UMMS Affiliation

Department of Biochemistry and Molecular Pharmacology

Publication Date

4-5-2005

Document Type

Article

Subjects

Biological Markers; Cell Line; Humans; MicroRNAs; Nucleic Acid Conformation; Promoter Regions (Genetics); *RNA Interference; RNA Polymerase II; RNA, Small Interfering; Ubiquitin C

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

RNA interference (RNAi) mediates gene silencing in many eukaryotes and has been widely used to investigate gene functions. A common method to induce sustained RNAi is introducing plasmids that synthesize short hairpin RNAs (shRNAs) using Pol III promoters. While these promoters synthesize shRNAs and elicit RNAi efficiently, they lack cell specificity. Monitoring shRNA expression levels in individual cells by Pol III promoters is also difficult. An alternative way to deliver RNAi is to use Pol II-directed synthesis of shRNA. Previous efforts in developing a Pol II system have been sparse and the results were conflicting, and the usefulness of those Pol II vectors has been limited due to low efficacy. Here we demonstrate a new Pol II system that directs efficient shRNA synthesis and mediates strong RNAi at levels that are comparable with the commonly used Pol III systems. In addition, this system synthesizes a marker protein under control of the same promoter as the shRNA, thus providing an unequivocal indicator, not only to the cells that express the shRNA, but also to the levels of the shRNA expression. This system may be adapted for in vivo shRNA expression and gene silencing.

Rights and Permissions

Citation: Nucleic Acids Res. 2005 Apr 1;33(6):e62. Link to article on publisher's site

DOI of Published Version

10.1093/nar/gni061

Related Resources

Link to Article in PubMed

Journal/Book/Conference Title

Nucleic acids research

PubMed ID

15805121

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