Evidence map›Paper›PMID 16143618›Full record

ArticleGenetics2005

The effect of polymorphisms in the enhancer of split gene complex on bristle number variation in a large wild-caught cohort of Drosophila melanogaster.

Stuart J Macdonald, Tomi Pastinen, Anthony D Long

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Genetics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  9. Review
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  13. Genetics. Life after GWA studies.Science (New York, N.Y.) · 2009
    Article
  14. Article
  15. An amino acid polymorphism in the couch potato gene forms the basis for climatic adaptation in Drosophila melanogaster.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  16. Article
  17. Review
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  19. Genetic variation in the cysteine biosynthesis pathway causes sensitivity to pharmacological compounds.Proceedings of the National Academy of Sciences of the United States of America · 2007
    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

3 authors at 2 institutions in 2 countries.

Stuart J MacdonaldDepartment of Ecology and Evolutionary Biology, University of California-Irvine, 321 Steinhaus Hall, Irvine, CA 92697-2525, USA. sjm@uci.edu
Tomi Pastinen
Anthony D Long
University of California, Irvine · USMcGill University and Génome Québec Innovation Centre · CA

Funding

USING DISEQUILIBRIUM MAPPING TO DISSECT COMPLEX TRAITSR01GM058564 · NIGMS · UNIVERSITY OF CALIFORNIA IRVINE · PI LONG, ANTHONY DOUGLAS · 1999 to 2003
$536k
NIGMS NIH HHS GM 58564NIGMS NIH HHS R01 GM058564
6 · The paper itself

Abstract

The Enhancer of split complex [E(spl)-C] in Drosophila encompasses a variety of functional elements controlling bristle patterning and on the basis of prior work is a strong candidate for harboring alleles having subtle effects on bristle number variation. Here we extend earlier studies identifying associations between complex phenotypes and polymorphisms segregating among inbred laboratory lines of Drosophila and test the influence of E(spl)-C on bristle number variation in a natural cohort. We describe results from an association mapping study using 203 polymorphisms spread throughout the E(spl)-C genotyped in 2000 wild-caught Drosophila melanogaster. Despite power to detect associations accounting for as little as 2% of segregating variation for bristle number, and saturating the region with single-nucleotide polymorphisms (SNPs), we identified no single SNP marker showing a significant (additive over loci) effect after correcting for multiple tests. Using a newly developed test we conservatively identify six regions of the E(spl)-C in which the insertion of transposable elements as a class contributes to variation in bristle number, apparently in a sex- or trait-limited fashion. Finally, we carry out all possible 20,503 two-way tests for epistasis and identify a slight excess of marginally significant interactions, although none survive multiple-testing correction. It may not be straightforward to extend the results of laboratory-based association studies to natural populations.

Indexed as

PhenotypePolymorphism, GeneticAnimalsAnimal StructuresBase SequenceBasic Helix-Loop-Helix ProteinsCaliforniaDNA Transposable ElementsDrosophila melanogasterDrosophila ProteinsEpistasis, GeneticGenetics, PopulationLinkage DisequilibriumMolecular Sequence DataRepressor ProteinsSequence Analysis, DNABasic Helix-Loop-Helix ProteinsDNA Transposable ElementsDrosophila ProteinsE(spl)m7-HLH protein, DrosophilaRepressor Proteins

Identifiers

PMID16143618
PMCPMC1456100
OpenAlexW2124425489

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.