Transsynaptic mapping of second-order taste neurons in flies by trans-Tango
Open accessAbstract
Mapping neural circuits across defined synapses is essential for understanding brain function. Here we describe trans-Tango, a technique for anterograde transsynaptic circuit tracing and manipulation. At the core of trans-Tango is a synthetic signaling pathway that is introduced into all neurons in the animal. This pathway converts receptor activation at the cell surface into reporter expression through site-specific proteolysis. Specific labeling is achieved by presenting a tethered ligand at the synapses of genetically defined neurons, thereby activating the pathway in their postsynaptic partners and providing genetic access to these neurons. We first validated trans-Tango in the Drosophila olfactory system and then implemented it in the gustatory system, where projections beyond the first-order receptor neurons are not fully characterized. We identified putative second-order neurons within the sweet circuit that include projection neurons targeting known neuromodulation centers in the brain. These experiments establish trans-Tango as a flexible platform for transsynaptic circuit analysis.
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Genetic trans-synaptic labeling methods may give false positives and negatives.
“However, the genetic methods may give false positives and negatives”
From A connectome and analysis of the adult Drosophila central brain (2020) · cites this paper as Talay et al., 2017
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Enzymatic assembly of DNA molecules up to several hundred kilobases
Gibson, D. G., Young, L., Chuang, R.-Y., Venter, J. C., Hutchison, C. A., & Smith, H. O. (2009) · Nature Methods · doi:10.1038/nmeth.1318 · Cited by 9,742 · see citing works
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
Brand, A. H., & Perrimon, N. (1993) · Development · doi:10.1242/dev.118.2.401 · Cited by 9,510 · see citing works
Ultrasensitive fluorescent proteins for imaging neuronal activity
Chen, T.-W., Wardill, T. J., Sun, Y., Pulver, S. R., Renninger, S. L., Baohan, A., Schreiter, E. R., Kerr, R. A., Orger, M. B., Jayaraman, V., et al. (2013) · Nature · doi:10.1038/nature12354 · Cited by 6,474 · see citing works
Lee, T., & Luo, L. (1999) · Neuron · doi:10.1016/s0896-6273(00)80701-1 · Cited by 2,540 · see citing works
An optimized transgenesis system for Drosophila using germ-line-specific φC31 integrases
Bischof, J., Maeda, R., Hediger, M., Karch, F., & Basler, K. (2007) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0611511104 · Cited by 1,959 · see citing works
A Photoactivatable GFP for Selective Photolabeling of Proteins and Cells
Patterson, G. H., & Lippincott‐Schwartz, J. (2002) · Science · doi:10.1126/science.1074952 · Cited by 1,612 · see citing works
Refinement of Tools for Targeted Gene Expression in Drosophila
Pfeiffer, B. D., Ngo, T.-T. B., Hibbard, K. L., Murphy, C., Jenett, A., Truman, J. W., & Rubin, G. M. (2010) · Genetics · doi:10.1534/genetics.110.119917 · Cited by 1,153 · see citing works
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 · see citing works
The Molecular Basis of Odor Coding in the Drosophila Antenna
Hallem, E. A., Ho, M. G.-R., & Carlson, J. R. (2004) · Cell · doi:10.1016/j.cell.2004.05.012 · Cited by 993 · see citing works
Tools for neuroanatomy and neurogenetics in Drosophila
Pfeiffer, B. D., Jenett, A., Hammonds, A. S., Ngo, T.-T. B., Misra, S., Murphy, C., Scully, A. L., Carlson, J. W., Wan, K. H., Laverty, T., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803697105 · Cited by 974 · see citing works
Construction of Transgenic Drosophila by Using the Site-Specific Integrase From Phage C31
Groth, A. C. (2004) · Genetics · doi:10.1534/genetics.166.4.1775 · Cited by 963 · see citing works
Molecular Architecture of Smell and Taste in Drosophila
Vosshall, L. B., & Stocker, R. F. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094306 · Cited by 860 · see citing works
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 · see citing works
A single class of olfactory neurons mediates behavioural responses to a Drosophila sex pheromone
Kurtović-Kozarić, A., Widmer, A., & Dickson, B. J. (2007) · Nature · doi:10.1038/nature05672 · Cited by 761 · see citing works
Zingg, B., Chou, X.-L., Zhang, Z., Mesik, L., Liang, F., Tao, H. W., & Zhang, L. I. (2016) · Neuron · doi:10.1016/j.neuron.2016.11.045 · Cited by 744 · see citing works
Feinberg, E. H., VanHoven, M. K., Bendesky, A., Wang, G., Fetter, R. D., Shen, K., & Bargmann, C. I. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.030 · Cited by 723 · see citing works
A chemosensory gene family encoding candidate gustatory and olfactory receptors in Drosophila.
