Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies

Am J Hum Genet. 2015 Nov 5;97(5):754-60. doi: 10.1016/j.ajhg.2015.09.012. Epub 2015 Oct 22.

Abstract

Autosomal-recessive optic neuropathies are rare blinding conditions related to retinal ganglion cell (RGC) and optic-nerve degeneration, for which only mutations in TMEM126A and ACO2 are known. In four families with early-onset recessive optic neuropathy, we identified mutations in RTN4IP1, which encodes a mitochondrial ubiquinol oxydo-reductase. RTN4IP1 is a partner of RTN4 (also known as NOGO), and its ortholog Rad8 in C. elegans is involved in UV light response. Analysis of fibroblasts from affected individuals with a RTN4IP1 mutation showed loss of the altered protein, a deficit of mitochondrial respiratory complex I and IV activities, and increased susceptibility to UV light. Silencing of RTN4IP1 altered the number and morphogenesis of mouse RGC dendrites in vitro and the eye size, neuro-retinal development, and swimming behavior in zebrafish in vivo. Altogether, these data point to a pathophysiological mechanism responsible for RGC early degeneration and optic neuropathy and linking RTN4IP1 functions to mitochondrial physiology, response to UV light, and dendrite growth during eye maturation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Carrier Proteins / antagonists & inhibitors
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Case-Control Studies
  • Cells, Cultured
  • Electron Transport Complex I
  • Female
  • Fibroblasts / metabolism
  • Fibroblasts / pathology*
  • Follow-Up Studies
  • Genes, Recessive
  • Humans
  • Male
  • Mice
  • Mitochondria / genetics
  • Mitochondria / pathology*
  • Mitochondrial Proteins / antagonists & inhibitors
  • Mitochondrial Proteins / genetics*
  • Mitochondrial Proteins / metabolism
  • Molecular Sequence Data
  • Mutation / genetics*
  • Nerve Degeneration
  • Optic Nerve Diseases / genetics*
  • Optic Nerve Diseases / pathology*
  • Pedigree
  • Prognosis
  • Retinal Ganglion Cells / metabolism
  • Retinal Ganglion Cells / pathology*
  • Sequence Homology, Amino Acid
  • Zebrafish / genetics
  • Zebrafish / growth & development
  • Zebrafish / metabolism

Substances

  • Carrier Proteins
  • Mitochondrial Proteins
  • RTN4IP1 protein, human
  • Electron Transport Complex I