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  • Review Article
  • Published:

Drosophila olfactory memory: single genes to complex neural circuits

Key Points

  • Fruit flies can learn to associate olfactory or visual cues with rewarding or punishing reinforcement. Fruitfly memory persists for hours or days, depending on the training protocol. Multiple spaced training trials form long-term memory that can persist for days.

  • Labour-intensive genetic screens and reverse genetic approaches over the last 30 years have identified more than 80 genes that are potentially involved in olfactory memory. These mutants provide a unique entry to the molecular processes that engender memory.

  • Localizing the memory-relevant gene products has primarily highlighted the mushroom body neurons as key neural circuit components of olfactory memory. This analysis also led to the identification of the two dorsal paired medial (DPM) neurons that innervate the mushroom bodies and are crucial for aversive and appetitive odour memory stability.

  • Genetic tools have been developed to precisely control transgene expression in space and time. These tools are essential to determine whether a gene product functions acutely in specific neurons in the adult fly brain as opposed to being required for brain development.

  • Interventionist approaches to stimulate or temporarily block synaptic transmission from genetically defined neurons have transformed studies of memory. These genetic tools permit a fine temporal dissection of the role of defined neurons in memory acquisition, consolidation and retrieval and have heralded a systems-level analysis of memory in the fly brain.

  • Monoamine function distinguishes between aversive and appetitive conditioning: aversive odour memory requires functional dopaminerigic neurons, whereas appetitive odour memory depends on octopamine. Current models posit that mushroom body neurons encode memory by integrating coincident odour information with a reward or punishment signal from the respective monoamine.

  • The fly employs parallel and sequential use of different mushroom body neurons to process memory. These findings suggest that memory processing in the fly is dynamic, and may more closely resemble memory processing in the mammalian brain than previously imagined.

  • Optical recording and physiology from genetically marked neurons in the brain of a live behaving fly has given a new dimension to the analysis of memory, filling the considerable gap between a dysfunctional gene and behavioural memory performance. Coupling these techniques with our large collection of memory defective mutants should further revolutionize our understanding of fly memory.

Abstract

A central goal of neuroscience is to understand how neural circuits encode memory and guide behaviour. Studying simple, genetically tractable organisms, such as Drosophila melanogaster, can illuminate principles of neural circuit organization and function. Early genetic dissection of D. melanogaster olfactory memory focused on individual genes and molecules. These molecular tags subsequently revealed key neural circuits for memory. Recent advances in genetic technology have allowed us to manipulate and observe activity in these circuits, and even individual neurons, in live animals. The studies have transformed D. melanogaster from a useful organism for gene discovery to an ideal model to understand neural circuit function in memory.

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Figure 1: Cartoon Drosophila melanogaster head.
Figure 2: Schematic of the adult fly olfactory system circuit.
Figure 3: Three-dimensional models of the mushroom bodies.
Figure 4: Dorsal paired medial neurons.
Figure 5: Model for aversive olfactory conditioning and DPM neuron-dependent memory processing.

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References

  1. McGuire, S. E., Deshazer, M. & Davis, R. L. Thirty years of olfactory learning and memory research in Drosophila melanogaster. Prog. Neurobiol. 76, 328–347 (2005).

    Article  CAS  PubMed  Google Scholar 

  2. Davis, R. L. Olfactory memory formation in Drosophila: from molecular to systems neuroscience. Annu. Rev. Neurosci. 28, 275–302 (2005).

    Article  CAS  PubMed  Google Scholar 

  3. Margulies, C., Tully, T. & Dubnau, J. Deconstructing memory in Drosophila. Curr. Biol. 15, R700–R713 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Venken, K. J. & Bellen, H. J. Emerging technologies for gene manipulation in Drosophila melanogaster. Nature Rev. Genet. 6, 167–178 (2005).

    Article  CAS  PubMed  Google Scholar 

  5. Kitamoto, T. Conditional modification of behavior in Drosophila by targeted expression of a temperature-sensitive shibire allele in defined neurons. J. Neurobiol. 47, 81–92 (2001).

    Article  CAS  PubMed  Google Scholar 

  6. Tobin, D. et al. Combinatorial expression of TRPV channel proteins defines their sensory functions and subcellular localization in C. elegans neurons. Neuron 35, 307–318 (2002).

    Article  CAS  PubMed  Google Scholar 

  7. Lima, S. Q. & Miesenbock, G. Remote control of behavior through genetically targeted photostimulation of neurons. Cell 121, 141–152 (2005). A spectacular demonstration of experimenter-controlled behaviour by photostimulation of genetically defined neurons in an intact living fly. A laser was used to activate an injected caged-ATP that depolarizes target neurons expressing a transgenically encoded mammalian ionotropic ATP receptor.

    Article  CAS  PubMed  Google Scholar 

  8. Marella, S. et al. Imaging taste responses in the fly brain reveals a functional map of taste category and behavior. Neuron 49, 285–295 (2006).

    Article  CAS  PubMed  Google Scholar 

  9. Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G. & Deisseroth, K. Millisecond-timescale, genetically targeted optical control of neural activity. Nature Neurosci. 8, 1263–1268 (2005).

    Article  CAS  PubMed  Google Scholar 

  10. Nagel, G. et al. Light activation of channel-rhodopsin-2 in excitable cells of Caenorhabditis elegans triggers rapid behavioral responses. Curr. Biol. 15, 2279–2284 (2005).

    Article  CAS  PubMed  Google Scholar 

  11. Schroll, C. et al. Light-induced activation of distinct modulatory neurons triggers appetitive or aversive learning in Drosophila larvae. Curr. Biol. 16, 1741–1747 (2006). In larval olfactory conditioning experiments the authors replaced US presentation with photostimulation of monoaminergic neurons expressing transgenic channelrhodopsin 2.

    Article  CAS  PubMed  Google Scholar 

  12. Fiala, A. et al. Genetically expressed cameleon in Drosophila melanogaster is used to visualize olfactory information in projection neurons. Curr. Biol. 12, 1877–1884 (2002).

    Article  CAS  PubMed  Google Scholar 

  13. Ng, M. et al. Transmission of olfactory information between three populations of neurons in the antennal lobe of the fly. Neuron 36, 463–474 (2002).

    Article  CAS  PubMed  Google Scholar 

  14. Wang, J. W., Wong, A. M., Flores, J., Vosshall, L. B. & Axel, R. Two-photon calcium imaging reveals an odor-evoked map of activity in the fly brain. Cell 112, 271–282 (2003).

