FB2024_02 , released April 23, 2024
Reference Report
Open Close
Reference
Citation
Wu, Y., Funato, Y., Meschi, E., Jovanoski, K.D., Miki, H., Waddell, S. (2020). Magnesium efflux from Drosophila Kenyon cells is critical for normal and diet-enhanced long-term memory.  eLife 9(): e61339.
FlyBase ID
FBrf0247921
Publication Type
Research paper
Abstract
Dietary magnesium (Mg2+) supplementation can enhance memory in young and aged rats. Memory-enhancing capacity was largely ascribed to increases in hippocampal synaptic density and elevated expression of the NR2B subunit of the NMDA-type glutamate receptor. Here we show that Mg2+ feeding also enhances long-term memory in Drosophila. Normal and Mg2+-enhanced fly memory appears independent of NMDA receptors in the mushroom body and instead requires expression of a conserved CNNM-type Mg2+-efflux transporter encoded by the unextended (uex) gene. UEX contains a putative cyclic nucleotide-binding homology domain and its mutation separates a vital role for uex from a function in memory. Moreover, UEX localization in mushroom body Kenyon cells (KCs) is altered in memory-defective flies harboring mutations in cAMP-related genes. Functional imaging suggests that UEX-dependent efflux is required for slow rhythmic maintenance of KC Mg2+. We propose that regulated neuronal Mg2+ efflux is critical for normal and Mg2+-enhanced memory.
PubMed ID
PubMed Central ID
PMC7843133 (PMC) (EuropePMC)
Related Publication(s)
Personal communication to FlyBase

Location data for uex[Δ].
Wu and Waddell, 2021.7.19, Location data for uex[Δ]. [FBrf0249519]

Note

A divalent boost from magnesium.
Laursen and Garrity, 2021, eLife 10: e65359 [FBrf0248020]

Associated Information
Comments
Associated Files
Other Information
Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    eLife
    Title
    eLife
    ISBN/ISSN
    2050-084X
    Data From Reference
    Alleles (32)
    Chemicals (1)
    Gene Groups (1)
    Genes (9)
    Natural transposons (1)
    Insertions (9)
    Experimental Tools (7)
    Transgenic Constructs (22)