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Auxin exposure disrupts feeding behavior and fatty acid metabolism in adult Drosophila .

Sophie A FleckPuja BiswasEmily D DeWittRebecca L KnutesonRobert C EismanTravis NemkovAngelo D'AlessandroJason M TennessenElizabeth J RideoutLesley N Weaver
Published in: eLife (2024)
The ease of genetic manipulation in Drosophila melanogaster using the Gal4/UAS system has been beneficial in addressing key biological questions. Current modifications of this methodology to temporally induce transgene expression require temperature changes or exposure to exogenous compounds, both of which have been shown to have detrimental effects on physiological processes. The recently described auxin-inducible gene expression system (AGES) utilizes the plant hormone auxin to induce transgene expression and is proposed to be the least toxic compound for genetic manipulation, with no obvious effects on Drosophila development and survival in one wild-type strain. Here, we show that auxin delays larval development in another widely used fly strain, and that short- and long-term auxin exposure in adult Drosophila induces observable changes in physiology and feeding behavior. We further reveal a dosage response to adult survival upon auxin exposure, and that the recommended auxin concentration for AGES alters feeding activity. Furthermore, auxin-fed male and female flies exhibit a significant decrease in triglyceride levels and display altered transcription of fatty acid metabolism genes. Although fatty acid metabolism is disrupted, auxin does not significantly impact adult female fecundity or progeny survival, suggesting AGES may be an ideal methodology for studying limited biological processes. These results emphasize that experiments using temporal binary systems must be carefully designed and controlled to avoid confounding effects and misinterpretation of results.
Keyphrases
  • arabidopsis thaliana
  • fatty acid
  • drosophila melanogaster
  • gene expression
  • genome wide
  • poor prognosis
  • dna methylation
  • transcription factor
  • young adults
  • childhood cancer
  • long non coding rna
  • binding protein