Evidence map›Paper›PMID 37774705›Full record

ArticleCell2023

Synthetic Par polarity induces cytoskeleton asymmetry in unpolarized mammalian cells.

Joseph L Watson, Lara K Krüger, Ariel J Ben-Sasson, Alice Bittleston, Marta N Shahbazi, Vicente Jose Planelles-Herrero, Joseph E Chambers, James D Manton, David Baker, Emmanuel Derivery

Open access · hybridAbstract read
In one paragraph

Article in Cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
11.5field-weighted citation impact, top 2% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

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  10. Neutrophil diversity and function in health and disease.Signal transduction and targeted therapy · 2024
    Review
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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 4 institutions in 2 countries.

Joseph L WatsonMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.
Lara K KrügerMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.
Ariel J Ben-SassonDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA; Institute for Protein Design, University of Washington, Seattle, WA 98195, USA.
Alice BittlestonMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.
Marta N ShahbaziMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.
Vicente Jose Planelles-HerreroMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.
Joseph E ChambersCambridge Institute for Medical Research, Department of Medicine, University of Cambridge, Hills Rd, Cambridge, UK.
James D MantonMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK.
David BakerDepartment of Biochemistry, University of Washington, Seattle, WA 98195, USA; Institute for Protein Design, University of Washington, Seattle, WA 98195, USA; Howard Hughes Medical Institute, University of Washington, Seattle, WA 98195, USA.
Emmanuel DeriveryMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, UK. Electronic address: derivery@mrc-lmb.cam.ac.uk.
MRC Laboratory of Molecular Biology · GBHoward Hughes Medical Institute · USUniversity of Cambridge · GBUniversity of Washington · US

Funding

Howard Hughes Medical InstituteMedical Research Council MC_UP_1201/13Medical Research Council MC_UP_1201/24Medical Research Council MR/V028669/1Wellcome TrustWellcome Trust 100140
6 · The paper itself

Abstract

Polarized cells rely on a polarized cytoskeleton to function. Yet, how cortical polarity cues induce cytoskeleton polarization remains elusive. Here, we capitalized on recently established designed 2D protein arrays to ectopically engineer cortical polarity of virtually any protein of interest during mitosis in various cell types. This enables direct manipulation of polarity signaling and the identification of the cortical cues sufficient for cytoskeleton polarization. Using this assay, we dissected the logic of the Par complex pathway, a key regulator of cytoskeleton polarity during asymmetric cell division. We show that cortical clustering of any Par complex subunit is sufficient to trigger complex assembly and that the primary kinetic barrier to complex assembly is the relief of Par6 autoinhibition. Further, we found that inducing cortical Par complex polarity induces two hallmarks of asymmetric cell division in unpolarized mammalian cells: spindle orientation, occurring via Par3, and central spindle asymmetry, depending on aPKC activity.

Indexed as

Adaptor Proteins, Signal TransducingCell PolarityCytological TechniquesMitosisAnimalsCytoskeletonMammalsMicrotubulesProtein Kinase CAdaptor Proteins, Signal TransducingProtein Kinase Casymmetric cell divisioncytoskeletonpolarityprotein designsynthetic biology

Identifiers

PMID37774705
PMCPMC10765089
OpenAlexW4387131807

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.