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OsJAZ9 overexpression improves potassium deficiency tolerance in rice by modulating jasmonic acid levels and signaling

https://doi.org/10.1101/440024
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What this work says

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

inferredcites →https://doi.org/10.1007/978-1-4612-4682-4_1openalex-snapshot
Potassium Dynamics in Soils
inferredcites →https://doi.org/10.1007/s00294-014-0438-xopenalex-snapshot
Identification and functional analysis of AG1-IA specific genes of Rhizoctonia solani
inferredcites →https://doi.org/10.1007/s00299-016-1984-0openalex-snapshot
Rice and chickpea GDPDs are preferentially influenced by low phosphate and CaGDPD1 encodes an active glycerophosphodiester phosphodiesterase enzyme
inferredcites →https://doi.org/10.1007/s00425-012-1698-7openalex-snapshot
Constitutive expression of rice WRKY30 gene increases the endogenous jasmonic acid accumulation, PR gene expression and resistance to fungal pathogens in rice
inferredcites →https://doi.org/10.1007/s10142-017-0556-xopenalex-snapshot
Morpho-physiological and transcriptome profiling reveal novel zinc deficiency-responsive genes in rice
inferredcites →https://doi.org/10.1007/s11103-009-9524-8openalex-snapshot
Identification and expression profiling analysis of TIFY family genes involved in stress and phytohormone responses in rice
inferredcites →https://doi.org/10.1007/s11103-016-0486-3openalex-snapshot
Jasmonate signaling is activated in the very early stages of iron deficiency responses in rice roots
inferredcites →https://doi.org/10.1016/b978-0-12-473542-2.x5000-7openalex-snapshot
Mineral Nutrition of Higher Plants
inferredcites →https://doi.org/10.1016/j.jplph.2012.05.002openalex-snapshot
The jasmonate receptor COI1 plays a role in jasmonate-induced lateral root formation and lateral root positioning in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.phytochem.2009.08.022openalex-snapshot
Top hits in contemporary JAZ: An update on jasmonate signaling
inferredcites →https://doi.org/10.1016/j.plantsci.2014.12.010openalex-snapshot
OsJAZ9 acts as a transcriptional regulator in jasmonate signaling and modulates salt stress tolerance in rice
inferredcites →https://doi.org/10.1016/j.tplants.2015.02.001openalex-snapshot
Diverse roles of jasmonates and ethylene in abiotic stress tolerance
inferredcites →https://doi.org/10.1023/a:1004883032383openalex-snapshot
Effect of potassium on drought resistance of Hibiscus rosa-sinensis cv. Leprechaun: Plant growth, leaf macro- and micronutrient content and root longevity
inferredcites →https://doi.org/10.1038/nature05960openalex-snapshot
JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling
inferredcites →https://doi.org/10.1038/nature06006openalex-snapshot
The JAZ family of repressors is the missing link in jasmonate signalling
inferredcites →https://doi.org/10.1038/nature08854openalex-snapshot
NINJA connects the co-repressor TOPLESS to jasmonate signalling
inferredcites →https://doi.org/10.1038/nature09430openalex-snapshot
Jasmonate perception by inositol-phosphate-potentiated COI1–JAZ co-receptor
inferredcites →https://doi.org/10.1038/ncomms4476openalex-snapshot
Jasmonic acid regulates spikelet development in rice
inferredcites →https://doi.org/10.1073/pnas.1201616109openalex-snapshot
Plant hormone jasmonate prioritizes defense over growth by interfering with gibberellin signaling cascade
inferredcites →https://doi.org/10.1073/pnas.89.15.6837openalex-snapshot
Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana mutant.
