Selection-free zinc-finger-nuclease engineering by context-dependent assembly (CoDA)

被引:321
作者
Sander, Jeffry D. [1 ,2 ,3 ]
Dahlborg, Elizabeth J. [1 ,2 ]
Goodwin, Mathew J. [1 ,2 ]
Cade, Lindsay [4 ]
Zhang, Feng [5 ,6 ]
Cifuentes, Daniel [7 ]
Curtin, Shaun J. [8 ]
Blackburn, Jessica S. [1 ,2 ,3 ]
Thibodeau-Beganny, Stacey [1 ,2 ]
Qi, Yiping [5 ,6 ]
Pierick, Christopher J. [5 ,6 ]
Hoffman, Ellen [7 ]
Maeder, Morgan L. [1 ,2 ,9 ]
Khayter, Cyd [1 ,2 ]
Reyon, Deepak [10 ,11 ]
Dobbs, Drena [10 ,11 ]
Langenau, David M. [1 ,3 ,9 ]
Stupar, Robert M. [8 ]
Giraldez, Antonio J. [7 ]
Voytas, Daniel F. [5 ,6 ]
Peterson, Randall T. [4 ,12 ,13 ]
Yeh, Jing-Ruey J. [4 ,12 ]
Joung, J. Keith [1 ,2 ,3 ,9 ]
机构
[1] Massachusetts Gen Hosp, Ctr Canc Res, Charlestown, MA USA
[2] Massachusetts Gen Hosp, Ctr Computat & Integrat Biol, Charlestown, MA USA
[3] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[4] Massachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA USA
[5] Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN USA
[6] Univ Minnesota, Ctr Genome Engn, Minneapolis, MN USA
[7] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA
[8] Univ Minnesota, Dept Agron & Plant Genet, St Paul, MN USA
[9] Harvard Univ, Sch Med, Biol & Biomed Sci Program, Boston, MA USA
[10] Iowa State Univ, Dept Genet Dev & Cell Biol, Ames, IA USA
[11] Iowa State Univ, Bioinformat & Computat Biol Program, Ames, IA USA
[12] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[13] Broad Inst, Cambridge, MA USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
TARGETED MUTAGENESIS;
D O I
10.1038/NMETH.1542
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Engineered zinc-finger nucleases (ZFNs) enable targeted genome modification. Here we describe context-dependent assembly (CoDA), a platform for engineering ZFNs using only standard cloning techniques or custom DNA synthesis. Using CoDA-generated ZFNs, we rapidly altered 20 genes in Danio rerio, Arabidopsis thaliana and Glycine max. The simplicity and efficacy of CoDA will enable broad adoption of ZFN technology and make possible large-scale projects focused on multigene pathways or genome-wide alterations.
引用
收藏
页码:67 / U94
页数:4
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