Inducible and neuron-specific gene expression in the adult mouse brain with the rtTA2S-M2 system

Genesis. 2005 Dec;43(4):205-12. doi: 10.1002/gene.20175.

Abstract

To achieve inducible and reversible gene expression in the adult mouse brain, we exploited an improved version of the tetracycline-controlled transactivator-based system (rtTA2(S)-M2, rtTA2 hereafter) and combined it with the forebrain-specific CaMKIIalpha promoter. Several independent lines of transgenic mice carrying the CaMKIIalpha promoter-rtTA2 gene were generated and examined for anatomical profile, doxycycline (dox)-dependence, time course, and reversibility of gene expression using several lacZ reporter lines. In two independent rtTA2-expressing lines, dox-treatment in the diet induced lacZ reporter expression in neurons of several forebrain structures including cortex, striatum, hippocampus, amygdala, and olfactory bulb. Gene expression was dose-dependent and was fully reversible. Further, a similar pattern of expression was obtained in three independent reporter lines, indicating the consistency of gene expression. Transgene expression could also be activated in the developing brain (P0) by dox-treatment of gestating females. These new rtTA2-expressing mice allowing inducible and reversible gene expression in the adult or developing forebrain represent useful models for future genetic studies of brain functions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism*
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium-Calmodulin-Dependent Protein Kinases / genetics
  • Doxycycline / pharmacology*
  • Female
  • Gene Expression Regulation
  • Genes, Reporter
  • Genetic Vectors
  • Lac Operon
  • Mice
  • Mice, Transgenic
  • Neurons / metabolism*
  • Pregnancy
  • Promoter Regions, Genetic
  • Prosencephalon / metabolism
  • Recombinant Fusion Proteins / genetics*
  • Repressor Proteins / genetics*
  • Trans-Activators / genetics*

Substances

  • Recombinant Fusion Proteins
  • Repressor Proteins
  • Trans-Activators
  • tetracycline resistance-encoding transposon repressor protein
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Doxycycline