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PHOSPHATE RESPONSE 1 family members act distinctly to regulate transcriptional responses to phosphate starvation

https://doi.org/10.1093/plphys/kiac521
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What this work says

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

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Identification of transcription factors that bind to the 5′-UTR of the barley PHO2 gene
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High-Efficiency Genome Editing in Arabidopsis Using YAO Promoter-Driven CRISPR/Cas9 System
inferredcites →https://doi.org/10.1016/j.molp.2019.08.002openalex-snapshot
Inositol Pyrophosphate InsP8 Acts as an Intracellular Phosphate Signal in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2020.06.009openalex-snapshot
TBtools: An Integrative Toolkit Developed for Interactive Analyses of Big Biological Data
inferredcites →https://doi.org/10.1016/j.molp.2021.12.005openalex-snapshot
Plant adaptation to low phosphorus availability: Core signaling, crosstalks, and applied implications
inferredcites →https://doi.org/10.1016/j.tplants.2020.04.013openalex-snapshot
Tightening the Phosphorus Cycle through Phosphorus-Efficient Crop Genotypes
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Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
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Metascape provides a biologist-oriented resource for the analysis of systems-level datasets
inferredcites →https://doi.org/10.1038/s41467-020-20681-4openalex-snapshot
Inositol pyrophosphates promote the interaction of SPX domains with the coiled-coil motif of PHR transcription factors to regulate plant phosphate homeostasis
inferredcites →https://doi.org/10.1038/s41477-021-00981-3openalex-snapshot
Live single-cell transcriptional dynamics via RNA labelling during the phosphate response in plants
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Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0505266102openalex-snapshot
A genome-wide transcriptional analysis using Arabidopsis thaliana Affymetrix gene chips determined plant responses to phosphate deprivation
inferredcites →https://doi.org/10.1093/aob/mct080openalex-snapshot
A phosphate starvation response regulator Ta-PHR1 is involved in phosphate signalling and increases grain yield in wheat
inferredcites →https://doi.org/10.1093/jxb/erx292openalex-snapshot
GmPHR25, a GmPHR member up-regulated by phosphate starvation, controls phosphate homeostasis in soybean
inferredcites →https://doi.org/10.1093/nar/gkx382openalex-snapshot
agriGO v2.0: a GO analysis toolkit for the agricultural community, 2017 update
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.103.021022openalex-snapshot
Phosphate Starvation Triggers Distinct Alterations of Genome Expression in Arabidopsis Roots and Leaves
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.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.107.111740openalex-snapshot
Firefly Luciferase Complementation Imaging Assay for Protein-Protein Interactions in Plants
inferredcites →https://doi.org/10.1104/pp.109.147280openalex-snapshot
Uncovering Small RNA-Mediated Responses to Phosphate Deficiency in Arabidopsis by Deep Sequencing
inferredcites →https://doi.org/10.1104/pp.111.183723openalex-snapshot
The Arabidopsis Purple Acid Phosphatase AtPAP10 Is Predominantly Associated with the Root Surface and Plays an Important Role in Plant Tolerance to Phosphate Limitation
inferredcites →https://doi.org/10.1104/pp.114.238725openalex-snapshot
Suppression of Photosynthetic Gene Expression in Roots Is Required for Sustained Root Growth under Phosphate Deficiency
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.18.00594openalex-snapshot
SPX4 Acts on PHR1-Dependent and -Independent Regulation of Shoot Phosphorus Status in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.12.11.2201openalex-snapshot
A Rab1 GTPase Is Required for Transport between the Endoplasmic Reticulum and Golgi Apparatus and for Normal Golgi Movement in Plants
inferredcites →https://doi.org/10.1105/tpc.17.00268openalex-snapshot
Light and Ethylene Coordinately Regulate the Phosphate Starvation Response through Transcriptional Regulation of PHOSPHATE STARVATION RESPONSE1
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Genome‐wide reprogramming of metabolism and regulatory networks of Arabidopsis in response to phosphorus
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Essential role of MYB transcription factor: PvPHR1 and microRNA: PvmiR399 in phosphorus‐deficiency signalling in common bean roots
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Opportunities for improving phosphorus‐use efficiency in crop plants
