Abstract
We have developed a nematode transformation vector carrying the bacterial neomycin resistance gene (NeoR) and shown that it could confer resistance to G-418 on both wild-type Caenorhabditis elegans and C. briggsae. This selection system allows hands-off maintenance and enrichment of transgenic worms carrying non-integrated transgenes on selective plates. We also show that this marker can be used for Mos1-mediated single-copy insertion in wild-type genetic backgrounds (MosSCI-biotic).
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Acknowledgements
Supported by the Program INSERM “Avenir” (D.D.), la Fondation Bettencourt-Schueller (D.D.), le Conseil Régional d'Aquitaine (D.D.), la Fondation pour la Recherche Médicale (D.D.), Natural Science and Engineering Research Council of Canada (D.B.) and le Ministère Français de l'Enseignement de la Recherche et des Technologies (R.G.-S.). We thank I.A. Hope, J. Ewbanks and J.L. Bessereau for discussions and access to facilities; and T. Leste-Lasserre and G. Drut for discussion about qPCR. EN5271 and EN5273 and MosSCI related plasmids were provided by J.L. Bessereau (INSERM U1024, Institute of Biology of the École Normale Supérieure). The Caenorhabditis Genetics Center, which is funded by the National Center for Research Resources of the US National Institutes of Health, provided the nematode species.
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S.M. and N.S. performed preliminary experiments under the supervision of M.V. D.D. designed and supervised the project and constructed the pDD04neo vector with N.S. Microinjections were performed by R.G.-S. and D.T. under the supervision of D.D., D.B. and R.J. R.G.-S. constructed MosSCI-biotic related vectors, characterized the transgenic worms and wrote the manuscript with D.D.
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Giordano-Santini, R., Milstein, S., Svrzikapa, N. et al. An antibiotic selection marker for nematode transgenesis. Nat Methods 7, 721–723 (2010). https://doi.org/10.1038/nmeth.1494
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DOI: https://doi.org/10.1038/nmeth.1494
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