The reverse tetracycline-controlled transactivator rtTA2S-S2 is toxic in mouse embryonic stem cells

被引:9
作者
Bryja, V
Pachernik, H
Kubala, L
Hampl, A
Dvorak, P
机构
[1] Charles Univ, Ctr Cell Therapy & Tissue Repair, Prague 15006, Czech Republic
[2] Acad Sci Czech Republ, Inst Expt Med, Dept Mol Embryol, Prague 14220, Czech Republic
[3] Mendel Univ Brno, Mol Embryol Lab, Brno 61300, Czech Republic
[4] Acad Sci Czech Republ, Inst Biophys, Lab Free Rad Pathophysiol, CS-61265 Brno, Czech Republic
来源
REPRODUCTION NUTRITION DEVELOPMENT | 2003年 / 43卷 / 06期
关键词
tetOn system; reverse tetracycline-controlled transactivator; embryonic stem cell; toxicity;
D O I
10.1051/rnd:2004001
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The efficient and reversible control of transgene expression is a powerful tool for the correct manipulation of embryonic stem cells in both cell therapy and transgenesis. The aim of this work was to investigate the possibilities of recently developed reverse tetracycline-controlled transactivator rtTA2(S)-S2. We show that the rtTA2(S)-S2 is useful for transient inducible expression of genes in embryonic stem cells. However, we found that it was not possible to establish mouse embryonic stem cell lines stably expressing this transactivator. Using the viral IRES sequence which couples the expression of rtTA2(S)-S2 and neomycin phosphotransferase, we found that embryonic stem cells expressing rtTA2(S)-S2 are not capable of growing in the presence of G418. Our results indicate that this transactivator is toxic to ES cells and raise the need for the development of other strategies for stable and inducible expression of genes in ES cells.
引用
收藏
页码:477 / 486
页数:10
相关论文
共 20 条
[1]   Tetracycline-controlled transcription in eukaryotes: Novel transactivators with graded transactivation potential [J].
Baron, U ;
Gossen, M ;
Bujard, H .
NUCLEIC ACIDS RESEARCH, 1997, 25 (14) :2723-2729
[2]   Latest developments and in vivo use of the Tet system:: ex vivo and in vivo delivery of tetracycline-regulated genes [J].
Corbel, SY ;
Rossi, FM .
CURRENT OPINION IN BIOTECHNOLOGY, 2002, 13 (05) :448-452
[3]  
DOETSCHMAN TC, 1985, J EMBRYOL EXP MORPH, V87, P27
[4]  
Elder D, 1999, RIV BIOL-BIOL FORUM, V92, P275
[5]   Regulated expression of P210 Bcr-Abl during embryonic stem cell differentiation stimulates multipotential progenitor expansion and myeloid cell fate [J].
Era, T ;
Witte, ON .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (04) :1737-1742
[6]   Tet-system for the regulation of gene expression during embryonic development [J].
Fedorov, LM ;
Tyrsin, OY ;
Krenn, V ;
Chernigovskaya, EV ;
Rapp, UR .
TRANSGENIC RESEARCH, 2001, 10 (03) :247-258
[7]   A syndrome of multiorgan hyperplasia with features of gigantism, tumorigenesis, and female sterility in p27(Kip1)-deficient mice [J].
Fero, ML ;
Rivkin, M ;
Tasch, M ;
Porter, P ;
Carow, CE ;
Firpo, E ;
Polyak, K ;
Tsai, LH ;
Broudy, V ;
Perlmutter, RM ;
Kaushansky, K ;
Roberts, JM .
CELL, 1996, 85 (05) :733-744
[8]   TEMPORAL CONTROL OF GENE-EXPRESSION IN TRANSGENIC MICE BY A TETRACYCLINE-RESPONSIVE PROMOTER [J].
FURTH, PA ;
STONGE, L ;
BOGER, H ;
GRUSS, P ;
GOSSEN, M ;
KISTNER, A ;
BUJARD, H ;
HENNIGHAUSEN, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (20) :9302-9306
[9]   Evaluation of an autoregulatory tetracycline regulated system [J].
Gallia, GL ;
Khalili, K .
ONCOGENE, 1998, 16 (14) :1879-1884
[10]   Use of the human EF-1α promoter for expression can significantly increase success in establishing stable cell lines with consistent expression:: a study using the tetracycline-inducible system in human cancer cells [J].
Gopalkrishnan, RV ;
Christiansen, KA ;
Goldstein, NI ;
DePinho, RA ;
Fisher, PB .
NUCLEIC ACIDS RESEARCH, 1999, 27 (24) :4775-4782