inferredcites →https://doi.org/10.1111/ppl.13503openalex-snapshot
SlPHL1 , a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response
inferredcites →https://doi.org/10.1126/science.aad9858openalex-snapshot
Control of eukaryotic phosphate homeostasis by inositol polyphosphate sensor domains
inferredcites →https://doi.org/10.1146/annurev-arplant-050213-035949openalex-snapshot
Phosphate Nutrition: Improving Low-Phosphate Tolerance in Crops
inferredcites →https://doi.org/10.11983/cbb19229openalex-snapshot
Luciferase Complementation Assay for Detecting Protein Interactions
inferredcites →https://doi.org/10.1242/dev.01595openalex-snapshot
Genetic and molecular identification of genes required for female gametophyte development and function in Arabidopsis
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
inferredcites →https://doi.org/10.1371/journal.pgen.1002021openalex-snapshot
Genetic Regulation by NLA and MicroRNA827 for Maintaining Nitrate-Dependent Phosphate Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pone.0044005openalex-snapshot
Brassica napus PHR1 Gene Encoding a MYB-Like Protein Functions in Response to Phosphate Starvation
inferredcites →https://doi.org/10.3389/fpls.2011.00083openalex-snapshot
Phosphate import in plants: focus on the PHT1 transporters
inferredcites →https://doi.org/10.3389/fpls.2018.01432openalex-snapshot
Functional Characterization of Arabidopsis PHL4 in Plant Response to Phosphate Starvation

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.4782305openalex-extracted
Tamyb-Cc5 Gene Specifically Expressed in Root Improve Tolerance of Phosphorus Deficiency and Drought Stress in Wheat
inferred← citeshttps://doi.org/10.2139/ssrn.4837258openalex-extracted
Genome-Wide Characterization and Expression of the Myb-Cc Gene Family in Salvia Miltiorrhiza Andsmmyb-Cc7-Mediated Response to Phosphate Starvation in Arabidopsis
inferred← citeshttps://doi.org/10.1002/advs.202502911openalex-snapshot
PHR‐Mediated Pi Starvation Response Mobile Messenger RNAs Represent Noncoding Transcripts in Recipient Tissues
inferred← citeshttps://doi.org/10.1002/mbo3.70307openalex-snapshot
Functional Metagenomics Insights Into the Allium ampeloprasum Rhizosphere Microbiome Under Different Fertilization Regimes
inferred← citeshttps://doi.org/10.1007/s00299-025-03461-6openalex-snapshot
Genome-wide identification of the SmPHR gene family in Salvia miltiorrhiza and SmPHR7-mediated response to phosphate starvation in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00299-025-03651-2openalex-snapshot
Genome-wide identification unravels the role of the MYB-CC family in cucumber stress response
inferred← citeshttps://doi.org/10.1007/s00425-026-05034-7openalex-snapshot
Transcription factors in phosphorus utilization: enhancing crop productivity and stress resilience
inferred← citeshttps://doi.org/10.1007/s10265-023-01513-0openalex-snapshot
Role of GARP family transcription factors in the regulatory network for nitrogen and phosphorus acquisition
inferred← citeshttps://doi.org/10.1007/s10265-024-01544-1openalex-snapshot
Update of phosphate transport regulations
inferred← citeshttps://doi.org/10.1007/s11104-026-08980-zopenalex-snapshot
Molecular and physiological mechanisms of the cadmium response in seedlings of two Theobroma cacao L. genotypes
inferred← citeshttps://doi.org/10.1007/s44154-026-00307-3openalex-snapshot
The SPX protein family in plants: from phosphate sensors to multifunctional signaling hubs
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2025.108686openalex-snapshot
Understanding low-phosphate stress responses in plants: Opportunities for genome editing to improve phosphorous use efficiency (PUE)
inferred← citeshttps://doi.org/10.1016/j.cell.2026.07.048openalex-snapshot
Mutually beneficial interactions between bacteria and Arabidopsis promote phosphorus nutrition and growth
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105646openalex-snapshot
Physiological and transcriptomic regulation of Populus simonii fine roots exposed to a heterogeneous phosphorus environment in soil
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.2024.139315openalex-snapshot
Transcription factor CaPHR3 enhances phosphate starvation tolerance by up-regulating the expression of the CaPHT1;4 phosphate transporter gene in pepper
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.ijbiomac.2026.151502openalex-snapshot
Evolutionary trajectory of Triticeae GATA transcription factors pinpoints TaGATA26-5A and TaGATA31.1-2B as regulators for drought and phosphorus tolerance
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.122857openalex-snapshot
Breaking the repulsive linkage between fiber strength and yield in a cotton (Gossypium hirsutum L.) MAGIC population suggests dampening starvation responses can increase yield
