Evidence map›Paper›PMID 19060186›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2008

Light-arousal and circadian photoreception circuits intersect at the large PDF cells of the Drosophila brain.

Yuhua Shang, Leslie C Griffith, Michael Rosbash

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 178 papers.

0numbers the graph read from it
0cells of the map it votes in
178citing papers in PubMed
6.3field-weighted citation impact, top 2% 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

178 citing papers in PubMed, 290 citations in OpenAlex.

  1. Article
  2. Article
  3. A day sleep promoting role of phototransduction inNeurobiology of sleep and circadian rhythms · 2026
    Article
  4. Article
  5. The use ofFrontiers in cell and developmental biology · 2026
    Review
  6. Sleep regulation inFrontiers in neuroscience · 2026
    Review
  7. Time-of-day modulation in mosquito response persistence to carbon dioxide is controlled by Pigment-Dispersing Factor.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Activity Monitoring for Analysis of Sleep inCold Spring Harbor protocols · 2024
    Article
  13. A four-oscillator model of seasonally adapted morning and evening activities in Drosophila melanogaster.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2024
    Review
  14. Review
  15. Differential regulation of sleep by blue, green, and red light inFrontiers in behavioral neuroscience · 2024
    Article
  16. Article
  17. Article
  18. Dissecting neuron-specific functions of circadian genes using modified cell-specific CRISPR approaches.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Article
  20. A phosphorylation-deficient mutant ofFrontiers in neuroscience · 2023
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Yuhua ShangHoward Hughes Medical Institute and National Center for Behavioral Genomics, Department of Biology, Brandeis University, Waltham, MA 02454, USA.
Leslie C Griffith
Michael Rosbash
Brandeis University · USHoward Hughes Medical Institute · US

Funding

THE MOLECULAR GENETIC BASIS OF SENSORY BEHAVIOR IN DROSOPHILAP01NS044232 · NINDS · BRANDEIS UNIVERSITY · PI GARRITY, PAUL · 2002 to 2011
$13.2M
Regulation of Intrinsic Plasticity in Neural CircuitsR01MH067284 · NIMH · BRANDEIS UNIVERSITY · PI GRIFFITH, LESLIE C · 2003 to 2025
$8.8M
Howard Hughes Medical InstituteNIMH NIH HHS R01 MH067284NINDS NIH HHS P01 NS044232NINDS NIH HHS P01 NS044232-06
6 · The paper itself

Abstract

The neural circuits that regulate sleep and arousal as well as their integration with circadian circuits remain unclear, especially in Drosophila. This issue intersects with that of photoreception, because light is both an arousal signal in diurnal animals and an entraining signal for the circadian clock. To identify neurons and circuits relevant to light-mediated arousal as well as circadian phase-shifting, we developed genetic techniques that link behavior to single cell-type resolution within the Drosophila central brain. We focused on the unknown function of the 10 PDF-containing large ventral lateral neurons (l-LNvs) of the Drosophila circadian brain network and show here that these cells function in light-dependent arousal. They also are important for phase shifting in the late-night (dawn), indicating that the circadian photoresponse is a network property and therefore non-cell-autonomous. The data further indicate that the circuits underlying light-induced arousal and circadian photoentrainment intersect at the l-LNvs and then segregate.

Indexed as

ArousalCircadian RhythmSleepAnimalsDrosophila melanogasterDrosophila ProteinsLateral VentriclesLightNerve NetPhotoreceptor Cells, InvertebrateReceptors, G-Protein-CoupledDrosophila ProteinsPDFR protein, DrosophilaReceptors, G-Protein-Coupled

Identifiers

PMID19060186
PMCPMC2596742
OpenAlexW2153041353

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.