Shortened snRNA promoters for efficient CRISPR/Cas-based multiplex genome editing in monocot plants-Reference-Cited by-同舟云学术

Shortened snRNA promoters for efficient CRISPR/Cas-based multiplex genome editing in monocot plants

Published:2020-01-14 Issue:6 Volume:63 Page:933-935
ISSN:1674-7305
Container-title:Science China Life Sciences
language:en
Short-container-title:Sci. China Life Sci.

Author:

Hao Yu,Zong Wubei,Zeng Dongchang,Han Jingluan,Chen Shuifu,Tang Jianian,Zhao Zhe,Li Xiaojuan,Ma Kun,Xie Xianrong,Zhu Qinlong,Chen Yuanling,Zhao Xiucai,Guo Jingxin,Liu Yao-Guang

Publisher

Springer Science and Business Media LLC

Subject

General Agricultural and Biological Sciences,General Environmental Science,General Biochemistry, Genetics and Molecular Biology

Link

http://link.springer.com/content/pdf/10.1007/s11427-019-1612-6.pdf

Reference11 articles.

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2. Cong, L., Ran, F.A., Cox, D., Lin, S., Barretto, R., Habib, N., Hsu, P.D., Wu, X., Jiang, W., Marraffini, L.A., et al. (2013). Multiplex genome engineering using CRISPR/Cas systems. Science 339, 819–823.

3. Connelly, S., Marshallsay, C., Leader, D., Brown, J.W., and Filipowicz, W. (1994). Small nuclear RNA genes transcribed by either RNA polymerase II or RNA polymerase III in monocot plants share three promoter elements and use a strategy to regulate gene expression different from that used by their dicot plant counterparts. Mol Cell Biol 14, 5910–5919.

4. Ding, D., Chen, K., Chen, Y., Li, H., and Xie, K. (2018). Engineering introns to express RNA guides for Cas9- and Cpf1-mediated multiplex genome editing. Mol Plant 11, 542–552.

5. Engler, C., Kandzia, R., and Marillonnet, S. (2008). A one pot, one step, precision cloning method with high throughput capability. PLoS ONE 3, e3647.

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