Evidence map›Paper›PMID 33901178›Full record

ArticlePLoS genetics2021

A complex genetic architecture in zebrafish relatives Danio quagga and D. kyathit underlies development of stripes and spots.

Braedan M McCluskey, Susumu Uji, Joseph L Mancusi, John H Postlethwait, David M Parichy

Abstract read
In one paragraph

Article in PLoS genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. The hybrid history of zebrafish.G3 (Bethesda, Md.) · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. 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

5 authors.

Braedan M McCluskeyDepartment of Biology, University of Virginia, Charlottesville, Virginia, United States of America.ORCID 0000-0001-6423-7048
Susumu UjiJapan Fisheries Research and Education Agency, Watarai, Japan.ORCID 0000-0003-3908-2990
Joseph L MancusiDepartment of Biology, University of Virginia, Charlottesville, Virginia, United States of America.ORCID 0000-0002-4808-4878
John H PostlethwaitInstitute of Neuroscience, University of Oregon, Eugene, Oregon, United States of America.ORCID 0000-0002-5476-2137
David M ParichyDepartment of Biology, University of Virginia, Charlottesville, Virginia, United States of America.ORCID 0000-0003-2771-6095

Funding

Graduate Training in Genetics Administrative Supplement - Career Curriculum DevelopmentT32GM007413 · NIGMS · UNIVERSITY OF OREGON · PI GUILLEMIN, KAREN J · 1985 to 2022
$7.8M
Fish facility enhancementR35GM122471 · NIGMS · UNIVERSITY OF WASHINGTON · PI DAVID M PARICHY · 2017 to 2026
$6.4M
Resources for Teleost Gene Duplicates and Human DiseaseR01OD011116 · OD · UNIVERSITY OF OREGON · PI POSTLETHWAIT, JOHN H. · 2012 to 2020
$5.4M
Morphogenesis of Pigmentation Patterns in Zebrafish and its Relatives: Testing the Genetic and Developmental Basis of Diverse Adult Phenotypes across EvolutionF32GM119202 · NIGMS · UNIVERSITY OF WASHINGTON · PI MCCLUSKEY, BRAEDAN MARSHALL · 2016 to 2018
$171k
NIGMS NIH HHS F32 GM119202NIGMS NIH HHS R35 GM122471NIGMS NIH HHS T32 GM007413NIH HHS R01 OD011116
6 · The paper itself

Abstract

Vertebrate pigmentation is a fundamentally important, multifaceted phenotype. Zebrafish, Danio rerio, has been a valuable model for understanding genetics and development of pigment pattern formation due to its genetic and experimental tractability, advantages that are shared across several Danio species having a striking array of pigment patterns. Here, we use the sister species D. quagga and D. kyathit, with stripes and spots, respectively, to understand how natural genetic variation impacts phenotypes at cellular and organismal levels. We first show that D. quagga and D. kyathit phenotypes resemble those of wild-type D. rerio and several single locus mutants of D. rerio, respectively, in a morphospace defined by pattern variation along dorsoventral and anteroposterior axes. We then identify differences in patterning at the cellular level between D. quagga and D. kyathit by repeated daily imaging during pattern development and quantitative comparisons of adult phenotypes, revealing that patterns are similar initially but diverge ontogenetically. To assess the genetic architecture of these differences, we employ reduced-representation sequencing of second-generation hybrids. Despite the similarity of D. quagga to D. rerio, and D. kyathit to some D. rerio mutants, our analyses reveal a complex genetic basis for differences between D. quagga and D. kyathit, with several quantitative trait loci contributing to variation in overall pattern and cellular phenotypes, epistatic interactions between loci, and abundant segregating variation within species. Our findings provide a window into the evolutionary genetics of pattern-forming mechanisms in Danio and highlight the complexity of differences that can arise even between sister species. Further studies of natural genetic diversity underlying pattern variation in D. quagga and D. kyathit should provide insights complementary to those from zebrafish mutant phenotypes and more distant species comparisons.

Indexed as

AnimalsCyprinidaeEmbryonic DevelopmentEmbryo, NonmammalianGene Expression Regulation, DevelopmentalMelanophoresMetamorphosis, BiologicalPhenotypePhylogenySkin PigmentationSpecies SpecificityZebrafish

Identifiers

PMID33901178
PMCPMC8102007

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.