Evidence map›Paper›PMID 25453760›Full record

ArticleMolecular cell2014

A negative feedback loop of transcription factors specifies alternative dendritic cell chromatin States.

Chamutal Bornstein, Deborah Winter, Zohar Barnett-Itzhaki, Eyal David, Sabah Kadri, Manuel Garber, Ido Amit

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2014. 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
2.5field-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

36 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. A lncRNA identifieseLife · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  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

7 authors at 3 institutions in 2 countries.

Chamutal BornsteinDepartment of Immunology, Weizmann Institute, Rehovot 76100, Israel.
Deborah WinterDepartment of Immunology, Weizmann Institute, Rehovot 76100, Israel.
Zohar Barnett-ItzhakiDepartment of Immunology, Weizmann Institute, Rehovot 76100, Israel.
Eyal DavidDepartment of Immunology, Weizmann Institute, Rehovot 76100, Israel.
Sabah KadriBroad Institute, 7 Cambridge Center, Cambridge, MA 02142, USA.
Manuel GarberProgram in Bioinformatics and Integrative Biology and Program in Molecular Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Ido AmitDepartment of Immunology, Weizmann Institute, Rehovot 76100, Israel. Electronic address: ido.amit@weizmann.ac.il.
Weizmann Institute of Science · ILBroad Institute · USUniversity of Massachusetts Chan Medical School · US

Funding

Center for Cell CircuitsP50HG006193 · NHGRI · BROAD INSTITUTE, INC. · PI REGEV, AVIV · 2011 to 2015
$15.6M
NHGRI NIH HHS 1P50HG006193NHGRI NIH HHS P50 HG006193
6 · The paper itself

Abstract

During hematopoiesis, cells originating from the same stem cell reservoir differentiate into distinct cell types. The mechanisms enabling common progenitors to differentiate into alternative cell fates are not fully understood. Here, we identify cell-fate-determining transcription factors (TFs) governing dendritic cell (DC) development by annotating the enhancer landscapes of the DC lineage. Combining these analyses with detailed overexpression, knockdown, and ChIP-Seq studies, we show that Irf8 functions as a plasmacytoid DC epigenetic and fate-determining TF, regulating massive, cell-specific chromatin changes in thousands of pDC enhancers. Importantly, Irf8 forms a negative feedback loop with Cebpb, a monocyte-derived DC epigenetic fate-determining TF. We show that using this circuit logic, a pulse of TF expression can stably define epigenetic and transcriptional states, regardless of the microenvironment. More broadly, our study proposes a general paradigm that allows closely related cells with a similar set of signal-dependent factors to generate differential and persistent enhancer landscapes.

Indexed as

Enhancer Elements, GeneticCCAAT-Enhancer-Binding Protein-betaChromatinDendritic CellsEpigenesis, GeneticFeedback, PhysiologicalHEK293 CellsHumansInterferon Regulatory Factor-8Interferon Regulatory FactorsProtein BindingTranscriptomeCCAAT-Enhancer-Binding Protein-betaCEBPB protein, humanChromatinInterferon Regulatory Factor-8Interferon Regulatory Factors

Identifiers

PMID25453760
PMCPMC4412443
OpenAlexW2007706803

What OpenQuestion holds

Textmetadata
LicenceTDM
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.