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Optimizing genome editing strategy by primer-extension-mediated sequencing

Efficient and precise genome editing is essential for clinical applications and generating animal models, which requires engineered nucleases with high editing ability while low off-target activity. Here we present a high-throughput sequencing method, primer-extension-mediated sequencing (PEM-seq),...

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Autores principales: Yin, Jianhang, Liu, Mengzhu, Liu, Yang, Wu, Jinchun, Gan, Tingting, Zhang, Weiwei, Li, Yinghui, Zhou, Yaxuan, Hu, Jiazhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434046/
https://www.ncbi.nlm.nih.gov/pubmed/30937179
http://dx.doi.org/10.1038/s41421-019-0088-8
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author Yin, Jianhang
Liu, Mengzhu
Liu, Yang
Wu, Jinchun
Gan, Tingting
Zhang, Weiwei
Li, Yinghui
Zhou, Yaxuan
Hu, Jiazhi
author_facet Yin, Jianhang
Liu, Mengzhu
Liu, Yang
Wu, Jinchun
Gan, Tingting
Zhang, Weiwei
Li, Yinghui
Zhou, Yaxuan
Hu, Jiazhi
author_sort Yin, Jianhang
collection PubMed
description Efficient and precise genome editing is essential for clinical applications and generating animal models, which requires engineered nucleases with high editing ability while low off-target activity. Here we present a high-throughput sequencing method, primer-extension-mediated sequencing (PEM-seq), to comprehensively assess both editing ability and specificity of engineered nucleases. We showed CRISPR/Cas9-generated breaks could lead to chromosomal translocations and large deletions by PEM-seq. We also found that Cas9 nickase possessed lower off-target activity while with some loss of target cleavage ability. However, high-fidelity Cas9 variants, including both eCas9 and the new FeCas9, could significantly reduce the Cas9 off-target activity with no obvious editing retardation. Moreover, we found AcrIIA4 inhibitor could greatly reduce the activities of Cas9, but off-target loci were not so effectively suppressed as the on-target sites. Therefore, PEM-seq fully evaluating engineered nucleases could help choose better genome editing strategy at given loci than other methods detecting only off-target activity.
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spelling pubmed-64340462019-04-01 Optimizing genome editing strategy by primer-extension-mediated sequencing Yin, Jianhang Liu, Mengzhu Liu, Yang Wu, Jinchun Gan, Tingting Zhang, Weiwei Li, Yinghui Zhou, Yaxuan Hu, Jiazhi Cell Discov Article Efficient and precise genome editing is essential for clinical applications and generating animal models, which requires engineered nucleases with high editing ability while low off-target activity. Here we present a high-throughput sequencing method, primer-extension-mediated sequencing (PEM-seq), to comprehensively assess both editing ability and specificity of engineered nucleases. We showed CRISPR/Cas9-generated breaks could lead to chromosomal translocations and large deletions by PEM-seq. We also found that Cas9 nickase possessed lower off-target activity while with some loss of target cleavage ability. However, high-fidelity Cas9 variants, including both eCas9 and the new FeCas9, could significantly reduce the Cas9 off-target activity with no obvious editing retardation. Moreover, we found AcrIIA4 inhibitor could greatly reduce the activities of Cas9, but off-target loci were not so effectively suppressed as the on-target sites. Therefore, PEM-seq fully evaluating engineered nucleases could help choose better genome editing strategy at given loci than other methods detecting only off-target activity. Nature Publishing Group UK 2019-03-26 /pmc/articles/PMC6434046/ /pubmed/30937179 http://dx.doi.org/10.1038/s41421-019-0088-8 Text en © The Author(s) 2019 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
Yin, Jianhang
Liu, Mengzhu
Liu, Yang
Wu, Jinchun
Gan, Tingting
Zhang, Weiwei
Li, Yinghui
Zhou, Yaxuan
Hu, Jiazhi
Optimizing genome editing strategy by primer-extension-mediated sequencing
title Optimizing genome editing strategy by primer-extension-mediated sequencing
title_full Optimizing genome editing strategy by primer-extension-mediated sequencing
title_fullStr Optimizing genome editing strategy by primer-extension-mediated sequencing
title_full_unstemmed Optimizing genome editing strategy by primer-extension-mediated sequencing
title_short Optimizing genome editing strategy by primer-extension-mediated sequencing
title_sort optimizing genome editing strategy by primer-extension-mediated sequencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434046/
https://www.ncbi.nlm.nih.gov/pubmed/30937179
http://dx.doi.org/10.1038/s41421-019-0088-8
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