Scott, K., Brady, R., Cravchik, A., Morozov, P., Rzhetsky, A., Zuker, C., & Axel, R. (2001) · Cell · doi:10.1016/s0092-8674(01)00263-x · Cited by 720 · see citing works
The genetic design of signaling cascades to record receptor activation
Barnea, G., Strapps, W. R., Herrada, G., Berman, Y. L., Ong, J., Kloss, B., Axel, R., & Lee, K. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710487105 · Cited by 673 · see citing works
Self-citationJefferis, G. S. X. E., Potter, C. J., Chan, A. M., Marin, E. C., Torsten Rohlfing, B., Maurer, C. R., & Luo, L. (2007) · Cell · doi:10.1016/j.cell.2007.01.040 · Cited by 647 · see citing works
A subset of dopamine neurons signals reward for odour memory in Drosophila
Liu, C., Plaçais, P.-Y., Yamagata, N., Pfeiffer, B. D., Aso, Y., Friedrich, A. B., Siwanowicz, I., Rubin, G. M., Préat, T., & Tanimoto, H. (2012) · Nature · doi:10.1038/nature11304 · Cited by 623 · see citing works
Candidate Taste Receptors in Drosophila
Clyne, P. J., Warr, C. G., & Carlson, J. R. (2000) · Science · doi:10.1126/science.287.5459.1830 · Cited by 616 · see citing works
Layered reward signalling through octopamine and dopamine in Drosophila
Burke, C. J., Huetteroth, W., Owald, D., Perisse, E., Krashes, M. J., Das, G., Gohl, D., Silies, M., Certel, S., & Waddell, S. (2012) · Nature · doi:10.1038/nature11614 · Cited by 614 · see citing works
A Systematic Nomenclature for the Insect Brain
Ito, K., Shinomiya, K., Ito, M., Armstrong, J. D., Boyan, G., Hartenstein, V., Harzsch, S., Heisenberg, M., Homberg, U., Jenett, A., et al. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.017 · Cited by 611 · see citing works
Genetic and Functional Subdivision of the Drosophila Antennal Lobe
Fishilevich, E., & Vosshall, L. B. (2005) · Current Biology · doi:10.1016/j.cub.2005.07.066 · Cited by 608 · see citing works
Potter, C. J., Tasic, B., Russler-Germain, E. V., Liang, L., & Luo, L. (2010) · Cell · doi:10.1016/j.cell.2010.02.025 · Cited by 605 · see citing works
SOME FEATURES OF THE SUBMICROSCOPIC MORPHOLOGY OF SYNAPSES IN FROG AND EARTHWORM
Robertis, E. D. P. D., & Bennett, H. S. (1955) · The Journal of Cell Biology · doi:10.1083/jcb.1.1.47 · Cited by 596 · see citing works
Nern, A., Pfeiffer, B. D., & Rubin, G. M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1506763112 · Cited by 584 · see citing works
Motor control in a Drosophila taste circuit
Gordon, M. D., & Scott, K. (2009) · Neuron · doi:10.1016/j.neuron.2008.12.033 · Cited by 531 · see citing works
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 · see citing works
Markstein, M., Pitsouli, C., Villalta, C., Celniker, S., & Perrimon, N. (2008) · Nature Genetics · doi:10.1038/ng.101 · Cited by 516 · see citing works
Use of a yeast site-specific recombinase to produce female germline chimeras in Drosophila.
Chou, T.-B., & Perrimon, N. (1992) · Genetics · doi:10.1093/genetics/131.3.643 · Cited by 493 · see citing works
Taste Representations in the Drosophila Brain
Wang, Z., Singhvi, A., Kong, P., & Scott, K. (2004) · Cell · doi:10.1016/j.cell.2004.06.011 · Cited by 489 · see citing works
Two Gr Genes Underlie Sugar Reception in Drosophila
Dahanukar, A. A., Lei, Y.-T., Kwon, J. Y., & Carlson, J. R. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.024 · Cited by 482 · see citing works
Construction of Transgenic Drosophila by Using the Site-Specific Integrase From Phage φC31
Groth, A. C., Fish, M., Nusse, R., & Calos, M. P. (2004) · Genetics · doi:10.1093/genetics/166.4.1775 · Cited by 423 · see citing works
Monosynaptic Circuit Tracing with Glycoprotein-Deleted Rabies Viruses
Callaway, E. M., & Luo, L. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0409-15.2015 · Cited by 418 · see citing works
Using translational enhancers to increase transgene expression in Drosophila
Pfeiffer, B. D., Truman, J. W., & Rubin, G. M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1204520109 · Cited by 397 · see citing works
The Drosophila pheromone cVA activates a sexually dimorphic neural circuit
Datta, S. R., Vasconcelos, M. L., Ruta, V., Luo, S. X., Wong, A. M., Demir, E., Flores, J., Balonze, K., Dickson, B. J., & Axel, R. (2008) · Nature · doi:10.1038/nature06808 · Cited by 383 · see citing works
The Mushroom Body of Adult Drosophila Characterized by GAL4 Drivers
Aso, Y., Grübel, K., Busch, S., Friedrich, A. B., Siwanowicz, I., & Tanimoto, H. (2009) · Journal of Neurogenetics · doi:10.1080/01677060802471718 · Cited by 381 · see citing works
A protocol for dissecting Drosophila melanogaster brains for live imaging or immunostaining
Wu, J., & Luo, L. (2006) · Nature Protocols · doi:10.1038/nprot.2006.336 · Cited by 368 · see citing works
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 · see citing works
Spatially restricted expression of candidate taste receptors in the Drosophila gustatory system
Dunipace, L., Meister, S., McNealy, C., & Amrein, H. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00258-5 · Cited by 360 · see citing works
Select Drosophila glomeruli mediate innate olfactory attraction and aversion
Semmelhack, J. L., & Wang, J. W. (2009) · Nature · doi:10.1038/nature07983 · Cited by 360 · see citing works
Cellular Organization of the Neural Circuit that Drives Drosophila Courtship Behavior
Yu, J. Y., Kanai, M. I., Demir, E., Jefferis, G. S. X. E., & Dickson, B. J. (2010) · Current Biology · doi:10.1016/j.cub.2010.08.025 · Cited by 349 · see citing works
A dimorphic pheromone circuit in Drosophila from sensory input to descending output
