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Updated: Aug 20, 2026

The Production of C. elegans Transgenes via Recombineering with the galK Selectable Marker
Published on: January 11, 2011
Controversial aspect of using GFP as a marker for the production of transgenic cattle
A M Duszewska1, D Lipiński, A Piliszek
1Department of Experimental Embryology, Polish Academy of Sciences, Strzeszyńska 32, 60-479 Poznań, Poland. duszewskaanna@hotmail.com
Abstract:
The objective of this study was to examine the feasibility of identification and selection of cattle embryos based on green fluorescence (GFP-positive) in order to obtain calves carrying an integrated transgene. The construct used (pbLGTNF-EGFP) contained the human tumor necrosis factor alpha (hTNFalpha) gene fused to the bovine beta-lactoglobulin promoter (bLG) in plasmid vector pCX-EGFP. In four experiments, 76 zygotes were injected; eight of them developed to the morulae/blastocysts stage of which only five were GFP positive (one of them 100%, one-50%, three- 25%). All of the GFP positive embryos were transferred to recipients. Two calves were born: one after transfer of the 100% GFP positive embryo and the other after transfer of one of the 25% GFP positive embryos. Both animals were healthy with normal weight when compared to two control calves. The integration of pbLGTNF-EGFP in the host genome could not be detected in either of the calves, suggesting that GFP is an unreliable marker for preimplantation screening of embryos.
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