Evidence map›Paper›PMID 26599497›Full record

ArticlePLoS genetics2015

The Multi-allelic Genetic Architecture of a Variance-Heterogeneity Locus for Molybdenum Concentration in Leaves Acts as a Source of Unexplained Additive Genetic Variance.

Simon K G Forsberg, Matthew E Andreatta, Xin-Yuan Huang, John Danku, David E Salt, Örjan Carlborg

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 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
6.9field-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

36 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
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  10. Review
  11. Microorganisms · 2023
    Review
  12. Article
  13. Article
  14. Genetics as a key to improving crop photosynthesis.Journal of experimental botany · 2022
    Article
  15. Article
  16. GWAS of longitudinal trajectories at biobank scale.American journal of human genetics · 2022
    Article
  17. Article
  18. Article
  19. Article
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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 2 countries.

Simon K G ForsbergDepartment of Clinical Sciences, Division of Computational Genetics, Swedish University of Agricultural Sciences, Uppsala, Sweden.
Matthew E AndreattaInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, Scotland, United Kingdom.
Xin-Yuan HuangInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, Scotland, United Kingdom.
John DankuInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, Scotland, United Kingdom.
David E SaltInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, Scotland, United Kingdom.
Örjan CarlborgDepartment of Clinical Sciences, Division of Computational Genetics, Swedish University of Agricultural Sciences, Uppsala, Sweden.
University of Aberdeen · GBSwedish University of Agricultural Sciences · SE

Funding

The Genetic Basis of Natural Ionomic VariationR01GM078536 · NIGMS · PURDUE UNIVERSITY · PI GUERINOT, MARY LOU · 2007 to 2014
$2.6M
Biotechnology and Biological Sciences Research Council BB/L000113/1NIGMS NIH HHS 2R01GM078536NIGMS NIH HHS R01 GM078536
6 · The paper itself

Abstract

Genome-wide association (GWA) analyses have generally been used to detect individual loci contributing to the phenotypic diversity in a population by the effects of these loci on the trait mean. More rarely, loci have also been detected based on variance differences between genotypes. Several hypotheses have been proposed to explain the possible genetic mechanisms leading to such variance signals. However, little is known about what causes these signals, or whether this genetic variance-heterogeneity reflects mechanisms of importance in natural populations. Previously, we identified a variance-heterogeneity GWA (vGWA) signal for leaf molybdenum concentrations in Arabidopsis thaliana. Here, fine-mapping of this association reveals that the vGWA emerges from the effects of three independent genetic polymorphisms that all are in strong LD with the markers displaying the genetic variance-heterogeneity. By revealing the genetic architecture underlying this vGWA signal, we uncovered the molecular source of a significant amount of hidden additive genetic variation or "missing heritability". Two of the three polymorphisms underlying the genetic variance-heterogeneity are promoter variants for Molybdate transporter 1 (MOT1), and the third a variant located ~25 kb downstream of this gene. A fourth independent association was also detected ~600 kb upstream of MOT1. Use of a T-DNA knockout allele highlights Copper Transporter 6; COPT6 (AT2G26975) as a strong candidate gene for this association. Our results show that an extended LD across a complex locus including multiple functional alleles can lead to a variance-heterogeneity between genotypes in natural populations. Further, they provide novel insights into the genetic regulation of ion homeostasis in A. thaliana, and empirically confirm that variance-heterogeneity based GWA methods are a valuable tool to detect novel associations of biological importance in natural populations.

Indexed as

Genome-Wide Association StudyAllelesAnion Transport ProteinsArabidopsisArabidopsis ProteinsGenetic HeterogeneityGenome, PlantGenotypeMembrane Transport ProteinsMolybdenumPlant LeavesPolymorphism, Single NucleotideQuantitative Trait LociSLC31 ProteinsAnion Transport ProteinsArabidopsis ProteinsCOPT6 protein, ArabidopsisMembrane Transport ProteinsMolybdenumMOT1 protein, ArabidopsisSLC31 Proteins

Identifiers

PMID26599497
PMCPMC4657900
OpenAlexW2181239459

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.