Ruta, V., Datta, S. R., Vasconcelos, M. L., Freeland, J., Looger, L. L., & Axel, R. (2010) · Nature · doi:10.1038/nature09554 · Cited by 344 · see citing works
Volume electron microscopy for neuronal circuit reconstruction
Briggman, K. L., & Bock, D. D. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.10.022 · Cited by 337 · see citing works
Inagaki, H. K., Ben-Tabou de-Leon, S., Wong, A. M., Jagadish, S., Ishimoto, H., Barnea, G., Kitamoto, T., Axel, R., & Anderson, D. J. (2012) · Cell · doi:10.1016/j.cell.2011.12.022 · Cited by 325 · see citing works
Self-citationFruitless specifies sexually dimorphic neural circuitry in the Drosophila brain
Kimura, K.-I., Oté, M., Tazawa, T., & Yamamoto, D. (2005) · Nature · doi:10.1038/nature04229 · Cited by 314 · see citing works
The Molecular Basis of Odor Coding in the Drosophila Larva
Kreher, S. A., Kwon, J. Y., & Carlson, J. R. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.007 · Cited by 301 · see citing works
Observations on the scratch‐reflex in the spinal dog
Sherrington, C. (1906) · The Journal of Physiology · doi:10.1113/jphysiol.1906.sp001139 · Cited by 298 · see citing works
Estructura de los centros nerviosos de las Aves
Ramon, Y., & Cajal, S. (1888) · Cited by 281 · see citing works
Factors that regulate insulin producing cells and their output in Drosophila
Nässel, D. R., Kubrak, O. I., Liu, Y., Luo, J., & Lushchak, O. V. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00252 · Cited by 268 · see citing works
Genetically encoded dendritic marker sheds light on neuronal connectivity in Drosophila
Nicolaï, L., Ramaekers, A., Raemaekers, T., Drozdzecki, A., Mauss, A. S., Yan, J., Landgraf, M., Annaert, W. G., & Hassan, B. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010198107 · Cited by 262 · see citing works
Multimodal Chemosensory Circuits Controlling Male Courtship in Drosophila
Clowney, E. J., Iguchi, S., Bussell, J. J., Scheer, E., & Ruta, V. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.025 · Cited by 255 · see citing works
Chemotaxis Behavior Mediated by Single Larval Olfactory Neurons in Drosophila
Fishilevich, E., Domingos, A. I., Asahina, K., Naef, F., Vosshall, L. B., & Louis, M. (2005) · Current Biology · doi:10.1016/j.cub.2005.11.016 · Cited by 253 · see citing works
Lo, L., & Anderson, D. J. (2011) · Neuron · doi:10.1016/j.neuron.2011.12.002 · Cited by 251 · see citing works
Living synaptic vesicle marker: Synaptotagmin‐GFP
Zhang, Y., Rodesch, C. K., & Broadie, K. S. (2002) · genesis · doi:10.1002/gene.10144 · Cited by 239 · see citing works
The Color-Vision Circuit in the Medulla of Drosophila
Morante, J., & Desplan, C. (2008) · Current Biology · doi:10.1016/j.cub.2008.02.075 · Cited by 215 · see citing works
Macpherson, L. J., Zaharieva, E. E., Kearney, P. J., Alpert, M. H., Lin, T., Turan, Z., Lee, C., & Gallio, M. (2015) · Nature Communications · doi:10.1038/ncomms10024 · Cited by 214 · see citing works
Elucidating the Neuronal Architecture of Olfactory Glomeruli in the Drosophila Antennal Lobe
Grabe, V., Baschwitz, A., Dweck, H. K. M., Lavista-Llanos, S., Hansson, B. S., & Sachse, S. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.08.063 · Cited by 186 · see citing works
Cell-type-Specific Labeling of Synapses In Vivo through Synaptic Tagging with Recombination
Chen, Y., Akin, O., Nern, A., Tsui, C. K., Pecot, M. Y., & Zipursky, S. L. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.021 · Cited by 179 · see citing works
Kapan, N., Lushchak, O. V., Luo, J., & Nässel, D. R. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1097-z · Cited by 169 · see citing works
Dual functions of wingless in the Drosophila leg imaginal disc
Wilder, E. L., & Perrimon, N. (1995) · Development · doi:10.1242/dev.121.2.477 · Cited by 166 · see citing works
Genetic and Neural Mechanisms that Inhibit Drosophila from Mating with Other Species
Fan, P., Manoli, D. S., Ahmed, O. M., Chen, Y., Agarwal, N., Kwong, S., Cai, A. G., Neitz, J., Renslo, A., Baker, B. S., et al. (2013) · Cell · doi:10.1016/j.cell.2013.06.008 · Cited by 164 · see citing works
Ramaekers, A., Magnenat, E., Marin, E. C., Gendre, N., Jefferis, G. S. X. E., Luo, L., & Stocker, R. F. (2005) · Current Biology · doi:10.1016/j.cub.2005.04.032 · Cited by 162 · see citing works
A Taste Circuit that Regulates Ingestion by Integrating Food and Hunger Signals
Yapici, N., Cohn, R., Schusterreiter, C., Ruta, V., & Vosshall, L. B. (2016) · Cell · doi:10.1016/j.cell.2016.02.061 · Cited by 162 · see citing works
Decoding odor quality and intensity in the Drosophila brain
Strutz, A., Sölter, J., Baschwitz, A., Farhan, A., Grabe, V., Rybak, J., Knaden, M., Schmuker, M., Hansson, B. S., & Sachse, S. (2014) · eLife · doi:10.7554/elife.04147 · Cited by 157 · see citing works
Seki, Y., Rybak, J., Wicher, D., Sachse, S., & Hansson, B. S. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00249.2010 · Cited by 147 · see citing works
Histamine and Its Receptors Modulate Temperature-Preference Behaviors inDrosophila
Hong, S.-T., Bang, S., Paik, D., Kang, J., Hwang, S., Jeon, K., Chun, B., Hyun, S., Lee, Y., & Kim, J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5426-05.2006 · Cited by 114 · see citing works
Representations of taste modality in the Drosophila brain
Harris, D. T., Kallman, B. R., Mullaney, B. C., & Scott, K. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.026 · Cited by 111 · see citing works
Distribution and functional anatomy of amine-containing neurons in decapod crustaceans
