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Osmotic stress inhibits leaf growth of Arabidopsis thaliana by enhancing ARF‐mediated auxin responses

https://doi.org/10.1111/nph.16490
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Outgoing claims: the papers this work cites, builds on, or argues with.

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X‐ray structure of ILL2, an auxin‐conjugate amidohydrolase from Arabidopsis thaliana
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A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
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Kinematic Analysis of Cell Division in Leaves of Mono- and Dicotyledonous Species: A Basis for Understanding Growth and Developing Refined Molecular Sampling Strategies
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Activation of a flavin monooxygenase gene YUCCA7 enhances drought resistance in Arabidopsis
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Water transport, perception, and response in plants
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Re-examination of the role of endoreduplication on cell-size control in leaves
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Dissecting regulatory pathways of G1/S control in Arabidopsis: common and distinct targets of CYCD3;1, E2Fa and E2Fc
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Effect of temperature on the dose–response curves for auxin-induced elongation growth in maize coleoptile segments
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Different Plant Hormones Regulate Similar Processes through Largely Nonoverlapping Transcriptional Responses
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Auxin: A Trigger for Change in Plant Development
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More from less: plant growth under limited water
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Plant Stress Tolerance Requires Auxin-Sensitive Aux/IAA Transcriptional Repressors
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The Auxin-Regulated CrRLK1L Kinase ERULUS Controls Cell Wall Composition during Root Hair Tip Growth
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Hormone balance and abiotic stress tolerance in crop plants
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ABA-dependent and ABA-independent signaling in response to osmotic stress in plants
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Leaf size control: complex coordination of cell division and expansion
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Indole-3-butyric acid in plant growth and development
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Control of root growth and development by cyclin expression
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Developmental regulation of CYCA2s contributes to tissue‐specific proliferation in Arabidopsis
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Systems‐based analysis of Arabidopsis leaf growth reveals adaptation to water deficit
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Efflux-dependent auxin gradients establish the apical–basal axis of Arabidopsis
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Survival and growth of Arabidopsis plants given limited water are not equal
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The auxin influx carrier LAX3 promotes lateral root emergence
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A mechanistic framework for auxin dependent Arabidopsis root hair elongation to low external phosphate
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Aluminium-induced reduction of plant growth in alfalfa (Medicago sativa) is mediated by interrupting auxin transport and accumulation in roots
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Fundamentals of Molecular Evolution (2nd edn)
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The AXR1 and AUX1 genes of Arabidopsis function in separate auxin‐response pathways
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Indole‐3‐glycerol phosphate, a branchpoint of indole‐3‐acetic acid biosynthesis from the tryptophan biosynthetic pathway in Arabidopsis thaliana
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Transcriptome analysis of sulfur depletion in Arabidopsis thaliana: interlacing of biosynthetic pathways provides response specificity
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ILR2, a novel gene regulating IAA conjugate sensitivity and metal transport in Arabidopsis thaliana
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Indole-3-Acetic Acid Protein Conjugates: Novel Players in Auxin Homeostasis
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Biochemical analyses of indole-3-acetaldoxime-dependent auxin biosynthesis in Arabidopsis
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The main auxin biosynthesis pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1201498109openalex-snapshot
Root gravitropism is regulated by a transient lateral auxin gradient controlled by a tipping-point mechanism
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GH3-mediated Auxin Homeostasis Links Growth Regulation with Stress Adaptation Response in Arabidopsis
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Auxin: Regulation, Action, and Interaction
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Fundamentals of Molecular Evolution
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The relationship of drought-related gene expression in Arabidopsis thaliana to hormonal and environmental factors
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Auxin conjugates: their role for plant development and in the evolution of land plants
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The pathway of auxin biosynthesis in plants
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Auxin biosynthesis and storage forms
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Auxin: simply complicated
inferredcites →https://doi.org/10.1093/mp/ssr104openalex-snapshot
Auxin Biosynthesis: A Simple Two-Step Pathway Converts Tryptophan to Indole-3-Acetic Acid in Plants
inferredcites →https://doi.org/10.1093/mp/sss100openalex-snapshot
Overexpression of Arabidopsis YUCCA6 in Potato Results in High-Auxin Developmental Phenotypes and Enhanced Resistance to Water Deficit
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a029387openalex-snapshot
Molecular Cloning and Characterization of Aldehyde Oxidases in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcs035openalex-snapshot
The Interaction and Integration of Auxin Signaling Components
inferredcites →https://doi.org/10.1093/pcp/pct173openalex-snapshot
UGT74D1 Catalyzes the Glucosylation of 2-Oxindole-3-Acetic Acid in the Auxin Metabolic Pathway in Arabidopsis
inferredcites →https://doi.org/10.1101/cshperspect.a001446openalex-snapshot
Cellular Responses to Auxin: Division versus Expansion
inferredcites →https://doi.org/10.1101/cshperspect.a001552openalex-snapshot
Auxin Transporters--Why So Many?
