A single gene defect causing claustrophobia

Transl Psychiatry. 2013 Apr 30;3(4):e254. doi: 10.1038/tp.2013.28.

Abstract

Claustrophobia, the well-known fear of being trapped in narrow/closed spaces, is often considered a conditioned response to traumatic experience. Surprisingly, we found that mutations affecting a single gene, encoding a stress-regulated neuronal protein, can cause claustrophobia. Gpm6a-deficient mice develop normally and lack obvious behavioral abnormalities. However, when mildly stressed by single-housing, these mice develop a striking claustrophobia-like phenotype, which is not inducible in wild-type controls, even by severe stress. The human GPM6A gene is located on chromosome 4q32-q34, a region linked to panic disorder. Sequence analysis of 115 claustrophobic and non-claustrophobic subjects identified nine variants in the noncoding region of the gene that are more frequent in affected individuals (P=0.028). One variant in the 3'untranslated region was linked to claustrophobia in two small pedigrees. This mutant mRNA is functional but cannot be silenced by neuronal miR124 derived itself from a stress-regulated transcript. We suggest that loosing dynamic regulation of neuronal GPM6A expression poses a genetic risk for claustrophobia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amygdala / chemistry
  • Animals
  • Behavior, Animal
  • Electroretinography
  • Female
  • Genetic Engineering / methods
  • Heterozygote
  • Humans
  • Male
  • Membrane Glycoproteins / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Nerve Tissue Proteins / genetics*
  • Phobic Disorders / genetics*
  • Psychological Tests
  • Reflex, Startle / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stress, Psychological / genetics

Substances

  • GPM6A protein, human
  • Gpm6a protein, mouse
  • Membrane Glycoproteins
  • Nerve Tissue Proteins