Beltz, B. S. (1999) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19990115/01)44:2/3 · Cited by 107 · see citing works
Leucine-rich repeat transmembrane proteins instruct discrete dendrite targeting in an olfactory map
Hong, W., Zhu, H., Potter, C. J., Barsh, G. R., Kurusu, M., Zinn, K., & Luo, L. (2009) · Nature Neuroscience · doi:10.1038/nn.2442 · Cited by 106 · see citing works
Long-range projection neurons in the taste circuit of Drosophila
Kim, H., Kirkhart, C. R., & Scott, K. (2017) · eLife · doi:10.7554/elife.23386 · Cited by 102 · see citing works
Secondary Taste Neurons that Convey Sweet Taste and Starvation in the Drosophila Brain
Kain, P., & Dahanukar, A. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.01.005 · Cited by 83 · see citing works
Structural basis for the hijacking of endosomal sorting nexin proteins by Chlamydia trachomatis
Paul, B., Kim, H. S., Kerr, M. C., Huston, W. M., Teasdale, R. D., & Collins, B. M. (2017) · eLife · doi:10.7554/elife.22311 · Cited by 81 · see citing works
A map of taste neuron projections in the Drosophila CNS
Kwon, J. Y., Dahanukar, A. A., Weiss, L. A., & Carlson, J. R. (2014) · Journal of Biosciences · doi:10.1007/s12038-014-9448-6 · Cited by 74 · see citing works
Thoma, V., Knapek, S., Arai, S., Hartl, M., Kohsaka, H., Sirigrivatanawong, P., Abe, A., Hashimoto, K., & Tanimoto, H. (2016) · Nature Communications · doi:10.1038/ncomms10678 · Cited by 74 · see citing works
Using the Q system in Drosophila melanogaster
Potter, C. J., & Luo, L. (2011) · Nature Protocols · doi:10.1038/nprot.2011.347 · Cited by 70 · see citing works
Fortin, J., Zhu, Y., Choi, C., Beinborn, M., Nitabach, M. N., & Kopin, A. S. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900149106 · Cited by 55 · see citing works
Identifying Functional Connections of the Inner Photoreceptors in Drosophila using Tango-Trace
Jagadish, S., Barnea, G., Clandinin, T. R., & Axel, R. (2014) · Neuron · doi:10.1016/j.neuron.2014.06.025 · Cited by 43 · see citing works
Self-citationMiyazaki, T., Lin, T.-Y., Ito, K., Lee, C.-H., & Stopfer, M. (2015) · Journal of Neurogenetics · doi:10.3109/01677063.2015.1054993 · Cited by 34 · see citing works
Krstenansky, J. L., Trivedi, D. B., Johnson, D., & Hruby, V. J. (1986) · Journal of the American Chemical Society · doi:10.1021/ja00267a053 · Cited by 34 · see citing works
Gene transfer in the nervous system and implications for transsynaptic neuronal tracing
Huh, Y., Oh, M. S., Leblanc, P. R., & Kim, K. (2010) · Expert Opinion on Biological Therapy · doi:10.1517/14712591003796538 · Cited by 27 · see citing works
Flagged first, then by citations
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- Nässel DR 1999 Histamine in the brain of insects: A review Microsc Res Tech 44 121 136 10084821
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Sorted by citations
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Scheffer, L. K., Xu, C. S., Januszewski, M., Lu, Z., Takemura, S.-Y., Hayworth, K. J., Huang, G. B., Shinomiya, K., Maitlin-Shepard, J., Berg, S., et al. (2020) · eLife · doi:10.7554/elife.57443 · Cited by 1,128 · see citing works
Genetic Dissection of Neural Circuits: A Decade of Progress
Luo, L., Callaway, E. M., & Svoboda, K. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.040 · Cited by 446 · see citing works
Architectures of neuronal circuits
Luo, L. (2021) · Science · doi:10.1126/science.abg7285 · Cited by 390 · see citing works
Hulse, B. K., Haberkern, H., Franconville, R., Turner-Evans, D., Takemura, S.-Y., Wolff, T., Noorman, M., Dreher, M., Dan, C., Parekh, R., et al. (2021) · eLife · doi:10.7554/elife.66039 · Cited by 392 · see citing works
Recent advances in neuropeptide signaling in Drosophila, from genes to physiology and behavior
Nässel, D. R., & Zandawala, M. (2019) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2019.02.003 · Cited by 367 · see citing works
Split-TurboID enables contact-dependent proximity labeling in cells
Cho, K. F., Branon, T. C., Rajeev, S., Svinkina, T., Udeshi, N. D., Thoudam, T., Kwak, C. S., Rhee, H., Lee, I., Carr, S. A., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1919528117 · Cited by 362 · see citing works
Algorithms for Olfactory Search across Species
Baker, K. L., Dickinson, M., Findley, T. M., Gire, D. H., Louis, M., Suver, M. P., Verhagen, J. V., Nagel, K. I., & Smear, M. C. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.1668-18.2018 · Cited by 177 · see citing works
The Neuroanatomical Ultrastructure and Function of a Biological Ring Attractor
Turner-Evans, D. B., Jensen, K. T., Ali, S., Paterson, T., Sheridan, A., Ray, R. P., Wolff, T., Lauritzen, J. S., Rubin, G. M., Bock, D. D., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.006 · Cited by 168 · see citing works
A Circadian Output Circuit Controls Sleep-Wake Arousal in Drosophila
Guo, F., Holla, M. R., Díaz, M. M., & Rosbash, M. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.002 · Cited by 173 · see citing works
Dolan, M.-J., Frechter, S., Bates, A. S., Dan, C., Huoviala, P., Roberts, R. J., Schlegel, P., Dhawan, S., Tabano, R., Dionne, H., et al. (2019) · eLife · doi:10.7554/elife.43079 · Cited by 169 · see citing works
The neuroanatomical ultrastructure and function of a biological ring attractor
Turner-Evans, D. B., Jensen, K. T., Ali, S., Paterson, T., Sheridan, A., Ray, R. P., Wolff, T., Lauritzen, S., Rubin, G. M., Bock, D., et al. (2019) · doi:10.1101/847152 · Cited by 166 · see citing works
