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

A Suite of Transgenic Driver and Reporter Mouse Lines with Enhanced Brain-Cell-Type Targeting and Functionality.
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DOI:
10.1016/j.cell.2018.06.035
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发表时间:
2018-07-12
期刊:
影响因子:
64.5
通讯作者:
Zeng H
Zeng H
中科院分区:
生物学1区
文献类型:
--
作者:
Daigle TL;Madisen L;Hage TA;Valley MT;Knoblich U;Larsen RS;Takeno MM;Huang L;Gu H;Larsen R;Mills M;Bosma-Moody A;Siverts LA;Walker M;Graybuck LT;Yao Z;Fong O;Nguyen TN;Garren E;Lenz GH;Chavarha M;Pendergraft J;Harrington J;Hirokawa KE;Harris JA;Nicovich PR;McGraw MJ;Ollerenshaw DR;Smith KA;Baker CA;Ting JT;Sunkin SM;Lecoq J;Lin MZ;Boyden ES;Murphy GJ;da Costa NM;Waters J;Li L;Tasic B;Zeng H

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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.
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