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Maintenance of phosphate homeostasis and root development are coordinately regulated by MYB1, an R2R3-type MYB transcription factor in rice

https://doi.org/10.1093/jxb/erx174
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What this work says

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

inferredcites →https://doi.org/10.1002/9781118958841.ch1openalex-snapshot
Phosphorus: Back to the Roots
inferredcites →https://doi.org/10.1007/s00122-004-1751-4openalex-snapshot
Phosphorus deficiency-induced root elongation and its QTL in rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1007/s00425-008-0754-9openalex-snapshot
PRD, an Arabidopsis AINTEGUMENTA-like gene, is involved in root architectural changes in response to phosphate starvation
inferredcites →https://doi.org/10.1007/s11103-016-0564-6openalex-snapshot
Phosphate starvation induced OsPHR4 mediates Pi-signaling and homeostasis in rice
inferredcites →https://doi.org/10.1007/s11104-004-2005-6openalex-snapshot
Phosphate Acquisition
inferredcites →https://doi.org/10.1016/j.copbio.2012.03.002openalex-snapshot
Bioengineering and management for efficient phosphorus utilization in crops and pastures
inferredcites →https://doi.org/10.1016/j.devcel.2015.02.007openalex-snapshot
Iron-Dependent Callose Deposition Adjusts Root Meristem Maintenance to Phosphate Availability
inferredcites →https://doi.org/10.1016/j.molp.2015.12.012openalex-snapshot
Complex Regulation of Plant Phosphate Transporters and the Gap between Molecular Mechanisms and Practical Application: What Is Missing?
inferredcites →https://doi.org/10.1016/j.pbi.2014.06.009openalex-snapshot
Control of phosphate homeostasis through gene regulation in crops
inferredcites →https://doi.org/10.1016/j.plaphy.2014.02.024openalex-snapshot
Overexpression of OsMYB4P, an R2R3-type MYB transcriptional activator, increases phosphate acquisition in rice
inferredcites →https://doi.org/10.1016/j.tplants.2011.05.006openalex-snapshot
Root developmental adaptation to phosphate starvation: better safe than sorry
inferredcites →https://doi.org/10.1038/cr.2013.123openalex-snapshot
Targeted mutagenesis in rice using CRISPR-Cas system
inferredcites →https://doi.org/10.1038/ng2041openalex-snapshot
Root tip contact with low-phosphate media reprograms plant root architecture
inferredcites →https://doi.org/10.1042/bj20070102openalex-snapshot
BHLH32 modulates several biochemical and morphological processes that respond to Pi starvation in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1404654111openalex-snapshot
SPX1 is a phosphate-dependent inhibitor of PHOSPHATE STARVATION RESPONSE 1 in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1404680111openalex-snapshot
Rice SPX1 and SPX2 inhibit phosphate starvation responses through interacting with PHR2 in a phosphate-dependent manner
inferredcites →https://doi.org/10.1093/jxb/erm221openalex-snapshot
Sucrose transport in the phloem: integrating root responses to phosphorus starvation
inferredcites →https://doi.org/10.1093/jxb/erv259openalex-snapshot
The paralogous R3 MYB proteins CAPRICE, TRIPTYCHON and ENHANCER OF TRY AND CPC1 play pleiotropic and partly non-redundant roles in the phosphate starvation response of Arabidopsis roots
inferredcites →https://doi.org/10.1093/jxb/erv515openalex-snapshot
OsWRKY74, a WRKY transcription factor, modulates tolerance to phosphate starvation in rice
inferredcites →https://doi.org/10.1093/jxb/erw444openalex-snapshot
Transport and homeostasis of potassium and phosphate: limiting factors for sustainable crop production
