References
Bi, H., and Yang, B. (2017). Gene editing with TALEN and CRISPR/Cas in rice. Prog Mol Biol Transl Sci 149, 81–98.
Boettcher, M., and McManus, M.T. (2015). Choosing the right tool for the job: RNAi, TALEN, or CRISPR. Mol Cell 58, 575–585.
Carroll, D. (2011). Genome engineering with zinc-finger nucleases. Genetics 188, 773–782.
Chen, J.S., Ma, E., Harrington, L.B., Da Costa, M., Tian, X., Palefsky, J.M., and Doudna, J.A. (2018). CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity. Science 360, 436–439.
Doudna, J.A., and Charpentier, E. (2014). The new frontier of genome engineering with CRISPR-Cas9. Science 346, 1258096.
English, M.A., Soenksen, L.R., Gayet, R.V., de Puig, H., Angenent-Mari, N.M., Mao, A.S., Nguyen, P.Q., and Collins, J.J. (2019). Programmable CRISPR-responsive smart materials. Science 365, 780–785.
Gootenberg, J.S., Abudayyeh, O.O., Kellner, M.J., Joung, J., Collins, J.J., and Zhang, F. (2018). Multiplexed and portable nucleic acid detection platform with Cas13, Cas12a, and Csm6. Science 360, 439–444.
Gootenberg, J.S., Abudayyeh, O.O., Lee, J.W., Essletzbichler, P., Dy, A.J., Joung, J., Verdine, V., Donghia, N., Daringer, N.M., Freije, C.A., et al. (2017). Nucleic acid detection with CRISPR-Cas13a/C2c2. Science 356, 438–442.
He, Z.Y., Men, K., Qin, Z., Yang, Y., Xu, T., and Wei, Y.Q. (2017). Non-viral and viral delivery systems for CRISPR-Cas9 technology in the biomedical field. Sci China Life Sci 60, 458–467.
Hsu, P.D., Lander, E.S., and Zhang, F. (2014). Development and applications of CRISPR-Cas9 for genome engineering. Cell 157, 1262–1278.
Knight, S.C., Tjian, R., and Doudna, J.A. (2018). Genomes in focus: development and applications of CRISPR-Cas9 imaging technologies. Angew Chem Int Ed 57, 4329–4337.
Knott, G.J., and Doudna, J.A. (2018). CRISPR-Cas guides the future of genetic engineering. Science 361, 866–869.
Li, S.Y., Cheng, Q.X., Liu, J.K., Nie, X.Q., Zhao, G.P., and Wang, J. (2018). CRISPR-Cas12a has both cis- and trans-cleavage activities on single-stranded DNA. Cell Res 28, 491–493.
Pardee, K., Green, A.A., Takahashi, M.K., Braff, D., Lambert, G., Lee, J. W., Ferrante, T., Ma, D., Donghia, N., Fan, M., et al. (2016). Rapid, low-cost detection of Zika virus using programmable biomolecular components. Cell 165, 1255–1266.
Ren, X., Holsteens, K., Li, H., Sun, J., Zhang, Y., Liu, L.P., Liu, Q., and Ni, J.Q. (2017). Genome editing in Drosophila melanogaster: from basic genome engineering to the multipurpose CRISPR-Cas9 system. Sci China Life Sci 60, 476–489.
Shen, L., Hua, Y., Fu, Y., Li, J., Liu, Q., Jiao, X., Xin, G., Wang, J., Wang, X., Yan, C., et al. (2017). Rapid generation of genetic diversity by multiplex CRISPR/Cas9 genome editing in rice. Sci China Life Sci 60, 506–515.
Singh, V., Braddick, D., and Dhar, P.K. (2017). Exploring the potential of genome editing CRISPR-Cas9 technology. Gene 599, 1–18.
Terns, R.M., and Terns, M.P. (2014). CRISPR-based technologies: prokaryotic defense weapons repurposed. Trends Genet 30, 111–118.
Wang, Y., Meng, Z., Liang, C., Meng, Z., Wang, Y., Sun, G., Zhu, T., Cai, Y., Guo, S., Zhang, R., et al. (2017). Increased lateral root formation by CRISPR/Cas9-mediated editing of arginase genes in cotton. Sci China Life Sci 60, 524–527.
Zhang, X., Wang, L., Liu, M., and Li, D. (2017). CRISPR/Cas9 system: a powerful technology for in vivo and ex vivo gene therapy. Sci China Life Sci 60, 468–475.
Author information
Authors and Affiliations
Corresponding author
Additional information
Compliance and ethics The author(s) declare that they have no conflict of interest.
Rights and permissions
About this article
Cite this article
Hong, W., Huang, M., Wei, Y. et al. A new and promising application of gene editing: CRISPR-controlled smart materials for tissue engineering, bioelectronics, and diagnostics. Sci. China Life Sci. 62, 1547–1549 (2019). https://doi.org/10.1007/s11427-019-1576-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11427-019-1576-0