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Molecular Architecture of Smell and Taste in Drosophila
Abstract
The chemical senses—smell and taste—allow animals to evaluate and distinguish valuable food resources from dangerous substances in the environment. The central mechanisms by which the brain recognizes and discriminates attractive and repulsive odorants and tastants, and makes behavioral decisions accordingly, are not well understood in any organism. Recent molecular and neuroanatomical advances in Drosophila have produced a nearly complete picture of the peripheral neuroanatomy and function of smell and taste in this insect. Neurophysiological experiments have begun to provide insight into the mechanisms by which these animals process chemosensory cues. Given the considerable anatomical and functional homology in smell and taste pathways in all higher animals, experimental approaches in Drosophila will likely provide broad insights into the problem of sensory coding. Here we provide a critical review of the recent literature in this field and comment on likely future directions.
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Cites
A novel multigene family may encode odorant receptors: A molecular basis for odor recognition
Buck, L., & Axel, R. (1991) · Cell · doi:10.1016/0092-8674(91)90418-x · Cited by 4,987
The organization of the chemosensory system in Drosophila melanogaster: a rewiew
Stocker, R. F. (1994) · Cell and Tissue Research · doi:10.1007/bf00305372 · Cited by 950
Self-citationExcitatory Local Circuits and Their Implications for Olfactory Processing in the Fly Antennal Lobe
Shang, Y., Claridge-Chang, A., Sjulson, L., Pypaert, M., & Miesenböck, G. (2007) · Cell · doi:10.1016/j.cell.2006.12.034 · Cited by 359
A Gr receptor is required for response to the sugar trehalose in taste neurons of Drosophila
Dahanukar, A., Foster, K., van der Goes van Naters, W. M., & Carlson, J. R. (2001) · Nature Neuroscience · doi:10.1038/nn765 · Cited by 286
Developmentally programmed remodeling of the Drosophila olfactory circuit
Marin, E. C., Watts, R. J., Tanaka, N. K., Ito, K., & Luo, L. (2005) · Development · doi:10.1242/dev.01614 · Cited by 177
Python, F., & Stocker, R. F. (2002) · Journal of Comparative Neurology · doi:10.1002/cne.10383 · Cited by 82
Self-citation
Cited by
A GAL4-Driver Line Resource for Drosophila Neurobiology
Jenett, A., Rubin, G. M., Ngo, T.-T. B., Shepherd, D., Murphy, C., Dionne, H., Pfeiffer, B. D., Cavallaro, A., Hall, D., Jeter, J., et al. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.09.011 · Cited by 1,449
The neuronal architecture of the mushroom body provides a logic for associative learning
Aso, Y., Hattori, D., Yu, Y., Johnston, R. M., Iyer, N. A., Ngo, T.-T., Dionne, H., Abbott, L., Axel, R., Tanimoto, H., et al. (2014) · eLife · doi:10.7554/elife.04577 · Cited by 1,051
Chiang, A.-S., Lin, C.-Y., Chuang, C.-C., Chang, H.-M., Hsieh, C.-H., Yeh, C.-W., Shih, C.-T., Wu, J.-J., Wang, G.-T., Chen, Y.-C., et al. (2011) · Current Biology · doi:10.1016/j.cub.2010.11.056 · Cited by 767
Presynaptic facilitation by neuropeptide signaling mediates odor-driven food search
Root, C. M., Ko, K. I., Jafari, A., & Wang, J. W. (2011) · Cell · doi:10.1016/j.cell.2011.02.008 · Cited by 526
Liman, E. R., Zhang, Y. V., & Montell, C. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.022 · Cited by 473
Distinct representations of olfactory information in different cortical centres
Sosulski, D. L., Bloom, M. L., Cutforth, T., Axel, R., & Datta, S. R. (2011) · Nature · doi:10.1038/nature09868 · Cited by 479
Random convergence of olfactory inputs in the Drosophila mushroom body
Caron, S. J. C., Ruta, V., Abbott, L. F., & Axel, R. (2013) · Nature · doi:10.1038/nature12063 · Cited by 409
Architectures of neuronal circuits
Luo, L. (2021) · Science · doi:10.1126/science.abg7285 · Cited by 390
Diversity and wiring variability of olfactory local interneurons in the Drosophila antennal lobe
Chou, Y.-H., Spletter, M. L., Yaksi, E., Leong, J. C. S., Wilson, R. I., & Luo, L. (2010) · Nature Neuroscience · doi:10.1038/nn.2489 · Cited by 361
Transsynaptic mapping of second-order taste neurons in flies by trans-Tango
Talay, M., Richman, E. B., Snell, N. J., Hartmann, G. G., Fisher, J. D., Sorkaç, A., Santoyo, J. F., Chou-Freed, C., Nair, N., Johnson, M., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.011 · Cited by 301
