Ubiquitin-dependent mitochondrial protein degradation.

Int J Biochem Cell Biol

Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.

Published: October 2011

AI Article Synopsis

  • Mitochondrial failure is linked to various age-related diseases due to the balance between energy production (ATP) and harmful byproducts (ROS).
  • Understanding how to maintain healthy mitochondria is crucial for preventing and treating these conditions.
  • One key protective mechanism involves the cytosolic ubiquitin/proteasome system, which helps degrade damaged mitochondrial proteins and shows promise for future research in disease management.

Article Abstract

Progressive mitochondrial failure is tightly associated with the onset of many age-related human pathologies. This tight connection results from the double-edged sword of mitochondrial respiration, which is responsible for generating both ATP and ROS, as well as from risks that are inherent to mitochondrial biogenesis. To prevent and treat these diseases, a precise understanding of the mechanisms that maintain functional mitochondria is necessary. Mitochondrial protein quality control is one of the mechanisms that protect mitochondrial integrity, and increasing evidence implicates the cytosolic ubiquitin/proteasome system (UPS) as part of this surveillance network. In this review, we will discuss our current understanding of UPS-dependent mitochondrial protein degradation, its roles in diseases progression, and insights into future studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163752PMC
http://dx.doi.org/10.1016/j.biocel.2011.06.002DOI Listing

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