Abstract
CRISPR-Cas9 and Cas12a (formerly Cpf1), RNA-guided DNA endonucleases found from adaptive immune system in prokaryotes, have been engineered and widely adopted as two of the most powerful genome editing systems in plants. Recently, we developed a single transcript unit (STU) CRISPR 2.0 toolbox for applications in plants, which contains two STU-Cas9 systems and one STU-Cas12a system. Here, we describe a detailed protocol about using the STU CRISPR 2.0 systems to achieve single and multiplex genome editing in rice.
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Acknowledgments
This work was supported by grants to Y.Z. from the Sichuan Youth Science and Technology Foundation (2017JQ0005), the National Science Foundation of China (31771486), the National Transgenic Major Project (2018ZX08022001-003), and the Fundamental Research Funds for the Central Universities (ZYGX2016J119 and ZYGX2016J122). This work was also partly supported by grants to Y.Q. from NSF (IOS-1758745), USDA-NIFA (2018-33522-28789), FFAR (593603), and Syngenta Biotechnology.
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Tang, X., Qi, Y., Zhang, Y. (2021). Single Transcript Unit CRISPR 2.0 Systems for Genome Editing in Rice. In: Bandyopadhyay, A., Thilmony, R. (eds) Rice Genome Engineering and Gene Editing. Methods in Molecular Biology, vol 2238. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-1068-8_12
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DOI: https://doi.org/10.1007/978-1-0716-1068-8_12
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