Evidence map›Paper›PMID 21746878›Full record

ArticleMolecular and cellular biology2011

Cooperative transcriptional activation by Klf4, Meis2, and Pbx1.

Glen A Bjerke, Cathy Hyman-Walsh, David Wotton

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

31 citing papers in PubMed, 50 citations in OpenAlex.

  1. Cell-Type-Specific Splicing of Transcription Regulators andThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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  2. Cell-type-specific splicing of transcription regulators andbioRxiv : the preprint server for biology · 2024
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  7. How "Neuronal" Are Human Skin Mast Cells?International journal of molecular sciences · 2022
    Review
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  9. PBX1: a key character of the hallmarks of cancer.Journal of molecular medicine (Berlin, Germany) · 2021
    Review
  10. Article
  11. Article
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  14. Review
  15. Article
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  18. Article
  19. Tgif1 and Tgif2 Repress Expression of the RabGAP Evi5l.Molecular and cellular biology · 2017
    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

3 authors at 1 institution in 1 country.

Glen A BjerkeDepartment of Biochemistry and Molecular Genetics and Center for Cell Signaling, University of Virginia, Charlottesville, Virginia 22908, USA.
Cathy Hyman-Walsh
David Wotton
University of Virginia · US

Funding

MOLECULAR ANALYSIS OF TRANSCRIPTIONAL REPRESSION BY TGIFR01HD039926 · NICHD · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI WOTTON, DAVID · 2001 to 2010
$2.5M
NICHD NIH HHS HD39926NICHD NIH HHS R01 HD039926
6 · The paper itself

Abstract

The Kruppel-like factor Klf4 is implicated in tumorigenesis and maintaining stem cell pluripotency, and Klf4 can both activate and repress gene expression. We show that the Pbx1 and Meis2 homeodomain proteins interact with Klf4 and can be recruited to DNA elements comprising a Klf4 site or GC box, with adjacent Meis and Pbx sites. Meis2d and Pbx1a activate expression of p15(Ink4a) and E-cadherin, dependent on the Meis2d transcriptional activation domain. In HepG2 cells, reducing expression of endogenous Meis2 or Pbx1 decreases p15 gene expression and increases the number of cells entering S phase. Although DNA binding by all three proteins contributes to full cooperative activation, the sequence requirements for binding by Meis2 and Pbx1 are variable. In the E-cadherin promoter, a Pbx-like site is required for full activation, whereas in the p15 promoter, the Klf4 site appears to play the major role. Through a bioinformatics search we identified additional genes with conserved binding sites for Klf4, Meis2, and Pbx1 and show that at least some of these genes can be activated cooperatively by Klf4 and Meis2/Pbx1. We suggest a model in which genes with Klf4 sites can be cooperatively activated by Meis2/Pbx1 and Klf4, dependent primarily on recruitment by Klf4. This provides a mechanism to modulate transcriptional regulation by the multifunctional Klf4 transcription factor.

Indexed as

Transcriptional ActivationAnimalsBase CompositionCadherinsCell CycleCell Line, TumorChlorocebus aethiopsChromatin ImmunoprecipitationCOS CellsCyclin-Dependent Kinase Inhibitor p15DNADNA-Binding ProteinsGene ExpressionGene Expression RegulationHeLa CellsHep G2 CellsCadherinsCyclin-Dependent Kinase Inhibitor p15DNADNA-Binding ProteinsHomeodomain ProteinsKLF4 protein, humanKlf4 protein, mouseKruppel-Like Factor 4Kruppel-Like Transcription FactorsMEIS2 protein, humanPBX1 protein, humanPre-B-Cell Leukemia Transcription Factor 1Proto-Oncogene ProteinsRNA, Small InterferingTranscription Factors

Identifiers

PMID21746878
PMCPMC3165729
OpenAlexW2113905214

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.