Partial complex I deficiency due to the CNS conditional ablation of Ndufa5 results in a mild chronic encephalopathy but no increase in oxidative damage

Hum Mol Genet. 2014 Mar 15;23(6):1399-412. doi: 10.1093/hmg/ddt526. Epub 2013 Oct 23.


Deficiencies in the complex I (CI; NADH-ubiquinone oxidoreductase) of the respiratory chain are frequent causes of mitochondrial diseases and have been associated with other neurodegenerative disorders, such as Parkinson's disease. The NADH-ubiquinone oxidoreductase 1 alpha subcomplex subunit 5 (NDUFA5) is a nuclear-encoded structural subunit of CI, located in the peripheral arm. We inactivated Ndufa5 in mice by the gene-trap methodology and found that this protein is required for embryonic survival. Therefore, we have created a conditional Ndufa5 knockout (KO) allele by introducing a rescuing Ndufa5 cDNA transgene flanked by loxP sites, which was selectively ablated in neurons by the CaMKIIα-Cre. At the age of 11 months, mice with a central nervous system knockout of Ndufa5 (Ndufa5 CNS-KO) showed lethargy and loss of motor skills. In these mice cortices, the levels of NDUFA5 protein were reduced to 25% of controls. Fully assembled CI levels were also greatly reduced in cortex and CI activity in homogenates was reduced to 60% of controls. Despite the biochemical phenotype, no oxidative damage, neuronal death or gliosis were detected in the Ndufa5 CNS-KO brain at this age. These results showed that a partial defect in CI in neurons can lead to late-onset motor phenotypes without neuronal loss or oxidative damage.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Damage, Chronic / pathology*
  • Cerebral Cortex / metabolism*
  • DNA Damage
  • Disease Models, Animal
  • Electron Transport Complex I / deficiency
  • Electron Transport Complex I / metabolism*
  • Embryo, Mammalian / metabolism
  • Mice
  • Mice, Knockout
  • NADH Dehydrogenase / drug effects
  • NADH Dehydrogenase / genetics
  • NADH Dehydrogenase / metabolism*
  • Neurons / metabolism*
  • Oxidative Stress*


  • NDUFA5 protein, mouse
  • NADH Dehydrogenase
  • Electron Transport Complex I