首页> 外文期刊>Translational psychiatry. >A single gene defect causing claustrophobia
【24h】

A single gene defect causing claustrophobia

机译:导致幽闭恐惧症的单基因缺陷

获取原文
           

摘要

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.
机译:幽闭恐惧症是众所周知的害怕被困在狭窄/封闭空间中的恐惧,通常被认为是对创伤经历的有条件反应。出乎意料的是,我们发现影响编码压力调节神经元蛋白的单个基因的突变会导致幽闭恐惧症。 Gpm6a缺陷型小鼠正常发育且缺乏明显的行为异常。但是,当通过单外壳轻微施加压力时,这些小鼠会出现惊人的幽闭恐惧症般的表型,即使在严重的压力下,在野生型对照中也无法诱导这种表型。人类GPM6A基因位于染色体4q32-q34上,该区域与恐慌症有关。 115位幽闭恐惧症和非幽闭恐惧症患者的序列分析确定了该基因非编码区中九种变异,这些变异在受影响的个体中更为常见(P = 0.028)。 3'非翻译区的一个变异与两个小谱系中的幽闭恐惧症有关。该突变mRNA是有功能的,但不能被源自压力调节转录本的神经元miR124沉默。我们建议,神经元GPM6A表达的动态调节丧失会导致幽闭恐惧症的遗传风险。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号