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Mitochondrial Proteases: Multifaceted Regulators of Mitochondrial Plasticity.
- Source :
-
Annual review of biochemistry [Annu Rev Biochem] 2020 Jun 20; Vol. 89, pp. 501-528. Date of Electronic Publication: 2020 Feb 19. - Publication Year :
- 2020
-
Abstract
- Mitochondria are essential metabolic hubs that dynamically adapt to physiological demands. More than 40 proteases residing in different compartments of mitochondria, termed mitoproteases, preserve mitochondrial proteostasis and are emerging as central regulators of mitochondrial plasticity. These multifaceted enzymes limit the accumulation of short-lived, regulatory proteins within mitochondria, modulate the activity of mitochondrial proteins by protein processing, and mediate the degradation of damaged proteins. Various signaling cascades coordinate the activity of mitoproteases to preserve mitochondrial homeostasis and ensure cell survival. Loss of mitoproteases severely impairs the functional integrity of mitochondria, is associated with aging, and causes pleiotropic diseases. Understanding the dual function of mitoproteases as regulatory and quality control enzymes will help unravel the role of mitochondrial plasticity in aging and disease.
- Subjects :
- Aging metabolism
Animals
Apoptosis genetics
Gene Expression Regulation
Homeostasis genetics
Humans
Lipid Metabolism genetics
Mitochondria enzymology
Mitochondrial Dynamics genetics
Mitochondrial Proteins genetics
Mitochondrial Proteins metabolism
Mitophagy genetics
Neoplasms enzymology
Neoplasms pathology
Neurodegenerative Diseases enzymology
Neurodegenerative Diseases pathology
Peptide Hydrolases genetics
Peptide Hydrolases metabolism
Phospholipids metabolism
Proteolysis
Proteostasis genetics
Aging genetics
Mitochondria genetics
Mitochondrial Proteins chemistry
Neoplasms genetics
Neurodegenerative Diseases genetics
Peptide Hydrolases chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1545-4509
- Volume :
- 89
- Database :
- MEDLINE
- Journal :
- Annual review of biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 32075415
- Full Text :
- https://doi.org/10.1146/annurev-biochem-062917-012739