#151474

DR3 KO Mouse

Cat. #151474

DR3 KO Mouse

Cat. #: 151474

Sub-type: Mouse

Availability: 6-8 weeks

Disease: Progressive neurological disease

Model: Knock-Out

This fee is applicable only for non-profit organisations. If you are a for-profit organisation or a researcher working on commercially-sponsored academic research, you will need to contact our licensing team for a commercial use license.

Contributor

Inventor: Eddie Wang ; Mike Owen

Institute: Cancer Research UK, London Research Institute: Lincoln's Inn Fields

Primary Citation: Wang et al. 2001. Mol Cell Biol. 21(10):3451-61. PMID: 11313471

Tool Details
Handling
Target Details
Application Details
References

Tool Details

*FOR RESEARCH USE ONLY

  • Tool name: DR3 KO Mouse
  • Tool sub type: Mouse
  • Disease: Progressive neurological disease
  • Model: Knock-Out
  • Conditional: No
  • Description: The DR3-/- mouse exhibits complete knockout of DR3, a death domain-containing tumour necrosis factor receptor, which mediates one of the key regulators of the cell division cycle. Negative selection and anti-CD3-induced apoptosis are significantly impaired in DR3-null mice. In contrast, both superantigen-induced negative selection and positive selection are normal. The pre-T-cell receptor-mediated checkpoint, which is dependent on TNFR signaling, is also unaffected in DR3-deficient mice. These data reveal a nonredundant in vivo role for this TNF receptor family member in the removal of self-reactive T cells in the thymus.
    Other behavioral studies on DR3 KO mice indicated that DR3 plays a key nonredundant role in the retention of normal motor control function during aging in mice and implicate DR3 in progressive neurological disease
  • Application: In vivo studies of DR3-induced apoptosis & function; in vivo studies of negative T cell selection and development
  • Genetic background: A DR3 targeting vector, replacing the entire DR3 coding region with a loxP flanked resistance cassette, was transfected into GK129 ES cells. Correctly targeted ES cells were injected into C57BL/6 blastocysts. Chimeric offspring were bred with C57BL/6 mice to yield mice heterozygous for the mutant allele.
  • Phenotype: Immune abnormalities (T cell development);
  • Zygosity: Homozygous
  • Production details: A DR3 targeting vector, replacing the entire DR3 coding region with a loxP flanked resistance cassette, was transfected into GK129 ES cells. Correctly targeted ES cells were injected into C57BL/6 blastocysts. Chimeric offspring were bred with C57BL/6 mice to yield mice heterozygous for the mutant allele.

Handling

  • Format: Embryo/Spermatoza
  • Shipping conditions: Dry Ice

Target Details

  • Target: DR3 (Death Domain Receptor 3)
  • Target background: DR3 (Ws1, Apo3, LARD, TRAMP, TNFSFR12) is a member of the death domain-containing tumor necrosis factor receptor (TNFR) superfamily, members of which mediate a variety of developmental events including the regulation of cell proliferation, differentiation, and apoptosis

Application Details

  • Application: In vivo studies of DR3-induced apoptosis & function; in vivo studies of negative T cell selection and development

References

  • Twohig et al. 2010. J Neurosci. 30(10):3782-92. PMID: 20220013
  • Wang et al. 2001. Mol Cell Biol. 21(10):3451-61. PMID: 11313471