Evidence map›Paper›PMID 25357003›Full record

ArticlePLoS genetics2014

Feeding state, insulin and NPR-1 modulate chemoreceptor gene expression via integration of sensory and circuit inputs.

Matthew Gruner, Dru Nelson, Ari Winbush, Rebecca Hintz, Leesun Ryu, Samuel H Chung, Kyuhyung Kim, Chrisopher V Gabel, Alexander M van der Linden

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.2field-weighted citation impact, top 27% 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

31 citing papers in PubMed, 51 citations in OpenAlex.

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  13. Chemical Signaling Regulates Axon Regeneration via the GPCR-Gqα Pathway inThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
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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

9 authors at 3 institutions in 2 countries.

Matthew GrunerDepartment of Biology, University of Nevada, Reno, Nevada, United States of America.
Dru NelsonDepartment of Biology, University of Nevada, Reno, Nevada, United States of America.
Ari WinbushDepartment of Biology, University of Nevada, Reno, Nevada, United States of America.
Rebecca HintzDepartment of Agriculture, Nutrition and Veterinary Sciences, University of Nevada, Reno, Nevada, United States of America.
Leesun RyuDepartment of Brain Science, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, Korea.
Samuel H ChungDepartment of Physiology and Biophysics, Boston University School of Medicine, Boston, Massachusetts, United States of America; Boston University Photonics Center, Boston, Massachusetts, United States of America.
Kyuhyung KimDepartment of Brain Science, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, Korea.
Chrisopher V GabelDepartment of Physiology and Biophysics, Boston University School of Medicine, Boston, Massachusetts, United States of America; Boston University Photonics Center, Boston, Massachusetts, United States of America.
Alexander M van der LindenDepartment of Biology, University of Nevada, Reno, Nevada, United States of America.
University of Nevada, Reno · USBoston University · USDaegu Gyeongbuk Institute of Science and Technology · KR

Funding

Outreach/Diversity/Pipeline ProjectP20GM103440 · NIGMS · UNIVERSITY OF NEVADA RENO · PI Eduardo A Robleto · 2012 to 2026
$58.0M
Virtual Reality and Augmented Reality CoreP20GM103650 · NIGMS · UNIVERSITY OF NEVADA RENO · PI WEBSTER, MICHAEL A · 2012 to 2022
$20.9M
C. elegans model for mammalian lesion-conditioned axon regenerationR21NS078580 · NINDS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GABEL, CHRISTOPHER V · 2012 to 2013
$419k
NIGMS NIH HHS P20 GM103440NIGMS NIH HHS P20GM103440NIGMS NIH HHS P20 GM103650NIGMS NIH HHS P20GM103650NINDS NIH HHS R21 NS078580NINDS NIH HHS R21NS078580
6 · The paper itself

Abstract

Feeding state and food availability can dramatically alter an animals' sensory response to chemicals in its environment. Dynamic changes in the expression of chemoreceptor genes may underlie some of these food and state-dependent changes in chemosensory behavior, but the mechanisms underlying these expression changes are unknown. Here, we identified a KIN-29 (SIK)-dependent chemoreceptor, srh-234, in C. elegans whose expression in the ADL sensory neuron type is regulated by integration of sensory and internal feeding state signals. We show that in addition to KIN-29, signaling is mediated by the DAF-2 insulin-like receptor, OCR-2 TRPV channel, and NPR-1 neuropeptide receptor. Cell-specific rescue experiments suggest that DAF-2 and OCR-2 act in ADL, while NPR-1 acts in the RMG interneurons. NPR-1-mediated regulation of srh-234 is dependent on gap-junctions, implying that circuit inputs regulate the expression of chemoreceptor genes in sensory neurons. Using physical and genetic manipulation of ADL neurons, we show that sensory inputs from food presence and ADL neural output regulate srh-234 expression. While KIN-29 and DAF-2 act primarily via the MEF-2 (MEF2) and DAF-16 (FOXO) transcription factors to regulate srh-234 expression in ADL neurons, OCR-2 and NPR-1 likely act via a calcium-dependent but MEF-2- and DAF-16-independent pathway. Together, our results suggest that sensory- and circuit-mediated regulation of chemoreceptor genes via multiple pathways may allow animals to precisely regulate and fine-tune their chemosensory responses as a function of internal and external conditions.

Indexed as

Feeding BehaviorAnimalsAnimals, Genetically ModifiedCaenorhabditis elegansCaenorhabditis elegans ProteinsGene Expression RegulationInsulinMutationProtein Serine-Threonine KinasesReceptor, InsulinReceptors, Neuropeptide YSensory Receptor CellsSignal TransductionTranscription FactorsCaenorhabditis elegans ProteinsDAF-2 protein, C elegansInsulinkin-29 protein, C elegansmef-2 protein, C elegansNPR-1 protein, C elegansProtein Serine-Threonine KinasesReceptor, InsulinReceptors, Neuropeptide YTranscription Factors

Identifiers

PMID25357003
PMCPMC4214617
OpenAlexW2087509846

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.