In vivo genome editing using a high-efficiency TALEN system

被引:712
作者
Bedell, Victoria M. [1 ]
Wang, Ying [2 ]
Campbell, Jarryd M. [1 ]
Poshusta, Tanya L. [1 ]
Starker, Colby G. [3 ,4 ]
Krug, Randall G., II [1 ]
Tan, Wenfang [3 ,4 ]
Penheiter, Sumedha G. [1 ]
Ma, Alvin C. [1 ,5 ]
Leung, Anskar Y. H. [5 ]
Fahrenkrug, Scott C. [3 ,4 ,6 ]
Carlson, Daniel F. [3 ,4 ,6 ]
Voytas, Daniel F. [3 ,4 ]
Clark, Karl J. [1 ]
Essner, Jeffrey J. [2 ]
Ekker, Stephen C. [1 ]
机构
[1] Mayo Clin, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[2] Iowa State Univ, Dept Genet Dev & Cell Biol, Ames, IA 50011 USA
[3] Univ Minnesota, Ctr Genome Engn, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Dept Anim Sci, Minneapolis, MN 55455 USA
[5] Univ Hong Kong, LKS Fac Med, Dept Med, Hong Kong, Hong Kong, Peoples R China
[6] Recombinetics Inc, St Paul, MN 55114 USA
基金
美国国家科学基金会;
关键词
ZINC-FINGER NUCLEASES; TARGETED GENE DISRUPTION; DNA-BINDING SPECIFICITY; ZEBRAFISH; EFFECTORS; CELLS;
D O I
10.1038/nature11537
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The zebrafish (Danio rerio) is increasingly being used to study basic vertebrate biology and human disease with a rich array of in vivo genetic and molecular tools. However, the inability to readily modify the genome in a targeted fashion has been a bottleneck in the field. Here we show that improvements in artificial transcription activator-like effector nucleases (TALENs) provide a powerful new approach for targeted zebrafish genome editing and functional genomic applications(1-5). Using the GoldyTALEN modified scaffold and zebrafish delivery system, we show that this enhanced TALEN toolkit has a high efficiency in inducing locus-specific DNA breaks in somatic and germline tissues. At some loci, this efficacy approaches 100%, including biallelic conversion in somatic tissues that mimics phenotypes seen using morpholino-based targeted gene knockdowns(6). With this updated TALEN system, we successfully used single-stranded DNA oligonucleotides to precisely modify sequences at predefined locations in the zebrafish genome through homology-directed repair, including the introduction of a custom-designed EcoRV site and a modified loxP (mloxP) sequence into somatic tissue in vivo. We further show successful germline transmission of both EcoRV and mloxP engineered chromosomes. This combined approach offers the potential to model genetic variation as well as to generate targeted conditional alleles.
引用
收藏
页码:114 / U133
页数:7
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