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PMID: 18470652 Published · ppublish English Journal Article

Conditional gene expression and knockdown using lentivirus vectors encoding shRNA.

Methods in molecular biology (Clifton, N.J.) ·Vol. 434 ·2008-00-00 ·Pages 291-309

Szulc J, Aebischer P

Abstract

Drug-inducible systems allowing the control of transgene expression and knockdown in mammalian cells are invaluable tools for genetic research, and could also play important roles in translational research or gene therapy. We and others have developed a lentivector-based, conditional gene expression system for drug-controllable expression of transgenes and small hairpin RNAs (shRNAs). This system is highly robust and versatile, governing tightly controlled expression of transgenes and endogenous cellular genes (through shRNAs) in various primary and established cell lines in vitro, as well as in vivo in the central nervous system or in human cancer cells xenotransplanted into nude mice. The goal of this article is to provide a concise methodology for construction and manipulation of this conditional lentiviral-based system, and quantitative analyses of drug-inducible transgene expression and gene knockdown both in vitro and in vivo.

MeSH Terms
Animals Breast Neoplasms/genetics,therapy Doxycycline/pharmacology Female Gene Expression Regulation, Neoplastic Gene Silencing Gene Targeting/methods Genetic Vectors/genetics Green Fluorescent Proteins/genetics,metabolism Humans Lentivirus/genetics Mice Mice, Nude RNA, Small Interfering/genetics Transfection Transgenes/physiology Tumor Suppressor Protein p53/antagonists & inhibitors,genetics,metabolism Xenograft Model Antitumor Assays
Chemicals
RNA, Small Interfering TP53 protein, human Tumor Suppressor Protein p53 Green Fluorescent Proteins Doxycycline
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Szulc Jolanta
Neurosciences Institute, Swiss Federal Institute of Technology Lausanne, Lausanne, Switzerland.
Aebischer Patrick
Article Info
Journal
Methods in molecular biology (Clifton, N.J.)
Abbr.
Methods Mol Biol
ISSN
1064-3745
Published
2008-00-00
Pages
291-309
Language
English
Region
United States
NLM ID
9214969
Subset
IM
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