Evidence map›Paper›PMID 21822054›Full record

ArticleCell cycle (Georgetown, Tex.)2011

tRNA genes protect a reporter gene from epigenetic silencing in mouse cells.

Thomas Ebersole, Jung-Hyun Kim, Alexander Samoshkin, Natalay Kouprina, Adam Pavlicek, Robert J White, Vladimir Larionov

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

40 citing papers in PubMed, 59 citations in OpenAlex.

  1. Rapid assembly of functional modules for generating human artificial chromosome constructs compatible with epigenetic centromere seeding.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Article
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  3. Viral and cellular insulators promote sustained HSV vector-mediated transgene expression in brain.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
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  9. Article
  10. Integrity of a heterochromatic domain ensured by its boundary elements.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  11. Article
  12. Experimental System to Study Instability of (CGG)Methods in molecular biology (Clifton, N.J.) · 2020
    Article
  13. Article
  14. Article
  15. Review
  16. Mechanisms of genetic instability caused by (CGG)Nature structural & molecular biology · 2018
    Article
  17. Article
  18. Article
  19. Article
  20. MIR retrotransposon sequences provide insulators to the human genome.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
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 1 institution in 1 country.

Thomas EbersoleLaboratory of Molecular Pharmacology, National Cancer Institute, Bethesda, MD, USA.
Jung-Hyun Kim
Alexander Samoshkin
Natalay Kouprina
Adam Pavlicek
Robert J White
Vladimir Larionov
National Cancer Institute · US

Funding

Study of hereditary prostate cancer and human artificial chromosomesZIABC010413 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LARIONOV, VLADIMIR · 2009 to 2025
$31.5M
Intramural NIH HHS
6 · The paper itself

Abstract

It is a well-established fact that the tRNA genes in yeast can function as chromatin barrier elements. However, so far there is no experimental evidence that tRNA and other Pol III-transcribed genes exhibit barrier activity in mammals. This study utilizes a recently developed reporter gene assay to test a set of Pol III-transcribed genes and gene clusters with variable promoter and intergenic regions for their ability to prevent heterochromatin-mediated reporter gene silencing in mouse cells. The results show that functional copies of mouse tRNA genes are effective barrier elements. The number of tRNA genes as well as their orientation influence barrier function. Furthermore, the DNA sequence composition of intervening and flanking regions affects barrier activity of tRNA genes. Barrier activity was maintained for much longer time when the intervening and flanking regions of tRNA genes were replaced by AT-rich sequences, suggesting a negative role of DNA methylation in the establishment of a functional barrier. Thus, our results suggest that tRNA genes are essential elements in establishment and maintenance of chromatin domain architecture in mammalian cells.

Indexed as

Epigenesis, GeneticGene SilencingAnimalsBase SequenceCell Line, TumorChromatin ImmunoprecipitationDNA MethylationDNA Polymerase IIIGenes, ReporterHeterochromatinMiceMultigene FamilyPromoter Regions, GeneticRNA, TransferSequence Analysis, DNATranscription, GeneticDNA Polymerase IIIHeterochromatinRNA, Transfer

Identifiers

PMID21822054
PMCPMC3219543
OpenAlexW2004852601

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.