A neurodevelopmental origin of behavioral individuality in the Drosophila visual system
Linneweber, G. A., Andriatsilavo, M., Dutta, S. B., Hellbruegge, L., Liu, G., Ejsmont, R. K., Fenk, L. M., Straw, A. D., Wernet, M. F., Hiesinger, P. R., et al. (2020) · Science · doi:10.1126/science.aaw7182 · Cited by 166 · see citing works
neuPrint: an open access tool for EM connectomics
Plaza, S. M., Clements, J., Dolafi, T., Umayam, L., Neubarth, N. N., Scheffer, L. K., & Berg, S. (2022) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2022.896292 · Cited by 145 · see citing works
Strategies for monitoring cell–cell interactions
Bechtel, T. J., Robles, T. R., Fadeyi, O., & Oslund, R. (2021) · Nature Chemical Biology · doi:10.1038/s41589-021-00790-x · Cited by 152 · see citing works
Kondo, S., Takahashi, T., Yamagata, N., Imanishi, Y., Katow, H., Hiramatsu, S., Lynn, K., Abe, A., Kumaraswamy, A., & Tanimoto, H. (2020) · Cell Reports · doi:10.1016/j.celrep.2019.12.018 · Cited by 154 · see citing works
A Connectome of the Adult Drosophila Central BrainPreprint
Xu, C. S., Januszewski, M., Lu, Z., Takemura, S.-Y., Hayworth, K. J., Huang, G. B., Shinomiya, K., Maitin-Shepard, J., Ackerman, D., Berg, S., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.21.911859 · Cited by 150 · see citing works
Sexual arousal gates visual processing during Drosophila courtship
Hindmarsh Sten, T., Li, R., Otopalik, A., & Ruta, V. (2021) · Nature · doi:10.1038/s41586-021-03714-w · Cited by 140 · see citing works
A neural circuit for wind-guided olfactory navigation
Matheson, A. M. M., Lanz, A. J., Medina, A. M., Licata, A. M., Currier, T. A., Syed, M. H., & Nagel, K. I. (2022) · Nature Communications · doi:10.1038/s41467-022-32247-7 · Cited by 136 · see citing works
Neural circuits driving larval locomotion in Drosophila
Clark, M. Q., Zarin, A. A., Carreira-Rosario, A., & Doe, C. Q. (2018) · Neural Development · doi:10.1186/s13064-018-0103-z · Cited by 124 · see citing works
A visual pathway for skylight polarization processing in Drosophila
Hardcastle, B. J., Omoto, J. J., Kandimalla, P., Nguyen, B.-C. M., Keleş, M. F., Boyd, N. K., Hartenstein, V., & Frye, M. A. (2021) · eLife · doi:10.7554/elife.63225 · Cited by 111 · see citing works
Building a functional connectome of the Drosophila central complex
Franconville, R., Beron, C. C., & Jayaraman, V. (2018) · eLife · doi:10.7554/elife.37017 · Cited by 123 · see citing works
Viral Vectors for Neural Circuit Mapping and Recent Advances in Trans-synaptic Anterograde Tracers
Xu, X., Holmes, T. C., Luo, M., Beier, K. T., Horwitz, G. D., Zhao, F., Zeng, W., Hui, M., Semler, B. L., & Sandri-Goldin, R. M. (2020) · Neuron · doi:10.1016/j.neuron.2020.07.010 · Cited by 120 · see citing works
Sensory Discrimination of Blood and Floral Nectar by Aedes aegypti Mosquitoes
Jové, V., Gong, Z., Hol, F. J. H., Zhao, Z., Sorrells, T. R., Carroll, T. S., Prakash, M., McBride, C. S., & Vosshall, L. B. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.019 · Cited by 109 · see citing works
Synaptic connectome of the Drosophila circadian clock
Reinhard, N., Fukuda, A., Manoli, G., Derksen, E., Saito, A., Möller, G., Sekiguchi, M., Rieger, D., Helfrich‐Förster, C., Yoshii, T., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-54694-0 · Cited by 110 · see citing works
Two brain pathways initiate distinct forward walking programs in Drosophila
Bidaye, S. S., Laturney, M., Chang, A. K., Liu, Y., Bockemühl, T., Büschges, A., & Scott, K. (2020) · Neuron · doi:10.1016/j.neuron.2020.07.032 · Cited by 109 · see citing works
Wang, H., Jing, M., & Li, Y. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.03.010 · Cited by 109 · see citing works
Modulation of Drosophila post-feeding physiology and behavior by the neuropeptide leucokinin
Zandawala, M., Yurgel, M. E., Liao, S., Texada, M. J., Rewitz, K., Keene, A. C., & Nässel, D. R. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007767 · Cited by 107 · see citing works
A Wake-Promoting Circadian Output Circuit in Drosophila
Lamaze, A., Krätschmer, P., Chen, K., Lowe, S. A., & Jepson, J. E. C. (2018) · Current Biology · doi:10.1016/j.cub.2018.07.024 · Cited by 106 · see citing works
Scopelliti, A., Bauer, C., Yu, Y., Zhang, T., Kruspig, B., Murphy, D. J., Vidal, M., Maddocks, O. D. K., & Cordero, J. B. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.09.021 · Cited by 106 · see citing works
Encoding of Wind Direction by Central Neurons in Drosophila
Suver, M. P., Matheson, A. M. M., Sarkar, S., Damiata, M., Schoppik, D., & Nagel, K. I. (2019) · Neuron · doi:10.1016/j.neuron.2019.03.012 · Cited by 99 · see citing works
Sleep in Drosophila and Its Context
Beckwith, E. J., & French, A. S. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01167 · Cited by 90 · see citing works
Endocrine cybernetics: neuropeptides as molecular switches in behavioural decisions
Nässel, D. R., & Zandawala, M. (2022) · Open Biology · doi:10.1098/rsob.220174 · Cited by 83 · see citing works
Liu, C., Meng, Z., Wiggin, T. D., Yu, J., Reed, M. L., Guo, F., Zhang, Y., Rosbash, M., & Griffith, L. C. (2019) · Current Biology · doi:10.1016/j.cub.2019.08.079 · Cited by 87 · see citing works
A neuropeptide regulates fighting behavior in Drosophila melanogaster
Wu, F., Deng, B., Xiao, N., Wang, T., Li, Y., Wang, R., Shi, K., Luo, D.-G., Rao, Y., & Zhou, C. (2020) · eLife · doi:10.7554/elife.54229 · Cited by 81 · see citing works
