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Vector Systems for the Delivery of Small Interfering RNAs: Managing the RISC
Author(s) -
Arendt Christopher W.,
Tang Guilin,
Zilberstein Asher
Publication year - 2003
Publication title -
chembiochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.05
H-Index - 126
eISSN - 1439-7633
pISSN - 1439-4227
DOI - 10.1002/cbic.200300695
Subject(s) - trans acting sirna , small interfering rna , rna interference , dicer , rna induced silencing complex , rna silencing , rna , biology , gene silencing , argonaute , small hairpin rna , rna induced transcriptional silencing , computational biology , microbiology and biotechnology , genetics , gene
Silence is golden : Recent breakthroughs in the field of RNA interference have made it feasible to engineer DNA vectors capable of selectively silencing the expression of genes in a wide variety of cell types. For example, lentiviral vectors containing an RNA polymerase III promoter such as U6 have been developed for the expression of small RNA hairpins. These RNA hairpin transcripts serve as substrates for the cytoplasmic ribonuclease Dicer, generating small interfering RNAs (siRNAs) capable of inducing RNA interference in association with the RNA‐induced silencing complex (RISC). A variety of vector strategies have been employed to achieve siRNA expression and long‐term gene suppression. Recent studies have provided new insights into how these vector strategies might be refined to achieve potent and specific gene suppression, while minimizing the risks associated with these approaches.

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