inferredcites →https://doi.org/10.1101/cshperspect.a001560openalex-snapshot
Modeling Auxin-regulated Development
inferredcites →https://doi.org/10.1101/gad.13.13.1678openalex-snapshot
Identification of an SCF ubiquitin-ligase complex required for auxin response in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.104.043398openalex-snapshot
A Novel Auxin Conjugate Hydrolase from Wheat with Substrate Specificity for Longer Side-Chain Auxin Amide Conjugates
inferredcites →https://doi.org/10.1104/pp.104.053884openalex-snapshot
Genome-Wide Analysis of Gene Expression Profiles Associated with Cell Cycle Transitions in Growing Organs of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.099895openalex-snapshot
STRESS RESPONSE SUPPRESSOR1 and STRESS RESPONSE SUPPRESSOR2, Two DEAD-Box RNA Helicases That Attenuate Arabidopsis Responses to Multiple Abiotic Stresses
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Functional Identification of Arabidopsis Stress Regulatory Genes Using the Controlled cDNA Overexpression System
inferredcites →https://doi.org/10.1104/pp.108.118224openalex-snapshot
Inactive Methyl Indole-3-Acetic Acid Ester Can Be Hydrolyzed and Activated by Several Esterases Belonging to the AtMES Esterase Family of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.148965openalex-snapshot
Developmental Stage Specificity and the Role of Mitochondrial Metabolism in the Response of Arabidopsis Leaves to Prolonged Mild Osmotic Stress
inferredcites →https://doi.org/10.1104/pp.110.157461openalex-snapshot
Conversion of Endogenous Indole-3-Butyric Acid to Indole-3-Acetic Acid Drives Cell Expansion in Arabidopsis Seedlings
inferredcites →https://doi.org/10.1104/pp.112.2.549openalex-snapshot
The Effects of Exogenous Auxins on Endogenous Indole-3-Acetic Acid Metabolism (The Implications for Carrot Somatic Embryogenesis)
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An in Vitro System from Maize Seedlings for Tryptophan-Independent Indole-3-Acetic Acid Biosynthesis1
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Hormonal Interactions in the Control of Arabidopsis Hypocotyl Elongation
inferredcites →https://doi.org/10.1104/pp.89.3.798openalex-snapshot
Turgor and Growth at Low Water Potentials
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Functional Analysis of Cyclin-Dependent Kinase Inhibitors of Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.010445openalex-snapshot
Genome-Wide Analysis of Core Cell Cycle Genes in Arabidopsis
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Induction of Arabidopsis Tryptophan Pathway Enzymes and Camalexin by Amino Acid Starvation, Oxidative Stress, and an Abiotic Elicitor
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Structure-Function Analysis of the Presumptive Arabidopsis Auxin Permease AUX1[W]
inferredcites →https://doi.org/10.1105/tpc.105.034959openalex-snapshot
An Indole-3-Acetic Acid Carboxyl Methyltransferase Regulates Arabidopsis Leaf Development
inferredcites →https://doi.org/10.1105/tpc.105.039651openalex-snapshot
The Balance between Cell Division and Endoreplication Depends on E2FC-DPB, Transcription Factors Regulated by the Ubiquitin-SCFSKP2A Pathway inArabidopsis
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ARF7 and ARF19 Regulate Lateral Root Formation via Direct Activation of LBD/ASL Genes in Arabidopsis
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Perturbation of Indole-3-Butyric Acid Homeostasis by the UDP-GlucosyltransferaseUGT74E2ModulatesArabidopsisArchitecture and Water Stress Tolerance
inferredcites →https://doi.org/10.1105/tpc.111.083071openalex-snapshot
Multiple Facets of Arabidopsis Seedling Development Require Indole-3-Butyric Acid–Derived Auxin
inferredcites →https://doi.org/10.1105/tpc.111.084160openalex-snapshot
Pause-and-Stop: The Effects of Osmotic Stress on Cell Proliferation during Early Leaf Development in Arabidopsis and a Role for Ethylene Signaling in Cell Cycle Arrest
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IAA-Ala Resistant3 , an Evolutionarily Conserved Target of miR167, Mediates Arabidopsis Root Architecture Changes during High Osmotic Stress
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AUX/LAX Genes Encode a Family of Auxin Influx Transporters That Perform Distinct Functions during Arabidopsis Development
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Auxin Regulates the Initiation and Radial Position of Plant Lateral Organs
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Genetic Components of Root Architecture Remodeling in Response to Salt Stress
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Cell and leaf size plasticity in Arabidopsis: what is the role of endoreduplication?
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Arabidopsis growth under prolonged high temperature and water deficit: independent or interactive effects?
