Evidence map›Paper›PMID 30270482›Full record

ArticleStem cells (Dayton, Ohio)2018

Histone Acetyltransferase KAT2A Stabilizes Pluripotency with Control of Transcriptional Heterogeneity.

Naomi Moris, Shlomit Edri, Denis Seyres, Rashmi Kulkarni, Ana Filipa Domingues, Tina Balayo, Mattia Frontini, Cristina Pina

Abstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Contributions of transcriptional noise to leukaemia evolution: KAT2A as a case-study.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Identification of HPV16-p16Epigenetics · 2021
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. MicroRNAs organize intrinsic variation into stem cell states.Proceedings of the National Academy of Sciences of the United States of America · 2020
    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

8 authors.

Naomi MorisDepartment of Genetics, University of Cambridge, Cambridge, United Kingdom.
Shlomit EdriDepartment of Genetics, University of Cambridge, Cambridge, United Kingdom.
Denis SeyresDepartment of Haematology, University of Cambridge, Cambridge, United Kingdom.
Rashmi KulkarniDepartment of Haematology, University of Cambridge, Cambridge, United Kingdom.
Ana Filipa DominguesDepartment of Haematology, University of Cambridge, Cambridge, United Kingdom.
Tina BalayoDepartment of Genetics, University of Cambridge, Cambridge, United Kingdom.
Mattia FrontiniDepartment of Haematology, University of Cambridge, Cambridge, United Kingdom.
Cristina PinaDepartment of Haematology, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-2575-6301

Funding

Biotechnology and Biological Sciences Research CouncilBritish Heart Foundation RE/13/6/30180British Heart Foundation Cambridge Centre of Excellence RE/13/6/30180
6 · The paper itself

Abstract

Cell fate transitions in mammalian stem cell systems have often been associated with transcriptional heterogeneity; however, existing data have failed to establish a functional or mechanistic link between the two phenomena. Experiments in unicellular organisms support the notion that transcriptional heterogeneity can be used to facilitate adaptability to environmental changes and have identified conserved chromatin-associated factors that modulate levels of transcriptional noise. Herein, we show destabilization of pluripotency-associated gene regulatory networks through increased transcriptional heterogeneity of mouse embryonic stem cells in which paradigmatic histone acetyl-transferase, and candidate noise modulator, Kat2a (yeast orthologue Gcn5), have been inhibited. Functionally, network destabilization associates with reduced pluripotency and accelerated mesendodermal differentiation, with increased probability of transitions into lineage commitment. Thus, we show evidence of a relationship between transcriptional heterogeneity and cell fate transitions through manipulation of the histone acetylation landscape of mouse embryonic stem cells, suggesting a general principle that could be exploited in other normal and malignant stem cell fate transitions. Stem Cells 2018;36:1828-11.

Indexed as

AnimalsCell DifferentiationGenetic HeterogeneityHistone AcetyltransferasesHumansMicep300-CBP-Associated FactorPluripotent Stem CellsHistone AcetyltransferasesKAT2A protein, humanp300-CBP-Associated FactorEmbryonic stem cellsEpigeneticsGene expression pluripotency

Identifiers

PMID30270482
PMCPMC6334525

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Registered trials

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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.