FB2026_03 , released September 17, 2026
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Citation
Ehaideb, S.N., Iyengar, A., Ueda, A., Iacobucci, G.J., Cranston, C., Bassuk, A.G., Gubb, D., Axelrod, J.D., Gunawardena, S., Wu, C.F., Manak, J.R. (2014). prickle modulates microtubule polarity and axonal transport to ameliorate seizures in flies.  Proc. Natl. Acad. Sci. U.S.A. 111(30): 11187--11192.
FlyBase ID
FBrf0225788
Publication Type
Research paper
Abstract
Recent analyses in flies, mice, zebrafish, and humans showed that mutations in prickle orthologs result in epileptic phenotypes, although the mechanism responsible for generating the seizures was unknown. Here, we show that Prickle organizes microtubule polarity and affects their growth dynamics in axons of Drosophila neurons, which in turn influences both anterograde and retrograde vesicle transport. We also show that enhancement of the anterograde transport mechanism is the cause of the seizure phenotype in flies, which can be suppressed by reducing the level of either of two Kinesin motor proteins responsible for anterograde vesicle transport. Additionally, we show that seizure-prone prickle mutant flies have electrophysiological defects similar to other fly mutants used to study seizures, and that merely altering the balance of the two adult prickle isoforms in neurons can predispose flies to seizures. These data reveal a previously unidentified pathway in the pathophysiology of seizure disorders and provide evidence for a more generalized cellular mechanism whereby Prickle mediates polarity by influencing microtubule-mediated transport.
PubMed ID
PubMed Central ID
PMC4121842 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Proc. Natl. Acad. Sci. U.S.A.
    Title
    Proceedings of the National Academy of Sciences of the United States of America
    Publication Year
    1915-
    ISBN/ISSN
    0027-8424
    Data From Reference
    Alleles (12)
    Genes (4)
    Human Disease Models (1)
    Natural transposons (1)
    Insertions (3)
    Experimental Tools (2)
    Transgenic Constructs (3)