Evidence map›Paper›PMID 24958088›Full record

ArticleCellular and molecular life sciences : CMLS2015

Using siRNA to define functional interactions between melanopsin and multiple G Protein partners.

Steven Hughes, Aarti Jagannath, Doron Hickey, Silvia Gatti, Matthew Wood, Stuart N Peirson, Russell G Foster, Mark W Hankins

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. A systematic comparison of optogenetic approaches to visual restoration.Molecular therapy. Methods & clinical development · 2022
    Article
  5. Functional Differentiation of BMP7 Genes in Zebrafish:Frontiers in cell and developmental biology · 2022
    Article
  6. Melanopsin phototransduction: beyond canonical cascades.The Journal of experimental biology · 2021
    Review
  7. Chimeric human opsins as optogenetic light sensitisers.The Journal of experimental biology · 2021
    Article
  8. Review
  9. Article
  10. Article
  11. Differential roles for cryptochromes in the mammalian retinal clock.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  12. Phototransduction in Retinal Ganglion Cells.The Yale journal of biology and medicine · 2018
    Review
  13. Long-term restoration of visual function in end-stage retinal degeneration using subretinal human melanopsin gene therapy.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  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

8 authors at 2 institutions in 2 countries.

Steven HughesNuffield Laboratory of Ophthalmology, University of Oxford, Oxford, OX3 9DU, UK.
Aarti Jagannath
Doron Hickey
Silvia Gatti
Matthew Wood
Stuart N Peirson
Russell G Foster
Mark W Hankins
University of Oxford · GBRoche (Switzerland) · CH

Funding

Biotechnology and Biological Sciences Research Council BB/I021086/1Wellcome Trust 098461
6 · The paper itself

Abstract

Melanopsin expressing photosensitive retinal ganglion cells (pRGCs) represent a third class of ocular photoreceptors and mediate a range of non-image forming responses to light. Melanopsin is a G protein coupled receptor (GPCR) and existing data suggest that it employs a membrane bound signalling cascade involving Gnaq/11 type G proteins. However, to date the precise identity of the Gα subunits involved in melanopsin phototransduction remains poorly defined. Here we show that Gnaq, Gna11 and Gna14 are highly co-expressed in pRGCs of the mouse retina. Furthermore, using RNAi based gene silencing we show that melanopsin can signal via Gnaq, Gna11 or Gna14 in vitro, and demonstrate that multiple members of the Gnaq/11 subfamily, including Gna14 and at least Gnaq or Gna11, can participate in melanopsin phototransduction in vivo and contribute to the pupillary light responses of mice lacking rod and cone photoreceptors. This diversity of G protein interactions suggests additional complexity in the melanopsin phototransduction cascade and may provide a basis for generating the diversity of light responses observed from pRGC subtypes.

Indexed as

AnimalsBlotting, WesternCalciumCells, CulturedFemaleGTP-Binding Protein alpha SubunitsImmunoenzyme TechniquesIntegrasesLightMaleMelanopsinMiceMice, Inbred C3HMice, Inbred C57BLMice, KnockoutPhotic StimulationCalciumCre recombinaseGTP-Binding Protein alpha SubunitsIntegrasesMelanopsinRNA, MessengerRNA, Small InterferingRod Opsins

Identifiers

PMID24958088
PMCPMC4282707
OpenAlexW2151707924

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.