    Article  CAS  PubMed  Google Scholar 

  15. Wang, Y. et al. Stereotyped odor-evoked activity in the mushroom body of Drosophila revealed by green fluorescent protein-based Ca2+ imaging. J. Neurosci. 24, 6507–6514 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Yu, D., Ponomarev, A. & Davis, R. L. Altered representation of the spatial code for odors after olfactory classical conditioning; memory trace formation by synaptic recruitment. Neuron 42, 437–449 (2004). The first study coupling live optical imaging of genetically defined neurons in the D. melanogaster brain with an olfactory conditioning protocol performed under the microscope. Conditioning changed odour-evoked activity in the antennal lobe.

    Article  CAS  PubMed  Google Scholar 

  17. Wilson, R. I., Turner, G. C. & Laurent, G. Transformation of olfactory representations in the Drosophila antennal lobe. Science 303, 366–370 (2003).

    Article  PubMed  CAS  Google Scholar 

  18. Schroder-Lang, S. et al. Fast manipulation of cellular cAMP level by light in vivo. Nature Methods 4, 39–42 (2007).

    Article  PubMed  CAS  Google Scholar 

  19. Quinn, W. G., Harris, W. A. & Benzer, S. Conditioned behavior in Drosophila melanogaster. Proc. Natl Acad. Sci. USA 71, 708–712 (1974).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Duerr, J. S. & Quinn, W. G. Three Drosophila mutations that block associative learning also affect habituation and sensitization. Proc. Natl Acad. Sci. USA 79, 3646–3650 (1982).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Tempel, B. L., Bonini, N., Dawson, D. R. & Quinn, W. G. Reward learning in normal and mutant Drosophila. Proc. Natl Acad. Sci. USA 80, 1482–1486 (1983).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Tully, T. & Quinn, W. G. Classical conditioning and retention in normal and mutant Drosophila melanogaster. J. Comp. Physiol. [A] 157, 263–277 (1985). The original description of the now standard olfactory conditioning procedure.

    Article  CAS  Google Scholar 

  23. Wolf, R. et al. Drosophila mushroom bodies are dispensable for visual, tactile, and motor learning. Learn. Mem. 5, 166–178 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Mery, F. & Kawecki, T. J. Experimental evolution of learning ability in fruit flies. Proc. Natl Acad. Sci. USA 99, 14274–14279 (2002).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Wustmann, G. & Heisenberg, M. Behavioral manipulation of retrieval in a spatial memory task for Drosophila melanogaster. Learn. Mem. 4, 328–336 (1997).

    Article  CAS  PubMed  Google Scholar 

  26. Schwaerzel, M. et al. Dopamine and octopamine differentiate between aversive and appetitive olfactory memories in Drosophila. J. Neurosci. 23, 10495–10502 (2003). This important paper demonstrated a differential requirement for dopamine and octopamine in aversive and appetitive conditioning.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Tully, T., Preat, T., Boynton, S. C. & Del, V. M. Genetic dissection of consolidated memory in Drosophila. Cell 79, 35–47 (1994). A landmark paper demonstrating that multiple spaced-training trials form protein synthesis-dependent long-term memory in D. melanogaster . This paper defined a new era of long-term memory study in D. melanogaster.

    Article  CAS  PubMed  Google Scholar 

  28. Quinn, W. G. & Dudai, Y. Memory phases in Drosophila. Nature 262, 576–577 (1976).

    Article  CAS  PubMed  Google Scholar 

  29. Folkers, E., Drain, P. & Quinn, W. G. Radish, a Drosophila mutant deficient in consolidated memory. Proc. Natl Acad. Sci. USA 90, 8123–8127 (1993).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Isabel, G., Pascual, A. & Preat, T. Exclusive consolidated memory phases in Drosophila. Science 304, 1024–1027 (2004).

    Article  CAS  PubMed  Google Scholar 

  31. Davis, R. L. Olfactory learning. Neuron 44, 31–48 (2004).

    Article  CAS  PubMed  Google Scholar 

  32. Clyne, P. J. et al. A novel family of divergent seven-transmembrane proteins: candidate odorant receptors in Drosophila. Neuron 22, 327–338 (1999).

    Article  CAS  PubMed  Google Scholar 

  33. Vosshall, L. B., Amrein, H., Morozov, P. S., Rzhetsky, A. & Axel, R. A spatial map of olfactory receptor expression in the Drosophila antenna. Cell 96, 725–736 (1999).

    Article  CAS  PubMed  Google Scholar 

  34. Gao, Q. & Chess, A. Identification of candidate Drosophila olfactory receptors from genomic DNA sequence. Genomics 60, 31–39 (1999).

    Article  CAS  PubMed  Google Scholar 

  35. Hallem, E. A. & Carlson, J. R. The odor coding system of Drosophila. Trends Genet. 20, 453–459 (2004).

    Article  CAS  PubMed  Google Scholar 

  36. Vosshall, L. B. The molecular logic of olfaction in Drosophila. Chem. Senses 26, 207–213 (2001).

    Article  CAS  PubMed  Google Scholar 

  37. de Bruyne, M., Clyne, P. J. & Carlson, J. R. Odor coding in a model olfactory organ: the Drosophila maxillary palp. J. Neurosci. 19, 4520–4532 (1999).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. de Bruyne, M., Foster, K. & Carlson, J. R. Odor coding in the Drosophila antenna. Neuron 30, 537–552 (2001).

    Article  CAS  PubMed  Google Scholar 

  39. Hallem, E. A., Ho, M. G. & Carlson, J. R. The molecular basis of odor coding in the Drosophila antenna. Cell 117, 965–979 (2004).

    Article  CAS  PubMed  Google Scholar 

  40. Hallem, E. A. & Carlson, J. R. Coding of odors by a receptor repertoire. Cell 125, 143–160 (2006).

    Article  CAS  PubMed  Google Scholar 

  41. Elmore, T., Ignell, R., Carlson, J. R. & Smith, D. P. Targeted mutation of a Drosophila odor receptor defines receptor requirement in a novel class of sensillum. J. Neurosci. 23, 9906–9912 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Larsson, M. C. et al. Or83b encodes a broadly expressed odorant receptor essential for Drosophila olfaction. Neuron 43, 703–714 (2004).

