Evidence map›Paper›PMID 25933381›Full record

ArticlePLoS genetics2015

Genetic Architecture of Abdominal Pigmentation in Drosophila melanogaster.

Lauren M Dembeck, Wen Huang, Michael M Magwire, Faye Lawrence, Richard F Lyman, Trudy F C Mackay

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing 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

57 citing papers in PubMed, 99 citations in OpenAlex.

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  15. Exercise-induced changes in climbing performance.Royal Society open science · 2021
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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

6 authors at 2 institutions in 1 country.

Lauren M DembeckDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, United States of America; Program in Genetics, North Carolina State University, Raleigh, North Carolina, United States of America; W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, North Carolina, United States of America.
Wen HuangDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, United States of America; Program in Genetics, North Carolina State University, Raleigh, North Carolina, United States of America; W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, North Carolina, United States of America.
Michael M MagwireSyngenta Biotechnology, Durham, North Carolina, United States of America.
Faye LawrenceDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, United States of America.
Richard F LymanDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, United States of America; Program in Genetics, North Carolina State University, Raleigh, North Carolina, United States of America; W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, North Carolina, United States of America.
Trudy F C MackayDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, United States of America; Program in Genetics, North Carolina State University, Raleigh, North Carolina, United States of America; W. M. Keck Center for Behavioral Biology, North Carolina State University, Raleigh, North Carolina, United States of America.
North Carolina State University · USSyngenta (United States) · US

Funding

NIGMS NIH HHS R01 GM455146
6 · The paper itself

Abstract

Pigmentation varies within and between species and is often adaptive. The amount of pigmentation on the abdomen of Drosophila melanogaster is a relatively simple morphological trait, which serves as a model for mapping the genetic basis of variation in complex phenotypes. Here, we assessed natural variation in female abdominal pigmentation in 175 sequenced inbred lines of the Drosophila melanogaster Genetic Reference Panel, derived from the Raleigh, NC population. We quantified the proportion of melanization on the two most posterior abdominal segments, tergites 5 and 6 (T5, T6). We found significant genetic variation in the proportion of melanization and high broad-sense heritabilities for each tergite. Genome-wide association studies identified over 150 DNA variants associated with the proportion of melanization on T5 (84), T6 (34), and the difference between T5 and T6 (35). Several of the top variants associated with variation in pigmentation are in tan, ebony, and bric-a-brac1, genes known to affect D. melanogaster abdominal pigmentation. Mutational analyses and targeted RNAi-knockdown showed that 17 out of 28 (61%) novel candidate genes implicated by the genome-wide association study affected abdominal pigmentation. Several of these genes are involved in developmental and regulatory pathways, chitin production, cuticle structure, and vesicle formation and transport. These findings show that genetic variation may affect multiple steps in pathways involved in tergite development and melanization. Variation in these novel candidates may serve as targets for adaptive evolution and sexual selection in D. melanogaster.

Indexed as

AnimalsDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEvolution, MolecularFemaleGenetic Association StudiesGenetic VariationLinkage DisequilibriumPhenotypePigmentationPolymorphism, Single NucleotideQuantitative Trait LociTranscription FactorsBric-a-brac protein 1, DrosophilaDNA-Binding ProteinsDrosophila ProteinsTranscription Factors

Identifiers

PMID25933381
PMCPMC4416719
OpenAlexW1981478316

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.