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Cytokinins regulate spatially-specific ethylene production to control root growth in Arabidopsis

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

inferredcites →https://doi.org/10.1002/smtd.201900267openalex-snapshot
Tools of the Ethylene Trade: A Chemical Kit to Influence Ethylene Responses in Plants and Its Use in Agriculture
inferredcites →https://doi.org/10.1007/978-1-61779-445-2_2openalex-snapshot
Combination of an AccQ·Tag-Ultra Performance Liquid Chromatographic Method with Tandem Mass Spectrometry for the Analysis of Amino Acids
inferredcites →https://doi.org/10.1007/s00425-005-0163-2openalex-snapshot
Progress report: ethylene signaling and responses
inferredcites →https://doi.org/10.1007/s00425-017-2651-6openalex-snapshot
Regulation of seedling growth by ethylene and the ethylene–auxin crosstalk
inferredcites →https://doi.org/10.1007/s004380000376openalex-snapshot
Characterisation of novel target promoters for the dexamethasone-inducible/tetracycline-repressible regulator TGV using luciferase and isopentenyl transferase as sensitive reporter genes
inferredcites →https://doi.org/10.1007/s11033-021-06802-2openalex-snapshot
Exogenous phytohormones in the regulation of growth and development of cereals under abiotic stresses
inferredcites →https://doi.org/10.1016/0092-8674(93)90119-bopenalex-snapshot
CTR1, a negative regulator of the ethylene response pathway in arabidopsis, encodes a member of the Raf family of protein kinases
inferredcites →https://doi.org/10.1016/j.cell.2015.09.037openalex-snapshot
EIN2-Directed Translational Regulation of Ethylene Signaling in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2018.02.024openalex-snapshot
The Soil-Borne Legacy
inferredcites →https://doi.org/10.1016/j.cub.2007.02.047openalex-snapshot
Cytokinins Determine Arabidopsis Root-Meristem Size by Controlling Cell Differentiation
inferredcites →https://doi.org/10.1016/j.cub.2022.03.019openalex-snapshot
Cytokinin promotes growth cessation in the Arabidopsis root
inferredcites →https://doi.org/10.1016/j.molp.2019.05.012openalex-snapshot
ETR1 Integrates Response to Ethylene and Cytokinins into a Single Multistep Phosphorelay Pathway to Control Root Growth
inferredcites →https://doi.org/10.1016/j.molp.2021.11.001openalex-snapshot
Lack of ethylene does not affect reproductive success and synergid cell death in Arabidopsis
inferredcites →https://doi.org/10.1016/j.pbi.2009.07.009openalex-snapshot
Ethylene signaling and response: where different regulatory modules meet
inferredcites →https://doi.org/10.1016/j.pbi.2020.08.005openalex-snapshot
Arabidopsis primary root growth: let it grow, can't hold it back anymore!
inferredcites →https://doi.org/10.1016/j.tplants.2018.02.004openalex-snapshot
The Root Transition Zone: A Hot Spot for Signal Crosstalk
inferredcites →https://doi.org/10.1016/s0092-8674(00)00095-7openalex-snapshot
A Viral Movement Protein Prevents Spread of the Gene Silencing Signal in Nicotiana benthamiana
inferredcites →https://doi.org/10.1038/cr.2012.145openalex-snapshot
Activation of ethylene signaling is mediated by nuclear translocation of the cleaved EIN2 carboxyl terminus
inferredcites →https://doi.org/10.1038/nature01984openalex-snapshot
Differential regulation of EIN3 stability by glucose and ethylene signalling in plants
inferredcites →https://doi.org/10.1038/ncomms13018openalex-snapshot
EIN2-dependent regulation of acetylation of histone H3K14 and non-canonical histone H3K23 in ethylene signalling
inferredcites →https://doi.org/10.1038/ncomms15758openalex-snapshot
Pyrazinamide and derivatives block ethylene biosynthesis by inhibiting ACC oxidase
inferredcites →https://doi.org/10.1038/ng.2725openalex-snapshot
Control of root system architecture by DEEPER ROOTING 1 increases rice yield under drought conditions
inferredcites →https://doi.org/10.1038/s41422-019-0239-3openalex-snapshot
Asymmetric distribution of cytokinins determines root hydrotropism in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/s41467-019-11483-4openalex-snapshot
Cytokinin functions as an asymmetric and anti-gravitropic signal in lateral roots
inferredcites →https://doi.org/10.1038/s41467-020-14313-0openalex-snapshot