    Article  CAS  PubMed  Google Scholar 

  43. Jones, W. D., Nguyen, T. A., Kloss, B., Lee, K. J. & Vosshall, L. B. Functional conservation of an insect odorant receptor gene across 250 million years of evolution. Curr. Biol. 15, R119–R121 (2005).

    Article  CAS  PubMed  Google Scholar 

  44. Goldman, A. L., Van der Goes van Naters, W., Lessing, D., Warr, C. G. & Carlson, J. R. Coexpression of two functional odor receptors in one neuron. Neuron 45, 661–666 (2005).

    Article  CAS  PubMed  Google Scholar 

  45. Jones, W. D., Cayirlioglu, P., Kadow, I. G. & Vosshall, L. B. Two chemosensory receptors together mediate carbon dioxide detection in Drosophila. Nature 445, 86–90 (2007).

    Article  CAS  PubMed  Google Scholar 

  46. Kwon, J. Y., Dahanukar, A., Weiss, L. A. & Carlson, J. R. The molecular basis of CO2 reception in Drosophila. Proc. Natl Acad. Sci. USA 104, 3574–3578 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  47. Vosshall, L. B., Wong, A. M. & Axel, R. An olfactory sensory map in the fly brain. Cell 102, 147–159 (2000).

    Article  CAS  PubMed  Google Scholar 

  48. Gao, Q., Yuan, B. & Chess, A. Convergent projections of Drosophila olfactory neurons to specific glomeruli in the antennal lobe. Nature Neurosci. 3, 780–785 (2000).

    Article  CAS  PubMed  Google Scholar 

  49. Couto, A., Alenius, M. & Dickson, B. J. Molecular, anatomical, and functional organization of the Drosophila olfactory system. Curr. Biol. 15, 1535–1547 (2005).

    Article  CAS  PubMed  Google Scholar 

  50. Fishilevich, E. & Vosshall, L. B. Genetic and functional subdivision of the Drosophila antennal lobe. Curr. Biol. 15, 1548–1553 (2005).

    Article  CAS  PubMed  Google Scholar 

  51. Stocker, R. F., Heimbeck, G., Gendre, N. & de Belle. J. S. Neuroblast ablation in Drosophila P[GAL4] lines reveals origins of olfactory interneurons. J. Neurobiol. 32, 443–456 (1997).

    Article  CAS  PubMed  Google Scholar 

  52. Jefferis, G. S., Marin, E. C., Stocker, R. F. & Luo, L. Target neuron prespecification in the olfactory map of Drosophila. Nature 414, 204–208 (2001).

    Article  CAS  PubMed  Google Scholar 

  53. Marin, E. C., Jefferis, G. S., Komiyama, T., Zhu, H. & Luo, L. Representation of the glomerular olfactory map in the Drosophila brain. Cell 109, 243–255 (2002).

    Article  CAS  PubMed  Google Scholar 

  54. Wilson, R. I. & Laurent, G. Role of GABAergic inhibition in shaping odor-evoked spatiotemporal patterns in the Drosophila antennal lobe. J. Neurosci. 25, 9069–9079 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Shang, Y., Claridge-Chang, A., Sjulson, L., Pypaert, M. & Miesenbock, G. Excitatory local circuits and their implications for olfactory processing in the fly antennal lobe. Cell 128, 601–612 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. Stocker, R. F. The organization of the chemosensory system in Drosophila melanogaster: a review. Cell Tissue Res. 275, 3–26 (1994).

    Article  CAS  PubMed  Google Scholar 

  57. Ito, K. et al. The organization of extrinsic neurons and their implications in the functional roles of the mushroom bodies in Drosophila melanogaster Meigen. Learn. Mem. 5, 52–77 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Miesenbock, G., De, A. D. A. & Rothman, J. E. Visualizing secretion and synaptic transmission with pH-sensitive green fluorescent proteins. Nature 394, 192–195 (1998).

    Article  CAS  PubMed  Google Scholar 

  59. Nakai, J., Ohkura, M. & Imoto, K. A high signal-to-noise Ca2+ probe composed of a single green fluorescent protein. Nature Biotechnol. 19, 137–141 (2001).

    Article  CAS  Google Scholar 

  60. Christensen, T. A. & Hildebrand, J. G. Pheromonal and host-odor processing in the insect antennal lobe: how different. Curr. Opin. Neurobiol. 12, 393–399 (2002).

    Article  CAS  PubMed  Google Scholar 

  61. Christensen, T. A., Lei, H. & Hildebrand, J. G. Coordination of central odor representations through transient, non-oscillatory synchronization of glomerular output neurons. Proc. Natl Acad. Sci. USA 100, 11076–11081 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  62. Friedrich, R. W. & Stopfer, M. Recent dynamics in olfactory population coding. Curr. Opin. Neurobiol. 11, 468–474 (2001).

    Article  CAS  PubMed  Google Scholar 

  63. Laurent, G. Olfactory network dynamics and the coding of multidimensional signals. Nature Rev. Neurosci. 3, 884–895 (2002).

    Article  CAS  Google Scholar 

  64. Laurent, G. et al. Odor encoding as an active, dynamical process: experiments, computation, and theory. Annu. Rev. Neurosci. 24, 263–297 (2001).

    Article  CAS  PubMed  Google Scholar 

  65. Menzel, R., Leboulle, G. & Eisenhardt, D. Small brains, bright minds. Cell 124, 237–239 (2006).

    Article  CAS  PubMed  Google Scholar 

  66. Hammer, M. & Menzel, R. Multiple sites of associative odor learning as revealed by local brain microinjections of octopamine in honeybees. Learn. Mem. 5, 146–156 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Faber, T., Joerges, J. & Menzel, R. Associative learning modifies neural representations of odors in the insect brain. Nature Neurosci. 2, 74–78 (1999).

    Article  CAS  PubMed  Google Scholar 

  68. Daly, K. C., Christensen, T. A., Lei, H., Smith, B. H. & Hildebrand, J. G. Learning modulates the ensemble representations for odors in primary olfactory networks. Proc. Natl Acad. Sci. USA 101, 10476–10481 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  69. Peele, P., Ditzen, M., Menzel, R. & Galizia, C. G. Appetitive odor learning does not change olfactory coding in a subpopulation of honeybee antennal lobe neurons. J. Comp. Physiol. A Neuroethol. Sens. Neural. Behav. Physiol. 192, 1083–1103 (2006).

