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通过CRISPR子宫内电穿孔在野生型啮齿动物发育大脑中进行基因敲除

Gene Knockout in the Developing Brain of Wild-Type Rodents by CRISPR In Utero Electroporation.

作者信息

Romanowski Andrea J, Richardson Ryan R, Plachez Celine, Erzurumlu Reha S, Poulopoulos Alexandros

机构信息

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.

出版信息

Methods Mol Biol. 2025;2910:221-238. doi: 10.1007/978-1-0716-4446-1_13.

Abstract

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.

摘要

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。

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