Localization of a short-term memory in Drosophila.

By T. Zars, M. Fischer, R. Schulz, Martin Heisenberg. 2000

618 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Ecology, Endocrine and Autonomic Systems

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Citations in the corpus

Dopaminergic neurons write and update memories with cell-type-specific rules (2016, background): “…involved in forming memories with different valence—that is, appetitive and aversive memories—and with different stabilities (Schwaerzel et al., 2003; Zars et al., 2000; Isabel et al., 2004; Blum et al., 2009; Krashes et al., 2009; Claridge-Chang et al., 2009; Aso et al., 2010; Sejourne et al.,…”
Mushroom body output neurons encode valence and guide memory-based action selection in Drosophila (2014, background): “…3 of 42 Research article cyclase encoded by the rutabaga gene, are required specifically in the KCs for memory formation (Livingstone et al., 1984; Zars et al., 2000; Schwaerzel et al., 2003; Kim et al., 2007; McGuire et al., 2003; Gervasi et al., 2010; Qin et al., 2012) and rutabaga was shown to…”
WRITING MEMORIES WITH LIGHT-ADDRESSABLE REINFORCEMENT CIRCUITRY (2009, background): “Of these, only the mushroom body has been implicated in response plasticity (Heisenberg et al., 1985; de Belle and Heisenberg, 1994; Zars et al., 2000; McGuire et al., 2003).”
A map of olfactory representation in the Drosophila mushroom body. (2007, neutral): “It has been shown that g KCs are critical for olfactory associated short-term memory and vertical a0/a lobes play a role in long-term memory formation (Zars et al., 2000; Pascual and Preat, 2001; Yu et al., 2006).”
A connectome of a learning and memory center in the adult Drosophila brain (2017, background): “Secondly, with the assumption that released dopamine diffuses locally, KC>MBON synapses would receive dopaminergic input close to the sites of vesicle release, consistent with the prevailing hypothesis that plasticity occurs at the presynaptic terminals of KCs (Heisenberg, 2003; McGuire et al., 2003”
Gustatory Learning and Processing in the Drosophila Mushroom Bodies (2015, background): “…memory (LTM), the / neurons are necessary for medium-term memory and LTM consolidation, and the neurons are required for short-term memory (STM) and courtship conditioning (Zars et al., 2000; McGuire et al., 2001; Keleman et al., 2007; Krashes et al., 2007; Blum et al., 2009; Trannoy et al., 2011).”
Operant conditioning in invertebrates. (2003, background): “Although the cAMP cascade and its downstream targets are both necessary and sufficient in the mushroom bodies for these tasks [15,22], in operant conditioning they are involved in neurons outside the mushroom bodies and in a different way than in classical conditioning [19 ].”
Sequential use of mushroom body neuron subsets during drosophila odor memory processing. (2007, neutral): “Although several complex behaviors in insects appear to require the MBs (Heisenberg et al., 1985; de Belle and Heisenberg, 1994; Martin et al., 1998; Liu et al., 1999; McBride et al., 1999; Tang and Guo, 2001; Pitman et al., 2006; Joiner et al., 2006) and a differential role for distinct MB neuron g”
Rapid Consolidation to a radish and Protein Synthesis-Dependent Long-Term Memory after Single-Session Appetitive Olfactory Conditioning in Drosophila (2008, methodology): “All resultant c739-GAL4;uas-dCreb2-b, c772GAL4/uas-dCreb2-b, and uas-dCreb2-b;MB247-GAL4 flies are heterozygous for each transgene.”
Short and Long-term memory in Drosophila require cAMP signaling in distinct neuron types (2009, methodology): “Together, the above findings are consistent with previous results [23, 24, 26] and the broadly accepted hypothesis that rutabaga-dependent cAMP signaling in MBs is sufficient to restore the aversive STM defect of the rutabaga mutant.”
γ neurons mediate dopaminergic input during aversive olfactory memory formation in Drosophila (2012, neutral): “Such findings have been interpreted as supporting the idea of independent signaling for parallel memory traces [9, 10, 23] as well as sequential action in different cell types to support a single memory mechanism [22].”
Structure and response patterns of olfactory interneurons in the honeybee, Apis mellifera (2001, background): “In Drosophila, the MBs are necessary for more flexible use of stored memories (Zars et al., 2000).”
Three Dopamine Pathways Induce Aversive Odor Memories with Different Stability (2012, background): “Considering parallel formation and the interaction of distinct memory components by different Kenyon cell populations [7,30,31,32,33,52], the latter scenario might be more likely.”
Limited taste discrimination in Drosophila (2010, background): “MB247 is expressed fairly specifically in the MBs, whereas c772 ismore broadly expressed (26).”
Olfactory representations by Drosophila mushroom body neurons. (2008, background): “Previous work suggests that the three classes play different roles in memory formation, possibly because they connect to different postsynaptic targets (Akalal et al. 2006; Krashes et al. 2007; Pascual and Preat 2001; Zars et al. 2000).”