Synaptic and peptidergic connectome of a neurosecretory center in the annelid brain
Open accessPublished version of a preprint
Abstract
Abstract Neurosecretory centres in animal brains use peptidergic signalling to influence physiology and behaviour. Understanding neurosecretory centre function requires mapping cell types, synapses, and peptidergic networks. Here we use electron microscopy and gene expression mapping to analyse the synaptic and peptidergic connectome of an entire neurosecretory centre. We mapped 78 neurosecretory neurons in the brain of larval Platynereis dumerilii , a marine annelid. These neurons form an anterior neurosecretory organ expressing many neuropeptides, including hypothalamic peptide orthologues and their receptors. Analysis of peptide-receptor pairs revealed sparsely connected networks linking specific neuronal subsets. We experimentally analysed one peptide-receptor pair and found that a neuropeptide can couple neurosecretory and synaptic brain signalling. Our study uncovered extensive non-synaptic signalling within a neurosecretory centre and its connection to the synaptic brain.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Four preprohormones of the GnRH superfamily were identified in Platynereis by transcriptomics, bioinformatics, and mass spectrometry.
“Four preprohormones of the gnrh superfamily were identified in Platynereis by a combination of transcriptomics, bioinformatics, and mass spectrometry analyses (refs. 53 and 54 and this study).”
From Corazonin signaling integrates energy homeostasis and lunar phase to regulate aspects of growth and sexual maturation in <i>Platynereis</i> (2020) · cites this paper as [54]
A GnRH-superfamily receptor with clear orthology to the Corazonin Receptor subfamily (CrzR) was identified and shown to interact with both CRZ1 and CRZ2.
“A GnRH-superfamily receptor with clear orthology to the Corazonin Receptor subfamily (CrzR) was identified and shown to interact with both CRZ1 and CRZ2 (54).”
From Corazonin signaling integrates energy homeostasis and lunar phase to regulate aspects of growth and sexual maturation in <i>Platynereis</i> (2020) · cites this paper as [54]
Both CrzRa and CrzRb were activated by CRZ1/GnRHL1 and CRZ2/GnRHL2 and, at higher concentration, also by GnRHL3.
“Both CrzRa and CrzRb were activated by CRZ1/GnRHL1 and CRZ2/GnRHL2 (Fig. 1B and SI Appendix, Fig. S3 C and D; see also ref. 54) and, at higher concentration, also by GnRHL3 (Fig. 1B and SI Appendix, Fig. S3 C and D).”
From Corazonin signaling integrates energy homeostasis and lunar phase to regulate aspects of growth and sexual maturation in <i>Platynereis</i> (2020) · cites this paper as [54]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Collective dynamics of ‘small-world’ networks
Watts, D. J., & Strogatz, S. H. (1998) · Nature · doi:10.1038/30918 · Cited by 43,060 · see citing works
Sakurai, T., Amemiya, A., Ishii, M., Matsuzaki, I., Chemelli, R. M., Tanaka, H., Williams, S. C., Richardson, J. A., Kozlowski, G. P., Wilson, S., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)80949-6 · Cited by 5,501 · see citing works
Detecting Novel Associations in Large Data Sets
Reshef, D. N., Reshef, Y., Finucane, H. K., Grossman, S. R., McVean, G., Turnbaugh, P. J., Lander, E. S., Mitzenmacher, M., & Sabeti, P. C. (2011) · Science · doi:10.1126/science.1205438 · Cited by 3,345 · see citing works
TrakEM2 Software for Neural Circuit Reconstruction
Cardona, A., Saalfeld, S., Schindelin, J., Arganda‐Carreras, I., Preibisch, S., Longair, M., Tomančák, P., Hartenstein, V., & Douglas, R. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038011 · Cited by 989 · see citing works
Neuromodulation of neuronal circuits: back to the future
Marder, E. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.010 · Cited by 904 · see citing works
A molecular census of arcuate hypothalamus and median eminence cell types
