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Environmental and Endogenous Control of Cortical Microtubule Orientation

https://doi.org/10.1016/j.tcb.2016.02.003

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1 of the 80 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1105/tpc.113.113472 (notice 2017-09-05).

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Microtubule severing

inferredcites →https://doi.org/10.1007/bf00391218openalex-snapshot

Re-formation of microtubules in Closterium ehrenbergii Meneghini after cold-induced depolymerization

inferredcites →https://doi.org/10.1007/bf00395959openalex-snapshot

Ethylene-induced microtubule reorientations: mediation by helical arrays

inferredcites →https://doi.org/10.1007/s00425-013-1941-xopenalex-snapshot

Rapid auxin-induced root growth inhibition requires the TIR and AFB auxin receptors

inferredcites →https://doi.org/10.1007/s11103-008-9426-1openalex-snapshot

Arabidopsis microtubule-associated protein AtMAP65-2 acts as a microtubule stabilizer

inferredcites →https://doi.org/10.1016/j.bpj.2012.01.008openalex-snapshot

Single-Molecule Analysis of the Microtubule Cross-Linking Protein MAP65-1 Reveals a Molecular Mechanism for Contact-Angle-Dependent Microtubule Bundling

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Arabidopsis Interdigitating Cell Growth Requires Two Antagonistic Pathways with Opposing Action on Cell Morphogenesis

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.2012.02.048openalex-snapshot

Mechanical Stress Acts via Katanin to Amplify Differences in Growth Rate between Adjacent Cells in Arabidopsis

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.cub.2013.03.053openalex-snapshot

Dynamic Regulation of Cortical Microtubule Organization through Prefoldin-DELLA Interaction

inferredcites →https://doi.org/10.1016/j.cub.2013.07.061openalex-snapshot

SPIRAL2 Determines Plant Microtubule Organization by Modulating Microtubule Severing

inferredcites →https://doi.org/10.1016/j.cub.2013.09.018openalex-snapshot

Microtubule Severing at Crossover Sites by Katanin Generates Ordered Cortical Microtubule Arrays in Arabidopsis

inferredcites →https://doi.org/10.1016/j.cub.2014.08.036openalex-snapshot

An Auxin-Mediated Shift toward Growth Isotropy Promotes Organ Formation at the Shoot Meristem in Arabidopsis

inferredcites →https://doi.org/10.1016/j.cub.2014.09.013openalex-snapshot

GCP-WD Mediates γ-TuRC Recruitment and the Geometry of Microtubule Nucleation in Interphase Arrays of Arabidopsis

inferredcites →https://doi.org/10.1016/j.devcel.2013.02.007openalex-snapshot

CLASP Interacts with Sorting Nexin 1 to Link Microtubules and Auxin Transport via PIN2 Recycling in Arabidopsis thaliana

inferredcites →https://doi.org/10.1016/j.tplants.2015.05.008openalex-snapshot

Auxin inhibits expansion rate independently of cortical microtubules

inferredcites →https://doi.org/10.1038/35079128openalex-snapshot

MOR1 is essential for organizing cortical microtubules in plants

inferredcites →https://doi.org/10.1038/35096571openalex-snapshot

Auxin transport inhibitors block PIN1 cycling and vesicle trafficking

inferredcites →https://doi.org/10.1038/nature05046openalex-snapshot

AtSNX1 defines an endosome for auxin-carrier trafficking in Arabidopsis

inferredcites →https://doi.org/10.1038/nature06520openalex-snapshot

A molecular framework for light and gibberellin control of cell elongation

inferredcites →https://doi.org/10.1038/nature13889openalex-snapshot

Inhibition of cell expansion by rapid ABP1-mediated auxin effect on microtubules

inferredcites →https://doi.org/10.1038/ncb1057openalex-snapshot

EB1 reveals mobile microtubule nucleation sites in Arabidopsis

inferredcites →https://doi.org/10.1038/ncb1886openalex-snapshot

Arabidopsis cortical microtubules position cellulose synthase delivery to the plasma membrane and interact with cellulose synthase trafficking compartments

inferredcites →https://doi.org/10.1038/ncb2110openalex-snapshot

Microtubule and katanin-dependent dynamics of microtubule nucleation complexes in the acentrosomal Arabidopsis cortical array

inferredcites →https://doi.org/10.1038/ncomms1444openalex-snapshot

A CLASP-modulated cell edge barrier mechanism drives cell-wide cortical microtubule organization in Arabidopsis

inferredcites →https://doi.org/10.1038/nrm1277openalex-snapshot

Microtubules and the shape of plants to come

inferredcites →https://doi.org/10.1038/nrm3064openalex-snapshot

Asymmetric cell division in land plants and algae: the driving force for differentiation

inferredcites →https://doi.org/10.1073/pnas.0808652105openalex-snapshot

Prefoldin 6 is required for normal microtubule dynamics and organization in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.1118560109openalex-snapshot

