Disorders from perturbations of nuclear-mitochondrial intergenomic cross-talk

J Intern Med. 2009 Feb;265(2):174-92. doi: 10.1111/j.1365-2796.2008.02059.x.

Abstract

In the course of evolution, mitochondria lost their independence, and mitochondrial DNA (mtDNA) became the 'slave' of nuclear DNA, depending on numerous nucleus-encoded factors for its integrity, replication and expression. Mutations in any of these factors may alter the cross-talk between the two genomes and cause Mendelian disorders characterized by qualitative (multiple deletions) or quantitative (depletion) alterations of mtDNA, or by defective translation of mtDNA-encoded respiratory chain components.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA, Mitochondrial / genetics*
  • Disease Models, Animal
  • Gene Deletion*
  • Humans
  • Mice
  • Mitochondrial Diseases / classification
  • Mitochondrial Diseases / genetics*
  • Mutation / genetics
  • Oxidative Phosphorylation

Substances

  • DNA, Mitochondrial