Abstract
The flip-excision switch (FLEX) system with an adeno-associated viral (AAV) vector allows expression of transgenes in specific cell populations having Cre recombinase. A significant issue with this system is non-specific expression of transgenes in tissues after vector injection. We show here that Cre-independent recombination events in the AAV genome carrying the FLEX sequence occur mainly during the production of viral vectors in packaging cells, which results in transgene expression in off-target populations. Introduction of a relatively longer nucleotide sequence between two recognition sites at the unilateral side of the transgene cassette, termed a unilateral spacer sequence (USS), is useful to suppress the recombination in the viral genome, leading to the protection of non-specific transgene expression with enhanced gene expression selectivity. Our FLEX/USS system offers a powerful strategy for highly specific Cre-dependent transgene expression, aiming at various applications for structural and functional analyses of target cell populations.
| Original language | English |
|---|---|
| Article number | 100393 |
| Journal | Cell Reports Methods |
| Volume | 3 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 27-02-2023 |
| Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Biotechnology
- Biochemistry
- Biochemistry, Genetics and Molecular Biology (miscellaneous)
- Genetics
- Radiology Nuclear Medicine and imaging
- Computer Science Applications
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