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Auxin-induced nanoclustering of membrane signaling complexes underlies cell polarity establishment in Arabidopsis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Cholesterol Depletion Using Methyl-β-cyclodextrin
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Ratiometric Fluorescence Live Imaging Analysis of Membrane Lipid Order in Arabidopsis Mitotic Cells Using a Lipid Order-Sensitive Probe
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Lipid Rafts: A Personal Account
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Rapid auxin-induced root growth inhibition requires the TIR and AFB auxin receptors
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Fronts propagating with curvature-dependent speed: Algorithms based on Hamilton-Jacobi formulations
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Ras nanoclusters: Versatile lipid-based signaling platforms
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Establishing and transducing cell polarity: common themes and variations
inferredcites →https://doi.org/10.1016/j.cell.2004.12.026openalex-snapshot
Arabidopsis Interdigitating Cell Growth Requires Two Antagonistic Pathways with Opposing Action on Cell Morphogenesis
inferredcites →https://doi.org/10.1016/j.cell.2008.01.047openalex-snapshot
TAA1-Mediated Auxin Biosynthesis Is Essential for Hormone Crosstalk and Plant Development
inferredcites →https://doi.org/10.1016/j.cell.2010.09.003openalex-snapshot
Cell Surface- and Rho GTPase-Based Auxin Signaling Controls Cellular Interdigitation in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2011.06.049openalex-snapshot
Cytoskeletal Control of CD36 Diffusion Promotes Its Receptor and Signaling Function
inferredcites →https://doi.org/10.1016/j.cell.2015.03.048openalex-snapshot
Transbilayer Lipid Interactions Mediate Nanoclustering of Lipid-Anchored Proteins
inferredcites →https://doi.org/10.1016/j.cell.2015.04.008openalex-snapshot
Membrane Nanoclusters—Tails of the Unexpected
inferredcites →https://doi.org/10.1016/j.cell.2016.04.037openalex-snapshot
Sterol-Rich Membrane Domains Define Fission Yeast Cell Polarity
inferredcites →https://doi.org/10.1016/j.cell.2016.11.059openalex-snapshot
Lipid-Sorting Specificity Encoded in K-Ras Membrane Anchor Regulates Signal Output
inferredcites →https://doi.org/10.1016/j.cell.2019.04.037openalex-snapshot
Integrin Mechano-chemical Signaling Generates Plasma Membrane Nanodomains that Promote Cell Spreading
inferredcites →https://doi.org/10.1016/j.celrep.2017.10.069openalex-snapshot
Gradients Of Rac1 Nanoclusters Support Spatial Patterns of Rac1 Signaling
inferredcites →https://doi.org/10.1016/j.cub.2009.08.052openalex-snapshot
A ROP GTPase Signaling Pathway Controls Cortical Microtubule Ordering and Cell Expansion in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2010.03.057openalex-snapshot
An S-Acylation Switch of Conserved G Domain Cysteines Is Required for Polarity Signaling by ROP GTPases
inferredcites →https://doi.org/10.1016/j.cub.2013.01.022openalex-snapshot
Rho GTPase Signaling Activates Microtubule Severing to Promote Microtubule Ordering in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2015.04.005openalex-snapshot
Spatiotemporal Dynamics of the BRI1 Receptor and its Regulation by Membrane Microdomains in Living Arabidopsis Cells
inferredcites →https://doi.org/10.1016/j.pbi.2012.10.004openalex-snapshot
