Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants

FEBS Lett. 2005 Jul 4;579(17):3770-6. doi: 10.1016/j.febslet.2005.05.035.

Abstract

The effect on the stability of alternative transcripts of different mutations of the NDUFS4 gene in patients with Leigh syndrome with complex I deficiency is presented. Normally, two NDUFS4 splice variants are degraded by nonsense mediated mRNA decay (NMD) while a third form does not trigger NMD degradation. In a patient with a premature termination codon in exon 1, all the three splice variants are up-regulated. The present is the first case of a nonsense mutation leading to the abrogation of NMD, which can represent an additional event to be considered in the evaluation of clinically relevant mutations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing*
  • Cells, Cultured
  • Codon, Nonsense / genetics*
  • Electron Transport Complex I / genetics
  • Fibroblasts / metabolism
  • Humans
  • Leigh Disease / genetics*
  • Mutation
  • NADH Dehydrogenase
  • NADH, NADPH Oxidoreductases / genetics*
  • Protein Biosynthesis / genetics
  • RNA Stability*
  • Transcription, Genetic

Substances

  • Codon, Nonsense
  • NADH, NADPH Oxidoreductases
  • NADH Dehydrogenase
  • Electron Transport Complex I
  • NDUFS4 protein, human