Genes and Dynamics of Memory Systems





Laboratoire Plasticité du Cerveau
Phone: 01 40 79 45 54
Fax: 01 40 79 47 57
Labex MemoLife, Idex PSL, EMBO


olfactory learning
long-term memory
Drosophila mutants
neuronal networks
Alzheimer's disease
Brain imaging
energy metabolism


Dolan, M.-J., Belliart-Guérin, G., Bates, A.S., Frechter, S. , Lampin-Saint-Amaux, A. , Aso, Y. , Roberts, R.J.V. , Schlegel, P., Wong, A., , Hammad, A. , Bock, D., Rubin, G.M., Preat, T., Plaçais, P.-Y.* and Jefferis, G.S.X.E.* (2018). Communication from learned to innate olfactory processing centers is required for memory retrieval in Drosophila. Neuron, 100: 1-18.

Pavlowsky, A., Schor , J., Plaçais, P.-Y., and Preat, T. (2018). A GABAergic feedback shapes dopaminergic input  on the Drosophila mushroom body  to promote appetitive long-term memory. Curr Biol, 28: 1–11.

Scheunemann, L., Plaçais, P.-Y., Dromard, Y., Schwärzel, M., and Preat, T. (2018). Dunce phosphodiesterase acts as a checkpoint for Drosophila long-term memory in a pair of serotonergic neurons. Neuron, 98:350-365.

Turrel, O., Goguel, V.* and Preat, T.* (2017). Drosophila neprilysin 1 rescues memory deficits caused by amyloid-β peptide. J Neurosci, 37(43):10334-10345.

Plaçais, P.-Y., de Tredern, E., Scheunemann, L., Trannoy, S., Goguel, V., Han, K.-A., Isabel, G., and Preat, T. (2017). Upregulated energy metabolism in the Drosophila mushroom body is the trigger for long-term memory. Nat Commun, 8:15510.

Musso, P.-Y., Tchenio, P.* and Preat, T.* (2015). Delayed dopamine signaling of energy level builds appetitive long-term memory in Drosophila. Cell Rep, 10: 1-9.

Plaçais, P.-Y. and Preat, T. (2013). To favor survival under food shortage, the brain disables costly memory. Science, 339(6118): 440-442.

Plaçais, P.-Y., Trannoy, S., Isabel, G., Aso, Y., Siwanowicz, I., Belliart-Guérin, G., Vernier, P., Birman, S., Tanimoto, H. and Preat, T. (2012). Slow oscillations in two pairs of dopaminergic neurons gate long-term memory formation in Drosophila. Nat Neurosci, 15(4): 592-599.

Séjourné, J., Plaçais, P.-Y., Aso, Y., Siwanowicz, I., Trannoy, S., Vladimiros, T., Tedjakumala, S.R., Rubin, G.M., Tchénio, P., Ito, K., Isabel, G., Tanimoto, H.* and Preat, T.* (2011). Mushroom body efferent neurons responsible for aversive olfactory memory retrieval in Drosophila. Nat Neurosci, 14(7): 903-910.

Fields of research

Neurophysiology / systems neuroscience

Research Theme


How are memories encoded in the brain? How do the different forms of memory interact? The major challenge faced by neuroscientists studying memory is to define the links between the various levels of brain organization. Powerful molecular genetics tools available in drosophila, along with the properties of its highly organized brain, make it a model of choice for such an integrated analysis. Our laboratory is engaged in top-down approach to unravel some of the general mechanisms involved in associative learning and memory. To study aversive memory we use conditioning protocols during which drosophila learns to associate an odor with electric shocks. Intensive conditioning with a rest interval between the stimulus presentations (spaced conditioning) leads to the formation of long-term memory (LTM). We also study appetitive memory, which forms in starved flies after odorant and sugar presentation. Our team has made major discoveries on the dynamics of memory phases in drosophila in the past two decades. We now focus onto two original questions, the analysis of the links between energy metabolism and memory, and the study of the APP-related pathways in learning and memory.


Memory and energy metabolism

The brain is the central regulator of energy homeostasis, and it prioritizes its own supply over peripheral organs. Intriguingly, a recent study rom our team provides novel evidence that the brain is also able to down-regulate its own activity under energy shortage conditions. Specifically, we showed that energetically costly aversive LTM is inhibited in starved flies to favor survival (Plaçais and Preat 2013; Plaçais et al. 2017). This brought us to study the interplay between memory formation and brain energy status. We follow an integrated approach to answer the following questions:

- how is memory dynamics modified by brain energetic status?

- what are the neuronal circuits that signal the energy level to the olfactory memory center, and how is their activity regulated?

- what are the molecular mechanisms that underlie the interaction between the energy level and memory formation?

- what is the energetic cost of LTM formation?

- how do the neuronal and glial networks interact to manage the energy fluxes underlying memory formation?


Drosophila memory as a read-out to study the early steps of Alzheimer’s disease

We use drosophila to study some aspects of Alzheimer’s disease (AD). While the main hypothesis for AD pathology centers on the amyloid peptide, generated by proteolytic processing of amyloid precursor protein (APP), little is known about the physiological function of APP and its derivatives in the adult brain. To gain information on the early stages of AD we think it is essential to better understand the physiological role of the molecular actors of the APP pathway in brain plasticity and memory. We studied the role of the drosophila ortholog APPL, and we showed that APPL-loss of function in the adult mushroom body affects LTM formation (Goguel et al. 2011). These data support the hypothesis that disruption of normal APP function may contribute to early AD cognitive impairment. We currently analyze in details the physiological implication of APPL protein in memory processing, and study several proteins that interact with APPL or its derivatives (Turrel et al. 2017).

Team members

Valérie Goguel
Pierre-Yves Plaçais
Alice Pavlowsky
Laure Pasquer
Lisa Scheunemann
Eloïse de Tredern
Julia Minatchy
Johann Schor
Olivier Mantha