Generation of the tamoxifen-inducible DBH-Cre transgenic mouse line DBH-CT

Genesis. 2011 Dec;49(12):935-41. doi: 10.1002/dvg.20773. Epub 2011 Aug 16.

Abstract

We generated transgenic mice bearing a tamoxifen-dependent Cre recombinase expressed under the control of the dopamine-β-hydroxylase promoter. By crossing to the ROSA26 reporter mice we show that tamoxifen-induced Cre recombinase in adult mice specifically activates β-galactosidase expression in differentiated noradrenergic neurons of the central and peripheral nervous system. Tamoxifen application in adult mice did not induce β-galactosidase activity in parasympathetic neurons that transiently express DBH during development. Thus, this transgenic mouse line represents a valuable tool to study gene function in mature noradrenergic neurons by conditional inactivation.

Publication types

  • Technical Report

MeSH terms

  • Adrenergic Neurons / cytology
  • Adrenergic Neurons / metabolism*
  • Animals
  • Cell Line
  • Crosses, Genetic
  • Dopamine beta-Hydroxylase / genetics*
  • Dopamine beta-Hydroxylase / metabolism
  • Gene Expression Regulation
  • Genes, Reporter
  • Genotype
  • In Situ Hybridization / methods
  • Integrases / metabolism
  • Mice
  • Mice, Transgenic*
  • Models, Animal
  • Neurons / cytology
  • Neurons / metabolism
  • Proteins / genetics
  • Proteins / metabolism
  • RNA, Untranslated
  • Recombination, Genetic
  • Tamoxifen / pharmacology*
  • beta-Galactosidase / genetics
  • beta-Galactosidase / metabolism

Substances

  • Gt(ROSA)26Sor non-coding RNA, mouse
  • Proteins
  • RNA, Untranslated
  • Tamoxifen
  • Dopamine beta-Hydroxylase
  • Cre recombinase
  • Integrases
  • beta-Galactosidase