inferredcites →https://doi.org/10.1074/mcp.ra117.000032openalex-snapshot
Large-scale Proteomics Combined with Transgenic Experiments Demonstrates An Important Role of Jasmonic Acid in Potassium Deficiency Response in Wheat and Rice
inferredcites →https://doi.org/10.1080/09168451.2016.1274638openalex-snapshot
Overexpression of TIFY genes promotes plant growth in rice through jasmonate signaling
inferredcites →https://doi.org/10.1081/pln-100001394openalex-snapshot
ENHANCEMENT OF GROWTH AND NORMAL GROWTH PARAMETERS BY FOLIAR APPLICATION OF POTASSIUM AND PHOSPHORUS IN TOMATO CULTIVARS GROWN AT HIGH (NaCl) SALINITY
inferredcites →https://doi.org/10.1093/aob/mct067openalex-snapshot
Jasmonates: biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany
inferredcites →https://doi.org/10.1093/jxb/erl199openalex-snapshot
Expressions of OsHKT1, OsHKT2, and OsVHA are differentially regulated under NaCl stress in salt-sensitive and salt-tolerant rice (Oryza sativa L.) cultivars
inferredcites →https://doi.org/10.1093/jxb/erw040openalex-snapshot
Characterization of aJAZ7activation-tagged Arabidopsis mutant with increased susceptibility to the fungal pathogenFusarium oxysporum
inferredcites →https://doi.org/10.1093/jxb/erw103openalex-snapshot
Overexpression of the rice AKT1 potassium channel affects potassium nutrition and rice drought tolerance
inferredcites →https://doi.org/10.1093/jxb/erw443openalex-snapshot
Jasmonates: biosynthesis, metabolism, and signaling by proteins activating and repressing transciption
inferredcites →https://doi.org/10.1093/pcp/pcs145openalex-snapshot
Involvement of OsJAZ8 in Jasmonate-Induced Resistance to Bacterial Blight in Rice
inferredcites →https://doi.org/10.1097/00010694-196406000-00004openalex-snapshot
POTTASIUM EXCHANGE AS AFFECTED BY CATION SIZE, PH, AND MINERAL STRUCTURE
inferredcites →https://doi.org/10.1097/00010694-196408000-00005openalex-snapshot
EFFECT OF CATION SIZE AND pH ON POTASSIUM EXCHANGE IN NASON SOIL
inferredcites →https://doi.org/10.1097/00010694-198604000-00011openalex-snapshot
Advances in Soil Science
inferredcites →https://doi.org/10.1104/pp.104.046482openalex-snapshot
The Potassium-Dependent Transcriptome of Arabidopsis Reveals a Prominent Role of Jasmonic Acid in Nutrient Signaling
inferredcites →https://doi.org/10.1104/pp.104.049213openalex-snapshot
Protection of Plasma Membrane K+ Transport by the Salt Overly Sensitive1 Na+-H+ Antiporter during Salinity Stress
inferredcites →https://doi.org/10.1104/pp.112.193771openalex-snapshot
NaJAZh Regulates a Subset of Defense Responses against Herbivores and Spontaneous Leaf Necrosis inNicotiana attenuataPlants
inferredcites →https://doi.org/10.1104/pp.113.218453openalex-snapshot
Plasticity of the Arabidopsis Root System under Nutrient Deficiencies
inferredcites →https://doi.org/10.1104/pp.17.00571openalex-snapshot
OsHAD1, a Haloacid Dehalogenase-Like APase, Enhances Phosphate Accumulation
inferredcites →https://doi.org/10.1104/pp.44.9.1350openalex-snapshot
Direct Determination of Potassium Ion Accumulation in Guard Cells in Relation to Stomatal Opening in Light
inferredcites →https://doi.org/10.1104/pp.51.1.43openalex-snapshot
Effects of Phosphorus Deficiency on the Photosynthesis and Respiration of Leaves of Sugar Beet
inferredcites →https://doi.org/10.1104/pp.51.4.783openalex-snapshot
Effects of Potassium Deficiency on the Photosynthesis and Respiration of Leaves of Sugar Beet
inferredcites →https://doi.org/10.1104/pp.91.1.249openalex-snapshot
Direct Measurement of K+ Channels in Thylakoid Membranes by Incorporation of Vesicles into Planar Lipid Bilayers
inferredcites →https://doi.org/10.1104/pp.97.2.580openalex-snapshot
Surface Charge-Mediated Effects of Mg2+ on K+ Flux across the Chloroplast Envelope Are Associated with Regulation of Stromal pH and Photosynthesis
inferredcites →https://doi.org/10.1105/tpc.010322openalex-snapshot
A Mutation in the Arabidopsis KT2/KUP2 Potassium Transporter Gene Affects Shoot Cell Expansion
inferredcites →https://doi.org/10.1105/tpc.6.5.751openalex-snapshot
Arabidopsis Mutants Selected for Resistance to the Phytotoxin Coronatine Are Male Sterile, Insensitive to Methyl Jasmonate, and Resistant to a Bacterial Pathogen.
