Evidence map›Paper›PMID 25062919›Full record

ArticleGenome biology and evolution2014

Epigenetics and the evolution of Darwin's Finches.

Michael K Skinner, Carlos Gurerrero-Bosagna, M Muksitul Haque, Eric E Nilsson, Jennifer A H Koop, Sarah A Knutie, Dale H Clayton

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

59 citing papers in PubMed, 118 citations in OpenAlex.

  1. Review
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  15. How is epigenetics predicted to contribute to climate change adaptation? What evidence do we need?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Article
  16. Review
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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

7 authors at 4 institutions in 2 countries.

Michael K SkinnerCenter for Reproductive Biology, School of Biological Sciences, Washington State University skinner@wsu.edu.
Carlos Gurerrero-BosagnaCenter for Reproductive Biology, School of Biological Sciences, Washington State UniversityPresent address: Department of Physics, Biology and Chemistry (IFM), Linköping University, Sweden.
M Muksitul HaqueCenter for Reproductive Biology, School of Biological Sciences, Washington State University.
Eric E NilssonCenter for Reproductive Biology, School of Biological Sciences, Washington State University.
Jennifer A H KoopDepartment of Biology, University of UtahPresent address: Department of Ecology and Evolutionary Biology, University of Arizona, Tucson, AZ.
Sarah A KnutieDepartment of Biology, University of Utah.
Dale H ClaytonDepartment of Biology, University of Utah.
Washington State University · USUniversity of Utah · USLinköping University · SEUniversity of Arizona · US

Funding

POST DOCTORAL EXCELLENCE IN RESEARCH AND TEACHINGK12GM000708 · NIGMS · UNIVERSITY OF ARIZONA · PI STRAUSFELD, NICHOLAS J · 2000 to 2018
$21.5M
EPIGENETIC TRANSGENERATIONAL ENDOCRINE DISRUPTOR ACTIONSR01ES012974 · NIEHS · WASHINGTON STATE UNIVERSITY · PI SKINNER, MICHAEL K · 2005 to 2018
$4.6M
NIEHS NIH HHS R01 ES012974NIGMS NIH HHS K12 GM000708
6 · The paper itself

Abstract

The prevailing theory for the molecular basis of evolution involves genetic mutations that ultimately generate the heritable phenotypic variation on which natural selection acts. However, epigenetic transgenerational inheritance of phenotypic variation may also play an important role in evolutionary change. A growing number of studies have demonstrated the presence of epigenetic inheritance in a variety of different organisms that can persist for hundreds of generations. The possibility that epigenetic changes can accumulate over longer periods of evolutionary time has seldom been tested empirically. This study was designed to compare epigenetic changes among several closely related species of Darwin's finches, a well-known example of adaptive radiation. Erythrocyte DNA was obtained from five species of sympatric Darwin's finches that vary in phylogenetic relatedness. Genome-wide alterations in genetic mutations using copy number variation (CNV) were compared with epigenetic alterations associated with differential DNA methylation regions (epimutations). Epimutations were more common than genetic CNV mutations among the five species; furthermore, the number of epimutations increased monotonically with phylogenetic distance. Interestingly, the number of genetic CNV mutations did not consistently increase with phylogenetic distance. The number, chromosomal locations, regional clustering, and lack of overlap of epimutations and genetic mutations suggest that epigenetic changes are distinct and that they correlate with the evolutionary history of Darwin's finches. The potential functional significance of the epimutations was explored by comparing their locations on the genome to the location of evolutionarily important genes and cellular pathways in birds. Specific epimutations were associated with genes related to the bone morphogenic protein, toll receptor, and melanogenesis signaling pathways. Species-specific epimutations were significantly overrepresented in these pathways. As environmental factors are known to result in heritable changes in the epigenome, it is possible that epigenetic changes contribute to the molecular basis of the evolution of Darwin's finches.

Indexed as

Epigenesis, GeneticAnimalsDNA MethylationFinchesMutationPhylogenySelection, GeneticSignal Transductionadaptive radiationBMPcopy number variationDNA methylationepimutationsmelanogenesisphylogenytoll

Identifiers

PMID25062919
PMCPMC4159007
OpenAlexW2113157204

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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.