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Transl Psychiatry ; 3: e254, 2013 Apr 30.
Article in English | MEDLINE | ID: mdl-23632458

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.


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