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Germline transgenesis in pigs by cytoplasmic microinjection of Sleeping Beauty transposons
Z. Ivics, W. Garrels, L. Mátés, TY. Yau, S. Bashir, V. Zidek, V. Landa, A. Geurts, M. Pravenec, T. Rülicke, WA. Kues, Z. Izsvák,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
ProQuest Central
od 2006-06-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2013-03-01 do 2015-12-31
Health & Medicine (ProQuest)
od 2006-06-01 do Před 1 rokem
PubMed
24625780
DOI
10.1038/nprot.2014.010
Knihovny.cz E-zdroje
- MeSH
- genetické vektory MeSH
- geneticky modifikovaná zvířata * MeSH
- genom MeSH
- mikroinjekce MeSH
- prasata genetika MeSH
- technika přenosu genů * MeSH
- transposasy MeSH
- transpozibilní elementy DNA * MeSH
- zárodečné buňky MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
The pig has emerged as an important large animal model in biomedical and pharmaceutical research. We describe a protocol for high-efficiency germline transgenesis and sustained transgene expression in pigs by using the Sleeping Beauty (SB) transposon system. The protocol is based on co-injection of a plasmid encoding the SB100X hyperactive transposase, together with a second plasmid carrying a transgene flanked by binding sites for the transposase, into the cytoplasm of porcine zygotes. The transposase mediates excision of the transgene cassette from the plasmid vector and its permanent insertion into the genome to produce stable transgenic animals. This method compares favorably in terms of both efficiency and reliable transgene expression to classic pronuclear microinjection or somatic cell nuclear transfer (SCNT), and it offers comparable efficacies to lentiviral approaches, without limitations on vector design, issues of transgene silencing and the toxicity and biosafety concerns of working with viral vectors. Microinjection of the vectors into zygotes and transfer of the embryos to recipient animals can be performed in 1 d; generation of germline-transgenic lines by using this protocol takes ∼1 year.
] Division of Medical Biotechnology Paul Ehrlich Institute Langen Germany [2]
] Friedrich Loeffler Institut Institut für Nutztiergenetik Neustadt Germany [2]
Biological Research Centre Hungarian Academy of Sciences Szeged Hungary
Department of Physiology Medical College of Wisconsin Milwaukee Wisconsin USA
Friedrich Loeffler Institut Institut für Nutztiergenetik Neustadt Germany
Institute of Laboratory Animal Science University of Veterinary Medicine Vienna Vienna Austria
Institute of Physiology Academy of Sciences of the Czech Republic Prague Czech Republic
Citace poskytuje Crossref.org
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