The pINDUCER lentiviral toolkit for inducible RNA interference in vitro and in vivo

Kristen L. Meerbrey, Guang Hu(National Institute of Environmental Health Sciences), Jessica D. Kessler, Kevin Roarty(Institut de Biologie Moléculaire et Cellulaire), Mamie Z. Li(Brigham and Women's Hospital), Justin E. Fang, Jason I. Herschkowitz(Institut de Biologie Moléculaire et Cellulaire), Anna E. Burrows(Brigham and Women's Hospital), Alberto Ciccia(Brigham and Women's Hospital), Tingting Sun, Earlene M. Schmitt, Ronald J. Bernardi(Pediatrics and Genetics), Xiaoyong Fu(Baylor College of Medicine), Christopher S. Bland(Bipar), Thomas A. Cooper(Bipar), Rachel Schiff(Baylor College of Medicine), Jeffrey M. Rosen(Institut de Biologie Moléculaire et Cellulaire), Thomas F. Westbrook(Pediatrics and Genetics), Stephen J. Elledge(Brigham and Women's Hospital)
Proceedings of the National Academy of Sciences
February 9, 2011
Cited by 709

Abstract

The discovery of RNAi has revolutionized loss-of-function genetic studies in mammalian systems. However, significant challenges still remain to fully exploit RNAi for mammalian genetics. For instance, genetic screens and in vivo studies could be broadly improved by methods that allow inducible and uniform gene expression control. To achieve this, we built the lentiviral pINDUCER series of expression vehicles for inducible RNAi in vivo. Using a multicistronic design, pINDUCER vehicles enable tracking of viral transduction and shRNA or cDNA induction in a broad spectrum of mammalian cell types in vivo. They achieve this uniform temporal, dose-dependent, and reversible control of gene expression across heterogenous cell populations via fluorescence-based quantification of reverse tet-transactivator expression. This feature allows isolation of cell populations that exhibit a potent, inducible target knockdown in vitro and in vivo that can be used in human xenotransplantation models to examine cancer drug targets.


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