Efficient in vitro and in vivo gene regulation of a retrovirally delivered pro-apoptotic factor under the control of the Drosophila HSP70 promoter

Gene Ther. 2001 Apr;8(8):600-7. doi: 10.1038/sj.gt.3301441.

Abstract

We have developed a self-inactivating retroviral vector system with an internal, inducible Drosophila HSP70 promoter. This vector system delivers the desired transgene into cells rapidly and efficiently. It generates mixed populations of transduced cells where the transgene is inducible, and does not require the isolation of specific clones. Since the transgene is not expressed (or poorly expressed) at the restrictive condition (34 degrees C), mixed populations can be selected in which tumor suppressors or other inhibitory genes can be strongly induced upon changing the conditions (39 degrees C or the plant amino acid L-canavanine). This retroviral vector should be very useful for the expression of sequences that are poorly tolerated by cells, and is also active in animals.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Apoptosis
  • Drosophila / genetics
  • Gene Expression Regulation, Viral
  • Genetic Therapy / methods*
  • Genetic Vectors / genetics
  • HSP70 Heat-Shock Proteins / genetics*
  • Male
  • Mice
  • Mice, Nude
  • Mutation
  • Promoter Regions, Genetic*
  • Prostatic Neoplasms / metabolism
  • Prostatic Neoplasms / pathology
  • Prostatic Neoplasms / therapy*
  • Receptor, IGF Type 1 / genetics*
  • Retroviridae / genetics*
  • Transduction, Genetic

Substances

  • HSP70 Heat-Shock Proteins
  • Receptor, IGF Type 1