Evidence map›Paper›PMID 26217193›Full record

ArticleFrontiers in neural circuits2015

A common evolutionary origin for the ON- and OFF-edge motion detection pathways of the Drosophila visual system.

Kazunori Shinomiya, Shin-ya Takemura, Patricia K Rivlin, Stephen M Plaza, Louis K Scheffer, Ian A Meinertzhagen

Abstract read
In one paragraph

Article in Frontiers in neural circuits, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Network Statistics of the Whole-Brain Connectome ofbioRxiv : the preprint server for biology · 2024
    Article
  6. Article
  7. Article
  8. How fly neurons compute the direction of visual motion.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. The Organization of the Second Optic Chiasm of theFrontiers in neural circuits · 2019
    Article
  13. Review
  14. Review
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Kazunori ShinomiyaDepartment of Psychology and Neuroscience, Life Sciences Centre, Dalhousie University Halifax, NS, Canada ; FlyEM Project Team, Howard Hughes Medical Institute, Janelia Research Campus Ashburn, VA, USA.
Shin-ya TakemuraFlyEM Project Team, Howard Hughes Medical Institute, Janelia Research Campus Ashburn, VA, USA.
Patricia K RivlinFlyEM Project Team, Howard Hughes Medical Institute, Janelia Research Campus Ashburn, VA, USA.
Stephen M PlazaFlyEM Project Team, Howard Hughes Medical Institute, Janelia Research Campus Ashburn, VA, USA.
Louis K SchefferFlyEM Project Team, Howard Hughes Medical Institute, Janelia Research Campus Ashburn, VA, USA.
Ian A MeinertzhagenDepartment of Psychology and Neuroscience, Life Sciences Centre, Dalhousie University Halifax, NS, Canada ; Department of Biology, Life Sciences Centre, Dalhousie University Halifax, NS, Canada.

Funding

Visual system synapses and circuitsR01EY003592 · NEI · DALHOUSIE UNIVERSITY · PI MEINERTZHAGEN, IAN A · 1985 to 2013
$2.8M
NEI NIH HHS EY-03592NEI NIH HHS R01 EY003592
6 · The paper itself

Abstract

Synaptic circuits for identified behaviors in the Drosophila brain have typically been considered from either a developmental or functional perspective without reference to how the circuits might have been inherited from ancestral forms. For example, two candidate pathways for ON- and OFF-edge motion detection in the visual system act via circuits that use respectively either T4 or T5, two cell types of the fourth neuropil, or lobula plate (LOP), that exhibit narrow-field direction-selective responses and provide input to wide-field tangential neurons. T4 or T5 both have four subtypes that terminate one each in the four strata of the LOP. Representatives are reported in a wide range of Diptera, and both cell types exhibit various similarities in: (1) the morphology of their dendritic arbors; (2) their four morphological and functional subtypes; (3) their cholinergic profile in Drosophila; (4) their input from the pathways of L3 cells in the first neuropil, or lamina (LA), and by one of a pair of LA cells, L1 (to the T4 pathway) and L2 (to the T5 pathway); and (5) their innervation by a single, wide-field contralateral tangential neuron from the central brain. Progenitors of both also express the gene atonal early in their proliferation from the inner anlage of the developing optic lobe, being alone among many other cell type progeny to do so. Yet T4 receives input in the second neuropil, or medulla (ME), and T5 in the third neuropil or lobula (LO). Here we suggest that these two cell types were originally one, that their ancestral cell population duplicated and split to innervate separate ME and LO neuropils, and that a fiber crossing-the internal chiasma-arose between the two neuropils. The split most plausibly occurred, we suggest, with the formation of the LO as a new neuropil that formed when it separated from its ancestral neuropil to leave the ME, suggesting additionally that ME input neurons to T4 and T5 may also have had a common origin.

Indexed as

Biological EvolutionAnimalsCholine O-AcetyltransferaseDrosophilaMotion PerceptionNeuronsNeuropilOrientationVesicular Inhibitory Amino Acid Transport ProteinsVisual PathwaysCholine O-Acetyltransferasevesicular GABA transporterVesicular Inhibitory Amino Acid Transport Proteinsdirectional selectivitylaminalobulamedullamotion sensitivity

Identifiers

PMID26217193
PMCPMC4496578

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.