Department of Neurobiology, Stanford University, Stanford, CA, USA.
Department of Medicine, Weill Cornell Medical College, New York, NY, USA.
Nat Neurosci. 2020 Sep;23(9):1168-1175. doi: 10.1038/s41593-020-0668-9. Epub 2020 Jul 20.
Many experimental approaches rely on controlling gene expression in select subsets of cells within an individual animal. However, reproducibly targeting transgene expression to specific fractions of a genetically defined cell type is challenging. We developed Sparse Predictive Activity through Recombinase Competition (SPARC), a generalizable toolkit that can express any effector in precise proportions of post-mitotic cells in Drosophila. Using this approach, we demonstrate targeted expression of many effectors in several cell types and apply these tools to calcium imaging of individual neurons and optogenetic manipulation of sparse cell populations in vivo.
许多实验方法都依赖于在个体动物的特定细胞亚群中控制基因表达。然而,有针对性地将转基因表达精确地靶向特定的遗传定义细胞类型的分数是具有挑战性的。我们开发了通过重组酶竞争进行稀疏预测活性(SPARC),这是一种可推广的工具包,可以在果蝇的有丝后细胞中以精确的比例表达任何效应物。使用这种方法,我们证明了许多效应物在几种细胞类型中的靶向表达,并将这些工具应用于单个神经元的钙成像和体内稀疏细胞群体的光遗传学操作。