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Functional Characterization of Arabidopsis PHL4 in Plant Response to Phosphate Starvation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
inferredcites →https://doi.org/10.1007/s00018-012-1090-6openalex-snapshot
Transcriptional regulation of phosphate acquisition by higher plants
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/10.1016/j.cub.2005.10.016openalex-snapshot
A miRNA Involved in Phosphate-Starvation Response in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2015.10.004openalex-snapshot
High-Efficiency Genome Editing in Arabidopsis Using YAO Promoter-Driven CRISPR/Cas9 System
inferredcites →https://doi.org/10.1016/j.pbi.2017.05.007openalex-snapshot
Novel signals in the regulation of Pi starvation responses in plants: facts and promises
inferredcites →https://doi.org/10.1016/j.semcdb.2017.06.013openalex-snapshot
Molecular mechanisms of phosphate transport and signaling in higher plants
inferredcites →https://doi.org/10.1016/s1369-5266(00)00062-5openalex-snapshot
Phosphate transport and signaling
inferredcites →https://doi.org/10.1016/s1369-5266(00)80063-1openalex-snapshot
Phosphate transport and signaling
inferredcites →https://doi.org/10.1038/36285openalex-snapshot
Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
inferredcites →https://doi.org/10.1038/ng2079openalex-snapshot
Target mimicry provides a new mechanism for regulation of microRNA activity
inferredcites →https://doi.org/10.1038/nmeth.1318openalex-snapshot
Enzymatic assembly of DNA molecules up to several hundred kilobases
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6050673.xopenalex-snapshot
The Arabidopsis ribonuclease gene RNS1 is tightly controlled in response to phosphate limitation
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
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A type 5 acid phosphatase gene from Arabidopsis thaliana is induced by phosphate starvation and by some other types of phosphate mobilising/oxidative stress conditions
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/10.1073/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/10.1073/pnas.93.19.10519openalex-snapshot
Phosphate transporters from the higher plant Arabidopsis thaliana.
inferredcites →https://doi.org/10.1074/jbc.m113.482281openalex-snapshot
Arabidopsis Ferritin 1 (AtFer1) Gene Regulation by the Phosphate Starvation Response 1 (AtPHR1) Transcription Factor Reveals a Direct Molecular Link between Iron and Phosphate Homeostasis
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/ert444openalex-snapshot
Coordination between zinc and phosphate homeostasis involves the transcription factor PHR1, the phosphate exporter PHO1, and its homologue PHO1;H3 in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/eru377openalex-snapshot
A major root-associated acid phosphatase in Arabidopsis, AtPAP10, is regulated by both local and systemic signals under phosphate starvation
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/pcp/pcw024openalex-snapshot
A Transcription Factor γMYB1 Binds to the P1BScis-Element and ActivatesPLA2-γExpression with its Co-Activator γMYB2
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.103.020941openalex-snapshot
Changes in Gene Expression in Arabidopsis Shoots during Phosphate Starvation and the Potential for Developing Smart Plants
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.106.090167openalex-snapshot
Genome-Wide Analysis of the Arabidopsis Leaf Transcriptome Reveals Interaction of Phosphate and Sugar Metabolism
inferredcites →https://doi.org/10.1104/pp.107.096958openalex-snapshot
Phosphorus Stress in Common Bean: Root Transcript and Metabolic Responses
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.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.112.209254openalex-snapshot
An RNA-Seq Transcriptome Analysis of Orthophosphate-Deficient White Lupin Reveals Novel Insights into Phosphorus Acclimation in Plants
inferredcites →https://doi.org/10.1104/pp.119.1.241openalex-snapshot
The Down-Regulation of Mt4-Like Genes by Phosphate Fertilization Occurs Systemically and Involves Phosphate Translocation to the Shoots1
inferredcites →https://doi.org/10.1104/pp.122.4.1003openalex-snapshot
Activation Tagging in Arabidopsis
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.97.3.1087openalex-snapshot
Mutant of Arabidopsis Deficient in Xylem Loading of Phosphate
inferredcites →https://doi.org/10.1105/tpc.112.096636openalex-snapshot
PHO2-Dependent Degradation of PHO1 Modulates Phosphate Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.116012openalex-snapshot
NITROGEN LIMITATION ADAPTATION, a Target of MicroRNA827, Mediates Degradation of Plasma Membrane–Localized Phosphate Transporters to Maintain Phosphate Homeostasis 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.114.123208openalex-snapshot
SPX4 Negatively Regulates Phosphate Signaling and Homeostasis through Its Interaction with PHR2 in Rice
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01608.xopenalex-snapshot
