Two novel adenovirus vector systems permitting regulated protein expression in gene transfer experiments

J Virol. 1998 Oct;72(10):8358-61. doi: 10.1128/JVI.72.10.8358-8361.1998.

Abstract

Two new adenovirus vector systems based on the tetracycline-regulated Tet-ON- (Gossen, M., et al., Science 268:1766-1769, 1995) and the RU 486-regulated progesterone antagonist (Wang, Y., et al., Proc. Natl. Acad. Sci. USA 91:8180-8184, 1994)-induced gene expression systems are described. We show that both systems permit a tight control of chloramphenicol acetyltransferase reporter gene expression in a variety of cell types, with induction levels of approximately 1,800-fold (Tet-ON system) and 600-fold (RU 486-regulated system), respectively. A significant advantage of our vector systems is that reporter protein expression can be adjusted over a wide range by varying the amount of inducer. The Tet-ON system is also shown to permit an efficient control of reporter gene expression in mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Adenoviridae / genetics*
  • Animals
  • COS Cells
  • Chloramphenicol O-Acetyltransferase / genetics
  • Gene Expression Regulation, Viral / drug effects*
  • Gene Transfer Techniques*
  • Genetic Vectors*
  • HeLa Cells
  • Hormone Antagonists / pharmacology
  • Humans
  • Mice
  • Mifepristone / pharmacology
  • Tetracycline / pharmacology

Substances

  • Hormone Antagonists
  • Mifepristone
  • Chloramphenicol O-Acetyltransferase
  • Tetracycline