Cre-dependent Cas9-expressing pigs enable efficient in vivo genome editing

Genome Res. 2017 Dec;27(12):2061-2071. doi: 10.1101/gr.222521.117. Epub 2017 Nov 16.

Abstract

Despite being time-consuming and costly, generating genome-edited pigs holds great promise for agricultural, biomedical, and pharmaceutical applications. To further facilitate genome editing in pigs, we report here establishment of a pig line with Cre-inducible Cas9 expression that allows a variety of ex vivo genome editing in fibroblast cells including single- and multigene modifications, chromosome rearrangements, and efficient in vivo genetic modifications. As a proof of principle, we were able to simultaneously inactivate five tumor suppressor genes (TP53, PTEN, APC, BRCA1, and BRCA2) and activate one oncogene (KRAS), achieved by delivering Cre recombinase and sgRNAs, which caused rapid lung tumor development. The efficient genome editing shown here demonstrates that these pigs can serve as a powerful tool for dissecting in vivo gene functions and biological processes in a temporal manner and for streamlining the production of genome-edited pigs for disease modeling.

MeSH terms

  • Animals
  • Animals, Genetically Modified*
  • Bacterial Proteins / genetics*
  • CRISPR-Associated Protein 9
  • CRISPR-Cas Systems / genetics
  • Endonucleases / genetics*
  • Female
  • Fibroblasts / metabolism
  • Gene Editing / methods*
  • Gene Rearrangement
  • Genes, Tumor Suppressor
  • Genome*
  • Humans
  • Integrases / metabolism
  • Lung Neoplasms / genetics
  • Male
  • Oncogenes
  • Swine
  • Swine, Miniature / genetics*
  • Transcription Activator-Like Effector Nucleases
  • Transcriptional Activation

Substances

  • Bacterial Proteins
  • Cre recombinase
  • Integrases
  • CRISPR-Associated Protein 9
  • Cas9 endonuclease Streptococcus pyogenes
  • Endonucleases
  • Transcription Activator-Like Effector Nucleases