Evidence map›Paper›PMID 27852783›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

An Array of Descending Visual Interneurons Encoding Self-Motion in Drosophila.

Marie P Suver, Ainul Huda, Nicole Iwasaki, Steve Safarik, Michael H Dickinson

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

64 citing papers in PubMed, 130 citations in OpenAlex.

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  4. How tp1, an indirect wing steering muscle, stabilizesbioRxiv : the preprint server for biology · 2025
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  13. Insect Flight: State of the Field and Future Directions.Integrative and comparative biology · 2024
    Article
  14. Comparative connectomics of the descending and ascending neurons of thebioRxiv : the preprint server for biology · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Descending control of motor sequences in Drosophila.Current opinion in neurobiology · 2024
    Review
  20. Fine-grained descending control of steering in walkingbioRxiv : the preprint server for biology · 2023
    Article

4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Marie P SuverDepartment of Biology, University of Washington, Seattle, Washington 98195.ORCID 0000-0003-4491-6996
Ainul HudaDepartment of Biology, University of Washington, Seattle, Washington 98195.ORCID 0000-0003-2073-6659
Nicole IwasakiDepartment of Biology, University of Washington, Seattle, Washington 98195.
Steve SafarikDepartment of Biology, University of Washington, Seattle, Washington 98195.
Michael H DickinsonDepartment of Biology, University of Washington, Seattle, Washington 98195, flyman@caltech.edu.ORCID 0000-0002-8587-9936
California Institute of Technology · USUniversity of Washington · USNeurosciences Institute · US

Funding

Integrative Functional Mapping of Sensory-Motor PathwaysU01NS090514 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI DICKINSON, MICHAEL H, HOLMES, PHILIP J · 2014 to 2018
$3.4M
NINDS NIH HHS U01 NS090514
6 · The paper itself

Abstract

The means by which brains transform sensory information into coherent motor actions is poorly understood. In flies, a relatively small set of descending interneurons are responsible for conveying sensory information and higher-order commands from the brain to motor circuits in the ventral nerve cord. Here, we describe three pairs of genetically identified descending interneurons that integrate information from wide-field visual interneurons and project directly to motor centers controlling flight behavior. We measured the physiological responses of these three cells during flight and found that they respond maximally to visual movement corresponding to rotation around three distinct body axes. After characterizing the tuning properties of an array of nine putative upstream visual interneurons, we show that simple linear combinations of their outputs can predict the responses of the three descending cells. Last, we developed a machine vision-tracking system that allows us to monitor multiple motor systems simultaneously and found that each visual descending interneuron class is correlated with a discrete set of motor programs. SIGNIFICANCE STATEMENT: Most animals possess specialized sensory systems for encoding body rotation, which they use for stabilizing posture and regulating motor actions. In flies and other insects, the visual system contains an array of specialized neurons that integrate local optic flow to estimate body rotation during locomotion. However, the manner in which the output of these cells is transformed by the downstream neurons that innervate motor centers is poorly understood. We have identified a set of three visual descending neurons that integrate the output of nine large-field visual interneurons and project directly to flight motor centers. Our results provide new insight into how the sensory information that encodes body motion is transformed into a code that is appropriate for motor actions.

Indexed as

AnimalsDrosophilaEfferent PathwaysFlight, AnimalInterneuronsOrientationPsychomotor PerformanceVisual PathwaysVisual Perceptionethologyflightself-motion estimationvision

Identifiers

PMID27852783
PMCPMC5125229
OpenAlexW2551255120

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.