Genome‐wide reprogramming of metabolism and regulatory networks of Arabidopsis in response to phosphorus
inferredcites →https://doi.org/10.1111/j.1365-3040.2007.01734.xopenalex-snapshot
Increased expression of the MYB‐related transcription factor, PHR1, leads to enhanced phosphate uptake in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1399-3054.2010.01384.xopenalex-snapshot
Global analysis of microRNA in Arabidopsis in response to phosphate starvation as studied by locked nucleic acid-based microarrays
inferredcites →https://doi.org/10.1111/j.1744-7909.2008.00709.xopenalex-snapshot
Signaling Components Involved in Plant Responses to Phosphate Starvation
inferredcites →https://doi.org/10.1111/jipb.12184openalex-snapshot
Comparative genetic analysis of Arabidopsis purple acid phosphatases AtPAP10, AtPAP12, and AtPAP26 provides new insights into their roles in plant adaptation to phosphate deprivation
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/10.1186/1471-2229-11-19openalex-snapshot
The transcription factor PHR1 plays a key role in the regulation of sulfate shoot-to-root flux upon phosphate starvation in Arabidopsis
inferredcites →https://doi.org/10.1186/s12864-016-2929-2openalex-snapshot
Systematic characterization of novel lncRNAs responding to phosphate starvation in Arabidopsis thaliana
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.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
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.4766567openalex-extracted
Egphl7, Egphr1 and Egphr2 Bind to P1bs and a Unique Motif, Agatwc, for Phosphate Starvation Transcriptional Regulation in Oil Palm
inferred← citeshttps://doi.org/10.1002/9781119672425.ch16openalex-snapshot
Genome Engineering Strategies for Quality Improvement in Tomato
inferred← citeshttps://doi.org/10.1002/9781119791461.ch4openalex-snapshot
Arsenic Induced Responses in Plants
inferred← citeshttps://doi.org/10.1002/pro.5214openalex-snapshot
The potent PHL4 transcription factor effector domain contains significant disorder
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/s00425-023-04325-7openalex-snapshot
A GARP transcription factor SlGCC positively regulates lateral root development in tomato via auxin-ethylene interplay
inferred← citeshttps://doi.org/10.1007/s00709-021-01702-5openalex-snapshot
Transgenic expression of rice OsPHR2 increases phosphorus uptake and yield in wheat
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/10.1016/b978-0-12-816091-6.00008-0openalex-snapshot
Root system architectural and growth responses of crop plants to mineral nutrition under moisture stress and its implications in drought tolerance
inferred← citeshttps://doi.org/10.1016/b978-0-12-821430-5.00006-7openalex-snapshot
Phosphorus and sulfur uptake, assimilation, and deprivation responses
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.11.298openalex-snapshot
Characterization and evolutionary analysis of phosphate starvation response genes in wheat and other major gramineous plants
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.molp.2021.12.005openalex-snapshot
Plant adaptation to low phosphorus availability: Core signaling, crosstalks, and applied implications
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111799openalex-snapshot
The MYB-CC transcription factor MdγMYB2 modulates shoot elongation in spur-type apples
inferred← citeshttps://doi.org/10.1016/j.plgene.2026.100589openalex-snapshot
EgPHL7, EgPHR1 and EgPHR2 bind to the P1BS and a unique motif, AGATACT for transcriptional regulation of phosphate-starvation inducible genes in oil palm
inferred← citeshttps://doi.org/10.1016/j.tplants.2022.10.004openalex-snapshot
Emerging trends in nitrogen and phosphorus signalling in photosynthetic eukaryotes
inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101627openalex-snapshot
PHR1-like 7 and phosphatidic acid oppositely regulate TAG degradation and seed oil accumulation in Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.2107558118openalex-snapshot
Genome accessibility dynamics in response to phosphate limitation is controlled by the PHR1 family of transcription factors in Arabidopsis
inferred← citeshttps://doi.org/10.1093/hr/uhag116openalex-snapshot
The transcription factor AebHLH89 activates AeGMP1 transcription to regulate L-ascorbic acid accumulation in kiwifruit ( Actinidia eriantha ) revealed by genome-wide association study
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/jxb/erz148openalex-snapshot
Perception, transduction, and integration of nitrogen and phosphorus nutritional signals in the transcriptional regulatory network in plants
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/plphys/kiac521openalex-snapshot
PHOSPHATE RESPONSE 1 family members act distinctly to regulate transcriptional responses to phosphate starvation
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/10.1101/467076openalex-snapshot
Two bifunctional inositol pyrophosphate kinases/phosphatases control plant phosphate homeostasis
