Evidence map›Paper›PMID 19657694›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society

A framework for detecting and characterizing genetic background-dependent imprinting effects.

Jason B Wolf, James M Cheverud

Open access · greenAbstract read
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

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  9. Bayesian mapping of genome-wide epistatic imprinted loci for quantitative traits.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2012
    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

2 authors at 2 institutions in 2 countries.

Jason B WolfFaculty of Life Sciences, University of Manchester, Manchester M139PT, UK. jason@evolutionarygenetics.org
James M Cheverud
University of Manchester · GBWashington University in St. Louis · US

Funding

A Mouse Model For Complex Human DiseasesR24RR015116 · NCRR · WASHINGTON UNIVERSITY · PI CHEVERUD, JAMES M · 2001 to 2009
$2.6M
Genetics Basis of Dietary Obesity in MiceR01DK055736 · NIDDK · WASHINGTON UNIVERSITY · PI CHEVERUD, JAMES M · 2000 to 2009
$2.1M
GENETIC BASIS OF DIETARY OBESITY IN MICER56DK055736 · NIDDK · WASHINGTON UNIVERSITY · PI CHEVERUD, JAMES M · 2010 to 2010
$354k
Biotechnology and Biological Sciences Research Council BB/C516936/1NCRR NIH HHS R24 RR015116NIDDK NIH HHS R01 DK055736NIDDK NIH HHS R56 DK055736
6 · The paper itself

Abstract

Genomic imprinting, where the effects of alleles depend on their parent-of-origin, can be an important component of the genetic architecture of complex traits. Although there has been a rapidly increasing number of studies of genetic architecture that have examined imprinting effects, none have examined whether imprinting effects depend on genetic background. Such effects are critical for the evolution of genomic imprinting because they allow the imprinting state of a locus to evolve as a function of genetic background. Here we develop a two-locus model of epistasis that includes epistatic interactions involving imprinting effects and apply this model to scan the mouse genome for loci that modulate the imprinting effects of quantitative trait loci (QTL). The inclusion of imprinting leads to nine orthogonal forms of epistasis, five of which do not appear in the usual two-locus decomposition of epistasis. Each form represents a change in the imprinting status of one locus across different classes of genotypes at the other locus. Our genome scan identified two different locus pairs that show complex patterns of epistasis, where the imprinting effect at one locus changes across genetic backgrounds at the other locus. Thus, our model provides a framework for the detection of genetic background-dependent imprinting effects that should provide insights into the background dependence and evolution of genomic imprinting. Our application of the model to a genome scan supports this assertion by identifying pairs of loci that show reciprocal changes in their imprinting status as the background provided by the other locus changes.

Indexed as

Epistasis, GeneticGenomic ImprintingQuantitative Trait LociAnimalsFemaleGenomeInbreedingMaleMiceMice, Inbred StrainsModels, GeneticPedigree

Identifiers

PMID19657694
PMCPMC2975584
OpenAlexW1975777966

What OpenQuestion holds

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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.