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Phenotypes Associated with This Genotype
Genotype
MGI:2663242
Allelic
Composition
Cittm1Fdc/Cittm1Fdc
Genetic
Background
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cittm1Fdc mutation (0 available); any Cit mutation (121 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most homozygotes died around 14 days of age (P14), none survived past P21

behavior/neurological
• relative to wild-type, mutants displayed a lower threshold for pentylenetetrazol-induced seizures
• after P8, mutants displayed tremors
• after P8, mutants displayed ataxia
• at P12, mutants showed a wide, uncoordinated gait, and frequently fell on their backs while walking
• at P12, mutants started to exhibit lethal seizures, typified by myoclonic jerks, loss of posture, and hyperextension of the trunk and hindlimbs

growth/size/body
• at ~P10, mutants began to exhibit failure to thrive
• at P12, mutants weighed 20% less than wild-type
• no correlation between mortality and reduced growth rate was observed

muscle
• at P12, mutants started to exhibit lethal seizures, typified by myoclonic jerks, loss of posture, and hyperextension of the trunk and hindlimbs

reproductive system
N
• the ovaries of mutant females appeared histologically normal
• mutant males exhibited embryonic and postnatal loss of undifferentiated germ cells
• the specification and migration of primordial germ cells appeared normal; however, the number of spermatogenic precursors was markedly reduced as early as E12.5
• in the first postnatal days, gonocytes and type A spermatogonia were still present but their number was severely reduced
• in mutant testes, cellular depletion was caused by increased apoptosis of undifferentiated and differentiating precursors
• gonocytes and spermatogonia with multiple nuclei were produced in the seminiferous tubules indicating a cytokinesis block

nervous system
• relative to wild-type, mutants displayed a lower threshold for pentylenetetrazol-induced seizures
• at P12, mutants started to exhibit lethal seizures, typified by myoclonic jerks, loss of posture, and hyperextension of the trunk and hindlimbs
• in mutant brains, depletion of specific microneurons in the olfactory bulb, hippocampus and cerebellum was caused by aberrant cytokinesis and massive apoptosis
• at P14, the overall average weight of mutant brains was reduced by 50%
• mutants displayed an average reduction of ~20% in the mesencephalon
• mutants displayed an average reduction of ~20% in the diencephalon and midbrain
• mutants displayed an average reduction of 50% in the cerebral hemispheres
• the dentate gyrus was almost completely absent
• in the mutant olfactory bulbs, the periglomerular interneurons, olfactory granular cells, and the external plexiform layer were almost completely absent
• mutants displayed an average reduction of 70% in the olfactory bulbs
• the monolayer architecture of Purkinje cells appeared disorganized with abnormal dendritic arborization
• the granule cell layer was significantly reduced
• in the mutant cerebellum, all major lobules were smaller than wild-type
• mutants displayed an average reduction of 70% in the cerebellum

cellular
• mutant males exhibited embryonic and postnatal loss of undifferentiated germ cells
• the specification and migration of primordial germ cells appeared normal; however, the number of spermatogenic precursors was markedly reduced as early as E12.5
• in the first postnatal days, gonocytes and type A spermatogonia were still present but their number was severely reduced
• in mutant testes, cellular depletion was caused by increased apoptosis of undifferentiated and differentiating precursors
• in mutant brains, depletion of specific microneurons in the olfactory bulb, hippocampus and cerebellum was caused by aberrant cytokinesis and massive apoptosis
• gonocytes and spermatogonia with multiple nuclei were produced in the seminiferous tubules indicating a cytokinesis block


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
04/09/2024
MGI 6.23
The Jackson Laboratory