Romanowski Andrea J, Richardson Ryan R, Plachez Celine, Erzurumlu Reha S, Poulopoulos Alexandros
Department of Pharmacology and Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Department of Neurobiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Methods Mol Biol. 2025;2910:221-238. doi: 10.1007/978-1-0716-4446-1_13.
CRISPR/Cas9 constructs can be delivered by in utero electroporation to knock out a gene of interest in neurons of the developing brain in wild-type rodents. This approach allows for high-throughput genetic screening, circuit-specific gene knockout, and knockout cell phenotyping using sparse labeling within a wild-type in vivo context. Here we outline the methods and steps of designing guide RNAs in silico, cloning guide RNAs into plasmid backbones, and introducing these plasmids into the developing mouse cortex and hippocampus.
CRISPR/Cas9构建体可通过子宫内电穿孔法导入,以敲除野生型啮齿动物发育中大脑神经元中感兴趣的基因。这种方法允许在野生型体内环境中进行高通量基因筛选、特定回路基因敲除以及使用稀疏标记进行敲除细胞表型分析。在此,我们概述了在计算机上设计引导RNA、将引导RNA克隆到质粒骨架中以及将这些质粒导入发育中的小鼠皮层和海马体的方法和步骤。