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Generating gene knockout rats by homologous recombination in embryonic stem cells.

Chang Tong | Guanyi Huang | Charles Ashton | Ping Li | Qi-Long Ying
Nature protocols | 2011

We describe here a detailed protocol for generating gene knockout rats by homologous recombination in embryonic stem (ES) cells. This protocol comprises the following procedures: derivation and expansion of rat ES cells, construction of gene-targeting vectors, generation of gene-targeted rat ES cells and, finally, production of gene-targeted rats. The major differences between this protocol and the classical mouse gene-targeting protocol include ES cell culture methods, drug selection scheme, colony picking and screening strategies. This ES cell-based gene-targeting technique allows sophisticated genetic modifications to be performed in the rat, as many laboratories have been doing in the mouse for the past two decades. Recently we used this protocol to generate Tp53 (also known as p53) gene knockout rats. The entire process requires ∼1 year to complete, from derivation of ES cells to generation of knockout rats.

Pubmed ID: 21637202

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Associated grants

  • Agency: NIH HHS, United States
    Id: R01 OD010926
  • Agency: NCRR NIH HHS, United States
    Id: R01 RR025881

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STOCK Dnmt1tm3Jae Hprt1 Tg(pPWL512hyg)1Ems/J (organism)

RRID:IMSR_JAX:003208

Mus musculus with name STOCK Dnmt1tm3Jae Hprt1 Tg(pPWL512hyg)1Ems/J from IMSR.

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Crl:CF1 (organism)

RRID:IMSR_CRL:023

Mus musculus with name Crl:CF1 from IMSR.

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