Cardiac Applications of CRISPR/AAV-Mediated Precise Genome Editing
Yanjiang Zheng, Joshua MayourianiD, Justin S. KingiD, Yifei LiiD, Vassilios J. BezzeridesiD, William T. PuiD, Nathan J. VanDuseniD
Abstract
The ability to efficiently make precise genome edits in somatic tissues will have profound implications for gene therapy and basic science. CRISPR/Cas9 mediated homology-directed repair (HDR) is one approach that is commonly used to achieve precise and efficient editing in cultured cells. Previously, we developed a platform capable of delivering CRISPR/Cas9 gRNAs and donor templates via adeno-associated virus to induce HDR (CASAAV-HDR). We demonstrated that CASAAV-HDR is capable of creating precise genome edits in vivo within mouse cardiomyocytes at the neonatal and adult stages. Here, we report several applications of CASAAV-HDR in cardiomyocytes. First, we show the utility of CASAAV-HDR for disease modeling applications by using CASAAV-HDR to create and precisely tag two pathological variants of the titin gene observed in cardiomyopathy patients. We used this approach to monitor the cellular localization of the variants, resulting in mechanistic insights into their pathological functions. Next, we utilized CASAAV-HDR to create another mutation associated with human cardiomyopathy, arginine 14 deletion (R14Del) within the N-terminus of Phospholamban (PLN). We assessed the localization of PLN-R14Del and quantified cardiomyocyte phenotypes associated with cardiomyopathy, including cell morphology, activation of PLN via phosphorylation, and calcium handling. After demonstrating CASAAV-HDR utility for disease modeling we next tested its utility for functional genomics, by targeted genomic insertion of a library of enhancers for a massively parallel reporter assay (MPRA). We show that MPRAs with genomically integrated enhancers are feasible, and can yield superior assay sensitivity compared to tests of the same enhancers in an AAV/episomal context. Collectively, our study showcases multiple applications for in vivo precise editing of cardiomyocyte genomes via CASAAV-HDR.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- Organism
- Assay
- Research Focus
- Approach
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
- An all-in-one AAV vector for cardiac-specific gene silencing by an adenine base editor
Zhanzhao Liu, Luzi Yang, … Yuxuan Guo·bioRxiv·Sep 30, 2024
- In vivo gene disruption and homology-directed repair in muscles and muscle stem cells using CRISPR/Cas9
Bryan L. Peacker, Kuan‐Hung Lin, … Amy J. Wagers·bioRxiv·Jul 1, 2026
- Efficient CRISPR/Cas9-mediated homology independent sequence replacement in vivo and non-dividing primary cells
Tu Dang, Alexandra Roman, … Ralf Kuehn·bioRxiv·Jul 24, 2026
- In vivo silencing of regulatory elements using a single AAV-CRISPRi vector
Patrick Laurette, C Cao, … Ralf Gilsbach·bioRxiv·Nov 5, 2023
- Striated muscle-specific base editing enables correction of mutations causing dilated cardiomyopathy
Markus Grosch, Laura Schraft, … Lars Michael Steinmetz·Nature CommunicationsPeer-reviewed·Jun 22, 2023
- MicroRNA-122-mediated liver detargeting enhances the tissue specificity of cardiac genome editing