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Optimization of CRISPR/Cas9 genome editing in cotton by improved sgRNA expression
BACKGROUND: When developing CRISPR/Cas9 systems for crops, it is crucial to invest time characterizing the genome editing efficiency of the CRISPR/Cas9 cassettes, especially if the transformation system is difficult or time-consuming. Cotton is an important crop for the production of fiber, oil, and...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169012/ https://www.ncbi.nlm.nih.gov/pubmed/30305839 http://dx.doi.org/10.1186/s13007-018-0353-0 |
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author | Long, Lu Guo, Dan-Dan Gao, Wei Yang, Wen-Wen Hou, Li-Pan Ma, Xiao-Nan Miao, Yu-Chen Botella, Jose Ramon Song, Chun-Peng |
author_facet | Long, Lu Guo, Dan-Dan Gao, Wei Yang, Wen-Wen Hou, Li-Pan Ma, Xiao-Nan Miao, Yu-Chen Botella, Jose Ramon Song, Chun-Peng |
author_sort | Long, Lu |
collection | PubMed |
description | BACKGROUND: When developing CRISPR/Cas9 systems for crops, it is crucial to invest time characterizing the genome editing efficiency of the CRISPR/Cas9 cassettes, especially if the transformation system is difficult or time-consuming. Cotton is an important crop for the production of fiber, oil, and biofuel. However, the cotton stable transformation is usually performed using Agrobacterium tumefaciens taking between 8 and 12 months to generate T(0) plants. Furthermore, cotton is a heterotetraploid and targeted mutagenesis is considered to be difficult as many genes are duplicated in this complex genome. The application of CRISPR/Cas9 in cotton is severely hampered by the long and technically challenging genetic transformation process, making it imperative to maximize its efficiency. RESULTS: In this study, we provide a new system to evaluate and validate the efficiency of CRISPR/Cas9 cassettes in cotton using a transient expression system. By using this system, we could select the most effective CRISPR/Cas9 cassettes before the stable transformation. We have also optimized the existing cotton CRISPR/Cas9 system to achieve vastly improved mutagenesis efficiency by incorporating an endogenous GhU6 promoter that increases sgRNA expression levels over the Arabidopsis AtU6-29 promoter. The 300 bp GhU6.3 promoter was cloned and validated using the transient expression system. When sgRNAs were expressed under the control of the GhU6.3 promoter in CRISPR/Cas9 cassettes, expression levels were 6–7 times higher than those provided by the AtU6-29 promoter and CRISPR/Cas9-mediated mutation efficiency was improved 4–6 times. CONCLUSIONS: This study provides essential improvements to maximize CRISPR/Cas9-mediated mutation efficiency by reducing risk and workload for the application of CRISPR/Cas9 approaches in the targeted mutagenesis of cotton. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-018-0353-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6169012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61690122018-10-10 Optimization of CRISPR/Cas9 genome editing in cotton by improved sgRNA expression Long, Lu Guo, Dan-Dan Gao, Wei Yang, Wen-Wen Hou, Li-Pan Ma, Xiao-Nan Miao, Yu-Chen Botella, Jose Ramon Song, Chun-Peng Plant Methods Methodology BACKGROUND: When developing CRISPR/Cas9 systems for crops, it is crucial to invest time characterizing the genome editing efficiency of the CRISPR/Cas9 cassettes, especially if the transformation system is difficult or time-consuming. Cotton is an important crop for the production of fiber, oil, and biofuel. However, the cotton stable transformation is usually performed using Agrobacterium tumefaciens taking between 8 and 12 months to generate T(0) plants. Furthermore, cotton is a heterotetraploid and targeted mutagenesis is considered to be difficult as many genes are duplicated in this complex genome. The application of CRISPR/Cas9 in cotton is severely hampered by the long and technically challenging genetic transformation process, making it imperative to maximize its efficiency. RESULTS: In this study, we provide a new system to evaluate and validate the efficiency of CRISPR/Cas9 cassettes in cotton using a transient expression system. By using this system, we could select the most effective CRISPR/Cas9 cassettes before the stable transformation. We have also optimized the existing cotton CRISPR/Cas9 system to achieve vastly improved mutagenesis efficiency by incorporating an endogenous GhU6 promoter that increases sgRNA expression levels over the Arabidopsis AtU6-29 promoter. The 300 bp GhU6.3 promoter was cloned and validated using the transient expression system. When sgRNAs were expressed under the control of the GhU6.3 promoter in CRISPR/Cas9 cassettes, expression levels were 6–7 times higher than those provided by the AtU6-29 promoter and CRISPR/Cas9-mediated mutation efficiency was improved 4–6 times. CONCLUSIONS: This study provides essential improvements to maximize CRISPR/Cas9-mediated mutation efficiency by reducing risk and workload for the application of CRISPR/Cas9 approaches in the targeted mutagenesis of cotton. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-018-0353-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-03 /pmc/articles/PMC6169012/ /pubmed/30305839 http://dx.doi.org/10.1186/s13007-018-0353-0 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Long, Lu Guo, Dan-Dan Gao, Wei Yang, Wen-Wen Hou, Li-Pan Ma, Xiao-Nan Miao, Yu-Chen Botella, Jose Ramon Song, Chun-Peng Optimization of CRISPR/Cas9 genome editing in cotton by improved sgRNA expression |
title | Optimization of CRISPR/Cas9 genome editing in cotton by improved sgRNA expression |
title_full | Optimization of CRISPR/Cas9 genome editing in cotton by improved sgRNA expression |
title_fullStr | Optimization of CRISPR/Cas9 genome editing in cotton by improved sgRNA expression |
title_full_unstemmed | Optimization of CRISPR/Cas9 genome editing in cotton by improved sgRNA expression |
title_short | Optimization of CRISPR/Cas9 genome editing in cotton by improved sgRNA expression |
title_sort | optimization of crispr/cas9 genome editing in cotton by improved sgrna expression |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169012/ https://www.ncbi.nlm.nih.gov/pubmed/30305839 http://dx.doi.org/10.1186/s13007-018-0353-0 |
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