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The AtGenExpress global stress expression data set: protocols, evaluation and model data analysis of UV‐B light, drought and cold stress responses
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Systematic analysis of cell‐cycle gene expression during Arabidopsis development
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The putative auxin efflux carrier OsPIN3t is involved in the drought stress response and drought tolerance
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A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
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A pair of receptor‐like kinases is responsible for natural variation in shoot growth response to mannitol treatment in A rabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1118642openalex-snapshot
Integration of Plant Responses to Environmentally Activated Phytohormonal Signals
inferredcites →https://doi.org/10.1126/science.1122847openalex-snapshot
AXR4 Is Required for Localization of the Auxin Influx Facilitator AUX1
inferredcites →https://doi.org/10.1126/science.273.5277.948openalex-snapshot
Arabidopsis AUX1 Gene: A Permease-Like Regulator of Root Gravitropism
inferredcites →https://doi.org/10.1126/science.7792599openalex-snapshot
ILR1, an Amidohydrolase That Releases Active Indole-3-Acetic Acid from Conjugates
inferredcites →https://doi.org/10.1146/annurev-arplant-050213-040000openalex-snapshot
Genetic Engineering and Breeding of Drought-Resistant Crops
inferredcites →https://doi.org/10.1146/annurev-genet-102108-134148openalex-snapshot
Mechanism of Auxin-Regulated Gene Expression in Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105444openalex-snapshot
TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES
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Auxin: The Looping Star in Plant Development
inferredcites →https://doi.org/10.1146/annurev.pp.27.060176.002203openalex-snapshot
Modeling of Plant Growth
inferredcites →https://doi.org/10.1146/annurev.pp.33.060182.002155openalex-snapshot
Chemistry and Physiology of the Bound Auxins
inferredcites →https://doi.org/10.1186/1746-4811-6-17openalex-snapshot
High-contrast three-dimensional imaging of the Arabidopsis leaf enables the analysis of cell dimensions in the epidermis and mesophyll
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Higher plant glycosyltransferases.
inferredcites →https://doi.org/10.1186/gb-2009-10-12-249openalex-snapshot
The PIN-FORMED (PIN) protein family of auxin transporters
inferredcites →https://doi.org/10.1199/tab.0132openalex-snapshot
The Biosynthetic Pathways for Shikimate and Aromatic Amino Acids in Arabidopsis thaliana
inferredcites →https://doi.org/10.1242/dev.030353openalex-snapshot
Auxin transport routes in plant development
inferredcites →https://doi.org/10.1371/annotation/457d7567-fc12-421c-9d79-880950ab10e1openalex-snapshot
Correction: UGT74D1 Is a Novel Auxin Glycosyltransferase from Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0061705openalex-snapshot
UGT74D1 Is a Novel Auxin Glycosyltransferase from Arabidopsis thaliana
inferredcites →https://doi.org/10.3389/fpls.2014.00151openalex-snapshot
Tolerance to drought and salt stress in plants: Unraveling the signaling networks
inferredcites →https://doi.org/10.3389/fpls.2014.00362openalex-snapshot
Leaf development: a cellular perspective
inferredcites →https://doi.org/10.3389/fpls.2015.00013openalex-snapshot
Facile high-throughput forward chemical genetic screening by in situ monitoring of glucuronidase-based reporter gene expression in Arabidopsis thaliana
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Perturbation of Auxin Homeostasis and Signaling by PINOID Overexpression Induces Stress Responses in Arabidopsis
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A Sweetpotato Auxin Response Factor Gene (IbARF5) Is Involved in Carotenoid Biosynthesis and Salt and Drought Tolerance in Transgenic Arabidopsis
inferredcites →https://doi.org/10.4161/psb.5.12.13941openalex-snapshot
Modulating plant hormones by enzyme action

What points at this work

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

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inferred← citeshttps://doi.org/10.1101/2020.10.20.347674openalex-snapshot
PSK signaling controls ABA homeostasis and signaling genes and maintains shoot growth under osmotic stress
inferred← citeshttps://doi.org/10.1101/cshperspect.a039917openalex-snapshot
Noncanonical Auxin Signaling
inferred← citeshttps://doi.org/10.1111/nph.19334openalex-snapshot
LTP2 hypomorphs show genotype‐by‐environment interaction in early seedling traits in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/ppl.13728openalex-snapshot
De novo transcriptome sequencing of Capsicum frutescens. L and comprehensive analysis of salt stress alleviating mechanism by Bacillus atrophaeus WU ‐9
inferred← citeshttps://doi.org/10.1111/ppl.14146openalex-snapshot
Modulation of phosphorylation status of MAP3 kinases under abiotic stress responses
inferred← citeshttps://doi.org/10.1111/tpj.17215openalex-snapshot
