Evidence map›Paper›PMID 23246434›Full record

ArticleMolecular cell2013

Latent regulatory potential of human-specific repetitive elements.

Michelle C Ward, Michael D Wilson, Nuno L Barbosa-Morais, Dominic Schmidt, Rory Stark, Qun Pan, Petra C Schwalie, Suraj Menon, Margus Lukk, Stephen Watt and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
10.5field-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

45 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Epigenomic insights into common human disease pathology.Cellular and molecular life sciences : CMLS · 2024
    Review
  4. Article
  5. Human Endogenous Retroviruses in Diseases.Sub-cellular biochemistry · 2023
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Humanising the mouse genome piece by piece.Nature communications · 2019
    Review
  16. Escape From X-Chromosome Inactivation: An Evolutionary Perspective.Frontiers in cell and developmental biology · 2019
    Review
  17. Mobile elements contribute to the uniqueness of human genome with 15,000 human-specific insertions and 14 Mbp sequence increase.DNA research : an international journal for rapid publication of reports on genes and genomes · 2018
    Article
  18. Article
  19. Article
  20. 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

16 authors at 4 institutions in 1 country.

Michelle C WardUniversity of Cambridge, Cancer Research UK-Cambridge Institute, Cambridge CB2 0RE, UK.
Michael D Wilson
Nuno L Barbosa-Morais
Dominic Schmidt
Rory Stark
Qun Pan
Petra C Schwalie
Suraj Menon
Margus Lukk
Stephen Watt
David Thybert
Claudia Kutter
Kristina Kirschner
Paul Flicek
Benjamin J Blencowe
Duncan T Odom
University of Cambridge · GBCancer Research UK · GBWellcome Trust · GBEuropean Bioinformatics Institute · GB

Funding

Cancer Research UK 15603Cancer Research UK A15603CIHREuropean Research Council 202218Wellcome TrustWellcome Trust WT062023Wellcome Trust WT098051
6 · The paper itself

Abstract

At least half of the human genome is derived from repetitive elements, which are often lineage specific and silenced by a variety of genetic and epigenetic mechanisms. Using a transchromosomic mouse strain that transmits an almost complete single copy of human chromosome 21 via the female germline, we show that a heterologous regulatory environment can transcriptionally activate transposon-derived human regulatory regions. In the mouse nucleus, hundreds of locations on human chromosome 21 newly associate with activating histone modifications in both somatic and germline tissues, and influence the gene expression of nearby transcripts. These regions are enriched with primate and human lineage-specific transposable elements, and their activation corresponds to changes in DNA methylation at CpG dinucleotides. This study reveals the latent regulatory potential of the repetitive human genome and illustrates the species specificity of mechanisms that control it.

Indexed as

DNA Transposable ElementsGene SilencingTranscriptional ActivationAnimalsChromosomes, Human, Pair 21DNA MethylationFemaleHistonesHumansKidneyLiverMaleMiceMice, Inbred C57BLOrgan SpecificityProtein BindingDNA Transposable ElementsHistonesTranscription Factors

Identifiers

PMID23246434
PMCPMC3560060
OpenAlexW1991360753

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.