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Precise, predictable multi-nucleotide deletions in rice and wheat using APOBEC–Cas9

Abstract

Short insertions and deletions can be produced in plant genomes using CRISPR–Cas editors, but reliable production of larger deletions in specific target sites has proven difficult to achieve. We report the development of a series of APOBEC–Cas9 fusion-induced deletion systems (AFIDs) that combine Cas9 with human APOBEC3A (A3A), uracil DNA-glucosidase and apurinic or apyrimidinic site lyase. In rice and wheat, AFID-3 generated deletions from 5′-deaminated C bases to the Cas9-cleavage site. Approximately one-third of deletions produced using AFID-3 in rice and wheat protoplasts (30.2%) and regenerated plants (34.8%) were predictable. We show that eAFID-3, in which the A3A in AFID-3 is replaced with truncated APOBEC3B (A3Bctd), produced more uniform deletions from the preferred TC motif to the double-strand break. AFIDs could be applied to study regulatory regions and protein domains to improve crop plants.

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Fig. 1: Characterization of the AFID system.
Fig. 2: AFID-3 induces predictable, multi-nucleotide-targeted deletions in protoplasts and regenerated plants.
Fig. 3: A3Bctd allows AFIDs to generate more uniform precise deletions within the protospacer.

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Data availability

NGS data have been deposited in the NCBI Sequence Read Archive database (accession no. PRJNA630559). Two plasmids encoding AFID-3 and eAFID-3 in the present study will be available through Addgene. All data supporting the findings of the present study are available in the article and its supplementary figures and tables, or from the corresponding author on request. For sequence data, OsAAT (LOC_Os01g55540), OsACC (LOC_Os05g22940), OsCDC48 (LOC_Os03g05730), OsEV (LOC_Os02g11010), OsNRT1.1B (LOC_Os10g40600), OsSPL14/OsIPA1 (LOC_Os08g39890) and OsSWEET14 (LOC_Os11g31190) are from Rice Genome Annotation Project (http://rice.plantbiology.msu.edu); TaMYB10 (AB191458.1, AB191459.1, AB191460.1) and TaVRN1 (AY747603.1, AY747604.1, AY747605.1) are from the NCBI (https://www.ncbi.nlm.nih.gov); TaF3H (TraesCS2A02G493500, TraesCS2B02G521500, TraesCS2D02G493400), TaGASR6 (TraesCS1A02G270100, TraesCS1D02G270100), TaPDS (TraesCS4A02G004900, TraesCS4B02G300100, TraesCS4D02G299000) and TaPMK (TraesCS5A02G449000, TraesCS5B02G453800, TraesCS5D02G455500) are from the International Wheat Genome Sequencing Consortium (https://urgi.versailles.inra.fr); and tae-Pri-miR160, tae-Pri-miR319, tae-Pri-miR396 and tae-Pri-miR444a are from miRBase (http://www.mirbase.org).

References

  1. Knott, G. J. & Doudna, J. A. CRISPR-Cas guides the future of genetic engineering. Science 361, 866–869 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  2. Chen, K., Wang, Y., Zhang, R., Zhang, H. & Gao, C. CRISPR/Cas genome editing and precision plant breeding in agriculture. Annu. Rev. Plant Biol. 70, 667–697 (2019).

    CAS  PubMed  Google Scholar 

  3. Jinek, M. et al. A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity. Science 337, 816–821 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  4. Chang, H. H. Y., Pannunzio, N. R., Adachi, N. & Lieber, M. R. Non-homologous DNA end joining and alternative pathways to double-strand break repair. Nat. Rev. Mol. Cell Biol. 18, 495–506 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  5. Stinson, B. M., Moreno, A. T., Walter, J. C. & Loparo, J. J. A mechanism to minimize errors during non-homologous end joining. Mol. Cell 77, 1080–1091 (2020).

    CAS  PubMed  Google Scholar 

  6. Taheri-Ghahfarokhi, A. et al. Decoding non-random mutational signatures at Cas9 targeted sites. Nucleic Acids Res. 46, 8417–8434 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  7. van Overbeek, M. et al. DNA repair profiling reveals nonrandom outcomes at Cas9-mediated breaks. Mol. Cell 63, 633–646 (2016).

    PubMed  Google Scholar 

  8. Burgess, D. G., Xu, J. & Freeling, M. Advances in understanding cis regulation of the plant gene with an emphasis on comparative genomics. Curr. Opin. Plant Biol. 27, 141–147 (2015).

