Evidence map›Paper›PMID 40392971›Full record

ArticleThe FEBS journal2025

Extreme multivalency and a composite short linear motif facilitate PCNA-binding, localisation and abundance of p21 (CDKN1A).

Signe Simonsen, Fia B Larsen, Caroline K Søgaard, Nicolas Jonsson, Kresten Lindorff-Larsen, Per Bruheim, Marit Otterlei, Rasmus Hartmann-Petersen, Birthe B Kragelund

Abstract read
In one paragraph

Article in The FEBS journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
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  4. Biomolecular NMR assignments · 2025
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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.

Signe SimonsenStructural Biology and NMR Laboratory, Linderstrøm-Lang Centre for Protein Science, Department of Biology, University of Copenhagen, Denmark.ORCID https://orcid.org/0000-0003-0376-7488
Fia B LarsenREPIN, University of Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-6787-3672
Caroline K SøgaardDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Nicolas JonssonStructural Biology and NMR Laboratory, Linderstrøm-Lang Centre for Protein Science, Department of Biology, University of Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-7838-1814
Kresten Lindorff-LarsenStructural Biology and NMR Laboratory, Linderstrøm-Lang Centre for Protein Science, Department of Biology, University of Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-4750-6039
Per BruheimDepartment of Biotechnology and Food Science, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Marit OtterleiDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.ORCID https://orcid.org/0000-0002-5232-1186
Rasmus Hartmann-PetersenREPIN, University of Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-4155-7791
Birthe B KragelundStructural Biology and NMR Laboratory, Linderstrøm-Lang Centre for Protein Science, Department of Biology, University of Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-7454-1761

Funding

Carlsbergfondet CF21-0392Natur og Univers, Det Frie Forskningsråd 10.46540/2032-00007BNatur og Univers, Det Frie Forskningsråd 9040-00164BNovo Nordisk Fonden NNF-0061734Novo Nordisk Fonden NNF18OC0033926Novo Nordisk Fonden NNF18OC0033950Novo Nordisk Fonden NNF21OC007105Trond-Mohn StiftelsenVillum Fonden
6 · The paper itself

Abstract

Cyclin-dependent kinase inhibitor 1 (CDKN1A; also known as p21) promotes cell cycle arrest and regulates DNA replication and DNA repair by high-affinity binding to proliferating cell nuclear antigen (PCNA) using a C-terminal short linear motif (SLiM). High-affinity binding to PCNA is driven by positively charged flanking regions of the SLiM, but the molecular details of their interaction as well as their roles for other p21 functions are not known. Using biophysics to study the interaction between PCNA and p21 variants with different Lys/Arg compositions in the flanking regions, as well as using D-amino acids, we find that the flanking regions of p21 bind to PCNA likely through an interaction driven by complementary charges without specific contacts. Although the exact Lys/Arg composition of the p21 flanking regions is unimportant for high-affinity PCNA binding, these positions are conserved in p21 orthologs, implying a conserved biological function. Accordingly, in cell-based experiments, we find that, while the flanking regions affect p21 abundance, both the context and the Lys/Arg composition of the N-terminal flanking region are crucial for p21 nuclear localisation. Such integration of SLiMs into a composite SLiM may be a widespread phenomenon and complicates the separation of function and drug development.

Indexed as

Cyclin-Dependent Kinase Inhibitor p21Proliferating Cell Nuclear AntigenAmino Acid MotifsAmino Acid SequenceBinding SitesCell NucleusDNA ReplicationHumansProtein BindingCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21PCNA protein, humanProliferating Cell Nuclear AntigenchargesconservationdegronIDPIDRITCNLSpolyelectrolyte

Identifiers

PMID40392971
PMCPMC12366268

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Registered trials

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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.