bioRxivNeurosciencePreprint
GEARBOCS: An Adeno Associated Virus Tool for In Vivo Gene Editing in Astrocytes
Dhanesh Sivadasan BinduiD, Justin T SavageiD, Nicholas BroseiD, Luke BradleyiD, Kylie Dimond, Christabel Xin TaniD, Çağla EroğluiD
Abstract
CRISPR/Cas9-based genome engineering enables rapid and precise gene manipulations in the CNS. Here, we developed a non-invasive astrocyte-specific method utilizing a single AAV vector, which we named GEARBOCS (Gene Editing in AstRocytes Based On CRISPR/Cas9 System). We verified GEARBOCS specificity to mouse cortical astrocytes and demonstrated its utility for three types of gene manipulations: knockout (KO); tagging (TagIn); and reporter knock-in (GeneTrap) strategies. Next, we deployed GEARBOCS in two test cases. First, we determined that astrocytes are a necessary source of the synaptogenic factor Sparcl1 for thalamocortical synapse maintenance in the mouse primary visual cortex. Second, we determined that cortical astrocytes express the synaptic vesicle associated Vamp2 protein and found that it is required for maintaining excitatory and inhibitory synapse numbers in the visual cortex. These results show that the GEARBOCS strategy provides a fast and efficient means to study astrocyte biology in vivo. MotivationAstrocytes are indispensable for brain development, function, and health. However, molecular tools to study astrocyte biology and function in vivo have been largely limited to genetically modified mice. Here, we developed a CRISPR/Cas9-based gene editing strategy within a single AAV vector that enables efficient genome manipulations in astrocytes. We designed and optimized this easy-to-use viral tool to understand gene expression, protein localization and function in astrocytes in vivo.
- organism: mouse
- research focus: gene regulatory network inference
- research focus: protein structure prediction
- research focus: drug response / drug discovery
- approach: experimental assay
- Citations
- 9
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Cell specific single viral vector CRISPR/Cas9 editing and genetically encoded tool delivery in the central and peripheral nervous systems
Jamie C. Moffa, India N. Bland, … Bryan A. Copits·eNeuroPeer-reviewed·Jun 13, 2024
- A toolbox of astrocyte-specific, serotype-independent adeno-associated viral vectors using microRNA targeting sequences.
Amy J. Gleichman, Riki Kawaguchi, … Stanley Thomas Carmichael·Nature CommunicationsPeer-reviewed·Nov 16, 2023
- Evaluating the efficacy of Optoα1AR activation in astrocytes in modulating basal hippocampal synaptic excitation and inhibition
Connor D. Courtney, Courtney A. Sobieski, … Catherine A. Christian·HippocampusPeer-reviewed·Sep 28, 2023
- Astrocytic modulation of population encoding in mouse visual cortex via GABA transporter 3 revealed by multiplexed CRISPR/Cas9 gene editing
Jiho Park, Grayson O. Sipe, … Mriganka Sur·eLifePeer-reviewed·Sep 30, 2025
- Efficient in vivo neuronal genome editing in the mouse brain using nanocapsules containing CRISPR-Cas9 ribonucleoproteins
Jeanette M. Metzger, Yuyuan Wang, … Shaoqin Gong·bioRxiv·Jul 24, 2022
- Enhancer-AAVs allow genetic access to oligodendrocytes and diverse populations of astrocytes across species
John K. Mich, Smrithi Sunil, … Boaz P. Levi·bioRxiv·Sep 20, 2023