Evidence map›Paper›PMID 35867833›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Superresolution microscopy localizes endogenous Dvl2 to Wnt signaling-responsive biomolecular condensates.

Antonia Schubert, Oksana Voloshanenko, Franziska Ragaller, Philipp Gmach, Dominique Kranz, Christian Scheeder, Thilo Miersch, Matthias Schulz, Lorenz Trümper, Claudia Binder and 3 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  8. Wnt signalosomes: What we know that we do not know.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  9. Frizzled receptors: gatekeepers of Wnt signaling in development and disease.Frontiers in cell and developmental biology · 2025
    Review
  10. Article
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  12. Article
  13. Article
  14. Article
  15. Article
  16. The interplay between Wnt signaling pathways and microtubule dynamics.In vitro cellular & developmental biology. Animal · 2024
    Review
  17. Review
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

13 authors at 4 institutions in 1 country.

Antonia SchubertDivision of Signaling and Functional Genomics, German Cancer Research Center and Department of Cell and Molecular Biology, Heidelberg University and BioQuant, 69120 Heidelberg, Germany.ORCID 0000-0002-7455-5047
Oksana VoloshanenkoDivision of Signaling and Functional Genomics, German Cancer Research Center and Department of Cell and Molecular Biology, Heidelberg University and BioQuant, 69120 Heidelberg, Germany.ORCID 0000-0002-0673-3278
Franziska RagallerDivision of Signaling and Functional Genomics, German Cancer Research Center and Department of Cell and Molecular Biology, Heidelberg University and BioQuant, 69120 Heidelberg, Germany.ORCID 0000-0002-4148-262X
Philipp GmachDivision of Signaling and Functional Genomics, German Cancer Research Center and Department of Cell and Molecular Biology, Heidelberg University and BioQuant, 69120 Heidelberg, Germany.ORCID 0000-0002-5258-0321
Dominique KranzDivision of Signaling and Functional Genomics, German Cancer Research Center and Department of Cell and Molecular Biology, Heidelberg University and BioQuant, 69120 Heidelberg, Germany.ORCID 0000-0003-3604-7647
Christian ScheederDivision of Signaling and Functional Genomics, German Cancer Research Center and Department of Cell and Molecular Biology, Heidelberg University and BioQuant, 69120 Heidelberg, Germany.ORCID 0000-0003-1786-4916
Thilo MierschDivision of Signaling and Functional Genomics, German Cancer Research Center and Department of Cell and Molecular Biology, Heidelberg University and BioQuant, 69120 Heidelberg, Germany.
Matthias SchulzDepartment of Hematology and Medical Oncology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Lorenz TrümperDepartment of Hematology and Medical Oncology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Claudia BinderDepartment of Hematology and Medical Oncology, University Medical Center Göttingen, 37075 Göttingen, Germany.
Marko LampeAdvanced Light Microscopy Facility, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.ORCID 0000-0002-4510-9048
Ulrike EngelNikon Imaging Center, BioQuant and Centre for Organismal Studies, Heidelberg University, 69120 Heidelberg, Germany.ORCID 0000-0002-6953-6845
Michael BoutrosDivision of Signaling and Functional Genomics, German Cancer Research Center and Department of Cell and Molecular Biology, Heidelberg University and BioQuant, 69120 Heidelberg, Germany.ORCID 0000-0002-9458-817X
German Cancer Research Center · DEUniversitätsmedizin Göttingen · DEEuropean Molecular Biology Laboratory · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During organismal development, homeostasis, and disease, Dishevelled (Dvl) proteins act as key signaling factors in beta-catenin-dependent and beta-catenin-independent Wnt pathways. While their importance for signal transmission has been genetically demonstrated in many organisms, our mechanistic understanding is still limited. Previous studies using overexpressed proteins showed Dvl localization to large, punctate-like cytoplasmic structures that are dependent on its DIX domain. To study Dvl's role in Wnt signaling, we genome engineered an endogenously expressed Dvl2 protein tagged with an mEos3.2 fluorescent protein for superresolution imaging. First, we demonstrate the functionality and specificity of the fusion protein in beta-catenin-dependent and beta-catenin-independent signaling using multiple independent assays. We performed live-cell imaging of Dvl2 to analyze the dynamic formation of the supramolecular cytoplasmic Dvl2_mEos3.2 condensates. While overexpression of Dvl2_mEos3.2 mimics the previously reported formation of abundant large "puncta," supramolecular condensate formation at physiological protein levels is only observed in a subset of cells with approximately one per cell. We show that, in these condensates, Dvl2 colocalizes with Wnt pathway components at gamma-tubulin and CEP164-positive centrosomal structures and that the localization of Dvl2 to these condensates is Wnt dependent. Single-molecule localization microscopy using photoactivated localization microscopy (PALM) of mEos3.2 in combination with DNA-PAINT demonstrates the organization and repetitive patterns of these condensates in a cell cycle-dependent manner. Our results indicate that the localization of Dvl2 in supramolecular condensates is coordinated dynamically and dependent on cell state and Wnt signaling levels. Our study highlights the formation of endogenous and physiologically regulated biomolecular condensates in the Wnt pathways at single-molecule resolution.

Indexed as

Biomolecular CondensatesDishevelled ProteinsWnt ProteinsWnt Signaling Pathwaybeta CateninHumansMicroscopy, FluorescenceProtein Domainsbeta CateninDishevelled ProteinsDVL2 protein, humanWnt Proteinsbiomolecular condensatesCRISPRDishevelledsuperresolution microscopyWnt signaling

Identifiers

PMID35867833
PMCPMC9335300
OpenAlexW4286587382

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.