Rapid "Open-Source" engineering of customized zinc-finger nucleases for highly efficient gene modification

被引:533
作者
Maeder, Morgan L. [1 ,2 ,3 ]
Thibodeau-Beganny, Stacey [1 ,2 ,3 ]
Osiak, Anna [5 ]
Wright, David A. [6 ]
Anthony, Reshma M. [8 ]
Eichtinger, Magdalena [1 ,2 ,3 ,9 ]
Jiang, Tao [1 ,2 ,3 ,9 ]
Foley, Jonathan E. [1 ,2 ,3 ]
Winfrey, Ronnie J. [6 ]
Townsend, Jeffrey A. [6 ]
Unger-Wallace, Erica [6 ]
Sander, Jeffry D. [6 ,7 ]
Mueller-Lerch, Felix [5 ]
Fu, Fengli [6 ,7 ]
Pearlberg, Joseph [10 ]
Goebel, Carl [1 ,2 ,3 ]
Dassie, Justin P. [8 ]
Pruett-Miller, Shondra M. [11 ]
Porteus, Matthew H. [11 ]
Sgroi, Dennis C. [1 ,2 ,9 ]
Iafrate, A. John [4 ,9 ]
Dobbs, Drena [6 ]
McCray, Paul B., Jr. [8 ]
Cathomen, Toni
Voytas, Daniel F. [6 ]
Joung, J. Keith [1 ,2 ,3 ,9 ]
机构
[1] Massachusetts Gen Hosp, Mol Pathol Unit, Boston, MA 02129 USA
[2] Massachusetts Gen Hosp, Ctr Canc Res, Boston, MA 02129 USA
[3] Massachusetts Gen Hosp, Ctr Computat & Integrat Biol, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Pathol Serv, Boston, MA 02114 USA
[5] Charite Univ Sch, Inst Virol CBF, D-12203 Berlin, Germany
[6] Iowa State Univ, Dept Genet Dev & Cell Biol, Ames, IA 50011 USA
[7] Iowa State Univ, Interdept Grad Program Bioinformat & Computat Bio, Ames, IA 50011 USA
[8] Univ Iowa, Dept Pediat, Carver Coll Med, Iowa City, IA 52242 USA
[9] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[10] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[11] Univ Texas SW Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA
关键词
D O I
10.1016/j.molcel.2008.06.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Custom-made zinc-finger nucleases (ZFNs) can induce targeted genome modifications with high efficiency in cell types including Drosophila, C. elegans, plants, and humans. A bottleneck in the application of ZFN technology has been the generation of highly specific engineered zinc-finger arrays. Here we describe OPEN (Oligomerized Pool ENgineering), a rapid, publicly available strategy for constructing multifinger arrays, which we show is more effective than the previously published modular assembly method. We used OPEN to construct 37 highly active ZFN pairs which induced targeted alterations with high efficiencies (1%-50%) at 11 different target sites located within three endogenous human genes (VEGF-A, HoxB13, and CFTR), an endogenous plant gene (tobacco SuRA), and a chromosomally integrated EGFP reporter gene. In summary, OPEN provides an "open-source" method for rapidly engineering highly active zinc-finger arrays, thereby enabling broader practice, development, and application of ZFN technology for biological research and gene therapy.
引用
收藏
页码:294 / 301
页数:8
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