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Highly efficient genome editing by CRISPR-Cpf1 using CRISPR RNA with a uridinylate-rich 3′-overhang

Genome editing has been harnessed through the development of CRISPR system, and the CRISPR from Prevotella and Francisella 1 (Cpf1) system has emerged as a promising alternative to CRISPR-Cas9 for use in various circumstances. Despite the inherent multiple advantages of Cpf1 over Cas9, the adoption...

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Autores principales: Bin Moon, Su, Lee, Jeong Mi, Kang, Jeong Gu, Lee, Nan-Ee, Ha, Dae-In, Kim, Do Yon, Kim, Sun Hee, Yoo, Kwangsun, Kim, Daesik, Ko, Jeong-Heon, Kim, Yong-Sam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128929/
https://www.ncbi.nlm.nih.gov/pubmed/30194297
http://dx.doi.org/10.1038/s41467-018-06129-w
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author Bin Moon, Su
Lee, Jeong Mi
Kang, Jeong Gu
Lee, Nan-Ee
Ha, Dae-In
Kim, Do Yon
Kim, Sun Hee
Yoo, Kwangsun
Kim, Daesik
Ko, Jeong-Heon
Kim, Yong-Sam
author_facet Bin Moon, Su
Lee, Jeong Mi
Kang, Jeong Gu
Lee, Nan-Ee
Ha, Dae-In
Kim, Do Yon
Kim, Sun Hee
Yoo, Kwangsun
Kim, Daesik
Ko, Jeong-Heon
Kim, Yong-Sam
author_sort Bin Moon, Su
collection PubMed
description Genome editing has been harnessed through the development of CRISPR system, and the CRISPR from Prevotella and Francisella 1 (Cpf1) system has emerged as a promising alternative to CRISPR-Cas9 for use in various circumstances. Despite the inherent multiple advantages of Cpf1 over Cas9, the adoption of Cpf1 has been unsatisfactory because of target-dependent insufficient indel efficiencies. Here, we report an engineered CRISPR RNA (crRNA) for highly efficient genome editing by Cpf1, which includes a 20-base target-complementary sequence and a uridinylate-rich 3′-overhang. When the crRNA is transcriptionally produced, crRNA with a 20-base target-complementary sequence plus a U(4)AU(4) 3′-overhang is the optimal configuration. U-rich crRNA also maximizes the utility of the AsCpf1 mutants and multiplexing genome editing using mRNA as the source of multiple crRNAs. Furthermore, U-rich crRNA enables a highly safe and specific genome editing using Cpf1 in human cells, contributing to the enhancement of a genome-editing toolbox.
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spelling pubmed-61289292018-09-10 Highly efficient genome editing by CRISPR-Cpf1 using CRISPR RNA with a uridinylate-rich 3′-overhang Bin Moon, Su Lee, Jeong Mi Kang, Jeong Gu Lee, Nan-Ee Ha, Dae-In Kim, Do Yon Kim, Sun Hee Yoo, Kwangsun Kim, Daesik Ko, Jeong-Heon Kim, Yong-Sam Nat Commun Article Genome editing has been harnessed through the development of CRISPR system, and the CRISPR from Prevotella and Francisella 1 (Cpf1) system has emerged as a promising alternative to CRISPR-Cas9 for use in various circumstances. Despite the inherent multiple advantages of Cpf1 over Cas9, the adoption of Cpf1 has been unsatisfactory because of target-dependent insufficient indel efficiencies. Here, we report an engineered CRISPR RNA (crRNA) for highly efficient genome editing by Cpf1, which includes a 20-base target-complementary sequence and a uridinylate-rich 3′-overhang. When the crRNA is transcriptionally produced, crRNA with a 20-base target-complementary sequence plus a U(4)AU(4) 3′-overhang is the optimal configuration. U-rich crRNA also maximizes the utility of the AsCpf1 mutants and multiplexing genome editing using mRNA as the source of multiple crRNAs. Furthermore, U-rich crRNA enables a highly safe and specific genome editing using Cpf1 in human cells, contributing to the enhancement of a genome-editing toolbox. Nature Publishing Group UK 2018-09-07 /pmc/articles/PMC6128929/ /pubmed/30194297 http://dx.doi.org/10.1038/s41467-018-06129-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bin Moon, Su
Lee, Jeong Mi
Kang, Jeong Gu
Lee, Nan-Ee
Ha, Dae-In
Kim, Do Yon
Kim, Sun Hee
Yoo, Kwangsun
Kim, Daesik
Ko, Jeong-Heon
Kim, Yong-Sam
Highly efficient genome editing by CRISPR-Cpf1 using CRISPR RNA with a uridinylate-rich 3′-overhang
title Highly efficient genome editing by CRISPR-Cpf1 using CRISPR RNA with a uridinylate-rich 3′-overhang
title_full Highly efficient genome editing by CRISPR-Cpf1 using CRISPR RNA with a uridinylate-rich 3′-overhang
title_fullStr Highly efficient genome editing by CRISPR-Cpf1 using CRISPR RNA with a uridinylate-rich 3′-overhang
title_full_unstemmed Highly efficient genome editing by CRISPR-Cpf1 using CRISPR RNA with a uridinylate-rich 3′-overhang
title_short Highly efficient genome editing by CRISPR-Cpf1 using CRISPR RNA with a uridinylate-rich 3′-overhang
title_sort highly efficient genome editing by crispr-cpf1 using crispr rna with a uridinylate-rich 3′-overhang
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128929/
https://www.ncbi.nlm.nih.gov/pubmed/30194297
http://dx.doi.org/10.1038/s41467-018-06129-w
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