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One-step CRISPR-Cas9 protocol for the generation of plug & play conditional knockouts in Drosophila melanogaster

This one-step method generates, for any locus, a conditional knockout allele in Drosophila. The allele carries a bright fluorescent marker for easy screening and an attP landing site for subsequent genetic manipulations. After removing the selectable marker with Cre, the attP site can be used to ins...

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Detalles Bibliográficos
Autores principales: Yu, Joyce J.S., Vincent, Jean-Paul, McGough, Ian J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165570/
https://www.ncbi.nlm.nih.gov/pubmed/34095868
http://dx.doi.org/10.1016/j.xpro.2021.100560
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author Yu, Joyce J.S.
Vincent, Jean-Paul
McGough, Ian J.
author_facet Yu, Joyce J.S.
Vincent, Jean-Paul
McGough, Ian J.
author_sort Yu, Joyce J.S.
collection PubMed
description This one-step method generates, for any locus, a conditional knockout allele in Drosophila. The allele carries a bright fluorescent marker for easy screening and an attP landing site for subsequent genetic manipulations. After removing the selectable marker with Cre, the attP site can be used to insert DNA fragments expressing tagged or mutant alleles to determine protein localization and function in a tissue- and stage-specific manner. Only a single round of CRISPR-Cas9-mediated editing is required. For complete details on the use and execution of this protocol, please refer to the DWnt4[cKO] example in Yu et al. (2020).
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spelling pubmed-81655702021-06-05 One-step CRISPR-Cas9 protocol for the generation of plug & play conditional knockouts in Drosophila melanogaster Yu, Joyce J.S. Vincent, Jean-Paul McGough, Ian J. STAR Protoc Protocol This one-step method generates, for any locus, a conditional knockout allele in Drosophila. The allele carries a bright fluorescent marker for easy screening and an attP landing site for subsequent genetic manipulations. After removing the selectable marker with Cre, the attP site can be used to insert DNA fragments expressing tagged or mutant alleles to determine protein localization and function in a tissue- and stage-specific manner. Only a single round of CRISPR-Cas9-mediated editing is required. For complete details on the use and execution of this protocol, please refer to the DWnt4[cKO] example in Yu et al. (2020). Elsevier 2021-05-25 /pmc/articles/PMC8165570/ /pubmed/34095868 http://dx.doi.org/10.1016/j.xpro.2021.100560 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Yu, Joyce J.S.
Vincent, Jean-Paul
McGough, Ian J.
One-step CRISPR-Cas9 protocol for the generation of plug & play conditional knockouts in Drosophila melanogaster
title One-step CRISPR-Cas9 protocol for the generation of plug & play conditional knockouts in Drosophila melanogaster
title_full One-step CRISPR-Cas9 protocol for the generation of plug & play conditional knockouts in Drosophila melanogaster
title_fullStr One-step CRISPR-Cas9 protocol for the generation of plug & play conditional knockouts in Drosophila melanogaster
title_full_unstemmed One-step CRISPR-Cas9 protocol for the generation of plug & play conditional knockouts in Drosophila melanogaster
title_short One-step CRISPR-Cas9 protocol for the generation of plug & play conditional knockouts in Drosophila melanogaster
title_sort one-step crispr-cas9 protocol for the generation of plug & play conditional knockouts in drosophila melanogaster
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165570/
https://www.ncbi.nlm.nih.gov/pubmed/34095868
http://dx.doi.org/10.1016/j.xpro.2021.100560
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