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Multistep allelic conversion in mouse pre-implantation embryos by AAV vectors
- 1.0598886 - ÚMG 2025 RIV US eng J - Journal Article
Nickl, Petr - Jeníčková, Irena - Eliáš, Jan - Kašpárek, Petr - Bařinka, Cyril - Kopkanová, Jana - Sedláček, Radislav
Multistep allelic conversion in mouse pre-implantation embryos by AAV vectors.
Scientific Reports. Roč. 14, č. 1 (2024), č. článku 20160. ISSN 2045-2322. E-ISSN 2045-2322
R&D Projects: GA MŠMT(CZ) LM2018126; GA MŠMT LM2023036; GA MŠMT LX22NPO5102
Institutional support: RVO:68378050 ; RVO:86652036
Keywords : gene * electroporation * zygotes * knockin * cells * aav * 3r * Gene delivery * Flp/FRT * ivf * Site-specific recombinase
OECD category: Biochemistry and molecular biology
Impact factor: 3.8, year: 2023 ; AIS: 1.061, rok: 2023
Method of publishing: Open access
Result website:
https://www.nature.com/articles/s41598-024-70853-1DOI: https://doi.org/10.1038/s41598-024-70853-1
Site-specific recombinases (SSRs) are critical for achieving precise spatiotemporal control of engineered alleles. These enzymes play a key role in facilitating the deletion or inversion of loci flanked by recombination sites, resulting in the activation or repression of endogenous genes, selection markers or reporter elements. However, multiple recombination in complex alleles can be laborious. To address this, a new and efficient method using AAV vectors has been developed to simplify the conversion of systems based on Cre, FLP, Dre and Vika recombinases. In this study, we present an effective method for ex vivo allele conversion using Cre, FLP (flippase), Dre, and Vika recombinases, employing adeno-associated viruses (AAV) as delivery vectors. AAVs enable efficient allele conversion with minimal toxicity in a reporter mouse line. Moreover, AAVs facilitate sequential allele conversion, essential for fully converting alleles with multiple recombination sites, typically found in conditional knockout mouse models. While simple allele conversions show a 100% efficiency rate, complex multiple conversions consistently achieve an 80% conversion rate. Overall, this strategy markedly reduces the need for animals and significantly speeds up the process of allele conversion, representing a significant improvement in genome engineering techniques.
Permanent Link: https://hdl.handle.net/11104/0356463
File Download Size Commentary Version Access s41598-024-70853-1 (1).pdf 0 3 MB Publisher’s postprint open-access
Number of the records: 1