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...
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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. |
doi_str_mv | 10.1038/s41438-021-00549-4 |
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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.</description><identifier>ISSN: 2662-6810</identifier><identifier>EISSN: 2052-7276</identifier><identifier>DOI: 10.1038/s41438-021-00549-4</identifier><identifier>PMID: 33931634</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/449/447/2311 ; 631/61/447/8 ; Agriculture ; Biomedical and Life Sciences ; Biotechnology ; CRISPR ; Cultivars ; Ecology ; Editing ; Fruit trees ; Gene sequencing ; Genetic diversity ; Genetic variance ; Genome editing ; Genomes ; Grapevines ; Life Sciences ; Mutation ; Mutation rates ; Nucleotides ; Plant Breeding/Biotechnology ; Plant Genetics and Genomics ; Plant Sciences ; Plant species ; Single-nucleotide polymorphism ; Target recognition ; Vitis vinifera ; Whole genome sequencing</subject><ispartof>Horticulture research, 2021-05, Vol.8 (1), p.114, Article 114</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c555t-5048d555abd32a92513a124dce8f83008a2b0f0dd0c439ecc556cffd3850f7bc3</citedby><cites>FETCH-LOGICAL-c555t-5048d555abd32a92513a124dce8f83008a2b0f0dd0c439ecc556cffd3850f7bc3</cites><orcidid>0000-0003-2445-3074 ; 0000-0003-4144-0099</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087786/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087786/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33931634$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Xianhang</creatorcontrib><creatorcontrib>Tu, Mingxing</creatorcontrib><creatorcontrib>Wang, Ya</creatorcontrib><creatorcontrib>Yin, Wuchen</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Wu, Hongsong</creatorcontrib><creatorcontrib>Gu, Yincong</creatorcontrib><creatorcontrib>Li, Zhi</creatorcontrib><creatorcontrib>Xi, Zhumei</creatorcontrib><creatorcontrib>Wang, Xiping</creatorcontrib><title>Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine</title><title>Horticulture research</title><addtitle>Hortic Res</addtitle><addtitle>Hortic Res</addtitle><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.</description><subject>631/449/447/2311</subject><subject>631/61/447/8</subject><subject>Agriculture</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>CRISPR</subject><subject>Cultivars</subject><subject>Ecology</subject><subject>Editing</subject><subject>Fruit trees</subject><subject>Gene sequencing</subject><subject>Genetic diversity</subject><subject>Genetic variance</subject><subject>Genome editing</subject><subject>Genomes</subject><subject>Grapevines</subject><subject>Life Sciences</subject><subject>Mutation</subject><subject>Mutation rates</subject><subject>Nucleotides</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Sciences</subject><subject>Plant species</subject><subject>Single-nucleotide polymorphism</subject><subject>Target recognition</subject><subject>Vitis vinifera</subject><subject>Whole genome sequencing</subject><issn>2662-6810</issn><issn>2052-7276</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kUlLBDEQhYMoKuof8CANnqOVrTt9EWRwA0FxQTyFTHelbZlJxqRnwH9vdFwvnlJQ731VqUfILoMDBkIfJsmk0BQ4owBK1lSukE0OitOKV-VqrsuS01Iz2CA7KT0DAFOSC1Wtkw0hasFKITfJ48NTmCDt0IcpFglf5uib3ndFxAXaSSqijVgE5-hgY4dDMZ0PduiDT0Xvi9HNxe31zeHIpppi2w_YFl20M1z0HrfJmssA3Pl8t8j96cnd6JxeXp1djI4vaaOUGqgCqdtc2XEruK25YsIyLtsGtdMCQFs-BgdtC40UNTbZVTbOtUIrcNW4EVvkaMmdzcdTzD4_RDsxs9hPbXw1wfbmb8f3T6YLC6NBV5UuM2D_ExBD_n4azHOYR593NlzxfFzOBMsqvlQ1MaQU0X1PYGDeEzHLRExOxHwkYmQ27f3e7dvydf8sEEtByi3fYfyZ_Q_2DY7cl4I</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Wang, Xianhang</creator><creator>Tu, Mingxing</creator><creator>Wang, Ya</creator><creator>Yin, Wuchen</creator><creator>Zhang, Yu</creator><creator>Wu, Hongsong</creator><creator>Gu, Yincong</creator><creator>Li, Zhi</creator><creator>Xi, Zhumei</creator><creator>Wang, Xiping</creator><general>Nature Publishing Group UK</general><general>Oxford University Press</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2445-3074</orcidid><orcidid>https://orcid.org/0000-0003-4144-0099</orcidid></search><sort><creationdate>20210501</creationdate><title>Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine</title><author>Wang, Xianhang ; 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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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33931634</pmid><doi>10.1038/s41438-021-00549-4</doi><orcidid>https://orcid.org/0000-0003-2445-3074</orcidid><orcidid>https://orcid.org/0000-0003-4144-0099</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/449/447/2311 631/61/447/8 Agriculture Biomedical and Life Sciences Biotechnology CRISPR Cultivars Ecology Editing Fruit trees Gene sequencing Genetic diversity Genetic variance Genome editing Genomes Grapevines Life Sciences Mutation Mutation rates Nucleotides Plant Breeding/Biotechnology Plant Genetics and Genomics Plant Sciences Plant species Single-nucleotide polymorphism Target recognition Vitis vinifera Whole genome sequencing |
title | Whole-genome sequencing reveals rare off-target mutations in CRISPR/Cas9-edited grapevine |
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