Evidence map›Paper›PMID 21067449›Full record

ReviewJournal of neurogenetics2010

The history of the Drosophila TRP channel: the birth of a new channel superfamily.

Baruch Minke

Open access · greenAbstract readHistorical ArticleReview
In one paragraph

Review in Journal of neurogenetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

51 citing papers in PubMed, 109 citations in OpenAlex.

  1. TRPA1 for Butterfly Eyespot Formation.International journal of molecular sciences · 2026
    Article
  2. Review
  3. Article
  4. Roles of TRPM channels in glioma.Cancer biology & therapy · 2024
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. TRPM2-mediated CaCell communication and signaling : CCS · 2023
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Mechanisms and significance of CaCurrent opinion in physiology · 2020
    Article
  18. Review
  19. TRPV4: A Physio and Pathophysiologically Significant Ion Channel.International journal of molecular sciences · 2020
    Review
  20. 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

1 author at 1 institution in 1 country.

Baruch MinkeDepartment of Medical Neurobiology, The Institute of Medical Research Israel-Canada, The Edmond and Lily Safra Center for Brain Sciences and the Kühne Minerva Center for Studies of Visual Transduction, Faculty of Medicine, The Hebrew University, Jerusalem 91120, Israel. baruchm@ekmd.huji.ac.il
Hebrew University of Jerusalem · IL

Funding

GENETIC DISSECTION OF PHOTOTRANSDUCTIONR01EY003529 · NEI · HEBREW UNIVERSITY OF JERUSALEM · PI MINKE, BARUCH · 1985 to 2011
$1.8M
NEI NIH HHS R01 EY003529NEI NIH HHS R01 EY 03529
6 · The paper itself

Abstract

Transient receptor potential (TRP) channels are polymodal cellular sensors involved in a wide variety of cellular processes, mainly by changing membrane voltage and increasing cellular Ca(2+). This review outlines in detail the history of the founding member of the TRP family, the Drosophila TRP channel. The field began with a spontaneous mutation in the trp gene that led to a blind mutant during prolonged intense light. It was this mutant that allowed for the discovery of the first TRP channels. A combination of electrophysiological, biochemical, Ca(2+) measurements, and genetic studies in flies and in other invertebrates pointed to TRP as a novel phosphoinositide-regulated and Ca(2+)-permeable channel. The cloning and sequencing of the trp gene provided its molecular identity. These seminal findings led to the isolation of the first mammalian homologues of the Drosophila TRP channels. We now know that TRP channel proteins are conserved through evolution and are found in most organisms, tissues, and cell-types. The TRP channel superfamily is classified into seven related subfamilies: TRPC, TRPM, TRPV, TRPA, TRPP, TRPML, and TRPN. A great deal is known today about participation of TRP channels in many biological processes, including initiation of pain, thermoregulation, salivary fluid secretion, inflammation, cardiovascular regulation, smooth muscle tone, pressure regulation, Ca(2+) and Mg(2+) homeostasis, and lysosomal function. The native Drosophila photoreceptor cells, where the founding member of the TRP channels superfamily was found, is still a useful preparation to study basic features of this remarkable channel.

Indexed as

AnimalsCalcium ChannelsDrosophilaDrosophila ProteinsEvolution, MolecularFemaleHistory, 20th CenturyHumansMammalsModels, AnimalTransient Receptor Potential ChannelsCalcium ChannelsDrosophila ProteinsTransient Receptor Potential Channelstrp protein, Drosophila

Identifiers

PMID21067449
PMCPMC3103766
OpenAlexW2045100549

What OpenQuestion holds

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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.