inferredcites →https://doi.org/10.1093/mp/ssn081openalex-snapshot
Phosphate Starvation Responses and Gibberellic Acid Biosynthesis are Regulated by the MYB62 Transcription Factor in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.204401openalex-snapshot
A conserved MYB transcription factor involved in phosphate starvation signaling both in vascular plants and in unicellular algae
inferredcites →https://doi.org/10.1104/pp.105.063115openalex-snapshot
OsPTF1, a Novel Transcription Factor Involved in Tolerance to Phosphate Starvation in Rice
inferredcites →https://doi.org/10.1104/pp.106.078063openalex-snapshot
pho2, a Phosphate Overaccumulator, Is Caused by a Nonsense Mutation in a MicroRNA399 Target Gene
inferredcites →https://doi.org/10.1104/pp.106.079707openalex-snapshot
PHO2, MicroRNA399, and PHR1 Define a Phosphate-Signaling Pathway in Plants
inferredcites →https://doi.org/10.1104/pp.106.093971openalex-snapshot
WRKY75 Transcription Factor Is a Modulator of Phosphate Acquisition and Root Development in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.101691openalex-snapshot
Phosphate Homeostasis and Root Development in Arabidopsis Are Synchronized by the Zinc Finger Transcription Factor ZAT6
inferredcites →https://doi.org/10.1104/pp.107.103788openalex-snapshot
Phosphate Starvation Root Architecture and Anthocyanin Accumulation Responses Are Modulated by the Gibberellin-DELLA Signaling Pathway in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.107.111443openalex-snapshot
OsPHR2 Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
inferredcites →https://doi.org/10.1104/pp.108.128504openalex-snapshot
A Recommendation for Naming Transcription Factor Proteins in the Grasses
inferredcites →https://doi.org/10.1104/pp.110.170209openalex-snapshot
LEAF TIP NECROSIS1 Plays a Pivotal Role in the Regulation of Multiple Phosphate Starvation Responses in Rice
inferredcites →https://doi.org/10.1104/pp.111.174581openalex-snapshot
Roles of Arbuscular Mycorrhizas in Plant Phosphorus Nutrition: Interactions between Pathways of Phosphorus Uptake in Arbuscular Mycorrhizal Roots Have Important Implications for Understanding and Manipulating Plant Phosphorus Acquisition
inferredcites →https://doi.org/10.1104/pp.111.175240openalex-snapshot
The Phosphate Transporter Gene OsPht1;8 Is Involved in Phosphate Homeostasis in Rice
inferredcites →https://doi.org/10.1104/pp.111.175281openalex-snapshot
Metabolic Adaptations of Phosphate-Starved Plants
inferredcites →https://doi.org/10.1104/pp.111.175380openalex-snapshot
Sugar Signaling in Root Responses to Low Phosphorus Availability
inferredcites →https://doi.org/10.1104/pp.111.181669openalex-snapshot
OsPHF1 Regulates the Plasma Membrane Localization of Low- and High-Affinity Inorganic Phosphate Transporters and Determines Inorganic Phosphate Uptake and Translocation in Rice
inferredcites →https://doi.org/10.1104/pp.112.194217openalex-snapshot
OsMYB2P-1 , an R2R3 MYB Transcription Factor, Is Involved in the Regulation of Phosphate-Starvation Responses and Root Architecture in Rice
inferredcites →https://doi.org/10.1104/pp.112.205922openalex-snapshot
Regulation of miR399f Transcription by AtMYB2 Affects Phosphate Starvation Responses in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.218453openalex-snapshot
Plasticity of the Arabidopsis Root System under Nutrient Deficiencies
inferredcites →https://doi.org/10.1104/pp.113.231183openalex-snapshot
ETHYLENE RESPONSE FACTOR070 Regulates Root Development and Phosphate Starvation-Mediated Responses
inferredcites →https://doi.org/10.1104/pp.113.235077openalex-snapshot
