Evidence map›Paper›PMID 12773395›Full record

ArticleThe EMBO journal2003

p53 represses RNA polymerase III transcription by targeting TBP and inhibiting promoter occupancy by TFIIIB.

Diane Crighton, Annette Woiwode, Cheng Zhang, Nihar Mandavia, Jennifer P Morton, Lorna J Warnock, Jo Milner, Robert J White, Deborah L Johnson

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

84 citing papers in PubMed, 141 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Activation of P53 pathway contributes toProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. RNA Polymerases I and III in development and disease.Seminars in cell & developmental biology · 2023
    Review
  11. Article
  12. Article
  13. tRNA dysregulation and disease.Nature reviews. Genetics · 2022
    Review
  14. Article
  15. Article
  16. Autophagy and apoptosis cascade: which is more prominent in neuronal death?Cellular and molecular life sciences : CMLS · 2021
    Review
  17. Review
  18. Article
  19. tRNAJournal of clinical laboratory analysis · 2021
    Article
  20. Article

24 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Diane CrightonInstitute of Biomedical and Life Sciences, Division of Biochemistry and Molecular Biology, Davidson Building, University of Glasgow, Glasgow G12 8QQ, UK.
Annette Woiwode
Cheng Zhang
Nihar Mandavia
Jennifer P Morton
Lorna J Warnock
Jo Milner
Robert J White
Deborah L Johnson
University of Glasgow · GB

Funding

TATA-binding protein, a novel target of EGFR signalingR01CA074138 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JOHNSON, DEBORAH L. · 1997 to 2015
$3.6M
NCI NIH HHS CA74138NCI NIH HHS R01 CA074138
6 · The paper itself

Abstract

The tumor suppressor p53 is a transcription factor that controls cellular growth and proliferation. p53 targets include RNA polymerase (pol) III-dependent genes encoding untranslated RNAs such as tRNA and 5S rRNA. These genes are repressed through interaction of p53 with TFIIIB, a TATA-binding protein (TBP)-containing factor. Although many studies have shown that p53 binds to TBP, the significance of this interaction has remained elusive. Here we demonstrate that the TBP-p53 interaction is of functional importance for regulating RNA pol III-transcribed genes. Unlike RNA pol II-dependent promoter repression, overexpressing TBP can reverse inhibition of tRNA gene transcription by p53. p53 does not disrupt the direct interaction between the TFIIIB subunits TBP and Brf1, but prevents the association of Brf1 complexes with TFIIIC2 and RNA pol III. Using chromatin immunoprecipitation assays, we found that TFIIIB occupancy on tRNA genes markedly decreases following p53 induction, whereas binding of TFIIIC2 to these genes is unaffected. Together our results support the idea that p53 represses RNA pol III transcription through direct interactions with TBP, preventing promoter occupancy by TFIIIB.

Indexed as

AnimalsBase SequenceBinding SitesDNA, NeoplasmGene ExpressionGenes, p53HeLa CellsHumansIn Vitro TechniquesMiceMice, KnockoutPromoter Regions, GeneticProtein BindingRNA Polymerase IIISaccharomyces cerevisiae ProteinsTATA-Binding Protein Associated FactorsBRF1 protein, humanBRF1 protein, S cerevisiaeDNA, NeoplasmRNA Polymerase IIISaccharomyces cerevisiae ProteinsTATA-Binding Protein Associated FactorsTATA-Box Binding ProteinTranscription Factors, TFIIITranscription Factor TFIIIBTranscription Factor TFIIICTumor Suppressor Protein p53

Identifiers

PMID12773395
PMCPMC156762
OpenAlexW2141902279

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.