An update of pTRIDENT multicistronic expression vectors: pTRIDENTs containing novel streptogramin-responsive promoters

被引:32
作者
Moser, S [1 ]
Schlatter, S [1 ]
Fux, C [1 ]
Rimann, M [1 ]
Bailey, JE [1 ]
Fussenegger, M [1 ]
机构
[1] Swiss Fed Inst Technol, Swiss Fed Inst Technol, Inst Biotechnol, CH-8093 Zurich, Switzerland
关键词
D O I
10.1021/bp000077r
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
We present an update on the pTRIDENT multicistronic mammalian expression vectors and their implications in various metabolic engineering and therapeutic applications. The pTRIDENT vector family has been expanded by construction of a new set of pTRPDENT-based vectors containing constitutive promoters of human origin (ubiquitin C and EF-1 alpha promoters) and selectable markers (zeocin resistance) and expressing different reporter genes (secreted alkaline phosphatase (SEAP) and the secreted single-chain urokinase-type plasminogen activator (low-M-r u-PA)). In addition, we have constructed pTRIDENT derivatives with novel streptogramin-repressible and streptogramin-inducible promoters for simultaneous and adjustable expression of three different transgenes. Streptogramin-inducible and tetracycline-repressible pTRIDENT derivatives were used to simultaneously control expression of three fluorescent proteins in mammalian cells: the enhanced cyan fluorescent protein (CFP), the recently isolated red fluorescent protein (RFP, also designated dsRed), and the enhanced yellow fluorescent protein (YFP). Owing to their modular structure, the pTRIDENT vector family represents a construction kit for the design of novel multicistronic expression constructs.
引用
收藏
页码:724 / 735
页数:12
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