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GhROP6 GTPase modulates auxin accumulation in cotton fibers by regulating cell-specific GhPIN3a localization

https://doi.org/10.1093/jxb/erac416
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What this work says

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

inferredcites →https://doi.org/10.1007/s00018-006-6116-5openalex-snapshot
Spatiotemporal asymmetric auxin distribution: a means to coordinate plant development
inferredcites →https://doi.org/10.1007/s00425-007-0580-5openalex-snapshot
Laser capture microdissection and cDNA microarrays used to generate gene expression profiles of the rapidly expanding fibre initial cells on the surface of cotton ovules
inferredcites →https://doi.org/10.1007/s11434-008-0290-9openalex-snapshot
SCFP, a novel fiber-specific promoter in cotton
inferredcites →https://doi.org/10.1016/j.cell.2007.07.033openalex-snapshot
Antagonistic Regulation of PIN Phosphorylation by PP2A and PINOID Directs Auxin Flux
inferredcites →https://doi.org/10.1016/j.cell.2009.03.001openalex-snapshot
Auxin: A Trigger for Change in Plant Development
inferredcites →https://doi.org/10.1016/j.cub.2005.09.052openalex-snapshot
Patterns of Auxin Transport and Gene Expression during Primordium Development Revealed by Live Imaging of the Arabidopsis Inflorescence Meristem
inferredcites →https://doi.org/10.1016/j.cub.2006.03.065openalex-snapshot
Regulation of AUXIN RESPONSE FACTOR3 by TAS3 ta-siRNA Affects Developmental Timing and Patterning in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2007.01.052openalex-snapshot
Clathrin-Mediated Constitutive Endocytosis of PIN Auxin Efflux Carriers 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.2011.01.036openalex-snapshot
PIN Polarity Maintenance by the Cell Wall in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2012.05.019openalex-snapshot
A ROP GTPase-Dependent Auxin Signaling Pathway Regulates the Subcellular Distribution of PIN2 in Arabidopsis Roots
inferredcites →https://doi.org/10.1016/j.cub.2012.05.020openalex-snapshot
ABP1 and ROP6 GTPase Signaling Regulate Clathrin-Mediated Endocytosis in Arabidopsis Roots
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.2013.10.036openalex-snapshot
Arabidopsis TOL Proteins Act as Gatekeepers for Vacuolar Sorting of PIN2 Plasma Membrane Protein
inferredcites →https://doi.org/10.1016/j.cub.2020.10.011openalex-snapshot
Auxin-Regulated Reversible Inhibition of TMK1 Signaling by MAKR2 Modulates the Dynamics of Root Gravitropism
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.molp.2021.03.021openalex-snapshot
Plant Rho GTPase signaling promotes autophagy
inferredcites →https://doi.org/10.1016/j.tplants.2018.03.009openalex-snapshot
Activation and Polarity Control of PIN-FORMED Auxin Transporters by Phosphorylation
inferredcites →https://doi.org/10.1016/j.tplants.2019.05.006openalex-snapshot
Auxin Metabolism Controls Developmental Decisions in Land Plants
inferredcites →https://doi.org/10.1016/s0092-8674(03)00003-5openalex-snapshot
The Arabidopsis GNOM ARF-GEF Mediates Endosomal Recycling, Auxin Transport, and Auxin-Dependent Plant Growth
inferredcites →https://doi.org/10.1016/s0092-8674(03)00924-3openalex-snapshot
Local, Efflux-Dependent Auxin Gradients as a Common Module for Plant Organ Formation
inferredcites →https://doi.org/10.1038/415806aopenalex-snapshot
Lateral relocation of auxin efflux regulator PIN3 mediates tropism in Arabidopsis
inferredcites →https://doi.org/10.1038/emboj.2010.181openalex-snapshot
The march of the PINs: developmental plasticity by dynamic polar targeting in plant cells
inferredcites →https://doi.org/10.1038/emboj.2012.310openalex-snapshot
SCFTIR1/AFB‐auxin signalling regulates PIN vacuolar trafficking and auxin fluxes during root gravitropism
inferredcites →https://doi.org/10.1038/msb.2011.72openalex-snapshot
Recycling, clustering, and endocytosis jointly maintain PIN auxin carrier polarity at the plasma membrane
inferredcites →https://doi.org/10.1038/nature02085openalex-snapshot
Efflux-dependent auxin gradients establish the apical–basal axis of Arabidopsis
inferredcites →https://doi.org/10.1038/nature06023openalex-snapshot
An ARF-GEF acting at the Golgi and in selective endocytosis in polarized plant cells
inferredcites →https://doi.org/10.1038/nbt.1843openalex-snapshot
Spatiotemporal manipulation of auxin biosynthesis in cotton ovule epidermal cells enhances fiber yield and quality
inferredcites →https://doi.org/10.1038/ncb1369openalex-snapshot
