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Implementing the CRISPR/Cas9 Technology in Eucalyptus Hairy Roots Using Wood-Related Genes

Eucalypts are the most planted hardwoods worldwide. The availability of the Eucalyptus grandis genome highlighted many genes awaiting functional characterization, lagging behind because of the lack of efficient genetic transformation protocols. In order to efficiently generate knock-out mutants to s...

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Autores principales: Dai, Ying, Hu, Guojian, Dupas, Annabelle, Medina, Luciano, Blandels, Nils, San Clemente, Hélène, Ladouce, Nathalie, Badawi, Myriam, Hernandez-Raquet, Guillermina, Mounet, Fabien, Grima-Pettenati, Jacqueline, Cassan-Wang, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7279396/
https://www.ncbi.nlm.nih.gov/pubmed/32408486
http://dx.doi.org/10.3390/ijms21103408
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author Dai, Ying
Hu, Guojian
Dupas, Annabelle
Medina, Luciano
Blandels, Nils
San Clemente, Hélène
Ladouce, Nathalie
Badawi, Myriam
Hernandez-Raquet, Guillermina
Mounet, Fabien
Grima-Pettenati, Jacqueline
Cassan-Wang, Hua
author_facet Dai, Ying
Hu, Guojian
Dupas, Annabelle
Medina, Luciano
Blandels, Nils
San Clemente, Hélène
Ladouce, Nathalie
Badawi, Myriam
Hernandez-Raquet, Guillermina
Mounet, Fabien
Grima-Pettenati, Jacqueline
Cassan-Wang, Hua
author_sort Dai, Ying
collection PubMed
description Eucalypts are the most planted hardwoods worldwide. The availability of the Eucalyptus grandis genome highlighted many genes awaiting functional characterization, lagging behind because of the lack of efficient genetic transformation protocols. In order to efficiently generate knock-out mutants to study the function of eucalypts genes, we implemented the powerful CRISPR/Cas9 gene editing technology with the hairy roots transformation system. As proofs-of-concept, we targeted two wood-related genes: Cinnamoyl-CoA Reductase1 (CCR1), a key lignin biosynthetic gene and IAA9A an auxin dependent transcription factor of Aux/IAA family. Almost all transgenic hairy roots were edited but the allele-editing rates and spectra varied greatly depending on the gene targeted. Most edition events generated truncated proteins, the prevalent edition types were small deletions but large deletions were also quite frequent. By using a combination of FT-IR spectroscopy and multivariate analysis (partial least square analysis (PLS-DA)), we showed that the CCR1-edited lines, which were clearly separated from the controls. The most discriminant wave-numbers were attributed to lignin. Histochemical analyses further confirmed the decreased lignification and the presence of collapsed vessels in CCR1-edited lines, which are characteristics of CCR1 deficiency. Although the efficiency of editing could be improved, the method described here is already a powerful tool to functionally characterize eucalypts genes for both basic research and industry purposes.
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spelling pubmed-72793962020-06-17 Implementing the CRISPR/Cas9 Technology in Eucalyptus Hairy Roots Using Wood-Related Genes Dai, Ying Hu, Guojian Dupas, Annabelle Medina, Luciano Blandels, Nils San Clemente, Hélène Ladouce, Nathalie Badawi, Myriam Hernandez-Raquet, Guillermina Mounet, Fabien Grima-Pettenati, Jacqueline Cassan-Wang, Hua Int J Mol Sci Article Eucalypts are the most planted hardwoods worldwide. The availability of the Eucalyptus grandis genome highlighted many genes awaiting functional characterization, lagging behind because of the lack of efficient genetic transformation protocols. In order to efficiently generate knock-out mutants to study the function of eucalypts genes, we implemented the powerful CRISPR/Cas9 gene editing technology with the hairy roots transformation system. As proofs-of-concept, we targeted two wood-related genes: Cinnamoyl-CoA Reductase1 (CCR1), a key lignin biosynthetic gene and IAA9A an auxin dependent transcription factor of Aux/IAA family. Almost all transgenic hairy roots were edited but the allele-editing rates and spectra varied greatly depending on the gene targeted. Most edition events generated truncated proteins, the prevalent edition types were small deletions but large deletions were also quite frequent. By using a combination of FT-IR spectroscopy and multivariate analysis (partial least square analysis (PLS-DA)), we showed that the CCR1-edited lines, which were clearly separated from the controls. The most discriminant wave-numbers were attributed to lignin. Histochemical analyses further confirmed the decreased lignification and the presence of collapsed vessels in CCR1-edited lines, which are characteristics of CCR1 deficiency. Although the efficiency of editing could be improved, the method described here is already a powerful tool to functionally characterize eucalypts genes for both basic research and industry purposes. MDPI 2020-05-12 /pmc/articles/PMC7279396/ /pubmed/32408486 http://dx.doi.org/10.3390/ijms21103408 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dai, Ying
Hu, Guojian
Dupas, Annabelle
Medina, Luciano
Blandels, Nils
San Clemente, Hélène
Ladouce, Nathalie
Badawi, Myriam
Hernandez-Raquet, Guillermina
Mounet, Fabien
Grima-Pettenati, Jacqueline
Cassan-Wang, Hua
Implementing the CRISPR/Cas9 Technology in Eucalyptus Hairy Roots Using Wood-Related Genes
title Implementing the CRISPR/Cas9 Technology in Eucalyptus Hairy Roots Using Wood-Related Genes
title_full Implementing the CRISPR/Cas9 Technology in Eucalyptus Hairy Roots Using Wood-Related Genes
title_fullStr Implementing the CRISPR/Cas9 Technology in Eucalyptus Hairy Roots Using Wood-Related Genes
title_full_unstemmed Implementing the CRISPR/Cas9 Technology in Eucalyptus Hairy Roots Using Wood-Related Genes
title_short Implementing the CRISPR/Cas9 Technology in Eucalyptus Hairy Roots Using Wood-Related Genes
title_sort implementing the crispr/cas9 technology in eucalyptus hairy roots using wood-related genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7279396/
https://www.ncbi.nlm.nih.gov/pubmed/32408486
http://dx.doi.org/10.3390/ijms21103408
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