Regulated multicistronic expression technology for mammalian metabolic engineering

被引:13
作者
Fussenegger, M [1 ]
Moser, S [1 ]
Bailey, JE [1 ]
机构
[1] Swiss Fed Inst Technol, ETH Zurich, Inst Biotechnol, CH-8093 Zurich, Switzerland
关键词
autoregulation; cell-cycle engineering; eukaryotic operon; IRES; multigene engineering; picornavirus; pTRIDENT; regulated expression;
D O I
10.1023/A:1008037916674
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
Contemporary basic research is rapidly revealing increasingly complex molecular regulatory networks which are often interconnected via key signal integrators. These connections among regulatory and catalytic networks often frustrate bioengineers as promising metabolic engineering strategies are bypassed by compensatory metabolic responses or cause unexpected, undesired outcomes such as apoptosis, product protein degradation or inappropriate post-translational modification. Therefore, for metabolic engineering to achieve greater success in mammalian cell culture processes and to become important for future applications such as gene therapy and tissue engineering, this technology must be enhanced to allow simultaneous, in cases conditional, reshaping of metabolic pathways to access difficult-to-attain cell states. Recent advances in this new territory of multigene metabolic engineering are intimately linked to the development of multicistronic expression technology which allows the simultaneous, and in some cases, regulated expression of several genes in mammalian cells. Here we review recent achievements in multicistronic expression technology in view of multigene metabolic engineering.
引用
收藏
页码:111 / 125
页数:15
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