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ITPK1-Dependent Inositol Polyphosphates Regulate Auxin Responses in Arabidopsis thaliana

https://doi.org/10.1101/2020.04.23.058487

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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/jcp.26017openalex-snapshot

Intimate connections: Inositol pyrophosphates at the interface of metabolic regulation and cell signaling

inferredcites →https://doi.org/10.1007/978-1-61779-197-0_12openalex-snapshot

Delete and Repeat: A Comprehensive Toolkit for Sequential Gene Knockout in the Budding Yeast Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1007/978-94-015-8394-7_20openalex-snapshot

Purification, Crystallization, and Preliminary X-ray Diffraction Analysis of a Condensing Enzyme

inferredcites →https://doi.org/10.1007/bf00262639openalex-snapshot

Comparison of mechanisms controlling uptake and accumulation of 2,4-dichlorophenoxy acetic acid, naphthalene-1-acetic acid, and indole-3-acetic acid in suspension-cultured tobacco cells

inferredcites →https://doi.org/10.1007/s004250000348openalex-snapshot

Abscisic acid-induced changes in inositol metabolism in Spirodela polyrrhiza

inferredcites →https://doi.org/10.1016/j.chembiol.2008.01.011openalex-snapshot

Inositol Hexakisphosphate Kinase Products Contain Diphosphate and Triphosphate Groups

inferredcites →https://doi.org/10.1016/j.cub.2011.04.017openalex-snapshot

A Mutually Inhibitory Interaction between Auxin and Cytokinin Specifies Vascular Pattern in Roots

inferredcites →https://doi.org/10.1016/j.febslet.2007.07.046openalex-snapshot

Arabidopsis thaliana inositol 1,3,4‐trisphosphate 5/6‐kinase 4 (AtITPK4) is an outlier to a family of ATP‐grasp fold proteins from Arabidopsis

inferredcites →https://doi.org/10.1016/j.febslet.2008.04.054openalex-snapshot

Metabolic and signaling properties of an Itpk gene family in Glycine max

inferredcites →https://doi.org/10.1016/j.molcel.2014.02.020openalex-snapshot

Inositol Pyrophosphates Mediate the DNA-PK/ATM-p53 Cell Death Pathway by Regulating CK2 Phosphorylation of Tti1/Tel2

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.tplants.2013.04.006openalex-snapshot

Lateral root development in Arabidopsis: fifty shades of auxin

inferredcites →https://doi.org/10.1016/j.tplants.2015.10.019openalex-snapshot

Structural Biology of Nuclear Auxin Action

inferredcites →https://doi.org/10.1016/j.tplants.2018.04.006openalex-snapshot

Adaptation to Phosphate Scarcity: Tips from Arabidopsis Roots

inferredcites →https://doi.org/10.1016/s0021-9258(18)53551-1openalex-snapshot

Turnover of inositol polyphosphate pyrophosphates in pancreatoma cells.

inferredcites →https://doi.org/10.1016/s0031-9422(02)00610-6openalex-snapshot

Seed phosphorus and inositol phosphate phenotype of barley low phytic acid genotypes

inferredcites →https://doi.org/10.1016/s0960-9822(00)80055-xopenalex-snapshot

Synthesis of diphosphoinositol pentakisphosphate by a newly identified family of higher inositol polyphosphate kinases

inferredcites →https://doi.org/10.1021/acschembio.9b00423openalex-snapshot

Arabidopsis ITPK1 and ITPK2 Have an Evolutionarily Conserved Phytic Acid Kinase Activity

inferredcites →https://doi.org/10.1038/35104500openalex-snapshot

Auxin regulates SCFTIR1-dependent degradation of AUX/IAA proteins

inferredcites →https://doi.org/10.1038/nature02081openalex-snapshot

Regulation of phyllotaxis by polar auxin transport

inferredcites →https://doi.org/10.1038/nature03542openalex-snapshot

The Arabidopsis F-box protein TIR1 is an auxin receptor

inferredcites →https://doi.org/10.1038/nature03543openalex-snapshot

The F-box protein TIR1 is an auxin receptor

inferredcites →https://doi.org/10.1038/nature05731openalex-snapshot

Mechanism of auxin perception by the TIR1 ubiquitin ligase

inferredcites →https://doi.org/10.1038/nature09430openalex-snapshot

Jasmonate perception by inositol-phosphate-potentiated COI1–JAZ co-receptor

inferredcites →https://doi.org/10.1038/nchembio.926openalex-snapshot

A combinatorial TIR1/AFB–Aux/IAA co-receptor system for differential sensing of auxin

