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Sub‐lethal UV‐C radiation induces callose, hydrogen peroxide and defence‐related gene expression in A rabidopsis thaliana

https://doi.org/10.1111/plb.12286
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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/jsfa.6227openalex-snapshot
Growth and phenolic compounds of Lactuca sativa L. grown in a closed‐type plant production system with UV ‐A, ‐B, or ‐C lamp
inferredcites →https://doi.org/10.1007/978-1-4614-0815-4_3openalex-snapshot
UV-B Radiation, Its Effects and Defense Mechanisms in Terrestrial Plants
inferredcites →https://doi.org/10.1007/bf00201815openalex-snapshot
Ultraviolet light and ozone stimulate accumulation of salicylic acid, pathogenesis-related proteins and virus resistance in tobacco
inferredcites →https://doi.org/10.1007/bf01281779openalex-snapshot
The effect of UV-B and UV-C radiation on sugar beet leaves
inferredcites →https://doi.org/10.1007/bf01282278openalex-snapshot
The time course of the induction of callose in wounded pea roots
inferredcites →https://doi.org/10.1007/bf02370718openalex-snapshot
Callose deposition in leaves of cowpea (Vigna unguiculata [L.] Walp.) as a sensitive response to high Mn supply
inferredcites →https://doi.org/10.1007/s00425-007-0654-4openalex-snapshot
Implication of reactive oxygen species and mitochondrial dysfunction in the early stages of plant programmed cell death induced by ultraviolet-C overexposure
inferredcites →https://doi.org/10.1007/s10142-006-0041-4openalex-snapshot
Suppression by ABA of salicylic acid and lignin accumulation and the expression of multiple genes, in Arabidopsis infected with Pseudomonas syringae pv. tomato
inferredcites →https://doi.org/10.1007/s10265-002-0031-0openalex-snapshot
Ethylene evolution from tobacco leaves irradiated with UV-B
inferredcites →https://doi.org/10.1007/s11103-008-9435-0openalex-snapshot
Role of plant hormones in plant defence responses
inferredcites →https://doi.org/10.1007/s11738-012-1103-yopenalex-snapshot
Callose: the plant cell wall polysaccharide with multiple biological functions
inferredcites →https://doi.org/10.1016/j.agrformet.2003.08.015openalex-snapshot
Field crop responses to ultraviolet-B radiation: a review
inferredcites →https://doi.org/10.1016/j.febslet.2011.04.039openalex-snapshot
Salicylic acid and its location in response to biotic and abiotic stress
inferredcites →https://doi.org/10.1016/j.jplph.2009.07.011openalex-snapshot
Changes of resveratrol and antioxidant enzymes during UV-induced plant defense response in peanut seedlings
inferredcites →https://doi.org/10.1016/j.plantsci.2005.12.017openalex-snapshot
Accumulation of cell-wall bound phenolic compounds and phytoalexin in Arabidopsis thaliana leaves following inoculation with pathovars of Pseudomonas syringae
inferredcites →https://doi.org/10.1016/j.plaphy.2004.03.007openalex-snapshot
Spread of oxidative damage and antioxidative response through cell layers of tobacco callus after UV-C treatment
inferredcites →https://doi.org/10.1016/j.pmpp.2008.08.005openalex-snapshot
Elucidation of defence responses and signalling pathways induced in Arabidopsis thaliana following challenge with Phytophthora cinnamomi
inferredcites →https://doi.org/10.1016/s0014-5793(98)01208-3openalex-snapshot
UV‐C radiation induces apoptotic‐like changes in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/s0027-5107(98)00043-8openalex-snapshot
DNA repair in higher plants
inferredcites →https://doi.org/10.1016/s0033-7560(66)80012-1openalex-snapshot
Effects of ultraviolet radiation on the leaves of higher plants
inferredcites →https://doi.org/10.1016/s0074-7696(08)60321-6openalex-snapshot
