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OsbHLH6 interacts with OsSPX4 and regulates the phosphate starvation response in rice

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What this work says

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

inferredcites →https://doi.org/10.1007/s11104-004-2005-6openalex-snapshot

Phosphate Acquisition

inferredcites →https://doi.org/10.1016/j.molp.2015.04.007openalex-snapshot

A Robust CRISPR/Cas9 System for Convenient, High-Efficiency Multiplex Genome Editing in Monocot and Dicot Plants

inferredcites →https://doi.org/10.1016/j.molp.2019.04.003openalex-snapshot

Two RING-Finger Ubiquitin E3 Ligases Regulate the Degradation of SPX4, An Internal Phosphate Sensor, for Phosphate Homeostasis and Signaling in Rice

inferredcites →https://doi.org/10.1016/j.pbi.2013.03.002openalex-snapshot

Improvement of phosphorus efficiency in rice on the basis of understanding phosphate signaling and homeostasis

inferredcites →https://doi.org/10.1038/nbt.3122openalex-snapshot

StringTie enables improved reconstruction of a transcriptome from RNA-seq reads

inferredcites →https://doi.org/10.1038/s41477-019-0384-1openalex-snapshot

Nitrate–NRT1.1B–SPX4 cascade integrates nitrogen and phosphorus signalling networks in plants

inferredcites →https://doi.org/10.1038/s41586-019-1057-yopenalex-snapshot

PTC-bearing mRNA elicits a genetic compensation response via Upf3a and COMPASS components

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.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/10.1093/bioinformatics/bth078openalex-snapshot

Open source clustering software

inferredcites →https://doi.org/10.1093/jxb/ert424openalex-snapshot

The paralogous SPX3 and SPX5 genes redundantly modulate Pi homeostasis in rice

inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot

MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods

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.106.080580openalex-snapshot

Genome-Wide Analysis of Basic/Helix-Loop-Helix Transcription Factor Family in Rice and Arabidopsis

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.107.111443openalex-snapshot

OsPHR2 Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants

inferredcites →https://doi.org/10.1104/pp.110.153593openalex-snapshot

Genome-Wide Classification and Evolutionary Analysis of the bHLH Family of Transcription Factors in Arabidopsis, Poplar, Rice, Moss, and Algae

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.113.235077openalex-snapshot

Arabidopsis WRKY45 Transcription Factor Activates PHOSPHATE TRANSPORTER1;1 Expression in Response to Phosphate Starvation

inferredcites →https://doi.org/10.1104/pp.114.253799openalex-snapshot

WRKY42 Modulates Phosphate Homeostasis through Regulating Phosphate Translocation and Acquisition 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/10.1105/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.114.123208openalex-snapshot

SPX4 Negatively Regulates Phosphate Signaling and Homeostasis through Its Interaction with PHR2 in Rice

inferredcites →https://doi.org/10.1105/tpc.114.126292openalex-snapshot

The bHLH142 Transcription Factor Coordinates with TDR1 to Modulate the Expression of EAT1 and Regulate Pollen Development in Rice

inferredcites →https://doi.org/10.1105/tpc.151140openalex-snapshot

Update on the Basic Helix-Loop-Helix Transcription Factor Gene Family in Arabidopsis thaliana

inferredcites →https://doi.org/10.1105/tpc.19.00038openalex-snapshot

OsSPL3, an SBP-Domain Protein, Regulates Crown Root Development 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.1365-313x.2008.03734.xopenalex-snapshot

Involvement of OsSPX1 in phosphate homeostasis in rice

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/jipb.12163openalex-snapshot

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

inferredcites →https://doi.org/10.1111/jipb.12922openalex-snapshot

A bHLH transcription activator regulates defense signaling by nucleo‐cytosolic trafficking in rice

inferredcites →https://doi.org/10.1111/nph.15155openalex-snapshot

Rice SPX6 negatively regulates the phosphate starvation response through suppression of the transcription factor PHR2

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/10.1146/annurev-arplant-042110-103849openalex-snapshot

