| Literature DB >> 33789083 |
Lucas T Graybuck1, Tanya L Daigle1, Adriana E Sedeño-Cortés1, Miranda Walker1, Brian Kalmbach2, Garreck H Lenz1, Elyse Morin1, Thuc Nghi Nguyen1, Emma Garren1, Jacqueline L Bendrick1, Tae Kyung Kim1, Thomas Zhou1, Marty Mortrud1, Shenqin Yao1, La' Akea Siverts1, Rachael Larsen1, Bryan B Gore1, Eric R Szelenyi1, Cameron Trader1, Pooja Balaram1, Cindy T J van Velthoven1, Megan Chiang1, John K Mich1, Nick Dee1, Jeff Goldy1, Ali H Cetin3, Kimberly Smith1, Sharon W Way1, Luke Esposito1, Zizhen Yao1, Viviana Gradinaru4, Susan M Sunkin1, Ed Lein5, Boaz P Levi1, Jonathan T Ting2, Hongkui Zeng1, Bosiljka Tasic6.
Abstract
Rapid cell type identification by new genomic single-cell analysis methods has not been met with efficient experimental access to these cell types. To facilitate access to specific neural populations in mouse cortex, we collected chromatin accessibility data from individual cells and identified enhancers specific for cell subclasses and types. When cloned into recombinant adeno-associated viruses (AAVs) and delivered to the brain, these enhancers drive transgene expression in specific cortical cell subclasses. We extensively characterized several enhancer AAVs to show that they label different projection neuron subclasses as well as a homologous neuron subclass in human cortical slices. We also show how coupling enhancer viruses expressing recombinases to a newly generated transgenic mouse, Ai213, enables strong labeling of three different neuronal classes/subclasses in the brain of a single transgenic animal. This approach combines unprecedented flexibility with specificity for investigation of cell types in the mouse brain and beyond.Entities:
Keywords: AAV; ATAC-seq; cell types; cortex; enhancer; recombinase; transgenic mouse
Mesh:
Year: 2021 PMID: 33789083 PMCID: PMC8610077 DOI: 10.1016/j.neuron.2021.03.011
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173