International Review of Cytology
inferredcites →https://doi.org/10.1016/s1360-1385(98)01215-1openalex-snapshot
Higher plants and UV-B radiation: balancing damage, repair and acclimation
inferredcites →https://doi.org/10.1016/s1360-1385(98)01355-7openalex-snapshot
Molecular genetics of DNA repair in higher plants
inferredcites →https://doi.org/10.1034/j.1399-3054.1990.780213.xopenalex-snapshot
Hydrogen peroxide formation in cultured rose cells in response to UV -C radiation
inferredcites →https://doi.org/10.1038/383826a0openalex-snapshot
The octadecanoid signalling pathway in plants mediates a response to ultraviolet radiation
inferredcites →https://doi.org/10.1038/nmeth.2089openalex-snapshot
NIH Image to ImageJ: 25 years of image analysis
inferredcites →https://doi.org/10.1039/c0pp90035dopenalex-snapshot
Effects of solar ultraviolet radiation on terrestrial ecosystems. Patterns, mechanisms, and interactions with climate change
inferredcites →https://doi.org/10.1046/j.1365-3040.1999.00499.xopenalex-snapshot
Ultraviolet‐B‐induced stress and changes in gene expression in Arabidopsis thaliana: role of signalling pathways controlled by jasmonic acid, ethylene and reactive oxygen species
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01474.xopenalex-snapshot
The impact of oxidative stress on Arabidopsis mitochondria
inferredcites →https://doi.org/10.1074/jbc.m704185200openalex-snapshot
Metacaspase-8 Modulates Programmed Cell Death Induced by Ultraviolet Light and H2O2 in Arabidopsis
inferredcites →https://doi.org/10.1093/emboj/cdf646openalex-snapshot
Distinct regulation of salinity and genotoxic stress responses by Arabidopsis MAP kinase phosphatase 1
inferredcites →https://doi.org/10.1093/jxb/41.11.1489openalex-snapshot
The Response of Bean Plants to UV-B Radiation Under Different Irradiances of Background Visible Light
inferredcites →https://doi.org/10.1093/jxb/erm144openalex-snapshot
AtMEK1 mediates stress-induced gene expression of CAT1 catalase by triggering H2O2 production in Arabidopsis
inferredcites →https://doi.org/10.1093/mp/ssn065openalex-snapshot
Accumulation of Flavonoids in an ntra ntrb Mutant Leads to Tolerance to UV-C
inferredcites →https://doi.org/10.1094/mpmi-23-3-0340openalex-snapshot
Ascorbic Acid Deficiency in Arabidopsis Induces Constitutive Priming That is Dependent on Hydrogen Peroxide, Salicylic Acid, and the NPR1 Gene
inferredcites →https://doi.org/10.1104/pp.102.2.671openalex-snapshot
Specificity and Photomorphogenic Nature of Ultraviolet-B-Induced Cotyledon Curling in Brassica napus L
inferredcites →https://doi.org/10.1104/pp.105.066803openalex-snapshot
Cauliflower mosaic virus, a Compatible Pathogen of Arabidopsis, Engages Three Distinct Defense-Signaling Pathways and Activates Rapid Systemic Generation of Reactive Oxygen Species
inferredcites →https://doi.org/10.1104/pp.105.4.1089openalex-snapshot
Ozone-Induced Expression of Stress-Related Genes in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.108.125435openalex-snapshot
UV-Induced DNA Damage Promotes Resistance to the Biotrophic Pathogen Hyaloperonospora parasitica in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.108.4.1673openalex-snapshot
Hydrogen Peroxide Stimulates Salicylic Acid Biosynthesis in Tobacco
inferredcites →https://doi.org/10.1104/pp.109.4.1159openalex-snapshot
Arabidopsis Mutants Lacking Phenolic Sunscreens Exhibit Enhanced Ultraviolet-B Injury and Oxidative Damage
inferredcites →https://doi.org/10.1104/pp.112.1.161openalex-snapshot
Solar Ultraviolet-B Radiation Affects Seedling Emergence, DNA Integrity, Plant Morphology, Growth Rate, and Attractiveness to Herbivore Insects in Datura ferox
inferredcites →https://doi.org/10.1104/pp.125.2.1074openalex-snapshot