Histidine kinase MHZ1/OsHK1 interacts with ethylene receptors to regulate root growth in rice
inferredcites →https://doi.org/10.1038/s41586-019-1203-6openalex-snapshot
An apical hypoxic niche sets the pace of shoot meristem activity
inferredcites →https://doi.org/10.1038/sj.emboj.7600337openalex-snapshot
The response regulator 2 mediates ethylene signalling and hormone signal integration in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.2000.00909.xopenalex-snapshot
Arabidopsis ARR1 and ARR2 response regulators operate as transcriptional activators
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01945.xopenalex-snapshot
Expression of cytokinin biosynthetic isopentenyltransferase genes in Arabidopsis : tissue specificity and regulation by auxin, cytokinin, and nitrate
inferredcites →https://doi.org/10.1071/bt06118openalex-snapshot
Roots of the Second Green Revolution
inferredcites →https://doi.org/10.1073/pnas.0900060106openalex-snapshot
Cytokinin regulates root meristem activity via modulation of the polar auxin transport
inferredcites →https://doi.org/10.1073/pnas.1707937114openalex-snapshot
EIN2 mediates direct regulation of histone acetylation in the ethylene response
inferredcites →https://doi.org/10.1073/pnas.1717649115openalex-snapshot
The plant hormone ethylene restricts Arabidopsis growth via the epidermis
inferredcites →https://doi.org/10.1073/pnas.2206291119openalex-snapshot
Tissue-specific regulation of lipid polyester synthesis genes controlling oxygen permeation into Lotus japonicus nodules
inferredcites →https://doi.org/10.1073/pnas.95.8.4766openalex-snapshot
Recessive and dominant mutations in the ethylene biosynthetic gene ACS 5 of Arabidopsis confer cytokinin insensitivity and ethylene overproduction, respectively
inferredcites →https://doi.org/10.1074/jbc.rev120.010854openalex-snapshot
Ethylene signaling in plants
inferredcites →https://doi.org/10.1093/aob/mci100openalex-snapshot
Ethylene Signal Transduction
inferredcites →https://doi.org/10.1093/aob/mcw101openalex-snapshot
Longitudinal zonation pattern inArabidopsisroot tip defined by a multiple structural change algorithm
inferredcites →https://doi.org/10.1093/aobpla/pls031openalex-snapshot
Advances in ethylene signalling: protein complexes at the endoplasmic reticulum membrane
inferredcites →https://doi.org/10.1093/jxb/48.2.201openalex-snapshot
The role of ethylene in the development of plant form
inferredcites →https://doi.org/10.1093/jxb/erab360openalex-snapshot
Hormonal orchestration of root apical meristem formation and maintenance in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/eri236openalex-snapshot
GAL4-GFP enhancer trap lines for genetic manipulation of lateral root development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/jxb/ers025openalex-snapshot
An altered hydrotropic response (ahr1) mutant of Arabidopsis recovers root hydrotropism with cytokinin
inferredcites →https://doi.org/10.1093/jxb/ert485openalex-snapshot
Hormonal control of cell division and elongation along differentiation trajectories in roots
inferredcites →https://doi.org/10.1098/rstb.2017.0042openalex-snapshot
Bilaterally symmetric axes with rhizoids composed the rooting structure of the common ancestor of vascular plants
inferredcites →https://doi.org/10.1101/2021.09.16.460643openalex-snapshot
AHK5 mediates ETR1-initiated multistep phosphorelay in Arabidopsis
inferredcites →https://doi.org/10.1101/cshperspect.a039990openalex-snapshot
Auxin Interactions with Other Hormones in Plant Development
inferredcites →https://doi.org/10.1101/gad.12.23.3703openalex-snapshot
Nuclear events in ethylene signaling: a transcriptional cascade mediated by ETHYLENE-INSENSITIVE3 and ETHYLENE-RESPONSE-FACTOR1
inferredcites →https://doi.org/10.1104/pp.104.049999openalex-snapshot
Unique and Overlapping Expression Patterns among the Arabidopsis 1-Amino-Cyclopropane-1-Carboxylate Synthase Gene Family Members
inferredcites →https://doi.org/10.1104/pp.107.106989openalex-snapshot
Recombinational Cloning with Plant Gateway Vectors
inferredcites →https://doi.org/10.1104/pp.107.4.1075openalex-snapshot
Cytokinin Action Is Coupled to Ethylene in Its Effects on the Inhibition of Root and Hypocotyl Elongation in Arabidopsis thaliana Seedlings
inferredcites →https://doi.org/10.1104/pp.109.135830openalex-snapshot
