Evidence map›Paper›PMID 25716787›Full record

ArticleProceedings. Biological sciences2015

Genome reorganization in F1 hybrids uncovers the role of retrotransposons in reproductive isolation.

Natacha Senerchia, François Felber, Christian Parisod

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings. Biological sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
12.9field-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

18 citing papers in PubMed, 46 citations in OpenAlex.

  1. Epigenetic signatures of migratory orientation in a songbird hybrid zone.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
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  9. Eukaryote hybrid genomes.PLoS genetics · 2019
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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

3 authors at 2 institutions in 1 country.

Natacha SenerchiaLaboratory of Evolutionary Botany, Institute of Biology, University of Neuchâtel, Rue Emile Argand 11, Neuchâtel 2000, Switzerland.
François FelberLaboratory of Evolutionary Botany, Institute of Biology, University of Neuchâtel, Rue Emile Argand 11, Neuchâtel 2000, Switzerland Musée et Jardins Botaniques Cantonaux, Lausanne 1007, Switzerland.
Christian ParisodLaboratory of Evolutionary Botany, Institute of Biology, University of Neuchâtel, Rue Emile Argand 11, Neuchâtel 2000, Switzerland christian.parisod@unine.ch.
University of Neuchâtel · CHMusée cantonal de zoologie de Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interspecific hybridization leads to new interactions among divergent genomes, revealing the nature of genetic incompatibilities having accumulated during and after the origin of species. Conflicts associated with misregulation of transposable elements (TEs) in hybrids expectedly result in their activation and genome-wide changes that may be key to species boundaries. Repetitive genomes of wild wheats have diverged under differential dynamics of specific long terminal repeat retrotransposons (LTR-RTs), offering unparalleled opportunities to address the underpinnings of plant genome reorganization by selfish sequences. Using reciprocal F1 hybrids between three Aegilops species, restructuring and epigenetic repatterning was assessed at random and LTR-RT sequences with amplified fragment length polymorphism and sequence-specific amplified polymorphisms as well as their methylation-sensitive counterparts, respectively. Asymmetrical reorganization of LTR-RT families predicted to cause conflicting interactions matched differential survival of F1 hybrids. Consistent with the genome shock model, increasing divergence of merged LTR-RTs yielded higher levels of changes in corresponding genome fractions and lead to repeated reorganization of LTR-RT sequences in F1 hybrids. Such non-random reorganization of hybrid genomes is coherent with the necessary repression of incompatible TE loci in support of hybrid viability and indicates that TE-driven genomic conflicts may represent an overlooked factor supporting reproductive isolation.

Indexed as

Genome, PlantReproductive IsolationRetroelementsTerminal Repeat SequencesAmplified Fragment Length Polymorphism AnalysisHybridization, GeneticPoaceaeRetroelementsAegilopsgenome shockhybridizationnucleocytoplasmic incompatibilitiesspeciationTEs

Identifiers

PMID25716787
PMCPMC4375867
OpenAlexW2035281648

What OpenQuestion holds

Textmetadata
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.