Evidence map›Paper›PMID 34645785›Full record

ArticleCell death & disease2021

p53 isoforms differentially impact on the POLι dependent DNA damage tolerance pathway.

Yitian Guo, Melanie Rall-Scharpf, Jean-Christophe Bourdon, Lisa Wiesmüller, Stephanie Biber

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. p53 Dysregulation in Breast Cancer: Insights on Mutations in theInternational journal of molecular sciences · 2023
    Article
  10. Article
  11. 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

5 authors at 2 institutions in 2 countries.

Yitian GuoDepartment of Obstetrics and Gynecology, Ulm University, Ulm, 89075, Germany.ORCID http://orcid.org/0000-0001-7926-4057
Melanie Rall-ScharpfDepartment of Obstetrics and Gynecology, Ulm University, Ulm, 89075, Germany.ORCID http://orcid.org/0000-0003-2991-5223
Jean-Christophe BourdonJacqui Wood Cancer Centre, School of Medicine, University of Dundee, Dundee, UK.ORCID http://orcid.org/0000-0003-4623-9386
Lisa Wiesmüller *Department of Obstetrics and Gynecology, Ulm University, Ulm, 89075, Germany. lisa.wiesmueller@uni-ulm.de.ORCID http://orcid.org/0000-0002-2397-5041
Stephanie Biber *Department of Obstetrics and Gynecology, Ulm University, Ulm, 89075, Germany. stephanie.biber@gmx.de.ORCID http://orcid.org/0000-0002-7403-484X
Universität Ulm · DEUniversity of Dundee · GB

Funding

China Scholarship Council (CSC) scholarship to Y.G.Deutsche Forschungsgemeinschaft (German Research Foundation) Research Training Group 2544Deutsche Krebshilfe (German Cancer Aid) Priority Program 'Translational Oncology' 70112504
6 · The paper itself

Abstract

The recently discovered p53-dependent DNA damage tolerance (DDT) pathway relies on its biochemical activities in DNA-binding, oligomerization, as well as complex formation with the translesion synthesis (TLS) polymerase iota (POLι). These p53-POLι complexes slow down nascent DNA synthesis for safe, homology-directed bypass of DNA replication barriers. In this study, we demonstrate that the alternative p53-isoforms p53β, p53γ, Δ40p53α, Δ133p53α, and Δ160p53α differentially affect this p53-POLι-dependent DDT pathway originally described for canonical p53α. We show that the C-terminal isoforms p53β and p53γ, comprising a truncated oligomerization domain (OD), bind PCNA. Conversely, N-terminally truncated isoforms have a reduced capacity to engage in this interaction. Regardless of the specific loss of biochemical activities required for this DDT pathway, all alternative isoforms were impaired in promoting POLι recruitment to PCNA in the chromatin and in decelerating DNA replication under conditions of enforced replication stress after Mitomycin C (MMC) treatment. Consistent with this, all alternative p53-isoforms no longer stimulated recombination, i.e., bypass of endogenous replication barriers. Different from the other isoforms, Δ133p53α and Δ160p53α caused a severe DNA replication problem, namely fork stalling even in untreated cells. Co-expression of each alternative p53-isoform together with p53α exacerbated the DDT pathway defects, unveiling impaired POLι recruitment and replication deceleration already under unperturbed conditions. Such an inhibitory effect on p53α was particularly pronounced in cells co-expressing Δ133p53α or Δ160p53α. Notably, this effect became evident after the expression of the isoforms in tumor cells, as well as after the knockdown of endogenous isoforms in human hematopoietic stem and progenitor cells. In summary, mimicking the situation found to be associated with many cancer types and stem cells, i.e., co-expression of alternative p53-isoforms with p53α, carved out interference with p53α functions in the p53-POLι-dependent DDT pathway.

Indexed as

DNA DamageDNA-Directed DNA PolymeraseDNA Polymerase iotaDNA ReplicationHumansK562 CellsMitomycinModels, BiologicalProliferating Cell Nuclear AntigenProtein BindingProtein IsoformsProtein MultimerizationRecombination, GeneticSubcellular FractionsTumor Suppressor Protein p53UbiquitinationDNA-Directed DNA PolymeraseDNA Polymerase iotaMitomycinPOLI protein, humanProliferating Cell Nuclear AntigenProtein IsoformsTumor Suppressor Protein p53

Identifiers

PMID34645785
PMCPMC8514551
OpenAlexW3205054410

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.