    CAS  PubMed  Google Scholar 

  9. Li, C. et al. A new rice breeding method: CRISPR/Cas9 system editing of the Xa13 promoter to cultivate transgene-free bacterial blight-resistant rice. Plant Biotech. J. 18, 313–315 (2020).

    Google Scholar 

  10. Li, M. et al. Reassessment of the four yield-related genes Gn1a, DEP1, GS3, and IPA1 in rice using a CRISPR/Cas9 system. Front. Plant Sci. 7, 377 (2016).

    PubMed  PubMed Central  Google Scholar 

  11. Zhang, X., Wang, L., Liu, M. & Li, D. CRISPR/Cas9 system: a powerful technology for in vivo and ex vivo gene therapy. Sci. China Life Sci. 60, 468–475 (2017).

    CAS  PubMed  Google Scholar 

  12. Zhou, J. et al. CRISPR-Cas9 based genome editing reveals new insights into microRNA function and regulation in rice. Front. Plant Sci. 8, 1598 (2017).

    PubMed  PubMed Central  Google Scholar 

  13. Bolukbasi, M. F. et al. Orthogonal Cas9–Cas9 chimeras provide a versatile platform for genome editing. Nat. Commun. 9, 4856 (2018).

    PubMed  PubMed Central  Google Scholar 

  14. Cong, L. et al. Multiplex genome engineering using CRISPR/Cas systems. Science 339, 819–823 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  15. Shou, J., Li, J., Liu, Y. & Wu, Q. Precise and predictable CRISPR chromosomal rearrangements reveal principles of Cas9-mediated nucleotide insertion. Mol. Cell 71, 498–509 (2018).

    CAS  PubMed  Google Scholar 

  16. Wolfs, J. M. et al. Biasing genome-editing events toward precise length deletions with an RNA-guided TevCas9 dual nuclease. Proc. Natl Acad. Sci. USA 113, 14988–14993 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  17. Čermák, T. et al. A multipurpose toolkit to enable advanced genome engineering in plants. Plant Cell 29, 1196–1217 (2017).

    PubMed  PubMed Central  Google Scholar 

  18. Zhang, Q., Yin, K., Liu, G., Li, S. & Qiu, J. L. Fusing T5 exonuclease with Cas9 and Cas12a increases the frequency and size of deletion at target sites. Sci. China Life Sci. https://doi.org/10.1007/s11427-020-1671-6 (2020).

  19. Anzalone, A. V. et al. Search-and-replace genome editing without double-strand breaks or donor DNA. Nature 576, 149–157 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  20. Lin, Q. et al. Prime genome editing in rice and wheat. Nat. Biotechnol. 38, 582–585 (2020).

    CAS  PubMed  Google Scholar 

  21. Rees, H. A. & Liu, D. R. Base editing: precision chemistry on the genome and transcriptome of living cells. Nat. Rev. Genet. 19, 770–788 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  22. Komor, A. C., Kim, Y. B., Packer, M. S., Zuris, J. A. & Liu, D. R. Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage. Nature 533, 420–424 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  23. Lei, L. et al. APOBEC3 induces mutations during repair of CRISPR-Cas9-generated DNA breaks. Nat. Struct. Mol. Biol. 25, 45–52 (2018).

    CAS  PubMed  Google Scholar 

  24. Que, Q. et al. Plant DNA repair pathways and their applications in genome engineering. Methods Protoc. 1917, 3–24 (2019).

    CAS  Google Scholar 

  25. Zong, Y. et al. Efficient C-to-T base editing in plants using a fusion of nCas9 and human APOBEC3A. Nat. Biotechnol. 36, 950–953 (2018).

    CAS  Google Scholar 

  26. Gisler, S. et al. Multiplexed Cas9 targeting reveals genomic location effects and gRNA-based staggered breaks influencing mutation efficiency. Nat. Commun. 10, 1598 (2019).

    PubMed  PubMed Central  Google Scholar 

  27. Zuo, Z. & Liu, J. Cas9-catalyzed DNA cleavage generates staggered ends: evidence from molecular dynamics simulations. Sci. Rep. 5, 37584 (2016).

    PubMed  PubMed Central  Google Scholar 

  28. Li, T., Liu, B., Spalding, M. H., Weeks, D. P. & Yang, B. High-efficiency TALEN-based gene editing produces disease-resistant rice. Nat. Biotechnol. 30, 390–392 (2012).

    CAS  PubMed  Google Scholar 

  29. Oliva, R. et al. Broad-spectrum resistance to bacterial blight in rice using genome editing. Nat. Biotechnol. 37, 1344–1350 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  30. Xu, Z. et al. Engineering broad-spectrum bacterial blight resistance by simultaneously disrupting variable TALE-binding elements of multiple susceptibility genes in rice. Mol. Plant 12, 1434–1446 (2019).

