Efficient gene targeting of the Rosa26 locus in mouse zygotes using TALE nucleases
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25241166
DOI
10.1016/j.febslet.2014.09.014
PII: S0014-5793(14)00689-9
Knihovny.cz E-resources
- Keywords
- Gene targeting, Homologous recombination, Rosa26 locus, Transcription activator-like effector nucleases, Transgenic, Zinc-finger nucleases,
- MeSH
- Endonucleases metabolism MeSH
- Genetic Loci genetics MeSH
- Gene Targeting methods MeSH
- Homologous Recombination MeSH
- Mice, Transgenic MeSH
- Mice MeSH
- Base Sequence MeSH
- Animals MeSH
- Zygote metabolism MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Endonucleases MeSH
Gene targeting in mice mainly employs homologous recombination (HR) in embryonic stem (ES) cells. Although it is a standard way for production of genetically modified mice, the procedure is laborious and time-consuming. This study describes targeting of the mouse Rosa26 locus by transcription activator-like effector nucleases (TALENs). We employed TALEN-assisted HR in zygotes to introduce constructs encoding TurboRFP and TagBFP fluorescent proteins into the first intron of the Rosa26 gene, and in this way generated two transgenic mice. We also demonstrated that these Rosa26-specific TALENs exhibit high targeting efficiency superior to that of zinc-finger nucleases (ZFNs) specific for the same targeting sequence. Moreover, we devised a reporter assay to assess TALENs activity and specificity to improve the quality of TALEN-assisted targeting.
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