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Targeted Gene Manipulation in Plants Using the CRISPR/Cas Technology
Abstract
The CRISPR/Cas technology is emerging as a revolutionary genome editing tool in diverse organisms including plants, and has quickly evolved into a suite of versatile tools for sequence-specific gene manipulations beyond genome editing. Here, we review the most recent applications of the CRISPR/Cas toolkit in plants and also discuss key factors for improving CRISPR/Cas performance and strategies for reducing the off-target effects. Novel technical breakthroughs in mammalian research regarding the CRISPR/Cas toolkit will also be incorporated into this review in hope to stimulate prospective users from the plant research community to fully explore the potential of these technologies.
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“These studies have already enabled identification of new therapeutic targets and disease mechanisms including the identification of the genes essential for the West-Nile-Virus induced cell death pathway [55,56].”
From Viral Delivery Systems for CRISPR (2019) · cites this paper as [56]
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Cites
Repurposing CRISPR as an RNA-Guided Platform for Sequence-Specific Control of Gene Expression
Qi, L. S., Larson, M. H., Gilbert, L. A., Doudna, J. A., Weissman, J. S., Arkin, A. P., & Lim, W. A. (2013) · Cell · doi:10.1016/j.cell.2013.02.022 · Cited by 5,016 · cited 1×
“Interestingly, although no cytotoxicity of SpCas9 has so far been reported in mammalian or plant cells, it often exhibits toxicity to E. coli (Qi et al., 2013; Johnson et al., 2015) and the single-cell alga Chlamydomonas reinhardtii even if its nuclease activities were disarmed (Jiang et al.,…”
BackgroundHigh-Frequency off-Target Mutagenesis Induced by CRISPR-Cas Nucleases in Human Cells
Fu, Y., Foden, J. A., Khayter, C., Maeder, M. L., Reyon, D., Joung, J. K., & Sander, J. D. (2013) · Nature Biotechnology · doi:10.1038/nbt.2623 · Cited by 3,292
Genome-scale transcriptional activation by an engineered CRISPR-Cas9 complex
Konermann, S., Brigham, M. D., Trevino, A. E., Joung, J., Abudayyeh, O. O., Barcena, C., Hsu, P. D., Habib, N., Gootenberg, J. S., Nishimasu, H., et al. (2015) · Nature · doi:10.1038/nature14136 · Cited by 2,825
In vivo genome editing using Staphylococcus aureus Cas9
Ran, F. A., Cong, L., Yan, W. X., Scott, D. A., Gootenberg, J. S., Kriz, A. J., Zetsche, B., Shalem, O., Wu, X., Makarova, K. S., et al. (2015) · Nature · doi:10.1038/nature14299 · Cited by 2,687
Rationally engineered Cas9 nucleases with improved specificity
Slaymaker, I. M., Gao, L., Zetsche, B., Scott, D. A., Yan, W. X., & Zhang, F. (2016) · Science · doi:10.1126/science.aad5227 · Cited by 2,414
Crystal structure of Cas9 in complex with guide RNA and target DNA
Nishimasu, H., Ran, F. A., Hsu, P. D., Konermann, S., Shehata, S. I., Dohmae, N., Ishitani, R., Zhang, F., & Nureki, O. (2014) · Cell · doi:10.1016/j.cell.2014.02.001 · Cited by 2,306
GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases
Tsai, S. Q., Zheng, Z., Nguyen, N. T., Liebers, M., Topkar, V. V., Thapar, V., Wyvekens, N., Khayter, C., Iafrate, A. J., Le, L. P., et al. (2015) · Nature Biotechnology · doi:10.1038/nbt.3117 · Cited by 2,268
Improving CRISPR-Cas nuclease specificity using truncated guide RNAs
Fu, Y., Sander, J. D., Reyon, D., Cascio, V. M., & Joung, J. K. (2014) · Nature Biotechnology · doi:10.1038/nbt.2808 · Cited by 1,993 · cited 1×
“For plants with fully sequenced genomes, the truncated sgRNA strategy (Fu et al., 2014) may also be used to reduce off-target effects: this strategy is based on the finding that truncating the 5’ end of a sgRNA by two nucleotides could retain a similar on-target editing efficiency as a full-length…”
BackgroundMali, P., Aach, J., Stranges, P. B., Esvelt, K. M., Moosburner, M., Kosuri, S., Yang, L., & Church, G. M. (2013) · Nature Biotechnology · doi:10.1038/nbt.2675 · Cited by 1,752 · cited 4×
“Pronounced activation had to rely on many sgRNAs targeting to the same promoter (Mali et al., 2013a; Perez-Pinera et al., 2013; Lowder et al., 2015), which dramatically reduces the total number of genes that can be activated concurrently due to M AN US CR IP T AC CE PT ED 16 the cloning and…”
BackgroundMethodInfluentialEngineered CRISPR-Cas9 nucleases with altered PAM specificities
Kleinstiver, B. P., Prew, M. S., Tsai, S. Q., Topkar, V. V., Nguyen, N. T., Zheng, Z., Gonzales, A. P. W., Li, Z., Peterson, R. T., Yeh, J.-R. J., et al. (2015) · Nature · doi:10.1038/nature14592 · Cited by 1,624
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Metadata
- Authors
- Zhang, D., Li, Z., & Li, J.-F.
- Venue
- Journal of Genetics and Genomics
- Publisher
- Elsevier BV
- Published
- 2016-05
- Volume
- 43
- Issue
- 5
- Pages
- 251-262
- ISSN
- 1673-8527
- Cited by
- 67
- References
- 10
- Language
- en
- Funders
- National Natural Science Foundation of China (31522006, 31570276)
- Sun Yat-sen University
- China's Thousand Young Talents Program
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