Arabidopsis WRKY45 Transcription Factor Activates PHOSPHATE TRANSPORTER1;1 Expression in Response to Phosphate Starvation
inferredcites →https://doi.org/10.1104/pp.114.245019openalex-snapshot
Activity of the Brassinosteroid Transcription Factors BRASSINAZOLE RESISTANT1 and BRASSINOSTEROID INSENSITIVE1-ETHYL METHANESULFONATE-SUPPRESSOR1/BRASSINAZOLE RESISTANT2 Blocks Developmental Reprogramming in Response to Low Phosphate Availability
inferredcites →https://doi.org/10.1104/pp.114.252338openalex-snapshot
Reducing the Genetic Redundancy of Arabidopsis PHOSPHATE TRANSPORTER1 Transporters to Study Phosphate Uptake and Signaling
inferredcites →https://doi.org/10.1104/pp.15.00736openalex-snapshot
Integrative Comparison of the Role of the PHOSPHATE RESPONSE1 Subfamily in Phosphate Signaling and Homeostasis in Rice
inferredcites →https://doi.org/10.1104/pp.15.01336openalex-snapshot
Arabidopsis PHL2 and PHR1 Act Redundantly as the Key Components of the Central Regulatory System Controlling Transcriptional Responses to Phosphate Starvation
inferredcites →https://doi.org/10.1104/pp.16.00278openalex-snapshot
Phosphate Deficiency Induces the Jasmonate Pathway and Enhances Resistance to Insect Herbivory
inferredcites →https://doi.org/10.1105/tpc.108.058719openalex-snapshot
Phosphate Availability Alters Lateral Root Development inArabidopsisby Modulating Auxin Sensitivity via a Mechanism Involving the TIR1 Auxin Receptor
inferredcites →https://doi.org/10.1105/tpc.108.064980openalex-snapshot
The WRKY6 Transcription Factor Modulates PHOSPHATE1 Expression in Response to Low Pi Stress in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.117325openalex-snapshot
Spatio-Temporal Transcript Profiling of Rice Roots and Shoots in Response to Phosphate Starvation and Recovery
inferredcites →https://doi.org/10.1105/tpc.114.132092openalex-snapshot
Brassinosteroid Regulates Cell Elongation by Modulating Gibberellin Metabolism in Rice
inferredcites →https://doi.org/10.1105/tpc.114.135335openalex-snapshot
The Rice CK2 Kinase Regulates Trafficking of Phosphate Transporters in Response to Phosphate Levels
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01405.xopenalex-snapshot
Identification of QTL controlling root growth response to phosphate starvation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02161.xopenalex-snapshot
Phosphate transport in Arabidopsis : Pht1;1 and Pht1;4 play a major role in phosphate acquisition from both low‐ and high‐phosphate environments
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03726.xopenalex-snapshot
Two rice phosphate transporters, OsPht1;2 and OsPht1;6, have different functions and kinetic properties in uptake and translocation
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04170.xopenalex-snapshot
OsSPX1 suppresses the function of OsPHR2 in the regulation of expression of OsPT2 and phosphate homeostasis in shoots of rice
inferredcites →https://doi.org/10.1111/j.1744-7909.2009.00819.xopenalex-snapshot
Overexpressing HRS1 Confers Hypersensitivity to Low Phosphate‐Elicited Inhibition of Primary Root Growth in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/jipb.12434openalex-snapshot
Improving crop nutrient efficiency through root architecture modifications
inferredcites →https://doi.org/10.1111/nph.12499openalex-snapshot
Auxin response factor (Os ARF 12), a novel regulator for phosphate homeostasis in rice (Oryza sativa)
inferredcites →https://doi.org/10.1111/pce.12001openalex-snapshot
OsARF16, a transcription factor, is required for auxin and phosphate starvation response in rice ( Oryza sativa L.)