Campbell, J. N., Macosko, E. Z., Fenselau, H., Pers, T. H., Lyubetskaya, A., Tenen, D., Goldman, M., Verstegen, A. M. J., Resch, J. M., McCarroll, S. A., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4495 · Cited by 817 · see citing works
Terakita, A. (2005) · Genome biology · doi:10.1186/gb-2005-6-3-213 · Cited by 632 · 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
Beyond the connectome: how neuromodulators shape neural circuits
Bargmann, C. I. (2012) · BioEssays · doi:10.1002/bies.201100185 · Cited by 505 · see citing works
Molecular interrogation of hypothalamic organization reveals distinct dopamine neuronal subtypes
Romanov, R. A., Zeisel, A., Bakker, J., Girach, F., Hellysaz, A., Tomer, R., Alpár, A., Mulder, J., Clotman, F., Keimpema, E., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4462 · Cited by 502 · see citing works
Ciliary photoreceptors with a vertebrate-type opsin in an invertebrate brain
Arendt, D., Tessmar-Raible, K., Snyman, H., Dorresteijn, A. W., & Wittbrodt, J. (2004) · Science · doi:10.1126/science.1099955 · Cited by 458 · see citing works
Global view of the evolution and diversity of metazoan neuropeptide signaling
Jékely, G. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221833110 · Cited by 451 · see citing works
Self-citationMolecular evolution of peptidergic signaling systems in bilaterians
Mirabeau, O., & Joly, J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219956110 · Cited by 423 · see citing works
Self-citationHigh-throughput spatial mapping of single-cell RNA-seq data to tissue of origin
Achim, K., Pettit, J.-B., Saraiva, L. R., Gavriouchkina, D., Larsson, T., Arendt, D., & Marioni, J. C. (2015) · Nature Biotechnology · doi:10.1038/nbt.3209 · Cited by 395 · see citing works
Tessmar-Raible, K., Raible, F., Christodoulou, F., Guy, K., Rembold, M., Hausen, H., & Arendt, D. (2007) · Cell · doi:10.1016/j.cell.2007.04.041 · Cited by 384 · see citing works
CATMAID: collaborative annotation toolkit for massive amounts of image data
Saalfeld, S., Cardona, A., Hartenstein, V., & Tomančák, P. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp266 · Cited by 384 · see citing works
Cardona, A., Saalfeld, S., Preibisch, S., Schmid, B., Cheng, A., Pulokas, J., Tomancak, P., & Hartenstein, V. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000502 · Cited by 372 · see citing works
Quantitative neuroanatomy for connectomics in Drosophila
Schneider-Mizell, C. M., Gerhard, S., Longair, M., Kazimiers, T., Li, F., Zwart, M. F., Champion, A., Midgley, F. M., Fetter, R. D., Saalfeld, S., et al. (2016) · eLife · doi:10.7554/elife.12059 · Cited by 332 · see citing works
TRP ion channels in the nervous system
Moran, M. M., Xu, H., & Clapham, D. E. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.05.003 · Cited by 328 · see citing works
Functional consequences of neuropeptide and small-molecule co-transmission
Nusbaum, M. P., Blitz, D. M., & Marder, E. E. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.56 · Cited by 304 · see citing works
Mechanism of phototaxis in marine zooplankton
Jékely, G., Colombelli, J., Hausen, H., Guy, K., Stelzer, E., Nédélec, F., & Arendt, D. (2008) · Nature · doi:10.1038/nature07590 · Cited by 298 · see citing works
Self-citationThe neuroendocrine system of invertebrates: a developmental and evolutionary perspective
Hartenstein, V. (2006) · Journal of Endocrinology · doi:10.1677/joe.1.06964 · Cited by 284 · see citing works
The Multilayer Connectome of Caenorhabditis elegans
Bentley, B., Branicky, R., Barnes, C. L., Chew, Y. L., Yemini, E., Bullmore, E. T., Vértes, P. E., & Schafer, W. R. (2016) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1005283 · Cited by 269 · see citing works
Smith, C. L., Varoqueaux, F., Kittelmann, M., Azzam, R. N., Cooper, B., Winters, C. A., Eitel, M., Fasshauer, D., & Reese, T. S. (2014) · Current Biology · doi:10.1016/j.cub.2014.05.046 · Cited by 254 · see citing works
