction enzymes (New England Biolabs, stored at -20 °C)
    1. DpnI (New England Biolabs, catalog number: R0176 )
    2. ApaI (New England Biolabs, catalog number: R0114 )
    3. SacI (New England Biolabs, catalog number: R0156 )
    4. PstI (New England Biolabs, catalog number: R3140S )
    5. KpnI (New England Biolabs, catalog number: R3142S )
    6. XbaI (New England Biolabs, catalog number: R0145S )
    7. MlyI (New England Biolabs, catalog number: R0610 )
  9. 10x Cutsmart buffer
  10. Antibiotics
    Ampicillin (AMRESCO, catalog number: 0339 )
    Kanamycin (AMRESCO, catalog number: 0408 )
    Rifampicin (Sigma-Aldrich, catalog number: R3501 )
  11. TIANprep Mini Plasmid Kit (TIANGEN Biotech, catalog number: DP103 ) for plasmid DNA extraction
  12. Ethanol (Beijing Chemical Factory, catalog number: B0301002 )
  13. T4 DNA polymerase (Thermo Fisher Scientific, Thermo ScientificTM, catalog number: EP0062 )
  14. dATP (Takara Bio, catalog number: 4026 )
  15. Chloroform (Sigma-Aldrich, catalog number: 1601383 )
  16. Phenol (Sigma-Aldrich, catalog number: P4557 )
  17. 3 M NaAc (Biovision, catalog number: 2118 )
  18. dTTP (Takara Bio, catalog number: 4029 )
  19. DNA Purification Kit (BioMED, catalog number: DH103-01 )
  20. T4 DNA ligase (Takara Bio, catalog number: 2011A )
  21. Tryptone (BD, BactoTM, catalog number: 211705 )
  22. Yeast extract (BD, BactoTM, catalog number: 212750 )
  23. Sodium chloride (NaCl) (Sigma-Aldrich, catalog number: 31434 )
  24. Magnesium chloride hexahydrate (MgCl2·6H2O) (Sigma-Aldrich, catalog number: M7304 )
  25. MES (Sigma-Aldrich, catalog number: M3671 )
  26. Potassium hydroxide (KOH)
  27. Acetosyringone (Solarbio, catalog number: A8110-1 )
  28. DMSO
  29. Sodium phosphate monobasic (NaH2PO4) (Sigma-Aldrich, catalog number: S3139 )
  30. Sodium phosphate dibasic (Na2HPO4) (Sigma-Aldrich, catalog number: S3264 )
  31. Sodium phosphate monobasic (NaH2PO4) (AMRESCO, catalog number: 0571 )
  32. Sodium phosphate dibasic (Na2HPO4) (AMRESCO, catalog number: 0404 )
  33. Sodium phosphate monobasic monohydrate (NaH2PO4·H2O)
  34. Sodium phosphate dibasic heptahydrate (Na2HPO4·7H2O)
  35. X-gluc (AMRESCO, catalog number: 0919 )
  36. Methanol (Beijing Chemical Factory, catalog number: B0301005 )
  37. Potassium ferricyanide (AMRESCO, catalog number: 0713 )
  38. Triton X-100 (Sigma-Aldrich, catalog number: T9284 )
  39. PEG 8000 (Sigma-Aldrich, catalog number: 89510 )
  40. Magnesium chloride hexahydrate (MgCl2·6H2O) (AMRESCO, catalog number: 0288 )
  41. Magnesium chloride hexahydrate (MgCl2·6H2O) (Sigma-Aldrich, catalog number: 63068 )
  42. MES (Sigma-Aldrich, catalog number: M3671 )
  43. Acetosyringone (Sigma-Aldrich, catalog number: D134406 )
  44. EasyTaq DNA polymerase (Beijing TransGen Biotech, catalog number: AP111 )
  45. DNAsecure Plant Kit (TIANGEN Biotech, catalog number: DP320 ) for genomic DNA extraction
  46. Luria-Bertani medium (see Recipes)
  47. MgCl2 (1 M stock) (see Recipes)
  48. MES (0.5 M stock) (see Recipes)
  49. Acetosyringone (1 M stock) (see Recipes)
  50. Infiltration buffer (see Recipes)
  51. 2x phosphate buffer (pH 7) (see Recipes)
  52. X-gluc substrate solution (see Recipes)
  53. PEG-MgCl2 solution (see Recipes)

Equipment

  1. Microcentrifuge (Eppendorf)
  2. PCR cycler (Bio-Rad Laboratories)
  3. 37 °C and 28 °C incubator; 37 °C and 28 °C shaker
  4. NanoDrop 1000 spectrophotometer (Thermo Fisher Scientific, model: NanoDrop 1000 ) (for measuring the concentration of the DNA)
  5. Electrophoresis apparatus (Junyi, Beijing)
  6. Vacuum apparatus (WILMAD-LABGLASS)
  7. Glass/plastic beaker
  8. Autoclave

Software

  1. ImageJ (https://imagej.nih.gov/ij)

Procedure

English
中文翻译

文章信息

版权信息

© 2017 The Authors; exclusive licensee Bio-protocol LLC.

如何引用

Yin, K., Han, T. and Liu, Y. (2017). Use of Geminivirus for Delivery of CRISPR/Cas9 Components to Tobacco by Agro-infiltration. Bio-protocol 7(7): e2209. DOI: 10.21769/BioProtoc.2209.

ris ris Download Citation in RIS Format

分类

植物科学 > 植物转化 > 农杆菌介导的转化方法

分子生物学 > DNA > 转化

分子生物学 > DNA > DNA 克隆

您对这篇实验方法有问题吗？

在此处发布您的问题，我们将邀请本文作者来回答。同时，我们会将您的问题发布到Bio-protocol Exchange，以便寻求社区成员的帮助。

post 发布问题
0 Q&A
pen 提交稿件