Molecular Responses to Aphid Feeding in Arabidopsis in Relation to Plant Defense Pathways
inferredcites →https://doi.org/10.1104/pp.127.3.1089openalex-snapshot
The Role of NDR1 in Avirulence Gene-Directed Signaling and Control of Programmed Cell Death in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.39.5.843openalex-snapshot
Callose Formation and Subsequent Disappearance: Studies in Ultrasound Stimulation
inferredcites →https://doi.org/10.1104/pp.77.3.544openalex-snapshot
Chitosan-Elicited Callose Synthesis in Soybean Cells as a Ca2+-Dependent Process
inferredcites →https://doi.org/10.1104/pp.80.1.7openalex-snapshot
Influence of Free Fatty Acids, Lysophosphatidylcholine, Platelet-Activating Factor, Acylcarnitine, and Echinocandin B on 1,3-β-d-Glucan Synthase and Callose Synthesis
inferredcites →https://doi.org/10.1105/tpc.010376openalex-snapshot
EDS5, an Essential Component of Salicylic Acid–Dependent Signaling for Disease Resistance in Arabidopsis, Is a Member of the MATE Transporter Family
inferredcites →https://doi.org/10.1105/tpc.016097openalex-snapshot
An Arabidopsis Callose Synthase, GSL5, Is Required for Wound and Papillary Callose Formation
inferredcites →https://doi.org/10.1105/tpc.10.12.2103openalex-snapshot
Concomitant Activation of Jasmonate and Ethylene Response Pathways Is Required for Induction of a Plant Defensin Gene in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.111.091033openalex-snapshot
Evidence for a SAL1-PAP Chloroplast Retrograde Pathway That Functions in Drought and High Light Signaling in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.2.5.437openalex-snapshot
Arabidopsis Is Susceptible to Infection by a Downy Mildew Fungus
inferredcites →https://doi.org/10.1105/tpc.5.2.171openalex-snapshot
Arabidopsis Flavonoid Mutants Are Hypersensitive to UV-B Irradiation.
inferredcites →https://doi.org/10.1105/tpc.7.2.203openalex-snapshot
UV-B-Induced PR-1 Accumulation Is Mediated by Active Oxygen Species
inferredcites →https://doi.org/10.1111/j.1365-2486.2009.01944.xopenalex-snapshot
Responses of plants in polar regions to UVB exposure: a meta‐analysis
inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03761.xopenalex-snapshot
The Arabidopsis glutathione transferase gene family displays complex stress regulation and co‐silencing multiple genes results in altered metabolic sensitivity to oxidative stress
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03794.xopenalex-snapshot
The ABC transporter BcatrB from Botrytis cinerea exports camalexin and is a virulence factor on Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1399-3054.2012.01661.xopenalex-snapshot
Beneficial effects of solar UV ‐B radiation on soybean yield mediated by reduced insect herbivory under field conditions
inferredcites →https://doi.org/10.1111/j.1744-7909.2007.00466.xopenalex-snapshot
Variations in Growth, Photosynthesis and Defense System Among Four Weed Species Under Increased UV‐B Radiation
inferredcites →https://doi.org/10.1111/j.1751-1097.2008.00433.xopenalex-snapshot
Ultraviolet Radiation as a Limiting Factor in Leaf Expansion and Development
inferredcites →https://doi.org/10.1111/ppl.12168openalex-snapshot
Dynamic changes in plant secondary metabolites during UV acclimation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1134/s1021443708040195openalex-snapshot
Role of salicylic acid in regulating ultraviolet radiation-induced oxidative stress in pepper leaves
inferredcites →https://doi.org/10.1146/annurev.arplant.47.1.127openalex-snapshot
THE FUNCTIONS AND REGULATION OF GLUTATHIONE S-TRANSFERASES IN PLANTS
inferredcites →https://doi.org/10.2307/3869583openalex-snapshot
Arabidopsis Flavonoid Mutants Are Hypersensitive to UV-B Irradiation