inferredcites →https://doi.org/10.1126/science.1068037openalex-snapshot
A Draft Sequence of the Rice Genome ( Oryza sativa L. ssp. indica )
inferredcites →https://doi.org/10.1126/science.1068275openalex-snapshot
A Draft Sequence of the Rice Genome ( Oryza sativa L. ssp. japonica )
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103849openalex-snapshot
Signaling Network in Sensing Phosphate Availability in Plants
inferredcites →https://doi.org/10.1146/annurev-arplant-050213-035949openalex-snapshot
Phosphate Nutrition: Improving Low-Phosphate Tolerance in Crops
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.665openalex-snapshot
PHOSPHATE ACQUISITION
inferredcites →https://doi.org/10.1371/journal.pgen.1001102openalex-snapshot
A Central Regulatory System Largely Controls Transcriptional Activation and Repression Responses to Phosphate Starvation in Arabidopsis

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/10.2139/ssrn.4137983openalex-extracted
Regulation of Stress Correlated Genes and Maintenance of Ionome Homeostasis in Rice Plants in Response to Arsenite Stress: Potential Connection between Transcriptomics and Ionomics
inferred← citeshttps://doi.org/10.1002/fes3.70068openalex-snapshot
Enhancing Crop Nutrition in Arid and Semiarid Regions of Africa Through Genome Editing Using CRISPR /Cas
inferred← citeshttps://doi.org/10.1002/fsn3.70561openalex-snapshot
Genome‐Wide Analyses of Phosphate Transporters in Wild Rice ( Oryza brachyantha ) Revealed Their Evolution and Regulatory Roles in Phosphate Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-031-81639-0_6openalex-snapshot
Crop Genome Editing for Nutrient Use Efficiency
inferred← citeshttps://doi.org/10.1007/s00122-019-03527-6openalex-snapshot
Improvement of nutrient use efficiency in rice: current toolbox and future perspectives
inferred← citeshttps://doi.org/10.1007/s00122-024-04728-4openalex-snapshot
Early exposure to phosphorus starvation induces genetically determined responses in Sorghum bicolor roots
inferred← citeshttps://doi.org/10.1007/s00344-023-11002-2openalex-snapshot
The Research Progress and Prospects of the NIGT1.2 Gene in Plants
inferred← citeshttps://doi.org/10.1007/s00344-024-11409-5openalex-snapshot
Regulation of Common Early and Late Stress Responses in Rice by Transcriptional and Antioxidant Mechanisms Under Salt Stress
inferred← citeshttps://doi.org/10.1007/s10534-023-00510-zopenalex-snapshot
Gene regulation and ionome homeostasis in rice plants in response to arsenite stress: potential connection between transcriptomics and ionomics
inferred← citeshttps://doi.org/10.1007/s10725-020-00688-zopenalex-snapshot
Characterization of two cis-acting elements, P1BS and W-box, in the regulation of OsPT6 responsive to phosphors deficiency
inferred← citeshttps://doi.org/10.1007/s10725-022-00922-wopenalex-snapshot
Rice MYB transcription factor OsMYB1R1 negatively regulates drought resistance
inferred← citeshttps://doi.org/10.1007/s11032-019-1059-3openalex-snapshot
Molecular control and genetic improvement of phosphorus use efficiency in rice
inferred← citeshttps://doi.org/10.1007/s11033-022-07354-9openalex-snapshot
Phosphorus homeostasis: acquisition, sensing, and long-distance signaling in plants
inferred← citeshttps://doi.org/10.1007/s11103-022-01254-zopenalex-snapshot
Transcriptome analysis of a near-isogenic line and its recurrent parent reveals the role of Pup1 QTL in phosphorus deficiency tolerance of rice at tillering stage
inferred← citeshttps://doi.org/10.1007/s11240-019-01716-1openalex-snapshot
SmMYB98b positive regulation to tanshinones in Salvia miltiorrhiza Bunge hairy roots
inferred← citeshttps://doi.org/10.1007/s11627-020-10108-6openalex-snapshot
Overexpression of annexin gene in rice (Oryza sativa L.) for salinity and water stress
inferred← citeshttps://doi.org/10.1007/s12042-024-09386-wopenalex-snapshot
Genome-Wide Analysis of the R2R3-MYB Gene Family in Durian (Durio zibethinus) and Potential Role in Nutrient Stress Response
inferred← citeshttps://doi.org/10.1007/s12298-024-01423-yopenalex-snapshot
Breeding rice for yield improvement through CRISPR/Cas9 genome editing method: current technologies and examples
