Generation of a Triple-Gene Knockout Mammalian Cell Line Using Engineered Zinc-Finger Nucleases

被引:82
作者
Liu, Pei-Qi [1 ]
Chan, Edmond M. [1 ]
Cost, Gregory J. [1 ]
Zhang, Lin [2 ]
Wang, Jianbin [1 ]
Miller, Jeffrey C. [1 ]
Guschin, Dmitry Y. [1 ]
Reik, Andreas [1 ]
Holmes, Michael C. [1 ]
Mott, John E. [2 ]
Collingwood, Trevor N. [3 ]
Gregory, Philip D. [1 ]
机构
[1] Sangamo BioSci Inc, Point Richmond Tech Ctr, Richmond, CA 94804 USA
[2] Pfizer Inc, Bioproc Res & Dev, Cell Line Dev, Chesterfield, MO 63017 USA
[3] Sigma Aldrich, St Louis, MO 63103 USA
关键词
zinc-finger nuclease; knockout; cell line engineering; GS; DHFR; Fut8; GLUTAMINE-SYNTHETASE; STEM-CELLS; GENOME; MECHANISM; ALPHA-1,6-FUCOSYL-TRANSFERASE; ESTABLISHMENT; MUTAGENESIS; DISRUPTION; CLEAVAGE; FUT8;
D O I
10.1002/bit.22654
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Mammalian cells with multi-gene knockouts could be of considerable utility in research, drug discovery, and cell-based therapeutics. However, existing methods for targeted gene deletion require sequential rounds of homologous recombination and drug selection to isolate rare desired events a process sufficiently laborious to limit application to individual loci. Here we present a solution to this problem. Firstly, we report the development of zinc-finger nucleases (ZFNs) targeted to cleave three independent genes with known null phenotypes. Mammalian cells exposed to each ZFN pair in turn resulted in the generation of cell lines harboring single, double, and triple gene knockouts, that is, the successful disruption of two, four, and six alleles. All three biallelic knockout events were obtained at frequencies of >1% without the use of selection, displayed the expected knockout phenotype(s), and harbored DNA mutations centered at the ZFN binding sites. These data demonstrate the utility of ZFNs in multi-locus genome engineering. Biotechnol. Bioeng. 2010;106: 97-105. (C) 2009 Wiley Periodicals, Inc.
引用
收藏
页码:97 / 105
页数:9
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