    Article  CAS  PubMed  Google Scholar 

  70. Ashraf, S. I., McLoon, A. L., Sclarsic, S. M. & Kunes, S. Synaptic protein synthesis associated with memory is regulated by the RISC pathway in Drosophila. Cell 124, 191–205 (2006).

    Article  CAS  PubMed  Google Scholar 

  71. Golic, K. G. & Lindquist, S. The FLP recombinase of yeast catalyzes site-specific recombination in the Drosophila genome. Cell 59, 499–509 (1989).

    Article  CAS  PubMed  Google Scholar 

  72. Lee, T. & Luo, L. Mosaic analysis with a repressible cell marker for studies of gene function in neuronal morphogenesis. Neuron 22, 451–461 (1999).

    Article  CAS  PubMed  Google Scholar 

  73. Wong, A. M., Wang, J. W. & Axel, R. Spatial representation of the glomerular map in the Drosophila protocerebrum. Cell 109, 229–241 (2002).

    Article  CAS  PubMed  Google Scholar 

  74. Jefferis, G. S. et al. Comprehensive maps of Drosophila higher olfactory centers: spatially segregated fruit and pheromone representation. Cell 128, 1187–1203 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  75. Zhu, H. et al. Dendritic patterning by Dscam and synaptic partner matching in the Drosophila antennal lobe. Nature Neurosci. 9, 349–355 (2006).

    Article  CAS  PubMed  Google Scholar 

  76. Tanaka, N. K., Awasaki, T., Shimada, T. & Ito, K. Integration of chemosensory pathways in the Drosophila second-order olfactory centers. Curr. Biol. 14, 449–457 (2004).

    Article  CAS  PubMed  Google Scholar 

  77. Lin, H., Lai, J. S., Chin, A., Chen, Y. & Chiang, A. A map of olfactory representation in the Drosophila mushroom body. Cell 128, 1205–1217 (2007).

    Article  CAS  PubMed  Google Scholar 

  78. Heimbeck, G., Bugnon, V., Gendre, N., Keller, A. & Stocker, R. F. A central neural circuit for experience-independent olfactory and courtship behavior in Drosophila melanogaster. Proc. Natl Acad. Sci. USA 98, 15336–15341 (2001).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  79. de Belle, J. S. & Heisenberg, M. Associative odor learning in Drosophila abolished by chemical ablation of mushroom bodies. Science 263, 692–695 (1994).

    Article  CAS  PubMed  Google Scholar 

  80. Wang, Y. et al. Blockade of neurotransmission in Drosophila mushroom bodies impairs odor attraction, but not repulsion. Curr. Biol. 13, 1900–1904 (2003).

    Article  CAS  PubMed  Google Scholar 

  81. Crittenden, J. R., Skoulakis, E. M., Han, K. A., Kalderon, D. & Davis, R. L. Tripartite mushroom body architecture revealed by antigenic markers. Learn. Mem. 5, 38–51 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  82. Lee, T., Lee, A. & Luo, L. Development of the Drosophila mushroom bodies: sequential generation of three distinct types of neurons from a neuroblast. Development 126, 4065–4076 (1999).

    Article  CAS  PubMed  Google Scholar 

  83. Yang, M. Y., Armstrong, J. D., Vilinsky, I., Strausfeld, N. J. & Kaiser, K. Subdivision of the Drosophila mushroom bodies by enhancer-trap expression patterns. Neuron 15, 45–54 (1995).

    Article  PubMed  Google Scholar 

  84. Strausfeld, N. J., Sinakevitch, I. & Vilinsky, I. The mushroom bodies of Drosophila melanogaster: an immunocytological and golgi study of Kenyon cell organization in the calyces and lobes. Microsc. Res. Tech. 62, 151–169 (2003).

    Article  PubMed  Google Scholar 

  85. Aceves-Pina, E. O. & Quinn, W. G. Learning in normal and mutant Drosophila larvae. Science 206, 93–96 (1979).

    Article  CAS  PubMed  Google Scholar 

  86. Gerber, B. & Stocker, R. F. The Drosophila larva as a model for studying chemosensation and chemosensory learning: a review. Chem. Senses 32, 65–89 (2007).

    Article  CAS  PubMed  Google Scholar 

  87. Scherer, S., Stocker, R. F. & Gerber, B. Olfactory learning in individually assayed Drosophila larvae. Learn. Mem. 10, 217–225 (2003).

    Article  PubMed  PubMed Central  Google Scholar 

  88. Hendel, T. et al. The carrot, not the stick: appetitive rather than aversive gustatory stimuli support associative olfactory learning in individually assayed Drosophila larvae. J. Comp. Physiol. A 191, 265–279 (2005).

    Article  Google Scholar 

  89. Tissot, M., Gendre, N., Hawken, A., Stortkuhl, K. F. & Stocker, R. F. Larval chemosensory projections and invasion of adult afferents in the antennal lobe of Drosophila. J. Neurobiol. 32, 281–297 (1997).

    Article  CAS  PubMed  Google Scholar 

  90. Ramaekers, A. et al. Glomerular maps without cellular redundancy at successive levels of the Drosophila larval olfactory circuit. Curr. Biol. 15, 982–992 (2005).

    Article  CAS  PubMed  Google Scholar 

  91. Masuda-Nakagawa, L. M., Tanaka, N. K. & O'Kane, C. J. Stereotypic and random patterns of connectivity in the larval mushroom body calyx of Drosophila. Proc. Natl Acad. Sci. USA 102, 19027–19032 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  92. Zhu, S., Chiang, A. S. & Lee, T. Development of the Drosophila mushroom bodies: elaboration, remodeling and spatial organization of dendrites in the calyx. Development 130, 2603–2610 (2003).

    Article  CAS  PubMed  Google Scholar 

  93. Yasuyama, K., Meinertzhagen, I. A. & Schurmann, F. W. Synaptic organization of the mushroom body calyx in Drosophila melanogaster. J. Comp. Neurol. 445, 211–226 (2002).

    Article  PubMed  Google Scholar 

  94. Perez-Orive, J. et al. Oscillations and sparsening of odor representations in the mushroom body. Science 297, 359–365 (2002).

