Efficient transgenesis in farm animals by lentiviral vectors

被引:205
作者
Hofmann, A
Kessler, B
Ewerling, S
Weppert, M
Vogg, B
Ludwig, H
Stojkovic, M
Boelhauve, M
Brem, G
Wolf, E
Pfeifer, A
机构
[1] Univ Munich, Gene Ctr, Inst Mol Anim Breeding, D-81377 Munich, Germany
[2] Univ Munich, Dept Pharm, Inst Pharmacol, Ctr Drug Res, D-81377 Munich, Germany
[3] ApoGene GmbH & Co KG, D-85354 Freising Weihenstephan, Germany
关键词
D O I
10.1038/sj.embor.7400007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microinjection of DNA is now the most widespread method for generating transgenic animals, but transgenesis rates achieved this way in higher mammals are extremely low. To address this long-standing problem, we used lentiviral vectors carrying a ubiquitously active promoter ( phosphoglycerate kinase, LV-PGK) to deliver transgenes to porcine embryos. Of the 46 piglets born, 32 (70%) carried the transgene DNA and 30 (94%) of these pigs expressed the transgene ( green fluorescent protein, GFP). Direct fluorescence imaging and immunohistochemistry showed that GFP was expressed in all tissues of LV-PGK transgenic pigs, including germ cells. Importantly, the transgene was transmitted through the germline. Tissue-specific transgene expression was achieved by infecting porcine embryos with lentiviral vectors containing the human keratin K14 promoter (LV-K14). LV-K14 transgenic animals expressed GFP specifically in basal keratinocytes of the skin. Finally, infection of bovine oocytes after and before in vitro fertilization with LV-PGK resulted in transgene expression in 45% and 92% of the infected embryos, respectively.
引用
收藏
页码:1054 / 1060
页数:7
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