Gene Targeting Using Homologous Recombination in Embryonic Stem Cells: The Future for Behavior Genetics?

被引:17
|
作者
Gerlai, Robert [1 ,2 ]
机构
[1] Univ Toronto, Dept Cell & Syst Biol, Mississauga, ON L5L 1C6, Canada
[2] Univ Toronto, Dept Psychol, Mississauga, ON L5L 1C6, Canada
来源
FRONTIERS IN GENETICS | 2016年 / 7卷
关键词
INBRED MOUSE STRAINS; FLP RECOMBINASE; MUTANT MICE; BRAIN; MEMORY; DNA; MUTATIONS; NUCLEASES; GENOME; CRISPR;
D O I
10.3389/fgene.2016.00043
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene targeting with homologous recombination in embryonic stem cells created a revolution in the analysis of the function of genes in behavioral brain research. The technology allowed unprecedented precision with which one could manipulate genes and study the effect of this manipulation on the central nervous system. With gene targeting, the uncertainty inherent in psychopharmacology regarding whether a particular compound would act only through a specific target was removed. Thus, gene targeting became highly popular. However, with this popularity came the realization that like other methods, gene targeting also suffered from some technical and principal problems. For example, two decades ago, issues about compensatory changes and about genetic linkage were raised. Since then, the technology developed, and its utility has been better delineated. This review will discuss the pros and cons of the technique along with these advancements from the perspective of the neuroscientist user. It will also compare and contrast methods that may represent novel alternatives to the homologous recombination based gene targeting approach, including the TALEN and the CRISPR/Cas9 systems. The goal of the review is not to provide detailed recipes, but to attempt to present a short summary of these approaches a behavioral geneticist or neuroscientist may consider for the analysis of brain function and behavior.
引用
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页数:10
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