4.7 Review

Disorders from perturbations of nuclear-mitochondrial intergenomic cross-talk

期刊

JOURNAL OF INTERNAL MEDICINE
卷 265, 期 2, 页码 174-192

出版社

WILEY
DOI: 10.1111/j.1365-2796.2008.02059.x

关键词

mitochondrial disorders; mitochondrial DNA; mtDNA depletion; mtDNA multiple deletions; oxidative phosphorylation

资金

  1. Pierfranco and Luisa Mariani Foundation
  2. Telethon-Italy Foundation [GGP07019]
  3. Italian Ministry of University and Research [RBLA038RMA]
  4. Italian Ministry of Health [RF2006 ex 56/05/21]
  5. MITOCIRCLE
  6. EUMITOCOMBAT [LSHM-CT-2004-503116]
  7. European Union Framework Program 6

向作者/读者索取更多资源

Spinazzola A, Zeviani M (C. Besta Neurological Institute, Foundation IRCCS, Milano, Italy). Disorders from perturbations of nuclear-mitochondrial intergenomic cross-talk (Review). J Intern Med 2009; 265: 174-192. 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.

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