Project Details
Projekt Print View

THAP1 regulates alpha-synuclein expression: Functional link of Dystonia with Parkinson’s disease pathways

Subject Area Molecular and Cellular Neurology and Neuropathology
Molecular Biology and Physiology of Neurons and Glial Cells
Term from 2019 to 2023
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 427402073
 
Final Report Year 2023

Final Report Abstract

Evidence from patients with Parkinson's disease (PD) and our previously reported α-synuclein (SNCA) transgenic rat model support the idea that increased SNCA protein is a substantial risk factor of PD pathogenesis. However, little is known about the transcription control of the human SNCA gene in the brain in vivo. Using cellular and animal models for DYT6 dystonia, we observed that THAP1 regulates the expression of SNCA in human and rat neurons most likely through regulating the activities of SNCA intronic enhancers. Increased SNCA expression was observed in brain of SNCA/THAP1 double transgenic rats compared to SNCA single transgenic rats. These observations support that down-regulation or mutation of THAP1 would protect against synuclein accumulation in the dopaminergic neuron, while increased THAP1 expression will lead to increased SNCA expression and may stimulate more pronounced synuclein accumulation and thus aggregation in dopaminergic neuron. We further observed that deletion of the SNCA intronic enhancers reduces its expression drastically in the brain, which may provide new therapeutic approaches to prevent its accumulation and thus related neurodegenerative diseases defined as synucleinopathies.

Publications

 
 

Additional Information

Textvergrößerung und Kontrastanpassung