Evidence map›Paper›PMID 22514277›Full record

ArticleThe Journal of biological chemistry2012

p53 basic C terminus regulates p53 functions through DNA binding modulation of subset of target genes.

Pierre-Jacques Hamard, Dana J Lukin, James J Manfredi

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

29 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. p53motifDB: integration of genomic information and tumour suppressor p53 binding motifs.Database : the journal of biological databases and curation · 2025
    Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. How p53 Molecules Solve the Target DNA Search Problem: A Review.International journal of molecular sciences · 2020
    Review
  12. Article
  13. The multiple mechanisms that regulate p53 activity and cell fate.Nature reviews. Molecular cell biology · 2019
    Review
  14. Transactivation domain of p53 regulates DNA repair and integrity in human iPS cells.American journal of physiology. Heart and circulatory physiology · 2018
    Article
  15. Article
  16. Article
  17. Article
  18. Mechanisms of transcriptional regulation by p53.Cell death and differentiation · 2018
    Review
  19. Article
  20. p16Molecular carcinogenesis · 2017
    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.

Pierre-Jacques HamardDepartment of Oncological Sciences, Mount Sinai School of Medicine, New York, New York 10029, USA.
Dana J Lukin
James J Manfredi
Icahn School of Medicine at Mount Sinai · US

Funding

PW1--A mediator of cell survival by NFKB and cell death by p53P01CA080058 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI AARONSON, STUART A · 2000 to 2016
$20.2M
NCI NIH HHS P01 CA080058
6 · The paper itself

Abstract

The p53 gene encodes a transcription factor that is composed of several functional domains: the N-terminal transactivation domain, the central sequence-specific DNA binding domain, the tetramerization domain, and the highly basic C-terminal regulatory domain (CTD). The p53 CTD is a nonspecific DNA binding domain that is subject to extensive post-translational modifications. However, the functional significance of the p53 CTD remains unclear. The role of this domain in the regulation of p53 functions is explored by comparing the activity of ectopically expressed wild-type (WT) p53 protein to that of a truncated mutant lacking the 24 terminal amino acids (Δ24). Using quantitative real time PCR and chromatin Immuno-Precipitation experiments, a p53 CTD deletion is shown to alter the p53-dependent induction of a subset of its target genes due to impaired specific DNA binding. Moreover, p53-induced growth arrest and apoptosis both require an intact p53 CTD. These data indicate that the p53 CTD is a positive regulator of p53 tumor suppressor functions.

Indexed as

Gene Expression RegulationAmino AcidsApoptosisBromodeoxyuridineCell LineCell LineageCell Line, TumorChromatin ImmunoprecipitationDNAHumansMicroscopy, FluorescencePlasmidsProtein BindingProtein Structure, TertiaryTranscription, GeneticTumor Suppressor Protein p53Amino AcidsBromodeoxyuridineDNATP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID22514277
PMCPMC3381199
OpenAlexW2128410594

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.