Differential second messenger signaling via dopamine neurons bidirectionally regulates memory retention

Proc Natl Acad Sci U S A. 2023 Sep 5;120(36):e2304851120. doi: 10.1073/pnas.2304851120. Epub 2023 Aug 28.

Abstract

Memory formation and forgetting unnecessary memory must be balanced for adaptive animal behavior. While cyclic AMP (cAMP) signaling via dopamine neurons induces memory formation, here we report that cyclic guanine monophosphate (cGMP) signaling via dopamine neurons launches forgetting of unconsolidated memory in Drosophila. Genetic screening and proteomic analyses showed that neural activation induces the complex formation of a histone H3K9 demethylase, Kdm4B, and a GMP synthetase, Bur, which is necessary and sufficient for forgetting unconsolidated memory. Kdm4B/Bur is activated by phosphorylation through NO-dependent cGMP signaling via dopamine neurons, inducing gene expression, including kek2 encoding a presynaptic protein. Accordingly, Kdm4B/Bur activation induced presynaptic changes. Our data demonstrate a link between cGMP signaling and synapses via gene expression in forgetting, suggesting that the opposing functions of memory are orchestrated by distinct signaling via dopamine neurons, which affects synaptic integrity and thus balances animal behavior.

Keywords: Drosophila; cGMP signaling; forgetting; gene expression; mushroom body.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dopaminergic Neurons*
  • Drosophila
  • Guanine
  • Histone Demethylases
  • Memory
  • Proteomics*
  • Second Messenger Systems
  • Signal Transduction

Substances

  • Guanine
  • Histone Demethylases