Article
The Parkinson's disease-associated mutation LRRK2 G2385R alters mitochondrial biogenesis via the PGC-1α-TFAM pathway.
Mitochondrion - 1 Nov 2023
Xue Jian, Zhang Jinbao, Zhang Jinru, Liu Junyi, Wang Fen, Li Kai, Liu Chunfeng
Abstract excerpt
Mutations in the Leucine-rich repeat protein kinase 2 (LRRK2) gene are the most frequent cause of familial Parkinson's disease (PD). Although LRRK2 has been extensively studied, the pathogenic mechanism of the LRRK2 G2385R mutation, which is most common in Asian populations, especially in the Chi...
Topics
- Humans
- DNA-Binding Proteins
- HEK293 Cells
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
- Mitochondrial Proteins
- Mutation
- Organelle Biogenesis
- Parkinson Disease
- Transcription Factors
- Mitochondria