Evidence map›Paper›PMID 38787854›Full record

ArticlePloS one2024

Regulation of YAP and Wnt signaling by the endosomal protein MAMDC4.

Christopher M Cox, Meng-Han Wu, Marco Padilla-Rodriguez, Isabella Blum, Samina Momtaz, Stefanie A T Mitchell, Jean M Wilson

Abstract read
In one paragraph

Article in PloS one, 2024. 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

7 authors.

Christopher M CoxDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States of America.ORCID 0009-0007-4543-7758
Meng-Han WuDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States of America.
Marco Padilla-RodriguezDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States of America.ORCID 0000-0003-1810-8573
Isabella BlumDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States of America.
Samina MomtazDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States of America.ORCID 0000-0002-1915-8727
Stefanie A T MitchellDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States of America.
Jean M WilsonDepartment of Cellular and Molecular Medicine, University of Arizona, Tucson, AZ, United States of America.

Funding

Autophagy and LC3-associated phagocytosis in intestinal epithelial cellsR01DK132074 · NIDDK · UNIVERSITY OF ARIZONA · PI Jean M Wilson · 2022 to 2026
$2.2M
Endocytic Regulation of Intestinal DevelopmentR01DK109701 · NIDDK · UNIVERSITY OF ARIZONA · PI WILSON, JEAN M · 2017 to 2021
$2.1M
NIDDK NIH HHS R01 DK109701NIDDK NIH HHS R01 DK132074
6 · The paper itself

Abstract

Maintenance of the intestinal epithelium requires constant self-renewal and regeneration. Tight regulation of proliferation and differentiation of intestinal stem cells within the crypt region is critical to maintaining homeostasis. The transcriptional co-factors β-catenin and YAP are required for proliferation during normal homeostasis as well as intestinal regeneration after injury: aberrant signaling activity results in over proliferation and tumorigenesis. Although both YAP and β-catenin activity are controlled along canonical pathways, it is becoming increasingly clear that non-canonical regulation of these transcriptional regulators plays a role in fine tuning their activity. We have shown previously that MAMDC4 (Endotubin, AEGP), an integral membrane protein present in endosomes, regulates both YAP and β-catenin activity in kidney epithelial cells and in the developing intestinal epithelium. Here we show that MAMDC4 interacts with members of the signalosome and mediates cross-talk between YAP and β-catenin. Interestingly, this cross-talk occurs through a non-canonical pathway involving interactions between AMOT:YAP and AMOT:β-catenin.

Indexed as

beta CateninEndosomesMembrane ProteinsTranscription FactorsWnt Signaling PathwayAdaptor Proteins, Signal TransducingAnimalsCell Cycle ProteinsGlycoproteinsHEK293 CellsHumansMicePhosphoproteinsProtein BindingYAP-Signaling ProteinsAdaptor Proteins, Signal Transducingbeta CateninCell Cycle ProteinsGlycoproteinsMAMDC4 protein, humanMembrane ProteinsPhosphoproteinsTranscription FactorsYAP-Signaling Proteins

Identifiers

PMID38787854
PMCPMC11125477

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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.