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Highly Efficient CRISPR-Associated Protein 9 Ribonucleoprotein-Based Genome Editing in Euglena gracilis

Euglena gracilis, a unicellular phytoflagellate microalga, is a promising biomaterial for foods, feeds, and biofuels. However, targeted mutagenesis in this species has been a long-standing challenge. We recently developed a transgene-free, highly efficient, genome editing method for E. gracilis usin...

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Detalles Bibliográficos
Autores principales: Nomura, Toshihisa, Yoshikawa, Mizuki, Suzuki, Kengo, Mochida, Keiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580193/
https://www.ncbi.nlm.nih.gov/pubmed/33111076
http://dx.doi.org/10.1016/j.xpro.2020.100023
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author Nomura, Toshihisa
Yoshikawa, Mizuki
Suzuki, Kengo
Mochida, Keiichi
author_facet Nomura, Toshihisa
Yoshikawa, Mizuki
Suzuki, Kengo
Mochida, Keiichi
author_sort Nomura, Toshihisa
collection PubMed
description Euglena gracilis, a unicellular phytoflagellate microalga, is a promising biomaterial for foods, feeds, and biofuels. However, targeted mutagenesis in this species has been a long-standing challenge. We recently developed a transgene-free, highly efficient, genome editing method for E. gracilis using CRISPR/Cas9 ribonucleoproteins (RNPs). Our method achieved mutagenesis rates of approximately 80% or more through an electroporation-based direct delivery of Cas9 RNPs. Therefore, this method is suitable for basic research and industrial applications, such as the breeding of Euglena. For complete details on the use and execution of this protocol, please refer to Nomura et al. (2019).
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spelling pubmed-75801932020-10-26 Highly Efficient CRISPR-Associated Protein 9 Ribonucleoprotein-Based Genome Editing in Euglena gracilis Nomura, Toshihisa Yoshikawa, Mizuki Suzuki, Kengo Mochida, Keiichi STAR Protoc Protocol Euglena gracilis, a unicellular phytoflagellate microalga, is a promising biomaterial for foods, feeds, and biofuels. However, targeted mutagenesis in this species has been a long-standing challenge. We recently developed a transgene-free, highly efficient, genome editing method for E. gracilis using CRISPR/Cas9 ribonucleoproteins (RNPs). Our method achieved mutagenesis rates of approximately 80% or more through an electroporation-based direct delivery of Cas9 RNPs. Therefore, this method is suitable for basic research and industrial applications, such as the breeding of Euglena. For complete details on the use and execution of this protocol, please refer to Nomura et al. (2019). Elsevier 2020-06-03 /pmc/articles/PMC7580193/ /pubmed/33111076 http://dx.doi.org/10.1016/j.xpro.2020.100023 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
Nomura, Toshihisa
Yoshikawa, Mizuki
Suzuki, Kengo
Mochida, Keiichi
Highly Efficient CRISPR-Associated Protein 9 Ribonucleoprotein-Based Genome Editing in Euglena gracilis
title Highly Efficient CRISPR-Associated Protein 9 Ribonucleoprotein-Based Genome Editing in Euglena gracilis
title_full Highly Efficient CRISPR-Associated Protein 9 Ribonucleoprotein-Based Genome Editing in Euglena gracilis
title_fullStr Highly Efficient CRISPR-Associated Protein 9 Ribonucleoprotein-Based Genome Editing in Euglena gracilis
title_full_unstemmed Highly Efficient CRISPR-Associated Protein 9 Ribonucleoprotein-Based Genome Editing in Euglena gracilis
title_short Highly Efficient CRISPR-Associated Protein 9 Ribonucleoprotein-Based Genome Editing in Euglena gracilis
title_sort highly efficient crispr-associated protein 9 ribonucleoprotein-based genome editing in euglena gracilis
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580193/
https://www.ncbi.nlm.nih.gov/pubmed/33111076
http://dx.doi.org/10.1016/j.xpro.2020.100023
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