Site-specific modification of the bovine genome using Cre recombinase-mediated gene targeting

被引:10
作者
AgResearch, Ruakura Research Centre, Hamilton, New Zealand [1 ]
机构
[1] AgResearch, Ruakura Research Centre, Hamilton
来源
Biotechnol. J. | 2009年 / 1卷 / 108-118期
关键词
Bovine; Cre; Recombinase-mediated cassette exchange; Transgenic;
D O I
10.1002/biot.200800200
中图分类号
学科分类号
摘要
Cre recombinase (Cre)-mediated targeted insertion of a transgene is a powerful technique that can be used to tailor genomes. When combined with somatic cell nuclear transfer it could offer an efficient way to generate transgenic livestock with site-specific genetic modifications that are free of antibiotic selection markers. We have engineered primary bovine fibroblasts to contain a chromosomal acceptor site with incompatible loxP/lox2272 sites for Cre-mediated cassette exchange and show for the first time that Cre-mediated targeting can be applied in these acceptor cells. Molecular characterization of the resulting cell clones revealed Cre-mediated transgene insertion efficiencies of up to 98% when antibiotic selection was used to identify transgene containing cell clones. Most clonal lines also contained random insertions of the targeting and Cre expression plasmids with only about 10% of the clones being exclusively modified by the intended targeted insertion. This targeting efficiency was sufficient to enable the isolation of correctly targeted clones without the help of antibiotic selection. Therefore, this recombinase-mediated insertion strategy has the potential to produce transgenic cattle from antibiotic selection marker-free somatic cells with transgenes inserted into proven genomic loci ensuring reliable expression levels. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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页码:108 / 118
页数:10
相关论文
共 30 条
[1]  
McCreath K.J., Howcroft J., Campbell K.H., Colman A., Et al., Production of gene-targeted sheep by nuclear transfer from cultured somatic cells, Nature, 405, pp. 1066-1069, (2000)
[2]  
Schnieke A.E., Kind A.J., Ritchie W.A., Mycock K., Et al., Human factor IX transgenic sheep produced by transfer of nuclei from transfected fetal fibroblasts, Science, 278, pp. 2130-2133, (1997)
[3]  
Wells D.N., Laible G., Cloning and Transgenesis to Redesign Livestock, (2007)
[4]  
Clark A.J., Bissinger P., Bullock D.W., Damak S., Et al., Chromosomal position effects and the modulation of transgene expression, Reprod. Fertil. Dev, 6, pp. 589-598, (1994)
[5]  
Doerfler W., Schubbert R., Heller H., Kammer C., Et al., Integration of foreign DNA and its consequences in mammalian systems, Trends Biotechnol, 15, pp. 297-301, (1997)
[6]  
Misra R.P., Duncan S.A., Gene targeting in the mouse: Advances in introduction of transgenes into the genome by homologous recombination, Endocrine, 19, pp. 229-238, (2002)
[7]  
Adams D.J., van der Weyden L., Contemporary approaches for modifying the mouse genome, Physiol. Genomics, 34, pp. 225-238, (2008)
[8]  
Clark A.J., Burl S., Denning C., Dickinson P., Gene targeting in livestock: A preview, Transgenic. Res, 9, pp. 263-275, (2000)
[9]  
Sorrell D.A., Kolb A.F., Targeted modification of mammalian genomes, Biotechnol. Adv, 23, pp. 431-469, (2005)
[10]  
Wirth D., Gama-Norton L., Riemer P., Sandhu U., Et al., Road to precision: Recombinase-based targeting technologies for genome engineering, Curr. Opin. Biotechnol, 18, pp. 411-419, (2007)