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SlPHL1 , a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response

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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.ch10openalex-snapshot

The Role of Intracellular and Secreted Purple Acid Phosphatases in Plant Phosphorus Scavenging and Recycling

inferredcites →https://doi.org/10.1002/9781119312994.apr0525openalex-snapshot

The Role of Intracellular and Secreted Purple Acid Phosphatases in Plant Phosphorus Scavenging and Recycling

inferredcites →https://doi.org/10.1007/978-1-4939-3115-6_5openalex-snapshot

Micro-Tom Tomato as an Alternative Plant Model System: Mutant Collection and Efficient Transformation

inferredcites →https://doi.org/10.1007/s00299-015-1759-zopenalex-snapshot

Molecular characterization of a tomato purple acid phosphatase during seed germination and seedling growth under phosphate stress

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/10.1016/0032-3861(78)90325-7openalex-snapshot

International journal of biological macromolecules

inferredcites →https://doi.org/10.1016/j.bbalip.2020.158763openalex-snapshot

Phosphate starvation causes different stress responses in the lipid metabolism of tomato leaves and roots

inferredcites →https://doi.org/10.1016/j.ijbiomac.2020.10.080openalex-snapshot

Identification, structure analysis, and transcript profiling of purple acid phosphatases under Pi deficiency in tomato (Solanum lycopersicum L.) and its wild relatives

inferredcites →https://doi.org/10.1016/j.jplph.2019.02.007openalex-snapshot

Gibberellins play dual roles in response to phosphate starvation of tomato seedlings, negatively in shoots but positively in roots

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.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.plantsci.2015.05.010openalex-snapshot

PHYTOCHROME-INTERACTING FACTOR 5 (PIF5) positively regulates dark-induced senescence and chlorophyll degradation in Arabidopsis

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/10.1038/nmeth1083openalex-snapshot

Bright far-red fluorescent protein for whole-body imaging

inferredcites →https://doi.org/10.1038/nprot.2007.199openalex-snapshot

Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis

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/10.1073/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.1711723115openalex-snapshot

Ethylene promotes root hair growth through coordinated EIN3/EIL1 and RHD6/RSL1 activity in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.96.26.15336openalex-snapshot

Psr1, a nuclear localized protein that regulates phosphorus metabolism in Chlamydomonas

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/ers295openalex-snapshot

Tomato SlDREB gene restricts leaf expansion and internode elongation by downregulating key genes for gibberellin biosynthesis

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/pcp/pcr004openalex-snapshot

TOMATOMA: A Novel Tomato Mutant Database Distributing Micro-Tom Mutant Collections

inferredcites →https://doi.org/10.1093/pcp/pcx041openalex-snapshot

OsPAP26 Encodes a Major Purple Acid Phosphatase and Regulates Phosphate Remobilization in Rice

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.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.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.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.18.01097openalex-snapshot

OsPHT1;3 Mediates Uptake, Translocation, and Remobilization of Phosphate under Extremely Low Phosphate Regimes

inferredcites →https://doi.org/10.1105/tpc.20.00361openalex-snapshot

The Transcription Factor NIGT1.2 Modulates Both Phosphate Uptake and Nitrate Influx during Phosphate Starvation in Arabidopsis and Maize

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.1438-8677.2010.00346.xopenalex-snapshot

Identification of rice purple acid phosphatases related to posphate starvation signalling

inferredcites →https://doi.org/10.1111/j.1744-7348.2001.tb00091.xopenalex-snapshot

Identification of mutants in phosphorus metabolism

inferredcites →https://doi.org/10.1111/j.1753-4887.1981.tb06752.xopenalex-snapshot

Proceedings of the National Academy of Sciences of the United States of America

inferredcites →https://doi.org/10.1111/jipb.12163openalex-snapshot

Molecular mechanisms underlying phosphate sensing, signaling, and adaptation in plants

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/10.1111/nph.16931openalex-snapshot

OsWRKY21 and OsWRKY108 function redundantly to promote phosphate accumulation through maintaining the constitutive expression of OsPHT1;1 under phosphate‐replete conditions

inferredcites →https://doi.org/10.1111/nph.17074openalex-snapshot

The molecular–physiological functions of mineral macronutrients and their consequences for deficiency symptoms in plants

inferredcites →https://doi.org/10.1111/nph.17139openalex-snapshot

SPX4 interacts with both PHR1 and PAP1 to regulate critical steps in phosphorus‐status‐dependent anthocyanin biosynthesis

inferredcites →https://doi.org/10.1111/pce.12794openalex-snapshot

OsPAP10c , a novel secreted acid phosphatase in rice, plays an important role in the utilization of external organic phosphorus

inferredcites →https://doi.org/10.1186/1471-2229-14-61openalex-snapshot

Genome-wide investigation and expression analysis suggest diverse roles and genetic redundancy of Pht1 family genes in response to Pi deficiency in tomato

inferredcites →https://doi.org/10.1186/1746-4811-5-16openalex-snapshot

Tape-Arabidopsis Sandwich - a simpler Arabidopsis protoplast isolation method

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.1006194openalex-snapshot

The Molecular Mechanism of Ethylene-Mediated Root Hair Development Induced by Phosphate Starvation

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.2020.00661openalex-snapshot