    Article  CAS  PubMed  Google Scholar 

  95. Perez-Orive, J., Bazhenov, M. & Laurent, G. Intrinsic and circuit properties favor coincidence detection for decoding oscillatory input. J. Neurosci. 24, 6037–6047 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  96. Miyawaki, A., Griesbeck, O., Heim, R. & Tsien, R. Y. Dynamic and quantitative Ca2+ measurements using improved cameleons. Proc. Natl Acad. Sci. USA 96, 2135–2140 (1999).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  97. Yu, D., Akalal, D. B. & Davis, R. L. Drosophila α/β mushroom body neurons form a branch-specific, long-term cellular memory trace after spaced olfactory conditioning. Neuron 52, 845–855 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  98. Hammer, M. An identified neuron mediates the unconditioned stimulus in associative olfactory learning in honeybees. Nature 366, 59–63 (1993).

    Article  CAS  PubMed  Google Scholar 

  99. Krashes, M. J., Keene, A. C., Leung, B., Armstrong, J. D. & Waddell, S. Sequential use of mushroom body neuron subsets during Drosophila odor memory processing. Neuron 53, 103–115 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  100. Scott, K. Taste recognition: food for thought. Neuron 48, 455–464 (2005).

    Article  CAS  PubMed  Google Scholar 

  101. Amrein, H. & Thorne, N. Gustatory perception and behavior in Drosophila melanogaster. Curr. Biol. 15, R673–R684 (2005).

    Article  CAS  PubMed  Google Scholar 

  102. Clyne, P. J., Warr, C. G. & Carlson, J. R. Candidate taste receptors in Drosophila. Science 287, 1830–1834 (2000).

    Article  CAS  PubMed  Google Scholar 

  103. Scott, K. et al. A chemosensory gene family encoding candidate gustatory and olfactory receptors in Drosophila. Cell 104, 661–673 (2001).

    Article  CAS  PubMed  Google Scholar 

  104. Chyb, S., Dahanukar, A., Wickens, A. & Carlson, J. R. Drosophila Gr5a encodes a taste receptor tuned to trehalose. Proc. Natl Acad. Sci. USA 100, 14526–14530 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  105. Wang, Z., Singhvi, A., Kong, P. & Scott, K. Taste representations in the Drosophila brain. Cell 117, 981–991 (2004).

    Article  CAS  PubMed  Google Scholar 

  106. Thorne, N., Chromey, C., Bray, S. & Amrein, H. Taste perception and coding in Drosophila. Curr. Biol. 14, 1065–1079 (2004).

    Article  CAS  PubMed  Google Scholar 

  107. Neckameyer, W. S. & White, K. Drosophila tyrosine hydroxylase is encoded by the pale locus. J. Neurogenet. 8, 189–199 (1993).

    Article  CAS  PubMed  Google Scholar 

  108. Livingstone, M. S. & Tempel, B. L. Genetic dissection of monoamine neurotransmitter synthesis in Drosophila. Nature 303, 67–70 (1983).

    Article  CAS  PubMed  Google Scholar 

  109. Friggi-Grelin, F. et al. Targeted gene expression in Drosophila dopaminergic cells using regulatory sequences from tyrosine hydroxylase. J. Neurobiol. 54, 618–627 (2003).

    Article  CAS  PubMed  Google Scholar 

  110. Riemensperger, T., Voller, T., Stock, P., Buchner, E. & Fiala, A. Punishment prediction by dopaminergic neurons in Drosophila. Curr. Biol. 15, 1953–1960 (2005).

    Article  CAS  PubMed  Google Scholar 

  111. Yellman, C., Tao, H., He, B. & Hirsh, J. Conserved and sexually dimorphic behavioral responses to biogenic amines in decapitated Drosophila. Proc. Natl Acad. Sci. USA 94, 4131–4136 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  112. Neckameyer, W. S. Dopamine and mushroom bodies in Drosophila: experience-dependent and-independent aspects of sexual behavior. Learn. Mem. 5, 157–165 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  113. Bainton, R. J. et al. Dopamine modulates acute responses to cocaine, nicotine and ethanol in Drosophila. Curr. Biol. 10, 187–194 (2000).

    Article  CAS  PubMed  Google Scholar 

  114. Andretic, R., van Swinderen, B. & Greenspan, R. J. Dopaminergic modulation of arousal in Drosophila. Curr. Biol. 15, 1165–1175 (2005).

    Article  CAS  PubMed  Google Scholar 

  115. Kume, K., Kume, S., Park, S. K., Hirsh, J. & Jackson, F. R. Dopamine is a regulator of arousal in the fruit fly. J. Neurosci. 25, 7377–7384 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  116. Sinakevitch, I. & Strausfeld, N. J. Comparison of octopamine-like immunoreactivity in the brains of the fruit fly and blow fly. J. Comp. Neurol. 494, 460–475 (2006).

    Article  CAS  PubMed  Google Scholar 

  117. Cole, S. H. et al. Two functional but noncomplementing Drosophila tyrosine decarboxylase genes: distinct roles for neural tyramine and octopamine in female fertility. J. Biol. Chem. 280, 14948–14955 (2005).

    Article  CAS  PubMed  Google Scholar 

  118. Heisenberg, M. Mushroom body memoir: from maps to models. Nature Rev. Neurosci. 4, 266–275 (2003).

    Article  CAS  Google Scholar 

  119. Han, K. A., Millar, N. S., Grotewiel, M. S. & Davis, R. L. DAMB, a novel dopamine receptor expressed specifically in Drosophila mushroom bodies. Neuron 16, 1127–1135 (1996).

    Article  CAS  PubMed  Google Scholar 

  120. Kim, Y. C., Lee, H. G., Seong, C. S. & Han, K. A. Expression of a D1 dopamine receptor dDA1/DmDOP1 in the central nervous system of Drosophila melanogaster. Gene Expr. Patterns 3, 237–245 (2003).

    Article  CAS  PubMed  Google Scholar 

  121. Han, K. A., Millar, N. S. & Davis, R. L. A novel octopamine receptor with preferential expression in Drosophila mushroom bodies. J. Neurosci. 18, 3650–3658 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  122. Heisenberg, M., Borst, A., Wagner, S. & Byers, D. Drosophila mushroom body mutants are deficient in olfactory learning. J. Neurogenet. 2, 1–30 (1985). The first paper suggesting a role for the D. melanogaster mushroom bodies in olfactory memory. Includes a nice discussion of the caveats of studying anatomically defective flies.

