AI Article Synopsis

  • Developed a refined tetracycline-controlled transactivator (rtTA2) system for reversible gene expression in adult mouse brains.
  • Created transgenic mice with the CaMKIIalpha promoter, demonstrating dox-dependent gene expression across various forebrain regions.
  • Confirmed that gene expression can be controlled in both adult and developing brains, which can facilitate future research on brain function and genetics.

Article 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.

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http://dx.doi.org/10.1002/gene.20175DOI Listing

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