Evidence map›Paper›PMID 27465027›Full record

ArticleThe Plant cell2016

Rapid Evolution of Genomic Imprinting in Two Species of the Brassicaceae.

Marcelinus R Hatorangan, Benjamin Laenen, Kim A Steige, Tanja Slotte, Claudia Köhler

Open access · greenAbstract read
In one paragraph

Article in The Plant cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
22.6field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 96 citations in OpenAlex.

  1. Pooled it
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  8. Review
  9. Parental dialectic: Epigenetic conversations in endosperm.Current opinion in plant biology · 2024
    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

5 authors at 3 institutions in 1 country.

Marcelinus R HatoranganDepartment of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences and Linnean Center for Plant Biology, 750 07 Uppsala, Sweden.
Benjamin LaenenDepartment of Ecology, Environment, and Plant Sciences, Science for Life Laboratory, Stockholm University, 114 18 Stockholm, Sweden.
Kim A SteigeDepartment of Ecology, Environment, and Plant Sciences, Science for Life Laboratory, Stockholm University, 114 18 Stockholm, Sweden Department of Ecology and Genetics, Evolutionary Biology Centre, Uppsala University, 75236 Uppsala, Sweden.
Tanja SlotteDepartment of Ecology, Environment, and Plant Sciences, Science for Life Laboratory, Stockholm University, 114 18 Stockholm, Sweden.
Claudia KöhlerDepartment of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences and Linnean Center for Plant Biology, 750 07 Uppsala, Sweden claudia.kohler@slu.se.ORCID 0000-0002-2619-4857
Stockholm University · SESwedish University of Agricultural Sciences · SEUppsala University · SE

Funding

European Research Council 280496
6 · The paper itself

Abstract

Genomic imprinting is an epigenetic phenomenon occurring in mammals and flowering plants that causes genes to adopt a parent-of-origin-specific mode of expression. While the imprinting status of genes is well conserved in mammals, clear estimates for the degree of conservation were lacking in plants. We therefore analyzed the genome-wide imprinting status of Capsella rubella, which shared a common recent ancestor with Arabidopsis thaliana ∼10 to 14 million years ago. However, only ∼14% of maternally expressed genes (MEGs) and ∼29% of paternally expressed genes (PEGs) in C. rubella were commonly imprinted in both species, revealing that genomic imprinting is a rapidly evolving phenomenon in plants. Nevertheless, conserved PEGs exhibited signs of selection, suggesting that a subset of imprinted genes play an important functional role and are therefore maintained in plants. Like in Arabidopsis, PEGs in C. rubella are frequently associated with the presence of transposable elements that preferentially belong to helitron and MuDR families. Our data further reveal that MEGs and PEGs differ in their targeting by 24-nucleotide small RNAs and asymmetric DNA methylation, suggesting different mechanisms establishing DNA methylation at MEGs and PEGs.

Indexed as

BrassicaceaeDNA MethylationDNA Transposable ElementsEvolution, MolecularGene Expression Regulation, PlantGenomic ImprintingPlant ProteinsDNA Transposable ElementsPlant Proteins

Identifiers

PMID27465027
PMCPMC5006707
OpenAlexW2503803182

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.