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Overexpression of MsGH3.5 inhibits shoot and root development through the auxin and cytokinin pathways in apple plants

https://doi.org/10.1111/tpj.14717
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s00299-007-0462-0openalex-snapshot
Overexpression of the Arabidopsis gai gene in apple significantly reduces plant size
inferredcites →https://doi.org/10.1007/s00425-006-0462-2openalex-snapshot
Arabidopsis thaliana GH3.9 influences primary root growth
inferredcites →https://doi.org/10.1007/s00425-012-1673-3openalex-snapshot
Effects of three auxin-inducible LBD members on lateral root formation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s11240-014-0599-9openalex-snapshot
BpGH3.5, an early auxin-response gene, regulates root elongation in Betula platyphylla × Betula pendula
inferredcites →https://doi.org/10.1007/s11627-999-0076-zopenalex-snapshot
Review the formation of adventitious roots: New concepts, new possibilities
inferredcites →https://doi.org/10.1016/j.cub.2019.02.022openalex-snapshot
The Lateral Root Cap Acts as an Auxin Sink that Controls Meristem Size
inferredcites →https://doi.org/10.1016/j.jplph.2004.08.007openalex-snapshot
Cytokinin inhibits lateral root initiation but stimulates lateral root elongation in rice (Oryza sativa)
inferredcites →https://doi.org/10.1016/j.molp.2015.11.006openalex-snapshot
The WUSCHEL Related Homeobox Protein WOX7 Regulates the Sugar Response of Lateral Root Development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.plantsci.2008.05.009openalex-snapshot
N,N′-bis-(2,3-Methylenedioxyphenyl)urea and N,N′-bis-(3,4-methylenedioxyphenyl)urea enhance adventitious rooting in Pinus radiata and affect expression of genes induced during adventitious rooting in the presence of exogenous auxin
inferredcites →https://doi.org/10.1016/j.plaphy.2019.03.006openalex-snapshot
miRNAs associated with auxin signaling, stress response, and cellular activities mediate adventitious root formation in apple rootstocks
inferredcites →https://doi.org/10.1016/j.tplants.2015.02.003openalex-snapshot
Cytokinin–auxin crosstalk in cell type specification
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/s0168-9452(98)00106-xopenalex-snapshot
Transformation of the apple rootstock M26 with the rolA gene and its influence on growth
inferredcites →https://doi.org/10.1016/s0176-1617(98)80164-8openalex-snapshot
Genetic transformation of the apple rootstock M26 with the RolB gene and its influence on rooting
inferredcites →https://doi.org/10.1016/s1673-8527(07)60018-6openalex-snapshot
Genetic Diversity of Volatile Components in Xinjiang Wild Apple (Malus sieversii)
inferredcites →https://doi.org/10.1038/nature06943openalex-snapshot
Cytokinin and auxin interaction in root stem-cell specification during early embryogenesis
inferredcites →https://doi.org/10.1038/ncomms9717openalex-snapshot
Cytokinin response factors regulate PIN-FORMED auxin transporters
inferredcites →https://doi.org/10.1038/nprot.2010.37openalex-snapshot
Quantitative analysis of major plant hormones in crude plant extracts by high-performance liquid chromatography–mass spectrometry
inferredcites →https://doi.org/10.1038/nrm2227openalex-snapshot
The ins and outs of the plant cell cycle
inferredcites →https://doi.org/10.1038/s41467-017-02088-wopenalex-snapshot
Structural absorption by barbule microstructures of super black bird of paradise feathers
inferredcites →https://doi.org/10.1038/s41467-018-03921-6openalex-snapshot
A B-ARR-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development
inferredcites →https://doi.org/10.1038/s41467-018-07508-zopenalex-snapshot
Plasmon induced thermoelectric effect in graphene
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/10.1046/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.2000.00762.xopenalex-snapshot
Transgenic tobacco plants co‐expressing Agrobacterium iaa and ipt genes have wild‐type hormone levels but display both auxin‐ and cytokinin‐overproducing phenotypes
inferredcites →https://doi.org/10.1046/j.1365-313x.2001.00957.xopenalex-snapshot
DFL1, an auxin-responsive GH3 gene homologue, negatively regulates shoot cell elongation and lateral root formation, and positively regulates the light response of hypocotyl length
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01973.xopenalex-snapshot