Spatial control of plasma membrane domains: ROP GTPase-based symmetry breaking
inferredcites →https://doi.org/10.1016/j.plaphy.2014.12.015openalex-snapshot
Di-4-ANEPPDHQ, a fluorescent probe for the visualisation of membrane microdomains in living Arabidopsis thaliana cells
inferredcites →https://doi.org/10.1016/j.semcdb.2009.03.006openalex-snapshot
Asymmetric localisation of planar polarity proteins: Mechanisms and consequences
inferredcites →https://doi.org/10.1016/j.tcb.2008.05.006openalex-snapshot
Using plasma membrane nanoclusters to build better signaling circuits
inferredcites →https://doi.org/10.1016/s0092-8674(00)81278-7openalex-snapshot
Origins of Cell Polarity
inferredcites →https://doi.org/10.1038/nature01602openalex-snapshot
Adaptation of core mechanisms to generate cell polarity
inferredcites →https://doi.org/10.1038/nature05731openalex-snapshot
Mechanism of auxin perception by the TIR1 ubiquitin ligase
inferredcites →https://doi.org/10.1038/ncb1342openalex-snapshot
Flotillin-1 defines a clathrin-independent endocytic pathway in mammalian cells
inferredcites →https://doi.org/10.1038/ncb1686openalex-snapshot
Sterol-dependent endocytosis mediates post-cytokinetic acquisition of PIN2 auxin efflux carrier polarity
inferredcites →https://doi.org/10.1038/nprot.2011.419openalex-snapshot
Quantitative imaging of membrane lipid order in cells and organisms
inferredcites →https://doi.org/10.1038/nrm.2017.11openalex-snapshot
Planar cell polarity in development and disease
inferredcites →https://doi.org/10.1038/nrm.2017.16openalex-snapshot
The mystery of membrane organization: composition, regulation and roles of lipid rafts
inferredcites →https://doi.org/10.1038/s41467-018-03582-5openalex-snapshot
AUX1-mediated root hair auxin influx governs SCFTIR1/AFB-type Ca2+ signaling
inferredcites →https://doi.org/10.1038/s41477-018-0190-1openalex-snapshot
Rapid and reversible root growth inhibition by TIR1 auxin signalling
inferredcites →https://doi.org/10.1038/s41586-019-1069-7openalex-snapshot
TMK1-mediated auxin signalling regulates differential growth of the apical hook
inferredcites →https://doi.org/10.1038/srep10082openalex-snapshot
The T cell receptor resides in ordered plasma membrane nanodomains that aggregate upon patching of the receptor
inferredcites →https://doi.org/10.1042/bc20090138openalex-snapshot
Host‐cell lipid rafts: a safe door for micro‐organisms?
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Fluorescence resonance energy transfer in living cells reveals dynamic membrane changes in the initiation of B cell signaling
inferredcites →https://doi.org/10.1073/pnas.171160298openalex-snapshot
Segregation of leading-edge and uropod components into specific lipid rafts during T cell polarization
inferredcites →https://doi.org/10.1074/jbc.273.52.34954openalex-snapshot
Cloning and Characterization of GEF-H1, a Microtubule-associated Guanine Nucleotide Exchange Factor for Rac and Rho GTPases
inferredcites →https://doi.org/10.1074/mcp.m800346-mcp200openalex-snapshot
Definition of Arabidopsis Sterol-rich Membrane Microdomains by Differential Treatment with Methyl-β-cyclodextrin and Quantitative Proteomics
inferredcites →https://doi.org/10.1091/mbc.e18-01-0051openalex-snapshot
Phosphatidylserine and GTPase activation control Cdc42 nanoclustering to counter dissipative diffusion
inferredcites →https://doi.org/10.1093/jxb/erv266openalex-snapshot
Pavement cells: a model system for non-transcriptional auxin signalling and crosstalks: Fig. 1.
