About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:5014212
Allelic
Composition
Tg(Gfap-rtTA,tetO-MAOB,-lacZ)1Jkan/0
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Gfap-rtTA,tetO-MAOB,-lacZ)1Jkan mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• induction increases microglia numbers by about 17%
• following induction, local microglial activation in the substantia nigra and striatum but not in the cortex
• following induction of transgene expression surviving tyrosine hydroxylase positive cells in mesencephalic cultures prepared from E14 embryos show significant loss of neurite processes
• induction of transgene expression results in significant loss of tyrosine hydroxylase positive cells in mesencephalic cultures prepared from E14 embryos
• a 2 week induction period results in a 40% loss of dopaminergic neurons in the substantia nigra
• loss of dopaminergic neurons is prevented by deprenyl co-treatment
• removal of doxycycline from the feed does not reverse cell loss
• irreversible dopaminergic substantia nigra neurodegeneration following induction of transgene expression
• following induction elevated levels of H2O2 are found in the media of cultures of mesencephalic cultures
• H2O2 levels are elevated in isolated ST dopaminergic synaptosomes following induction of transgene expression
• elevated levels of mitochondrial O2- levels in dopaminergic neurons following induction

behavior/neurological
• locomotor activity is reduced following 2 weeks of doxycycline treatment

hematopoietic system
• induction increases microglia numbers by about 17%
• following induction, local microglial activation in the substantia nigra and striatum but not in the cortex

immune system
• induction increases microglia numbers by about 17%
• following induction, local microglial activation in the substantia nigra and striatum but not in the cortex

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Parkinson's disease DOID:14330 OMIM:PS168600
J:132679


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
10/29/2024
MGI 6.24
The Jackson Laboratory