Intracellular trafficking and proteolysis of the Arabidopsis auxin-efflux facilitator PIN2 are involved in root gravitropism
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00321.xopenalex-snapshot
Auxin and ethylene promote root hair elongation in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0808073105openalex-snapshot
Differential degradation of PIN2 auxin efflux carrier by retromer-dependent vacuolar targeting
inferredcites →https://doi.org/10.1073/pnas.1016260107openalex-snapshot
ADP-ribosylation factor machinery mediates endocytosis in plant cells
inferredcites →https://doi.org/10.1073/pnas.1614380114openalex-snapshot
Dynamic PIN-FORMED auxin efflux carrier phosphorylation at the plasma membrane controls auxin efflux-dependent growth
inferredcites →https://doi.org/10.1083/jcb.200409140openalex-snapshot
A Rho family GTPase controls actin dynamics and tip growth via two counteracting downstream pathways in pollen tubes
inferredcites →https://doi.org/10.1093/emboj/20.11.2779openalex-snapshot
Arabidopsis thaliana Rop GTPases are localized to tips of root hairs and control polar growth
inferredcites →https://doi.org/10.1093/jxb/ern240openalex-snapshot
Post-transcriptional regulation of auxin transport proteins: cellular trafficking, protein phosphorylation, protein maturation, ubiquitination, and membrane composition
inferredcites →https://doi.org/10.1093/jxb/erv282openalex-snapshot
Tricho- and atrichoblast cell files show distinct PIN2 auxin efflux carrier exploitations and are jointly required for defined auxin-dependent root organ growth
inferredcites →https://doi.org/10.1093/jxb/erw216openalex-snapshot
Regulation of polar auxin transport by protein and lipid kinases
inferredcites →https://doi.org/10.1093/jxb/erz162openalex-snapshot
Cytokinin inhibits cotton fiber initiation by disrupting PIN3a-mediated asymmetric accumulation of auxin in the ovule epidermis
inferredcites →https://doi.org/10.1093/pcp/pcw203openalex-snapshot
Auxin Regulates Cotton Fiber Initiation via GhPIN-Mediated Auxin Transport
inferredcites →https://doi.org/10.1093/pcp/pcx118openalex-snapshot
BEN3/BIG2 ARF GEF is Involved in Brefeldin A-Sensitive Trafficking at the trans-Golgi Network/Early Endosome in Arabidopsis thaliana
inferredcites →https://doi.org/10.1101/cshperspect.a001552openalex-snapshot
Auxin Transporters--Why So Many?
inferredcites →https://doi.org/10.1104/pp.010724openalex-snapshot
Cotton Fiber Growth in Planta and in Vitro. Models for Plant Cell Elongation and Cell Wall Biogenesis
inferredcites →https://doi.org/10.1104/pp.112.213165openalex-snapshot
The Arabidopsis Rho of Plants GTPase AtROP6 Functions in Developmental and Pathogen Response Pathways
inferredcites →https://doi.org/10.1104/pp.16.01243openalex-snapshot
The Microtubule-Associated Protein MAP18 Affects ROP2 GTPase Activity during Root Hair Growth
inferredcites →https://doi.org/10.1105/tpc.001537openalex-snapshot
The ROP2 GTPase Controls the Formation of Cortical Fine F-Actin and the Early Phase of Directional Cell Expansion during Arabidopsis Organogenesis
inferredcites →https://doi.org/10.1105/tpc.006437openalex-snapshot
Regulation of Root Hair Initiation and Expansin Gene Expression in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.010359openalex-snapshot
The Arabidopsis Rop2 GTPase Is a Positive Regulator of Both Root Hair Initiation and Tip Growth
inferredcites →https://doi.org/10.1105/tpc.108.064865openalex-snapshot
The ESCRT-Related CHMP1A and B Proteins Mediate Multivesicular Body Sorting of Auxin Carriers in Arabidopsis and Are Required for Plant Development
inferredcites →https://doi.org/10.1105/tpc.110.074211openalex-snapshot
Phospholipase A2 Is Required for PIN-FORMED Protein Trafficking to the Plasma Membrane in theArabidopsisRoot
inferredcites →https://doi.org/10.1105/tpc.114.127902openalex-snapshot
ROP3 GTPase Contributes to Polar Auxin Transport and Auxin Responses and Is Important for Embryogenesis and Seedling Growth inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.134874openalex-snapshot
PIN-Dependent Auxin Transport: Action, Regulation, and Evolution
inferredcites →https://doi.org/10.1105/tpc.114.135400openalex-snapshot
Arabidopsis RIC1 Severs Actin Filaments at the Apex to Regulate Pollen Tube Growth
inferredcites →https://doi.org/10.1105/tpc.12.4.507openalex-snapshot
Auxin Regulates the Initiation and Radial Position of Plant Lateral Organs
inferredcites →https://doi.org/10.1105/tpc.15.00306openalex-snapshot
