Evidence map›Paper›PMID 24371809›Full record

ArticleStem cell reports2013

Identification of transcription factors for lineage-specific ESC differentiation.

Kohei Yamamizu, Yulan Piao, Alexei A Sharov, Veronika Zsiros, Hong Yu, Kazu Nakazawa, David Schlessinger, Minoru S H Ko

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

49 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. The Role of FoxG1 in the Inner Ear.Frontiers in cell and developmental biology · 2020
    Review
  20. 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

8 authors at 3 institutions in 2 countries.

Kohei YamamizuLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Yulan PiaoLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Alexei A SharovLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Veronika ZsirosUnit on Genetics of Cognition and Behavior, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.
Hong YuLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Kazu NakazawaUnit on Genetics of Cognition and Behavior, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.
David SchlessingerLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Minoru S H KoLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA ; Department of Systems Medicine, Sakaguchi Laboratory, Keio University School of Medicine, Tokyo 160-8582, Japan ; Japan Science and Technology Agency, CREST, Tokyo160-8582, Japan.
National Institutes of Health · USNational Institute of Mental Health · USNational Institute on Aging · US

Funding

Systematic analysis of gene regulatory networksZIAAG000656 · NIA · NATIONAL INSTITUTE ON AGING · PI SCHLESSINGER, DAVID · 2009 to 2016
$3.9M
6 · The paper itself

Abstract

A network of transcription factors (TFs) determines cell identity, but identity can be altered by overexpressing a combination of TFs. However, choosing and verifying combinations of TFs for specific cell differentiation have been daunting due to the large number of possible combinations of ∼2,000 TFs. Here, we report the identification of individual TFs for lineage-specific cell differentiation based on the correlation matrix of global gene expression profiles. The overexpression of identified TFs-Myod1, Mef2c, Esx1, Foxa1, Hnf4a, Gata2, Gata3, Myc, Elf5, Irf2, Elf1, Sfpi1, Ets1, Smad7, Nr2f1, Sox11, Dmrt1, Sox9, Foxg1, Sox2, or Ascl1-can direct efficient, specific, and rapid differentiation into myocytes, hepatocytes, blood cells, and neurons. Furthermore, transfection of synthetic mRNAs of TFs generates their appropriate target cells. These results demonstrate both the utility of this approach to identify potent TFs for cell differentiation, and the unanticipated capacity of single TFs directly guides differentiation to specific lineage fates.

Indexed as

AnimalsBlood CellsCell DifferentiationCell LineCell LineageEmbryonic Stem CellsGene Expression ProfilingGene Expression RegulationHepatocytesMiceMuscle CellsNeuronsRNA, MessengerTranscription FactorsRNA, MessengerTranscription Factors

Identifiers

PMID24371809
PMCPMC3871400
OpenAlexW2047771164

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.