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CRISPR-Cas9-Mediated Genomic Deletions Protocol in Zebrafish

Since its first application for site-directed mutagenesis, the CRISPR-Cas9 system has revolutionized genome engineering. Here, we present a validated workflow for the generation of targeted genomic deletions in zebrafish, including the design, cloning, and synthesis of single-guide RNAs and Cas9 mRN...

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Autores principales: Amorim, João Pedro, Bordeira-Carriço, Renata, Gali-Macedo, Ana, Perrod, Chiara, Bessa, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757680/
https://www.ncbi.nlm.nih.gov/pubmed/33377102
http://dx.doi.org/10.1016/j.xpro.2020.100208
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author Amorim, João Pedro
Bordeira-Carriço, Renata
Gali-Macedo, Ana
Perrod, Chiara
Bessa, José
author_facet Amorim, João Pedro
Bordeira-Carriço, Renata
Gali-Macedo, Ana
Perrod, Chiara
Bessa, José
author_sort Amorim, João Pedro
collection PubMed
description Since its first application for site-directed mutagenesis, the CRISPR-Cas9 system has revolutionized genome engineering. Here, we present a validated workflow for the generation of targeted genomic deletions in zebrafish, including the design, cloning, and synthesis of single-guide RNAs and Cas9 mRNA, followed by microinjection in zebrafish embryos and subsequent genotype screening for the establishment of a mutant line. The versatility and efficiency of this pipeline makes the generation of zebrafish models a widely used approach in functional genetics. For complete details on the use and execution of this protocol, please refer to Amorim et al. (2020).
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spelling pubmed-77576802020-12-28 CRISPR-Cas9-Mediated Genomic Deletions Protocol in Zebrafish Amorim, João Pedro Bordeira-Carriço, Renata Gali-Macedo, Ana Perrod, Chiara Bessa, José STAR Protoc Protocol Since its first application for site-directed mutagenesis, the CRISPR-Cas9 system has revolutionized genome engineering. Here, we present a validated workflow for the generation of targeted genomic deletions in zebrafish, including the design, cloning, and synthesis of single-guide RNAs and Cas9 mRNA, followed by microinjection in zebrafish embryos and subsequent genotype screening for the establishment of a mutant line. The versatility and efficiency of this pipeline makes the generation of zebrafish models a widely used approach in functional genetics. For complete details on the use and execution of this protocol, please refer to Amorim et al. (2020). Elsevier 2020-12-10 /pmc/articles/PMC7757680/ /pubmed/33377102 http://dx.doi.org/10.1016/j.xpro.2020.100208 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Amorim, João Pedro
Bordeira-Carriço, Renata
Gali-Macedo, Ana
Perrod, Chiara
Bessa, José
CRISPR-Cas9-Mediated Genomic Deletions Protocol in Zebrafish
title CRISPR-Cas9-Mediated Genomic Deletions Protocol in Zebrafish
title_full CRISPR-Cas9-Mediated Genomic Deletions Protocol in Zebrafish
title_fullStr CRISPR-Cas9-Mediated Genomic Deletions Protocol in Zebrafish
title_full_unstemmed CRISPR-Cas9-Mediated Genomic Deletions Protocol in Zebrafish
title_short CRISPR-Cas9-Mediated Genomic Deletions Protocol in Zebrafish
title_sort crispr-cas9-mediated genomic deletions protocol in zebrafish
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757680/
https://www.ncbi.nlm.nih.gov/pubmed/33377102
http://dx.doi.org/10.1016/j.xpro.2020.100208
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