inferredcites →https://doi.org/10.1038/ncomms10269openalex-snapshot

HSP90 regulates temperature-dependent seedling growth in Arabidopsis by stabilizing the auxin co-receptor F-box protein TIR1

inferredcites →https://doi.org/10.1038/nplants.2015.190openalex-snapshot

Molecular and genetic control of plant thermomorphogenesis

inferredcites →https://doi.org/10.1038/nprot.2006.337openalex-snapshot

Extraction and analysis of soluble inositol polyphosphates from yeast

inferredcites →https://doi.org/10.1038/nrm2020openalex-snapshot

Auxin in action: signalling, transport and the control of plant growth and development

inferredcites →https://doi.org/10.1038/s41467-017-02195-8openalex-snapshot

A 1-phytase type III effector interferes with plant hormone signaling

inferredcites →https://doi.org/10.1038/s41586-018-0837-0openalex-snapshot

High levels of auxin signalling define the stem-cell organizer of the vascular cambium

inferredcites →https://doi.org/10.1042/bj20090241openalex-snapshot

Inositol pyrophosphates modulate hydrogen peroxide signalling

inferredcites →https://doi.org/10.1042/bj20130118openalex-snapshot

Inositol pyrophosphates: between signalling and metabolism

inferredcites →https://doi.org/10.1042/bj20140798openalex-snapshot

Inositol pyrophosphates regulate RNA polymerase I-mediated rRNA transcription in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1042/bj3180279openalex-snapshot

Inositol phosphates in barley (Hordeum vulgare L.) aleurone tissue are stereochemically similar to the products of breakdown of InsP6in vitro by wheat-bran phytase

inferredcites →https://doi.org/10.1073/pnas.0504172102openalex-snapshot

Generation of phytate-free seeds in Arabidopsis through disruption of inositol polyphosphate kinases

inferredcites →https://doi.org/10.1073/pnas.0509839103openalex-snapshot

An auxin-driven polarized transport model for phyllotaxis

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/10.1074/jbc.m805686200openalex-snapshot

Structural Analysis and Detection of Biological Inositol Pyrophosphates Reveal That the Family of VIP/Diphosphoinositol Pentakisphosphate Kinases Are 1/3-Kinases

inferredcites →https://doi.org/10.1074/jbc.ra119.007848openalex-snapshot

The inositol hexakisphosphate kinases IP6K1 and -2 regulate human cellular phosphate homeostasis, including XPR1-mediated phosphate export

inferredcites →https://doi.org/10.1093/nar/20.6.1425openalex-snapshot

Improved method for high efficiency transformation of intact yeast cells

inferredcites →https://doi.org/10.1098/rsob.150014openalex-snapshot

A novel method for the purification of inositol phosphates from biological samples reveals that no phytate is present in human plasma or urine

inferredcites →https://doi.org/10.1101/gad.12.2.198openalex-snapshot

The TIR1 protein of Arabidopsis functions in auxin response and is related to human SKP2 and yeast Grr1p

inferredcites →https://doi.org/10.1101/gad.1402406openalex-snapshot

Control of leaf vascular patterning by polar auxin transport

inferredcites →https://doi.org/10.1104/pp.106.078063openalex-snapshot

pho2, a Phosphate Overaccumulator, Is Caused by a Nonsense Mutation in a MicroRNA399 Target Gene

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.107.1.207openalex-snapshot

Characterization of a Phosphate-Accumulator Mutant of Arabidopsis thaliana

inferredcites →https://doi.org/10.1104/pp.121.4.1179openalex-snapshot

Auxin Is Required for Leaf Vein Pattern in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.16.00694openalex-snapshot

Inositol Polyphosphate Binding Specificity of the Jasmonate Receptor Complex

inferredcites →https://doi.org/10.1104/pp.18.01377openalex-snapshot

A Mobile Auxin Signal Connects Temperature Sensing in Cotyledons with Growth Responses in Hypocotyls

inferredcites →https://doi.org/10.1104/pp.65.1.57openalex-snapshot

Establishment of an Experimental System for the Study of Tracheary Element Differentiation from Single Cells Isolated from the Mesophyll of Zinnia elegans

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.114.133744openalex-snapshot

SCF TIR1/AFB -Based Auxin Perception: Mechanism and Role in Plant Growth and Development

inferredcites →https://doi.org/10.1105/tpc.114.135160openalex-snapshot

VIH2 Regulates the Synthesis of Inositol Pyrophosphate InsP8 and Jasmonate-Dependent Defenses in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.16.00351openalex-snapshot

