Conferring DNA virus resistance with high specificity in plants using virus-inducible genome-editing system
The CRISPR/Cas9 system has recently been engineered to confer resistance to geminiviruses in plants. However, we show here that the usefulness of this antiviral strategy is undermined by off-target effects identified by deep sequencing in Arabidopsis . We construct two virus-inducible CRISPR/Cas9 ve...
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| Published in | Genome Biology Vol. 19; no. 1; p. 197 |
|---|---|
| Main Authors | , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
London
BioMed Central
15.11.2018
Springer Nature B.V BMC |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1474-760X 1474-7596 1474-760X |
| DOI | 10.1186/s13059-018-1580-4 |
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| Abstract | The CRISPR/Cas9 system has recently been engineered to confer resistance to geminiviruses in plants. However, we show here that the usefulness of this antiviral strategy is undermined by off-target effects identified by deep sequencing in
Arabidopsis
. We construct two virus-inducible CRISPR/Cas9 vectors that efficiently inhibit beet severe curly top virus (BSCTV) accumulation in both transient assays (
Nicotiana benthamiana
) and transgenic lines (
Arabidopsis
). Deep sequencing detects no off-target effect in candidate sites of the transgenic
Arabidopsis
. This kind of virus-inducible genome-editing system should be widely applicable for generating virus-resistant plants without off-target costs. |
|---|---|
| AbstractList | The CRISPR/Cas9 system has recently been engineered to confer resistance to geminiviruses in plants. However, we show here that the usefulness of this antiviral strategy is undermined by off-target effects identified by deep sequencing in Arabidopsis. We construct two virus-inducible CRISPR/Cas9 vectors that efficiently inhibit beet severe curly top virus (BSCTV) accumulation in both transient assays (Nicotiana benthamiana) and transgenic lines (Arabidopsis). Deep sequencing detects no off-target effect in candidate sites of the transgenic Arabidopsis. This kind of virus-inducible genome-editing system should be widely applicable for generating virus-resistant plants without off-target costs. The CRISPR/Cas9 system has recently been engineered to confer resistance to geminiviruses in plants. However, we show here that the usefulness of this antiviral strategy is undermined by off-target effects identified by deep sequencing in Arabidopsis . We construct two virus-inducible CRISPR/Cas9 vectors that efficiently inhibit beet severe curly top virus (BSCTV) accumulation in both transient assays ( Nicotiana benthamiana ) and transgenic lines ( Arabidopsis ). Deep sequencing detects no off-target effect in candidate sites of the transgenic Arabidopsis . This kind of virus-inducible genome-editing system should be widely applicable for generating virus-resistant plants without off-target costs. The CRISPR/Cas9 system has recently been engineered to confer resistance to geminiviruses in plants. However, we show here that the usefulness of this antiviral strategy is undermined by off-target effects identified by deep sequencing in Arabidopsis. We construct two virus-inducible CRISPR/Cas9 vectors that efficiently inhibit beet severe curly top virus (BSCTV) accumulation in both transient assays (Nicotiana benthamiana) and transgenic lines (Arabidopsis). Deep sequencing detects no off-target effect in candidate sites of the transgenic Arabidopsis. This kind of virus-inducible genome-editing system should be widely applicable for generating virus-resistant plants without off-target costs.The CRISPR/Cas9 system has recently been engineered to confer resistance to geminiviruses in plants. However, we show here that the usefulness of this antiviral strategy is undermined by off-target effects identified by deep sequencing in Arabidopsis. We construct two virus-inducible CRISPR/Cas9 vectors that efficiently inhibit beet severe curly top virus (BSCTV) accumulation in both transient assays (Nicotiana benthamiana) and transgenic lines (Arabidopsis). Deep sequencing detects no off-target effect in candidate sites of the transgenic Arabidopsis. This kind of virus-inducible genome-editing system should be widely applicable for generating virus-resistant plants without off-target costs. Abstract The CRISPR/Cas9 system has recently been engineered to confer resistance to geminiviruses in plants. However, we show here that the usefulness of this antiviral strategy is undermined by off-target effects identified by deep sequencing in Arabidopsis. We construct two virus-inducible CRISPR/Cas9 vectors that efficiently inhibit beet severe curly top virus (BSCTV) accumulation in both transient assays (Nicotiana benthamiana) and transgenic lines (Arabidopsis). Deep sequencing detects no off-target effect in candidate sites of the transgenic Arabidopsis. This kind of virus-inducible genome-editing system should be widely applicable for generating virus-resistant plants without off-target costs. |
| ArticleNumber | 197 |
| Author | Zhang, Yi Si, Xiaomin Gao, Caixia Ji, Xiang Zhang, Huawei Zhang, Feng |
| Author_xml | – sequence: 1 givenname: Xiang surname: Ji fullname: Ji, Xiang organization: State Key Laboratory of Plant Cell and Chromosome Engineering, Center for Genome Editing, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences – sequence: 2 givenname: Xiaomin surname: Si fullname: Si, Xiaomin organization: State Key Laboratory of Plant Cell and Chromosome Engineering, Center for Genome Editing, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences – sequence: 3 givenname: Yi surname: Zhang fullname: Zhang, Yi organization: Key Laboratory of Plant Stress Research, College of Life Science, Shandong Normal University – sequence: 4 givenname: Huawei surname: Zhang fullname: Zhang, Huawei organization: State Key Laboratory of Plant Cell and Chromosome Engineering, Center for Genome Editing, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences – sequence: 5 givenname: Feng surname: Zhang fullname: Zhang, Feng organization: Department of Plant and Microbial Biology, University of Minnesota, Center for Precision Plant Genomics, University of Minnesota – sequence: 6 givenname: Caixia orcidid: 0000-0003-3169-8248 surname: Gao fullname: Gao, Caixia email: cxgao@genetics.ac.cn organization: State Key Laboratory of Plant Cell and Chromosome Engineering, Center for Genome Editing, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30442181$$D View this record in MEDLINE/PubMed |
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| Keywords | Geminivirus Off-target Virus-resistance CRISPR/Cas9 system Virus-inducible |
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| Snippet | The CRISPR/Cas9 system has recently been engineered to confer resistance to geminiviruses in plants. However, we show here that the usefulness of this... Abstract The CRISPR/Cas9 system has recently been engineered to confer resistance to geminiviruses in plants. However, we show here that the usefulness of this... |
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| SubjectTerms | Animal Genetics and Genomics Arabidopsis Beet severe curly top virus Bioinformatics Biomedical and Life Sciences CRISPR CRISPR-Cas Systems CRISPR/Cas9 system Deoxyribonucleic acid Disease Resistance DNA Evolutionary Biology Geminiviridae Geminivirus gene editing Gene Editing - methods Gene expression genetically modified organisms genome Genomes Human Genetics Immune system Infections Insights from Genome Editing Life Sciences Microbial Genetics and Genomics Nicotiana Nicotiana benthamiana Off-target Plant Genetics and Genomics Plant viruses Short Report Transgenic plants Virology Virus-inducible Virus-resistance Viruses |
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| Title | Conferring DNA virus resistance with high specificity in plants using virus-inducible genome-editing system |
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