Evidence map›Paper›PMID 34463728›Full record

ArticleDevelopment (Cambridge, England)2021

New mouse models for high resolution and live imaging of planar cell polarity proteins in vivo.

Lena P Basta, Michael Hill-Oliva, Sarah V Paramore, Rishabh Sharan, Audrey Goh, Abhishek Biswas, Marvin Cortez, Katherine A Little, Eszter Posfai, Danelle Devenport

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Lena P BastaDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544USA.ORCID 0000-0002-9756-9628
Michael Hill-OlivaDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544USA.ORCID 0000-0001-5581-7120
Sarah V ParamoreDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544USA.ORCID 0000-0001-9466-7380
Rishabh SharanDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544USA.ORCID 0000-0002-7579-7670
Audrey GohDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544USA.ORCID 0000-0003-3682-5189
Abhishek BiswasDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544USA.ORCID 0000-0002-8074-2543
Marvin CortezDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544USA.ORCID 0000-0002-9774-2128
Katherine A LittleDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544USA.ORCID 0000-0001-6993-5312
Eszter PosfaiDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544USA.ORCID 0000-0002-4871-6652
Danelle DevenportDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544USA.ORCID 0000-0002-5464-259X
Princeton University · US

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007388 · NIGMS · PRINCETON UNIVERSITY · PI CRISTEA, ILEANA M. · 1985 to 2022
$27.4M
Multiscale coordination of planar cell polarityR01AR066070 · NIAMS · PRINCETON UNIVERSITY · PI DEVENPORT, DANELLE N · 2015 to 2025
$5.7M
Cell-cycle control of cell polarity in epidermal patterning and differentiationR01AR068320 · NIAMS · PRINCETON UNIVERSITY · PI Danelle N Devenport · 2016 to 2026
$3.8M
Investigating the Establishment and Propagation of Planar Cell PolarityF31AR077407 · NIAMS · PRINCETON UNIVERSITY · PI BASTA, JELENA POPOVIC · 2020 to 2022
$138k
NIAMS NIH HHS F31 AR077407NIAMS NIH HHS R01 AR066070NIAMS NIH HHS R01 AR068320NIGMS NIH HHS T32 GM007388
6 · The paper itself

Abstract

The collective polarization of cellular structures and behaviors across a tissue plane is a near universal feature of epithelia known as planar cell polarity (PCP). This property is controlled by the core PCP pathway, which consists of highly conserved membrane-associated protein complexes that localize asymmetrically at cell junctions. Here, we introduce three new mouse models for investigating the localization and dynamics of transmembrane PCP proteins: Celsr1, Fz6 and Vangl2. Using the skin epidermis as a model, we characterize and verify the expression, localization and function of endogenously tagged Celsr1-3xGFP, Fz6-3xGFP and tdTomato-Vangl2 fusion proteins. Live imaging of Fz6-3xGFP in basal epidermal progenitors reveals that the polarity of the tissue is not fixed through time. Rather, asymmetry dynamically shifts during cell rearrangements and divisions, while global, average polarity of the tissue is preserved. We show using super-resolution STED imaging that Fz6-3xGFP and tdTomato-Vangl2 can be resolved, enabling us to observe their complex localization along junctions. We further explore PCP fusion protein localization in the trachea and neural tube, and discover new patterns of PCP expression and localization throughout the mouse embryo.

Indexed as

AnimalsBody PatterningCell PolarityDiagnostic ImagingEmbryo, MammalianEpidermal CellsEpidermisEpitheliumFrizzled ReceptorsMembrane ProteinsMiceMice, Inbred C57BLModels, AnimalNerve Tissue ProteinsNeural TubeReceptors, G-Protein-CoupledFrizzled ReceptorsMembrane ProteinsNerve Tissue ProteinsReceptors, G-Protein-CoupledCelsr1EpidermisFrizzled 6Planar cell polaritySuper resolutionVangl2

Identifiers

PMID34463728
PMCPMC8487645
OpenAlexW3196761297

What OpenQuestion holds

Textmetadata
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.