    Article  CAS  PubMed  Google Scholar 

  123. Dudai, Y., Jan, Y. N., Byers, D., Quinn, W. G. & Benzer, S. dunce, a mutant of Drosophila deficient in learning. Proc. Natl Acad. Sci. USA 73, 1684–1688 (1976). dunce was the first identified learning mutant. This paper contains an important discussion of the specificity of the mutant phenotype.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  124. Byers, D., Davis, R. L. & Kiger, J. A. J. Defect in cyclic AMP phosphodiesterase due to the dunce mutation of learning in Drosophila melanogaster. Nature 289, 79–81 (1981).

    Article  CAS  PubMed  Google Scholar 

  125. Davis, R. L. & Kiger, J. A. J. Dunce mutants of Drosophila melanogaster: mutants defective in the cyclic AMP phosphodiesterase enzyme system. J. Cell Biol. 90, 101–107 (1981).

    Article  CAS  PubMed  Google Scholar 

  126. Chen, C. N., Denome, S. & Davis, R. L. Molecular analysis of cDNA clones and the corresponding genomic coding sequences of the Drosophila dunce+ gene, the structural gene for cAMP phosphodiesterase. Proc. Natl Acad. Sci. USA 83, 9313–9317 (1986).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  127. Qiu, Y. H. et al. Characterization of the memory gene dunce of Drosophila melanogaster. J. Mol. Biol. 222, 553–565 (1991).

    Article  CAS  PubMed  Google Scholar 

  128. Livingstone, M. S., Sziber, P. P. & Quinn, W. G. Loss of calcium/calmodulin responsiveness in adenylate cyclase of rutabaga, a Drosophila learning mutant. Cell 37, 205–215 (1984).

    Article  CAS  PubMed  Google Scholar 

  129. Levin, L. R. et al. The Drosophila learning and memory gene rutabaga encodes a Ca2+/Calmodulin-responsive adenylyl cyclase. Cell 68, 479–489 (1992).

    Article  CAS  PubMed  Google Scholar 

  130. Nighorn, A., Healy, M. J. & Davis, R. L. The cyclic AMP phosphodiesterase encoded by the Drosophila dunce gene is concentrated in the mushroom body neuropil. Neuron 6, 455–467 (1991).

    Article  CAS  PubMed  Google Scholar 

  131. Han, P. L., Levin, L. R., Reed, R. R. & Davis, R. L. Preferential expression of the Drosophila rutabaga gene in mushroom bodies, neural centers for learning in insects. Neuron 9, 619–627 (1992).

    Article  CAS  PubMed  Google Scholar 

  132. Skoulakis, E. M., Kalderon, D. & Davis, R. L. Preferential expression in mushroom bodies of the catalytic subunit of protein kinase A and its role in learning and memory. Neuron 11, 197–208 (1993).

    Article  CAS  PubMed  Google Scholar 

  133. Folkers, E., Waddell, S. & Quinn, W. G. The Drosophila radish gene encodes a protein required for anesthesia-resistant memory. Proc. Natl Acad. Sci. USA (2006).

    Google Scholar 

  134. Zars, T., Fischer, M., Schulz, R. & Heisenberg, M. Localization of a short-term memory in Drosophila. Science 288, 672–675 (2000).

    Article  CAS  PubMed  Google Scholar 

  135. McGuire, S. E., Le, P. T., Osborn, A. J., Matsumoto, K. & Davis, R. L. Spatiotemporal rescue of memory dysfunction in Drosophila. Science 302, 1765–1768 (2003). The description and use of TARGET: a system that permits spatial and temporal control of transgene expression based on a temperature sensitive variant of the GAL80 repressor of GAL4. Using this method, and that detailed in reference 136, the authors restrict expression of a rutabaga transgene to adulthood in rut mutant flies and determine that RUT adenylate cyclase functions acutely in the adult mushroom bodies.

    Article  CAS  PubMed  Google Scholar 

  136. Mao, Z., Roman, G., Zong, L. & Davis, R. L. Pharmacogenetic rescue in time and space of the rutabaga memory impairment by using Gene-Switch. Proc. Natl Acad. Sci. USA 101, 198–203 (2004).

    Article  CAS  PubMed  Google Scholar 

  137. Connolly, J. B. et al. Associative learning disrupted by impaired Gs signaling in Drosophila mushroom bodies. Science 274, 2104–2107 (1996).

    Article  CAS  PubMed  Google Scholar 

  138. Grotewiel, M. S., Beck, C. D., Wu, K. H., Zhu, X. R. & Davis, R. L. Integrin-mediated short-term memory in Drosophila. Nature 391, 455–460 (1998).

    Article  CAS  PubMed  Google Scholar 

  139. Cheng, Y. et al. Drosophila fasciclinII is required for the formation of odor memories and for normal sensitivity to alcohol. Cell 105, 757–768 (2001).

    Article  CAS  PubMed  Google Scholar 

  140. Dubnau, J. et al. The staufen/pumilio pathway is involved in Drosophila long-term memory. Curr. Biol. 13, 286–296 (2003). Reports a large screen for long-term memory-defective flies. This mutant collection provides a considerable resource for future study.

    Article  CAS  PubMed  Google Scholar 

  141. Qiu, Y. & Davis, R. L. Genetic dissection of the learning/memory gene dunce of Drosophila melanogaster. Genes Dev. 7, 1447–1458 (1993).

    Article  CAS  PubMed  Google Scholar 

  142. Kalidas, S. & Smith, D. P. Novel genomic cDNA hybrids produce effective RNA interference in adult Drosophila. Neuron 33, 177–184 (2002).

    Article  CAS  PubMed  Google Scholar 

  143. Didelot, G. et al. Tequila, a neurotrypsin ortholog, regulates long-term memory formation in Drosophila. Science 313, 851–853 (2006).

    Article  CAS  PubMed  Google Scholar 

  144. Dubnau, J., Grady, L., Kitamoto, T. & Tully, T. Disruption of neurotransmission in Drosophila mushroom body blocks retrieval but not acquisition of memory. Nature 411, 476–480 (2001). Along with reference 145, this study employed the UAS– shibirets1 transgene expressed in mushroom bodies to test the role of mushroom body neuron activity in memory acquisition, storage and retrieval.

    Article  CAS  PubMed  Google Scholar 

  145. McGuire, S. E., Le, P. T. & Davis, R. L. The role of Drosophila mushroom body signaling in olfactory memory. Science 293, 1330–1333 (2001).

