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Pig transgenesis by Sleeping Beauty DNA transposition
Authors:Jannik E Jakobsen  Juan Li  Peter M Kragh  Brian Moldt  Lin Lin  Ying Liu  Mette Schmidt  Kjeld Dahl Winther  Brian Dall Schyth  Ida E Holm  G��bor Vajta  Lars Bolund  Henrik Callesen  Arne Lund J?rgensen  Anders Lade Nielsen  Jacob Giehm Mikkelsen
Institution:1. Department of Human Genetics, University of Aarhus, Wilh. Meyers All?? 1240, 8000, Aarhus C, Denmark
2. Department of Genetics and Biotechnology, Faculty of Agricultural Sciences, University of Aarhus, 8830, Tjele, Denmark
3. Department of Veterinary Reproduction and Obstetrics, Faculty of Life Sciences, University of Copenhagen, 1870, Frederiksberg C, Denmark
4. Danish Agriculture and Food Council, Knowledge Center on Pig Production, 1609, Copenhagen V, Denmark
5. National Veterinary Institute, Technical University of Denmark, 8200, Aarhus N, Denmark
6. Department of Pathology, Randers Hospital, 8900, Randers, Denmark
7. Danish Neuroscience Center, Aarhus University Hospital, 8000, Aarhus C, Denmark
Abstract:Modelling of human disease in genetically engineered pigs provides unique possibilities in biomedical research and in studies of disease intervention. Establishment of methodologies that allow efficient gene insertion by non-viral gene carriers is an important step towards development of new disease models. In this report, we present transgenic pigs created by Sleeping Beauty DNA transposition in primary porcine fibroblasts in combination with somatic cell nuclear transfer by handmade cloning. Göttingen minipigs expressing green fluorescent protein are produced by transgenesis with DNA transposon vectors carrying the transgene driven by the human ubiquitin C promoter. These animals carry multiple copies (from 8 to 13) of the transgene and show systemic transgene expression. Transgene-expressing pigs carry both transposase-catalyzed insertions and at least one copy of randomly inserted plasmid DNA. Our findings illustrate critical issues related to DNA transposon-directed transgenesis, including coincidental plasmid insertion and relatively low Sleeping Beauty transposition activity in porcine fibroblasts, but also provide a platform for future development of porcine disease models using the Sleeping Beauty gene insertion technology.
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