Transcriptional Regulation of the Ethylene Response Factor LeERF2 in the Expression of Ethylene Biosynthesis Genes Controls Ethylene Production in Tomato and Tobacco
inferredcites →https://doi.org/10.1104/pp.112.196790openalex-snapshot
Histidine Kinase Activity of the Ethylene Receptor ETR1 Facilitates the Ethylene Response in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.112.202853openalex-snapshot
Proteome Analysis in Arabidopsis Reveals Shoot- and Root-Specific Targets of Cytokinin Action and Differential Regulation of Hormonal Homeostasis
inferredcites →https://doi.org/10.1104/pp.112.213207openalex-snapshot
Nomenclature for Members of the Two-Component Signaling Pathway of Plants
inferredcites →https://doi.org/10.1104/pp.124.4.1718openalex-snapshot
STUNTED PLANT 1 Mediates Effects of Cytokinin, But Not of Auxin, on Cell Division and Expansion in the Root of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.125.2.519openalex-snapshot
In the Early Response of Arabidopsis Roots to Ethylene, Cell Elongation Is Up- and Down-Regulated and Uncoupled from Differentiation
inferredcites →https://doi.org/10.1104/pp.15.00415openalex-snapshot
Ethylene Inhibits Cell Proliferation of the Arabidopsis Root Meristem
inferredcites →https://doi.org/10.1104/pp.18.00199openalex-snapshot
Root Engineering in Barley: Increasing Cytokinin Degradation Produces a Larger Root System, Mineral Enrichment in the Shoot and Improved Drought Tolerance
inferredcites →https://doi.org/10.1105/tpc.006882openalex-snapshot
The eto1 , eto2 , and eto3 Mutations and Cytokinin Treatment Increase Ethylene Biosynthesis in Arabidopsis by Increasing the Stability of ACS Protein
inferredcites →https://doi.org/10.1105/tpc.112.103044openalex-snapshot
Spatiotemporal Regulation of Lateral Root Organogenesis in Arabidopsis by Cytokinin
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02731.xopenalex-snapshot
Two‐hybrid protein–protein interaction analysis in Arabidopsis protoplasts: establishment of a heterodimerization map of group C and group S bZIP transcription factors
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03711.xopenalex-snapshot
Regulation of ACS protein stability by cytokinin and brassinosteroid
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.04060.xopenalex-snapshot
A rapid and non‐destructive screenable marker, FAST, for identifying transformed seeds of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1399-3054.1982.tb06318.xopenalex-snapshot
Effects of α‐aminoisobutyric acid and D‐ and L‐amino acids on ethylene production and content of 1‐aminocyclopropane‐1‐carboxylic acid in cotyledonary segments of cocklebur seeds
inferredcites →https://doi.org/10.1111/j.1399-3054.1983.tb02779.xopenalex-snapshot
α‐Aminoisabutyric acid, propyl gallate and cobalt ion and the mode of inhibition of ethylene production by cotyledonary segments of cocklebur seeds
inferredcites →https://doi.org/10.1111/j.1399-3054.2005.00445.xopenalex-snapshot
The interaction of cytokinin with other signals
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04100.xopenalex-snapshot
Ethylene in vegetative development: a tale with a riddle
inferredcites →https://doi.org/10.1111/jipb.12929openalex-snapshot
Asymmetric cytokinin signaling opposes gravitropism in roots
inferredcites →https://doi.org/10.1111/nph.16873openalex-snapshot
The regulation of ethylene biosynthesis: a complex multilevel control circuitry
inferredcites →https://doi.org/10.1111/pce.13494openalex-snapshot
Cytokinin action in response to abiotic and biotic stresses in plants
inferredcites →https://doi.org/10.1111/pce.14266openalex-snapshot
Genetic and molecular mechanisms underlying root architecture and function under heat stress—A hidden story
inferredcites →https://doi.org/10.1111/tpj.13585openalex-snapshot
Regulation of the turnover of ACC synthases by phytohormones and heterodimerization in Arabidopsis
inferredcites →https://doi.org/10.1126/science.1143409openalex-snapshot
Ethylene Modulates Stem Cell Division in the Arabidopsis thaliana Root
inferredcites →https://doi.org/10.1126/science.1146265openalex-snapshot
A High-Resolution Root Spatiotemporal Map Reveals Dominant Expression Patterns
inferredcites →https://doi.org/10.1126/science.284.5423.2148openalex-snapshot
