D-026
DNA damage repair proteins as molecular sensors of sleep in Drosophila
Canela Pedreira-González1,2, Emiliano Kalesnik-Vissio1,2, Agustina Bruno-Vignolo1,2, Ivana Ducrey1,2, Florencia Fernandez-Chiappe1, Marina Propato-Lots1,3, Luis de Lecea4, Nara I. Muraro1
  1. Biomedicine Research Institute of Buenos Aires-CONICET-Partner Institute of the Max Planck Society, Buenos Aires, Argentina.
  2. PhD program of the Faculty of Exact and Natural Sciences, University of Buenos Aires, Argentina.
  3. Biological Sciences Student of the Faculty of Exact and Natural Sciences, University of Buenos Aires, Argentina.
  4. Department of Psychiatry and Behavioral Sciences, Stanford Medicine, California, United States of America.
Presenting Author:
Canela Pedreira-González
canelaghia@gmail.com
What are the evolutionary advantages of sleep? Although it is well established that sleep is a highly conserved behavior throughout the animal kingdom, its precise biological purpose is still unclear. Several theories have been put forward to explain its role. For instance, sleep has been linked to processes such as memory consolidation, synaptic remodeling, and the clearance of neurotoxic by-products that accumulate in the extracellular space during periods of wakefulness. More recently, a novel hypothesis has emerged suggesting that the repair of DNA damage accumulated while awake constitutes a core function of sleep in zebrafish. Could this mechanism be conserved across other animals? Might DNA repair proteins serve as critical molecular sensors in the regulation of sleep? We propose that DNA repair proteins contribute to the molecular machinery of the sleep homeostat in Drosophila. To investigate this idea, we employ new approaches to induce DNA damage and subsequently assess alterations in sleep patterns. Furthermore, we are evaluating whether PARP1, a protein identified as a key detector of DNA double-strand breaks and mediator of sleep induction in fish, also fulfills this role in insects. Future investigations will explore whether additional DNA repair factors, including Rad51, Ku70, and Ku80, participate in shaping sleep regulation in fruit flies.