ydk1‐D , an auxin‐responsive GH3 mutant that is involved in hypocotyl and root elongation
inferredcites →https://doi.org/10.1073/pnas.0402504101openalex-snapshot
Auxin regulation of cytokinin biosynthesis in Arabidopsis thaliana : A factor of potential importance for auxin–cytokinin-regulated development
inferredcites →https://doi.org/10.1073/pnas.1604458113openalex-snapshot
Dynamic regulation of auxin oxidase and conjugating enzymes AtDAO1 and GH3 modulates auxin homeostasis
inferredcites →https://doi.org/10.1073/pnas.1620749114openalex-snapshot
Cytokinin induces genome-wide binding of the type-B response regulator ARR10 to regulate growth and development in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1705833114openalex-snapshot
Auxin minimum triggers the developmental switch from cell division to cell differentiation in the Arabidopsis root
inferredcites →https://doi.org/10.1074/jbc.m610524200openalex-snapshot
GH3-mediated Auxin Homeostasis Links Growth Regulation with Stress Adaptation Response in Arabidopsis
inferredcites →https://doi.org/10.1079/ivp2002335openalex-snapshot
Rooting of microcuttings: Theory and practice
inferredcites →https://doi.org/10.1093/aob/mci083openalex-snapshot
Auxin: Regulation, Action, and Interaction
inferredcites →https://doi.org/10.1093/jxb/ers300openalex-snapshot
A GH3 family member, OsGH3-2, modulates auxin and abscisic acid levels and differentially affects drought and cold tolerance in rice
inferredcites →https://doi.org/10.1093/jxb/eru026openalex-snapshot
Identification of new adventitious rooting mutants amongst suppressors of the Arabidopsis thaliana superroot2 mutation
inferredcites →https://doi.org/10.1093/jxb/erv478openalex-snapshot
Strigolactones spatially influence lateral root development through the cytokinin signaling network
inferredcites →https://doi.org/10.1093/jxb/erw001openalex-snapshot
A new three-locus model for rootstock-induced dwarfing in apple revealed by genetic mapping of root bark percentage
inferredcites →https://doi.org/10.1093/pcp/pcm165openalex-snapshot
Three Type-B Response Regulators, ARR1, ARR10 and ARR12, Play Essential but Redundant Roles in Cytokinin Signal Transduction Throughout the Life Cycle of Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcn029openalex-snapshot
Effects of Conditional IPT-Dependent Cytokinin Overproduction on Root Architecture of Arabidopsis Seedlings
inferredcites →https://doi.org/10.1093/treephys/21.7.457openalex-snapshot
Distinct effects of auxin and light on adventitious root development in Eucalyptus saligna and Eucalyptus globulus
inferredcites →https://doi.org/10.1093/treephys/tpx118openalex-snapshot
The WUSCHEL-related homeobox 5a (PtoWOX5a) is involved in adventitious root development in poplar
inferredcites →https://doi.org/10.1098/rstb.2011.0232openalex-snapshot
Multiple AUX/IAA–ARF modules regulate lateral root formation: the role of Arabidopsis SHY2/IAA3-mediated auxin signalling
inferredcites →https://doi.org/10.1104/pp.005504openalex-snapshot
Two-Component Signal Transduction Pathways in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.137505openalex-snapshot
The Cytokinin Type-B Response Regulator PtRR13 Is a Negative Regulator of Adventitious Root Development inPopulus
inferredcites →https://doi.org/10.1104/pp.109.146803openalex-snapshot
Altered Architecture and Enhanced Drought Tolerance in Rice via the Down-Regulation of Indole-3-Acetic Acid by TLD1/OsGH3.13 Activation
inferredcites →https://doi.org/10.1104/pp.110.163774openalex-snapshot
Manipulating Broad-Spectrum Disease Resistance by Suppressing Pathogen-Induced Auxin Accumulation in Rice
inferredcites →https://doi.org/10.1104/pp.111.1.9openalex-snapshot
Early Genes and Auxin Action
inferredcites →https://doi.org/10.1104/pp.112.203166openalex-snapshot
Pattern of Auxin and Cytokinin Responses for Shoot Meristem Induction Results from the Regulation of Cytokinin Biosynthesis by AUXIN RESPONSE FACTOR3
inferredcites →https://doi.org/10.1104/pp.112.208736openalex-snapshot
Functional Characterization of Type-B Response Regulators in the Arabidopsis Cytokinin Response
inferredcites →https://doi.org/10.1104/pp.113.217026openalex-snapshot
Identification of Cytokinin-Responsive Genes Using Microarray Meta-Analysis and RNA-Seq in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.16.00129openalex-snapshot
