Evidence map›Paper›PMID 23617951›Full record

ArticleBMC genomics2013

Genome-wide association study of sleep in Drosophila melanogaster.

Susan T Harbison, Lenovia J McCoy, Trudy F C Mackay

Abstract read
In one paragraph

Article in BMC genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
–field-weighted citation impact
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

102 citing papers in PubMed.

  1. Article
  2. Female genetic variation controlling timing of mating plug ejection inbioRxiv : the preprint server for biology · 2026
    Article
  3. Inferring the genetic basis of sleep states inbioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Early life sleep is associated with longevity inbioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. A genome-wide association study implicates the olfactory system inbioRxiv : the preprint server for biology · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The genetic basis of incipient sexual isolation inProceedings. Biological sciences · 2024
    Article
  18. Article
  19. bioRxiv : the preprint server for biology · 2024
    Article
  20. iScience · 2024
    Article

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

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

3 authors.

Susan T HarbisonDepartment of Genetics, North Carolina State University, Raleigh, North Carolina 27695, USA. susan.harbison@nih.gov
Lenovia J McCoy
Trudy F C Mackay

Funding

Verification of Polymorphisms Impacting SleepZIAHL006146 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI HARBISON, SUSAN · 2012 to 2025
$12.4M
QUANTITATIVE TRAIT LOCI IN DROSOPHILAR01GM045146 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI ANHOLT, ROBERT R. H, MACKAY, TRUDY F. · 1991 to 2012
$5.1M
Intramural NIH HHSNIGMS NIH HHS R01 GM45146
6 · The paper itself

Abstract

backgroundSleep is a highly conserved behavior, yet its duration and pattern vary extensively among species and between individuals within species. The genetic basis of natural variation in sleep remains unknown.

resultsWe used the Drosophila Genetic Reference Panel (DGRP) to perform a genome-wide association (GWA) study of sleep in D. melanogaster. We identified candidate single nucleotide polymorphisms (SNPs) associated with differences in the mean as well as the environmental sensitivity of sleep traits; these SNPs typically had sex-specific or sex-biased effects, and were generally located in non-coding regions. The majority of SNPs (80.3%) affecting sleep were at low frequency and had moderately large effects. Additive models incorporating multiple SNPs explained as much as 55% of the genetic variance for sleep in males and females. Many of these loci are known to interact physically and/or genetically, enabling us to place them in candidate genetic networks. We confirmed the role of seven novel loci on sleep using insertional mutagenesis and RNA interference.

conclusionsWe identified many SNPs in novel loci that are potentially associated with natural variation in sleep, as well as SNPs within genes previously known to affect Drosophila sleep. Several of the candidate genes have human homologues that were identified in studies of human sleep, suggesting that genes affecting variation in sleep are conserved across species. Our discovery of genetic variants that influence environmental sensitivity to sleep may have a wider application to all GWA studies, because individuals with highly plastic genotypes will not have consistent phenotypes.

Indexed as

AnimalsDrosophila melanogasterFemaleGenes, InsectGenome-Wide Association StudyGenotypeHumansMaleMutagenesis, InsertionalPhenotypePolymorphism, Single NucleotideRNA InterferenceSleepSleep Wake Disorders

Identifiers

PMID23617951
PMCPMC3644253

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.