Mice homozygous for the Ifngr1tm1 knock-out mutation have normal T cell responses but are defective in natural resistance, evidenced by an increased susceptibility to infection by Listeria monocytogenes and vaccinia virus. Mouse mutants involving this gene have been used in studies of Zika virus pathogenesis. Note: these mice carry the same allele as 'G129' mice, although on a congenic C57BL/6, not 129, genetic background.
IMR Colony, The Jackson Laboratory
Mice homozygous for the Ifngr1tm1 targeted mutation are viable and fertile with no overt abnormalities. They have normal T cell responses but are defective in natural resistance, evidenced by an increased susceptibility to infection by Listeria monocytogenes and vaccinia virus.
A targeting vector containing a neo cassette was used to disrupt exon 5. The construct was electroporated into 129S7/SvEvBrd-Hprt1+ derived AB1 embryonic stem (ES) cells. Correctly targeted ES cells were injected into recipient blastocysts. The resulting chimeric male animals were crossed to 129SvEv female mice, and then backcrossed to C57BL/6J for 10 generations.
|Allele Name||targeted mutation 1, Michel Aguet|
|Allele Type||Targeted (Null/Knockout)|
|Allele Synonym(s)||G129; IFn type II receptor; IFN-gamma R-; IFN-gamma R0; IFN-gammaR-; IFNgammaR KO; IFN-gammaR KO; IFN-gamma-R KO; IFN-gammaR-; IFN-gammaR0; IFN-gammaR1-; IFN-gammaRalpha_; Ifngr-; IFNgR KO; Ifngr1-|
|Gene Symbol and Name||Ifngr1, interferon gamma receptor 1|
|Strain of Origin||129S7/SvEvBrd-Hprt+|
|Molecular Note||Insertion of a neomycin cassette into exon V, which encodes an extracellular membrane-proximal portion of the receptor.|
|Mutations Made By|| |
Dr. Michel Aguet, EPFL, Ecole polytechnique fédérale de Lausanne
When using the Ifngr KO mouse strain in a publication, please cite the originating article(s) and include JAX stock #003288 in your Materials and Methods section.