Evidence map›Paper›PMID 18777163›Full record

ArticleMolecular and cellular biochemistry2009

Notch signaling regulates the FOXP3 promoter through RBP-J- and Hes1-dependent mechanisms.

Hai-Feng Ou-Yang, Hong-Wei Zhang, Chang-Gui Wu, Ping Zhang, Jian Zhang, Jun-Chang Li, Li-Hong Hou, Fei He, Xin-Yu Ti, Li-Qiang Song and 4 more

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

27 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. FOXP3 expression is modulated by TGF‑β1/NOTCH1 pathway in human melanoma.International journal of molecular medicine · 2018
    Article
  5. Article
  6. Phosphatase and tensin homolog-β-catenin signaling modulates regulatory T cells and inflammatory responses in mouse liver ischemia/reperfusion injury.Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society · 2017
    Article
  7. Article
  8. Review
  9. Article
  10. Notch Signaling and Immune Regulation in Alloimmunity.Current transplantation reports · 2016
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. A Bone Anabolic Effect of RANKL in a Murine Model of Osteoporosis Mediated Through FoxP3+ CD8 T Cells.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2015
    Article
  16. Review
  17. Article
  18. Article
  19. 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

14 authors at 2 institutions in 1 country.

Hai-Feng Ou-YangDepartment of Respiratory Diseases, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Hong-Wei Zhang
Chang-Gui Wu
Ping Zhang
Jian Zhang
Jun-Chang Li
Li-Hong Hou
Fei He
Xin-Yu Ti
Li-Qiang Song
Su-Zhen Zhang
Lei Feng
Hao-Wen Qi
Hua Han
Air Force Medical University · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence has shown that Notch signaling modulates CD4(+)CD25(+) regulatory T-cells (Tregs). As transcription factor Foxp3 acts as a master molecule governing the development and function of Tregs, we investigated whether Notch signaling might directly regulate Foxp3 expression. Here, we provide evidence that Notch signaling can modulate the FOXP3 promoter through RBP-J- and Hes1-dependent mechanisms. A conserved RBP-J-binding site and N-box sites were identified within the FOXP3 promoter. We show that the Notch intracellular domain (NIC), the active form of Notch receptors, activates a reporter driven by the FOXP3 promoter. Dissection of the FOXP3 promoter revealed bipartite effects of the RBP-J-binding site and the N-boxes: the RBP-J-binding site positively, while the N-boxes negatively regulated the FOXP3 promoter activity. Moreover, in freshly isolated Tregs, NIC-RBP-J complex is bound to the FOXP3 promoter in Tregs. Our results suggest that Notch signaling might be involved in the development and function of Tregs through regulating Foxp3 expression.

Indexed as

Forkhead Transcription FactorsGene Expression RegulationPromoter Regions, GeneticAnimalsBase SequenceBasic Helix-Loop-Helix ProteinsCD4-Positive T-LymphocytesGenes, ReporterHeLa CellsHomeodomain ProteinsHumansImmunoglobulin J Recombination Signal Sequence-Binding ProteinJurkat CellsMiceMolecular Sequence DataMutagenesis, Site-DirectedBasic Helix-Loop-Helix ProteinsForkhead Transcription FactorsFoxp3 protein, mouseHes1 protein, mouseHomeodomain ProteinsImmunoglobulin J Recombination Signal Sequence-Binding ProteinRbpj protein, mouseReceptors, NotchTranscription Factor HES-1

Identifiers

PMID18777163
OpenAlexW2007401120

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.