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Silencing a dehydration‐responsive element‐binding gene enhances the resistance of plants to a phloem‐feeding herbivore

https://doi.org/10.1111/pce.14569
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Mechanisms of callose deposition in rice regulated by exogenous abscisic acid and its involvement in rice resistance to Nilaparvata lugens Stål (Hemiptera: Delphacidae)
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Arabidopsis Plants Overexpressing the MsDREB2C Exhibit Increased Susceptibility to Alternaria mali Infection
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Effects of intraspecific variation in rice resistance to aboveground herbivore, brown planthopper, and rice root nematodes on plant yield, labile pools of plant, and rhizosphere soil
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Rice DREB1B promoter shows distinct stress-specific responses, and the overexpression of cDNA in tobacco confers improved abiotic and biotic stress tolerance
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How plants handle multiple stresses: hormonal interactions underlying responses to abiotic stress and insect herbivory
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Autophagy and Programmed Cell Death Are Critical Pathways in Jasmonic Acid Mediated Saline Stress Tolerance in Oryza sativa
inferredcites →https://doi.org/10.1007/s12033-011-9477-4openalex-snapshot
ENAC1, a NAC Transcription Factor, is an Early and Transient Response Regulator Induced by Abiotic Stress in Rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1007/s12298-022-01185-5openalex-snapshot
Identification and characterization of drought-tolerant local pigmented rice from Indonesia
inferredcites →https://doi.org/10.1016/j.bbrc.2009.07.026openalex-snapshot
OsBWMK1 mediates SA-dependent defense responses by activating the transcription factor OsWRKY33
inferredcites →https://doi.org/10.1016/j.biocontrol.2013.06.011openalex-snapshot
Biological control of rice insect pests in China
inferredcites →https://doi.org/10.1016/j.jinsphys.2011.07.002openalex-snapshot
Planthopper “adaptation” to resistant rice varieties: Changes in amino acid composition over time
inferredcites →https://doi.org/10.1016/j.pbi.2022.102242openalex-snapshot
Rapid systemic responses to herbivory
inferredcites →https://doi.org/10.1016/j.pestbp.2009.07.001openalex-snapshot
Effects of jasmonic acid-induced resistance in rice on the plant brownhopper, Nilaparvata lugens Stål (Homoptera: Delphacidae)
inferredcites →https://doi.org/10.1016/j.plantsci.2018.10.009openalex-snapshot
A DREB1 gene from zoysiagrass enhances Arabidopsis tolerance to temperature stresses without growth inhibition
inferredcites →https://doi.org/10.1016/j.pld.2018.06.006openalex-snapshot
Current understanding of maize and rice defense against insect herbivores
inferredcites →https://doi.org/10.1016/j.rsci.2021.05.013openalex-snapshot
Understanding Brown Planthopper Resistance in Rice: Genetics, Biochemical and Molecular Breeding Approaches
inferredcites →https://doi.org/10.1016/j.tplants.2021.12.010openalex-snapshot
Plant defense strategies against attack by multiple herbivores
inferredcites →https://doi.org/10.1038/s41598-020-64925-1openalex-snapshot
Interactions between brown planthopper (Nilaparvata lugens) and salinity stressed rice (Oryza sativa) plant are cultivar-specific
inferredcites →https://doi.org/10.1038/s41598-020-80704-4openalex-snapshot
Elevated temperatures diminish the effects of a highly resistant rice variety on the brown planthopper
inferredcites →https://doi.org/10.1038/srep39819openalex-snapshot
Arabidopsis CBF3 and DELLAs positively regulate each other in response to low temperature
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01661.xopenalex-snapshot
OsDREB genes in rice, Oryza sativa L., encode transcription activators that function in drought‐, high‐salt‐ and cold‐responsive gene expression
inferredcites →https://doi.org/10.1074/mcp.m115.049759openalex-snapshot
Comparative Study of Early Cold-Regulated Proteins by Two-Dimensional Difference Gel Electrophoresis Reveals a Key Role for Phospholipase Dα1 in Mediating Cold Acclimation Signaling Pathway in Rice
inferredcites →https://doi.org/10.1080/07388551.2019.1710459openalex-snapshot
Phytohormones regulate convergent and divergent responses between individual and combined drought and pathogen infection
inferredcites →https://doi.org/10.1080/07388551.2020.1768509openalex-snapshot
Advances in AP2/ERF super-family transcription factors in plant
inferredcites →https://doi.org/10.1080/07388551.2022.2053056openalex-snapshot
Cold stress regulates accumulation of flavonoids and terpenoids in plants by phytohormone, transcription process, functional enzyme, and epigenetics
inferredcites →https://doi.org/10.1080/15592324.2016.1169357openalex-snapshot
OsWRKY53, a versatile switch in regulating herbivore-induced defense responses in rice
inferredcites →https://doi.org/10.1093/jxb/err210openalex-snapshot
Role of DREBs in regulation of abiotic stress responses in plants
inferredcites →https://doi.org/10.1093/jxb/erx118openalex-snapshot
Dehydration responsive element binding transcription factors and their applications for the engineering of stress tolerance
inferredcites →https://doi.org/10.1093/mp/ssn012openalex-snapshot
Rice Gene Network Inferred from Expression Profiling of Plants Overexpressing OsWRKY13, a Positive Regulator of Disease Resistance
inferredcites →https://doi.org/10.1093/mp/ssu085openalex-snapshot
Contrasting Effects of Ethylene Biosynthesis on Induced Plant Resistance against a Chewing and a Piercing-Sucking Herbivore in Rice
inferredcites →https://doi.org/10.1093/pcp/pci230openalex-snapshot
Functional Analysis of Rice DREB1/CBF-type Transcription Factors Involved in Cold-responsive Gene Expression in Transgenic Rice
inferredcites →https://doi.org/10.1093/pcp/pct087openalex-snapshot
Isolation and Characterization of Dehydration-Responsive Element-Binding Factor 2C (MsDREB2C) from Malus sieversii Roem.
