Mitochondrial Proteases: Multifaceted Regulators of Mitochondrial Plasticity

Annu Rev Biochem. 2020 Jun 20:89:501-528. doi: 10.1146/annurev-biochem-062917-012739. Epub 2020 Feb 19.

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.

Keywords: aging; mitochondria; mitochondrial proteases; mitochondrial quality control; neurodegeneration; proteostasis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aging / genetics*
  • Aging / metabolism
  • Animals
  • Apoptosis / genetics
  • Gene Expression Regulation
  • Homeostasis / genetics
  • Humans
  • Lipid Metabolism / genetics
  • Mitochondria / enzymology
  • Mitochondria / genetics*
  • Mitochondrial Dynamics / genetics
  • Mitochondrial Proteins / chemistry*
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Mitophagy / genetics
  • Neoplasms / enzymology
  • Neoplasms / genetics*
  • Neoplasms / pathology
  • Neurodegenerative Diseases / enzymology
  • Neurodegenerative Diseases / genetics*
  • Neurodegenerative Diseases / pathology
  • Peptide Hydrolases / chemistry*
  • Peptide Hydrolases / genetics
  • Peptide Hydrolases / metabolism
  • Phospholipids / metabolism
  • Proteolysis
  • Proteostasis / genetics

Substances

  • Mitochondrial Proteins
  • Phospholipids
  • Peptide Hydrolases