Evidence map›Paper›PMID 35228718›Full record

ReviewNature reviews. Molecular cell biology2022

Roles of transposable elements in the regulation of mammalian transcription.

Raquel Fueyo, Julius Judd, Cedric Feschotte, Joanna Wysocka

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Molecular cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 277 papers.

0numbers the graph read from it
0cells of the map it votes in
277citing papers in PubMed
100.2field-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

277 citing papers in PubMed, 451 citations in OpenAlex.

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  19. Transposable Element-Driven PIEZO Mutation Enhances Locust Flight in Plateau Hypoxia.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  20. The Encyclopedia of DNA Elements.bioRxiv : the preprint server for biology · 2026
    Article

217 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 3 institutions in 2 countries.

Raquel Fueyo *Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA.
Julius Judd *Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0002-4602-0205
Cedric FeschotteDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA. cf458@cornell.edu.ORCID http://orcid.org/0000-0002-8772-6976
Joanna WysockaDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA, USA. wysocka@stanford.edu.
Cornell University · USHoward Hughes Medical Institute · USStanford University · US

Funding

Regulatory Crosstalk Between Human Endogenous Retroviruses, HIV, and EBV, in LymphomaR01CA260691 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CESARMAN, ETHEL, NIXON, DOUGLAS F · 2021 to 2025
$5.8M
Genomic and Physiological Impact of Transposable Elements.R35GM122550 · NIGMS · CORNELL UNIVERSITY · PI Cedric Feschotte · 2017 to 2026
$4.4M
Uncovering fundamentals of gene regulation by enhancersR35GM131757 · NIGMS · STANFORD UNIVERSITY · PI Joanna Wysocka · 2019 to 2026
$3.1M
Connecting transposable elements and regulatory innovation using ENCODE dataU01HG009391 · NHGRI · WASHINGTON UNIVERSITY · PI COHEN, BARAK A, FESCHOTTE, CEDRIC · 2017 to 2021
$2.4M
Interrogating Enhancer Function and Cooperation by Systematic Perturbation of Transposable ElementsF31HG010820 · NHGRI · CORNELL UNIVERSITY · PI JUDD, JULIUS A. · 2019 to 2021
$107k
Howard Hughes Medical InstituteNCI NIH HHS R01 CA260691NHGRI NIH HHS F31 HG010820NHGRI NIH HHS U01 HG009391NIGMS NIH HHS R35 GM122550NIGMS NIH HHS R35 GM131757
6 · The paper itself

Abstract

Transposable elements (TEs) comprise about half of the mammalian genome. TEs often contain sequences capable of recruiting the host transcription machinery, which they use to express their own products and promote transposition. However, the regulatory sequences carried by TEs may affect host transcription long after the TEs have lost the ability to transpose. Recent advances in genome analysis and engineering have facilitated systematic interrogation of the regulatory activities of TEs. In this Review, we discuss diverse mechanisms by which TEs contribute to transcription regulation. Notably, TEs can donate enhancer and promoter sequences that influence the expression of host genes, modify 3D chromatin architecture and give rise to novel regulatory genes, including non-coding RNAs and transcription factors. We discuss how TEs spur regulatory evolution and facilitate the emergence of genetic novelties in mammalian physiology and development. By virtue of their repetitive and interspersed nature, TEs offer unique opportunities to dissect the effects of mutation and genomic context on the function and evolution of cis-regulatory elements. We argue that TE-centric studies hold the key to unlocking general principles of transcription regulation and evolution.

Indexed as

DNA Transposable ElementsRegulatory Sequences, Nucleic AcidAnimalsEvolution, MolecularGene Expression RegulationMammalsPromoter Regions, GeneticTranscription FactorsDNA Transposable ElementsTranscription Factors

Identifiers

PMID35228718
PMCPMC10470143
OpenAlexW4214672693

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.