inferredcites →https://doi.org/10.1093/plcell/koac009openalex-snapshot
Molecular tug-of-war: Plant immune recognition of herbivory
inferredcites →https://doi.org/10.1094/mpmi-20-5-0492openalex-snapshot
OsWRKY13 Mediates Rice Disease Resistance by Regulating Defense-Related Genes in Salicylate- and Jasmonate-Dependent Signaling
inferredcites →https://doi.org/10.1104/pp.104.059147openalex-snapshot
Arabidopsis CBF3/DREB1A and ABF3 in Transgenic Rice Increased Tolerance to Abiotic Stress without Stunting Growth
inferredcites →https://doi.org/10.1104/pp.110.154617openalex-snapshot
DREB2C Interacts with ABF2, a bZIP Protein Regulating Abscisic Acid-Responsive Gene Expression, and Its Overexpression Affects Abscisic Acid Sensitivity
inferredcites →https://doi.org/10.1104/pp.111.183749openalex-snapshot
The Chloroplast-Localized Phospholipases D α4 and α5 Regulate Herbivore-Induced Direct and Indirect Defenses in Rice
inferredcites →https://doi.org/10.1104/pp.15.01090openalex-snapshot
The rice transcription factor WRKY53 suppresses herbivore-induced defenses by acting as a negative feedback modulator of map kinase activity
inferredcites →https://doi.org/10.1105/tpc.10.8.1391openalex-snapshot
Two Transcription Factors, DREB1 and DREB2, with an EREBP/AP2 DNA Binding Domain Separate Two Cellular Signal Transduction Pathways in Drought- and Low-Temperature-Responsive Gene Expression, Respectively, in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03988.xopenalex-snapshot
Silencing OsHI‐LOX makes rice more susceptible to chewing herbivores, but enhances resistance to a phloem feeder
inferredcites →https://doi.org/10.1111/jipb.13204openalex-snapshot
Integrated view of plant metabolic defense with particular focus on chewing herbivores
inferredcites →https://doi.org/10.1111/mec.14067openalex-snapshot
Comparative analysis of the transcriptional responses to low and high temperatures in three rice planthopper species
inferredcites →https://doi.org/10.1111/nph.15989openalex-snapshot
Plant immunity in signal integration between biotic and abiotic stress responses
inferredcites →https://doi.org/10.1111/nph.16111openalex-snapshot
Novel crosstalk between ethylene‐ and jasmonic acid‐pathway responses to a piercing–sucking insect in rice
inferredcites →https://doi.org/10.1111/nph.17251openalex-snapshot
Molecular dissection of rice phytohormone signaling involved in resistance to a piercing‐sucking herbivore
inferredcites →https://doi.org/10.1111/pce.14341openalex-snapshot
The lipoxygenase gene OsRCI‐1 is involved in the biosynthesis of herbivore‐induced JAs and regulates plant defense and growth in rice
inferredcites →https://doi.org/10.1111/phen.12356openalex-snapshot
Brown planthopper infestations alter sugar metabolism in the rice plant as well as brown planthopper
inferredcites →https://doi.org/10.1111/tpj.15124openalex-snapshot
Multiple levels of crosstalk in hormone networks regulating plant defense
inferredcites →https://doi.org/10.1146/annurev-arplant-050718-095910openalex-snapshot
Molecular Interactions Between Plants and Insect Herbivores
inferredcites →https://doi.org/10.1146/annurev-ento-010715-023851openalex-snapshot
The Layers of Plant Responses to Insect Herbivores
inferredcites →https://doi.org/10.1186/s12870-016-0771-yopenalex-snapshot
Plant hormone-mediated regulation of stress responses
inferredcites →https://doi.org/10.1371/journal.pgen.1002767openalex-snapshot
Dual-Level Regulation of ACC Synthase Activity by MPK3/MPK6 Cascade and Its Downstream WRKY Transcription Factor during Ethylene Induction in Arabidopsis
inferredcites →https://doi.org/10.2135/cropsci2006.11.0712openalex-snapshot
Genetic Engineering of Maize with the Arabidopsis DREB1A/CBF3 Gene Using Split‐Seed Explants
inferredcites →https://doi.org/10.3389/fpls.2017.01647openalex-snapshot
Transcriptome Profiling Reveals the Negative Regulation of Multiple Plant Hormone Signaling Pathways Elicited by Overexpression of C-Repeat Binding Factors
