Targeted genome engineering techniques in Drosophila

被引:60
作者
Beumer, Kelly J. [1 ]
Carroll, Dana [1 ]
机构
[1] Univ Utah, Sch Med, Dept Biochem, Salt Lake City, UT 84112 USA
关键词
TALEN; CRISPR; Zinc finger nuclease; Gene targeting; Drosophila; Nuclease; NHEJ; Homologous recombination; ZINC-FINGER NUCLEASES; TAL EFFECTOR NUCLEASES; SITE-SPECIFIC RECOMBINATION; GUIDED CAS9 NUCLEASE; HIGHLY EFFICIENT; HOMOLOGOUS RECOMBINATION; GENE REPLACEMENT; DNA ENDONUCLEASE; III EFFECTORS; HUMAN-CELLS;
D O I
10.1016/j.ymeth.2013.12.002
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
For a century, Drosophila has been a favored organism for genetic research. However, the array of materials and methods available to the Drosophila worker has expanded dramatically in the last decade. The most common gene targeting tools, zinc finger nucleases, TALENs, and RNA-guided CRISPR/Cas9, have all been adapted for use in Drosophila, both for simple mutagenesis and for gene editing via homologous recombination. For each tool, there exist a number of web sites, design applications, and delivery methods. The successful application of any of these tools also requires an understanding of methods for detecting successful genome modifications. This article provides an overview of the available gene targeting tools and their application in Drosophila. In lieu of simply providing a protocol for gene targeting, we direct the researcher to resources that will allow access to the latest research in this rapidly evolving field. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:29 / 37
页数:9
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