Evidence map›Paper›PMID 41279358›Full record

ArticlebioRxiv : the preprint server for biology2025

WNK kinase regulates plasma membrane levels of the WNT inhibitor RNF43: A WNK-RNF43 circuit regulates WNT signal suppression.

Gabriele Colozza, Ingrid Jordens, Eric Sosa, Jeongmin Ha, Szu-Hsien Sam Wu, Katherina Tavernini, Andrea Català-Bordes, Fiona Farnhammer, Noelia Urbán, Madelon M Maurice and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Gabriele ColozzaDepartment of Biology, Unit of Cell and Developmental Biology, University of Pisa, S.S. 12 Abetone e Brennero 4, 56127 Pisa, Italy.ORCID 0000-0003-4517-3389
Ingrid JordensOncode Institute and Centre for Molecular Medicine, University Medical Centre Utrecht, Utrecht, Netherlands.
Eric SosaDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.ORCID 0000-0001-5965-3477
Jeongmin HaCenter for Genome Engineering, Institute for Basic Science, Daejeon 34126, Republic of Korea.
Szu-Hsien Sam WuInstitute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna Biocenter Campus (VBC), Dr. Bohr Gasse 3, 1030 Vienna, Austria.
Katherina TaverniniInstitute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna Biocenter Campus (VBC), Dr. Bohr Gasse 3, 1030 Vienna, Austria.
Andrea Català-BordesInstitute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna Biocenter Campus (VBC), Dr. Bohr Gasse 3, 1030 Vienna, Austria.
Fiona FarnhammerInstitute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna Biocenter Campus (VBC), Dr. Bohr Gasse 3, 1030 Vienna, Austria.
Noelia UrbánInstitute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna Biocenter Campus (VBC), Dr. Bohr Gasse 3, 1030 Vienna, Austria.ORCID 0000-0003-4813-9274
Madelon M MauriceOncode Institute and Centre for Molecular Medicine, University Medical Centre Utrecht, Utrecht, Netherlands.
Bon-Kyoung KooCenter for Genome Engineering, Institute for Basic Science, Daejeon 34126, Republic of Korea.

Funding

Medical Scientist Training ProgramT32GM149364 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Myles H. Akabas · 2023 to 2026
$7.5M
Defining the gene regulatory roles of non-coding variants in the pathogenesis of autismF31MH131380 · NIMH · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SOSA, ERIC ALEXANDER · 2022 to 2025
$213k
NIGMS NIH HHS T32 GM149364NIMH NIH HHS F31 MH131380
6 · The paper itself

Abstract

The E3 ubiquitin ligases RNF43 and ZNRF3 are key negative regulators of canonical WNT signaling, promoting turnover of the WNT receptors FRIZZLED and LRP5/6 at the plasma membrane. While their mechanism of action is well established, how RNF43/ZNRF3 themselves are regulated remains unclear. Here, we identify WNK kinases as novel upstream regulators of RNF43 through proximity labeling proteomics. Using gain- and loss-of-function approaches, we show that WNKs control RNF43 surface localization and thereby its ability to ubiquitinate and downregulate WNT receptors. Pharmacological inhibition of WNKs increases RNF43 membrane abundance and enhances WNT suppression - an effect abolished in RNF43/ZNRF3 double knockout cells and organoids. Mechanistically, WNK inhibition alters RNF43 trafficking and ubiquitination, revealing a role for WNKs in regulating its plasma membrane distribution. These findings define a new regulatory axis linking the pro-WNT activity of WNKs to RNF43/ZNRF3-mediated feedback inhibition. Targeting WNK now offers a novel therapeutic strategy to restore WNT pathway control in cancers with RSPO fusions or RNF43 mutations.

Identifiers

PMID41279358
PMCPMC12632470

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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.