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.140114openalex-snapshot
Galactinol synthase 1, AtGolS1, affects arsenate tolerance by modulating phosphate homeostasis in sensitive ecotype Slavi-1 of Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jplph.2024.154382openalex-snapshot
PHR1 negatively regulates nitrate reductase activity by directly inhibiting the transcription of NIA1 in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.ncrops.2024.100064openalex-snapshot
Molecular mechanisms underlying plant responses to low phosphate stress and potential applications in crop improvement
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112389openalex-snapshot
Transcription factors PHR1 and PHR1-like 1 regulate ABA-mediated inhibition of seed germination and stomatal opening in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2026.112986openalex-snapshot
MeJA regulates plant root growth, development and phosphorus uptake to adapt to low phosphorus stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.107801openalex-snapshot
SlPHL1 is involved in low phosphate stress promoting anthocyanin biosynthesis by directly upregulation of genes SlF3H, SlF3′H, and SlLDOX in tomato
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108128openalex-snapshot
Two PHOSPHATE-TRANSPORTER1 genes in cotton enhance tolerance to phosphorus starvation
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109011openalex-snapshot
TaMYB-CC5 gene specifically expressed in root improve tolerance of phosphorus deficiency and drought stress in wheat
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109608openalex-snapshot
AtPHR1 and SlPHL1 positively regulate phosphorus remobilization in response to phosphate starvation by directly facilitating the transcription of genes encoding S-like ribonucleases in Arabidopsis and tomato, respectively
inferred← citeshttps://doi.org/10.1016/j.scienta.2026.115017openalex-snapshot
Stage-specific root–microbiome interactions enhance phosphorus acquisition in tomato under straw amendment
inferred← citeshttps://doi.org/10.1016/j.stress.2025.101069openalex-snapshot
Tissue-specific phosphorus stress adaptation in Brassica rapa: WGCNA reveals root hormonal triad and leaf lipid remodeling as key tolerance mechanisms
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101220openalex-snapshot
HvPHR1 as a key gene in maintaining phosphate homeostasis in barley
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.101140openalex-snapshot
A PHR-dependent reciprocal antagonistic interplay between UV response and P-deficiency adaptation in plants
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/10.1021/acs.jafc.5c12270openalex-snapshot
Purple Acid Phosphatase Gene PpPAP17a Confers Phosphate Starvation Tolerance in Pennisetum purpureum by Mediating Organic Phosphate Utilization
inferred← citeshttps://doi.org/10.1038/s41467-023-40773-1openalex-snapshot
Phosphate starvation response precedes abscisic acid response under progressive mild drought in plants
inferred← citeshttps://doi.org/10.1038/s41467-025-59331-yopenalex-snapshot
N 6-methyladenosine modifications stabilize phosphate starvation response–related mRNAs in plant adaptation to nutrient-deficient stress
inferred← citeshttps://doi.org/10.1038/s41579-024-01073-7openalex-snapshot
Cross-kingdom nutrient exchange in the plant–arbuscular mycorrhizal fungus–bacterium continuum
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/uhag114openalex-snapshot
The chromosome-level genomes of two Macaranga species provide insights into the molecular mechanism of nervonic acid accumulation
inferred← citeshttps://doi.org/10.1093/jxb/erae041openalex-snapshot
The centrality of redox regulation and sensing of reactive oxygen species in abiotic and biotic stress acclimatization
inferred← citeshttps://doi.org/10.1093/jxb/erae367openalex-snapshot
Sink strength, nutrient allocation, cannabinoid yield, and associated transcript profiles vary in two drug-type Cannabis chemovars
inferred← citeshttps://doi.org/10.1093/jxb/erag002openalex-snapshot
Phosphate starvation response 1 (PHR1): a versatile master regulator shaping plant resilience beyond phosphate deprivation
inferred← citeshttps://doi.org/10.1093/pcp/pcaf069openalex-snapshot
Phosphate deficiency reduces nodule formation through a phosphate starvation response-like protein in Phaseolus vulgaris
inferred← citeshttps://doi.org/10.1093/plcell/koad071openalex-snapshot
Coordinating phosphorus and jasmonate signaling: PHR1 partners with transcriptional regulators
inferred← citeshttps://doi.org/10.1093/plcell/koad326openalex-snapshot
Milestones in understanding transport, sensing, and signaling of the plant nutrient phosphorus
inferred← citeshttps://doi.org/10.1093/plcell/koaf138openalex-snapshot
