Genome Engineering With Zinc-Finger Nucleases

被引:705
作者
Carroll, Dana [1 ]
机构
[1] Univ Utah, Sch Med, Dept Biochem, Salt Lake City, UT 84112 USA
基金
美国国家卫生研究院;
关键词
DOUBLE-STRAND BREAKS; TARGETED GENE DISRUPTION; DNA-BINDING SPECIFICITY; HOMOLOGOUS RECOMBINATION; KNOCKOUT RATS; RESTRICTION ENZYMES; MAMMALIAN GENOME; STEM-CELLS; I-SCEI; MUTAGENESIS;
D O I
10.1534/genetics.111.131433
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Zinc-finger nucleases (ZFNs) are targetable DNA cleavage reagents that have been adopted as gene-targeting tools. ZFN-induced double-strand breaks are subject to cellular DNA repair processes that lead to both targeted mutagenesis and targeted gene replacement at remarkably high frequencies. This article briefly reviews the history of ZFN development and summarizes applications that have been made to genome editing in many different organisms and situations. Considerable progress has been made in methods for deriving zinc-finger sets for new genomic targets, but approaches to design and selection are still being perfected. An issue that needs more attention is the extent to which available mechanisms of double-strand break repair limit the scope and utility of ZFN-initiated events. The bright prospects for future applications of ZFNs, including human gene therapy, are discussed.
引用
收藏
页码:773 / 782
页数:10
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