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Efficient CRISPR/Cas9-based genome editing in carrot cells
KEY MESSAGE: The first report presenting successful and efficient carrot genome editing using CRISPR/Cas9 system. ABSTRACT: Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated (Cas9) is a powerful genome editing tool that has been widely adopted in model organisms re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852178/ https://www.ncbi.nlm.nih.gov/pubmed/29332168 http://dx.doi.org/10.1007/s00299-018-2252-2 |
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author | Klimek-Chodacka, Magdalena Oleszkiewicz, Tomasz Lowder, Levi G. Qi, Yiping Baranski, Rafal |
author_facet | Klimek-Chodacka, Magdalena Oleszkiewicz, Tomasz Lowder, Levi G. Qi, Yiping Baranski, Rafal |
author_sort | Klimek-Chodacka, Magdalena |
collection | PubMed |
description | KEY MESSAGE: The first report presenting successful and efficient carrot genome editing using CRISPR/Cas9 system. ABSTRACT: Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated (Cas9) is a powerful genome editing tool that has been widely adopted in model organisms recently, but has not been used in carrot—a model species for in vitro culture studies and an important health-promoting crop grown worldwide. In this study, for the first time, we report application of the CRISPR/Cas9 system for efficient targeted mutagenesis of the carrot genome. Multiplexing CRISPR/Cas9 vectors expressing two single-guide RNA (gRNAs) targeting the carrot flavanone-3-hydroxylase (F3H) gene were tested for blockage of the anthocyanin biosynthesis in a model purple-colored callus using Agrobacterium-mediated genetic transformation. This approach allowed fast and visual comparison of three codon-optimized Cas9 genes and revealed that the most efficient one in generating F3H mutants was the Arabidopsis codon-optimized AteCas9 gene with up to 90% efficiency. Knockout of F3H gene resulted in the discoloration of calli, validating the functional role of this gene in the anthocyanin biosynthesis in carrot as well as providing a visual marker for screening successfully edited events. Most resulting mutations were small Indels, but long chromosome fragment deletions of 116–119 nt were also generated with simultaneous cleavage mediated by two gRNAs. The results demonstrate successful site-directed mutagenesis in carrot with CRISPR/Cas9 and the usefulness of a model callus culture to validate genome editing systems. Given that the carrot genome has been sequenced recently, our timely study sheds light on the promising application of genome editing tools for boosting basic and translational research in this important vegetable crop. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00299-018-2252-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5852178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-58521782018-03-21 Efficient CRISPR/Cas9-based genome editing in carrot cells Klimek-Chodacka, Magdalena Oleszkiewicz, Tomasz Lowder, Levi G. Qi, Yiping Baranski, Rafal Plant Cell Rep Original Article KEY MESSAGE: The first report presenting successful and efficient carrot genome editing using CRISPR/Cas9 system. ABSTRACT: Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated (Cas9) is a powerful genome editing tool that has been widely adopted in model organisms recently, but has not been used in carrot—a model species for in vitro culture studies and an important health-promoting crop grown worldwide. In this study, for the first time, we report application of the CRISPR/Cas9 system for efficient targeted mutagenesis of the carrot genome. Multiplexing CRISPR/Cas9 vectors expressing two single-guide RNA (gRNAs) targeting the carrot flavanone-3-hydroxylase (F3H) gene were tested for blockage of the anthocyanin biosynthesis in a model purple-colored callus using Agrobacterium-mediated genetic transformation. This approach allowed fast and visual comparison of three codon-optimized Cas9 genes and revealed that the most efficient one in generating F3H mutants was the Arabidopsis codon-optimized AteCas9 gene with up to 90% efficiency. Knockout of F3H gene resulted in the discoloration of calli, validating the functional role of this gene in the anthocyanin biosynthesis in carrot as well as providing a visual marker for screening successfully edited events. Most resulting mutations were small Indels, but long chromosome fragment deletions of 116–119 nt were also generated with simultaneous cleavage mediated by two gRNAs. The results demonstrate successful site-directed mutagenesis in carrot with CRISPR/Cas9 and the usefulness of a model callus culture to validate genome editing systems. Given that the carrot genome has been sequenced recently, our timely study sheds light on the promising application of genome editing tools for boosting basic and translational research in this important vegetable crop. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00299-018-2252-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-01-13 2018 /pmc/articles/PMC5852178/ /pubmed/29332168 http://dx.doi.org/10.1007/s00299-018-2252-2 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. |
spellingShingle | Original Article Klimek-Chodacka, Magdalena Oleszkiewicz, Tomasz Lowder, Levi G. Qi, Yiping Baranski, Rafal Efficient CRISPR/Cas9-based genome editing in carrot cells |
title | Efficient CRISPR/Cas9-based genome editing in carrot cells |
title_full | Efficient CRISPR/Cas9-based genome editing in carrot cells |
title_fullStr | Efficient CRISPR/Cas9-based genome editing in carrot cells |
title_full_unstemmed | Efficient CRISPR/Cas9-based genome editing in carrot cells |
title_short | Efficient CRISPR/Cas9-based genome editing in carrot cells |
title_sort | efficient crispr/cas9-based genome editing in carrot cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852178/ https://www.ncbi.nlm.nih.gov/pubmed/29332168 http://dx.doi.org/10.1007/s00299-018-2252-2 |
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