inferredcites →https://doi.org/10.1111/j.1399-3054.1962.tb08052.xopenalex-snapshot
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
inferredcites →https://doi.org/10.1111/j.1399-3054.1974.tb03660.xopenalex-snapshot
Effect of Potassium Supply on the Transport of Photosynthates to the Fruits of Tomatoes (Lycopersicon esculentum)
inferredcites →https://doi.org/10.1111/j.1467-7652.2011.00658.xopenalex-snapshot
Gateway‐compatible vectors for high‐throughput gene functional analysis in switchgrass ( Panicum virgatum L.) and other monocot species
inferredcites →https://doi.org/10.1111/j.1469-8137.1984.tb04103.xopenalex-snapshot
A HYPOTHESIS RELATING CRITICAL POTASSIUM CONCENTRATIONS FOR GROWTH TO THE DISTRIBUTION AND FUNCTIONS OF THIS ION IN THE PLANT CELL
inferredcites →https://doi.org/10.1111/pbi.12699openalex-snapshot
Improvement in phosphate acquisition and utilization by a secretory purple acid phosphatase (OsPAP21b) in rice
inferredcites →https://doi.org/10.1186/1471-2229-10-172openalex-snapshot
Potassium deficiency induces the biosynthesis of oxylipins and glucosinolates in Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/1471-2229-12-161openalex-snapshot
Transcriptome analysis of rice root responses to potassium deficiency
inferredcites →https://doi.org/10.1371/journal.pone.0070321openalex-snapshot
Gene Expression Analysis of Rice Seedling under Potassium Deprivation Reveals Major Changes in Metabolism and Signaling Components
inferredcites →https://doi.org/10.30061/ceb.201209.0002openalex-snapshot
Nitric Oxide is Involved in Methyl Jasmonate- induced Lateral Root Formation in Rice
inferredcites →https://doi.org/10.3389/fpls.2015.00975openalex-snapshot
JAZ Repressors: Potential Involvement in Nutrients Deficiency Response in Rice and Chickpea
inferredcites →https://doi.org/10.3389/fpls.2015.01077openalex-snapshot
Exploring Jasmonates in the Hormonal Network of Drought and Salinity Responses
inferredcites →https://doi.org/10.3390/ijms14047370openalex-snapshot
The Critical Role of Potassium in Plant Stress Response
inferredcites →https://doi.org/10.4161/psb.24409openalex-snapshot
Global transcriptome profile of rice root in response to essential macronutrient deficiency

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.jplph.2020.153137openalex-snapshot
Transcriptome analysis of rice (Oryza sativa L.) in response to ammonium resupply reveals the involvement of phytohormone signaling and the transcription factor OsJAZ9 in reprogramming of nitrogen uptake and metabolism
inferred← citeshttps://doi.org/10.1016/j.plgene.2021.100335openalex-snapshot
Hormone mediated cell signaling in plants under changing environmental stress
inferred← citeshttps://doi.org/10.1111/pce.70165openalex-snapshot
Potassium Deficiency and Hormone Signalling in Plants
inferred← citeshttps://doi.org/10.3390/ijms21072433openalex-snapshot
Genome-Wide Analysis Reveals Stress and Hormone Responsive Patterns of JAZ Family Genes in Camellia Sinensis
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