Zhang, C., Daubnerová, I., Jang, Y.-H., Kondo, S., Žitňan, D., & Kim, Y. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2016878118 · Cited by 83 · see citing works
Kim, C. K., Cho, K. F., Kim, M. W., & Ting, A. Y. (2019) · eLife · doi:10.7554/elife.43826 · Cited by 78 · see citing works
Neuronal constituents and putative interactions within the Drosophila Ellipsoid Body Neuropil
Omoto, J. J., Nguyen, B.-C. M., Kandimalla, P., Lovick, J. K., Donlea, J. M., & Hartenstein, V. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00103 · Cited by 72 · see citing works
Zeng, H. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.03.003 · Cited by 73 · see citing works
Distributed control of motor circuits for backward walking in Drosophila
Feng, K., Sen, R., Minegishi, R., Dübbert, M., Bockemühl, T., Büschges, A., & Dickson, B. J. (2020) · Nature Communications · doi:10.1038/s41467-020-19936-x · Cited by 69 · see citing works
A neuroendocrine pathway modulating osmotic stress in Drosophila
Zandawala, M., Nguyen, T., Balanyà-Segura, M., Johard, H. A. D., Amcoff, M., Wegener, C., Paluzzi, J.-P. V., & Nässel, D. R. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009425 · Cited by 77 · see citing works
Combinatorial Pharyngeal Taste Coding for Feeding Avoidance in Adult Drosophila
Chen, Y., Park, S. J., Joseph, R. M., Ja, W. W., & Dahanukar, A. A. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.09.036 · Cited by 66 · see citing works
Gap junctions desynchronize a neural circuit to stabilize insect flight
Hürkey, S., Niemeyer, N., Schleimer, J.-H., Ryglewski, S., Schreiber, S., & Duch, C. (2023) · Nature · doi:10.1038/s41586-023-06099-0 · Cited by 64 · see citing works
A neuronal ensemble encoding adaptive choice during sensory conflict in Drosophila
Sareen, P., McCurdy, L. Y., & Nitabach, M. N. (2021) · Nature Communications · doi:10.1038/s41467-021-24423-y · Cited by 66 · see citing works
Chemosensory sensilla of the Drosophila wing express a candidate ionotropic pheromone receptor
He, Z., Luo, Y., Shang, X., Sun, J. S., & Carlson, J. R. (2019) · PLoS Biology · doi:10.1371/journal.pbio.2006619 · Cited by 57 · see citing works
A circadian output center controlling feeding:fasting rhythms in Drosophila
Dreyer, A. P., Martin, M. M., Fulgham, C. V., Jabr, D. A., Bai, L., Beshel, J., & Cavanaugh, D. J. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008478 · Cited by 63 · see citing works
Sensory processing during sleep in Drosophila melanogaster
French, A. S., Geissmann, Q., Beckwith, E. J., & Gilestro, G. F. (2021) · Nature · doi:10.1038/s41586-021-03954-w · Cited by 61 · see citing works
Kiral, F. R., Linneweber, G. A., Mathejczyk, T. F., Georgiev, S. V., Wernet, M. F., Hassan, B. A., von Kleist, M., & Hiesinger, P. R. (2020) · Nature Communications · doi:10.1038/s41467-020-14781-4 · Cited by 59 · see citing works
Anatomy and Neural Pathways Modulating Distinct Locomotor Behaviors in Drosophila Larva
Gowda, S. B. M., Salim, S., & Mohammad, F. (2021) · Biology · doi:10.3390/biology10020090 · Cited by 59 · see citing works
Non-canonical Receptive Field Properties and Neuromodulation of Feature-Detecting Neurons in Flies
Städele, C., Keleş, M. F., Mongeau, J.-M., & Frye, M. A. (2020) · Current Biology · doi:10.1016/j.cub.2020.04.069 · Cited by 52 · see citing works
Brain connectivity inversely scales with developmental temperature in Drosophila
Kiral, F. R., Dutta, S. B., Linneweber, G. A., Hilgert, S., Poppa, C., Duch, C., von Kleist, M., Hassan, B. A., & Hiesinger, P. R. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110145 · Cited by 58 · see citing works
Transsynaptic mapping of Drosophila mushroom body output neurons
Scaplen, K. M., Talay, M., Fisher, J. D., Cohn, R., Sorkaç, A., Aso, Y., Barnea, G., & Kaun, K. R. (2021) · eLife · doi:10.7554/elife.63379 · Cited by 56 · see citing works
Self-citationA subset of DN1p neurons integrates thermosensory inputs to promote wakefulness via CNMa signaling
Jin, X., Tian, Y., Zhang, Z. C., Gu, P., Liu, C., & Han, J. (2021) · Current Biology · doi:10.1016/j.cub.2021.02.048 · Cited by 63 · see citing works
Zhang, C., Kim, A. J., Rivera-Perez, C., Noriega, F. G., & Kim, Y. (2022) · Nature Communications · doi:10.1038/s41467-022-28592-2 · Cited by 57 · see citing works
Taste quality and hunger interactions in a feeding sensorimotor circuit
Shiu, P. K., Sterne, G. R., Engert, S., Dickson, B. J., & Scott, K. (2022) · eLife · doi:10.7554/elife.79887 · Cited by 56 · see citing works
Social attraction in Drosophila is regulated by the mushroom body and serotonergic system
Sun, Y., Qiu, R., Li, X., Cheng, Y., Gao, S., Kong, F., Liu, L., & Zhu, Y. (2020) · Nature Communications · doi:10.1038/s41467-020-19102-3 · Cited by 55 · see citing works
Meiselman, M. R., Alpert, M. H., Cui, X., Shea, J., Gregg, I., Gallio, M., & Yapici, N. (2022) · Current Biology · doi:10.1016/j.cub.2022.01.061 · Cited by 55 · see citing works
Circuits that encode and guide alcohol-associated preference
Scaplen, K. M., Talay, M., Salamon, S., Nuñez, K. M., Waterman, A. G., Gang, S., Song, S. L., Barnea, G., & Kaun, K. R. (2020) · eLife · doi:10.7554/elife.48730 · Cited by 61 · see citing works
Self-citationOf what use is connectomics? A personal perspective on the<i>Drosophila</i>connectome
Meinertzhagen, I. A. (2018) · Journal of Experimental Biology · doi:10.1242/jeb.164954 · Cited by 53 · see citing works
Hulse, B. K., Haberkern, H., Franconville, R., Turner-Evans, D. B., Takemura, S., Wolff, T., Noorman, M., Dreher, M., Dan, C., Parekh, R., et al. (2020) · doi:10.1101/2020.12.08.413955 · Cited by 392 · see citing works
