Evidence map›Paper›PMID 23085759›Full record

ArticleOncogene2013

The Cul4A-DDB1 E3 ubiquitin ligase complex represses p73 transcriptional activity.

M Malatesta, A Peschiaroli, E M Memmi, J Zhang, A Antonov, D R Green, N A Barlev, A V Garabadgiu, P Zhou, G Melino and 1 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 29 citations in OpenAlex.

  1. ABCC1 Is a ΔNp63 Target Gene Overexpressed in Squamous Cell Carcinoma.International journal of molecular sciences · 2024
    Article
  2. Article
  3. Review
  4. Review
  5. Mechanisms of Functional Pleiotropy of p73 in Cancer and Beyond.Frontiers in cell and developmental biology · 2021
    Review
  6. Review
  7. Review
  8. The emerging role for Cullin 4 family of E3 ligases in tumorigenesis.Biochimica et biophysica acta. Reviews on cancer · 2019
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. 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

11 authors at 5 institutions in 4 countries.

M MalatestaDepartment of Experimental Medicine and Surgery, University of Rome 'Tor Vergata', Rome, Italy.
A Peschiaroli
E M Memmi
J Zhang
A Antonov
D R Green
N A Barlev
A V Garabadgiu
P Zhou
G Melino
F Bernassola
University of Rome Tor Vergata · ITCornell University · USSt. Petersburg State Technological Institute · RUUniversity of Leicester · GBSt. Jude Children's Research Hospital · US

Funding

Regulation of Nucleotide Excision Repair by ProteolysisR01CA098210 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ZHOU, PENGBO · 2003 to 2013
$3.3M
Ubiquitin-Proteolytic Control of HOXA9 in LeukemogenesisR01CA118085 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ZHOU, PENGBO · 2006 to 2010
$1.5M
Medical Research Council MC_U132670600NCI NIH HHS 2R01CA098210NCI NIH HHS 5R01CA 118085
6 · The paper itself

Abstract

The Cullin4A (cul4A)-dependent ligase (CDL4A) E3 has been implicated in a variety of biological processes, including cell cycle progression and DNA damage response. Remarkably, CDL4A exerts its function through both proteolytic and non-proteolytic events. Here, we show that the p53 family member p73 is able to interact with the CDL4A complex through its direct binding to the receptor subunit DNA-binding protein 1 (DDB1). As a result, the CDL4A complex is able to monoubiquitylate p73. Modification of p73 by CDL4A-mediated ubiquitylation does not affect p73 protein stability, but negatively regulates p73-dependent transcriptional activity. Indeed, genetic or RNA interference-mediated depletion of DDB1 induces the expression of several p73 target genes in a p53-independent manner. In addition, by exploiting a bioinformatic approach, we found that elevated expression of Cul4A in human breast carcinomas is associated with repression of p73 target genes. In conclusion, our findings add a novel insight into the regulation of p73 by the CDL4A complex, through the inhibition of its transcriptional function.

Indexed as

Transcription, GeneticAnimalsBreast NeoplasmsCarcinomaCarrier ProteinsCell LineCullin ProteinsDNA-Binding ProteinsFemaleGene Expression Regulation, NeoplasticHEK293 CellsHumansMiceMultiprotein ComplexesNeoplasm ProteinsNuclear ProteinsCarrier ProteinsCUL4A protein, humanCullin ProteinsDDB1 protein, humanDNA-Binding ProteinsMultiprotein ComplexesNeoplasm ProteinsNuclear ProteinsRBX1 protein, humanTP53 protein, humanTP73 protein, humanTrp73 protein, mouseTumor Protein p73Tumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID23085759
OpenAlexW1972814805

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.