inferred← citeshttps://doi.org/10.1007/s12298-024-01479-wopenalex-snapshot
Opportunity for genome engineering to enhance phosphate homeostasis in crops
inferred← citeshttps://doi.org/10.1007/s13562-022-00788-zopenalex-snapshot
Overexpression of AtMYB115 gene in transgenic rice exhibits increased early regeneration and results in dwarf phenotype
inferred← citeshttps://doi.org/10.1016/b978-0-12-819334-1.00011-3openalex-snapshot
Transcription factors and their roles in phosphorus stress tolerance in crop plants
inferred← citeshttps://doi.org/10.1016/b978-0-443-21793-7.00026-xopenalex-snapshot
Genome editing for stress tolerance in rice
inferred← citeshttps://doi.org/10.1016/b978-0-443-33465-8.00033-5openalex-snapshot
Next-generation biotechnology for improving abiotic stress tolerance in rice
inferred← citeshttps://doi.org/10.1016/j.agwat.2022.108120openalex-snapshot
Assessment and Mitigation of Soil Water Stress of Rainfed Lentil (Lens Culinaries Medik) Through Sowing Time, Tillage and Potassic Fertilization Disparities
inferred← citeshttps://doi.org/10.1016/j.copbio.2024.103180openalex-snapshot
Bioengineering and management for efficient and sustainable utilization of phosphorus in crops
inferred← citeshttps://doi.org/10.1016/j.cropd.2025.100095openalex-snapshot
Genome-wide association study identifies loci and candidate genes for root traits in rice grown in Brazil
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2020.104223openalex-snapshot
Ectopic expression of BrALDH7B2 gene encoding an antiquitin from Brassica rapa confers tolerance to abiotic stresses and improves photosynthetic performance under salt stress in tobacco
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105120openalex-snapshot
Breeding and genomics approaches for improving phosphorus-use efficiency in grain legumes
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2022.105130openalex-snapshot
Transcriptome-Wide Analysis of M6a Methylation Reveals Genetic Responses to Cadmium Stress at Germination Stage in Rice
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105257openalex-snapshot
NtPIN3 positively regulates low phosphorus tolerance by changing root elongation, Pi concentration and antioxidant capacity in tobacco
inferred← citeshttps://doi.org/10.1016/j.foodchem.2021.129699openalex-snapshot
Selenium and anthocyanins share the same transcription factors R2R3MYB and bHLH in wheat
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.136652openalex-snapshot
MYB transcription factors in plants: A comprehensive review of their discovery, structure, classification, functional diversity and regulatory mechanism
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144539openalex-snapshot
Optimizing plant phosphate uptake: Advances in the core regulatory mechanisms of phosphate starvation response proteins and their macromolecular partners: A review
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.122155openalex-snapshot
Identification of key candidate genes and pathways responding to nitrogen stress in sugarcane
inferred← citeshttps://doi.org/10.1016/j.jare.2020.01.012openalex-snapshot
Tanshinone and salvianolic acid biosynthesis are regulated by SmMYB98 in Salvia miltiorrhiza hairy roots
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2021.127106openalex-snapshot
Novel phytase PvPHY1 from the As-hyperaccumulator Pteris vittata enhances P uptake and phytate hydrolysis, and inhibits As translocation in Plant
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2022.129430openalex-snapshot
Arsenic-induced up-regulation of P transporters PvPht1;3–1;4 enhances both As and P uptake in As-hyperaccumulator Pteris vittata
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.134640openalex-snapshot
Multiomics analysis reveals a substantial decrease in nanoplastics uptake and associated impacts by nano zinc oxide in fragrant rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.134867openalex-snapshot
Novel phosphatase PvPAP1 from the As-hyperaccumulator Pteris vittata promotes organic P utilization and plant growth: Extracellular exudation and phytate hydrolysis
inferred← citeshttps://doi.org/10.1016/j.jplph.2026.154815openalex-snapshot
Phytohormonal orchestration of plant phosphate starvation responses
