Evidence map›Paper›PMID 37294634›Full record

ArticleCell reports2023

Co-option of endogenous retroviruses through genetic escape from TRIM28 repression.

Rocio Enriquez-Gasca, Poppy A Gould, Hale Tunbak, Lucia Conde, Javier Herrero, Alexandra Chittka, Christine R Beck, Robert Gifford, Helen M Rowe

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
8.3field-weighted citation impact, top 3% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. KAP1 in antiviral immunity: dual roles in viral silencing and immune regulation.Frontiers in cellular and infection microbiology · 2025
    Review
  8. Article
  9. Article
  10. The Molecular Impacts of Retrotransposons in Development and Diseases.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Review
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

9 authors at 4 institutions in 2 countries.

Rocio Enriquez-GascaCentre for Immunobiology, Blizard Institute, Queen Mary University of London, London E1 2AT, UK. Electronic address: r.enriquez-gasca@qmul.ac.uk.
Poppy A GouldCentre for Immunobiology, Blizard Institute, Queen Mary University of London, London E1 2AT, UK.
Hale TunbakCentre for Immunobiology, Blizard Institute, Queen Mary University of London, London E1 2AT, UK.
Lucia CondeBill Lyons Informatics Centre, UCL Cancer Institute, London WC1E 6DD, UK.
Javier HerreroBill Lyons Informatics Centre, UCL Cancer Institute, London WC1E 6DD, UK.
Alexandra ChittkaCentre for Immunobiology, Blizard Institute, Queen Mary University of London, London E1 2AT, UK.
Christine R BeckDepartment of Genetics and Genome Sciences, University of Connecticut Health Center, The Jackson Laboratory for Genomic Medicine, Connecticut, JAX CT, Farmington, CT 06032, USA.
Robert GiffordMRC-University of Glasgow Centre for Virus Research, Glasgow G611QH, UK.
Helen M RoweCentre for Immunobiology, Blizard Institute, Queen Mary University of London, London E1 2AT, UK. Electronic address: h.rowe@qmul.ac.uk.
Queen Mary University of London · GBUniversity College London · GBJackson Laboratory · USMRC University of Glasgow Centre for Virus Research · GB

Funding

Repetitive sequences drive genome variation and plasticityR35GM133600 · NIGMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI Christine R Beck · 2019 to 2026
$3.0M
NIGMS NIH HHS R35 GM133600Wellcome TrustWellcome Trust 101200/Z/13/Z
6 · The paper itself

Abstract

Endogenous retroviruses (ERVs) have rewired host gene networks. To explore the origins of co-option, we employed an active murine ERV, IAPEz, and an embryonic stem cell (ESC) to neural progenitor cell (NPC) differentiation model. Transcriptional silencing via TRIM28 maps to a 190 bp sequence encoding the intracisternal A-type particle (IAP) signal peptide, which confers retrotransposition activity. A subset of "escapee" IAPs (∼15%) exhibits significant genetic divergence from this sequence. Canonical repressed IAPs succumb to a previously undocumented demarcation by H3K9me3 and H3K27me3 in NPCs. Escapee IAPs, in contrast, evade repression in both cell types, resulting in their transcriptional derepression, particularly in NPCs. We validate the enhancer function of a 47 bp sequence within the U3 region of the long terminal repeat (LTR) and show that escapee IAPs convey an activating effect on nearby neural genes. In sum, co-opted ERVs stem from genetic escapees that have lost vital sequences required for both TRIM28 restriction and autonomous retrotransposition.

Indexed as

Endogenous RetrovirusesTripartite Motif-Containing Protein 28AnimalsCell DifferentiationEmbryonic Stem CellsHistonesMiceTerminal Repeat SequencesHistonesTripartite Motif-Containing Protein 28cancerco-optionCP: Developmental biologyCP: Stem cell researchendogenous retrovirusesenhancersepigenetic silencingERVsexaptationIAPsintracisternal A-type particlesKRAB-zinc finger proteinsretrotranspositionretrotransposonTRIM28

Identifiers

PMID37294634
PMCPMC11980785
OpenAlexW4379741373

What OpenQuestion holds

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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.