Larval body patterning and apical organs are conserved in animal evolution
Marlow, H. Q., Tosches, M. A., Tomer, R., Steinmetz, P. R. H., Lauri, A., Larsson, T., & Arendt, D. (2014) · BMC Biology · doi:10.1186/1741-7007-12-7 · Cited by 207 · see citing works
The apical sensory organ of a gastropod veliger is a receptor for settlement cues
Hadfield, M., Meleshkevitch, E., & Boudko, D. (2000) · The Biological Bulletin · doi:10.2307/1542804 · Cited by 176 · see citing works
Six3 demarcates the anterior-most developing brain region in bilaterian animals
Steinmetz, P. R. H., Urbach, R., Posnien, N., Eriksson, J., Kostyuchenko, R. P., Brena, C., Guy, K., Akam, M. E., Bucher, G., & Arendt, D. (2010) · EvoDevo · doi:10.1186/2041-9139-1-14 · Cited by 172 · see citing works
The neuropeptide complement of the marine annelid Platynereis dumerilii
Conzelmann, M., Williams, E. A., Krug, K., Franz-Wachtel, M., Macek, B., & Jékely, G. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-906 · Cited by 165 · see citing works
Self-citationConserved MIP receptor–ligand pair regulates <i>Platynereis</i> larval settlement
Conzelmann, M., Williams, E. A., Tunaru, S., Randel, N., Shahidi, R., Asadulina, A., Berger, J., Offermanns, S., & Jékely, G. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1220285110 · Cited by 155 · see citing works
Self-citationLarge-Scale Combinatorial Deorphanization of Platynereis Neuropeptide GPCRs
Bauknecht, P., & Jékely, G. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.06.052 · Cited by 154 · see citing works
Self-citationSynaptic transmission parallels neuromodulation in a central food-intake circuit
Schlegel, P., Texada, M. J., Miroschnikow, A., Schoofs, A., Hückesfeld, S., Peters, M., Schneider-Mizell, C. M., Lacin, H., Li, F., Fetter, R. D., et al. (2016) · eLife · doi:10.7554/elife.16799 · Cited by 151 · see citing works
Circadian and circalunar clock interactions in a marine annelid
Zantke, J., Ishikawa-Fujiwara, T., Arboleda, E., Lohs, C., Schipany, K., Hallay, N., Straw, A. D., Todo, T., & Tessmar-Raible, K. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.08.031 · Cited by 148 · see citing works
Different Proctolin Neurons Elicit Distinct Motor Patterns from a Multifunctional Neuronal Network
Blitz, D. M., Christie, A. E., Coleman, M. J., Norris, B. J., Marder, E. E., & Nusbaum, M. P. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05449.1999 · Cited by 148 · see citing works
Neuropeptides regulate swimming depth of Platynereis larvae
Conzelmann, M., Offenburger, S.-L., Asadulina, A., Keller, T., Münch, T. A., & Jékely, G. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109085108 · Cited by 136 · see citing works
Self-citationMelatonin Signaling Controls Circadian Swimming Behavior in Marine Zooplankton
Tosches, M. A., Bucher, D. B., Vopálenský, P., & Arendt, D. (2014) · Cell · doi:10.1016/j.cell.2014.07.042 · Cited by 134 · see citing works
Morphology of the nervous system of Polychaeta (Annelida)
Orrhage, L., & Müller, M. C. M. (2005) · Springer eBooks · doi:10.1007/1-4020-3240-4_6 · Cited by 131 · see citing works
Morphology of the nervous system of Polychaeta (Annelida)
Orrhage, L., & Müller, M. C. M. (2005) · Hydrobiologia · doi:10.1007/s10750-004-4375-4 · Cited by 126 · see citing works
Neuronal connectome of a sensory-motor circuit for visual navigation
Randel, N., Asadulina, A., Bezares-Calderón, L. A., Verasztó, C., Williams, E. A., Conzelmann, M., Shahidi, R., & Jékely, G. (2014) · eLife · doi:10.7554/elife.02730 · Cited by 119 · see citing works
Self-citationSense organs in polychaetes (Annelida)
Purschke, G. (2005) · Hydrobiologia · doi:10.1007/s10750-004-4358-5 · Cited by 115 · see citing works
Ciliomotor circuitry underlying whole-body coordination of ciliary activity in the Platynereis larva
