A novel tetracycline-dependent transactivator with E2F4 transcriptional activation domain

被引:30
作者
Akagi, Kiwamu [1 ]
Kanai, Masayuki [1 ]
Saya, Hideyuki [2 ,3 ]
Kozu, Tomoko [1 ]
Berns, Anton [4 ]
机构
[1] Saitama Canc Ctr, Res Inst, Ina, Saitama 3620806, Japan
[2] Kumamoto Univ, Dept Tumor Genet & Biol, Sch Med, Kumamoto 8600811, Japan
[3] Netherlands Canc Inst, Div Mol Genet, NL-1066 CX Amsterdam, Netherlands
[4] Netherlands Canc Inst, Ctr Biomed Genet, NL-1066 CX Amsterdam, Netherlands
关键词
D O I
10.1093/nar/29.4.e23
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A tetracycline-controlled gene expression system provides a powerful tool to dissect the functions of gene products. However, it often appears difficult to establish cell lines or transgenic animals stably expressing tetracycline-dependent transactivators, possibly as a result of toxicity of the transactivator domains used. In order to overcome this problem, we developed a novel tetracycline-dependent transactivator that works efficiently in mammalian cells. This transactivator is a fusion of the tet reverse repressor mutant and the transcriptional activating domain of human E2F4, which is ubiquitously expressed in vivo. We demonstrate here that this tetracycline-regulated gene expression system provides a two log transcriptional activation in mammalian cells as assessed by northern blot and luciferase analyses. Combining this system with green fluorescent protein reporter systems or microarray gene expression profiling will facilitate the study of gene function.
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页数:5
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