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miR-218 Inhibits Mitochondrial Clearance by Targeting PRKN E3 Ubiquitin Ligase
- Source :
- International Journal of Molecular Sciences, International Journal of Molecular Sciences, Vol 21, Iss 1, p 355 (2020), Volume 21, Issue 1
- Publication Year :
- 2020
- Publisher :
- MDPI AG, 2020.
-
Abstract
- The selective elimination of dysfunctional mitochondria through mitophagy is crucial for preserving mitochondrial quality and cellular homeostasis. The most described mitophagy pathway is regulated by a positive ubiquitylation feedback loop in which the PINK1 (PTEN induced kinase 1) kinase phosphorylates both ubiquitin and the E3 ubiquitin ligase PRKN (Parkin RBR E3 ubiquitin ligase), also known as PARKIN. This event recruits PRKN to the mitochondria, thus amplifying ubiquitylation signal. Here we report that miR-218 targets PRKN and negatively regulates PINK1/PRKN-mediated mitophagy. Overexpression of miR-218 reduces PRKN mRNA levels, thus also reducing protein content and deregulating the E3 ubiquitin ligase action. In fact, following miR-218 overexpression, mitochondria result less ubiquitylated and the autophagy machinery fails to proceed with correct mitochondrial clearance. Since mitophagy defects are associated with various human diseases, these results qualify miR-218 as a promising therapeutic target for human diseases. &nbsp
- Subjects :
- Ubiquitin-Protein Ligases
miR-218
PARKIN/PRKN
Cellular homeostasis
PINK1
Mitochondrion
Article
Catalysis
Parkin
lcsh:Chemistry
Inorganic Chemistry
Ubiquitin
Mitophagy
Humans
Physical and Theoretical Chemistry
lcsh:QH301-705.5
Molecular Biology
Spectroscopy
microRNA
biology
Chemistry
Organic Chemistry
Autophagy
Autophagosomes
mitochondria
mitophagy
General Medicine
Computer Science Applications
Cell biology
Ubiquitin ligase
MicroRNAs
HEK293 Cells
lcsh:Biology (General)
lcsh:QD1-999
biology.protein
Subjects
Details
- ISSN :
- 14220067
- Volume :
- 21
- Database :
- OpenAIRE
- Journal :
- International Journal of Molecular Sciences
- Accession number :
- edsair.doi.dedup.....78f12aebe797e34e97d6cd1eff0a5d5e
- Full Text :
- https://doi.org/10.3390/ijms21010355