Flexible Accelerated STOP Tetracycline Operator-Knockin (FAST): A Versatile and Efficient New Gene Modulating System

被引:86
作者
Tanaka, Kenji F. [1 ,2 ,3 ,4 ]
Ahmari, Susanne E. [1 ,2 ]
Leonardo, E. David [1 ,2 ]
Richardson-Jones, Jesse W. [1 ,2 ]
Budreck, Elaine C. [5 ]
Scheiffele, Peter [5 ]
Sugio, Shouta [4 ]
Inamura, Naoko [3 ]
Ikenaka, Kazuhiro [3 ,4 ]
Hen, Rene [1 ,2 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Neurosci, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Pharmacol & Psychiat, New York, NY 10032 USA
[3] Natl Inst Physiol Sci, Div Neurobiol & Bioinformat, Okazaki, Aichi 444, Japan
[4] Grad Univ Adv Studies SOKENDAI, Sch Life Sci, Dept Physiol Sci, Kanagawa, Japan
[5] Univ Basel, Biozentrum, Dept Cell Biol, Basel, Switzerland
关键词
Animal model; conditional modulation of gene expression; developmental change; gene targeting; genetics; mouse; MICE; EXPRESSION; PROMOTERS; MUTATIONS; MOUSE;
D O I
10.1016/j.biopsych.2009.12.020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We created the Flexible Accelerated STOP Tetracycline Operator (tetO)-knockin (FAST) system, an efficient method for manipulating gene expression in vivo to rapidly screen animal models of disease. A single gene targeting event yields two distinct knockin mice STOP-tetO and tetO knockin that permit generation of multiple strains with variable expression patterns: 1) knockout, 2) Cre-mediated rescue, 3) tetracycline-controlled transcriptional activator (tTA)-mediated misexpression, 4) tetracycline-controlled transcriptional activator (tTA)mediated overexpression, and 5) tetracycline-controlled transcriptional silencer (tTS)-mediated conditional knockout/knockdown. Using the FAST system, multiple gain-of-function and loss-of-function strains can therefore be generated on a time scale not previously achievable. These strains can then be screened for clinically relevant abnormalities. We demonstrate the flexibility and broad applicability of the FAST system by targeting several genes encoding proteins implicated in neuropsychiatric disorders: Mid, neuroligin 3, the serotonin 1 A receptor, and the serotonin 1B receptor.
引用
收藏
页码:770 / 773
页数:4
相关论文
共 16 条
[1]  
DEUSCHLE U, 1995, MOL CELL BIOL, V15, P1907
[2]   Conditional mutagenesis in mice with heat shock promoter-driven cre transgenes [J].
Dietrich, P ;
Dragatsis, I ;
Xuan, SH ;
Zeitlin, S ;
Efstratiadis, A .
MAMMALIAN GENOME, 2000, 11 (03) :196-205
[3]  
Farley FW, 2000, GENESIS, V28, P106, DOI 10.1002/1526-968X(200011/12)28:3/4<106::AID-GENE30>3.0.CO
[4]  
2-T
[5]   TIGHT CONTROL OF GENE-EXPRESSION IN MAMMALIAN-CELLS BY TETRACYCLINE-RESPONSIVE PROMOTERS [J].
GOSSEN, M ;
BUJARD, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (12) :5547-5551
[6]   Serotonin1A receptor acts during development to establish normal anxiety-like behaviour in the adult [J].
Gross, C ;
Zhuang, XX ;
Stark, K ;
Ramboz, S ;
Oosting, R ;
Kirby, L ;
Santarelli, L ;
Beck, S ;
Hen, R .
NATURE, 2002, 416 (6879) :396-400
[7]   Reversal of neurological defects in a mouse model of Rett syndrome [J].
Guy, Jacky ;
Gan, Jian ;
Selfridge, Jim ;
Cobb, Stuart ;
Bird, Adrian .
SCIENCE, 2007, 315 (5815) :1143-1147
[8]   Cortex-restricted disruption of NMDAR1 impairs neuronal patterns in the barrel cortex [J].
Iwasato, T ;
Datwani, A ;
Wolf, AM ;
Nishiyama, H ;
Taguchi, Y ;
Tonegawa, S ;
Knöpfel, T ;
Erzurumlu, RS ;
Itohara, S .
NATURE, 2000, 406 (6797) :726-731
[9]   Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism [J].
Jamain, S ;
Quach, H ;
Betancur, C ;
Råstam, M ;
Colineaux, C ;
Gillberg, IC ;
Soderstrom, H ;
Giros, B ;
Leboyer, M ;
Gillberg, C ;
Bourgeron, T ;
Gillberg, C ;
Råstam, M ;
Gillberg, C ;
Nydén, A ;
Söderström, H ;
Leboyer, M ;
Betancur, C ;
Philippe, A ;
Giros, B ;
Colineaux, C ;
Cohen, D ;
Chabane, N ;
Mouren-Siméoni, MC ;
Brice, A ;
Sponheim, E ;
Spurkland, I ;
Skjeldal, OH ;
Coleman, M ;
Pearl, PL ;
Cohen, IL ;
Tsiouris, J ;
Zappella, M ;
Menchetti, G ;
Pompella, A ;
Aschauer, H ;
Van Maldergem, L .
NATURE GENETICS, 2003, 34 (01) :27-29
[10]   TARGETED ONCOGENE ACTIVATION BY SITE-SPECIFIC RECOMBINATION IN TRANSGENIC MICE [J].
LAKSO, M ;
SAUER, B ;
MOSINGER, B ;
LEE, EJ ;
MANNING, RW ;
YU, SH ;
MULDER, KL ;
WESTPHAL, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6232-6236