CRISPR/Cas9 for potato functional genomics and breeding

Cultivated potato (Solanum tuberosum L.) is one of the most important staple food crops worldwide. Its tetraploid and highly heterozygous nature pose a great challenge to its basic research and trait improvement through traditional mutagenesis and/or crossbreeding. The establishment of the clustered...

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Main Authors: Gonzalez, Matías Nicolás, Massa, Gabriela Alejandra, Andersson, Mariette, Storani, Leonardo, Olsson, Niklas, Decima Oneto, Cecilia Andrea, Hofvander, Per, Feingold, Sergio Enrique
Format: Capítulo de libro
Language:Inglés
Published: Humana Press (Springer) 2024
Subjects:
Online Access:http://hdl.handle.net/20.500.12123/17657
https://link.springer.com/protocol/10.1007/978-1-0716-3131-7_21
https://doi.org/10.1007/978-1-0716-3131-7_21
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author Gonzalez, Matías Nicolás
Massa, Gabriela Alejandra
Andersson, Mariette
Storani, Leonardo
Olsson, Niklas
Decima Oneto, Cecilia Andrea
Hofvander, Per
Feingold, Sergio Enrique
author_browse Andersson, Mariette
Decima Oneto, Cecilia Andrea
Feingold, Sergio Enrique
Gonzalez, Matías Nicolás
Hofvander, Per
Massa, Gabriela Alejandra
Olsson, Niklas
Storani, Leonardo
author_facet Gonzalez, Matías Nicolás
Massa, Gabriela Alejandra
Andersson, Mariette
Storani, Leonardo
Olsson, Niklas
Decima Oneto, Cecilia Andrea
Hofvander, Per
Feingold, Sergio Enrique
author_sort Gonzalez, Matías Nicolás
collection INTA Digital
description Cultivated potato (Solanum tuberosum L.) is one of the most important staple food crops worldwide. Its tetraploid and highly heterozygous nature pose a great challenge to its basic research and trait improvement through traditional mutagenesis and/or crossbreeding. The establishment of the clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated protein 9 (Cas9) as a gene-editing tool has allowed the alteration of specific gene sequences and their concomitant gene function, providing powerful technology for potato gene functional analysis and improvement of elite cultivars. This technology relies on a short RNA molecule called single guide RNA (sgRNA) that directs the Cas9 nuclease to induce a site-specific double-stranded break (DSB). Further, repair of the DSB by the error-prone non-homologous end joining (NHEJ) mechanism, leads to the introduction of targeted mutations, which can be used to produce the loss of function of specific gene/s. In this chapter, we describe experimental procedures to apply the CRISPR/Cas9 technology for potato genome editing. First, we provide strategies for target selection and sgRNA design and describe a Golden Gate-based cloning system to obtain a sgRNA/Cas9-encoding binary vector. We also describe an optimized protocol for ribonucleoprotein complexes (RNP) assembly. The binary vector can be used for both Agrobacterium-mediated transformation and transient expression in potato protoplasts, while the RNP complexes are intended to obtain edited potato lines through protoplast transfection and plant regeneration. Finally, we describe procedures to identify the gene-edited potato lines. The methods described here are suitable for potato gene functional analysis and breeding.