Cellulose synthase interactive protein 1 (CSI1) links microtubules and cellulose synthase complexes

inferredcites →https://doi.org/10.1073/pnas.1500365112openalex-snapshot

Auxin binding protein 1 (ABP1) is not required for either auxin signaling or Arabidopsis development

inferredcites →https://doi.org/10.1073/pnas.91.13.6050openalex-snapshot

Dynamic reorientation of cortical microtubules, from transverse to longitudinal, in living plant cells.

inferredcites →https://doi.org/10.1073/pnas.95.12.7197openalex-snapshot

High temperature promotes auxin-mediated hypocotyl elongation in Arabidopsis

inferredcites →https://doi.org/10.1091/mbc.e08-06-0665openalex-snapshot

CLASP Modulates Microtubule-Cortex Interaction during Self-Organization of Acentrosomal Microtubules

inferredcites →https://doi.org/10.1093/jxb/eru325openalex-snapshot

Microtubule array reorientation in response to hormones does not involve changes in microtubule nucleation modes at the periclinal cell surface

inferredcites →https://doi.org/10.1093/mp/ssp016openalex-snapshot

Prefoldins 3 and 5 Play an Essential Role in Arabidopsis Tolerance to Salt Stress

inferredcites →https://doi.org/10.1093/mp/ssu038openalex-snapshot

Visualization of Microtubule Organization and Dynamics in Living Arabidopsis Embryonic Cells

inferredcites →https://doi.org/10.1093/pcp/pcu094openalex-snapshot

Microtubule Initiation from the Nuclear Surface Controls Cortical Microtubule Growth Polarity and Orientation in Arabidopsis thaliana

inferredcites →https://doi.org/10.1104/pp.104.040493openalex-snapshot

Disorganization of Cortical Microtubules Stimulates Tangential Expansion and Reduces the Uniformity of Cellulose Microfibril Alignment among Cells in the Root of Arabidopsis

inferredcites →https://doi.org/10.1104/pp.104.051623openalex-snapshot

In Vivo Dynamics and Differential Microtubule-Binding Activities of MAP65 Proteins

inferredcites →https://doi.org/10.1104/pp.104.051748openalex-snapshot

Plant-Specific Microtubule-Associated Protein SPIRAL2 Is Required for Anisotropic Growth in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.104.052456openalex-snapshot

Two Microtubule-Associated Proteins of the Arabidopsis MAP65 Family Function Differently on Microtubules

inferredcites →https://doi.org/10.1104/pp.108.120196openalex-snapshot

Genetic Evidence That Cellulose Synthase Activity Influences Microtubule Cortical Array Organization

inferredcites →https://doi.org/10.1104/pp.113.225607openalex-snapshot

Purification and Characterization of Novel Microtubule-Associated Proteins from Arabidopsis Cell Suspension Cultures

inferredcites →https://doi.org/10.1104/pp.116.3.1043openalex-snapshot

Extending the Microtubule/Microfibril Paradigm1

inferredcites →https://doi.org/10.1104/pp.15.00609openalex-snapshot

Ethylene Regulates the Arabidopsis Microtubule-Associated Protein WAVE-DAMPENED2-LIKE5 in Etiolated Hypocotyl Elongation

inferredcites →https://doi.org/10.1104/pp.99.4.1302openalex-snapshot

Auxin Redistribution during First Positive Phototropism in Corn Coleoptiles

inferredcites →https://doi.org/10.1105/tpc.010402openalex-snapshot

The Arabidopsis TONNEAU 2 Gene Encodes a Putative Novel Protein Phosphatase 2A Regulatory Subunit Essential for the Control of the Cortical Cytoskeleton

inferredcites →https://doi.org/10.1105/tpc.104.026930openalex-snapshot

Encounters between Dynamic Cortical Microtubules Promote Ordering of the Cortical Array through Angle-Dependent Modifications of Microtubule Behavior[W]

inferredcites →https://doi.org/10.1105/tpc.106.048579openalex-snapshot

Arabidopsis MICROTUBULE-ASSOCIATED PROTEIN18 Functions in Directional Cell Growth by Destabilizing Cortical Microtubules

inferredcites →https://doi.org/10.1105/tpc.107.053777openalex-snapshot

The Arabidopsis CLASP Gene Encodes a Microtubule-Associated Protein Involved in Cell Expansion and Division

inferredcites →https://doi.org/10.1105/tpc.109.069716openalex-snapshot

ArabidopsisCortical Microtubules Are Initiated along, as Well as Branching from, Existing Microtubules

inferredcites →https://doi.org/10.1105/tpc.109.069906openalex-snapshot

Auxin Response inArabidopsisunder Cold Stress: Underlying Molecular Mechanisms

inferredcites →https://doi.org/10.1105/tpc.111.092684openalex-snapshot

MDP25, A Novel Calcium Regulatory Protein, Mediates Hypocotyl Cell Elongation by Destabilizing Cortical Microtubules inArabidopsis

