| Literature DB >> 35005091 |
Haojie Sun1,2,3, Ming Yi1,2,3, You Wan1,2,3.
Abstract
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 cbp (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 in vitro, 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.Entities:
Keywords: Adeno-associated virus; CRISPR-SaCas9; Gene editing; Infralimbic cortex; Memory
Year: 2021 PMID: 35005091 PMCID: PMC8678550 DOI: 10.21769/BioProtoc.4246
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325