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Zinc-finger nickase-mediated insertion of the lysostaphin gene into the beta-casein locus in cloned cows

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  • Xu Liu

    (College of Veterinary Medicine, Northwest A&F University
    Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University)

  • Yongsheng Wang

    (College of Veterinary Medicine, Northwest A&F University
    Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University)

  • Wenjiang Guo

    (College of Veterinary Medicine, Northwest A&F University
    Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University)

  • Bohao Chang

    (College of Veterinary Medicine, Northwest A&F University
    Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University)

  • Jun Liu

    (College of Veterinary Medicine, Northwest A&F University
    Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University)

  • Zekun Guo

    (College of Veterinary Medicine, Northwest A&F University
    Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University)

  • Fusheng Quan

    (College of Veterinary Medicine, Northwest A&F University
    Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University)

  • Yong Zhang

    (College of Veterinary Medicine, Northwest A&F University
    Key Laboratory of Animal Biotechnology, Ministry of Agriculture, Northwest A&F University)

Abstract

Zinc-finger nickases (ZFNickases) are a type of programmable nuclease that can be engineered from zinc-finger nucleases to induce site-specific single-strand breaks or nicks in genomic DNA, which result in homology-directed repair. Although zinc-finger nuclease-mediated gene disruption has been demonstrated in pigs and cattle, they have not been used to target gene addition into an endogenous gene locus in any large domestic species. Here we show in bovine fetal fibroblasts that targeting ZFNickases to the endogenous β-casein (CSN2) locus stimulates lysostaphin gene addition by homology-directed repair. We find that ZFNickase-treated cells can be successfully used in somatic cell nuclear transfer, resulting in live-born gene-targeted cows. Furthermore, the gene-targeted cows secrete lysostaphin in their milk and in vitro assays demonstrate the milk’s ability to kill Staphylococcus aureus. Our success with this strategy will facilitate new transgenic technologies beneficial to both agriculture and biomedicine.

Suggested Citation

  • Xu Liu & Yongsheng Wang & Wenjiang Guo & Bohao Chang & Jun Liu & Zekun Guo & Fusheng Quan & Yong Zhang, 2013. "Zinc-finger nickase-mediated insertion of the lysostaphin gene into the beta-casein locus in cloned cows," Nature Communications, Nature, vol. 4(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms3565
    DOI: 10.1038/ncomms3565
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