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The GB4.0 Platform, an All-In-One Tool for CRISPR/Cas-Based Multiplex Genome Engineering in Plants
CRISPR/Cas ability to target several loci simultaneously (multiplexing) is a game-changer in plant breeding. Multiplexing not only accelerates trait pyramiding but also can unveil traits hidden by functional redundancy. Furthermore, multiplexing enhances dCas-based programmable gene expression and e...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284049/ https://www.ncbi.nlm.nih.gov/pubmed/34276739 http://dx.doi.org/10.3389/fpls.2021.689937 |
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author | Vazquez-Vilar, Marta Garcia-Carpintero, Víctor Selma, Sara Bernabé-Orts, Joan M. Sanchez-Vicente, Javier Salazar-Sarasua, Blanca Ressa, Arianna de Paola, Carmine Ajenjo, María Quintela, Jose Carlos Fernández-del-Carmen, Asun Granell, Antonio Orzáez, Diego |
author_facet | Vazquez-Vilar, Marta Garcia-Carpintero, Víctor Selma, Sara Bernabé-Orts, Joan M. Sanchez-Vicente, Javier Salazar-Sarasua, Blanca Ressa, Arianna de Paola, Carmine Ajenjo, María Quintela, Jose Carlos Fernández-del-Carmen, Asun Granell, Antonio Orzáez, Diego |
author_sort | Vazquez-Vilar, Marta |
collection | PubMed |
description | CRISPR/Cas ability to target several loci simultaneously (multiplexing) is a game-changer in plant breeding. Multiplexing not only accelerates trait pyramiding but also can unveil traits hidden by functional redundancy. Furthermore, multiplexing enhances dCas-based programmable gene expression and enables cascade-like gene regulation. However, the design and assembly of multiplex constructs comprising tandemly arrayed guide RNAs (gRNAs) requires scarless cloning and is still troublesome due to the presence of repetitive sequences, thus hampering a more widespread use. Here we present a comprehensive extension of the software-assisted cloning platform GoldenBraid (GB), in which, on top of its multigene cloning software, we integrate new tools for the Type IIS-based easy and rapid assembly of up to six tandemly-arrayed gRNAs with both Cas9 and Cas12a, using the gRNA-tRNA-spaced and the crRNA unspaced approaches, respectively. As stress tests for the new tools, we assembled and used for Agrobacterium-mediated stable transformation a 17 Cas9-gRNAs construct targeting a subset of the Squamosa-Promoter Binding Protein-Like (SPL) gene family in Nicotiana tabacum. The 14 selected genes are targets of miR156, thus potentially playing an important role in juvenile-to-adult and vegetative-to-reproductive phase transitions. With the 17 gRNAs construct we generated a collection of Cas9-free SPL edited T(1) plants harboring up to 9 biallelic mutations and showing leaf juvenility and more branching. The functionality of GB-assembled dCas9 and dCas12a-based CRISPR/Cas activators and repressors using single and multiplexing gRNAs was validated using a Luciferase reporter with the Solanum lycopersicum Mtb promoter or the Agrobacterium tumefaciens nopaline synthase promoter in transient expression in Nicotiana benthamiana. With the incorporation of the new web-based tools and the accompanying collection of DNA parts, the GB4.0 genome edition turns an all-in-one open platform for plant genome engineering. |
format | Online Article Text |
id | pubmed-8284049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82840492021-07-17 The GB4.0 Platform, an All-In-One Tool for CRISPR/Cas-Based Multiplex Genome Engineering in Plants Vazquez-Vilar, Marta Garcia-Carpintero, Víctor Selma, Sara Bernabé-Orts, Joan M. Sanchez-Vicente, Javier Salazar-Sarasua, Blanca Ressa, Arianna de Paola, Carmine Ajenjo, María Quintela, Jose Carlos Fernández-del-Carmen, Asun Granell, Antonio Orzáez, Diego Front Plant Sci Plant Science CRISPR/Cas ability to target several loci simultaneously (multiplexing) is a game-changer in plant breeding. Multiplexing not only accelerates trait pyramiding but also can unveil traits hidden by functional redundancy. Furthermore, multiplexing enhances dCas-based programmable gene expression and enables cascade-like gene regulation. However, the design and assembly of multiplex constructs comprising tandemly arrayed guide RNAs (gRNAs) requires scarless cloning and is still troublesome due to the presence of repetitive sequences, thus hampering a more widespread use. Here we present a comprehensive extension of the software-assisted cloning platform GoldenBraid (GB), in which, on top of its multigene cloning software, we integrate new tools for the Type IIS-based easy and rapid assembly of up to six tandemly-arrayed gRNAs with both Cas9 and Cas12a, using the gRNA-tRNA-spaced and the crRNA unspaced approaches, respectively. As stress tests for the new tools, we assembled and used for Agrobacterium-mediated stable transformation a 17 Cas9-gRNAs construct targeting a subset of the Squamosa-Promoter Binding Protein-Like (SPL) gene family in Nicotiana tabacum. The 14 selected genes are targets of miR156, thus potentially playing an important role in juvenile-to-adult and vegetative-to-reproductive phase transitions. With the 17 gRNAs construct we generated a collection of Cas9-free SPL edited T(1) plants harboring up to 9 biallelic mutations and showing leaf juvenility and more branching. The functionality of GB-assembled dCas9 and dCas12a-based CRISPR/Cas activators and repressors using single and multiplexing gRNAs was validated using a Luciferase reporter with the Solanum lycopersicum Mtb promoter or the Agrobacterium tumefaciens nopaline synthase promoter in transient expression in Nicotiana benthamiana. With the incorporation of the new web-based tools and the accompanying collection of DNA parts, the GB4.0 genome edition turns an all-in-one open platform for plant genome engineering. Frontiers Media S.A. 2021-07-01 /pmc/articles/PMC8284049/ /pubmed/34276739 http://dx.doi.org/10.3389/fpls.2021.689937 Text en Copyright © 2021 Vazquez-Vilar, Garcia-Carpintero, Selma, Bernabé-Orts, Sanchez-Vicente, Salazar-Sarasua, Ressa, de Paola, Ajenjo, Quintela, Fernández-del-Carmen, Granell and Orzáez. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Vazquez-Vilar, Marta Garcia-Carpintero, Víctor Selma, Sara Bernabé-Orts, Joan M. Sanchez-Vicente, Javier Salazar-Sarasua, Blanca Ressa, Arianna de Paola, Carmine Ajenjo, María Quintela, Jose Carlos Fernández-del-Carmen, Asun Granell, Antonio Orzáez, Diego The GB4.0 Platform, an All-In-One Tool for CRISPR/Cas-Based Multiplex Genome Engineering in Plants |
title | The GB4.0 Platform, an All-In-One Tool for CRISPR/Cas-Based Multiplex Genome Engineering in Plants |
title_full | The GB4.0 Platform, an All-In-One Tool for CRISPR/Cas-Based Multiplex Genome Engineering in Plants |
title_fullStr | The GB4.0 Platform, an All-In-One Tool for CRISPR/Cas-Based Multiplex Genome Engineering in Plants |
title_full_unstemmed | The GB4.0 Platform, an All-In-One Tool for CRISPR/Cas-Based Multiplex Genome Engineering in Plants |
title_short | The GB4.0 Platform, an All-In-One Tool for CRISPR/Cas-Based Multiplex Genome Engineering in Plants |
title_sort | gb4.0 platform, an all-in-one tool for crispr/cas-based multiplex genome engineering in plants |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284049/ https://www.ncbi.nlm.nih.gov/pubmed/34276739 http://dx.doi.org/10.3389/fpls.2021.689937 |
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