    Article  CAS  PubMed  Google Scholar 

  146. Schwaerzel, M., Heisenberg, M. & Zars, T. Extinction antagonizes olfactory memory at the subcellular level. Neuron 35, 951–960 (2002).

    Article  CAS  PubMed  Google Scholar 

  147. Akalal, D. B. et al. Roles for Drosophila mushroom body neurons in olfactory learning and memory. Learn. Mem. 13, 659–668 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  148. Waddell, S., Armstrong, J. D., Kitamoto, T., Kaiser, K. & Quinn, W. G. The amnesiac gene product is expressed in two neurons in the Drosophila brain that are critical for memory. Cell 103, 805–813 (2000). Describes the identification of DPM neurons and the demonstration that their function is vital for memory stability in adult flies.

    Article  CAS  PubMed  Google Scholar 

  149. Quinn, W. G., Sziber, P. P. & Booker, R. The Drosophila memory mutant amnesiac. Nature 277, 212–214 (1979).

    Article  CAS  PubMed  Google Scholar 

  150. Feany, M. B. & Quinn, W. G. A neuropeptide gene defined by the Drosophila memory mutant amnesiac. Science 268, 869–873 (1995).

    Article  CAS  PubMed  Google Scholar 

  151. Moore, M. S. et al. Ethanol intoxication in Drosophila: genetic and pharmacological evidence for regulation by the cAMP signaling pathway. Cell 93, 997–1007 (1998).

    Article  CAS  PubMed  Google Scholar 

  152. Tamura, T. et al. Aging specifically impairs amnesiac-dependent memory in Drosophila. Neuron 40, 1003–1011 (2003).

    Article  CAS  PubMed  Google Scholar 

  153. Keene, A. C. et al. Diverse odor-conditioned memories require uniquely timed dorsal paired medial neuron output. Neuron 44, 521–533 (2004).

    Article  CAS  PubMed  Google Scholar 

  154. Keene, A. C., Krashes, M. J., Leung, B., Bernard, J. A. & Waddell, S. Drosophila dorsal paired medial neurons provide a general mechanism for memory consolidation. Curr. Biol. 16, 1524–1530 (2006).

    Article  CAS  PubMed  Google Scholar 

  155. Yu, D., Keene, A. C., Srivatsan, A., Waddell, S. & Davis, R. L. Drosophila DPM neurons form a delayed and branch-specific memory trace after olfactory classical conditioning. Cell 123, 945–957 (2005). Coupled live optical imaging of DPM neurons with an olfactory learning protocol performed under the microscope. An odour-specific memory trace formed with a similar delayed temporal kinetic to the behavioural memory requirement for DPM neuron activity.

    Article  CAS  PubMed  Google Scholar 

  156. Gu, H. & O'Dowd, D. K. Cholinergic synaptic transmission in adult Drosophila Kenyon cells in situ. J. Neurosci. 26, 265–272 (2006).

    Article  CAS  PubMed  Google Scholar 

  157. Perry, T., McKenzie, J. A. & Batterham, P. A Dα6 knockout strain of Drosophila melanogaster confers a high level of resistance to spinosad. Insect Biochem. Mol. Biol. 37, 184–188 (2007).

    Article  CAS  PubMed  Google Scholar 

  158. Fayyazuddin, A., Zaheer, M. A., Hiesinger, P. R. & Bellen, H. J. The nicotinic acetylcholine receptor Dα7 is required for an escape behavior in Drosophila. PLoS Biol. 4, e63 (2006).

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  159. Millar, N. S. et al. Functional expression of a cloned Drosophila muscarinic acetylcholine receptor in a stable Drosophila cell line. J. Exp. Biol. 198, 1843–1850 (1995).

    Article  CAS  PubMed  Google Scholar 

  160. Cordova, D., Delpech, V. R., Sattelle, D. B. & Rauh, J. J. Spatiotemporal calcium signaling in a Drosophila melanogaster cell line stably expressing a Drosophila muscarinic acetylcholine receptor. Invert. Neurosci. 5, 19–28 (2003).

    Article  CAS  PubMed  Google Scholar 

  161. Ponsioen, B. et al. Detecting cAMP-induced Epac activation by fluorescence resonance energy transfer: Epac as a novel cAMP indicator. EMBO Rep. 5, 1176–1180 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  162. Lai, S. L. & Lee, T. Genetic mosaic with dual binary transcriptional systems in Drosophila. Nature Neurosci. 9, 703–709 (2006).

    Article  CAS  PubMed  Google Scholar 

  163. Miesenbock, G. & Kevrekidis, I. G. Optical imaging and control of genetically designated neurons in functioning circuits. Annu. Rev. Neurosci. 28, 533–563 (2005).

    Article  PubMed  CAS  Google Scholar 

  164. Awasaki, T. et al. The Drosophila trio plays an essential role in patterning of axons by regulating their directional extension. Neuron 26, 119–131 (2000).

    Article  CAS  PubMed  Google Scholar 

  165. Choi, K. W., Smith, R. F., Buratowski, R. M. & Quinn, W. G. Deficient protein kinase C activity in turnip, a Drosophila learning mutant. J. Biol. Chem. 266, 15999–15606 (1991).

    Article  CAS  PubMed  Google Scholar 

  166. Goodwin, S. F. et al. Defective learning in mutants of the Drosophila gene for a regulatory subunit of cAMP-dependent protein kinase. J. Neurosci. 17, 8817–8827 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  167. Guo, H. F., Tong, J., Hannan, F., Luo, L. & Zhong, Y. A neurofibromatosis-1-regulated pathway is required for learning in Drosophila. Nature 403, 895–898 (2000).

    Article  CAS  PubMed  Google Scholar 

  168. Skoulakis, E. M. & Davis, R. L. Olfactory learning deficits in mutants for leonardo, a Drosophila gene encoding a 14–3-3 protein. Neuron 17, 931–944 (1996).

    Article  CAS  PubMed  Google Scholar 

  169. Putz, G., Bertolucci, F., Raabe, T., Zars, T. & Heisenberg, M. The S6KII (rsk) gene of Drosophila melanogaster differentially affects an operant and a classical learning task. J. Neurosci. 24, 9745–9751 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  170. Boynton, S. & Tully, T. latheo, a new gene involved in associative learning and memory in Drosophila melanogaster, identified from P element mutagenesis. Genetics 131, 655–672 (1992).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  171. DeZazzo, J. et al. nalyot, a mutation of the Drosophila myb-related Adf1 transcription factor, disrupts synapse formation and olfactory memory. Neuron 27, 145–158 (2000).

