Evidence map›Paper›PMID 24755983›Full record

ReviewHeredity2014

The evolution of genomic imprinting: theories, predictions and empirical tests.

M M Patten, L Ross, J P Curley, D C Queller, R Bonduriansky, J B Wolf

Abstract readReview
In one paragraph

Review in Heredity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing 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

83 citing papers in PubMed.

  1. Review
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  13. Brinkmanship in intragenomic conflict.Proceedings. Biological sciences · 2025
    Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Parental dialectic: Epigenetic conversations in endosperm.Current opinion in plant biology · 2024
    Review
  19. Article
  20. Review

23 more citing papers are in PubMed but not listed here.

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.

M M PattenDepartment of Biology, Georgetown University, Washington, DC, USA.
L RossSchool of Biological Sciences, Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK.
J P CurleyPsychology Department, Columbia University, New York, NY, USA.
D C QuellerDepartment of Biology, Washington University, St Louis, MO, USA.
R BondurianskyEvolution & Ecology Research Centre and School of Biological, Earth and Environmental Sciences, University of New South Wales, Sydney, New South Wales, Australia.
J B WolfDepartment of Biology and Biochemistry, University of Bath, Bath, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/C516936/1
6 · The paper itself

Abstract

The epigenetic phenomenon of genomic imprinting has motivated the development of numerous theories for its evolutionary origins and genomic distribution. In this review, we examine the three theories that have best withstood theoretical and empirical scrutiny. These are: Haig and colleagues' kinship theory; Day and Bonduriansky's sexual antagonism theory; and Wolf and Hager's maternal-offspring coadaptation theory. These theories have fundamentally different perspectives on the adaptive significance of imprinting. The kinship theory views imprinting as a mechanism to change gene dosage, with imprinting evolving because of the differential effect that gene dosage has on the fitness of matrilineal and patrilineal relatives. The sexual antagonism and maternal-offspring coadaptation theories view genomic imprinting as a mechanism to modify the resemblance of an individual to its two parents, with imprinting evolving to increase the probability of expressing the fitter of the two alleles at a locus. In an effort to stimulate further empirical work on the topic, we carefully detail the logic and assumptions of all three theories, clarify the specific predictions of each and suggest tests to discriminate between these alternative theories for why particular genes are imprinted.

Indexed as

Biological EvolutionGenomic ImprintingAdaptation, BiologicalAnimalsFemaleGene DosageGene Expression RegulationHumansMaleModels, GeneticOrgan SpecificitySelection, Genetic

Identifiers

PMID24755983
PMCPMC4105453

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.