Genome Engineering of Drosophila with the CRISPR RNA-Guided Cas9 Nuclease

被引:801
作者
Gratz, Scott J. [1 ]
Cummings, Alexander M. [2 ]
Nguyen, Jennifer N. [3 ]
Hamm, Danielle C. [4 ]
Donohue, Laura K. [2 ]
Harrison, Melissa M. [4 ,6 ]
Wildonger, Jill [3 ]
O'Connor-Giles, Kate M. [1 ,2 ,5 ]
机构
[1] Univ Wisconsin, Genet Training Program, Madison, WI 53706 USA
[2] Univ Wisconsin, Genet Lab, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[4] Univ Wisconsin, Integrated Program Biochem, Madison, WI 53706 USA
[5] Univ Wisconsin, Lab Cell & Mol Biol, Madison, WI 53706 USA
[6] Univ Wisconsin, Sch Med & Publ Hlth, Dept Biomol Chem, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
ZINC-FINGER NUCLEASES; INDUCED GAP REPAIR; HOMOLOGOUS RECOMBINATION; GENE; EFFICIENT; MELANOGASTER; MUTAGENESIS; ENDONUCLEASE; INTERFERENCE; REPLACEMENT;
D O I
10.1534/genetics.113.152710
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have adapted a bacterial CRISPR RNA/Cas9 system to precisely engineer the Drosophila genome and report that Cas9-mediated genomic modifications are efficiently transmitted through the germline. This RNA-guided Cas9 system can be rapidly programmed to generate targeted alleles for probing gene function in Drosophila.
引用
收藏
页码:1029 / +
页数:17
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