inferredcites →https://doi.org/10.1093/mp/ssn062openalex-snapshot
Cellular and Molecular Requirements for Polar PIN Targeting and Transcytosis in Plants
inferredcites →https://doi.org/10.1101/269647openalex-snapshot
FERONIA’s sensing of cell wall pectin activates ROP GTPase signaling in Arabidopsis
inferredcites →https://doi.org/10.1101/cshperspect.a002964openalex-snapshot
Planar Cell Polarity Signaling: The Developing Cell's Compass
inferredcites →https://doi.org/10.1101/cshperspect.a004697openalex-snapshot
Membrane Organization and Lipid Rafts
inferredcites →https://doi.org/10.1101/gad.14.12.1471openalex-snapshot
FACKEL is a sterol C-14 reductase required for organized cell division and expansion in Arabidopsis embryogenesis
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A critical role of sterols in embryonic patterning and meristem programming revealed by thefackelmutants ofArabidopsis thaliana
inferredcites →https://doi.org/10.1101/gad.1511207openalex-snapshot
Microtubule-induced cortical cell polarity
inferredcites →https://doi.org/10.1105/tpc.001248openalex-snapshot
hydra Mutants of Arabidopsis Are Defective in Sterol Profiles and Auxin and Ethylene Signaling
inferredcites →https://doi.org/10.1105/tpc.110.082131openalex-snapshot
A Barley ROP GTPase ACTIVATING PROTEIN Associates with Microtubules and Regulates Entry of the Barley Powdery Mildew Fungus into Leaf Epidermal Cells
inferredcites →https://doi.org/10.1105/tpc.111.093575openalex-snapshot
POM-POM2/CELLULOSE SYNTHASE INTERACTING1 Is Essential for the Functional Association of Cellulose Synthase and Microtubules in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.112.095695openalex-snapshot
A Membrane Microdomain-Associated Protein, Arabidopsis Flot1, Is Involved in a Clathrin-Independent Endocytic Pathway and Is Required for Seedling Development
inferredcites →https://doi.org/10.1105/tpc.114.133744openalex-snapshot
SCF TIR1/AFB -Based Auxin Perception: Mechanism and Role in Plant Growth and Development
inferredcites →https://doi.org/10.1111/imm.12617openalex-snapshot
Lipid rafts in immune signalling: current progress and future perspective
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04423.xopenalex-snapshot
Dynamics of auxin‐dependent Ca2+ and pH signaling in root growth revealed by integrating high‐resolution imaging with automated computer vision‐based analysis
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.03100.xopenalex-snapshot
The mechanics behind plant development
inferredcites →https://doi.org/10.1111/j.1600-0854.2004.0178.xopenalex-snapshot
Molecular Dynamics and Interactions for Creation of Stimulation‐Induced Stabilized Rafts from Small Unstable Steady‐State Rafts
inferredcites →https://doi.org/10.1111/tpj.13480openalex-snapshot
Membrane microdomains and the cytoskeleton constrain At HIR 1 dynamics and facilitate the formation of an At HIR 1‐associated immune complex
inferredcites →https://doi.org/10.1126/science.1222597openalex-snapshot
Initiation of Cell Wall Pattern by a Rho- and Microtubule-Driven Symmetry Breaking
inferredcites →https://doi.org/10.1126/science.1245125openalex-snapshot
Cell Surface ABP1-TMK Auxin-Sensing Complex Activates ROP GTPase Signaling
inferredcites →https://doi.org/10.1126/science.aaa5619openalex-snapshot
Membrane potential modulates plasma membrane phospholipid dynamics and K-Ras signaling
inferredcites →https://doi.org/10.1126/science.aav9959openalex-snapshot
Developmental control of plant Rho GTPase nano-organization by the lipid phosphatidylserine
inferredcites →https://doi.org/10.1128/mcb.00186-18openalex-snapshot
Rac1 Nanoscale Organization on the Plasma Membrane Is Driven by Lipid Binding Specificity Encoded in the Membrane Anchor
inferredcites →https://doi.org/10.1128/mcb.00333-17openalex-snapshot
Corrected and Republished from: Activation Status-Coupled Transient S-Acylation Determines Membrane Partitioning of a Plant Rho-Related GTPase
inferredcites →https://doi.org/10.1128/mcb.01059-06openalex-snapshot
Clustering of Raft-Associated Proteins in the External Membrane Leaflet Modulates Internal Leaflet H-Ras Diffusion and Signaling
