Evidence map›Paper›PMID 31697683›Full record

ArticlePLoS genetics2019

Role of α-Catenin and its mechanosensing properties in regulating Hippo/YAP-dependent tissue growth.

Ritu Sarpal, Victoria Yan, Lidia Kazakova, Luka Sheppard, Jessica C Yu, Rodrigo Fernandez-Gonzalez, Ulrich Tepass

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.8field-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

28 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Mechanobiology of the Hippo-YAP Signaling Network.Cold Spring Harbor perspectives in biology · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Cortical tension promotes Kibra degradation via Par-1.Molecular biology of the cell · 2024
    Article
  11. Turn-On Protein Switches for Controlling Actin Binding in Cells.bioRxiv : the preprint server for biology · 2023
    Article
  12. Article
  13. Article
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  15. Article
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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

7 authors at 1 institution in 1 country.

Ritu SarpalDepartment of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada.
Victoria YanDepartment of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0003-1982-9145
Lidia KazakovaDepartment of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0001-9963-9776
Luka SheppardDepartment of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0001-7311-6854
Jessica C YuInstitute of Biomaterials and Biomedical Engineering, University of Toronto, Toronto, Ontario, Canada.
Rodrigo Fernandez-GonzalezDepartment of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0003-0770-744X
Ulrich TepassDepartment of Cell and Systems Biology, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-7494-5942
University of Toronto · CA

Funding

CIHR PJT-153249
6 · The paper itself

Abstract

α-catenin is a key protein of adherens junctions (AJs) with mechanosensory properties. It also acts as a tumor suppressor that limits tissue growth. Here we analyzed the function of Drosophila α-Catenin (α-Cat) in growth regulation of the wing epithelium. We found that different α-Cat levels led to a differential activation of Hippo/Yorkie or JNK signaling causing tissue overgrowth or degeneration, respectively. α-Cat can modulate Yorkie-dependent tissue growth through recruitment of Ajuba, a negative regulator of Hippo signaling to AJs but also through a mechanism independent of Ajuba recruitment to AJs. Both mechanosensory regions of α-Cat, the M region and the actin-binding domain (ABD), contribute to growth regulation. Whereas M is dispensable for α-Cat function in the wing, individual M domains (M1, M2, M3) have opposing effects on growth regulation. In particular, M1 limits Ajuba recruitment. Loss of M1 causes Ajuba hyper-recruitment to AJs, promoting tissue-tension independent overgrowth. Although M1 binds Vinculin, Vinculin is not responsible for this effect. Moreover, disruption of mechanosensing of the α-Cat ABD affects tissue growth, with enhanced actin interactions stabilizing junctions and leading to tissue overgrowth. Together, our findings indicate that α-Cat acts through multiple mechanisms to control tissue growth, including regulation of AJ stability, mechanosensitive Ajuba recruitment, and dynamic direct F-actin interactions.

Indexed as

Actin CytoskeletonActinsAdherens Junctionsalpha CateninAnimalsCell DeathCytoskeletonDrosophila melanogasterDrosophila ProteinsEpitheliumHippo KinasesIntracellular Signaling Peptides and ProteinsLIM Domain ProteinsMAP Kinase Signaling SystemMechanotransduction, CellularNuclear ProteinsActinsalpha CateninDrosophila ProteinsHippo Kinaseshpo protein, DrosophilaIntracellular Signaling Peptides and Proteinsjub protein, DrosophilaLIM Domain ProteinsNuclear ProteinsProtein Serine-Threonine KinasesTrans-ActivatorsVinculinYAP-Signaling ProteinsYki protein, Drosophila

Identifiers

PMID31697683
PMCPMC6863567
OpenAlexW2985074328

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.