Basic Principles of RNA Interference: Nucleic Acid Types and In Vitro Intracellular Delivery Methods

被引:6
作者
Isenmann, Marie [1 ,2 ]
Stoddart, Martin James [1 ,2 ]
Schmelzeisen, Rainer [1 ]
Gross, Christian [1 ]
Della Bella, Elena [2 ]
Rothweiler, Rene Marcel [1 ,2 ]
机构
[1] Univ Freiburg, Fac Med, Dept Oral & Maxillofacial Surg, Hugstetterstr 55, D-79106 Freiburg, Germany
[2] AO Res Inst Davos, Clavadelerstr 8, CH-7270 Davos, Switzerland
关键词
RNA interference; siRNA; miRNA; shRNA; piRNA; ASO; gene silencing; CONDITIONALLY REPLICATING ADENOVIRUSES; HUMAN HEMATOPOIETIC STEM; TOBACCO-MOSAIC-VIRUS; SHORT HAIRPIN RNAS; GENE-EXPRESSION; FUSOGENIC LIPOSOMES; STRUCTURAL BASIS; MESSENGER-RNA; TRANSFECTION EFFICIENCY; DEPENDENT STIMULATION;
D O I
10.3390/mi14071321
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Since its discovery in 1989, RNA interference (RNAi) has become a widely used tool for the in vitro downregulation of specific gene expression in molecular biological research. This basically involves a complementary RNA that binds a target sequence to affect its transcription or translation process. Currently, various small RNAs, such as small interfering RNA (siRNA), micro RNA (miRNA), small hairpin RNA (shRNA), and PIWI interacting RNA (piRNA), are available for application on in vitro cell culture, to regulate the cells' gene expression by mimicking the endogenous RNAi-machinery. In addition, several biochemical, physical, and viral methods have been established to deliver these RNAs into the cell or nucleus. Since each RNA and each delivery method entail different off-target effects, limitations, and compatibilities, it is crucial to understand their basic mode of action. This review is intended to provide an overview of different nucleic acids and delivery methods for planning, interpreting, and troubleshooting of RNAi experiments.
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页数:22
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