Characterization of Purple Acid Phosphatase Family and Functional Analysis of GmPAP7a/7b Involved in Extracellular ATP Utilization in Soybean

inferredcites →https://doi.org/10.3390/genes10121018openalex-snapshot

Plant PHR Transcription Factors: Put on A Map

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/10.2139/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/10.1007/s00299-022-02902-wopenalex-snapshot

An Agrobacterium-mediated transient expression method contributes to functional analysis of a transcription factor and potential application of gene editing in Chenopodium quinoa

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/s00425-022-03952-wopenalex-snapshot

PHR1 positively regulates phosphate starvation-induced anthocyanin accumulation through direct upregulation of genes F3’H and LDOX in Arabidopsis

inferred← citeshttps://doi.org/10.1007/s11105-024-01512-yopenalex-snapshot

Pup1 QTL-Mediated Tissue-Specific Differential Expression of Transcription Factors Help Mitigate Deleterious Effects of Phosphorus-Starvation in Rice (Oryza sativa L.)

inferred← citeshttps://doi.org/10.1007/s40502-026-01020-zopenalex-snapshot

Multifaceted roles of phosphate starvation response (PHRs) transcription factors: beyond phosphate acquisition and homeostasis

inferred← citeshttps://doi.org/10.1007/s44154-022-00035-4openalex-snapshot

High transcriptome plasticity drives phosphate starvation responses in tomato

inferred← citeshttps://doi.org/10.1016/j.envres.2022.114282openalex-snapshot

Plant responses to drought stress: microRNAs in action

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.138588openalex-snapshot

MYB proteins: Versatile regulators of plant development, stress responses, and secondary metabolite biosynthetic pathways

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.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.plantsci.2023.111723openalex-snapshot

Silencing of SlSPX1 and SlSPX2 promote growth and root mycorrhization in tomato (Solanum lycopersicum L.) seedlings

inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112889openalex-snapshot

SlWRKY23 is a positive regulator of phosphate starvation response in tomato

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.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.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.scienta.2022.111767openalex-snapshot

Genome-wide identification and characterization of SPX domain-containing proteins and their responses to phosphorus and/or nitrogen deficiency in apple (Malus domestica Borkh.)

inferred← citeshttps://doi.org/10.1016/j.stress.2026.101379openalex-snapshot

TaPHL7–TaSOD7-4A regulatory pair enhances drought tolerance in wheat (Triticum aestivum L.)

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/10.1038/s41467-025-63406-1openalex-snapshot

A cis-natural antisense RNA regulates alternative polyadenylation of SlSPX5 under Pi starvation in tomato

inferred← citeshttps://doi.org/10.1038/s41598-026-39117-yopenalex-snapshot

Machine learning model provides stress biomarkers for the classification of abiotic stress in Micro-Tom

inferred← citeshttps://doi.org/10.1079/9781800626638.0003openalex-snapshot

Gene Pyramiding to Increase the Sustainability of Crops Under Biotic and Abiotic Stresses

inferred← citeshttps://doi.org/10.1093/jxb/erae451openalex-snapshot

SlMIPS2, a myo -inositol phosphate synthase, regulates phosphate homeostasis by influencing SlPHL1 and SlSPX2 levels in tomato seedlings

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/erag259openalex-snapshot

The link between phosphate starvation-triggered anthocyanin biosynthesis and jasmonate-driven regulation in tomato

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/kiac521openalex-snapshot

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

inferred← citeshttps://doi.org/10.1093/plphys/kiag070openalex-snapshot

The regulatory module MsSPX4/MsPHL11–MsWRKY91 mediates low-phosphorus-induced anthocyanin synthesis in Malus spectabilis leaves

inferred← citeshttps://doi.org/10.1101/2023.11.29.569173openalex-snapshot

Lack of Purple Acid Phosphatase SlPAP26b compromises the phosphorus starvation response in tomato independent of SlPHR1 and SlPHL1

inferred← citeshttps://doi.org/10.1111/pce.15007openalex-snapshot

Genetic and functional traits limit the success of colonisation by arbuscular mycorrhizal fungi in a tomato wild relative

inferred← citeshttps://doi.org/10.1111/pce.70779openalex-snapshot

Transcription Factors Regulating Nutrient and Ion Uptake in Plants Exposed to Abiotic and Biotic Stress Conditions

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/10.1186/s12870-026-08320-4openalex-snapshot

Genome-wide characterization of the PHT gene family in Uncaria rhynchophylla identified UrPHT1;11 as a key regulator to low phosphorus response

inferred← citeshttps://doi.org/10.3389/fgene.2022.894928openalex-snapshot

Identification and Analysis of MYB Gene Family for Discovering Potential Regulators Responding to Abiotic Stresses in Curcuma wenyujin

inferred← citeshttps://doi.org/10.3389/fpls.2023.1120777openalex-snapshot

Comparative physiological, metabolomic, and transcriptomic analyses reveal mechanisms of apple dwarfing rootstock root morphogenesis under nitrogen and/or phosphorus deficient conditions

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/genes16030322openalex-snapshot

Genome-Wide Identification and Comprehensive Analysis of the GARP Transcription Factor Superfamily in Populus deltoides

inferred← citeshttps://doi.org/10.48130/vegres-0025-0032openalex-snapshot

SlRLK55 negatively regulates phosphate starvation response in tomato

inferred← citeshttps://doi.org/10.5338/kjea.2025.44.07openalex-snapshot

Effects of Nitrogen or Phosphorus Deficiency and Light Treatment on Anthocyanin Biosynthesis in Tomato Hypocotyls

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