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Efficient Genome Editing Using CRISPR/Cas9 Technology in Chicory.

Identifieur interne : 000122 ( Main/Exploration ); précédent : 000121; suivant : 000123

Efficient Genome Editing Using CRISPR/Cas9 Technology in Chicory.

Auteurs : Guillaume Bernard [France] ; David Gagneul [France] ; Harmony Alves Dos Santos [France] ; Audrey Etienne [France] ; Jean-Louis Hilbert [France] ; Caroline Rambaud [France]

Source :

RBID : pubmed:30845784

Descripteurs français

English descriptors

Abstract

CRISPR/Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR associated with protein CAS9) is a genome-editing tool that has been extensively used in the last five years because of its novelty, affordability, and feasibility. This technology has been developed in many plant species for gene function analysis and crop improvement but has never been used in chicory (Cichorium intybus L.). In this study, we successfully applied CRISPR/Cas9-mediated targeted mutagenesis to chicory using Agrobacterium rhizogenes-mediated transformation and protoplast transfection methods. A U6 promoter (CiU6-1p) among eight predicted U6 promoters in chicory was selected to drive sgRNA expression. A binary vector designed to induce targeted mutations in the fifth exon of the chicory phytoene desaturase gene (CiPDS) was then constructed and used to transform chicory. The mutation frequency was 4.5% with the protoplast transient expression system and 31.25% with A. rhizogenes-mediated stable transformation. Biallelic mutations were detected in all the mutant plants. The use of A. rhizogenes-mediated transformation seems preferable as the regeneration of plants is faster and the mutation frequency was shown to be higher. With both transformation methods, foreign DNA was integrated in the plant genome. Hence, selection of vector (transgene)-free segregants is required. Our results showed that genome editing with CRISPR/Cas9 system can be efficiently used with chicory, which should facilitate and accelerate genetic improvement and functional biology.

DOI: 10.3390/ijms20051155
PubMed: 30845784
PubMed Central: PMC6429391


Affiliations:


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Le document en format XML

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<term>Agrobacterium (physiology)</term>
<term>CRISPR-Cas Systems (MeSH)</term>
<term>Chicory (genetics)</term>
<term>Chicory (microbiology)</term>
<term>Gene Editing (methods)</term>
<term>Mutation (MeSH)</term>
<term>Oxidoreductases (genetics)</term>
<term>Plant Proteins (genetics)</term>
<term>Promoter Regions, Genetic (MeSH)</term>
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<term>Agrobacterium (physiologie)</term>
<term>Chicorée (génétique)</term>
<term>Chicorée (microbiologie)</term>
<term>Mutation (MeSH)</term>
<term>Oxidoreductases (génétique)</term>
<term>Protéines végétales (génétique)</term>
<term>Régions promotrices (génétique) (MeSH)</term>
<term>Systèmes CRISPR-Cas (MeSH)</term>
<term>Édition de gène (méthodes)</term>
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<term>Oxidoreductases</term>
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<div type="abstract" xml:lang="en">CRISPR/Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR associated with protein CAS9) is a genome-editing tool that has been extensively used in the last five years because of its novelty, affordability, and feasibility. This technology has been developed in many plant species for gene function analysis and crop improvement but has never been used in chicory (
<i>Cichorium intybus</i>
L.). In this study, we successfully applied CRISPR/Cas9-mediated targeted mutagenesis to chicory using
<i>Agrobacterium rhizogenes</i>
-mediated transformation and protoplast transfection methods. A
<i>U6</i>
promoter (
<i>CiU6</i>
-1p) among eight predicted
<i>U6</i>
promoters in chicory was selected to drive sgRNA expression. A binary vector designed to induce targeted mutations in the fifth exon of the chicory
<i>phytoene desaturase</i>
gene
<i>(CiPDS)</i>
was then constructed and used to transform chicory. The mutation frequency was 4.5% with the protoplast transient expression system and 31.25% with
<i>A. rhizogenes</i>
-mediated stable transformation. Biallelic mutations were detected in all the mutant plants. The use of
<i>A. rhizogenes</i>
-mediated transformation seems preferable as the regeneration of plants is faster and the mutation frequency was shown to be higher. With both transformation methods, foreign DNA was integrated in the plant genome. Hence, selection of vector (transgene)-free segregants is required. Our results showed that genome editing with CRISPR/Cas9 system can be efficiently used with chicory, which should facilitate and accelerate genetic improvement and functional biology.</div>
</front>
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<AbstractText>CRISPR/Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR associated with protein CAS9) is a genome-editing tool that has been extensively used in the last five years because of its novelty, affordability, and feasibility. This technology has been developed in many plant species for gene function analysis and crop improvement but has never been used in chicory (
<i>Cichorium intybus</i>
L.). In this study, we successfully applied CRISPR/Cas9-mediated targeted mutagenesis to chicory using
<i>Agrobacterium rhizogenes</i>
-mediated transformation and protoplast transfection methods. A
<i>U6</i>
promoter (
<i>CiU6</i>
-1p) among eight predicted
<i>U6</i>
promoters in chicory was selected to drive sgRNA expression. A binary vector designed to induce targeted mutations in the fifth exon of the chicory
<i>phytoene desaturase</i>
gene
<i>(CiPDS)</i>
was then constructed and used to transform chicory. The mutation frequency was 4.5% with the protoplast transient expression system and 31.25% with
<i>A. rhizogenes</i>
-mediated stable transformation. Biallelic mutations were detected in all the mutant plants. The use of
<i>A. rhizogenes</i>
-mediated transformation seems preferable as the regeneration of plants is faster and the mutation frequency was shown to be higher. With both transformation methods, foreign DNA was integrated in the plant genome. Hence, selection of vector (transgene)-free segregants is required. Our results showed that genome editing with CRISPR/Cas9 system can be efficiently used with chicory, which should facilitate and accelerate genetic improvement and functional biology.</AbstractText>
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