The Systemic Acquired Resistance Regulator OsNPR1 Attenuates Growth by Repressing Auxin Signaling through Promoting IAA-Amido Synthase Expression
inferredcites →https://doi.org/10.1104/pp.17.00878openalex-snapshot
Type B Response Regulators Act As Central Integrators in Transcriptional Control of the Auxin Biosynthesis Enzyme TAA1
inferredcites →https://doi.org/10.1104/pp.17.01713openalex-snapshot
The ARF7 and ARF19 Transcription Factors Positively Regulate PHOSPHATE STARVATION RESPONSE1 in Arabidopsis Roots
inferredcites →https://doi.org/10.1105/tpc.010289openalex-snapshot
AUX/IAA Proteins Are Active Repressors, and Their Stability and Activity Are Modulated by Auxin
inferredcites →https://doi.org/10.1105/tpc.018978openalex-snapshot
Type-A Arabidopsis Response Regulators Are Partially Redundant Negative Regulators of Cytokinin Signaling[W]
inferredcites →https://doi.org/10.1105/tpc.104.026690openalex-snapshot
Characterization of an Arabidopsis Enzyme Family That Conjugates Amino Acids to Indole-3-Acetic Acid
inferredcites →https://doi.org/10.1105/tpc.105.031625openalex-snapshot
Auxin and Light Control of Adventitious Rooting in Arabidopsis Require ARGONAUTE1
inferredcites →https://doi.org/10.1105/tpc.105.035451openalex-snapshot
Multiple Type-B Response Regulators Mediate Cytokinin Signal Transduction in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.047761openalex-snapshot
ARF7 and ARF19 Regulate Lateral Root Formation via Direct Activation of LBD/ASL Genes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.055657openalex-snapshot
Activation of the Indole-3-Acetic Acid–Amido Synthetase GH3-8 Suppresses Expansin Expression and Promotes Salicylate- and Jasmonate-Independent Basal Immunity in Rice
inferredcites →https://doi.org/10.1105/tpc.107.055863openalex-snapshot
Cytokinins Act Directly on Lateral Root Founder Cells to Inhibit Root Initiation
inferredcites →https://doi.org/10.1105/tpc.108.064758openalex-snapshot
Phenotypic Plasticity of Adventitious Rooting in Arabidopsis Is Controlled by Complex Regulation of AUXIN RESPONSE FACTOR Transcripts and MicroRNA Abundance
inferredcites →https://doi.org/10.1105/tpc.109.072694openalex-snapshot
Root-Specific Reduction of Cytokinin Causes Enhanced Root Growth, Drought Tolerance, and Leaf Mineral Enrichment inArabidopsisand Tobacco
inferredcites →https://doi.org/10.1105/tpc.110.074856openalex-snapshot
Cytokinin Regulation of Auxin Synthesis in Arabidopsis Involves a Homeostatic Feedback Loop Regulated via Auxin and Cytokinin Signal Transduction
inferredcites →https://doi.org/10.1105/tpc.114.122887openalex-snapshot
WOX11 and 12 Are Involved in the First-Step Cell Fate Transition during de Novo Root Organogenesis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.13.12.2809openalex-snapshot
AUX/IAA Proteins Are Active Repressors, and Their Stability and Activity Are Modulated by Auxin
inferredcites →https://doi.org/10.1111/j.1365-313x.2001.00957.xopenalex-snapshot
DFL1, an auxin‐responsive GH3 gene homologue, negatively regulates shoot cell elongation and lateral root formation, and positively regulates the light response of hypocotyl length
inferredcites →https://doi.org/10.1111/pbi.12980openalex-snapshot
The auxin receptor TIR 1 homolog (Pag FBL 1) regulates adventitious rooting through interactions with Aux/ IAA 28 in Populus
inferredcites →https://doi.org/10.1111/pbi.13209openalex-snapshot
OsNAC2 integrates auxin and cytokinin pathways to modulate rice root development
inferredcites →https://doi.org/10.1111/ppl.12171openalex-snapshot
Auxin is a central player in the hormone cross‐talks that control adventitious rooting
inferredcites →https://doi.org/10.1111/ppl.12817openalex-snapshot
Inhibition of adventitious root development in apple rootstocks by cytokinin is based on its suppression of adventitious root primordia formation
inferredcites →https://doi.org/10.1111/tpj.12939openalex-snapshot
OsPIN5b modulates rice (Oryza sativa) plant architecture and yield by changing auxin homeostasis, transport and distribution
inferredcites →https://doi.org/10.1111/tpj.13401openalex-snapshot
Overexpression of Ms DREB 6.2 results in cytokinin‐deficient developmental phenotypes and enhances drought tolerance in transgenic apple plants
inferredcites →https://doi.org/10.1111/tpj.13945openalex-snapshot
