Evidence map›Paper›PMID 22346759›Full record

ArticlePLoS genetics2012

Gene expression and stress response mediated by the epigenetic regulation of a transposable element small RNA.

Andrea D McCue, Saivageethi Nuthikattu, Sarah H Reeder, R Keith Slotkin

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
29.0field-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

102 citing papers in PubMed, 217 citations in OpenAlex.

  1. Review
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  3. Review
  4. Review
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  9. Comprehensive in-silico characterization and expression pattern of calmodulin genes under various abiotic and biotic stresses in Indian mustard (Physiology and molecular biology of plants : an international journal of functional plant biology · 2025
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  10. Transposons disrupt genomic stability and trigger cancers.Frontiers in cellular and infection microbiology · 2025
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  12. OsALKBH9-mediated mPlant biotechnology journal · 2024
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  14. Review
  15. Article
  16. Phased secondary small interfering RNAs inNAR genomics and bioinformatics · 2023
    Article
  17. Article
  18. Review
  19. Article
  20. Article

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

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

4 authors at 1 institution in 1 country.

Andrea D McCueDepartment of Molecular Genetics, The Ohio State University, Columbus, Ohio, USA.
Saivageethi Nuthikattu
Sarah H Reeder
R Keith Slotkin
The Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epigenetic activity of transposable elements (TEs) can influence the regulation of genes; though, this regulation is confined to the genes, promoters, and enhancers that neighbor the TE. This local cis regulation of genes therefore limits the influence of the TE's epigenetic regulation on the genome. TE activity is suppressed by small RNAs, which also inhibit viruses and regulate the expression of genes. The production of TE heterochromatin-associated endogenous small interfering RNAs (siRNAs) in the reference plant Arabidopsis thaliana is mechanistically distinct from gene-regulating small RNAs, such as microRNAs or trans-acting siRNAs (tasiRNAs). Previous research identified a TE small RNA that potentially regulates the UBP1b mRNA, which encodes an RNA-binding protein involved in stress granule formation. We demonstrate that this siRNA, siRNA854, is under the same trans-generational epigenetic control as the Athila family LTR retrotransposons from which it is produced. The epigenetic activation of Athila elements results in a shift in small RNA processing pathways, and new 21-22 nucleotide versions of Athila siRNAs are produced by protein components normally not responsible for processing TE siRNAs. This processing results in siRNA854's incorporation into ARGONAUTE1 protein complexes in a similar fashion to gene-regulating tasiRNAs. We have used reporter transgenes to demonstrate that the UPB1b 3' untranslated region directly responds to the epigenetic status of Athila TEs and the accumulation of siRNA854. The regulation of the UPB1b 3' untranslated region occurs both on the post-transcriptional and translational levels when Athila TEs are epigenetically activated, and this regulation results in the phenocopy of the ubp1b mutant stress-sensitive phenotype. This demonstrates that a TE's epigenetic activity can modulate the host organism's stress response. In addition, the ability of this TE siRNA to regulate a gene's expression in trans blurs the lines between TE and gene-regulating small RNAs.

Indexed as

3' Untranslated RegionsArabidopsisArabidopsis ProteinsArgonaute ProteinsBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsEpigenesis, GeneticGene Expression RegulationGene Expression Regulation, PlantGene SilencingHumansMicroRNAsMutationOrgan SpecificityPlants, Genetically ModifiedPollen3' Untranslated RegionsAGO1 protein, ArabidopsisArabidopsis ProteinsArgonaute ProteinsBasic Helix-Loop-Helix ProteinsDDM1 protein, ArabidopsisDNA-Binding ProteinsMicroRNAsRetroelementsRNA, Small InterferingTranscription FactorsUPBEAT1 protein, Arabidopsis

Identifiers

PMID22346759
PMCPMC3276544
OpenAlexW2074137164

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.