Nogo provides a molecular marker for diagnosis of amyotrophic lateral sclerosis

Neurobiol Dis. 2002 Aug;10(3):358-65. doi: 10.1006/nbdi.2002.0522.

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurological disorder characterized by the selective degeneration of upper and lower motor neurons. The lack of a molecular diagnostic marker is of increasing concern in view of the therapeutic strategies in development. Using an unbiased subtractive suppressive hybridization screen we have identified a clone encoding the neurite outgrowth inhibitor Nogo and shown that its isoforms display a characteristic altered expression in ALS. This was first confirmed by analyzing Nogo isoform expression in a transgenic ALS model at early asymptomatic stages where we found increased levels of Nogo-A and decreased Nogo-C and importantly, not following experimentally induced denervation. Furthermore, we confirmed these changes in both post-mortem and biopsy samples from diagnosed ALS patients but not control patients. Thus, the alteration in Nogo expression pattern, common to sporadic and familial ALS, represents a potential diagnosis tool and points strongly to Nogo having a central role in disease.

Publication types

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

MeSH terms

  • Amyotrophic Lateral Sclerosis / diagnosis*
  • Amyotrophic Lateral Sclerosis / genetics
  • Amyotrophic Lateral Sclerosis / metabolism*
  • Animals
  • Genetic Markers / physiology
  • Humans
  • Male
  • Mice
  • Mice, Transgenic
  • Muscle, Skeletal / metabolism
  • Mutation, Missense / genetics
  • Myelin Proteins / biosynthesis*
  • Myelin Proteins / genetics
  • Nogo Proteins
  • Protein Isoforms / biosynthesis
  • Protein Isoforms / genetics
  • Spinal Cord / metabolism

Substances

  • Genetic Markers
  • Myelin Proteins
  • Nogo Proteins
  • Protein Isoforms
  • RTN4 protein, human
  • Rtn4 protein, mouse