Verasztó, C., Ueda, N., Bezares-Calderón, L. A., Panzera, A., Williams, E. A., Shahidi, R., & Jékely, G. (2017) · eLife · doi:10.7554/elife.26000 · Cited by 113 · see citing works
Self-citationNeuropeptidergic integration of behavior in <i>Trichoplax adhaerens</i>, an animal without synapses
Senatore, A., Reese, T. S., & Smith, C. L. (2017) · Journal of Experimental Biology · doi:10.1242/jeb.162396 · Cited by 113 · see citing works
Neuropeptides Modulate Female Chemosensory Processing upon Mating in Drosophila
Hussain, A., Üçpunar, H. K., Zhang, M., Loschek, L. F., & Kadow, I. C. G. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002455 · Cited by 111 · see citing works
Neural circuits and motivational processes for hunger
Sternson, S. M., Nicholas Betley, J., & Cao, Z. F. H. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.04.006 · Cited by 108 · see citing works
Ultrastructure of Nuchal Organs in Polychaetes (Annelida) — New Results and Review
Purschke, G. (1997) · Acta Zoologica · doi:10.1111/j.1463-6395.1997.tb01133.x · Cited by 107 · see citing works
The bilaterian forebrain: an evolutionary chimaera
Tosches, M. A., & Arendt, D. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.09.005 · Cited by 106 · see citing works
The evolution and nomenclature of GnRH-type and corazonin-type neuropeptide signaling systems
Zandawala, M., Tian, S., & Elphick, M. R. (2018) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2017.06.007 · Cited by 105 · see citing works
The long and the short of it – a perspective on peptidergic regulation of circuits and behaviour
Jékely, G., Melzer, S., Beets, I., Kadow, I. C. G., Koene, J. M., Haddad, S., & Holden-Dye, L. M. (2018) · Journal of Experimental Biology · doi:10.1242/jeb.166710 · Cited by 102 · see citing works
Self-citationBioinformatic prediction of Trichoplax adhaerens regulatory peptides
Nikitin, M. (2015) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2014.03.049 · Cited by 93 · see citing works
Vergara, H. M., Bertucci, P. Y., Hantz, P., Tosches, M. A., Achim, K., Vopálenský, P., & Arendt, D. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610602114 · Cited by 84 · see citing works
Urbilaterian origin of paralogous GnRH and corazonin neuropeptide signalling pathways
Tian, S., Zandawala, M., Beets, I., Baytemur, E., Slade, S. E., Scrivens, J. H., & Elphick, M. R. (2016) · Scientific Reports · doi:10.1038/srep28788 · Cited by 79 · see citing works
Divergent co‐transmitter actions underlie motor pattern activation by a modulatory projection neuron
Stein, W., DeLong, N. D., Wood, D. E., & Nusbaum, M. P. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05744.x · Cited by 74 · see citing works
Thirumalai, V., & Marder, E. E. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-05-01874.2002 · Cited by 68 · see citing works
Conzelmann, M., & Jékely, G. (2012) · EvoDevo · doi:10.1186/2041-9139-3-23 · Cited by 67 · see citing works
Self-citationA serial multiplex immunogold labeling method for identifying peptidergic neurons in connectomes
Shahidi, R., Williams, E. A., Conzelmann, M., Asadulina, A., Verasztó, C., Jasek, S., Bezares-Calderón, L. A., & Jékely, G. (2015) · eLife · doi:10.7554/elife.11147 · Cited by 65 · see citing works
Self-citationA Hormone-Activated Central Pattern Generator for Courtship
Wagenaar, D. A., Hamilton, M. S., Huang, T., Kristan, W. B., & French, K. A. (2010) · Current Biology · doi:10.1016/j.cub.2010.02.027 · Cited by 62 · see citing works
Circadian Rhythms: In the Loop at Last
Gelder, R. N. V., Herzog, E. D., Schwartz, W. J., & Taghert, P. H. (2003) · Science · doi:10.1126/science.1085446 · Cited by 62 · see citing works
Inter-individual stereotypy of the Platynereis larval visual connectome
Randel, N., Shahidi, R., Verasztó, C., Bezares-Calderón, L. A., Schmidt, S., & Jékely, G. (2015) · eLife · doi:10.7554/elife.08069 · Cited by 56 · see citing works