Synergism between Inositol Polyphosphates and TOR Kinase Signaling in Nutrient Sensing, Growth Control, and Lipid Metabolism in Chlamydomonas

inferredcites →https://doi.org/10.1105/tpc.2.11.1071openalex-snapshot

Growth and Development of the axr1 Mutants of Arabidopsis

inferredcites →https://doi.org/10.1107/s1744309106041728openalex-snapshot

Crystallization and preliminary X-ray diffraction analysis of phospholipid-bound Sfh1p, a member of theSaccharomyces cerevisiaeSec14p-like phosphatidylinositol transfer protein family

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04803.xopenalex-snapshot

Quantitative analysis of venation patterns of Arabidopsis leaves by supervised image analysis

inferredcites →https://doi.org/10.1111/nph.14731openalex-snapshot

Response of the plant hormone network to boron deficiency

inferredcites →https://doi.org/10.1111/tpj.12650openalex-snapshot

Arabidopsis inositol pentakisphosphate 2‐kinase, A t IPK 1, is required for growth and modulates phosphate homeostasis at the transcriptional level

inferredcites →https://doi.org/10.1111/tpj.12669openalex-snapshot

Two inositol hexakisphosphate kinases drive inositol pyrophosphate synthesis in plants

inferredcites →https://doi.org/10.1111/tpj.13974openalex-snapshot

Arabidopsis inositol phosphate kinases IPK 1 and ITPK 1 constitute a metabolic pathway in maintaining phosphate homeostasis

inferredcites →https://doi.org/10.1126/science.1139099openalex-snapshot

A Conserved Family of Enzymes That Phosphorylate Inositol Hexakisphosphate

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-043015-112122openalex-snapshot

Transcriptional Responses to the Auxin Hormone

inferredcites →https://doi.org/10.1271/bbb.70216openalex-snapshot

Improved Gateway Binary Vectors: High-Performance Vectors for Creation of Fusion Constructs in Transgenic Analysis of Plants

inferredcites →https://doi.org/10.1371/journal.pcbi.1006896openalex-snapshot

Toward a 3D model of phyllotaxis based on a biochemically plausible auxin-transport mechanism

inferredcites →https://doi.org/10.1371/journal.pone.0005580openalex-snapshot

Inositol Pyrophosphates and Their Unique Metabolic Complexity: Analysis by Gel Electrophoresis

inferredcites →https://doi.org/10.7554/elife.43582openalex-snapshot

Two bifunctional inositol pyrophosphate kinases/phosphatases control plant phosphate homeostasis

inferredcites →https://doi.org/10.7554/elife.54740openalex-snapshot

Genetic analysis of the Arabidopsis TIR1/AFB auxin receptors reveals both overlapping and specialized functions

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s00299-021-02812-3openalex-snapshot

Arabidopsis inositol polyphosphate kinases IPK1 and ITPK1 modulate crosstalk between SA-dependent immunity and phosphate-starvation responses

inferred← citeshttps://doi.org/10.1016/j.jbior.2020.100782openalex-snapshot

Inositol phosphate kinases in the eukaryote landscape

inferred← citeshttps://doi.org/10.1016/j.molp.2021.07.011openalex-snapshot

ITPK1 is an InsP6/ADP phosphotransferase that controls phosphate signaling in Arabidopsis

inferred← citeshttps://doi.org/10.1021/acs.biochem.2c00145openalex-snapshot

Arabidopsis PFA-DSP-Type Phosphohydrolases Target Specific Inositol Pyrophosphate Messengers

inferred← citeshttps://doi.org/10.1101/2020.10.02.323584openalex-snapshot

Arabidopsis inositol polyphosphate kinase activities regulate COP9 deneddylation functions in phosphate-homeostasis

inferred← citeshttps://doi.org/10.1101/2022.05.02.489396openalex-snapshot

Translational approach to increase phosphate accumulation in two plant species through perturbance of inositol pyrophosphates

inferred← citeshttps://doi.org/10.3389/fpls.2022.944515openalex-snapshot

Regulation of plant biotic interactions and abiotic stress responses by inositol polyphosphates

inferred← citeshttps://doi.org/10.3390/agronomy12020285openalex-snapshot

Root Growth and Architecture of Wheat and Brachypodium Vary in Response to Algal Fertilizer in Soil and Solution

inferred← citeshttps://doi.org/10.3390/metabo13091021openalex-snapshot

Non-Targeted Metabolomic Analysis of Arabidopsis thaliana (L.) Heynh: Metabolic Adaptive Responses to Stress Caused by N Starvation

inferred← citeshttps://doi.org/10.3791/61495openalex-snapshot

Extraction and Quantification of Soluble, Radiolabeled Inositol Polyphosphates from Different Plant Species using SAX-HPLC

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