The wiring diagram of a glomerular olfactory system
Berck, M. E., Khandelwal, A., Claus, L., Hernandez-Nunez, L., Si, G., Tabone, C. J., Li, F., Truman, J. W., Fetter, R. D., Louis, M., et al. (2016) · eLife · doi:10.7554/elife.14859 · Cited by 209
An odorant-binding protein required for suppression of sweet taste by bitter chemicals
Jeong, Y. T., Shim, J., Oh, S. R., Yoon, H. I., Kim, C. H., Moon, S. J., & Montell, C. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.025 · Cited by 223
Plasticity of local GABAergic interneurons drives olfactory habituation
Das, S., Sadanandappa, M. K., Dervan, A., Larkin, A., Lee, J. A., Sudhakaran, I. P., Priya, R., Heidari, R., Holohan, E. E., Pimentel, A., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106411108 · Cited by 219
Cell-Surface Proteomic Profiling in the Fly Brain Uncovers Wiring Regulators
Li, J., Han, S., Li, H., Udeshi, N. D., Svinkina, T., Mani, D. R., Xu, C., Guajardo, R., Xie, Q., Li, T., et al. (2020) · Cell · doi:10.1016/j.cell.2019.12.029 · Cited by 204
Information flow, cell types and stereotypy in a full olfactory connectome
Schlegel, P., Bates, A. S., Stürner, T., Jagannathan, S. R., Drummond, N., Hsu, J., Serratosa Capdevila, L., Javier, A., Marin, E. C., Barth-Maron, A., et al. (2021) · eLife · doi:10.7554/elife.66018 · Cited by 178
Molecular vibration-sensing component in Drosophila melanogaster olfaction
Franco, M. I., Turin, L., Mershin, A., & Skoulakis, E. M. C. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1012293108 · Cited by 183
Testing Odor Response Stereotypy in the Drosophila Mushroom Body
Murthy, M., Fiete, I., & Laurent, G. (2008) · Neuron · doi:10.1016/j.neuron.2008.07.040 · Cited by 163
Quantitative Proteomics by Metabolic Labeling of Model Organisms
Gouw, J. W., Krijgsveld, J., & Heck, A. J. R. (2010) · Molecular & Cellular Proteomics · doi:10.1074/mcp.r900001-mcp200 · Cited by 151
Chemoreceptor co-expression in Drosophila melanogaster olfactory neurons
Task, D., Lin, C.-C., Vulpe, A., Afify, A., Ballou, S., Brbic, M., Schlegel, P., Raji, J., Jefferis, G. S., Li, H., et al. (2022) · eLife · doi:10.7554/elife.72599 · Cited by 141
Drosophila sensory receptors—a set of molecular Swiss Army Knives
Montell, C. (2021) · Genetics · doi:10.1093/genetics/iyaa011 · Cited by 140
Nässel, D. R. (2009) · Invertebrate Neuroscience · doi:10.1007/s10158-009-0090-1 · Cited by 125
Simultaneous Encoding of Odors by Channels with Diverse Sensitivity to Inhibition
Hong, E. J., & Wilson, R. I. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.040 · Cited by 93
Motor neurons controlling fluid ingestion in Drosophila
Manzo, A., Silies, M., Gohl, D. M., & Scott, K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120305109 · Cited by 69
The Ol1mpiad: concordance of behavioural faculties of stage 1 and stage 3 Drosophila larvae
Almeida-Carvalho, M. J., Berh, D., Braun, A., Chen, Y.-C., Eichler, K., Eschbach, C., Fritsch, P. M. J., Gerber, B., Hoyer, N., Jiang, X., et al. (2017) · Journal of Experimental Biology · doi:10.1242/jeb.156646 · Cited by 51
A resource for the Drosophila antennal lobe provided by the connectome of glomerulus VA1v
Horne, J. A., Langille, C., McLin, S., Wiederman, M., Lu, Z., Xu, C. S., Plaza, S. M., Scheffer, L. K., Hess, H. F., & Meinertzhagen, I. A. (2018) · eLife · doi:10.7554/elife.37550 · Cited by 46
Complex representation of taste quality by second-order gustatory neurons in Drosophila
Snell, N. J., Fisher, J. D., Hartmann, G. G., Zolyomi, B., Talay, M., & Barnea, G. (2022) · Current Biology · doi:10.1016/j.cub.2022.07.048 · Cited by 39
Miyazaki, T., Lin, T.-Y., Ito, K., Lee, C.-H., & Stopfer, M. (2015) · Journal of Neurogenetics · doi:10.3109/01677063.2015.1054993 · Cited by 34
Mating-driven variability in olfactory local interneuron wiring
Chou, Y.-H., Yang, C.-J., Huang, H.-W., Liou, N.-F., Panganiban, M. R., Luginbuhl, D., Yin, Y., Taisz, I., Liang, L., Jefferis, G. S. X. E., et al. (2022) · Science Advances · doi:10.1126/sciadv.abm7723 · Cited by 9
Metadata
- Authors
- Vosshall, L. B., & Stocker, R. F.
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 2007-07-01
- Volume
- 30
- Issue
- 1
- Pages
- 505-533
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- OpenAlex
- W2118398316
- Cited by
- 870
- References
- 6
- FWCI
- 2.07
- Type
- journal article
- Language
- en
- Open access
- closed
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