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Phenotypes Associated with This Genotype
Genotype
MGI:6416112
Allelic
Composition
Eif2b5tm1.1Sidr/Eif2b5tm1.1Sidr
Genetic
Background
B6(Cg)-Eif2b5tm1.1Sidr
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eif2b5tm1.1Sidr mutation (0 available); any Eif2b5 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• mice fail to gain weight after 1 week of age
• mice treated with a small molecule Eif2b activator, 2BAct, catch up to wild-type weights 2 weeks after beginning treatment

behavior/neurological
• in a beam-crossing test, mice show increased beam-crossing time and more foot slips and falls from the beam at 23 weeks, but not 8-19 weeks, and by 26 weeks, some mice completely fail to cross the beam within the trail time
• mice treated with 2BAct show normal performance on the beam-crossing test
• mice begin to show a trend towards shorter hang times at 23 weeks of age and significant decrease in hang time at 26 weeks of age, indicating progressive strength deficits
• mice treated with 2BAct show normal performance on the inverted grid test

nervous system
• mice show increased reactive gliosis in the corpus callosum and spinal cord
• 2BAct treatment prevents reactive gliosis
• marker analysis indicates that the integrated stress response is induced at 2.5, 5, and 7 months, but not at P14, in the cerebellum, forebrain, midbrain, and hindbrain; stress response precedes the appearance of pathology
• greater integrated stress response is seen in the spinal cord than in the cerebellum and the integrated stress response is activated in astrocytes and myelinating oligodendrocytes
• treatment with 2BAct abolishes integrated stress response in the cerebellum and spinal cord
• reduction in myelin, with a 33% reduction in corpus callosum and 58% reduction in cervical/thoracic spinal cord
• 2BAct treatment maintains myelin levels at 91% and 85% of wild-type in the corpus callosum and spinal cord, respectively, indicating prevention of myelin loss

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
leukoencephalopathy with vanishing white matter DOID:0060868 OMIM:PS603896
J:278928


Contributing Projects:
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
04/23/2024
MGI 6.23
The Jackson Laboratory