Evidence map›Paper›PMID 26393419›Full record

ArticleeLife2015

A novel GSK3-regulated APC:Axin interaction regulates Wnt signaling by driving a catalytic cycle of efficient βcatenin destruction.

Mira I Pronobis, Nasser M Rusan, Mark Peifer

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

72 citing papers in PubMed, 108 citations in OpenAlex.

  1. Article
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  8. Review
  9. Review
  10. Wnt signalosomes: What we know that we do not know.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  11. Article
  12. Review
  13. Review
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  15. Review
  16. Article
  17. Review
  18. To condense or not to condense: Wnt regulation by centrosome-nucleated biomolecular condensates.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. Article
  20. Superresolution microscopy localizes endogenous Dvl2 to Wnt signaling-responsive biomolecular condensates.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article

12 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

3 authors at 2 institutions in 1 country.

Mira I PronobisCurriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, United States.
Nasser M RusanCell Biology and Physiology Center, National Heart, Lung, and Blood Institute, Bethesda, United States.
Mark PeiferCurriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill, Chapel Hill, United States.
University of North Carolina at Chapel Hill · USNational Heart Lung and Blood Institute · US

Funding

Regulation of Centrosome Asymmetry in Stem CellsZIAHL006126 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI RUSAN, NASSER · 2011 to 2025
$19.4M
Cell adhesion, signal transduction and cytoskeletal regulation in DrosophilaR01GM047857 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PEIFER, MARK A. · 1992 to 2016
$5.2M
A model system to study the tumor suppressor APCR01GM067236 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PEIFER, MARK A. · 2002 to 2015
$2.8M
Howard Hughes Medical InstituteIntramural NIH HHS ZIA HL006126NIGMS NIH HHS R01 GM047857NIGMS NIH HHS R01 GM067236NIGMS NIH HHS R01 GM47857
6 · The paper itself

Abstract

APC, a key negative regulator of Wnt signaling in development and oncogenesis, acts in the destruction complex with the scaffold Axin and the kinases GSK3 and CK1 to target βcatenin for destruction. Despite 20 years of research, APC's mechanistic function remains mysterious. We used FRAP, super-resolution microscopy, functional tests in mammalian cells and flies, and other approaches to define APC's mechanistic role in the active destruction complex when Wnt signaling is off. Our data suggest APC plays two roles: (1) APC promotes efficient Axin multimerization through one known and one novel APC:Axin interaction site, and (2) GSK3 acts through APC motifs R2 and B to regulate APC:Axin interactions, promoting high-throughput of βcatenin to destruction. We propose a new dynamic model of how the destruction complex regulates Wnt signaling and how this goes wrong in cancer, providing insights into how this multiprotein signaling complex is assembled and functions via multivalent interactions.

Indexed as

Protein MultimerizationWnt Signaling PathwayAdenomatous Polyposis Coli ProteinAnimalsAxin Proteinbeta CateninCell LineDrosophilaGlycogen Synthase Kinase 3HumansMicroscopy, FluorescenceProtein Interaction MappingProteolysisAdenomatous Polyposis Coli ProteinAxin Proteinbeta CateninGlycogen Synthase Kinase 3APCAxinbeta-catenincell biologyD. melanogasterhumanhuman biologymedicineWnt signaling

Identifiers

PMID26393419
PMCPMC4568445
OpenAlexW2185657910

What OpenQuestion holds

Textmetadata
LicenceCC0
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.