Evidence map›Paper›PMID 26561855›Full record

ArticlePLoS genetics2015

Enhancer Runaway and the Evolution of Diploid Gene Expression.

Frédéric Fyon, Aurélie Cailleau, Thomas Lenormand

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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Why recombination hotspots?PLoS genetics · 2026
    Review
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  8. The integrative biology of genetic dominance.Biological reviews of the Cambridge Philosophical Society · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Evolutionary mysteries in meiosis.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Review
  15. Molecular evolution: Regulatory runaways.Nature reviews. Genetics · 2016
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Frédéric FyonUMR 5175 CEFE, CNRS, Université Montpellier, Université P. Valéry, EPHE, Montpellier, France.
Aurélie CailleauUMR 5175 CEFE, CNRS, Université Montpellier, Université P. Valéry, EPHE, Montpellier, France.
Thomas LenormandUMR 5175 CEFE, CNRS, Université Montpellier, Université P. Valéry, EPHE, Montpellier, France.
Centre National de la Recherche Scientifique · FRUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence is mounting that the evolution of gene expression plays a major role in adaptation and speciation. Understanding the evolution of gene regulatory regions is indeed an essential step in linking genotypes and phenotypes and in understanding the molecular mechanisms underlying evolutionary change. The common view is that expression traits (protein folding, expression timing, tissue localization and concentration) are under natural selection at the individual level. Here, we use a theoretical approach to show that, in addition, in diploid organisms, enhancer strength (i.e., the ability of enhancers to activate transcription) may increase in a runaway process due to competition for expression between homologous enhancer alleles. These alleles may be viewed as self-promoting genetic elements, as they spread without conferring a benefit at the individual level. They gain a selective advantage by getting associated to better genetic backgrounds: deleterious mutations are more efficiently purged when linked to stronger enhancers. This process, which has been entirely overlooked so far, may help understand the observed overrepresentation of cis-acting regulatory changes in between-species phenotypic differences, and sheds a new light on investigating the contribution of gene expression evolution to adaptation.

Indexed as

Enhancer Elements, GeneticEvolution, MolecularModels, TheoreticalAllelesAnimalsDiploidyGene Expression RegulationSelection, GeneticSequence Deletion

Identifiers

PMID26561855
PMCPMC4642963
OpenAlexW2113871673

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.