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Egphl7, Egphr1 and Egphr2 Bind to P1bs and a Unique Motif, Agatwc, for Phosphate Starvation Transcriptional Regulation in Oil Palm

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Is H3K4me3 instructive for transcription activation?
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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
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H3K4 trimethylation dynamics impact diverse developmental and environmental responses in plants
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Characterization of two cis-acting elements, P1BS and W-box, in the regulation of OsPT6 responsive to phosphors deficiency
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Plant hormones and nutrient signaling
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Genetic manipulation of a high-affinity PHR1 target cis-element to improve phosphorous uptake in Oryza sativa L.
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Phosphate starvation induced OsPHR4 mediates Pi-signaling and homeostasis in rice
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Phosphate Acquisition
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Expression of several genes involved in sucrose/starch metabolism as affected by different strategies to induce phosphate deficiency in Arabidopsis
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Genome-wide molecular characterization of Phosphate Transporter 1 and Phosphate Starvation Response gene families in Elaeis guineensis Jacq. and their transcriptional response under different levels of phosphate starvation
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High transcriptome plasticity drives phosphate starvation responses in tomato
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Introduction to Transcription Factor Structure and Function
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Crosstalk among Histone Modifications
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TaMADS2-3D, a MADS transcription factor gene, regulates phosphate starvation responses in plants
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Patterning chromatin: form and function for H2A.Z variant nucleosomes
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Complex Regulation of Plant Phosphate Transporters and the Gap between Molecular Mechanisms and Practical Application: What Is Missing?
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H2A.Z Represses Gene Expression by Modulating Promoter Nucleosome Structure and Enhancer Histone Modifications in Arabidopsis
inferredcites →https://doi.org/10.1016/j.molp.2019.08.002openalex-extracted
Inositol Pyrophosphate InsP8 Acts as an Intracellular Phosphate Signal in Arabidopsis
inferredcites →https://doi.org/10.1016/j.pbi.2010.11.005openalex-extracted
Histone variants and modifications in plant gene regulation
inferredcites →https://doi.org/10.1016/j.pbi.2013.03.002openalex-extracted
Improvement of phosphorus efficiency in rice on the basis of understanding phosphate signaling and homeostasis
inferredcites →https://doi.org/10.1016/j.pbi.2017.07.006openalex-extracted
The world according to GARP transcription factors
inferredcites →https://doi.org/10.1016/j.plaphy.2018.04.004openalex-extracted
Functional characterization of the gene promoter for an Elaeis guineensis phosphate starvation-inducible, high affinity phosphate transporter in both homologous and heterologous model systems
inferredcites →https://doi.org/10.1016/j.plaphy.2021.09.045openalex-extracted
Identification of SPX family genes in the maize genome and their expression under different phosphate regimes
inferredcites →https://doi.org/10.1016/j.semcdb.2017.06.013openalex-extracted
Molecular mechanisms of phosphate transport and signaling in higher plants
inferredcites →https://doi.org/10.1016/j.stem.2012.11.003openalex-extracted
H2A.Z Facilitates Access of Active and Repressive Complexes to Chromatin in Embryonic Stem Cell Self-Renewal and Differentiation
inferredcites →https://doi.org/10.1016/j.tibs.2022.04.014openalex-extracted
H2A.Z's ‘social’ network: functional partners of an enigmatic histone variant
inferredcites →https://doi.org/10.1016/j.ygeno.2015.05.005openalex-extracted
Genome-wide histone acetylation correlates with active transcription in maize
inferredcites →https://doi.org/10.1016/j.ygeno.2020.09.052openalex-extracted
The histone modification H3K4me3 marks functional genes in soybean nodules
inferredcites →https://doi.org/10.1016/s0176-1617(00)80225-4openalex-extracted
Sucrose Metabolism in Leaves and Roots of Bean (Phaseolus vulgaris L.) during Phosphate Deficiency
inferredcites →https://doi.org/10.1038/emboj.2010.85openalex-extracted
Essential role of p18Hamlet/SRCAP‐mediated histone H2A.Z chromatin incorporation in muscle differentiation
inferredcites →https://doi.org/10.1038/nature07324openalex-extracted
Histone H2A.Z and DNA methylation are mutually antagonistic chromatin marks