Signaling Network in Sensing Phosphate Availability in Plants

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

inferredcites →https://doi.org/10.1371/journal.pone.0194628openalex-snapshot

Rice OsMYB5P improves plant phosphate acquisition by regulation of phosphate transporter

inferredcites →https://doi.org/10.3389/fpls.2018.01432openalex-snapshot

Functional Characterization of Arabidopsis PHL4 in Plant Response to Phosphate Starvation

inferredcites →https://doi.org/10.7554/elife.14577openalex-snapshot

A novel role for the root cap in phosphate uptake and homeostasis

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.4854565openalex-extracted

Tabahd35-1b Positively Regulates Phosphate Starvation Response in Wheat

inferred← citeshttps://doi.org/10.1007/978-981-19-5817-5_12openalex-snapshot

Molecular Mechanisms of Nutrient Deficiency Stress Tolerance in Legumes

inferred← citeshttps://doi.org/10.1007/s00122-022-04182-0openalex-snapshot

Fine mapping and characterization of a major QTL for grain weight on wheat chromosome arm 5DL

inferred← citeshttps://doi.org/10.1007/s00122-024-04738-2openalex-snapshot

Tracing post-domestication historical events and screening pre-breeding germplasm from large gene pools in wheat in the absence of phenotype data

inferred← citeshttps://doi.org/10.1007/s00299-026-03997-1openalex-snapshot

OsbHLH6 regulates OsMADS57 and amino acid metabolism to impair cold tolerance in rice

inferred← citeshttps://doi.org/10.1007/s00344-023-11011-1openalex-snapshot

Flavonoids Mediate the Modulation of Phosphate Uptake and Phosphate-Starvation Signaling in Tobacco

inferred← citeshttps://doi.org/10.1007/s00344-024-11610-6openalex-snapshot

Strigolactone-Mediated Positive Regulation of Phosphate Stress in Anoectochilus roxburghii Through Reducing the Oxidative Damage of Roots

inferred← citeshttps://doi.org/10.1007/s00344-025-11979-yopenalex-snapshot

HmbHLH42, a Light-induced Transcription Factor, Positively Regulates Anthocyanin Biosynthesis in Sepals of Hydrangea Macrophylla

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/s11032-022-01301-zopenalex-snapshot

Functional study and elite haplotype identification of soybean phosphate starvation response transcription factors GmPHR14 and GmPHR32

inferred← citeshttps://doi.org/10.1007/s11104-023-05976-xopenalex-snapshot

Emerging roles of inositol pyrophosphates in signaling plant phosphorus status and phytohormone signaling

inferred← citeshttps://doi.org/10.1016/j.cell.2025.07.027openalex-snapshot

NRT1.1B acts as an abscisic acid receptor in integrating compound environmental cues for plants

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.2025.144611openalex-snapshot

Open stomata 1 and phosphate starvation response 1 regulate tomato root system architecture during heterogeneous phosphate availability

inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.123234openalex-snapshot

DgbHLH2 positively regulates cold tolerance by activating DgGST expression to mediate ROS scavenging in chrysanthemum

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.molp.2023.07.004openalex-snapshot

Phosphate-dependent regulation of vacuolar trafficking of OsSPX-MFSs is critical for maintaining intracellular phosphate homeostasis in rice

inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111618openalex-snapshot

Transcription factor OsNAC016 negatively regulates phosphate-starvation response in rice

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.plantsci.2026.113069openalex-snapshot

Overexpression of PbWRKY66 negatively regulate phosphate uptake and root-to-shoot distribution in Arabidopsis

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.2026.111357openalex-snapshot

OsPHR2 activates OsPAP23 to promote organic phosphorus utilization in rice

inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111715openalex-snapshot

OsPHO2 promotes the ubiquitin-dependent degradation of OsHMGB1 to fine-tune phosphate homeostasis in rice

inferred← citeshttps://doi.org/10.1016/j.stress.2025.101054openalex-snapshot

ZmLBD1 confers multi-abiotic stress tolerance in Arabidopsis by enhancing root growth

inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101680openalex-snapshot

Unfolding of RNA secondary structure impairs RNA stability to fine-tune phosphate starvation responses in rice roots

inferred← citeshttps://doi.org/10.1038/s41467-024-55324-5openalex-snapshot

A root system architecture regulator modulates OsPIN2 polar localization in rice

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/pcp/pcab011openalex-snapshot

Phosphate Uptake and Transport in Plants: An Elaborate Regulatory System

inferred← citeshttps://doi.org/10.1093/plcell/koae159openalex-snapshot

Multiomic analyses reveal key sectors of jasmonate-mediated defense responses in rice

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/plcell/koag191openalex-snapshot

Functional specialization of two jasmonic acid-amido synthetases in rice defense and spikelet development

inferred← citeshttps://doi.org/10.1093/plphys/kiab343openalex-snapshot

Intracellular phosphate sensing and regulation of phosphate transport systems in plants

inferred← citeshttps://doi.org/10.1093/plphys/kiac404openalex-snapshot

PtoWRKY40 interacts with PtoPHR1-LIKE3 while regulating the phosphate starvation response in poplar

inferred← citeshttps://doi.org/10.1093/plphys/kiaf390openalex-snapshot

Function and regulatory mechanism of HvSPX4 in maintaining phosphate homeostasis in barley

