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A phosphate starvation response‐regulated receptor‐like kinase, OsADK1, is required for mycorrhizal symbiosis and phosphate starvation responses

https://doi.org/10.1111/nph.18546
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What this work says

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

inferredcites →https://doi.org/10.1016/j.cell.2021.09.030openalex-snapshot
A phosphate starvation response-centered network regulates mycorrhizal symbiosis
inferredcites →https://doi.org/10.1016/j.chom.2014.01.011openalex-snapshot
CYCLOPS, A DNA-Binding Transcriptional Activator, Orchestrates Symbiotic Root Nodule Development
inferredcites →https://doi.org/10.1016/j.cub.2012.09.043openalex-snapshot
A Common Signaling Process that Promotes Mycorrhizal and Oomycete Colonization of Plants
inferredcites →https://doi.org/10.1016/j.cub.2012.09.044openalex-snapshot
A GRAS-Type Transcription Factor with a Specific Function in Mycorrhizal Signaling
inferredcites →https://doi.org/10.1016/j.cub.2016.01.069openalex-snapshot
A CCaMK-CYCLOPS-DELLA Complex Activates Transcription of RAM1 to Regulate Arbuscule Branching
inferredcites →https://doi.org/10.1016/j.cub.2016.07.059openalex-snapshot
Symbiotic Fungi Control Plant Root Cortex Development through the Novel GRAS Transcription Factor MIG1
inferredcites →https://doi.org/10.1016/j.cub.2017.03.003openalex-snapshot
A Transcriptional Program for Arbuscule Degeneration during AM Symbiosis Is Regulated by MYB1
inferredcites →https://doi.org/10.1016/j.cub.2019.11.038openalex-snapshot
LCO Receptors Involved in Arbuscular Mycorrhiza Are Functional for Rhizobia Perception in Legumes
inferredcites →https://doi.org/10.1016/j.molp.2017.07.012openalex-snapshot
Nutrient Exchange and Regulation in Arbuscular Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1016/j.molp.2018.09.006openalex-snapshot
Medicago AP2-Domain Transcription Factor WRI5a Is a Master Regulator of Lipid Biosynthesis and Transfer during Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1016/j.molp.2019.10.015openalex-snapshot
A LysM Receptor Heteromer Mediates Perception of Arbuscular Mycorrhizal Symbiotic Signal in Rice
inferredcites →https://doi.org/10.1038/cr.2013.167openalex-snapshot
A DELLA protein complex controls the arbuscular mycorrhizal symbiosis in plants
inferredcites →https://doi.org/10.1038/nature03608openalex-snapshot
Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1038/nature03610openalex-snapshot
Nitrogen transfer in the arbuscular mycorrhizal symbiosis
inferredcites →https://doi.org/10.1038/nature09622openalex-snapshot
Fungal lipochitooligosaccharide symbiotic signals in arbuscular mycorrhiza
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1038/nplants.2015.208openalex-snapshot
Genes conserved for arbuscular mycorrhizal symbiosis identified through phylogenomics
inferredcites →https://doi.org/10.1038/nprot.2017.055openalex-snapshot
Mapping genome-wide transcription-factor binding sites using DAP-seq
inferredcites →https://doi.org/10.1038/nrmicro1987openalex-snapshot
Arbuscular mycorrhiza: the mother of plant root endosymbioses
inferredcites →https://doi.org/10.1038/nrmicro2990openalex-snapshot
Speak, friend, and enter: signalling systems that promote beneficial symbiotic associations in plants
inferredcites →https://doi.org/10.1038/s41467-022-27976-8openalex-snapshot
PHOSPHATE STARVATION RESPONSE transcription factors enable arbuscular mycorrhiza symbiosis
inferredcites →https://doi.org/10.1073/pnas.0508883103openalex-snapshot
A nucleoporin is required for induction of Ca 2+ spiking in legume nodule development and essential for rhizobial and fungal symbiosis
inferredcites →https://doi.org/10.1073/pnas.0806858105openalex-snapshot
CYCLOPS, a mediator of symbiotic intracellular accommodation
inferredcites →https://doi.org/10.1073/pnas.1812275115openalex-snapshot