inferredcites →https://doi.org/10.1038/s41467-020-16457-5openalex-extracted
Integrative analysis of reference epigenomes in 20 rice varieties
inferredcites →https://doi.org/10.1038/s41467-020-20681-4openalex-extracted
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/s41598-017-11490-9openalex-extracted
Identification of Purple Acid Phosphatases in Chickpea and Potential Roles of CaPAP7 in Seed Phytate Accumulation
inferredcites →https://doi.org/10.1080/01490451.2019.1654043openalex-extracted
Phosphorus and phosphate solubilizing bacteria: Keys for sustainable agriculture
inferredcites →https://doi.org/10.1080/15592324.2019.1686236openalex-extracted
Epigenetic regulation: another layer in plant nutrition
inferredcites →https://doi.org/10.1093/aob/mct080openalex-extracted
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/erv025openalex-extracted
Differentiating phosphate-dependent and phosphate-independent systemic phosphate-starvation response networks in Arabidopsis thaliana through the application of phosphite
inferredcites →https://doi.org/10.1093/jxb/erx292openalex-extracted
GmPHR25, a GmPHR member up-regulated by phosphate starvation, controls phosphate homeostasis in soybean
inferredcites →https://doi.org/10.1093/jxb/ery244openalex-extracted
Rice H2A.Z negatively regulates genes responsive to nutrient starvation but promotes expression of key housekeeping genes
inferredcites →https://doi.org/10.1093/molbev/msab120openalex-extracted
MEGA11: Molecular Evolutionary Genetics Analysis Version 11
inferredcites →https://doi.org/10.1093/mp/ssp120openalex-extracted
Regulation of Phosphate Starvation Responses in Plants: Signaling Players and Cross-Talks
inferredcites →https://doi.org/10.1093/pcp/pcab007openalex-extracted
A Citrus Phosphate Starvation Response Factor CsPHL3 Negatively Regulates Carotenoid Metabolism
inferredcites →https://doi.org/10.1093/pcp/pcab011openalex-extracted
Phosphate Uptake and Transport in Plants: An Elaborate Regulatory System
inferredcites →https://doi.org/10.1093/pcp/pch056openalex-extracted
Low Phosphorus Tolerance Mechanisms: Phosphorus Recycling and Photosynthate Partitioning in the Tropical Forage Grass, Brachiaria Hybrid Cultivar Mulato Compared with Rice
inferredcites →https://doi.org/10.1093/pcp/pcw100openalex-extracted
Characterization of theAtSPX3Promoter Elucidates its Complex Regulation in Response to Phosphorus Deficiency
inferredcites →https://doi.org/10.1093/pcp/pcy148openalex-extracted
Sensing and Signaling of Phosphate Starvation: From Local to Long Distance
inferredcites →https://doi.org/10.1101/2019.12.13.875393openalex-extracted
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/10.1101/467076openalex-extracted
Two bifunctional inositol pyrophosphate kinases/phosphatases control plant phosphate homeostasis
inferredcites →https://doi.org/10.1101/gad.204401openalex-extracted
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.104.045823openalex-extracted
Promoter Analysis of the Barley Pht1;1 Phosphate Transporter Gene Identifies Regions Controlling Root Expression and Responsiveness to Phosphate Deprivation
inferredcites →https://doi.org/10.1104/pp.107.111443openalex-extracted
OsPHR2 Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
inferredcites →https://doi.org/10.1104/pp.109.145532openalex-extracted
Histone H2A.Z Regulates the Expression of Several Classes of Phosphate Starvation Response Genes But Not as a Transcriptional Activator
inferredcites →https://doi.org/10.1104/pp.111.178459openalex-extracted
Phosphate Utilization Efficiency Correlates with Expression of Low-Affinity Phosphate Transporters and Noncoding RNA, IPS1, in Barley
inferredcites →https://doi.org/10.1104/pp.15.00736openalex-extracted
Integrative Comparison of the Role of the PHOSPHATE RESPONSE1 Subfamily in Phosphate Signaling and Homeostasis in Rice
inferredcites →https://doi.org/10.1104/pp.15.01005openalex-extracted
OsSPX-MFS3, a vacuolar phosphate efflux transporter, is involved in maintaining Pi homeostasis in rice
inferredcites →https://doi.org/10.1104/pp.15.01336openalex-extracted
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.19.01153openalex-extracted
Low-Phosphate Chromatin Dynamics Predict a Cell Wall Remodeling Network in Rice Shoots
inferredcites →https://doi.org/10.1105/tpc.105.036640openalex-extracted
PHOSPHATE TRANSPORTER TRAFFIC FACILITATOR1 Is a Plant-Specific SEC12-Related Protein That Enables the Endoplasmic Reticulum Exit of a High-Affinity Phosphate Transporter in Arabidopsis [W]
inferredcites →https://doi.org/10.1105/tpc.13.5.1231openalex-extracted
The Maize Golden2 Gene Defines a Novel Class of Transcriptional Regulators in Plants
inferredcites →https://doi.org/10.1105/tpc.19.00685openalex-extracted
PROTEIN PHOSPHATASE95 Regulates Phosphate Homeostasis by Affecting Phosphate Transporter Trafficking in Rice
inferredcites →https://doi.org/10.1111/febs.14846openalex-extracted
Structural basis for the Target DNA recognition and binding by the MYB domain of phosphate starvation response 1
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01608.xopenalex-extracted