Regulation of glucosylceramide synthase and sphingolipid remodeling in the plant response to phosphate deficiency
inferred← citeshttps://doi.org/10.1093/plcell/koaf171openalex-snapshot
A PHR transcription factor-directed gene network reveals key regulators of phosphate metabolism and starvation responses in tomato
inferred← citeshttps://doi.org/10.1093/plphys/kiaf277openalex-snapshot
Transcription factor MdHB52 mediates phosphorus uptake by regulating methyl jasmonate secretion in apple rootstock
inferred← citeshttps://doi.org/10.1093/plphys/kiag676openalex-snapshot
SgPHR1-SgPAE1 module modulates root growth and increases low phosphorus tolerance in Stylosanthes guianensis
inferred← citeshttps://doi.org/10.1101/2023.03.11.532192openalex-snapshot
PHR1 and PHL1 mediate rapid high-light responses and acclimation to high photosynthetic activity
inferred← citeshttps://doi.org/10.1111/nph.19869openalex-snapshot
The phosphate starvation response regulator PHR2 antagonizes arbuscule maintenance in Medicago
inferred← citeshttps://doi.org/10.1111/pce.70527openalex-snapshot
ZmPHR1 and ZmPHR2 Mediate Metabolic and Microbial Regulation of Maize Adaptation to Phosphorus Heterogeneity
inferred← citeshttps://doi.org/10.1111/ppl.14197openalex-snapshot
SlPHL1 positively modulates acid phosphatase in response to phosphate starvation by directly activating the genes SlPAP10b and SlPAP15 in tomato
inferred← citeshttps://doi.org/10.1111/ppl.70264openalex-snapshot
Hydrogen Peroxide Positively Regulates Phosphate Starvation Responses in Rice
inferred← citeshttps://doi.org/10.1111/tpj.70901openalex-snapshot
PHR1 mediates rapid high light responses and acclimation to high photosynthetic activity
inferred← citeshttps://doi.org/10.1111/tpj.71068openalex-snapshot
The PHR1 – RSL2 module regulates root hair elongation induced by phosphate deficiency
inferred← citeshttps://doi.org/10.1186/s12284-025-00840-1openalex-snapshot
Genetic Dissection of Rice Plant-Specific Non-ε Group 14-3-3 Proteins in Response to Phosphate Starvation
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011135openalex-snapshot
ZmARF1 positively regulates low phosphorus stress tolerance via modulating lateral root development in maize
inferred← citeshttps://doi.org/10.2139/ssrn.5384457openalex-snapshot
Hvphr1 as a Key Gene in Maintaining Phosphate Homeostasis in Barley
inferred← citeshttps://doi.org/10.22201/fesz.23958723e.2024.659openalex-snapshot
PHR1 como componente central en el balance entre la respuesta a la deficiencia de fosfato y la respuesta inmune en plantas
inferred← citeshttps://doi.org/10.3389/fpls.2024.1379562openalex-snapshot
Comparative functional analyses of PHR1, PHL1, and PHL4 transcription factors in regulating Arabidopsis responses to phosphate starvation
inferred← citeshttps://doi.org/10.3389/fpls.2025.1557118openalex-snapshot
Physiological and transcriptional analyses of Arabidopsis primary root growth in response to phosphate starvation under light and dark conditions
inferred← citeshttps://doi.org/10.3389/fpls.2026.1825102openalex-snapshot
Mesophyll protoplasts: a key tool for deciphering plant nutrient starvation pathways
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/agronomy16201999openalex-snapshot
Genome-Wide Identification and Characterization of the C3H Gene Family in Maize (Zea mays L.) and Expression Profiling Under Low-Phosphorus and High-Nitrogen Conditions
inferred← citeshttps://doi.org/10.3390/ijms252312894openalex-snapshot
Physiological and Transcriptional Responses to Phosphorus Deficiency and Glucose-6-Phosphate Supplementation in Neopyropia yezoensis
inferred← citeshttps://doi.org/10.3390/ijms26072958openalex-snapshot
Decoding PHR-Orchestrated Stress Adaptation: A Genome-Wide Integrative Analysis of Transcriptional Regulation Under Abiotic Stress in Eucalyptus grandis
inferred← citeshttps://doi.org/10.3390/ijms27156824openalex-snapshot
Coordinated MBW, GIS, and RSL Regulatory Networks in Plant Epidermal Patterning Under Environmental Cues
inferred← citeshttps://doi.org/10.3390/plants14030461openalex-snapshot
Identification and Expression Analysis of Acid Phosphatase Gene (PAP) in Brassica napus: Effects of cis-Acting Elements on Two BnaPAP10 Genes in Response to Phosphorus Stress
inferred← citeshttps://doi.org/10.3390/plants14101443openalex-snapshot
Genome-Wide Identification of the PHR Gene Family in Six Cucurbitaceae Species and Its Expression Analysis in Cucurbita moschata
inferred← citeshttps://doi.org/10.3390/plants14233556openalex-snapshot
Integrating RNA-Seq and Metabolomic Perspectives Reveals the Mechanism of Response to Phosphorus Stress of Potamogeton wrightii
inferred← citeshttps://doi.org/10.34133/research.0405openalex-snapshot
Link between Plant Phosphate and Drought Stress Responses
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