Transgenic mouse having a genome comprising a homozygous disruption of the endogenous MFN2 gene expression in the dopaminergic neurons
An animal model for Parkinson's disease has a disrupted Mfn2 gene in dopaminergic neurons. The Mfn2 gene disruption results in severe movement disorder attributed to progressive degeneration of the nigrostriatal circuit as found in Parkinson's disease. The animal model having exogenous suppression of the Mfn2 gene in dopaminergic neurons is a suitable animal model for studying Parkinson's disease.
1. A transgenic mouse having a genome comprising a homozygous disruption of the endogenous Mfn2 gene expression in the dopaminergic neurons, wherein the transgenic mouse exhibits locomotive defects compared to a mouse having a wildtype Mfn2 genotype.
2. The transgenic mouse of claim 1 , wherein the homozygous disruption of the endogenous Mfn2 gene expression comprises a nucleic acid sequence inserted within the endogenous Mfn2 gene.
3. The transgenic mouse of claim 2 , wherein the nucleic acid sequence encodes for a photo-activatable fluorescent protein that is capable of targeting mitochondria.
4. The transgenic mouse of claim 1 , wherein the locomotive defects comprise bradykinesia and/or postural defects.
5. The transgenic mouse of claim 1 , wherein the transgenic mouse has decreased dopaminergic innervation compared to a mouse having a wildtype Mfn2 genotype.