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
收藏
页数:10
相关论文
共 50 条
  • [31] PRODUCTION OF A MUTATION IN MOUSE EN-2 GENE BY HOMOLOGOUS RECOMBINATION IN EMBRYONIC STEM-CELLS
    JOYNER, AL
    SKARNES, WC
    ROSSANT, J
    NATURE, 1989, 338 (6211) : 153 - 156
  • [32] TARGETED DISRUPTION OF THE PTH PTHRP RECEPTOR GENE BY HOMOLOGOUS RECOMBINATION IN MOUSE EMBRYONIC STEM-CELLS
    LANSKE, BKM
    KARAPLIS, AC
    KRONENBERG, HM
    JOURNAL OF BONE AND MINERAL RESEARCH, 1993, 8 : S189 - S189
  • [33] GENE TARGETING IN EMBRYONIC STEM-CELLS
    RAMIREZSOLIS, R
    DAVIS, AC
    BRADLEY, A
    GUIDE TO TECHNIQUES IN MOUSE DEVELOPMENT, 1993, 225 : 855 - 878
  • [34] Gene targeting by homologous recombination in Drosophila
    Rong, YS
    Golic, KG
    SCIENCE, 2000, 288 (5473) : 2013 - 2018
  • [35] GENE REPLACEMENT OF THE P53 GENE WITH THE LACZ GENE IN MOUSE EMBRYONIC STEM-CELLS AND MICE BY USING 2 STEPS OF HOMOLOGOUS RECOMBINATION
    GONDO, Y
    NAKAMURA, K
    NAKAO, K
    SASAOKA, T
    ITO, K
    KIMURA, M
    KATSUKI, M
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 202 (02) : 830 - 837
  • [36] GENETICS OF GENETICS IN DROSOPHILA - P-ELEMENTS SERVING THE STUDY OF HOMOLOGOUS RECOMBINATION, GENE CONVERSION AND TARGETING
    LANKENAU, DH
    CHROMOSOMA, 1995, 103 (10) : 659 - 668
  • [37] Is homologous recombination in stem cells a realistic approach to gene therapy?
    Rahemtulla, A
    Leung, R
    BLOOD, 1999, 94 (10) : 415B - 415B
  • [38] CFTR gene targeting in mouse embryonic stem cells mediated by Small Fragment Homologous Replacement (SFHR)
    Sangiuolo, Federica
    Scaldaferri, Maria Lucia
    Filareto, Antonio
    Spitalieri, Paola
    Guerra, Lorenzo
    Favia, Maria
    Caroppo, Rosa
    Mango, Ruggiero
    Bruscia, Emanuela
    Gruenert, Dieter C.
    Casavola, Valeria
    De Felici, Massimo
    Novelli, Giuseppe
    FRONTIERS IN BIOSCIENCE-LANDMARK, 2008, 13 : 2989 - 2999
  • [39] THE ROLE AND FATE OF DNA ENDS FOR HOMOLOGOUS RECOMBINATION IN EMBRYONIC STEM-CELLS
    HASTY, P
    RIVERAPEREZ, J
    BRADLEY, A
    MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (06) : 2464 - 2474
  • [40] Efficient gene targeting in mouse embryonic stem cells
    Templeton, NS
    Roberts, DD
    Safer, B
    GENE THERAPY, 1997, 4 (07) : 700 - 709