inferred← citeshttps://doi.org/10.1101/2024.05.22.595400openalex-snapshot

Nitrogen starvation response in hornworts and liverworts provides little evidence for complex priming to the cyanobiont

inferred← citeshttps://doi.org/10.1111/nph.18933openalex-snapshot

The good, the bad, and the phosphate: regulation of beneficial and detrimental plant–microbe interactions by the plant phosphate status

inferred← citeshttps://doi.org/10.1111/nph.19189openalex-snapshot

Rice chromatin protein OsHMGB1 is involved in phosphate homeostasis and plant growth by affecting chromatin accessibility

inferred← citeshttps://doi.org/10.1111/pce.14457openalex-snapshot

Molecular mechanisms and genetic improvement of low‐phosphorus tolerance in rice

inferred← citeshttps://doi.org/10.1111/pce.14920openalex-snapshot

A bamboo bHLH transcription factor PeRHL4 has dual functions in enhancing drought and phosphorus starvation tolerance

inferred← citeshttps://doi.org/10.1111/tpj.17124openalex-snapshot

OsbHLH6 , a basic helix–loop–helix transcription factor, confers arsenic tolerance and root‐to‐shoot translocation in rice

inferred← citeshttps://doi.org/10.1186/s12284-023-00645-0openalex-snapshot

Pan-transcriptomic Profiling Demarcates Serendipita Indica-Phosphorus Mediated Tolerance Mechanisms in Rice Exposed to Arsenic Toxicity

inferred← citeshttps://doi.org/10.1186/s12870-022-03556-2openalex-snapshot

GmSPX8, a nodule-localized regulator confers nodule development and nitrogen fixation under phosphorus starvation in soybean

inferred← citeshttps://doi.org/10.1186/s12870-025-06577-9openalex-snapshot

MmPHR1 enhances low phosphorus stress tolerance by activating MmPHT1;5 in an elite apple rootstock -Malus mandshurica

inferred← citeshttps://doi.org/10.1186/s40538-026-00929-9openalex-snapshot

Integrative analysis of metagenomics and metabolomics reveals rhizospheric regulatory strategies for soybean adaptation to gradient phosphorus stress

inferred← citeshttps://doi.org/10.3389/fpls.2025.1654599openalex-snapshot

OSH45, a homeobox transcription factor, coordinates low-phosphate adaptation 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

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Transcriptome-Wide Identification and Expression Profiling of SPX Domain-Containing Members in Responses to Phosphorus Deprivation of Pinus massoniana

inferred← citeshttps://doi.org/10.3390/ijms242216305openalex-snapshot

The Basic/Helix-Loop-Helix Transcription Factor Family Gene RcbHLH112 Is a Susceptibility Gene in Gray Mould Resistance of Rose (Rosa Chinensis)

inferred← citeshttps://doi.org/10.3390/plants12112146openalex-snapshot

Biocuration of a Transcription Factors Network Involved in Submergence Tolerance during Seed Germination and Coleoptile Elongation in Rice (Oryza sativa)

inferred← citeshttps://doi.org/10.6084/m9.figshare.26599438openalex-snapshot

Additional file 1 of Pan-transcriptomic Profiling Demarcates Serendipita Indica-Phosphorus Mediated Tolerance Mechanisms in Rice Exposed to Arsenic Toxicity

inferred← citeshttps://doi.org/10.6084/m9.figshare.26599441openalex-snapshot

Additional file 2 of Pan-transcriptomic Profiling Demarcates Serendipita Indica-Phosphorus Mediated Tolerance Mechanisms in Rice Exposed to Arsenic Toxicity

inferred← citeshttps://doi.org/10.7287/peerj.13981v0.1/reviews/1openalex-snapshot

Peer Review #1 of "Genome-wide identification and transcriptional profiling of the basic helix-loop-helix gene family in tung tree (Vernicia fordii) (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.13981v0.1/reviews/2openalex-snapshot

Peer Review #2 of "Genome-wide identification and transcriptional profiling of the basic helix-loop-helix gene family in tung tree (Vernicia fordii) (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.13981v0.2/reviews/1openalex-snapshot

Peer Review #1 of "Genome-wide identification and transcriptional profiling of the basic helix-loop-helix gene family in tung tree (Vernicia fordii) (v0.2)"

inferred← citeshttps://doi.org/10.7287/peerj.13981v0.2/reviews/2openalex-snapshot

Peer Review #2 of "Genome-wide identification and transcriptional profiling of the basic helix-loop-helix gene family in tung tree (Vernicia fordii) (v0.2)"

inferred← citeshttps://doi.org/10.7717/peerj.13981openalex-snapshot

Genome-wide identification and transcriptional profiling of the basic helix-loop-helix gene family in tung tree ( Vernicia fordii )

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