Inhibitory neuron-specific Cre-dependent red fluorescent labeling using VGAT BAC-based transgenic mouse lines with identified transgene integration sites

J Comp Neurol. 2018 Feb 15;526(3):373-396. doi: 10.1002/cne.24343. Epub 2017 Nov 11.

Abstract

Inhibitory neurons are crucial for shaping and regulating the dynamics of the entire network, and disturbances in these neurons contribute to brain disorders. Despite the recent progress in genetic labeling techniques, the heterogeneity of inhibitory neurons requires the development of highly characterized tools that allow accurate, convenient, and versatile visualization of inhibitory neurons in the mouse brain. Here, we report a novel genetic technique to visualize the vast majority and/or sparse subsets of inhibitory neurons in the mouse brain without using techniques that require advanced skills. We developed several lines of Cre-dependent tdTomato reporter mice based on the vesicular GABA transporter (VGAT)-BAC, named VGAT-stop-tdTomato mice. The most useful line (line #54) was selected for further analysis based on two characteristics: the inhibitory neuron-specificity of tdTomato expression and the transgene integration site, which confers efficient breeding and fewer adverse effects resulting from transgene integration-related genomic disruption. Robust and inhibitory neuron-specific expression of tdTomato was observed in a wide range of developmental and cellular contexts. By breeding the VGAT-stop-tdTomato mouse (line #54) with a novel Cre driver mouse line, Galntl4-CreER, sparse labeling of inhibitory neurons was achieved following tamoxifen administration. Furthermore, another interesting line (line #58) was generated through the unexpected integration of the transgene into the X-chromosome and will be used to map X-chromosome inactivation of inhibitory neurons. Taken together, our studies provide new, well-characterized tools with which multiple aspects of inhibitory neurons can be studied in the mouse.

Keywords: Cre; RRID: AB_10000343; RRID: AB_10000347; RRID: AB_1587367; RRID: AB_2179313; RRID: AB_2255365; RRID: AB_2571622; RRID: AB_2571847; RRID: AB_2631185; RRID: AB_442102; RRID: AB_477652; RRID: AB_88410; X-chromosome inactivation; inhibitory neuron; reporter mouse; tdTomato; transgene integration site.

MeSH terms

  • Animals
  • Brain / cytology
  • Estrogen Antagonists / pharmacology
  • Gene Expression Regulation / genetics
  • Glutamate Decarboxylase / genetics
  • Glutamate Decarboxylase / metabolism
  • Integrases / genetics
  • Integrases / metabolism*
  • Ki-67 Antigen / metabolism
  • Luminescent Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Mutation / genetics
  • N-Acetylgalactosaminyltransferases / genetics
  • N-Acetylgalactosaminyltransferases / metabolism
  • Nerve Tissue Proteins / metabolism
  • Neural Inhibition / genetics*
  • PAX2 Transcription Factor / metabolism
  • Polypeptide N-acetylgalactosaminyltransferase
  • RGS Proteins / genetics
  • RGS Proteins / metabolism
  • Somatostatin / metabolism
  • Tamoxifen / pharmacology
  • Vesicular Inhibitory Amino Acid Transport Proteins / genetics
  • Vesicular Inhibitory Amino Acid Transport Proteins / metabolism*

Substances

  • Estrogen Antagonists
  • Ki-67 Antigen
  • Luminescent Proteins
  • Nerve Tissue Proteins
  • PAX2 Transcription Factor
  • Pax2 protein, mouse
  • RGS Proteins
  • RGS8 protein, mouse
  • Vesicular Inhibitory Amino Acid Transport Proteins
  • Viaat protein, mouse
  • Tamoxifen
  • Somatostatin
  • N-Acetylgalactosaminyltransferases
  • Cre recombinase
  • Integrases
  • Glutamate Decarboxylase
  • glutamate decarboxylase 2