    CAS  PubMed  Google Scholar 

  31. Zong, Y. et al. Precise base editing in rice, wheat and maize with a Cas9-cytidine deaminase fusion. Nat. Biotechnol. 35, 438–440 (2017).

    CAS  PubMed  Google Scholar 

  32. Gehrke, J. M. et al. An APOBEC3A-Cas9 base editor with minimized bystander and off-target activities. Nat. Biotechnol. 36, 977–982 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  33. St. Martin, A. et al. A fluorescent reporter for quantification and enrichment of DNA editing by APOBEC-Cas9 or cleavage by Cas9 in living cells. Nucleic Acids Res. 46, e84 (2018).

    Google Scholar 

  34. Siriwardena, S. U., Guruge, T. A. & Bhagwat, A. S. Characterization of the catalytic domain of human APOBEC3B and the critical structural role for a conserved methionine. J. Mol. Biol. 427, 3042–3055 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  35. Omidbakhshfard, M., Proost, S., Fujikura, U. & Mueller-Roeber, B. Growth-regulating factors (GRFs): a small transcription factor family with important functions in plant biology. Mol. Plant 8, 998–1010 (2015).

    CAS  PubMed  Google Scholar 

  36. Shen, M. W. et al. Predictable and precise template-free CRISPR editing of pathogenic variants. Nature 563, 646–651 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  37. Allen, F. et al. Predicting the mutations generated by repair of Cas9-induced double-strand breaks. Nat. Biotechnol. 37, 64–72 (2018).

    Google Scholar 

  38. Leenay, R. T. et al. Large dataset enables prediction of repair after CRISPR-Cas9 editing in primary T cells. Nat. Biotechnol. 37, 1034–1037 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  39. Turonyi, B. W. et al. Continuous evolution of base editors with expanded target compatibility and improved activity. Nat. Biotechnol. 37, 1070–1079 (2019).

    Google Scholar 

  40. He, W. et al. De novo identification of essential protein domains from CRISPR-Cas9 tiling-sgRNA knockout screens. Nat. Commun. 46, 505–529 (2019).

    Google Scholar 

  41. Xing, H. L. et al. A CRISPR/Cas9 toolkit for multiplex genome editing in plants. BMC Plant Biol. 14, 327 (2014).

    PubMed  PubMed Central  Google Scholar 

  42. Shan, Q. et al. Targeted genome modification of crop plants using a CRISPR-Cas system. Nat. Biotechnol. 31, 686–688 (2013).

    CAS  PubMed  Google Scholar 

  43. Wang, Y. et al. Simultaneous editing of three homoeoalleles in hexaploid bread wheat confers heritable resistance to powdery mildew. Nat. Biotechnol. 32, 947–951 (2014).

    CAS  PubMed  Google Scholar 

  44. Zhang, Y., Zhang, Q. & Chen, Q. J. Agrobacterium-mediated delivery of CRISPR/Cas reagents for genome editing in plants enters an era of ternary vector systems. Sci. China Life Sci. https://doi.org/10.1007/s11427-020-1685-9 (2020).

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Acknowledgements

We thank Professor G. Chen (Shanghai Jiao Tong University) for providing the PH strain containing the TAL effector AvaXa7 for evaluation of bacterial blight resistance. This work was supported by grants from the Strategic Priority Research Program of the Chinese Academy of Sciences (Precision Seed Design and Breeding, grant no. XDA24020100), the National Transgenic Science and Technology Program (grant no. 2016ZX08010002), the National Natural Science Foundation of China (grant no. 31788103, 31971370), the National Key Research and Development Program of China (grant no. 2016YFD0101804), the Chinese Academy of Sciences (grant no. QYZDY-SSW-SMC030) and the Postdoctoral Innovative Talent Support Program of China (grant no. BX20190365).

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S.W., H.Z. and C.G. designed the project. S.W., Y.Z., Q.L., H.Z., Z.C., K.C. and D.Z. performed the experiments. C.G. supervised the project. S.W., Y.Z., Q.L., H.Z, J.-L.Q. and C.G. wrote the manuscript.

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Correspondence to Caixia Gao.

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Supplementary Figs. 1–9, Tables 1 and 2 and Sequences 1 and 2.

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Wang, S., Zong, Y., Lin, Q. et al. Precise, predictable multi-nucleotide deletions in rice and wheat using APOBEC–Cas9. Nat Biotechnol 38, 1460–1465 (2020). https://doi.org/10.1038/s41587-020-0566-4

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