inferred← citeshttps://doi.org/10.1016/j.molp.2020.02.005openalex-snapshot
Enhanced Vitamin C Production Mediated by an ABA-Induced PTP-like Nucleotidase Improves Plant Drought Tolerance in Arabidopsis and Maize
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Crop designs: The ideal root architecture for future crop breeding
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112415openalex-snapshot
Tolerance of Oryza sativa to low phosphate is associated with adaptive changes in root architecture and metabolic exudates
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.113449openalex-snapshot
MYB transcription factors coordinate plant growth, metabolism and environmental adaptation
inferred← citeshttps://doi.org/10.1016/j.plaphy.2021.09.045openalex-snapshot
Identification of SPX family genes in the maize genome and their expression under different phosphate regimes
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108006openalex-snapshot
Polyphosphate promotes oxidation resistance of ppk-expressing transgenic rice in low phosphorus culture
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109918openalex-snapshot
Sulfur and phosphorus transporters in plants: Integrating mechanisms for optimized nutrient supply
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.03.010openalex-snapshot
The potential application of genome editing by using CRISPR/Cas9, and its engineered and ortholog variants for studying the transcription factors involved in the maintenance of phosphate homeostasis in model plants
inferred← citeshttps://doi.org/10.1021/acs.est.2c04367openalex-snapshot
Novel Mycorrhiza-Specific P Transporter PvPht1;6 Contributes to As Accumulation at the Symbiotic Interface of As-Hyperaccumulator Pteris vittata
inferred← citeshttps://doi.org/10.1021/acs.est.3c09335openalex-snapshot
Novel Phosphate Transporter-B PvPTB1;1/1;2 Contribute to Efficient Phosphate Uptake and Arsenic Accumulation in As-Hyperaccumulator Pteris vittata
inferred← citeshttps://doi.org/10.1021/acs.est.5c08760openalex-snapshot
Phytate-Mediated Arsenic Hyperaccumulation in Pteris vittata : Synthesis, Sequestration, and Exudation
inferred← citeshttps://doi.org/10.1038/s41598-019-45511-6openalex-snapshot
Sequencing and comparative analysis of three Chlorella genomes provide insights into strain-specific adaptation to wastewater
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inferred← citeshttps://doi.org/10.1093/aob/mcag034openalex-snapshot
ZmPHR1 coordinates root–rhizosphere processes and phosphorus allocation to enhance phosphorus efficiency and yield in maize
inferred← citeshttps://doi.org/10.1093/hr/uhac282openalex-snapshot
SlMYB1regulates the accumulation of lycopene, fruit shape, and resistance toBotrytis cinereain tomato
inferred← citeshttps://doi.org/10.1093/hr/uhaf058openalex-snapshot
Molecular mechanism of SmMYB53 activates the expression of SmCYP71D375, thereby modulating tanshinone accumulation in Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.1093/jxb/erab177openalex-snapshot
Integrating transcriptome, co-expression and QTL-seq analysis reveals that primary root growth in maize is regulated via flavonoid biosynthesis and auxin signal transduction
inferred← citeshttps://doi.org/10.1093/jxb/erab300openalex-snapshot
Sulfoquinovosyl diacylglycerol synthase 1 impairs glycolipid accumulation and photosynthesis in phosphate-deprived rice
inferred← citeshttps://doi.org/10.1093/jxb/erac247openalex-snapshot
The transcription factor OsGATA6 regulates rice heading date and grain number per panicle
inferred← citeshttps://doi.org/10.1093/jxb/erac456openalex-snapshot
The transcription factor OsWRKY10 inhibits phosphate uptake via suppressingOsPHT1;2expression under phosphate-replete conditions in rice
inferred← citeshttps://doi.org/10.1093/jxb/ery163openalex-snapshot
Are we ready to improve phosphorus homeostasis in rice?
inferred← citeshttps://doi.org/10.1093/jxb/erz540openalex-snapshot
MYB57 transcriptionally regulates MAPK11 to interact with PAL2;3 and modulate rice allelopathy
inferred← citeshttps://doi.org/10.1093/pcp/pcag053openalex-snapshot
