Homozygous p.V116* mutation in C12orf65 results in Leigh syndrome

J Neurol Neurosurg Psychiatry. 2016 Feb;87(2):212-6. doi: 10.1136/jnnp-2014-310084. Epub 2015 May 20.

Abstract

Background: Leigh syndrome (LS) is an early-onset progressive neurodegenerative disorder associated with mitochondrial dysfunction. LS is characterised by elevated lactate and pyruvate and bilateral symmetric hyperintense lesions in the basal ganglia, thalamus, brainstem, cerebral white matter or spinal cord on T2-weighted MRI. LS is a genetically heterogeneous disease, and to date mutations in approximately 40 genes related to mitochondrial function have been linked to the disorder.

Methods: We investigated a pair of female monozygotic twins diagnosed with LS from consanguineous healthy parents of Indian origin. Their common clinical features included optic atrophy, ophthalmoplegia, spastic paraparesis and mild intellectual disability. High-blood lactate and high-intensity signal in the brainstem on T2-weighted MRI were consistent with a clinical diagnosis of LS. To identify the genetic cause of their condition, we performed whole exome sequencing.

Results: We identified a homozygous nonsense mutation in C12orf65 (NM_001143905; c.346delG, p.V116*) in the affected twins. Interestingly, the identical mutation was previously reported in an Indian family with Charcot-Marie Tooth disease type 6, which displayed some overlapping clinical features with the twins.

Conclusions: We demonstrate that the identical nonsense mutation in C12orf65 can result in different clinical features, suggesting the involvement of unknown modifiers.

Keywords: MITOCHONDRIAL DISORDERS; NEUROGENETICS.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Twin Study

MeSH terms

  • Adolescent
  • Age of Onset
  • Asian People
  • Brain / pathology
  • Charcot-Marie-Tooth Disease / genetics
  • Child
  • Codon, Nonsense / genetics
  • Consanguinity
  • Exome / genetics
  • Female
  • Humans
  • Jews
  • Leigh Disease / genetics*
  • Leigh Disease / pathology
  • Magnetic Resonance Imaging
  • Male
  • Mitochondrial Proteins / genetics*
  • Muscle, Skeletal / pathology
  • Pedigree
  • Peptide Termination Factors / genetics*
  • Sequence Analysis, DNA

Substances

  • C12orf65 protein, human
  • Codon, Nonsense
  • Mitochondrial Proteins
  • Peptide Termination Factors