Development of a species-specific RNA polymerase I-based shRNA expression vector
Author(s) -
Maria S. Brenz Verca,
Peter Weber,
Christine Mayer,
C. Graf,
Damián Refojo,
Ralf Kühn,
Ingrid Grummt,
Beat Lutz
Publication year - 2006
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkl1045
Subject(s) - rna polymerase iii , biology , small hairpin rna , rna interference , rna polymerase i , microbiology and biotechnology , trans acting sirna , small interfering rna , rna polymerase ii , transcription (linguistics) , rna induced transcriptional silencing , rna silencing , rna dependent rna polymerase , polymerase , rna , gene expression , promoter , genetics , gene , linguistics , philosophy
RNA interference (RNAi) can be induced in vitro either by application of synthetic short interfering RNAs (siRNAs), or by intracellular expression of siRNAs or short hairpin RNAs (shRNAs) from trans- fected vectors. The most widely used promoters for siRNA/shRNA expression are based on polymerase III (Pol III)-dependent transcription. We developed an alternative vector for siRNA/shRNA expression, using a mouse RNA polymerase I (Pol I) promoter. Pol I-dependent transcription serves in cells for pro- duction of ribosomal RNA (rRNA), and as such, is ubiquitously and stably active in different cell types. As Pol I-dependent transcription is highly species- specific, Pol I-based system provides an important biosafety advantage with respect to silencing of genes with unknown functions.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom