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Contributor Information

  • Name Tomas Lindahl
  • Institute Cancer Research UK, London Research Institute: Clare Hall Laboratories

Tool Details

  • Tool name: UNG Mouse
  • Tool type: Experimental models
  • Tool sub-type: Mouse
  • Cancer type: B cell lymphoma
  • Disease: Cancer
  • Conditional: No
  • Conditional description:
  • Genetic background and cross history: A ung targeting vector, replacing exon 4 with a resistance cassette, was transfected into 129 ES cells. Properly targeted ES cells containing a homologous recombination event were selected, cloned, and injected into C57BL6 blastocysts. Chimeric mice were mated with C57BL6 mice to generate heterozygotes. Heterozygous mice were crossed to generate homozygous Ung-/- mice.
  • Phenotype:
  • Zygosity: Homozygous
  • Description: In vivo study of UNG knockout and DNA mismatch mutation during DNA synthesis. Mice develop B cell lymphoma and are abnormally defective in their immune response. There are also mouse embryonic fibroblasts from this line available.
  • Research area: Cancer; DNA Damage and Repair; Genetic studies; Immunology
  • Production details: A ung targeting vector, replacing exon 4 with a resistance cassette, was transfected into 129 ES cells. Properly targeted ES cells containing a homologous recombination event were selected, cloned, and injected into C57BL6 blastocysts. Chimeric mice were mated with C57BL6 mice to generate heterozygotes. Heterozygous mice were crossed to generate homozygous Ung-/- mice.
  • Additional notes:

  • For Research Use Only

Target Details

  • Target: Uracil-DNA Glycosylase (UNG)

Application Details

Handling

  • Shipping conditions: Embryo/Spermatoza- Dry Ice

Documentation

  • Available on request

References

  •   Nilsen et al. 2003. Oncogene. 22(35):5381-6. PMID: 12934097.
  •   Gene-targeted mice lacking the Ung uracil-DNA glycosylase develop B-cell lymphomas.
  •   Nilsen et al. 2000. Mol Cell. 5(6):1059-65. PMID: 10912000.
  •   Uracil-DNA glycosylase (UNG)-deficient mice reveal a primary role of the enzyme during DNA replication.