Evidence map›Paper›PMID 35864192›Full record

ArticleNature genetics2022

Hijacking of transcriptional condensates by endogenous retroviruses.

Vahid Asimi, Abhishek Sampath Kumar, Henri Niskanen, Christina Riemenschneider, Sara Hetzel, Julian Naderi, Nina Fasching, Niko Popitsch, Manyu Du, Helene Kretzmer and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Nature genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
15.8field-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

64 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 4 institutions in 3 countries.

Vahid Asimi *Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Abhishek Sampath Kumar *Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Henri Niskanen *Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Christina Riemenschneider *Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Sara HetzelDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.ORCID http://orcid.org/0000-0002-4783-3814
Julian NaderiDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Nina FaschingInstitute of Molecular Biotechnology (IMBA), Vienna BioCenter (VBC), Vienna, Austria.
Niko PopitschInstitute of Molecular Biotechnology (IMBA), Vienna BioCenter (VBC), Vienna, Austria.
Manyu DuDepartment of Physics, Massachusetts Institute of Technology (MIT), Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-5737-3578
Helene KretzmerDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Zachary D SmithBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Raha WeigertDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Maria WaltherDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Sainath MamdeDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
David MeierhoferMax Planck Institute for Molecular Genetics, Mass Spectrometry Facility, Berlin, Germany.
Lars WittlerDepartment of Developmental Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.
René BuschowMicroscopy Core Facility, Max Planck Institute for Molecular Genetics, Berlin, Germany.ORCID http://orcid.org/0000-0002-9800-2578
Bernd TimmermannSequencing Core Facility, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Ibrahim I CisseDepartment of Physics, Massachusetts Institute of Technology (MIT), Cambridge, MA, USA.
Stefan L AmeresInstitute of Molecular Biotechnology (IMBA), Vienna BioCenter (VBC), Vienna, Austria.
Alexander MeissnerDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.ORCID http://orcid.org/0000-0001-8646-7469
Denes HniszDepartment of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany. hnisz@molgen.mpg.de.ORCID http://orcid.org/0000-0002-6256-1693
Max Planck Institute for Molecular Genetics · DEInstitute of Molecular Biotechnology · ATBroad Institute · USMax Planck Institute of Immunobiology and Epigenetics · DE

Funding

Center for Cell CircuitsP50HG006193 · NHGRI · BROAD INSTITUTE, INC. · PI REGEV, AVIV · 2011 to 2015
$15.6M
Nuclear Organization and Dynamics of Mediator and RNA Polymerase II in Living Stem CellsR01GM134734 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GORE, JEFF · 2019 to 2022
$1.2M
NHGRI NIH HHS P50 HG006193NIGMS NIH HHS R01 GM134734
6 · The paper itself

Abstract

Most endogenous retroviruses (ERVs) in mammals are incapable of retrotransposition; therefore, why ERV derepression is associated with lethality during early development has been a mystery. Here, we report that rapid and selective degradation of the heterochromatin adapter protein TRIM28 triggers dissociation of transcriptional condensates from loci encoding super-enhancer (SE)-driven pluripotency genes and their association with transcribed ERV loci in murine embryonic stem cells. Knockdown of ERV RNAs or forced expression of SE-enriched transcription factors rescued condensate localization at SEs in TRIM28-degraded cells. In a biochemical reconstitution system, ERV RNA facilitated partitioning of RNA polymerase II and the Mediator coactivator into phase-separated droplets. In TRIM28 knockout mouse embryos, single-cell RNA-seq analysis revealed specific depletion of pluripotent lineages. We propose that coding and noncoding nascent RNAs, including those produced by retrotransposons, may facilitate 'hijacking' of transcriptional condensates in various developmental and disease contexts.

Indexed as

Endogenous RetrovirusesAnimalsEmbryonic Stem CellsHeterochromatinMammalsMiceNuclear BodiesRetroelementsHeterochromatinRetroelements

Identifiers

PMID35864192
PMCPMC9355880
OpenAlexW4286497619

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.