LBD 18 uses a dual mode of a positive feedback loop to regulate ARF expression and transcriptional activity in Arabidopsis
inferredcites →https://doi.org/10.1126/science.1065201openalex-snapshot
ARR1, a Transcription Factor for Genes Immediately Responsive to Cytokinins
inferredcites →https://doi.org/10.1126/science.1164147openalex-snapshot
A Genetic Framework for the Control of Cell Division and Differentiation in the Root Meristem
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112308openalex-snapshot
Auxin Biosynthesis and Its Role in Plant Development
inferredcites →https://doi.org/10.1186/1471-2164-14-297openalex-snapshot
Genome-wide analysis of the GH3 family in apple (Malus × domestica)
inferredcites →https://doi.org/10.1186/1471-2164-15-104openalex-snapshot
An evaluation of genotyping by sequencing (GBS) to map the Breviaristatum-e (ari-e) locus in cultivated barley
inferredcites →https://doi.org/10.1186/1471-2164-15-296openalex-snapshot
WUSCHEL-related Homeobox genes in Populus tomentosa: diversified expression patterns and a functional similarity in adventitious root formation
inferredcites →https://doi.org/10.1186/1746-4811-1-13openalex-snapshot
Transient expression vectors for functional genomics, quantification of promoter activity and RNA silencing in plants
inferredcites →https://doi.org/10.1186/s12864-016-2484-xopenalex-snapshot
Transcriptome analysis reveals the effects of sugar metabolism and auxin and cytokinin signaling pathways on root growth and development of grafted apple
inferredcites →https://doi.org/10.1186/s12864-016-3041-3openalex-snapshot
Characterizing the population structure and genetic diversity of maize breeding germplasm in Southwest China using genome-wide SNP markers
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/10.1242/dev.152132openalex-snapshot
Non-canonical WOX11 -mediated root branching contributes to plasticity in Arabidopsis root system architecture
inferredcites →https://doi.org/10.17660/ejhs.2015/80.3.3openalex-snapshot
Root growth, yield and fruit quality of 'Red Fuji' apple trees in relation to planting depth of dwarfing interstock on the Loess Plateau
inferredcites →https://doi.org/10.3389/fpls.2017.01059openalex-snapshot
High miR156 Expression Is Required for Auxin-Induced Adventitious Root Formation via MxSPL26 Independent of PINs and ARFs in Malus xiaojinensis
inferredcites →https://doi.org/10.3390/plants8040094openalex-snapshot
Cytokinin-Dependent Control of GH3 Group II Family Genes in the Arabidopsis Root

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/10.1093/hr/uhaf101openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/plphys/kiad099openalex-snapshot
MicroRNA156ab regulates apple plant growth and drought tolerance by targeting transcription factor MsSPL13
inferred← citeshttps://doi.org/10.1093/plphys/kiae025openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/tpj.15631openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/tpj.16082openalex-snapshot
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Genome-Wide Analysis of GRETCHEN HAGEN3 Genes and Characterization of IAA-Amido Synthetase Gene CsGH3.1 in Rhizome Proliferation in Cymbidium sinense ‘Qijianbaimo’
inferred← citeshttps://doi.org/10.3390/plants14111627openalex-snapshot
The Overexpression of ORR3 Negatively Regulates the Growth of Young Rice Roots by Reducing the Cell Size and the Number in the Root Meristematic Zone
inferred← citeshttps://doi.org/10.48130/opr-0024-0024openalex-snapshot
Overexpression of HmWOX8 promotes callus proliferation and shoot regeneration by regulating hormone signaling and shoot development-related genes
inferred← citeshttps://doi.org/10.6084/m9.figshare.26066115openalex-snapshot
Additional file 1 of Physiological and transcriptome analysis of changes in endogenous hormone and sugar content during the formation of tender asparagus stems
inferred← citeshttps://doi.org/10.6084/m9.figshare.26066185openalex-snapshot
Additional file 2 of Physiological and transcriptome analysis of changes in endogenous hormone and sugar content during the formation of tender asparagus stems
inferred← citeshttps://doi.org/10.67443/pt-2026-01010003openalex-snapshot
Light Spectrum, Intensity, and Photoperiod as Drivers of Redox Regulation in Primary and Secondary Plant Metabolism: Central Roles of LED Lighting Systems
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