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Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine
The CRISPR (clustered regularly interspaced short palindromic repeats)-associated protein 9 (Cas9) system is a powerful tool for targeted genome editing, with applications that include plant biotechnology and functional genomics research. However, the specificity of Cas9 targeting is poorly investig...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087786/ https://www.ncbi.nlm.nih.gov/pubmed/33931634 http://dx.doi.org/10.1038/s41438-021-00549-4 |
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author | Wang, Xianhang Tu, Mingxing Wang, Ya Yin, Wuchen Zhang, Yu Wu, Hongsong Gu, Yincong Li, Zhi Xi, Zhumei Wang, Xiping |
author_facet | Wang, Xianhang Tu, Mingxing Wang, Ya Yin, Wuchen Zhang, Yu Wu, Hongsong Gu, Yincong Li, Zhi Xi, Zhumei Wang, Xiping |
author_sort | Wang, Xianhang |
collection | PubMed |
description | The CRISPR (clustered regularly interspaced short palindromic repeats)-associated protein 9 (Cas9) system is a powerful tool for targeted genome editing, with applications that include plant biotechnology and functional genomics research. However, the specificity of Cas9 targeting is poorly investigated in many plant species, including fruit trees. To assess the off-target mutation rate in grapevine (Vitis vinifera), we performed whole-genome sequencing (WGS) of seven Cas9-edited grapevine plants in which one of two genes was targeted by CRISPR/Cas9 and three wild-type (WT) plants. In total, we identified between 202,008 and 272,397 single nucleotide polymorphisms (SNPs) and between 26,391 and 55,414 insertions/deletions (indels) in the seven Cas9-edited grapevine plants compared with the three WT plants. Subsequently, 3272 potential off-target sites were selected for further analysis. Only one off-target indel mutation was identified from the WGS data and validated by Sanger sequencing. In addition, we found 243 newly generated off-target sites caused by genetic variants between the Thompson Seedless cultivar and the grape reference genome (PN40024) but no true off-target mutations. In conclusion, we observed high specificity of CRISPR/Cas9 for genome editing of grapevine. |
format | Online Article Text |
id | pubmed-8087786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80877862021-05-05 Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine Wang, Xianhang Tu, Mingxing Wang, Ya Yin, Wuchen Zhang, Yu Wu, Hongsong Gu, Yincong Li, Zhi Xi, Zhumei Wang, Xiping Hortic Res Article The CRISPR (clustered regularly interspaced short palindromic repeats)-associated protein 9 (Cas9) system is a powerful tool for targeted genome editing, with applications that include plant biotechnology and functional genomics research. However, the specificity of Cas9 targeting is poorly investigated in many plant species, including fruit trees. To assess the off-target mutation rate in grapevine (Vitis vinifera), we performed whole-genome sequencing (WGS) of seven Cas9-edited grapevine plants in which one of two genes was targeted by CRISPR/Cas9 and three wild-type (WT) plants. In total, we identified between 202,008 and 272,397 single nucleotide polymorphisms (SNPs) and between 26,391 and 55,414 insertions/deletions (indels) in the seven Cas9-edited grapevine plants compared with the three WT plants. Subsequently, 3272 potential off-target sites were selected for further analysis. Only one off-target indel mutation was identified from the WGS data and validated by Sanger sequencing. In addition, we found 243 newly generated off-target sites caused by genetic variants between the Thompson Seedless cultivar and the grape reference genome (PN40024) but no true off-target mutations. In conclusion, we observed high specificity of CRISPR/Cas9 for genome editing of grapevine. Nature Publishing Group UK 2021-05-01 /pmc/articles/PMC8087786/ /pubmed/33931634 http://dx.doi.org/10.1038/s41438-021-00549-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wang, Xianhang Tu, Mingxing Wang, Ya Yin, Wuchen Zhang, Yu Wu, Hongsong Gu, Yincong Li, Zhi Xi, Zhumei Wang, Xiping Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine |
title | Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine |
title_full | Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine |
title_fullStr | Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine |
title_full_unstemmed | Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine |
title_short | Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine |
title_sort | whole-genome sequencing reveals rare off-target mutations in crispr/cas9-edited grapevine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087786/ https://www.ncbi.nlm.nih.gov/pubmed/33931634 http://dx.doi.org/10.1038/s41438-021-00549-4 |
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