“…(GRASP) (Xie et al., 2017) and trans-Tango (Omoto et al., 2018), methods that are limited in accuracy and reliability (Lee et al., 2017; Talay et al., 2017), have also been used to infer synaptic connectivity in the fly CX. Optogenetic stimulation of one candidate neural population and…”
Transcriptional readout of neuronal activity via an engineered Ca 2+ -activated protease
Sánchez, M. I., Nguyen, Q.-A., Wang, W., Soltész, I., & Ting, A. Y. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2006521117 · Cited by 51 · see citing works
Inhibitory Interactions and Columnar Inputs to an Object Motion Detector in Drosophila
Keleş, M. F., Hardcastle, B. J., Städele, C., Xiao, Q., & Frye, M. A. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.061 · Cited by 50 · see citing works
Tracing neuronal circuits in transgenic animals by transneuronal control of transcription (TRACT)
Huang, T.-H., Niesman, P. J., Arasu, D., Lee, D., Cruz, A. L. D. L., Callejas, A., Hong, E. J., & Lois, C. (2017) · eLife · doi:10.7554/elife.32027 · Cited by 43 · see citing works
Neuropeptides in modulation of Drosophila behavior: how to get a grip on their pleiotropic actions
Nässel, D. R., Pauls, D., & Huetteroth, W. (2019) · Current Opinion in Insect Science · doi:10.1016/j.cois.2019.03.002 · Cited by 48 · see citing works
The Neurotransmitters Involved in Drosophila Alcohol-Induced Behaviors
Chvilicek, M. M., Titos, I., & Rothenfluh, A. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.607700 · Cited by 45 · see citing works
Gao, J., Zhang, S., Deng, P., Wu, Z., Lemaître, B., Zhai, Z., & Guo, Z. (2024) · Nature Communications · doi:10.1038/s41467-024-47465-4 · Cited by 43 · see citing works
BAcTrace, a tool for retrograde tracing of neuronal circuits in Drosophila
Cachero, S., Gkantia, M., Bates, A. S., Frechter, S., Blackie, L., McCarthy, A., Sutcliffe, B., Strano, A., Aso, Y., & Jefferis, G. S. X. E. (2020) · Nature Methods · doi:10.1038/s41592-020-00989-1 · Cited by 45 · see citing works
Circadian clock disruption promotes the degeneration of dopaminergic neurons in male Drosophila
Dorcikova, M. M., Duret, L. C., Pottié, E., & Nagoshi, E. (2023) · Nature Communications · doi:10.1038/s41467-023-41540-y · Cited by 42 · see citing works
On the cutting edge: protease-based methods for sensing and controlling cell biology
Chung, H. K., & Lin, M. Z. (2020) · Nature Methods · doi:10.1038/s41592-020-0891-z · Cited by 43 · see citing works
Nässel, D. R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041940 · Cited by 42 · see citing works
Doszyn, O., Dulski, T., & Zmorzyńska, J. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1358844 · Cited by 41 · see citing works
Musso, P.-Y., Junca, P., & Gordon, M. D. (2021) · Science Advances · doi:10.1126/sciadv.abj0186 · Cited by 41 · see citing works
The Neuronal Circuit of the Dorsal Circadian Clock Neurons in Drosophila melanogaster
Reinhard, N., Schubert, F. K., Bertolini, E., Hagedorn, N., Manoli, G., Sekiguchi, M., Yoshii, T., Rieger, D., & Helfrich‐Förster, C. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.886432 · Cited by 40 · see citing works
Recurrent circadian circuitry regulates central brain activity to maintain sleep
Sun, L., Jiang, R. H., Ye, W., Rosbash, M., & Guo, F. (2022) · Neuron · doi:10.1016/j.neuron.2022.04.010 · Cited by 40 · see citing works
Recent Advances in the Genetic Dissection of Neural Circuits in Drosophila
Guo, C., Pan, Y., & Gong, Z. (2019) · Neuroscience Bulletin · doi:10.1007/s12264-019-00390-9 · Cited by 40 · see citing works
Functional architecture of neural circuits for leg proprioception in Drosophila
Chen, C., Agrawal, S., Mark, B., Mamiya, A., Sustar, A., Phelps, J. S., Lee, W.-C. A., Dickson, B. J., Card, G. M., & Tuthill, J. C. (2021) · Current Biology · doi:10.1016/j.cub.2021.09.035 · Cited by 39 · see citing works
Modality-Specific Circuits for Skylight Orientation in the Fly Visual System
Sancer, G., Kind, E., Plazaola-Sasieta, H., Balke, J., Pham, T., Hasan, A., Münch, L. O., Courgeon, M., Mathejczyk, T. F., & Wernet, M. F. (2019) · Current Biology · doi:10.1016/j.cub.2019.07.020 · Cited by 36 · see citing works
Circadian Structural Plasticity Drives Remodeling of E Cell Output
Duhart, J. M., Herrero, A., de la Cruz, G., Ispizua, J. I., Pírez, N., & Ceriani, M. F. (2020) · Current Biology · doi:10.1016/j.cub.2020.09.057 · Cited by 37 · see citing works
Dense Circuit Reconstruction to Understand Neuronal Computation: Focus on Zebrafish
Friedrich, R. W., & Wanner, A. A. (2021) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-110220-013050 · Cited by 33 · see citing works
A neural circuit integrates pharyngeal sensation to control feeding
Yang, T., Yuan, Z., Liu, C., Liu, T., & Zhang, W. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109983 · Cited by 35 · see citing works
Reinhard, N., Bertolini, E., Saito, A., Sekiguchi, M., Yoshii, T., Rieger, D., & Helfrich‐Förster, C. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25294 · Cited by 35 · see citing works
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 · see citing works
Self-citationretro-Tango enables versatile retrograde circuit tracing in Drosophila
Sorkaç, A., Moșneanu, R. A., Crown, A. M., Savaş, D., Okoro, A. M., Memiş, E., Talay, M., & Barnea, G. (2022) · bioRxiv · doi:10.7554/elife.85041 · Cited by 21 · see citing works
