We have identified two classes of neural circuits that encode aversive and appetitive valences and act antagonistically in olfactory memory formation of Drosophila.
We are who we are because we remember and forget
“Learning and memory are two of the most magical capabilities of our mind. Learning is the biological process of acquiring new knowledge about the world, and memory is the process of retaining and reconstructing that knowledge over time. Most of our knowledge of the world and most of our skills are not innate but learned. Thus, we are who we are in large part because of what we have learned and what we remember and forget.” Eric Kandel et al., 2014, Cell.
Drosophila can form an association between a particular odor and an electric shock, acquiring a conditional avoidance response to the odor. This is a simple form of memory termed aversive memory. Similarly, Drosophila can form a memory by associating an odor with the taste of sugar in a process called appetitive memory. The research in my laboratory focuses primarily on the question of how and where a memory is formed, stored and retrieved in the Drosophila brain. The study of Drosophila olfactory learning offers the advantages of simple eural circuits and advanced molecular genetics, allowing us to identify the synapses that provide plasticity and transduce critical signals. We are currently focusing on the neuropile called the mushroom body, which is thought to function as a coincidence detector during olfactory learning. The mushroom body consists of many types of neurons. Each plays a role in a different step of memory formation— for example, acquisition, consolidation and retrieval—and in a different context indicating that memory formation can be divided into several stages and that each of these stages is performed by a distinct unit. Our projects include identification of the cellular and molecular mechanisms underlying these processes. To this end, we utilize various strategies and techniques, such as behavior assay, optogenetics, functional imaging and electrophysiology.
- Two parallel pathways assign opposing odor valences during Drosophila memory formation. Yamazaki, D., Hiroi, M., Abe, T., Shimizu, K., Minami-Ohtsubo, M., Maeyama, Y., Horiuchi, J. and Tabata, T. Cell Reports 22, 2346–2358, 2018.
- Suppression of a single pair of mushroom body output neurons in Drosophila triggers aversive associations. Ueoka Y, Hiroi M, Abe T, Tabata T.
FEBS Open Bio. 22;7(4):562-576, 2017.
- Abe, T., Yamazaki, D., Murakami, S., Hiroi, M., Nitta, Y., Maeyama, Y., and Tabata, T. Sickie, a human NAV2 homolog., regulates F-actin-mediated axonal growth in Drosophila mushroom body neurons via the non-canonical Rac-Cofilin pathway. Development, 141, 4716-4728, 2014.
- Hiroi, M., Ohkura, M., Nakai., J, Masuda, N., Hashimoto, K., Inoue, K., Fiala, A., Tabata, T. Principal component analysis of odor coding at the level of third-order olfactory neurons in Drosophila. Genes Cells, 18, 1070-1081, 2013.
- Shimizu, K., Sato, M. and Tabata, T. The Wnt5/Planar cell polarity pathway regulates axonal development of the Drosophila mushroom body neuron. J. Neuroscience, 31, 4944-4954, 2011.
- Sato, M., Umetsu, D., Murakami, S., Yasugi, T. and Tabata, T. DWnt4 regulates the dorsoventral specificity of retinal projections in the Drosophila visual system. Nature Neuroscience 9 (1) 67-75, 2006
- Tabata, T. Genetics of morphogen gradients. Nature Reviews Genetics, 2, 620-630, 2001.
- Tanimoto, H., Itoh, S., ten Dijke, P., and Tabata, T. Hedgehog creates a gradient of Dpp activity in Drosophila wing imaginal discs. Mol. Cell, 5, 59-71, 2000.
- Minami, M., Kinoshita, N., Kamoshida, Y., Tanimoto, H., Tabata, T. brinker is a target of Dpp in Drosophila that negatively regulates Dpp-dependent genes. Nature, 398, 242-246, 1999.
- Tsuneizumi, K., Nakayama, T., Kamoshida, Y., Kornberg, T.B., Christian, J. L., and Tabata, T. Daughters against dpp modulates dpp organizing activity in Drosophila wing development. Nature, 389, 627-631, 1997.
Graduate School of Science