FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Tamberg, L., Jaago, M., Säälik, K., Sirp, A., Tuvikene, J., Shubina, A., Kiir, C.S., Nurm, K., Sepp, M., Timmusk, T., Palgi, M. (2020). Daughterless, the Drosophila orthologue of TCF4, is required for associative learning and maintenance of the synaptic proteome.  Dis. Model Mech. 13(7): dmm042747.
FlyBase ID
FBrf0246472
Publication Type
Research paper
Abstract
Mammalian transcription factor 4 (TCF4) has been linked to schizophrenia and intellectual disabilities, such as Pitt-Hopkins syndrome (PTHS). Here, we show that similarly to mammalian TCF4, fruit fly orthologue Daughterless (Da) is expressed widely in the Drosophila brain. Furthermore, silencing of da, using several central nervous system-specific Gal4 driver lines, impairs appetitive associative learning of the larvae and leads to decreased levels of the synaptic proteins Synapsin (Syn) and Discs large 1 (Dlg1), suggesting the involvement of Da in memory formation. Here, we demonstrate that Syn and dlg1 are direct target genes of Da in adult Drosophila heads, as Da binds to the regulatory regions of these genes and the modulation of Da levels alter the levels of Syn and dlg1 mRNA. Silencing of da also affects negative geotaxis of the adult flies, suggesting the impairment of locomotor function. Overall, our findings suggest that Da regulates Drosophila larval memory and adult negative geotaxis, possibly via its synaptic target genes Syn and dlg1 These behavioural phenotypes can be further used as a PTHS model to screen for therapeutics.This article has an associated First Person interview with the first author of the paper.
PubMed ID
PubMed Central ID
PMC7406316 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Dis. Model Mech.
    Title
    Disease models & mechanisms
    ISBN/ISSN
    1754-8403 1754-8411
    Data From Reference
    Alleles (13)
    Genes (7)
    Human Disease Models (1)
    Insertions (5)
    Experimental Tools (2)
    Transgenic Constructs (8)