Cytochrome c levels link mitochondrial function to plant growth and stress responses through changes in SnRK1 pathway activity
inferred← citeshttps://doi.org/10.1186/s12870-022-03918-wopenalex-snapshot
Leaf transcriptome analysis of Medicago ruthenica revealed its response and adaptive strategy to drought and drought recovery
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2946229/v1openalex-snapshot
Function analysis of transcription factor OSR1 regulating osmotic stress resistance in maize
inferred← citeshttps://doi.org/10.2174/9789815305845124020007openalex-snapshot
New-Generation Plant Growth Regulators
inferred← citeshttps://doi.org/10.3389/fgene.2024.1394091openalex-snapshot
Role of transcriptional regulation in auxin-mediated response to abiotic stresses
inferred← citeshttps://doi.org/10.3389/fpls.2022.902902openalex-snapshot
Design, Synthesis, and Action Mechanism of 1,3-Benzodioxole Derivatives as Potent Auxin Receptor Agonists and Root Growth Promoters
inferred← citeshttps://doi.org/10.3389/fpls.2023.1099587openalex-snapshot
Identification of a pluripotency-inducing small compound, PLU, that induces callus formation via Heat Shock Protein 90-mediated activation of auxin signaling
inferred← citeshttps://doi.org/10.3390/agronomy14030610openalex-snapshot
Influence of Nutrient Solutions in an NGS® Soilless System on the Yield, Quality and Shelf Life of Fresh-Cut Commercial Mint at Different Harvest Times
inferred← citeshttps://doi.org/10.3390/app12031360openalex-snapshot
Auxin Response Factors Are Ubiquitous in Plant Growth and Development, and Involved in Crosstalk between Plant Hormones: A Review
inferred← citeshttps://doi.org/10.3390/biology14121774openalex-snapshot
Genome-Wide Discovery and Characterization of the Auxin Response Factor (ARF) Gene Family in Avicennia marina That Regulates Phytohormone Levels and Responds to Salt and Auxin Treatments
inferred← citeshttps://doi.org/10.3390/cells11203250openalex-snapshot
Melatonin and Indole-3-Acetic Acid Synergistically Regulate Plant Growth and Stress Resistance
inferred← citeshttps://doi.org/10.3390/ijms23041933openalex-snapshot
Auxin/Cytokinin Antagonistic Control of the Shoot/Root Growth Ratio and Its Relevance for Adaptation to Drought and Nutrient Deficiency Stresses
inferred← citeshttps://doi.org/10.3390/ijms23105309openalex-snapshot
Genome-Wide Identification of Auxin Response Factors in Peanut (Arachis hypogaea L.) and Functional Analysis in Root Morphology
inferred← citeshttps://doi.org/10.3390/ijms231911108openalex-snapshot
Identification and Characterization of AUXIN Response Factor Gene Family Reveals Their Regulatory Network to Respond the Multi-Hormones Crosstalk during GA-Induced Grape Parthenocarpic Berry
inferred← citeshttps://doi.org/10.3390/ijms24010756openalex-snapshot
Identification and Functional Validation of Auxin-Responsive Tabzip Genes from Wheat Leaves in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms25020806openalex-snapshot
A Comprehensive Analysis of Auxin Response Factor Gene Family in Melastoma dodecandrum Genome
inferred← citeshttps://doi.org/10.3390/nano12122099openalex-snapshot
Potassium Chloroaurate-Mediated In Vitro Synthesis of Gold Nanoparticles Improved Root Growth by Crosstalk with Sucrose and Nutrient-Dependent Auxin Homeostasis in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/plants13202940openalex-snapshot
Genome-Wide Identification and Characterization of the Aux/IAA Gene Family in Strawberry Species
inferred← citeshttps://doi.org/10.3390/plants14071108openalex-snapshot
Transcriptional Dynamics Underlying Somatic Embryogenesis in Coffea canephora
inferred← citeshttps://doi.org/10.3390/plants14152277openalex-snapshot
Identification of Auxin-Associated Genes in Wheat Through Comparative Transcriptome Analysis and Validation of the Candidate Receptor-like Kinase Gene TaPBL7-2B in Arabidopsis
inferred← citeshttps://doi.org/10.7287/peerj.14938v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Functional verification of the JmLFY gene associated with the flowering of Juglans mandshurica Maxim. (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.14938v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Functional verification of the JmLFY gene associated with the flowering of Juglans mandshurica Maxim. (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.14938v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Functional verification of the JmLFY gene associated with the flowering of Juglans mandshurica Maxim. (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.14938v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Functional verification of the JmLFY gene associated with the flowering of Juglans mandshurica Maxim. (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.14938v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Functional verification of the JmLFY gene associated with the flowering of Juglans mandshurica Maxim. (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.14938openalex-snapshot
Functional verification of the JmLFY gene associated with the flowering of Juglans mandshurica Maxim.
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.