FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Androschuk, A., He, R.X., Weber, S., Rosenfelt, C., Bolduc, F.V. (2018). Stress Odorant Sensory Response Dysfunction in Drosophila Fragile X Syndrome Mutants.  Front. Mol. Neurosci. 11(): 242.
FlyBase ID
FBrf0239856
Publication Type
Research paper
Abstract
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 (FMR1) gene leads to Fragile X syndrome (FXS), the most common single gene cause of ID and ASD. Drosophila have a highly conserved FMR1 ortholog, dfmr1. dfmr1 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 Drosophila stress odorant (dSO) to gain a better understanding of the molecular basis of SPD in FXS. Here, we show that dfmr1 mutant flies present significant defects in dSO response. We found that dfmr1 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 dfmr1 mutant flies.
PubMed ID
PubMed Central ID
PMC6092503 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Front. Mol. Neurosci.
    Title
    Frontiers in molecular neuroscience
    ISBN/ISSN
    1662-5099
    Data From Reference
    Chemicals (4)
    Genes (4)
    Human Disease Models (1)