Mirabilis jalapa mannanase-mediated mannose promotes root development in Arabidopsis via the MYB41-DWF4 module regulating brassinosteroid signaling pathways
inferred← citeshttps://doi.org/10.1093/plcell/koad268openalex-snapshot
The transcription factor MYB110 regulates plant height, lodging resistance, and grain yield in rice
inferred← citeshttps://doi.org/10.1093/plphys/kiae495openalex-snapshot
Developmental responses of roots to limited phosphate availability: Research progress and application in cereals
inferred← citeshttps://doi.org/10.1111/jipb.13053openalex-snapshot
Potassium and phosphorus transport and signaling in plants
inferred← citeshttps://doi.org/10.1111/jipb.13496openalex-snapshot
NIGT1 represses plant growth and mitigates phosphate starvation signaling to balance the growth response tradeoff in rice
inferred← citeshttps://doi.org/10.1111/jipb.13932openalex-snapshot
Recent advances in improving yield and immunity through transcription factor engineering
inferred← citeshttps://doi.org/10.1111/nph.16931openalex-snapshot
OsWRKY21 and OsWRKY108 function redundantly to promote phosphate accumulation through maintaining the constitutive expression of OsPHT1;1 under phosphate‐replete conditions
inferred← citeshttps://doi.org/10.1111/nph.17534openalex-snapshot
TaPHT1;9‐4B and its transcriptional regulator TaMYB4‐7D contribute to phosphate uptake and plant growth in bread wheat
inferred← citeshttps://doi.org/10.1111/nph.70430openalex-snapshot
GA ‐ DELLA ‐ OsMYB48 ‐1 module–mediated regulation of inorganic phosphate uptake in rice
inferred← citeshttps://doi.org/10.1111/pbi.13516openalex-snapshot
Genome‐wide association coupled gene to gene interaction studies unveil novel epistatic targets among major effect loci impacting rice grain chalkiness
inferred← citeshttps://doi.org/10.1111/pce.15540openalex-snapshot
OsMYB67 Knockout Promotes Rice Heading and Yield by Facilitating Copper Distribution in Panicles
inferred← citeshttps://doi.org/10.1111/ppl.71005openalex-snapshot
Powering Genome Editing in Rice by Harnessing Promising Gene Resources: A Comprehensive Roadmap
inferred← citeshttps://doi.org/10.1111/tpj.14637openalex-snapshot
Nitrate‐inducible NIGT1 proteins modulate phosphate uptake and starvation signalling via transcriptional regulation of SPX genes
inferred← citeshttps://doi.org/10.1152/physrev.00008.2019openalex-snapshot
Phosphate Transport in Epithelial and Nonepithelial Tissue
inferred← citeshttps://doi.org/10.1155/2019/4168045openalex-snapshot
Discovery of Functional SNPs via Genome-Wide Exploration of Malaysian Pigmented Rice Varieties
inferred← citeshttps://doi.org/10.1186/s12284-018-0262-xopenalex-snapshot
Molecular Mechanisms of Root Development in Rice
inferred← citeshttps://doi.org/10.1186/s12870-019-1914-8openalex-snapshot
Transcriptome analysis reveals candidate genes related to phosphorus starvation tolerance in sorghum
inferred← citeshttps://doi.org/10.1186/s12870-020-02585-zopenalex-snapshot
Genome-wide sRNA and mRNA transcriptomic profiling insights into dynamic regulation of taproot thickening in radish (Raphanus sativus L.)
inferred← citeshttps://doi.org/10.1186/s12870-021-03015-4openalex-snapshot
Characterization of contrasting rice (Oryza sativa L.) genotypes reveals the Pi-efficient schema for phosphate starvation tolerance
inferred← citeshttps://doi.org/10.1270/jsbbs.20102openalex-snapshot
Modulation of plant root traits by nitrogen and phosphate: transporters, long-distance signaling proteins and peptides, and potential artificial traps
inferred← citeshttps://doi.org/10.1360/ssv-2023-0048openalex-snapshot
Molecular regulation network of phosphorus starvation signaling and genetic improvement of phosphorus efficiency in plants
inferred← citeshttps://doi.org/10.19103/as.2020.0075.03openalex-snapshot
The development of crop root architecture and optimization of nutrition acquisition: the case of rice
inferred← citeshttps://doi.org/10.20944/preprints202306.0686.v1openalex-snapshot
Molecular Regulation for Maintenance of Plant Phosphate Homeostasis in Crop Plants as Basis for Precision Genome Engineering
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2401090/v1openalex-snapshot
Structural and functional analysis of 31 HbMYB gene family members in rubber tree leaves