Self-citationChia, F. S., & Koss, R. (1984) · Zoomorphology · doi:10.1007/bf00312131 · Cited by 56 · see citing works
Apical Sensory Organ in Larvae of the PatellogastropodTectura scutum
Page, L. R. (2002) · Biological Bulletin · doi:10.2307/1543218 · Cited by 55 · see citing works
Hunnekuhl, V. S., & Akam, M. E. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.09.020 · Cited by 54 · see citing works
The evolution of neurosecretory centers in bilaterian forebrains: insights from protostomes
Tessmar-Raible, K. (2007) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2007.04.007 · Cited by 53 · see citing works
Growth Hormone Secretagogues and Hypothalamic Networks
Bluet‐Pajot, M., Tolle, V., Zizzari, P., Robert, C., Hammond, C., Mitchell, V. A., Beauvillain, J., Viollet, C., Epelbaum, J., & Kordon, C. (2001) · Endocrine · doi:10.1385/endo:14:1:001 · Cited by 52 · see citing works
Whole-body gene expression pattern registration in Platynereis larvae
Asadulina, A., Panzera, A., Verasztó, C., Liebig, C., & Jékely, G. (2012) · EvoDevo · doi:10.1186/2041-9139-3-27 · Cited by 52 · see citing works
Self-citationCoexpression analysis of nine neuropeptides in the neurosecretory preoptic area of larval zebrafish
Herget, U., & Ryu, S. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00002 · Cited by 49 · see citing works
Getting Nervous: An Evolutionary Overhaul for Communication
Varoqueaux, F., & Fasshauer, D. (2017) · Annual Review of Genetics · doi:10.1146/annurev-genet-120116-024648 · Cited by 47 · see citing works
Garcia, V. J., Daur, N., Temporal, S., Schulz, D. J., & Bucher, D. M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0171-15.2015 · Cited by 44 · see citing works
The animal sensorimotor organization: a challenge for the environmental complexity thesis
Keijzer, F., & Arnellos, A. (2017) · Biology & Philosophy · doi:10.1007/s10539-017-9565-3 · Cited by 43 · see citing works
Towards a systems-level understanding of development in the marine annelid Platynereis dumerilii
Williams, E. A., & Jékely, G. (2016) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2016.07.005 · Cited by 38 · see citing works
Self-citationNeuromodulatory connectivity defines the structure of a behavioral neural network
Diao, F., Elliott, A. D., Diao, F., Shah, S., & White, B. H. (2017) · eLife · doi:10.7554/elife.29797 · Cited by 38 · see citing works
Thorndyke, M. C., Crawford, B. D., & Burke, R. D. (1992) · Acta Zoologica · doi:10.1111/j.1463-6395.1992.tb01084.x · Cited by 37 · see citing works
Mayorova, T. D., Tian, S., Cai, W., Semmens, D. C., Odekunle, E., Zandawala, M., Badi, Y. E., Rowe, M. L., Egertová, M., & Elphick, M. R. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00553 · Cited by 37 · see citing works
Carbohydrate uptake by quiescent and reactivated mouse blastocysts
Spindler, R. E., Renfree, M. B., & Gardner, D. K. (1996) · Journal of Experimental Zoology · doi:10.1002/(sici)1097-010x(19961001)276:2 · Cited by 24 · see citing works
Identifying Cell Types from Spatially Referenced Single-Cell Expression Datasets
Pettit, J.-B., Tomer, R., Achim, K., Richardson, S., Azizi, L., & Marioni, J. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003824 · Cited by 23 · see citing works
Aros, B., Béla, V. I. G. H., & Vigh‐Teichmann, I. (1977) · Cell and Tissue Research · doi:10.1007/bf00220174 · Cited by 14 · see citing works
Rosalind’s Ghost: Biology, Collaboration, and the Female
Wagner, C. S. (2016) · PLoS Biology · doi:10.1371/journal.pbio.2001003 · Cited by 13 · see citing works
Object-based representation and analysis of light and electron microscopic volume data using Blender
Asadulina, A., Conzelmann, M., Williams, E. A., et al. (2015) · BMC Bioinformatics · doi:10.1186/s12859-015-0652-7 · Cited by 12 · see citing works
Self-citationHomology of insect corpora allata and vertebrate adenohypophysis?
