Human mitochondrial nucleases.

Abstract

Mitochondria are cytosolic organelles that have many essential roles including ATP production via oxidative phosphorylation, apoptosis, iron-sulfur cluster biogenesis, heme and steroid synthesis, calcium homeostasis, and regulation of cellular redox state. One of the unique features of these organelles is the presence of an extrachromosomal mitochondrial genome (mtDNA), together with all the machinery required to replicate and transcribe mtDNA. The accurate maintenance of mitochondrial gene expression is essential for correct organellar metabolism, and is in part dependent on the levels of mtDNA and mtRNA, which are regulated by balancing synthesis against degradation. It is clear that although a number of mitochondrial nucleases have been identified, not all those responsible for the degradation of DNA or RNA have been characterized. Recent investigations, however, have revealed the contribution that mutations in the genes coding for these enzymes has made to causing pathogenic mitochondrial diseases.

• Authors: Francesco Bruni, Robert N Lightowlers, Zofia M Chrzanowska-Lightowlers
• Journal: The FEBS journal (FEBS J) Vol. 284 Issue 12 Pg. 1767-1777 (06 2017) ISSN: 1742-4658 [Electronic] England
• PMID: 27926991 (Publication Type: Journal Article, Review, Research Support, Non-U.S. Gov't)
• Copyright: © 2016 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.

Chemical References

• Mitochondrial Proteins
• Endonucleases

Topics

• Endonucleases (metabolism)
• Humans
• Mitochondria (enzymology)
• Mitochondrial Diseases (enzymology, pathology)
• Mitochondrial Proteins (metabolism)