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-extracted
Increased expression of the MYB‐related transcription factor, PHR1, leads to enhanced phosphate uptake in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03734.xopenalex-extracted
Involvement of OsSPX1 in phosphate homeostasis in rice
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03795.xopenalex-extracted
Arabidopsis ING and Alfin1‐like protein families localize to the nucleus and bind to H3K4me3/2 via plant homeodomain fingers
inferredcites →https://doi.org/10.1111/nph.12194openalex-extracted
ALFIN ‐ LIKE 6 is involved in root hair elongation during phosphate deficiency in Arabidopsis
inferredcites →https://doi.org/10.1111/nph.15306openalex-extracted
Epigenetic regulation of anthocyanin biosynthesis by an antagonistic interaction between H2A.Z and H3K4me3
inferredcites →https://doi.org/10.1111/pbi.12699openalex-extracted
Improvement in phosphate acquisition and utilization by a secretory purple acid phosphatase (OsPAP21b) in rice
inferredcites →https://doi.org/10.1111/ppl.13503openalex-extracted
SlPHL1 , a MYB‐CC transcription factor identified from tomato, positively regulates the phosphate starvation response
inferredcites →https://doi.org/10.1111/tpj.13549openalex-extracted
WRI 1‐1, ABI 5, NF ‐ YA 3 and NF ‐ YC 2 increase oil biosynthesis in coordination with hormonal signaling during fruit development in oil palm
inferredcites →https://doi.org/10.1111/tpj.15868openalex-extracted
H3K4me3 plays a key role in establishing permissive chromatin states during bud dormancy and bud break in apple
inferredcites →https://doi.org/10.1128/mcb.05017-11openalex-extracted
Histone H3 Lysine 4 Hypermethylation Prevents Aberrant Nucleosome Remodeling at the PHO5 Promoter
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103849openalex-extracted
Signaling Network in Sensing Phosphate Availability in Plants
inferredcites →https://doi.org/10.1186/1746-4811-3-11openalex-extracted
Chromatin immunoprecipitation: optimization, quantitative analysis and data normalization
inferredcites →https://doi.org/10.1186/s12863-021-00962-7openalex-extracted
Comparative transcriptome analysis reveals novel insights into transcriptional responses to phosphorus starvation in oil palm (Elaeis guineensis) root
inferredcites →https://doi.org/10.1186/s12864-021-08242-5openalex-extracted
New insights into the evolution of SPX gene family from algae to legumes; a focus on soybean
inferredcites →https://doi.org/10.1371/journal.pbio.0030384openalex-extracted
Variant Histone H2A.Z Is Globally Localized to the Promoters of Inactive Yeast Genes and Regulates Nucleosome Positioning
inferredcites →https://doi.org/10.1371/journal.pgen.1001102openalex-extracted
A Central Regulatory System Largely Controls Transcriptional Activation and Repression Responses to Phosphate Starvation in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pgen.1009601openalex-extracted
Crosstalk between H2A variant-specific modifications impacts vital cell functions
inferredcites →https://doi.org/10.1371/journal.pone.0083556openalex-extracted
A Rapid, Highly Efficient and Economical Method of Agrobacterium-Mediated In planta Transient Transformation in Living Onion Epidermis
inferredcites →https://doi.org/10.1371/journal.pone.0194628openalex-extracted
Rice OsMYB5P improves plant phosphate acquisition by regulation of phosphate transporter
inferredcites →https://doi.org/10.1590/1678-4499.0408openalex-extracted
Determination of optimum levels of nitrogen, phosphorus and potassium of oil palm seedlings in solution culture
inferredcites →https://doi.org/10.21894/jopr.2020.0042openalex-extracted
ECONOMIC FEASIBILITY OF CLONAL OIL PALM PLANTING MATERIAL
inferredcites →https://doi.org/10.3389/fpls.2018.01186openalex-extracted
Overexpression of a Phosphate Starvation Response AP2/ERF Gene From Physic Nut in Arabidopsis Alters Root Morphological Traits and Phosphate Starvation-Induced Anthocyanin Accumulation
inferredcites →https://doi.org/10.3389/fpls.2018.01432openalex-extracted
Functional Characterization of Arabidopsis PHL4 in Plant Response to Phosphate Starvation
inferredcites →https://doi.org/10.3389/fpls.2019.00095openalex-extracted
An Overview of Sucrose Synthases in Plants
inferredcites →https://doi.org/10.3389/fpls.2021.700651openalex-extracted
Transcription Factor GmWRKY46 Enhanced Phosphate Starvation Tolerance and Root Development in Transgenic Plants
inferredcites →https://doi.org/10.3389/fpls.2021.761059openalex-extracted
Profiling of H3K4me3 and H3K27me3 and Their Roles in Gene Subfunctionalization in Allotetraploid Cotton
inferredcites →https://doi.org/10.3390/ijms222212348openalex-extracted
Phosphate (Pi) Starvation Up-Regulated GmCSN5A/B Participates in Anthocyanin Synthesis in Soybean (Glycine max) Dependent on Pi Availability
inferredcites →https://doi.org/10.3390/metabo11040217openalex-extracted
The Dynamic Responses of Oil Palm Leaf and Root Metabolome to Phosphorus Deficiency
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