Androschuk Alaura, He Richard X, Weber Savannah, Rosenfelt Cory, Bolduc Francois V
Department of Pediatrics, University of Alberta, Edmonton, AB, Canada.
Neuroscience and Mental Health Institute, University of Alberta, Edmonton, AB, Canada.
Front Mol Neurosci. 2018 Aug 8;11:242. doi: 10.3389/fnmol.2018.00242. eCollection 2018.
Sensory processing dysfunction (SPD) is present in most patients with intellectual disability (ID) and autism spectrum disorder (ASD). Silencing expression of the Fragile X mental retardation 1 () gene leads to Fragile X syndrome (FXS), the most common single gene cause of ID and ASD. have a highly conserved FMR1 ortholog, . mutants display cognitive and social defects reminiscent of symptoms seen in individuals with FXS. We utilized a robust behavioral assay for sensory processing of the stress odorant (dSO) to gain a better understanding of the molecular basis of SPD in FXS. Here, we show that mutant flies present significant defects in dSO response. We found that expression in mushroom bodies is required for dSO processing. We also show that cyclic adenosine monophosphate (cAMP) signaling via PKA is activated after exposure to dSO and that several drugs regulating both cAMP and cyclic guanosine monophosphate (cGMP) levels significantly improved defects in dSO processing in mutant flies.
感觉处理功能障碍(SPD)存在于大多数智力残疾(ID)和自闭症谱系障碍(ASD)患者中。脆性X智力低下1( )基因的表达沉默会导致脆性X综合征(FXS),这是ID和ASD最常见的单基因病因。 有一个高度保守的FMR1直系同源基因,即 。 突变体表现出认知和社交缺陷,让人联想到FXS患者的症状。我们利用一种针对应激气味剂(dSO)感觉处理的强大行为测定法,以更好地了解FXS中SPD的分子基础。在这里,我们表明 突变果蝇在dSO反应中存在显著缺陷。我们发现蘑菇体中的 表达是dSO处理所必需的。我们还表明,暴露于dSO后,通过蛋白激酶A(PKA)的环磷酸腺苷(cAMP)信号被激活,并且几种调节cAMP和环磷酸鸟苷(cGMP)水平的药物显著改善了 突变果蝇在dSO处理中的缺陷。