Wirmer, A., Bradler, S., & Heinrich, R. (2012) · Arthropod Structure & Development · doi:10.1016/j.asd.2012.04.003 · Cited by 12 · see citing works
Haamedi, S. N., Karten, H. J., & Djamgoz, M. B. A. (2001) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20010319)431:4 · Cited by 8 · see citing works
Achim, K., Eling, N., Vergara, H. M., Bertucci, P. Y., Brunet, T., Collier, P. G., Beneš, V., Marioni, J. C., & Arendt, D. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/167742 · Cited by 3 · see citing works
Verasztó, C., Ueda, N., Bezares-Calderón, L. A., et al. (2017) · doi:10.7554/elife.26000.040 · Cited by 1 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Allostasis: A brain-centered, predictive mode of physiological regulation
Schulkin, J., & Sterling, P. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.07.010 · Cited by 265 · see citing works
Cephalopod Brains: An Overview of Current Knowledge to Facilitate Comparison With Vertebrates
Shigeno, S., Andrews, P. L. R., Ponte, G., & Fiorito, G. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00952 · Cited by 182 · see citing works
Miroschnikow, A., Schlegel, P., Schoofs, A., Hueckesfeld, S., Li, F., Schneider-Mizell, C. M., Fetter, R. D., Truman, J. W., Cardona, A., & Pankratz, M. J. (2018) · eLife · doi:10.7554/elife.40247 · Cited by 84 · see citing works
Verasztó, C., Jasek, S., Gühmann, M., Shahidi, R., Ueda, N., Beard, J. D., Mendes, S., Heinz, K., Bezares-Calderón, L. A., Williams, E., et al. (2020) · doi:10.1101/2020.08.21.260984 · Cited by 54 · see citing works
Self-citationAndreatta, G., Broyart, C., Borghgraef, C., Vadiwala, K., Kozin, V., Polo, A., Bileck, A., Beets, I., Schoofs, L., Gerner, C., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1910262116 · Cited by 61 · see citing works
Ramirez, M. D., Bui, T. N., & Katz, P. S. (2024) · Journal of Comparative Neurology · doi:10.1002/cne.25628 · Cited by 10 · see citing works
- Authors
- Williams, E. A., Verasztó, C., Jasek, S., Conzelmann, M., Shahidi, R., Bauknecht, P., Mirabeau, O., & Jékely, G.
- Affiliations
- Max Planck Institute for Developmental Biology (DE)
- University of Exeter (GB)
- Inserm (FR)
- Corresponding author
- Jékely, Gáspár
- ORCID
- Venue
- eLife
- Publisher
- eLife Sciences Publications, Ltd
- Published
- 2017-12-04
- Volume
- 6
- ISSN
- 2050-084X (ISSN-L)
- PMC
- PMC5747525
- OpenAlex
- W2611412176
- Cited by
- 119
- References
- 80
- Citations by year
- 2026: 5 · 2025: 11 · 2024: 34 · 2023: 20 · 2022: 5 · 2021: 11 · 2020: 8 · 2019: 7 · 2018: 14 · 2017: 4
- FWCI
- 4.41
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- eLife (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Open Research Exeter (University of Exeter) (acceptedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Max Planck Digital Library (submittedVersion)
- Figshare (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- Max-Planck-Gesellschaft
- Deutsche Forschungsgemeinschaft (JE 777/1-1)
- 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 › Neuropeptides and Animal Physiology
- Keywords
- peptidergic signaling, synaptic connectivity, connectome, neuropeptides, neuropeptide receptors, hypothalamic neuropeptides, Platynereis dumerilii, larval brain, single-cell transcriptome, neurosecretory cells
- MeSH terms
- Animals, Brain, Neuropeptides, Neurosecretory Systems, Polychaeta, Gene Expression Profiling, Microscopy, Electron, Transmission, Connectome
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 ›
Are you an author, or do you see a problem with this page? Request a review