Evidence map›Paper›PMID 28591649›Full record

ArticleStem cell reports2017

Activation of Lineage Regulators and Transposable Elements across a Pluripotent Spectrum.

Jamie A Hackett, Toshihiro Kobayashi, Sabine Dietmann, M Azim Surani

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. 3'-tRNA Fragments Target Domesticated LTR-Retrotransposons.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Transposons disrupt genomic stability and trigger cancers.Frontiers in cellular and infection microbiology · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Article
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  13. Article
  14. Loss ofLife science alliance · 2021
    Article
  15. Article
  16. Article
  17. 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

4 authors at 2 institutions in 2 countries.

Jamie A HackettWellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK; European Molecular Biology Laboratory (EMBL) - Monterotondo, via Ramarini 32, 00015, Rome, Italy.
Toshihiro KobayashiWellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK.
Sabine DietmannWellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK.
M Azim SuraniWellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK. Electronic address: a.surani@gurdon.cam.ac.uk.
University of Cambridge · GBWellcome/Cancer Research UK Gurdon Institute · GB

Funding

Cancer Research UK C6946/A14492Wellcome Trust 092096Wellcome Trust 096738
6 · The paper itself

Abstract

Embryonic stem cells (ESCs) are characterized by the pluripotent capacity to generate all embryonic lineages. Here, we show that ESCs can occupy a spectrum of distinct transcriptional and epigenetic states in response to varied extrinsic conditions. This spectrum broadly corresponds to a developmental continuum of pluripotency and is coupled with a gradient of increasing global DNA methylation. Each pluripotent state is linked with activation of distinct classes of transposable elements (TEs), which in turn influence ESCs through generating chimeric transcripts. Moreover, varied ESC culture parameters differentially license heterogeneous activation of master lineage regulators, including Sox1, Gata4, or Blimp1, and influence differentiation. Activation of Blimp1 is prevalent in 2i (without LIF) conditions, and marks a dynamic primordial germ cell (PGC)-like sub-state that is directly repressed by Klf4 downstream of LIF/STAT3 signaling. Thus, extrinsic cues establish a spectrum of pluripotent states, in part by modulating sub-populations, as well as directing the transcriptome, epigenome, and TE.

Indexed as

AnimalsCell DifferentiationCell LineCell LineageCRISPR-Cas SystemsDNA MethylationDNA Transposable ElementsGATA4 Transcription FactorKruppel-Like Factor 4Kruppel-Like Transcription FactorsLeukemia Inhibitory FactorMaleMiceMice, Inbred C57BLMouse Embryonic Stem CellsPluripotent Stem CellsDNA Transposable ElementsGata4 protein, mouseGATA4 Transcription FactorKlf4 protein, mouseKruppel-Like Factor 4Kruppel-Like Transcription FactorsLeukemia Inhibitory FactorPositive Regulatory Domain I-Binding Factor 1Prdm1 protein, mouseSox1 protein, mouseSOXB1 Transcription FactorsStat3 protein, mouseSTAT3 Transcription FactorTranscription Factorschimeric transcriptsDNA methylationembryonic stem cellheterogeneityimprintsKLF4PGCpluripotencySTAT3transposable element

Identifiers

PMID28591649
PMCPMC5470235
OpenAlexW2622954142

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.