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spelling INTA176572024-05-08T11:28:39Z CRISPR/Cas9 for potato functional genomics and breeding Gonzalez, Matías Nicolás Massa, Gabriela Alejandra Andersson, Mariette Storani, Leonardo Olsson, Niklas Decima Oneto, Cecilia Andrea Hofvander, Per Feingold, Sergio Enrique Papa Edición de Genes Genómica Funcional Agrobacterium tumefaciens Proteínas Mejoramiento Genético Potatoes Gene Editing Functional Genomics Proteins Genetic Improvement CRISPR Repeticiones Palindrómicas Cortas Agrupadas y Regularmente Interespaciadas Cultivated potato (Solanum tuberosum L.) is one of the most important staple food crops worldwide. Its tetraploid and highly heterozygous nature pose a great challenge to its basic research and trait improvement through traditional mutagenesis and/or crossbreeding. The establishment of the clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated protein 9 (Cas9) as a gene-editing tool has allowed the alteration of specific gene sequences and their concomitant gene function, providing powerful technology for potato gene functional analysis and improvement of elite cultivars. This technology relies on a short RNA molecule called single guide RNA (sgRNA) that directs the Cas9 nuclease to induce a site-specific double-stranded break (DSB). Further, repair of the DSB by the error-prone non-homologous end joining (NHEJ) mechanism, leads to the introduction of targeted mutations, which can be used to produce the loss of function of specific gene/s. In this chapter, we describe experimental procedures to apply the CRISPR/Cas9 technology for potato genome editing. First, we provide strategies for target selection and sgRNA design and describe a Golden Gate-based cloning system to obtain a sgRNA/Cas9-encoding binary vector. We also describe an optimized protocol for ribonucleoprotein complexes (RNP) assembly. The binary vector can be used for both Agrobacterium-mediated transformation and transient expression in potato protoplasts, while the RNP complexes are intended to obtain edited potato lines through protoplast transfection and plant regeneration. Finally, we describe procedures to identify the gene-edited potato lines. The methods described here are suitable for potato gene functional analysis and breeding. EEA Balcarce Fil: González, Matías Nicolás Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Balcarce; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Instituto de Innovación para la Producción Agropecuaria y el Desarrollo Sostenible Balcarce; Argentina Fil: Massa, Gabriela Alejandra. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Balcarce; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Instituto de Innovación para la Producción Agropecuaria y el Desarrollo Sostenible Balcarce; Argentina Fil: Massa, Gabriela Alejandra. Universidad Nacional de Mar del Plata. Facultad de Ciencias Agrarias; Argentina Fil: Andersson, Mariette. Swedish University Of Agricultural Sciences; Suecia Fil: Storani, Leonardo. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Balcarce; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Instituto de Innovación para la Producción Agropecuaria y el Desarrollo Sostenible Balcarce; Argentina Fil: Olsson, Niklas. Swedish University Of Agricultural Sciences; Suecia Fil: Décima Oneto, Cecilia Andrea. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Balcarce; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Instituto de Innovación para la Producción Agropecuaria y el Desarrollo Sostenible Balcarce; Argentina Fil: Décima Oneto, Cecilia Andrea.Universidad Nacional de Mar del Plata. Facultad de Ciencias Agrarias; Argentina Fil: Hofvander, Per. Swedish University Of Agricultural Sciences; Suecia Fil: Feingold, Sergio. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Balcarce; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Instituto de Innovación para la Producción Agropecuaria y el Desarrollo Sostenible Balcarce; Argentina 2024-05-08T11:14:58Z 2024-05-08T11:14:58Z 2023-03-31 info:ar-repo/semantics/parte de libro info:eu-repo/semantics/bookPart info:eu-repo/semantics/publishedVersion http://hdl.handle.net/20.500.12123/17657 https://link.springer.com/protocol/10.1007/978-1-0716-3131-7_21 978-1-0716-3130-0 978-1-0716-3131-7 https://doi.org/10.1007/978-1-0716-3131-7_21 eng info:eu-repo/semantics/restrictedAccess http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) application/pdf Humana Press (Springer) Plant Genome engineering / Yang, B.; Harwood, W.; Que, Q. (editors). New York: Humana Press, 2023. Chapter 21, p. 333-361
spellingShingle Papa
Edición de Genes
Genómica Funcional
Agrobacterium tumefaciens
Proteínas
Mejoramiento Genético
Potatoes
Gene Editing
Functional Genomics
Proteins
Genetic Improvement
CRISPR
Repeticiones Palindrómicas Cortas Agrupadas y Regularmente Interespaciadas
Gonzalez, Matías Nicolás
Massa, Gabriela Alejandra
Andersson, Mariette
Storani, Leonardo
Olsson, Niklas
Decima Oneto, Cecilia Andrea
Hofvander, Per
Feingold, Sergio Enrique
CRISPR/Cas9 for potato functional genomics and breeding
title CRISPR/Cas9 for potato functional genomics and breeding
title_full CRISPR/Cas9 for potato functional genomics and breeding
title_fullStr CRISPR/Cas9 for potato functional genomics and breeding
title_full_unstemmed CRISPR/Cas9 for potato functional genomics and breeding
title_short CRISPR/Cas9 for potato functional genomics and breeding
title_sort crispr cas9 for potato functional genomics and breeding
topic Papa
Edición de Genes
Genómica Funcional
Agrobacterium tumefaciens
Proteínas
Mejoramiento Genético
Potatoes
Gene Editing
Functional Genomics
Proteins
Genetic Improvement
CRISPR
Repeticiones Palindrómicas Cortas Agrupadas y Regularmente Interespaciadas
url http://hdl.handle.net/20.500.12123/17657
https://link.springer.com/protocol/10.1007/978-1-0716-3131-7_21
https://doi.org/10.1007/978-1-0716-3131-7_21
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