immune system
• macrophages exhibit a modest decrease in response to Sendai virus compared with wild-type cells
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Allele Symbol Allele Name Allele ID |
Sting1tm1Gnb targeted mutation 1, Glen N Barber MGI:3817418 |
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Summary |
4 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• macrophages exhibit a modest decrease in response to Sendai virus compared with wild-type cells
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mouse embryonic fibroblasts (MEF) are defective in initiating immune defenses (i.e. interferon-beta induction ) in response to negative strand viruses such as vesicular stomatitis virus (VSV) and the Sendai virus or the DNA herpes simplex virus 1
• b-form DNA, interferon stimulatory DNA, and the bacteria Listeria monocytogenes also fail to elicit a response in mutant MEFs
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• MEFs produce less interferon-beta in response to herpes simplex-1 virus
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• MEFs infected with vesicular stomatitis virus (VSV) have 100-fold higher titer number than controls 24 to 36 hours after infection
• MEFs produce less interferon-beta in response to VSV and the Sendai viruses
• less susceptibility to VSV is observed in bone marrow-derived dendritic cells or macrophages
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• mice are either perinatal lethal or survive after birth; survival is at 6% of expected frequency with 2% of pups surviving weaning
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• surviving mice are about 70% in body size and weight compared to controls
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• surviving mice are about 70% in body size and weight compared to controls
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• white patches show lack of melanin in hair shafts
• however, skin histology from white patches in normal
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• all viable mice present a ventral white spotting phenotype and white hind- and forepaws from birth which remains through life
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• E13.5 and E15.5 embryos exhibit increased LINE-1 retroelement DNA levels in cytosolic extract, however, no elevation in L1 ORF1 protein is seen
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• white patches show lack of melanin in hair shafts
• however, skin histology from white patches in normal
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• all viable mice present a ventral white spotting phenotype and white hind- and forepaws from birth which remains through life
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• mice fail to produce offspring
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N |
• no abnormalities or inflammation in internal organs, including the brain, are seen in viable mice and expression of interferon-stimulated genes is restored to normal levels
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
N |
• mice exhibit normal survival unlike Trex1tm1Tld homozygotes
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N |
• mice do not exhibit multi-organ inflammation unlike Trex1tm1Tld homozygotes
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 11/19/2024 MGI 6.24 |
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