Evidence map›Paper›PMID 26154367›Full record

ArticlePLoS genetics2015

Sensory Neurons Arouse C. elegans Locomotion via Both Glutamate and Neuropeptide Release.

Seungwon Choi, Kelsey P Taylor, Marios Chatzigeorgiou, Zhitao Hu, William R Schafer, Joshua M Kaplan

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

38 citing papers in PubMed, 58 citations in OpenAlex.

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  18. Behavioral States.Genetics · 2020
    Review
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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 at 4 institutions in 2 countries.

Seungwon ChoiDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Neurobiology, Harvard Medical School, Boston, Massachusetts, United States of America; Biological and Biomedical Sciences program, Harvard Medical School, Boston, Massachusetts, United States of America.
Kelsey P TaylorDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Neurobiology, Harvard Medical School, Boston, Massachusetts, United States of America; Biological and Biomedical Sciences program, Harvard Medical School, Boston, Massachusetts, United States of America.
Marios ChatzigeorgiouCell Biology Division, MRC Laboratory of Molecular Biology, Cambridge, United Kingdom.
Zhitao HuDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Neurobiology, Harvard Medical School, Boston, Massachusetts, United States of America.
William R SchaferCell Biology Division, MRC Laboratory of Molecular Biology, Cambridge, United Kingdom.
Joshua M KaplanDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Neurobiology, Harvard Medical School, Boston, Massachusetts, United States of America; Biological and Biomedical Sciences program, Harvard Medical School, Boston, Massachusetts, United States of America.
Massachusetts General Hospital · USHarvard University · USMRC Laboratory for Molecular Cell Biology · GBMRC Laboratory of Molecular Biology · GB

Funding

Regulation of insulin secretion C. elegansR01DK080215 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI KAPLAN, JOSHUA M · 2008 to 2016
$3.3M
Medical Research Council MC_U105185857NIDDK NIH HHS DK80215NIDDK NIH HHS R01 DK080215Wellcome Trust 103784
6 · The paper itself

Abstract

C. elegans undergoes periods of behavioral quiescence during larval molts (termed lethargus) and as adults. Little is known about the circuit mechanisms that establish these quiescent states. Lethargus and adult locomotion quiescence is dramatically reduced in mutants lacking the neuropeptide receptor NPR-1. Here, we show that the aroused locomotion of npr-1 mutants results from the exaggerated activity in multiple classes of sensory neurons, including nociceptive (ASH), touch sensitive (ALM and PLM), and stretch sensing (DVA) neurons. These sensory neurons accelerate locomotion via both neuropeptide and glutamate release. The relative contribution of these sensory neurons to arousal differs between larval molts and adults. Our results suggest that a broad network of sensory neurons dictates transitions between aroused and quiescent behavioral states.

Indexed as

AnimalsArousalBehavior, AnimalCaenorhabditis elegansCaenorhabditis elegans ProteinsCell MovementGlutamic AcidNeuropeptidesNociceptorsReceptors, Neuropeptide YSensory Receptor CellsSleepCaenorhabditis elegans ProteinsGlutamic AcidNeuropeptidesNPR-1 protein, C elegansReceptors, Neuropeptide Y

Identifiers

PMID26154367
PMCPMC4495980
OpenAlexW808554464

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.