Sun Haojie, Yi Ming, Wan You
Department of Neurobiology, School of Basic Medical Sciences, Peking University, Beijing 100083, China.
Neuroscience Research Institute, Peking University, Beijing 100083, China.
Bio Protoc. 2021 Dec 5;11(23):e4246. doi: 10.21769/BioProtoc.4246.
The CRISPR-Cas9 enables efficient gene editing in various cell types, including post-mitotic neurons. However, neuronal ensembles in the same brain region can still be functionally or anatomically different, and such heterogeneity requires gene editing in specific neuronal populations. We recently developed a CRISPR-SaCas9 system-based technique. Combined with activity-dependent cell-labeling methods and anterograde/retrograde adeno-associated virus (AAV) vectors, this technique achieves function- and projection-specific gene editing in the mammalian brain. We showed that perturbing (CREB-binding protein) in extinction-ensemble neurons among amygdala-projecting infralimbic cortex (IL) cells impaired fear extinction learning, demonstrating the high efficiency in regulation of extinction learning with CRISPR-Cas9. Here, we describe a detailed protocol of gene perturbation in presynaptic extinction-ensemble neurons in adult rats, including gRNA design, gRNA evaluation , stereotaxic AAV injection, and contextual fear conditioning. The high specificity and efficiency of projection- and function-specific CRISPR-SaCas9 system can be widely applied in neural circuitry studies.
CRISPR-Cas9能够在包括有丝分裂后神经元在内的各种细胞类型中实现高效的基因编辑。然而,同一脑区的神经元集群在功能或解剖结构上仍可能存在差异,这种异质性需要在特定的神经元群体中进行基因编辑。我们最近开发了一种基于CRISPR-SaCas9系统的技术。结合活动依赖的细胞标记方法和顺行/逆行腺相关病毒(AAV)载体,该技术在哺乳动物大脑中实现了功能和投射特异性的基因编辑。我们发现,在杏仁核投射的边缘下皮质(IL)细胞中的消退集群神经元中干扰(CREB结合蛋白)会损害恐惧消退学习,这证明了使用CRISPR-Cas9调节消退学习的高效率。在这里,我们描述了成年大鼠突触前消退集群神经元中基因干扰的详细方案,包括gRNA设计、gRNA评估、立体定位AAV注射和情境恐惧条件反射。投射和功能特异性CRISPR-SaCas9系统的高特异性和效率可广泛应用于神经回路研究。