Evidence map›Paper›PMID 31735672›Full record

ArticleCurrent biology : CB2019

Polymodal Nociception in Drosophila Requires Alternative Splicing of TrpA1.

Pengyu Gu, Jiaxin Gong, Ye Shang, Fei Wang, Kendra T Ruppell, Zhiguo Ma, Amy E Sheehan, Marc R Freeman, Yang Xiang

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 61 citations in OpenAlex.

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  16. Multiple mechanisms of action of an extremely painful venom.bioRxiv : the preprint server for biology · 2024
    Article
  17. iScience · 2024
    Article
  18. Review
  19. Article
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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 1 institution in 1 country.

Pengyu GuDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Jiaxin GongDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Ye ShangDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Fei WangDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Kendra T RuppellDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Zhiguo MaDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Amy E SheehanDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Marc R FreemanDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Yang XiangDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, MA 01605, USA. Electronic address: yang.xiang@umassmed.edu.
University of Massachusetts Chan Medical School · US

Funding

Astrocyte control of neural circuits and behaviorR37NS053538 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FREEMAN, MARC R · 2016 to 2022
$2.9M
Molecular Mechanisms of nociceptor sensitizationR01NS089787 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI XIANG, YANG · 2015 to 2019
$1.8M
Cellular and molecular mechanisms underlying neuronal activity-controlled regeneration specificityR21NS107924 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI XIANG, YANG · 2018 to 2019
$481k
NINDS NIH HHS R01 NS089787NINDS NIH HHS R21 NS107924NINDS NIH HHS R37 NS053538
6 · The paper itself

Abstract

Transcripts of noxious stimulus-detecting TrpA1 channels are alternatively spliced. Despite the importance of nociception for survival, the in vivo significance of expressing different TrpA1 isoforms is largely unknown. Here, we develop a novel genetic approach to generate Drosophila knockin strains expressing single TrpA1 isoforms. Drosophila TrpA1 mediates heat and UVC-triggered nociception. We show that TrpA1-C and TrpA1-D, two alternative isoforms, are co-expressed in nociceptors. When examined in heterologous cells, both TrpA1-C and TrpA1-D are activated by heat and UVC. By contrast, analysis of knockin flies reveals the striking functional specificity; TrpA1-C mediates UVC-nociception, whereas TrpA1-D mediates heat-nociception. Therefore, in vivo functions of TrpA1-C and TrpA1-D are different from each other and are different from their in vitro properties. Our results indicate that a given sensory stimulus preferentially activates a single TrpA1 isoform in vivo and that polymodal nociception requires co-expression of TrpA1 isoforms, providing novel insights of how alternative splicing regulates nociception.

Indexed as

Alternative SplicingNociceptionAnimalsDrosophila melanogasterDrosophila ProteinsIon ChannelsProtein IsoformsSingle-Cell AnalysisDrosophila ProteinsIon ChannelsProtein IsoformsTrpA1 protein, Drosophilaalternative splicingDrosophilagenome engineeringnociceptionpolymodal nociceptorsthermogeneticstransient receptor potentialtranslational reportersTrpA1

Identifiers

PMID31735672
PMCPMC6938258
OpenAlexW2987719291

What OpenQuestion holds

Textmetadata
LicenceTDM
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.