NeuronDevelopmental BiologyPeer-reviewed journal article
Unlimited genetic switches for cell-type specific manipulation
Jorge García‐MarquésiD, Ching-Po Yang, Isabel Espinosa-MedinaiD, Kent Mok, Minoru KoyamaiD, Tzumin LeeiD
Abstract
Gaining independent genetic access to discrete cell types is critical to interrogate their biological functions, as well as to deliver precise gene therapy. Transcriptome analyses have allowed us to profile cell populations with extraordinary precision, revealing that cell types are typically defined by a unique combination of genetic markers. Given the lack of adequate tools to target cell types based on multiple markers, most cell types have remained inaccessible to genetic manipulation. Here, we present CaSSA, a platform to create unlimited genetic switches based on CRISPR/Cas9 (Ca) and the DNA repair mechanism known as single-strand annealing (SSA). CaSSA allows engineering of independent genetic switches that each respond to a specific gRNA. Expressing multiple gRNAs in specific patterns enables multiplex cell type-specific manipulations and combinatorial genetic targeting. CaSSA is thus a new genetic tool that conceptually works as an unlimited number of recombinases and will facilitate genetic access to cell types in diverse organisms.
- Citations
- 37
- FWCI
- 1.99
- Field percentile
- top 13%
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
- Sequential Activation of Guide RNAs for Algorithmic Multiplexing of Cas9 Activities
Ryan Clarke, Alexander R. Terry, … Bradley J. Merrill·bioRxiv·Jun 20, 2020
- Cell-specific CRISPR/Cas9 activation by microRNA-dependent expression of anti-CRISPR proteins
Mareike Daniela Hoffmann, Sabine Aschenbrenner, … Dominik Niopek·Nucleic Acids ResearchPeer-reviewed·Apr 5, 2019
- Multiplex, single-cell CRISPRa screening for cell type specific regulatory elements
Florence M. Chardon, Troy A. McDiarmid, … Jay Shendure·Nature CommunicationsPeer-reviewed·Sep 18, 2024
- Upgraded CRISPR/Cas9 Tools for Tissue-Specific Mutagenesis in Drosophila
Gabriel T. Koreman, Yineng Xu, … Chun Han·Proceedings of the National Academy of SciencesPeer-reviewed·Mar 29, 2021
- 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 unified genetic perturbation language for human cellular programming
Austin Hartman, Oliver Takacsi-Nagy, … Theodore L. Roth·bioRxiv·Nov 20, 2025