inferredcites →https://doi.org/10.3389/fpls.2020.528550openalex-snapshot
Overexpression Levels of LbDREB6 Differentially Affect Growth, Drought, and Disease Tolerance in Poplar
inferredcites →https://doi.org/10.3389/fpls.2021.770794openalex-snapshot
Phospholipase Dα1 Acts as a Negative Regulator of High Mg2+-Induced Leaf Senescence in Arabidopsis
inferredcites →https://doi.org/10.3390/ijms17060697openalex-snapshot
The Transcription Factor OsWRKY45 Negatively Modulates the Resistance of Rice to the Brown Planthopper Nilaparvata lugens
inferredcites →https://doi.org/10.3390/ijms19092744openalex-snapshot
Overexpression of OsGID1 Enhances the Resistance of Rice to the Brown Planthopper Nilaparvata lugens
inferredcites →https://doi.org/10.3390/ijms20123023openalex-snapshot
OsMKK3, a Stress-Responsive Protein Kinase, Positively Regulates Rice Resistance to Nilaparvata lugens via Phytohormone Dynamics
inferredcites →https://doi.org/10.3390/ijms222212182openalex-snapshot
Silencing a Simple Extracellular Leucine-Rich Repeat Gene OsI-BAK1 Enhances the Resistance of Rice to Brown Planthopper Nilaparvata lugens
inferredcites →https://doi.org/10.3390/ijms222313020openalex-snapshot
Silencing an E3 Ubiquitin Ligase Gene OsJMJ715 Enhances the Resistance of Rice to a Piercing-Sucking Herbivore by Activating ABA and JA Signaling Pathways
inferredcites →https://doi.org/10.3390/ijms23052690openalex-snapshot
Plant Secondary Metabolites as Defense Tools against Herbivores for Sustainable Crop Protection
inferredcites →https://doi.org/10.3390/ijms23169439openalex-snapshot
Overexpression of PgCBF3 and PgCBF7 Transcription Factors from Pomegranate Enhances Freezing Tolerance in Arabidopsis under the Promoter Activity Positively Regulated by PgICE1
inferredcites →https://doi.org/10.3390/insects10020057openalex-snapshot
Influence of Abscisic Acid-Biosynthesis Inhibitor Fluridone on the Feeding Behavior and Fecundity of Nilaparvata lugens
inferredcites →https://doi.org/10.3390/insects13040355openalex-snapshot
Physiological and Population Responses of Nilaparvata lugens after Feeding on Drought-Stressed Rice
inferredcites →https://doi.org/10.7554/elife.04805openalex-snapshot
Prioritizing plant defence over growth through WRKY regulation facilitates infestation by non-target herbivores
inferredcites →https://doi.org/10.7554/elife.07295openalex-snapshot
Negative regulation of ABA signaling by WRKY33 is critical for Arabidopsis immunity towards Botrytis cinerea 2100

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.4769846openalex-extracted
Fine-Mapping and Candidate Analysis of a New Brown Planthopper Resistance Locus in an Indian Landrace of Rice, Paedai Kalibungga
inferred← citeshttps://doi.org/10.1002/ps.70082openalex-snapshot
Knocking out a wound‐induced vascular plant one‐zinc finger gene enhances plant defense against phloem‐feeding herbivores
inferred← citeshttps://doi.org/10.1007/s11032-024-01485-6openalex-snapshot
Identification and candidate analysis of a new brown planthopper resistance locus in an Indian landrace of rice, paedai kalibungga
inferred← citeshttps://doi.org/10.1007/s44297-024-00027-yopenalex-snapshot
Advances in molecular interactions between rice and insect herbivores
inferred← citeshttps://doi.org/10.1016/j.tplants.2025.07.009openalex-snapshot
Climate change effects on plant immune activation
inferred← citeshttps://doi.org/10.1093/plphys/kiaf577openalex-snapshot
The OsDREB1C-OsNAC3-OsGH3.2 module regulates seed germination in rice
inferred← citeshttps://doi.org/10.1111/pce.14689openalex-snapshot
Trade‐offs in plant responses to the environment
inferred← citeshttps://doi.org/10.1126/sciadv.adw0421openalex-snapshot
Feedback transcription regulation between OsNAC3 and OsDREB1A promotes postgermination growth in rice
inferred← citeshttps://doi.org/10.3390/plants14233673openalex-snapshot
Knockout of the OsNAC113 Transcription Factor Causes High Salt Resistance in Rice
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