Evidence map›Paper›PMID 19187253›Full record

ArticleEvolution; international journal of organic evolution2009

Relative contribution of additive, dominance, and imprinting effects to phenotypic variation in body size and growth between divergent selection lines of mice.

Reinmar Hager, James M Cheverud, Jason B Wolf

Abstract read
In one paragraph

Article in Evolution; international journal of organic evolution, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Bayesian mapping of genome-wide epistatic imprinted loci for quantitative traits.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2012
    Article
  8. Article
  9. Article
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  18. Article
  19. Metabolic syndrome components in murine models.Endocrine, metabolic & immune disorders drug targets · 2010
    Review
  20. A framework for detecting and characterizing genetic background-dependent imprinting effects.Mammalian genome : official journal of the International Mammalian Genome Society
    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.

Reinmar HagerThe University of Manchester, Manchester M13 9PT, UK. reinmar.hager@cantab.net
James M Cheverud
Jason B Wolf

Funding

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/C516936/1NIDDK NIH HHS DK055736NIDDK NIH HHS R01 DK055736NIDDK NIH HHS R56 DK055736
6 · The paper itself

Abstract

Epigenetic effects attributed to genomic imprinting are increasingly recognized as an important source of variation in quantitative traits. However, little is known about their relative contribution to phenotypic variation compared to those of additive and dominance effects, and almost nothing about their role in phenotypic evolution. Here we address these questions by investigating the relative contribution of additive, dominance, and imprinting effects of quantitative trait loci (QTL) to variation in "early" and "late" body weight in an intercross of mice selected for divergent adult body weight. We identified 18 loci on 13 chromosomes; additive effects accounted for most of the phenotypic variation throughout development, and imprinting effects were always small. Genetic effects on early weight showed more dominance, less additive, and, surprisingly, less imprinting variation than that of late weight. The predominance of additivity of QTL effects on body weight follows the expectation that additive effects account for the evolutionary divergence between selection lines. We hypothesize that the appearance of more imprinting effects on late body weight may be a consequence of divergent selection on adult body weight, which may have indirectly selected for alleles showing partial imprinting effects due to their associated additive effects, highlighting a potential role of genomic imprinting in the response to selection.

Indexed as

Genomic ImprintingPhenotypeSelection, GeneticAnimalsBiological EvolutionBody SizeBody WeightEpigenesis, GeneticFemaleGenetic VariationGenotypeGrowthMaleMiceMice, Inbred StrainsModels, Genetic

Identifiers

PMID19187253
PMCPMC3846273

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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.