Evidence map›Paper›PMID 18687026›Full record

ArticlePLoS biology2008

A novel molecular solution for ultraviolet light detection in Caenorhabditis elegans.

Stacey L Edwards, Nicole K Charlie, Marie C Milfort, Brandon S Brown, Christen N Gravlin, Jamie E Knecht, Kenneth G Miller

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 184 papers.

0numbers the graph read from it
0cells of the map it votes in
184citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

184 citing papers in PubMed, 318 citations in OpenAlex.

  1. ThebioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Non-visual light modulates behavioral memory and gene expression inbioRxiv : the preprint server for biology · 2025
    Article
  11. Phenotypic and metabonomics studies of FMOs in C. elegans and their roles in lifespan extension.Metabolomics : Official journal of the Metabolomic Society · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. The effects of intense light onbioRxiv : the preprint server for biology · 2025
    Article
  16. Article
  17. Food sensing controlsScience advances · 2025
    Article
  18. Review
  19. Review
  20. Article

124 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Stacey L EdwardsGenetic Models of Disease Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, United States of America.
Nicole K Charlie
Marie C Milfort
Brandon S Brown
Christen N Gravlin
Jamie E Knecht
Kenneth G Miller
Oklahoma Medical Research Foundation · US

Funding

Signaling Pathways that Regulate Synaptic TransmissionR01GM080765 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI MILLER, KENNETH GEORGE · 2007 to 2015
$2.7M
NIGMS NIH HHS R01 GM080765
6 · The paper itself

Abstract

For many organisms the ability to transduce light into cellular signals is crucial for survival. Light stimulates DNA repair and metabolism changes in bacteria, avoidance responses in single-cell organisms, attraction responses in plants, and both visual and nonvisual perception in animals. Despite these widely differing responses, in all of nature there are only six known families of proteins that can transduce light. Although the roundworm Caenorhabditis elegans has none of the known light transduction systems, we show here that C. elegans strongly accelerates its locomotion in response to blue or shorter wavelengths of light, with maximal responsiveness to ultraviolet light. Our data suggest that C. elegans uses this light response to escape the lethal doses of sunlight that permeate its habitat. Short-wavelength light drives locomotion by bypassing two critical signals, cyclic adenosine monophosphate (cAMP) and diacylglycerol (DAG), that neurons use to shape and control behaviors. C. elegans mutants lacking these signals are paralyzed and unresponsive to harsh physical stimuli in ambient light, but short-wavelength light rapidly rescues their paralysis and restores normal levels of coordinated locomotion. This light response is mediated by LITE-1, a novel ultraviolet light receptor that acts in neurons and is a member of the invertebrate Gustatory receptor (Gr) family. Heterologous expression of the receptor in muscle cells is sufficient to confer light responsiveness on cells that are normally unresponsive to light. Our results reveal a novel molecular solution for ultraviolet light detection and an unusual sensory modality in C. elegans that is unlike any previously described light response in any organism.

Indexed as

Ultraviolet RaysAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCyclic AMPDiglyceridesLocomotionMembrane ProteinsMotor NeuronsMuscle CellsMutationSignal TransductionCaenorhabditis elegans ProteinsCyclic AMPDiglycerideslite-1 protein, C elegansMembrane Proteins

Identifiers

PMID18687026
PMCPMC2494560
OpenAlexW1970489875

What OpenQuestion holds

Textmetadata
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.