inferred← citeshttps://doi.org/10.1111/jipb.70278openalex-snapshot
SlMED25‐SlPHR3‐SlSPX2 module fine‐tunes SlPHR3‐mediated transcriptional activation of phosphate starvation response in tomato
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/10.1111/tpj.15061openalex-snapshot
OsbHLH6 interacts with OsSPX4 and regulates the phosphate starvation response in rice
inferred← citeshttps://doi.org/10.1111/tpj.17134openalex-snapshot
Defense‐related callose synthase PMR4 promotes root hair callose deposition and adaptation to phosphate deficiency in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/tpj.70445openalex-snapshot
Organ‐specific transcriptional and metabolic adaptations of potato plants to limited phosphate availability prior and after tuberization
inferred← citeshttps://doi.org/10.1126/sciadv.aec5607openalex-snapshot
Lotus japonicus VIH2 is an inositol pyrophosphate synthase that regulates arbuscular mycorrhiza
inferred← citeshttps://doi.org/10.1134/s1021443722060152openalex-snapshot
Genome-Wide Identification and Characterization of MYB-CC Gene Factor Family in Sorghum and Their Response to Phosphate Starvation
inferred← citeshttps://doi.org/10.1186/s12863-021-00962-7openalex-snapshot
Comparative transcriptome analysis reveals novel insights into transcriptional responses to phosphorus starvation in oil palm (Elaeis guineensis) root
inferred← citeshttps://doi.org/10.1186/s12870-020-02595-xopenalex-snapshot
Long non-coding RNAs: emerging players regulating plant abiotic stress response and adaptation
inferred← citeshttps://doi.org/10.1186/s12870-025-07423-8openalex-snapshot
Genome-wide identification and expression analysis of the GARP superfamily in response to abiotic stresses in alfalfa (Medicago sativa L.)
inferred← citeshttps://doi.org/10.1186/s40538-024-00648-zopenalex-snapshot
Dicranopteris dichotoma rhizosphere-derived Bacillus sp. MQB12 acts as an enhancer of plant growth via increasing phosphorus utilization, hormone synthesis, and rhizosphere microbial abundance
inferred← citeshttps://doi.org/10.1371/journal.ppat.1013601openalex-snapshot
Starve or share? Phosphate availability shapes plant–microbe interactions
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/10.3389/fpls.2022.878796openalex-snapshot
Increasing Expression of PnGAP and PnEXPA4 Provides Insights Into the Enlargement of Panax notoginseng Root Size From Qing Dynasty to Cultivation Era
inferred← citeshttps://doi.org/10.3389/fpls.2022.947072openalex-snapshot
Genome-Wide Identification and Characterization of GARP Transcription Factor Gene Family Members Reveal Their Diverse Functions in Tea Plant (Camellia sinensis)
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.2025.1586547openalex-snapshot
Genome-wide identification of GDPD gene family in foxtail millet (Setaria italica L.) and functional characterization of SiGDPD14 under low phosphorus stress
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/genes10121018openalex-snapshot
Plant PHR Transcription Factors: Put on A Map
inferred← citeshttps://doi.org/10.3390/ijms23042273openalex-snapshot
The Ubiquitin E3 Ligase PRU2 Modulates Phosphate Uptake in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms23042353openalex-snapshot
The Genetic Basis of Phosphorus Utilization Efficiency in Plants Provide New Insight into Woody Perennial Plants Improvement
inferred← citeshttps://doi.org/10.3390/plants14243869openalex-snapshot
Glucose-6-Phosphate 1-Epimerase Responds to Phosphate Starvation by Regulating Carbohydrate Homeostasis in Rice and Arabidopsis
inferred← citeshttps://doi.org/10.48130/frures-0025-0007openalex-snapshot
Analysis of the SPX gene family in Vitis vinifera and Vitis amurensis and its expression under phosphorus stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.13725230openalex-snapshot
Additional file 1 of Comparative transcriptome analysis reveals novel insights into transcriptional responses to phosphorus starvation in oil palm (Elaeis guineensis) root
inferred← citeshttps://doi.org/10.6084/m9.figshare.13725233openalex-snapshot
Additional file 2 of Comparative transcriptome analysis reveals novel insights into transcriptional responses to phosphorus starvation in oil palm (Elaeis guineensis) root
inferred← citeshttps://doi.org/10.70675/5461667cz5fd4z47f2zb3a4zd5d54c2ea194openalex-snapshot
Real-time imaging of transcription to study phosphate sensing in plants
inferred← citeshttps://doi.org/10.7287/peerj.12882v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Genome-wide evolution and expression analysis of the MYB-CC gene family in Brassica spp. (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12882v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Genome-wide evolution and expression analysis of the MYB-CC gene family in Brassica spp. (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.12882openalex-snapshot
Genome-wide evolution and expression analysis of the MYB-CC gene family in Brassica spp.
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