An alternative strategy for targeted gene replacement in plants using a dual-sgRNA/Cas9 design-Reference-Cited by-同舟云学术

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An alternative strategy for targeted gene replacement in plants using a dual-sgRNA/Cas9 design

Published:2016-04 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Zhao Yongping,Zhang Congsheng,Liu Wenwen,Gao Wei,Liu Changlin,Song Gaoyuan,Li Wen-Xue,Mao Long,Chen Beijiu,Xu Yunbi,Li Xinhai,Xie Chuanxiao

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep23890.pdf

Reference46 articles.

1. Gao, H. et al. Heritable targeted mutagenesis in maize using a designed endonuclease. The Plant Journal 61, 176–187, doi: 10.1111/j.1365-313X.2009.04041.x (2009).

2. Porteus, M. H. & Carroll, D. Gene targeting using zinc finger nucleases. Nat Biotech 23, 967–973 (2005).

3. Reyon, D. et al. FLASH assembly of TALENs for high-throughput genome editing. Nat Biotech 30, 460–465 (2012).

4. Jinek, M. et al. A programmable dual-RNA–guided DNA endonuclease in adaptive bacterial immunity. Science 337, 816–821, doi: 10.1126/science.1225829 (2012).

5. Feng, Z. et al. Efficient genome editing in plants using a CRISPR/Cas system. Cell Res 23, 1229–1232, doi: 10.1038/cr.2013.114 (2013).

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