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A Suite of Transgenic Driver and Reporter Mouse Lines with Enhanced Brain-Cell-Type Targeting and Functionality.

Cell | 2018

Modern genetic approaches are powerful in providing access to diverse cell types in the brain and facilitating the study of their function. Here, we report a large set of driver and reporter transgenic mouse lines, including 23 new driver lines targeting a variety of cortical and subcortical cell populations and 26 new reporter lines expressing an array of molecular tools. In particular, we describe the TIGRE2.0 transgenic platform and introduce Cre-dependent reporter lines that enable optical physiology, optogenetics, and sparse labeling of genetically defined cell populations. TIGRE2.0 reporters broke the barrier in transgene expression level of single-copy targeted-insertion transgenesis in a wide range of neuronal types, along with additional advantage of a simplified breeding strategy compared to our first-generation TIGRE lines. These novel transgenic lines greatly expand the repertoire of high-precision genetic tools available to effectively identify, monitor, and manipulate distinct cell types in the mouse brain.

Pubmed ID: 30007418 RIS Download

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Associated grants

  • Agency: NIDA NIH HHS, United States
    Id: R01 DA036909
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS078067
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH085500
  • Agency: NIGMS NIH HHS, United States
    Id: P50 GM107615
  • Agency: NIMH NIH HHS, United States
    Id: U01 MH105982
  • Agency: NIDA NIH HHS, United States
    Id: R01 DA028298

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STAR (tool)

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