inferred← citeshttps://doi.org/10.2139/ssrn.5398308openalex-snapshot
Mirman-Mediated Mannose Regulates Lateral Root Development Through Hormone Signaling Pathways In Arabidopsis Thaliana
inferred← citeshttps://doi.org/10.31390/gradschool_dissertations.5904openalex-snapshot
Genetic Dissection and QTL Pyramiding to Enhance Salinity Tolerance in Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.3389/fgene.2022.900897openalex-snapshot
Genome Editing Targets for Improving Nutrient Use Efficiency and Nutrient Stress Adaptation
inferred← citeshttps://doi.org/10.3389/fpls.2019.00168openalex-snapshot
Overexpression of a MYB Family Gene, OsMYB6, Increases Drought and Salinity Stress Tolerance in Transgenic Rice
inferred← citeshttps://doi.org/10.3389/fpls.2022.1083374openalex-snapshot
Genetic analysis of grapevine root system architecture and loci associated gene networks
inferred← citeshttps://doi.org/10.3389/fpls.2022.863283openalex-snapshot
CBL-Interacting Protein Kinase OsCIPK18 Regulates the Response of Ammonium Toxicity in Rice Roots
inferred← citeshttps://doi.org/10.3389/fpls.2025.1527547openalex-snapshot
From genes to traits: maximizing phosphorus utilization efficiency in crop plants
inferred← citeshttps://doi.org/10.3389/fpls.2025.1653514openalex-snapshot
Overexpression of OsMYBS1 affect leaf morphology, photosynthesis, and agronomic performance in rice
inferred← citeshttps://doi.org/10.3389/fpls.2025.1668800openalex-snapshot
Research progress on the synergistic regulation of MYB transcription factor-mediated developmental plasticity and stress responses in rice
inferred← citeshttps://doi.org/10.3389/fpls.2026.1877859openalex-snapshot
Adaptation mechanisms of low-phosphorus stress in plants: physiological responses, molecular regulation, and future perspectives
inferred← citeshttps://doi.org/10.3390/agronomy13123007openalex-snapshot
The Analysis of Short-Term Differential Expression of Transcription Factor Family Genes in Diploid and Tetraploid Rice (Oryza sativa L.) Varieties during Blast Fungus Infection
inferred← citeshttps://doi.org/10.3390/f14040710openalex-snapshot
Genome-Wide Identification and Expression Analysis of the R2R3-MYB Gene Family in Rubber Trees
inferred← citeshttps://doi.org/10.3390/genes12121891openalex-snapshot
Overexpression of Orange Gene (OsOr-R115H) Enhances Heat Tolerance and Defense-Related Gene Expression in Rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.3390/ijms21010333openalex-snapshot
Gluconacetobacter diazotrophicus Changes The Molecular Mechanisms of Root Development in Oryza sativa L. Growing Under Water Stress
inferred← citeshttps://doi.org/10.3390/ijms23169262openalex-snapshot
MYB Transcription Factors Becoming Mainstream in Plant Roots
inferred← citeshttps://doi.org/10.3390/ijms232314549openalex-snapshot
A Novel R2R3-MYB Transcription Factor FtMYB22 Negatively Regulates Salt and Drought Stress through ABA-Dependent Pathway
inferred← citeshttps://doi.org/10.3390/ijms24065107openalex-snapshot
Phenotypes and Molecular Mechanisms Underlying the Root Response to Phosphate Deprivation in Plants
inferred← citeshttps://doi.org/10.3390/ijms25042209openalex-snapshot
OsMYB58 Negatively Regulates Plant Growth and Development by Regulating Phosphate Homeostasis
inferred← citeshttps://doi.org/10.3390/ijms26178385openalex-snapshot
Multi-Stage Transcriptome Analysis Identifies Key Molecular Pathways for Soybean Under Phosphorus-Limited Conditions
inferred← citeshttps://doi.org/10.3390/life15060962openalex-snapshot
OsMYBR1, a 1R-MYB Family Transcription Factor Regulates Starch Biosynthesis in Rice Endosperm
inferred← citeshttps://doi.org/10.3390/plants11060788openalex-snapshot
Novel QTL Associated with Aerenchyma-Mediated Radial Oxygen Loss (ROL) in Rice (Oryza sativa L.) under Iron (II) Sulfide
inferred← citeshttps://doi.org/10.3390/plants11151928openalex-snapshot
Genome-Wide Identification of R2R3-MYB Transcription Factor and Expression Analysis under Abiotic Stress in Rice
inferred← citeshttps://doi.org/10.48130/frures-2023-0026openalex-snapshot
Functional identification of the bHLH transcription factor MdSAT1 in the phosphate deficiency response
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