Polyswitch Lentivectors: "All-in-One" Lentiviral Vectors for Drug-Inducible Gene Expression, Live Selection, and Recombination Cloning

被引:19
|
作者
Giry-Laterriere, Marc [1 ]
Cherpin, Ophelie [1 ]
Kim, Yong-Sik [2 ]
Jensen, Jan [2 ]
Salmon, Patrick [1 ]
机构
[1] CMU, Dept Neurosci, Fac Med, CH-1211 Geneva 4, Switzerland
[2] Cleveland Clin, Lerner Res Inst, Dept Stem Cell Biol & Regenerat Med, Cleveland, OH 44195 USA
关键词
TIGHT CONTROL; TRANSGENE EXPRESSION; REGULATED EXPRESSION; MAMMALIAN-CELLS; DNA CLONING; SYSTEM; VIVO; GENERATION; PROMOTER; TRANSACTIVATOR;
D O I
10.1089/hum.2010.179
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Lentiviral vectors are now widely considered one of the safest and most efficient tools for gene delivery and stable gene expression. Even though inducible gene expression cassettes are mandatory for many genetic engineering strategies, most current systems suffer from various issues, such as the requirement of two vectors, which decreases the overall efficiency of the tran.sduction, leakiness and/or insufficient levels of activation of the inducible promoter, lack of selectable marker, low titers, or general issues associated with the cloning of large plasmids. In this article, we describe the design and functional characterization of a set of "all-in-one" multicistronic autoinducible lentivectors. They combine: (1) an optimized drug-inducible promoter; (2) a multicistronic strategy to express living color, selectable marker, and transactivator; and (3) acceptor sites for easy recombination cloning of genes of interest. These polyswitch lentivectors have good titers, very low basal activity, and reversible high induced activity, and can accept a growing number of genes already cloned in entry plasmids. These combined features make them a novel, powerful, and versatile tool for current and future genetic engineering approaches.
引用
收藏
页码:1255 / 1267
页数:13
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