AP2 transcription factor CBX1 with a specific function in symbiotic exchange of nutrients in mycorrhizal Lotus japonicus
inferredcites →https://doi.org/10.1073/pnas.2023738118openalex-snapshot
Discriminating symbiosis and immunity signals by receptor competition in rice
inferredcites →https://doi.org/10.1093/nar/gku365openalex-snapshot
deepTools: a flexible platform for exploring deep-sequencing data
inferredcites →https://doi.org/10.1093/pcp/pcu129openalex-snapshot
The Bifunctional Plant Receptor, OsCERK1, Regulates Both Chitin-Triggered Immunity and Arbuscular Mycorrhizal Symbiosis in Rice
inferredcites →https://doi.org/10.1094/mpmi-11-21-0270-ropenalex-snapshot
Colonization of Mutualistic Mycorrhizal and Parasitic Blast Fungi Requires OsRAM2-Regulated Fatty Acid Biosynthesis in Rice
inferredcites →https://doi.org/10.1094/mpmi-20-8-0912openalex-snapshot
A Novel Nuclear Protein Interacts With the Symbiotic DMI3 Calcium- and Calmodulin-Dependent Protein Kinase of Medicago truncatula
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.103.024380openalex-snapshot
Mycorrhizal Fungi Can Dominate Phosphate Supply to Plants Irrespective of Growth Responses
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.107.111443openalex-snapshot
OsPHR2 Is Involved in Phosphate-Starvation Signaling and Excessive Phosphate Accumulation in Shoots of Plants
inferredcites →https://doi.org/10.1104/pp.112.195990openalex-snapshot
Transcriptional Responses toward Diffusible Signals from Symbiotic Microbes Reveal MtNFP- and MtDMI3-Dependent Reprogramming of Host Gene Expression by Arbuscular Mycorrhizal Fungal Lipochitooligosaccharides
inferredcites →https://doi.org/10.1104/pp.114.255430openalex-snapshot
Network of GRAS Transcription Factors Involved in the Control of Arbuscule Development inLotus japonicus
inferredcites →https://doi.org/10.1104/pp.15.00310openalex-snapshot
The Petunia GRAS Transcription Factor ATA/RAM1 Regulates Symbiotic Gene Expression and Fungal Morphogenesis in Arbuscular Mycorrhiza
inferredcites →https://doi.org/10.1105/tpc.105.035410openalex-snapshot
Arbuscular Mycorrhizal Fungi Elicit a Novel Intracellular Apparatus in Medicago truncatula Root Epidermal Cells before Infection[W]
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01095.xopenalex-snapshot
The Arum–Paris continuum of mycorrhizal symbioses
inferredcites →https://doi.org/10.1111/nph.13427openalex-snapshot
Combined genetic and transcriptomic analysis reveals three major signalling pathways activated by Myc‐ LCO s in Medicago truncatula
inferredcites →https://doi.org/10.1111/nph.15891openalex-snapshot
The Medicago truncatula LysM receptor‐like kinase LYK9 plays a dual role in immunity and the arbuscular mycorrhizal symbiosis
inferredcites →https://doi.org/10.1111/nph.17979openalex-snapshot
OsADK1, a novel kinase regulating arbuscular mycorrhizal symbiosis in rice
inferredcites →https://doi.org/10.1111/tpj.12723openalex-snapshot
The receptor kinase CERK 1 has dual functions in symbiosis and immunity signalling
inferredcites →https://doi.org/10.1126/science.aam9970openalex-snapshot
Plants transfer lipids to sustain colonization by mutualistic mycorrhizal and parasitic fungi
inferredcites →https://doi.org/10.1126/science.aan0081openalex-snapshot
Fatty acids in arbuscular mycorrhizal fungi are synthesized by the host plant
inferredcites →https://doi.org/10.1126/science.abg0929openalex-snapshot
Lipid exchanges drove the evolution of mutualism during plant terrestrialization
inferredcites →https://doi.org/10.1146/annurev-phyto-080516-035521openalex-snapshot
Mechanisms Underlying Establishment of Arbuscular Mycorrhizal Symbioses
inferredcites →https://doi.org/10.1186/gb-2008-9-9-r137openalex-snapshot
Model-based Analysis of ChIP-Seq (MACS)
inferredcites →https://doi.org/10.1371/journal.pbio.0040226openalex-snapshot
Strigolactones Stimulate Arbuscular Mycorrhizal Fungi by Activating Mitochondria
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

