Evidence map›Paper›PMID 24166496›Full record

ArticleOncogene2014

Prohibitin is required for transcriptional repression by the WT1-BASP1 complex.

E Toska, J Shandilya, S J Goodfellow, K F Medler, S G E Roberts

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

  1. Reactivation of the silencedProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. When PIPFrontiers in cell and developmental biology · 2022
    Review
  5. Cholesterol is required for transcriptional repression by BASP1.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Phospholipid regulation of the nuclear receptor superfamily.Advances in biological regulation · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. A role of WT1 in cell division and genomic stability.Cell cycle (Georgetown, Tex.) · 2015
    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

5 authors at 3 institutions in 2 countries.

E ToskaDepartment of Biological Sciences, University at Buffalo, Buffalo, NY, USA.
J ShandilyaDepartment of Biological Sciences, University at Buffalo, Buffalo, NY, USA.
S J GoodfellowWellcome Trust Centre for Gene Regulation, University of Dundee, Dundee, UK.
K F MedlerDepartment of Biological Sciences, University at Buffalo, Buffalo, NY, USA.
S G E Roberts1] Department of Biological Sciences, University at Buffalo, Buffalo, NY, USA [2] School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
University at Buffalo, State University of New York · USUniversity of Bristol · GBUniversity of Dundee · GB

Funding

Functional analysis of the WT1-BASP1 transcriptional repressor complexR01GM098609 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MEDLER, KATHRYN, ROBERTS, STEFAN · 2012 to 2015
$1.2M
Cancer Research UK A6630Cancer Research UK C1356/A6630NIGMS NIH HHS 1R01GM098609NIGMS NIH HHS R01 GM098609
6 · The paper itself

Abstract

The Wilms' tumor-1 protein (WT1) is a transcriptional regulator that can either activate or repress genes controlling cell growth, apoptosis and differentiation. The transcriptional corepressor BASP1 interacts with WT1 and mediates WT1's transcriptional repression activity. BASP1 is contained within large complexes, suggesting that it works in concert with other factors. Here we report that the transcriptional repressor prohibitin is part of the WT1-BASP1 transcriptional repression complex. Prohibitin interacts with BASP1, colocalizes with BASP1 in the nucleus, and is recruited to the promoter region of WT1 target genes to elicit BASP1-dependent transcriptional repression. We demonstrate that prohibitin and BASP1 cooperate to recruit the chromatin remodeling factor BRG1 to WT1-responsive promoters and that this results in the dissociation of CBP from the promoter region of WT1 target genes. As seen with BASP1, prohibitin can associate with phospholipids. We demonstrate that the recruitment of PIP2 and HDAC1 to WT1 target genes is also dependent on the concerted activity of BASP1 and prohibitin. Our findings provide new insights into the function of prohibitin in transcriptional regulation and uncover a BASP1-prohibitin complex that plays an essential role in the PIP2-dependent recruitment of chromatin remodeling activities to the promoter.

Indexed as

Transcription, GeneticCell Line, TumorCell NucleusChromatin Assembly and DisassemblyGene Expression Regulation, NeoplasticHeLa CellsHumansK562 CellsMCF-7 CellsMembrane ProteinsNerve Tissue ProteinsPhospholipidsProhibitinsPromoter Regions, GeneticRepressor ProteinsWT1 ProteinsBASP1 protein, humanMembrane ProteinsNerve Tissue ProteinsPhospholipidsProhibitinsRepressor ProteinsWT1 protein, humanWT1 Proteins

Identifiers

PMID24166496
PMCPMC4002674
OpenAlexW2149805582

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.