    Article  CAS  PubMed  Google Scholar 

  172. Dura, J. M., Preat, T. & Tully, T. Identification of linotte, a new gene affecting learning and memory in Drosophila melanogaster. J. Neurogenet. 9, 1–14 (1993).

    Article  CAS  PubMed  Google Scholar 

  173. Xia, S. et al. NMDA receptors mediate olfactory learning and memory in Drosophila. Curr. Biol. 15, 603–615 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  174. Yin, J. C. et al. Induction of a dominant negative CREB transgene specifically blocks long-term memory in Drosophila. Cell 79, 49–58 (1994).

    Article  CAS  PubMed  Google Scholar 

  175. Chang, K. T., Shi, Y. J. & Min, K. T. The Drosophila homolog of Down's syndrome critical region 1 gene regulates learning: implications for mental retardation. Proc. Natl Acad. Sci. USA 100, 15794–15799 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  176. Presente, A., Boyles, R. S., Serway, C. N., de Belle, J. S. & Andres, A. J. Notch is required for long-term memory in Drosophila. Proc. Natl Acad. Sci. USA 101, 1764–1768 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  177. Ge, X. et al. Notch signaling in Drosophila long-term memory formation. Proc. Natl Acad. Sci. USA 101, 10172–10176 (2004).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  178. Comas, D., Petit, F. & Preat, T. Drosophila long-term memory formation involves regulation of cathepsin activity. Nature 430, 460–463 (2004).

    Article  CAS  PubMed  Google Scholar 

  179. Drier, E. A. et al. Memory enhancement and formation by atypical PKM activity in Drosophila melanogaster. Nature Neurosci. 5, 316–324 (2002).

    Article  CAS  PubMed  Google Scholar 

  180. Michels, B. et al. A role for Synapsin in associative learning: the Drosophila larva as a study case. Learn. Mem. 12, 224–231 (2005).

    Article  PubMed  PubMed Central  Google Scholar 

  181. Brand, A. H. & Perrimon, N. Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development 118, 401–415 (1993).

    Article  CAS  PubMed  Google Scholar 

  182. Sweeney, S. T., Broadie, K., Keane, J., Niemann, H. & O'Kane, C. J. Targeted expression of tetanus toxin light chain in Drosophila specifically eliminates synaptic transmission and causes behavioral defects. Neuron 14, 341–351 (1995).

    Article  CAS  PubMed  Google Scholar 

  183. Ferris, J., Ge, H., Liu, L. & Roman, G. G(o) signaling is required for Drosophila associative learning. Nature Neurosci. 9, 1036–1040 (2006).

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We thank B. Leung for the confocal images used to produce Figures 3 and 4. We also thank V. Budnik, B. Leung and M. Krashes for discussion and comments on the manuscript. We acknowledge the contribution of our colleagues in the field, R. Davis, B. Gerber and M. Heisenberg, in shaping our thought process. We apologize to those authors whose work we were unable to cite due to space limitations. This work was supported by a grant to S.W. from the National Institutes of Health MH09883 and a National Research Service Award MH073311 to A.C.K.

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FURTHER INFORMATION

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Glossary

Conditioned stimulus

A stimulus — odour, in olfactory conditioning — that gains meaning following pairing with an unconditioned stimulus.

Unconditioned stimulus

A stimulus that generates an unlearned behavioural response: the shock or sugar in fly olfactory conditioning.

Long-term memory

Consolidated memory that is formed following multiple spaced training trials and requires new protein synthesis after training.

Short-term memory

A phase of fly memory that lasts a few minutes and is sensitive to anaesthetic disruption.

Middle-term memory

A phase of fly memory that lasts a few hours, is sensitive to anaesthetic disruption and is dependent on the amnesiac gene.

Anaesthesia-resistant memory

Consolidated fly memory that is resistant to anaesthetic disruption, develops during the first 30 minutes after training and is dependent on the radish gene.

Mushroom bodies

Mushroom bodies, or Corpora pedunculata, are paired neural structures in the insect brain that morphologically resemble mushrooms and are required for olfactory memory.

Glomeruli

Morphologically distinguishable areas in the antennal lobe that contain the presynaptic terminals of olfactory sensory neurons that express the same olfactory receptor and dendrites of postsynaptic projection neurons.

Labelled line

A simple one-to-one-to-one neural connectivity model that transfers sensory information from the periphery to deeper layers of the brain via a faithful linear arrangement of connected neurons. Sensory signals are thereby represented as activity in 'labelled lines' in the brain.

Neural ensemble

A population of neurons involved in a particular computational process.

Tethered fly preparation

The fly is alive but immobilized for viewing under the confocal microscope. A window is cut in the head capsule so that the brain can be visualized.

Enhancer-trap

Insertion of a P-element transposon harbouring the GAL4 transcription factor in a region of the genome in which a neighbouring transcriptional enhancer element confers region-specific GAL4 expression.

Calyx

A compartment of the mushroom bodies where the presynaptic projection neurons synapse with the dendrites of the Kenyon cells.

Kenyon cells

The neurons comprising the mushroom bodies.

GAL4/UAS system

A genetic system for controlling the induction of gene expression. An activator line that expresses the yeast transcriptional activator GAL4 gene under the control of a tissue-specific promoter is crossed to an effector line that carries the DNA-binding motif of GAL4 (upstream activating sequence, UAS) fused to the gene of interest. As a result, the progeny of this cross expresses the gene of interest in a region-specific manner.

Neuropil

The interior of the fly brain that is rich in axonal material, synaptic connections and intervening glia. The majority of cell bodies, or perikarya, in the fly brain are located on the periphery in the rind.

Golgi-impregnation

A classic histological staining technique developed in 1873 by Camillo Golgi that allows one to visualize the fine detail of single neurons.

Peduncle

The fasciculated axon bundle or 'stalk' of Kenyon cells between the dendritic calyx and presynaptic compartment in the mushroom body lobes.

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Keene, A., Waddell, S. Drosophila olfactory memory: single genes to complex neural circuits. Nat Rev Neurosci 8, 341–354 (2007). https://doi.org/10.1038/nrn2098

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