inferredcites →https://doi.org/10.1128/mcb.01227-13openalex-snapshot
Signal Integration by Lipid-Mediated Spatial Cross Talk between Ras Nanoclusters
inferredcites →https://doi.org/10.1128/mcb.01615-09openalex-snapshot
Epidermal Growth Factor Receptor Activation Remodels the Plasma Membrane Lipid Environment To Induce Nanocluster Formation
inferredcites →https://doi.org/10.1128/mcb.05570-11openalex-snapshot
Raft Protein Clustering Alters N-Ras Membrane Interactions and Activation Pattern
inferredcites →https://doi.org/10.1128/mmbr.63.1.54-105.1999openalex-snapshot
Cdc42: An Essential Rho-Type GTPase Controlling Eukaryotic Cell Polarity
inferredcites →https://doi.org/10.1146/annurev-genet-102108-134148openalex-snapshot
Mechanism of Auxin-Regulated Gene Expression in Plants
inferredcites →https://doi.org/10.1242/jcs.01596openalex-snapshot
Polarized sorting in epithelial cells: raft clustering and the biogenesis of the apical membrane
inferredcites →https://doi.org/10.1242/jcs.028753openalex-snapshot
EGF induces coalescence of different lipid rafts
inferredcites →https://doi.org/10.1242/jcs.146340openalex-snapshot
Nanoclustering as a dominant feature of plasma membrane organization
inferredcites →https://doi.org/10.1242/jcs.164715openalex-snapshot
Complementary probes reveal that phosphatidylserine is required for the proper transbilayer distribution of cholesterol
inferredcites →https://doi.org/10.1371/journal.pbio.1000516openalex-snapshot
Alignment between PIN1 Polarity and Microtubule Orientation in the Shoot Apical Meristem Reveals a Tight Coupling between Morphogenesis and Auxin Transport
inferredcites →https://doi.org/10.1371/journal.pbio.1001299openalex-snapshot
ROP GTPase-Dependent Actin Microfilaments Promote PIN1 Polarization by Localized Inhibition of Clathrin-Dependent Endocytosis
inferredcites →https://doi.org/10.1371/journal.pone.0060990openalex-snapshot
The TMK Subfamily of Receptor-Like Kinases in Arabidopsis Display an Essential Role in Growth and a Reduced Sensitivity to Auxin
inferredcites →https://doi.org/10.1371/journal.pone.0169905openalex-snapshot
Visualization of BRI1 and SERK3/BAK1 Nanoclusters in Arabidopsis Roots
inferredcites →https://doi.org/10.15252/embj.201899652openalex-snapshot
Avidity‐driven polarity establishment via multivalent lipid–GTPase module interactions
inferredcites →https://doi.org/10.1529/biophysj.105.064816openalex-snapshot
Cholesterol-Enriched Lipid Domains Can Be Visualized by di-4-ANEPPDHQ with Linear and Nonlinear Optics
inferredcites →https://doi.org/10.7554/elife.06587openalex-snapshot
Glycosylphosphatidylinositol-anchored proteins as chaperones and co-receptors for FERONIA receptor kinase signaling in Arabidopsis
inferredcites →https://doi.org/10.7554/elife.19891openalex-snapshot
Protein sorting by lipid phase-like domains supports emergent signaling function in B lymphocyte plasma membranes
inferredcites →https://doi.org/10.7554/elife.25114openalex-snapshot
Plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.xplc.2020.100048openalex-snapshot
All Roads Lead to Auxin: Post-translational Regulation of Auxin Transport by Multiple Hormonal Pathways
inferred← citeshttps://doi.org/10.1093/plphys/kiaa082openalex-snapshot
Function of membrane domains in rho-of-plant signaling
inferred← citeshttps://doi.org/10.1093/plphys/kiad444openalex-snapshot
Membrane microdomains: Structural and signaling platforms for establishing membrane polarity
inferred← citeshttps://doi.org/10.1104/pp.19.01349openalex-snapshot
The Nanoscale Organization of the Plasma Membrane and Its Importance in Signaling: A Proteolipid Perspective
inferred← citeshttps://doi.org/10.1111/jipb.12904openalex-snapshot
Cell polarity: Regulators and mechanisms in plants
inferred← citeshttps://doi.org/10.18174/511017openalex-snapshot
Proteomics perspective on auxin biology
inferred← citeshttps://doi.org/10.70675/a6fd7ae1z6cc4z4278z9f0bze0db404d751bopenalex-snapshot
Role of PI4Kalpha1 complex in plasma membrane identity and development in Arabidopsis thaliana
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