EIN2, a Bifunctional Transducer of Ethylene and Stress Responses in Arabidopsis
inferredcites →https://doi.org/10.1126/science.abf3013openalex-snapshot
Plant roots sense soil compaction through restricted ethylene diffusion
inferredcites →https://doi.org/10.1146/annurev.arplant.35.1.155openalex-snapshot
Ethylene Biosynthesis and its Regulation in Higher Plants
inferredcites →https://doi.org/10.1186/1471-2229-12-208openalex-snapshot
Identification of genes involved in the ACC-mediated control of root cell elongation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/1746-4811-8-7openalex-snapshot
Identifying biological landmarks using a novel cell measuring image analysis tool: Cell-o-Tape
inferredcites →https://doi.org/10.1186/s12864-017-3929-6openalex-snapshot
Ethylene induces combinatorial effects of histone H3 acetylation in gene expression in Arabidopsis
inferredcites →https://doi.org/10.1186/s12870-014-0214-6openalex-snapshot
Cadmium-induced ethylene production and responses in Arabidopsis thaliana rely on ACS2 and ACS6 gene expression
inferredcites →https://doi.org/10.1242/dev.132035openalex-snapshot
Cytokinin acts through the auxin influx carrier AUX1 to regulate cell elongation in the root
inferredcites →https://doi.org/10.1242/dev.149344openalex-snapshot
Cytokinin signaling in plant development
inferredcites →https://doi.org/10.1371/journal.pone.0212056openalex-snapshot
ARR22 overexpression can suppress plant Two-Component Regulatory Systems
inferredcites →https://doi.org/10.14348/molcells.2018.0092openalex-snapshot
Arabidopsis ACC Oxidase 1 Coordinated by Multiple Signals Mediates Ethylene Biosynthesis and Is Involved in Root Development.
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3389/fpls.2013.00442openalex-snapshot
Root traits contributing to plant productivity under drought
inferredcites →https://doi.org/10.3389/fpls.2014.00296openalex-snapshot
A novel phylogeny and morphological reconstruction of the PIN genes and first phylogeny of the ACC-oxidases (ACOs)
inferredcites →https://doi.org/10.3389/fpls.2019.00695openalex-snapshot
1-Aminocyclopropane-1-Carboxylic Acid Oxidase (ACO): The Enzyme That Makes the Plant Hormone Ethylene
inferredcites →https://doi.org/10.3389/fpls.2021.644823openalex-snapshot
Signal Integration in Plant Abiotic Stress Responses via Multistep Phosphorelay Signaling
inferredcites →https://doi.org/10.3390/ijms19124051openalex-snapshot
Supraoptimal Cytokinin Content Inhibits Rice Seminal Root Growth by Reducing Root Meristem Size and Cell Length via Increased Ethylene Content
inferredcites →https://doi.org/10.3390/ijms19124060openalex-snapshot
Deciphering Auxin-Ethylene Crosstalk at a Systems Level
inferredcites →https://doi.org/10.3390/plants10071458openalex-snapshot
Meeting at the DNA: Specifying Cytokinin Responses through Transcription Factor Complex Formation
inferredcites →https://doi.org/10.3390/plants8120590openalex-snapshot
New Insights into Multistep-Phosphorelay (MSP)/Two-Component System (TCS) Regulation: Are Plants and Bacteria That Different?

What points at this work

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

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Dissecting chickpea genomic loci associated with the root penetration responsive traits in compacted soil
inferred← citeshttps://doi.org/10.1007/s11103-024-01534-wopenalex-snapshot
Regulatory mechanisms of trichome and root hair development in Arabidopsis
inferred← citeshttps://doi.org/10.1101/2024.02.01.578397openalex-snapshot
1-Aminocyclopropane-1-carboxylic acid oxidase determines the fate of ethylene biosynthesis in a tissue-specific way to fine-tune development and stress resilience
inferred← citeshttps://doi.org/10.1111/nph.19878openalex-snapshot
A UPLC ‐ MS / MS method for quantification of metabolites in the ethylene biosynthesis pathway and its biological validation in Arabidopsis
inferred← citeshttps://doi.org/10.1186/s12870-024-05817-8openalex-snapshot
Identification of two postharvest ripening regulatory models in kiwifruit: based on plant hormones, physiology, and transcriptome analysis
inferred← citeshttps://doi.org/10.3390/ijms25063335openalex-snapshot
New Hybrid Ethylenediurea (EDU) Derivatives and Their Phytoactivity
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