Phytosulfokine Regulates Growth in Arabidopsis through a Response Module at the Plasma Membrane That Includes CYCLIC NUCLEOTIDE-GATED CHANNEL17, H+-ATPase, and BAK1
inferredcites →https://doi.org/10.1105/tpc.19.00869openalex-snapshot
Arabidopsis Flippases Cooperate with ARF GTPase Exchange Factors to Regulate the Trafficking and Polarity of PIN Auxin Transporters
inferredcites →https://doi.org/10.1105/tpc.20.00440openalex-snapshot
A Fully Functional ROP Fluorescent Fusion Protein Reveals Roles for This GTPase in Subcellular and Tissue-Level Patterning
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03144.xopenalex-snapshot
GhDET2, a steroid 5α‐reductase, plays an important role in cotton fiber cell initiation and elongation
inferredcites →https://doi.org/10.1111/nph.14844openalex-snapshot
Genetics and evolution of MIXTA genes regulating cotton lint fiber development
inferredcites →https://doi.org/10.1111/tra.12425openalex-snapshot
Ikarugamycin: A Natural Product Inhibitor of Clathrin‐Mediated Endocytosis
inferredcites →https://doi.org/10.1126/science.179.4077.1003openalex-snapshot
Hormonal Regulation of Growth in Unfertilized Cotton Ovules
inferredcites →https://doi.org/10.1155/2009/451357openalex-snapshot
Techniques to Study Autophagy in Plants
inferredcites →https://doi.org/10.1242/dev.030353openalex-snapshot
Auxin transport routes in plant development
inferredcites →https://doi.org/10.1242/dev.168088openalex-snapshot
PIN-FORMED and PIN-LIKES auxin transport facilitators
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.pgen.1003540openalex-snapshot
Cell Polarity and Patterning by PIN Trafficking through Early Endosomal Compartments in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0153988openalex-snapshot
Characterization of a Novel Cotton Subtilase Gene GbSBT1 in Response to Extracellular Stimulations and Its Role in Verticillium Resistance
inferredcites →https://doi.org/10.2307/3871050openalex-snapshot
Control of Pollen Tube Tip Growth by a Rop GTPase-Dependent Pathway That Leads to Tip-Localized Calcium Influx
inferredcites →https://doi.org/10.3389/fpls.2020.581983openalex-snapshot
Auxin Directly Upregulates GhRAC13 Expression to Promote the Onset of Secondary Cell Wall Deposition in Cotton Fibers

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4480360openalex-extracted
Synergism of Vesicle Trafficking and Cytoskeleton During Regulation of Plant Growth and Development: A Mechanistic Outlook
inferred← citeshttps://doi.org/10.1007/s00122-025-05043-2openalex-snapshot
Genetic basis and role of exotic accessions in cultivated cotton fiber quality improvement
inferred← citeshttps://doi.org/10.1007/s11032-024-01500-wopenalex-snapshot
Simultaneous improvement of fiber yield and quality in upland cotton (Gossypium hirsutum L.) by integration of auxin transport and synthesis
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e21976openalex-snapshot
RETRACTED: Synergism of vesicle trafficking and cytoskeleton during regulation of plant growth and development: A mechanistic outlook
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.143662openalex-snapshot
GhIAA14-GhARF7 module coordinates auxin-mediated cellulose biosynthesis during secondary cell wall thickening in cotton fibers
inferred← citeshttps://doi.org/10.1093/jxb/erae162openalex-snapshot
Crosstalk between Rho of Plants GTPase signalling and plant hormones
inferred← citeshttps://doi.org/10.1093/plcell/koaf237openalex-snapshot
A light-governed cascade of ubiquitin modifications regulates cotton fiber development by coordinating PIN3a proteolysis
inferred← citeshttps://doi.org/10.1111/jipb.70213openalex-snapshot
Recent advances in genetic control of fiber length in upland cotton
inferred← citeshttps://doi.org/10.1111/nph.20286openalex-snapshot
Natural variation in GhROPGEF5 contributes to longer and stronger cotton fibers
inferred← citeshttps://doi.org/10.1111/tpj.70064openalex-snapshot
Spatial transcriptome and single‐cell RNA sequencing reveal the molecular basis of cotton fiber initiation development
inferred← citeshttps://doi.org/10.3390/agronomy14061208openalex-snapshot
Genetic and Molecular Regulation of Cotton Fiber Initiation and Elongation
inferred← citeshttps://doi.org/10.3390/ijms24010843openalex-snapshot
Regulation of PIN-FORMED Protein Degradation
inferred← citeshttps://doi.org/10.3390/plants13081127openalex-snapshot
Comparative Transcriptomic Analysis of Gossypium hirsutum Fiber Development in Mutant Materials (xin w 139) Provides New Insights into Cotton Fiber Development
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