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.111.094367openalex-snapshot

TONNEAU2/FASS Regulates the Geometry of Microtubule Nucleation and Cortical Array Organization in Interphase Arabidopsis Cells

inferredcites →https://doi.org/10.1105/tpc.112.103838openalex-snapshot

Arabidopsis MICROTUBULE DESTABILIZING PROTEIN40 Is Involved in Brassinosteroid Regulation of Hypocotyl Elongation

inferredcites →https://doi.org/10.1105/tpc.112.104182openalex-snapshot

Phosphatidic Acid Regulates Microtubule Organization by Interacting with MAP65-1 in Response to Salt Stress in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.112.107326openalex-snapshot

Progressive Transverse Microtubule Array Organization in Hormone-InducedArabidopsisHypocotyl Cells

inferredcites →https://doi.org/10.1105/tpc.113.113472openalex-snapshot

RETRACTED:ArabidopsisAUGMIN Subunit8 Is a Microtubule Plus-End Binding Protein That Promotes Microtubule Reorientation in Hypocotyls

inferredcites →https://doi.org/10.1105/tpc.114.126193openalex-snapshot

The jiaoyao1 Mutant Is an Allele of korrigan1 That Abolishes Endoglucanase Activity and Affects the Organization of Both Cellulose Microfibrils and Microtubules in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.15.00442openalex-snapshot

CELLULOSE SYNTHASE INTERACTIVE1 Is Required for Fast Recycling of Cellulose Synthase Complexes to the Plasma Membrane in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02761.xopenalex-snapshot

Katanin's severing activity favors bundling of cortical microtubules in plants

inferredcites →https://doi.org/10.1126/science.1083529openalex-snapshot

Sustained Microtubule Treadmilling in Arabidopsis Cortical Arrays

inferredcites →https://doi.org/10.1126/science.1123542openalex-snapshot

PIN Proteins Perform a Rate-Limiting Function in Cellular Auxin Efflux

inferredcites →https://doi.org/10.1126/science.1126551openalex-snapshot

Visualization of Cellulose Synthase Demonstrates Functional Association with Microtubules

inferredcites →https://doi.org/10.1126/science.1165594openalex-snapshot

Developmental Patterning by Mechanical Signals in Arabidopsis

inferredcites →https://doi.org/10.1126/science.1245533openalex-snapshot

A Mechanism for Reorientation of Cortical Microtubule Arrays Driven by Microtubule Severing

inferredcites →https://doi.org/10.1126/science.138.3548.1404openalex-snapshot

Mechanism for Plant Cellular Morphogenesis

inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105329openalex-snapshot

MICROTUBULE DYNAMICS AND ORGANIZATION IN THE PLANT CORTICAL ARRAY

inferredcites →https://doi.org/10.1146/annurev.cb.01.110185.001045openalex-snapshot

Microtubule Organizing Centers

inferredcites →https://doi.org/10.1242/dev.041939openalex-snapshot

A conditional mutation in Arabidopsis thaliana separase induces chromosome non-disjunction, aberrant morphogenesis and cyclin B1;1 stability

inferredcites →https://doi.org/10.1242/jcs.109.3.561openalex-snapshot

Katanin, the microtubule-severing ATPase, is concentrated at centrosomes

inferredcites →https://doi.org/10.1242/jcs.113.16.2821openalex-snapshot

Cellular Samurai: katanin and the severing of microtubules

inferredcites →https://doi.org/10.12688/f1000research.7143.1openalex-snapshot

Embryo-lethal phenotypes in early abp1 mutants are due to disruption of the neighboring BSM gene

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.pone.0036210openalex-snapshot

Hypocotyl Transcriptome Reveals Auxin Regulation of Growth-Promoting Genes through GA-Dependent and -Independent Pathways

inferredcites →https://doi.org/10.1371/journal.pone.0093981openalex-snapshot

Molecular Modeling and Imaging of Initial Stages of Cellulose Fibril Assembly: Evidence for a Disordered Intermediate Stage

inferredcites →https://doi.org/10.3732/ajb.93.10.1415openalex-snapshot

Biomechanics of plant growth

inferredcites →https://doi.org/10.4161/psb.28337openalex-snapshot

Phospholipids

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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