Self-citationA single photoreceptor splits perception and entrainment by cotransmission
Xiao, N., Shuang, X., Li, Z., Tang, M., Mao, R., Tian, Y., Ma, S.-X., Wang, P.-H., Li, M.-T., Sunilkumar, A., et al. (2023) · Nature · doi:10.1038/s41586-023-06681-6 · Cited by 34 · see citing works
A pair of commissural command neurons induces Drosophila wing grooming
Zhang, N., & Simpson, J. H. (2022) · iScience · doi:10.1016/j.isci.2022.103792 · Cited by 25 · see citing works
Molecular and cellular mechanisms of teneurin signaling in synaptic partner matching
Xu, C., Li, Z., Lyu, C., Hu, Y., McLaughlin, C. N., Wong, K. K. L., Xie, Q., Luginbuhl, D. J., Li, H., Udeshi, N. D., et al. (2024) · Cell · doi:10.1016/j.cell.2024.06.022 · Cited by 32 · see citing works
Wiring patterns from auditory sensory neurons to the escape and song-relay pathways in fruit flies
Kim, H., Horigome, M., Ishikawa, Y., Li, F., Lauritzen, J. S., Card, G., Bock, D. D., & Kamikouchi, A. (2020) · Journal of Comparative Neurology · doi:10.1002/cne.24877 · Cited by 27 · see citing works
Ehrhardt, E., Whitehead, S. C., Namiki, S., Minegishi, R., Siwanowicz, I., Feng, K., Otsuna, H., FlyLight Project Team, Meissner, G. W., Stern, D., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.31.542897 · Cited by 29 · see citing works
Differential Role for a Defined Lateral Horn Neuron Subset in Naïve Odor Valence in Drosophila
Lerner, H., Rozenfeld, E., Rozenman, B., Huetteroth, W., & Parnas, M. (2020) · Scientific Reports · doi:10.1038/s41598-020-63169-3 · Cited by 27 · see citing works
Liu, Y., Hasegawa, E., Nose, A., Zwart, M., & Kohsaka, H. (2023) · eLife · doi:10.7554/elife.83328 · Cited by 31 · see citing works
Daily rewiring of a neural circuit generates a predictive model of environmental light
Song, B. J., Sharp, S. J., & Rogulja, D. (2021) · Science Advances · doi:10.1126/sciadv.abe4284 · Cited by 28 · see citing works
Dopamine and GPCR-mediated modulation of DN1 clock neurons gates the circadian timing of sleep
Schlichting, M., Richhariya, S., Herndon, N., Ma, D., Xin, J., Lenh, W., Abruzzi, K. C., & Rosbash, M. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2206066119 · Cited by 29 · see citing works
Takagi, S., Sancer, G., Abuin, L., Stupski, S. D., Arguello, J. R., Prieto-Godino, L. L., Stern, D. L., Cruchet, S., Álvarez-Ocaña, R., Wienecke, C. F. R., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-50808-w · Cited by 29 · see citing works
González-Segarra, A. J., Pontes, G. B., Jourjine, N., Toro, A. D., & Scott, K. (2023) · eLife · doi:10.7554/elife.88143.3 · Cited by 27 · see citing works
A neural pathway underlying hunger modulation of sexual receptivity in Drosophila females
Sun, M., Ma, M., Deng, B., Li, N., Peng, Q., & Pan, Y. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113243 · Cited by 31 · see citing works
Extended Flight Bouts Require Disinhibition from GABAergic Mushroom Body Neurons
Manjila, S. B., Kuruvilla, M., Ferveur, J., Sane, S. P., & Hasan, G. (2018) · Current Biology · doi:10.1016/j.cub.2018.11.070 · Cited by 23 · see citing works
Mushroom body output differentiates memory processes and distinct memory-guided behaviors
Ichinose, T., Kanno, M., Wu, H., Yamagata, N., Sun, H., Abe, A., & Tanimoto, H. (2021) · Current Biology · doi:10.1016/j.cub.2020.12.032 · Cited by 28 · see citing works
A disinhibitory mechanism biases Drosophila innate light preference
Zhao, W., Zhou, P., Gong, C., Ouyang, Z., Wang, J., Zheng, N., & Gong, Z. (2019) · Nature Communications · doi:10.1038/s41467-018-07929-w · Cited by 25 · see citing works
Oikawa, I., Kondo, S., Hashimoto, K., Yoshida, A., Hamajima, M., Tanimoto, H., Furukubo-Tokunaga, K., & Honjo, K. (2023) · eLife · doi:10.7554/elife.85760 · Cited by 26 · see citing works
Li, H., Li, Z., Yuan, X., Tian, Y. L., Ye, W., Zeng, P., Li, X., & Guo, F. (2024) · Nature Communications · doi:10.1038/s41467-024-47278-5 · Cited by 24 · see citing works
Kubrak, O. I., Jørgensen, A. F., Koyama, T., Lassen, M., Nagy, S., Hald, J., Mazzoni, G., Madsen, D., Hansen, J. B., Larsen, M. R., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-50468-w · Cited by 30 · see citing works
- Authors
- 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., Szymanski, J. R., & Barnea, G.
- Affiliations
- Brown University (US)
- Corresponding author
- Barnea, Gilad
- ORCID
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2017-11
- Volume
- 96
- Issue
- 4
- Pages
- 783-795.e4
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC5693608
- OpenAlex
- W2765562046
- Cited by
- 301
- References
- 82
- Citations by year
- 2026: 26 · 2025: 31 · 2024: 53 · 2023: 39 · 2022: 35 · 2021: 40 · 2020: 38 · 2019: 18 · 2018: 20 · 2017: 1
- FWCI
- 10.44
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH (R21DCO14333, R01MH086920, R01MH105368, R01DC013561)
- Brown University: BIBS Innovation Award
- OVPR Salomon and Seed Awards
- Pew Charitable Trus
- Suna & İnan Kıraç Foundation
- BIBS
- Karen T. Romer UTRA (DGE1058262)
- National Science Foundation Graduate Research Fellowship Program
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Keywords
- gustatory system, Drosophila, site-specific proteolysis, tethered ligand, projection neurons, neuromodulation, olfactory system, neural circuit mapping
- MeSH terms
- Animals, Drosophila, Neural Pathways, Neurons, Olfactory Pathways, Animals, Genetically Modified, Taste Perception, Neuroanatomical Tract-Tracing Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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