Evidence map›Paper›PMID 32238817›Full record

ArticleNature communications2020

The translational landscape of ground state pluripotency.

Yaser Atlasi, Seyed Mehdi Jafarnejad, Christos G Gkogkas, Michiel Vermeulen, Nahum Sonenberg, Hendrik G Stunnenberg

Abstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Science advances · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Translational control of stem cell function.Nature reviews. Molecular cell biology · 2021
    Review
  16. Article
  17. Article
  18. 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

6 authors.

Yaser Atlasi *Department of Molecular Biology, Faculty of Science, Radboud University, Radboud Institute for Molecular Life Sciences (RIMLS), 6525 GA, Nijmegen, The Netherlands. yaser.atlasi@ncmls.ru.nl.
Seyed Mehdi Jafarnejad *Patrick G. Johnston Centre for Cancer Research, Queen's University Belfast, Belfast, UK.
Christos G GkogkasCentre for Discovery Brain Sciences, and The Patrick Wild Centre, The University of Edinburgh, Edinburgh, UK.
Michiel VermeulenDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Oncode Institute, Radboud University Nijmegen, Nijmegen, The Netherlands.
Nahum SonenbergDepartment of Biochemistry and Goodman Cancer Research Centre, McGill University, Montreal, QC, H3A 1A3, Canada. nahum.sonenberg@mcgill.ca.
Hendrik G StunnenbergDepartment of Molecular Biology, Faculty of Science, Radboud University, Radboud Institute for Molecular Life Sciences (RIMLS), 6525 GA, Nijmegen, The Netherlands. h.stunnenberg@ncmls.ru.nl.ORCID http://orcid.org/0000-0002-0066-1576

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Translational control plays a central role in regulation of gene expression and can lead to significant divergence between mRNA- and protein-abundance. Here, we used genome-wide approaches combined with time-course analysis to measure the mRNA-abundance, mRNA-translation rate and protein expression during the transition of naïve-to-primed mouse embryonic stem cells (ESCs). We find that the ground state ESCs cultured with GSK3-, MEK-inhibitors and LIF (2iL) display higher ribosome density on a selective set of mRNAs. This set of mRNAs undergo strong translational buffering to maintain stable protein expression levels in 2iL-ESCs. Importantly, we show that the global alteration of cellular proteome during the transition of naïve-to-primed pluripotency is largely accompanied by transcriptional rewiring. Thus, we provide a comprehensive and detailed overview of the global changes in gene expression in different states of ESCs and dissect the relative contributions of mRNA-transcription, translation and regulation of protein stability in controlling protein abundance.

Indexed as

AnimalsEmbryonic Stem CellsGene Expression RegulationGlycogen Synthase Kinase 3Metabolic Networks and PathwaysMiceMouse Embryonic Stem CellsPolyribosomesProteomeRibosomesRNA, MessengerTranscriptomeGlycogen Synthase Kinase 3ProteomeRNA, Messenger

Identifiers

PMID32238817
PMCPMC7113317

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.