Distinct memory traces for two visual features in the Drosophila brain
By Gang Liu, Holger Seiler, A-Li Wen, T. Zars, Kei Ito, R. Wolf, Martin Heisenberg, Li Liu. 2006
437 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Ecology, Evolution, Behavior and Systematics, Genetics
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cellular and Molecular Neuroscience
- Yoshinori Aso
- Gerald M. Rubin
- Hiromu Tanimoto
- P. Plaçais
- T. Préat
- Severine Trannoy
- S. Waddell
- Stephan Knapek
In Ecology, Evolution, Behavior and Systematics
In Genetics
- Gerald M. Rubin
- Yoshinori Aso
- P. Plaçais
- Hiromu Tanimoto
- T. Préat
- Severine Trannoy
- Gero Miesenböck
- Qingzhong Ren
Citations in the corpus
- The neuronal architecture of the mushroom body provides a logic for associative learning (2014, background): “In Drosophila melanogaster, a number of different forms of learning have been observed in response to sensory stimuli (Siegel and Hall, 1979; Liu et al., 1999, 2006; Masek and Scott, 2010; Schnaitmann et al., 2010; Ofstad et al., 2011; Vogt et al., 2014).”
- WRITING MEMORIES WITH LIGHT-ADDRESSABLE REINFORCEMENT CIRCUITRY (2009, background): “Action-contingent olfactory learning depended, like Pavlovian olfactory conditioning (Figure 2B) and some forms of visually cued learning (Liu et al., 2006; Brembs and Plendl, 2008), on a functional rutabaga gene (Figure 3C, column b), but it required less reinforcement to achieve the same level of ”
- Neural dynamics for landmark orientation and angular path integration (2015, neutral): “The number of trials (in brackets) for each fly for each of these conditions was: (i) 1(7), 2(6), 3(9), 4(11), 5(15), 6(13), 7(3), 8(7), 9(7), 10(6), 11(5), 12(9), 13(9), 14(10), 15(6); (ii) 1(12), 2(8), 3(10), 4(3), 5(6), 6(8), 7(16); (iii) 1(6) (same as fly 1 in (ii)), 2(2) (same as fly 2 in (ii))”
- Systematic analysis of neural projections reveals clonal composition of the Drosophila brain. (2013, neutral): “Specific visual characteristics are processed by the clonally associated neurons in the mammalian visual cortex [5, 6] and clonally organized layers in the fly FB [30].”
- A connectome of the Drosophila central complex reveals network motifs suitable for flexible navigation and context-dependent action selection (2020, background): “, 2020), form short- and long-term visual memories that aid in spatial navigation (Kuntz et al., 2017; Liu et al., 2006; Neuser et al., 2008; Ofstad et al., 2011), use internal models of their body size when performing motor tasks (Krause et al.”
- Appetitive and Aversive Visual Learning in Freely Moving Drosophila (2009, background): “In particular, presentation of complex visual objects as landmarks is possible (Liu et al., 2006).”
- Parallel Pathways for Cross-Modal Memory Retrieval in Drosophila (2013, methodology): “The visual elevation memory trace is found in layer 5 (F5) of the fan-shaped body (Liu et al., 2006; Wang et al., 2008b), which is the largest component of the central complex in Drosophila.”
- Shared mushroom body circuits underlie visual and olfactory memories in Drosophila (2014, background): “Shock before test is dispensable at high temperature, however, requirement of MBs remains.”
- Shared Visual Attention and Memory Systems in the Drosophila Brain (2009, background): “. Visual learning appears to reside in another brain area, the central complex”
- Competing dopamine neurons drive oviposition choice for ethanol in Drosophila (2013, background): “(F) Decreasing DopR1 and DopR2 expression in the EB increases oviposition preference for ethanol [DopR1: n = 18 per strain; ANOVA: F(2,50) = 9.”
- Specific requirement of NMDA receptors for long-term memory consolidation in Drosophila ellipsoid body (2007, background): “The strong expression of dNR2 in ellipsoid body interested us, as another closely-related substructure of the central complex, the fan-shaped body, appears to subserve a short-term memory trace for visual learnin”
- Mushroom bodies regulate habit formation in Drosophila. (2008, positive): “Sensorimotor learning interfering with behavioral flexibility (‘‘habit interference’’) is a well-known phenomenon [8], and the balance between interference and transfer/generalization is a popular research topic [9].”
- Eight Different Types of Dopaminergic Neurons Innervate the Drosophila Mushroom Body Neuropil: Anatomical and Physiological Heterogeneity (2009, neutral): “The central complex of the Drosophila is involved in controlling locomotion (Strauss, 2002) and may also be involved in learning and memory (Liu et al., 2006).”
- Dopamine Signalling in Mushroom Bodies Regulates Temperature-Preference Behaviour in Drosophila (2011, background): “The central complex is involved in behaviours such as locomotion, visual flight, courtship, and olfactory learning task [20,21].”
- cAMP signalling in mushroom bodies modulates temperature preference behaviour in Drosophila (2008, background): “The central complex is involved in behaviours such as locomotion, visual flight, courtship, and olfactory learning task [20,21].”