Evidence map›Paper›PMID 24019486›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Ets-1 facilitates nuclear entry of NFAT proteins and their recruitment to the IL-2 promoter.

Hsiao-Wei Tsao, Tzong-Shyuan Tai, William Tseng, Hui-Hsin Chang, Roland Grenningloh, Shi-Chuen Miaw, I-Cheng Ho

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. 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
2.1field-weighted citation impact, top 13% 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, 52 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. ETS1 Function in Leukemia and Lymphoma.Advances in experimental medicine and biology · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. SilencingAging · 2020
    Article
  19. Long Noncoding RNA-CERNA1 Stabilized Atherosclerotic Plaques in apolipoprotein EJournal of cardiovascular translational research · 2019
    Article
  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

7 authors at 3 institutions in 2 countries.

Hsiao-Wei TsaoGraduate Institute of Immunology, National Taiwan University College of Medicine, Taipei 10051, Taiwan.
Tzong-Shyuan Tai
William Tseng
Hui-Hsin Chang
Roland Grenningloh
Shi-Chuen Miaw
I-Cheng Ho
Brigham and Women's Hospital · USNational Taiwan University · TWVA Boston Healthcare System · US

Funding

Regulation of IL-2 expression by the transcription factor Ets-1R03AI081052 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI HO, I-CHENG · 2009 to 2010
$178k
NIAID NIH HHS AI081052NIAID NIH HHS R03 AI081052
6 · The paper itself

Abstract

E26 transformation-specific sequence 1 (Ets-1), the prototype of the ETS family of transcription factors, is critical for the expression of IL-2 by murine Th cells; however, its mechanism of action is still unclear. Here we show that Ets-1 is also essential for optimal production of IL-2 by primary human Th cells. Although Ets-1 negatively regulates the expression of Blimp1, a known suppressor of IL-2 expression, ablation of B lymphocyte-induced maturation protein 1 (Blimp1) does not rescue the expression of IL-2 by Ets-1-deficient Th cells. Instead, Ets-1 physically and functionally interacts with the nuclear factor of activated T-cells (NFAT) and is required for the recruitment of NFAT to the IL-2 promoter. In addition, Ets-1 is located in both the nucleus and cytoplasm of resting Th cells. Nuclear Ets-1 quickly exits the nucleus in response to calcium-dependent signals and competes with NFAT proteins for binding to protein components of noncoding RNA repressor of NFAT complex (NRON), which serves as a cytoplasmic trap for phosphorylated NFAT proteins. This nuclear exit of Ets-1 precedes rapid nuclear entry of NFAT and Ets-1 deficiency results in impaired nuclear entry, but not dephosphorylation, of NFAT proteins. Thus, Ets-1 promotes the expression of IL-2 by modulating the activity of NFAT.

Indexed as

Promoter Regions, GeneticAnimalsBase SequenceCalciumCell NucleusGene Knockout TechniquesHumansInterleukin-2MiceMolecular Sequence DataMultiprotein ComplexesNFATC Transcription FactorsPositive Regulatory Domain I-Binding Factor 1Protein BindingProtein TransportProto-Oncogene Protein c-ets-1CalciumETS1 protein, humanEts1 protein, mouseInterleukin-2Multiprotein ComplexesNFATC Transcription FactorsPositive Regulatory Domain I-Binding Factor 1Prdm1 protein, mouseProto-Oncogene Protein c-ets-1Transcription Factors

Identifiers

PMID24019486
PMCPMC3785780
OpenAlexW2002740312

What OpenQuestion holds

Textmetadata
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.