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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
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.
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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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