Evidence map›Paper›PMID 40377178›Full record

ArticleDevelopment (Cambridge, England)2025

Regulation of Hippo signaling and planar cell polarity via distinct regions of the Fat intracellular domain.

Cole R Julick, Nattapon Thanintorn, Hongtao Zhang, Yonit Tsatskis, Megan Glaeser, Yi Qu, Jannette Rusch, Helen McNeill

Abstract read
In one paragraph

Article in Development (Cambridge, England), 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

8 authors.

Cole R JulickDepartment of Developmental Biology, Washington University School of Medicine, St Louis, MO 63110, USA.ORCID 0009-0000-6078-0975
Nattapon ThanintornDepartment of Developmental Biology, Washington University School of Medicine, St Louis, MO 63110, USA.
Hongtao ZhangSchool of Life Sciences, Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, Shandong 266237, China.
Yonit TsatskisCell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.ORCID 0000-0003-2580-0728
Megan GlaeserDepartment of Developmental Biology, Washington University School of Medicine, St Louis, MO 63110, USA.
Yi QuLunenfeld-Tanenbaum Research Institute, Sinai Health Systems, Toronto, ON M5G 1X5, Canada.ORCID 0000-0002-1420-7753
Jannette RuschDepartment of Developmental Biology, Washington University School of Medicine, St Louis, MO 63110, USA.
Helen McNeillDepartment of Developmental Biology, Washington University School of Medicine, St Louis, MO 63110, USA.ORCID 0000-0003-1126-5154

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Dissecting Fat cadherin function in vivoR01GM138853 · NIGMS · WASHINGTON UNIVERSITY · PI MCNEILL, HELEN · 2020 to 2023
$1.8M
NCI NIH HHS P30 CA091842NIGMS NIH HHS R01 GM138853NIH HHS GM138853ANIH HHS P40 OD018537NIH HHS R01GM138853
6 · The paper itself

Abstract

The large Drosophila protocadherin Fat (Ft) is a receptor for signal transduction pathways that control growth (Hippo signaling), planar cell polarity (PCP), metabolism and the proximodistal patterning of appendages. The intracellular domain (ICD) of Ft is crucial in implementing its biological functions. Six regions of high conservation (named A-F) within the ICD have been identified, as well as distinct regions mediating Hippo pathway activity that have been functionally characterized via transgenic expression rescue assays. Here, we make targeted deletions of these highly conserved residues and the putative Hippo- and PCP-regulating domains of endogenous Ft using CRISPR/Cas9. Through transcriptomic, developmental and phenotypic analyses, we show that different regions of Ft contribute uniquely to chromatin dynamics, tissue morphogenesis, PCP and metabolic regulation. We also demonstrate that different regions of Ft regulate growth in opposite directions, with regions B and F promoting growth and region D inhibiting growth. Strikingly, conserved regions D and F are key regulators of the function of Ft in Hippo activity - exhibiting opposing effects on Hippo pathway modulation - and of the conserved regions, and D is the main regulator of PCP.

Indexed as

CadherinsCell PolarityDrosophila melanogasterDrosophila ProteinsIntracellular Signaling Peptides and ProteinsProtein Serine-Threonine KinasesSignal TransductionAnimalsCell Adhesion MoleculesGene Expression Regulation, DevelopmentalHippo KinasesHippo Signaling PathwayProtein DomainsCadherinsCell Adhesion MoleculesDrosophila Proteinsft protein, DrosophilaHippo Kinaseshpo protein, DrosophilaIntracellular Signaling Peptides and ProteinsProtein Serine-Threonine KinasesDrosophilaFatHippoPlanar cell polarity

Identifiers

PMID40377178
PMCPMC12188247

What OpenQuestion holds

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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.