Evidence map›Paper›PMID 27242129›Full record

ArticleeLife2016

Hyperosmotic stress memory in Arabidopsis is mediated by distinct epigenetically labile sites in the genome and is restricted in the male germline by DNA glycosylase activity.

Anjar Wibowo, Claude Becker, Gianpiero Marconi, Julius Durr, Jonathan Price, Jorg Hagmann, Ranjith Papareddy, Hadi Putra, Jorge Kageyama, Jorg Becker and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 155 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
155citing papers in PubMed, 1 pooled it
80.2field-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

155 citing papers in PubMed, 1 synthesis or guideline pooled it, 364 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 4 countries.

Anjar Wibowo *School of Life Sciences, University of Warwick, Coventry, United Kingdom.
Claude Becker *Department of Molecular Biology, Max Planck Institute for Developmental Biology, Tübingen, Germany.ORCID http://orcid.org/0000-0003-3406-4670
Gianpiero MarconiSchool of Life Sciences, University of Warwick, Coventry, United Kingdom.ORCID http://orcid.org/0000-0003-2669-0399
Julius DurrSchool of Life Sciences, University of Warwick, Coventry, United Kingdom.
Jonathan PriceSchool of Life Sciences, University of Warwick, Coventry, United Kingdom.
Jorg HagmannDepartment of Molecular Biology, Max Planck Institute for Developmental Biology, Tübingen, Germany.
Ranjith PapareddySchool of Life Sciences, University of Warwick, Coventry, United Kingdom.
Hadi PutraSchool of Life Sciences, University of Warwick, Coventry, United Kingdom.
Jorge KageyamaDepartment of Molecular Biology, Max Planck Institute for Developmental Biology, Tübingen, Germany.
Jorg BeckerInstituto Gulbenkian de Ciencia, Oeiras, Portugal.
Detlef WeigelDepartment of Molecular Biology, Max Planck Institute for Developmental Biology, Tübingen, Germany.ORCID http://orcid.org/0000-0002-2114-7963
Jose Gutierrez-MarcosSchool of Life Sciences, University of Warwick, Coventry, United Kingdom.ORCID http://orcid.org/0000-0002-5441-9080
University of Warwick · GBMax Planck Institute for Developmental Biology · DEInstituto Gulbenkian de Ciência · PTUniversity of Perugia · IT

Funding

Biotechnology and Biological Sciences Research Council BB/F008082
6 · The paper itself

Abstract

Inducible epigenetic changes in eukaryotes are believed to enable rapid adaptation to environmental fluctuations. We have found distinct regions of the Arabidopsis genome that are susceptible to DNA (de)methylation in response to hyperosmotic stress. The stress-induced epigenetic changes are associated with conditionally heritable adaptive phenotypic stress responses. However, these stress responses are primarily transmitted to the next generation through the female lineage due to widespread DNA glycosylase activity in the male germline, and extensively reset in the absence of stress. Using the CNI1/ATL31 locus as an example, we demonstrate that epigenetically targeted sequences function as distantly-acting control elements of antisense long non-coding RNAs, which in turn regulate targeted gene expression in response to stress. Collectively, our findings reveal that plants use a highly dynamic maternal 'short-term stress memory' with which to respond to adverse external conditions. This transient memory relies on the DNA methylation machinery and associated transcriptional changes to extend the phenotypic plasticity accessible to the immediate offspring.

Indexed as

Gene Expression Regulation, PlantGenome, PlantInheritance PatternsOsmotic PressureArabidopsisArabidopsis ProteinsChromosome MappingDNA GlycosylasesDNA MethylationEpigenesis, GeneticGenetic LociGerm CellsSodium ChlorideStress, PhysiologicalArabidopsis ProteinsDNA GlycosylasesSodium Chlorideadaptationcomputational biologyenvironmentepigeneticevolutionary biologygenomics<i>a. thaliana</i>memorysystems biology

Identifiers

PMID27242129
PMCPMC4887212
OpenAlexW2415322025

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.