Daughterless, the Drosophila orthologue of TCF4, is required for associative learning and maintenance of the synaptic proteome

Dis Model Mech. 2020 Jul 30;13(7):dmm042747. doi: 10.1242/dmm.042747.

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.

Keywords: Appetitive associative learning; Daughterless; Drosophila melanogaster; Intellectual disability; Negative geotaxis; Pitt–Hopkins syndrome; TCF4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Association Learning*
  • Basic Helix-Loop-Helix Proteins / genetics
  • Basic Helix-Loop-Helix Proteins / metabolism*
  • Behavior, Animal*
  • Brain / embryology
  • Brain / metabolism*
  • Brain / physiopathology
  • Disease Models, Animal
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / embryology
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / metabolism*
  • Facies
  • Gene Expression Regulation, Developmental
  • HEK293 Cells
  • Humans
  • Hyperventilation / genetics
  • Hyperventilation / metabolism*
  • Hyperventilation / physiopathology
  • Intellectual Disability / genetics
  • Intellectual Disability / metabolism*
  • Intellectual Disability / physiopathology
  • Larva / genetics
  • Larva / metabolism
  • Motor Activity
  • Neurons / metabolism*
  • Proteome*
  • Signal Transduction
  • Synapses / genetics
  • Synapses / metabolism*
  • Synapsins / genetics
  • Synapsins / metabolism
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / metabolism

Substances

  • Basic Helix-Loop-Helix Proteins
  • Drosophila Proteins
  • Proteome
  • Synapsins
  • Tumor Suppressor Proteins
  • Da protein, Drosophila
  • Syn protein, Drosophila
  • dlg1 protein, Drosophila

Supplementary concepts

  • Pitt-Hopkins syndrome