What points at this work

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

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Symrk Significantly Affected Am Fungal Symbiosis and Plant Growth in Maize
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Mycorrhizal Symbiosis: Evolution, Opportunities, Challenges, and Prospects
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Hidden Allies: Exploring the Cutting-Edge Insights into the Role of Mycorrhizal Fungi in Plant Health
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A transcriptomic perspective of P trade in mycorrhizal grapevine
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IPD3, a master regulator of arbuscular mycorrhizal symbiosis, affects genes for immunity and metabolism of non-host Arabidopsis when restored long after its evolutionary loss
inferred← citeshttps://doi.org/10.1007/s11104-024-07047-1openalex-snapshot
Arbuscular mycorrhizal fungi enhance Leymus chinensis resistance to salinity predominantly through regulating root endosphere bacteria
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The Underlying Molecular Mechanisms of Agriculturally Important Microbes: Role in Global Sustainable Development Through Agricultural and Environmental Interventions
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Multifaceted roles of phosphate starvation response (PHRs) transcription factors: beyond phosphate acquisition and homeostasis
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Novel insights into phosphate starvation response in plants from mycorrhiza perspective
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Networks of the symbiosis-immunity continuum in plants
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Root exudate-mediated nutrient exchange in the rhizosphere: multi-element networks, dynamic regulation, and implications for sustainable agriculture
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Deciphering Plant-Microbe Symbioses: A Molecular Blueprint for Precision Agriculture
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Mixed cropping enhances the nitrogen and phosphorus purification efficiency of sewage in wetland ecosystems
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Presymbiotic activation of karrikin signaling creates a permissive state for arbuscular mycorrhizal symbiosis by derepressing the NSP1–NSP2–SLR1 transcriptional complex in rice
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The hormonal, metabolic, and environmental regulation of plant shoot branching
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112427openalex-snapshot
SYMRK significantly affected AMF symbiosis and plant growth in maize
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111523openalex-snapshot
Interkingdom signaling dynamics in the cereal holobiont: microbiome-mediated pathways to drought resilience
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Methane Emission from Rice Fields: Necessity for Molecular Approach for Mitigation
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Phosphorus/nitrogen sensing and signaling in diverse root–fungus symbioses
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CARK3-mediated phosphorylation of bHLH106 inhibits iron uptake by repressing the expression of IRT1 in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41477-023-01453-6openalex-snapshot
The strigolactone pathway plays a crucial role in integrating metabolic and nutritional signals in plants
inferred← citeshttps://doi.org/10.1073/pnas.2416345122openalex-snapshot
OsNLP3 and OsPHR2 orchestrate direct and mycorrhizal pathways for nitrate uptake by regulating NAR2.1–NRT2s complexes in rice
inferred← citeshttps://doi.org/10.1093/hr/uhae228openalex-snapshot
The transcription factor MYC2 positively regulates terpene trilactone biosynthesis through activating GbGGPPS expression in Ginkgo biloba
inferred← citeshttps://doi.org/10.1093/jxb/eraf404openalex-snapshot
Integrating single-cell omic techniques to resolve the spatio-temporal complexity of arbuscular mycorrhizal symbiosis
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/plcell/koad050openalex-snapshot
ARBUSCULAR MYCORRHIZA-INDUCED KINASES AMK8 and AMK24 associate with the receptor-like kinase KINASE3 to regulate arbuscular mycorrhizal symbiosis in Lotus japonicus
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Re-engineering a lost trait: IPD3 , a master regulator of arbuscular mycorrhizal symbiosis, affects genes for immunity and metabolism of non-host Arabidopsis when restored long after its evolutionary loss
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Nitrogen starvation response in hornworts and liverworts provides little evidence for complex priming to the cyanobiont
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The good, the bad, and the phosphate: regulation of beneficial and detrimental plant–microbe interactions by the plant phosphate status
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Microbe‐dependent and independent nitrogen and phosphate acquisition and regulation in plants
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Walking on a tightrope: cell wall‐associated kinases act as sensors and regulators of immunity and symbiosis
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Convergent losses of arbuscular mycorrhizal symbiosis in carnivorous plants
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E3 ligase ATL17 is a key regulator of abscisic acid signaling that mediates AHG1 degradation in Arabidopsis thaliana
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Unravelling the Molecular Dialogue of Beneficial Microbe−Plant Interactions
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OsPHR2‐OsDIR55 Module Enhances Root Barrier Integrity and Rice Tolerance to Phosphate Deficiency
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Phosphate Levels: The Hidden Gatekeepers of the Rice–Blast Pathosystem
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Outsmarted by fungi
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Molecular regulation network of phosphorus starvation signaling and genetic improvement of phosphorus efficiency in plants
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Regulation of arbuscular mycorrhiza development by environmental stimuli: Many roads lead to strigolactones
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Efficiently recording and processing data from arbuscular mycorrhizal colonization assays using AMScorer and AMReader
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Functional Overview of Plant Genes Essential for Arbuscular Mycorrhizal Symbiosis
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Identification of genetic loci related to low phosphorus tolerance at the seedling stage in wheat and analysis of candidate genes
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