inferredcites →https://doi.org/10.3389/fpls.2011.00047openalex-snapshot
Rewiring of the jasmonate signaling pathway in Arabidopsis during insect herbivory

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.4788802openalex-extracted
Priming for Drought Resistance: Uv-C Flashes Triggered Pipecolate Accumulation and Dehydration Avoidance in Capsicum Chinense But Induced No Growth or Metabolic Cost
inferred← citeshttps://doi.org/10.1002/ps.4655openalex-snapshot
Mechanisms of callose deposition in rice regulated by exogenous abscisic acid and its involvement in rice resistance to Nilaparvata lugens Stål (Hemiptera: Delphacidae)
inferred← citeshttps://doi.org/10.1007/s00299-025-03604-9openalex-snapshot
Deciphering UV-C-induced transcriptomic shifts in tomato: defence mechanisms, stress responses, and photoreceptor regulation
inferred← citeshttps://doi.org/10.1007/s00344-026-12109-yopenalex-snapshot
Illuminating Ultraviolet-C on Plants: Insights into Mechanism, Regulation and Response
inferred← citeshttps://doi.org/10.1007/s10658-025-03037-wopenalex-snapshot
UV-C treatment has a higher efficacy on reducing germination of spores rather than mycelium growth
inferred← citeshttps://doi.org/10.1007/s10725-016-0205-8openalex-snapshot
Quantitation of ascorbic acid in Arabidopsis thaliana reveals distinct differences between organs and growth phases
inferred← citeshttps://doi.org/10.1007/s11103-017-0594-8openalex-snapshot
Genome-wide analysis of expansin superfamily in wild Arachis discloses a stress-responsive expansin-like B gene
inferred← citeshttps://doi.org/10.1007/s42535-022-00390-7openalex-snapshot
Sub-lethal effect of diesel fuel on the development of in vitro produced callus culture of Tagetes patula L. (Marigold-Nemo mix)
inferred← citeshttps://doi.org/10.1016/j.cropro.2015.12.018openalex-snapshot
Nanostructured liquid crystalline particle assisted delivery of 2,4-dichlorophenoxyacetic acid to weeds, crops and model plants
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105873openalex-snapshot
Priming for drought resistance: UV-C flashes triggered pipecolate accumulation and dehydration avoidance in Capsicum chinense Jacq. but induced no growth or metabolic costs
inferred← citeshttps://doi.org/10.1016/j.funbio.2018.12.002openalex-snapshot
UV-C irradiation compromises conidial germination, formation of appressoria, and induces transcription of three putative photolyase genes in the barley powdery mildew fungus, Blumeria graminis f. sp. hordei
inferred← citeshttps://doi.org/10.1016/j.funeco.2018.05.006openalex-snapshot
Hormonal and physiological changes driven by fungal endophytes increase Antarctic plant performance under UV-B radiation
inferred← citeshttps://doi.org/10.1016/j.plaphy.2018.05.031openalex-snapshot
The influence of ascorbic acid on root growth and the root apical meristem in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.spaceh.2025.100005openalex-snapshot
Functional foods for astronauts: Enhancing health and performance in microgravity and extreme environments
inferred← citeshttps://doi.org/10.1038/s41467-025-59542-3openalex-snapshot
Machine-learning meta-analysis reveals ethylene as a central component of the molecular core in abiotic stress responses in Arabidopsis
inferred← citeshttps://doi.org/10.1071/fp16266openalex-snapshot
Active defence by an Australian native host, Lomandra longifolia, provides resistance against Phytophthora cinnamomi
inferred← citeshttps://doi.org/10.1073/pnas.2612171123openalex-snapshot
Arabidopsis YEATS domain proteins facilitate DNA double-strand break repair via homology-directed pathways
inferred← citeshttps://doi.org/10.1093/jxb/erw261openalex-snapshot
Hormone-controlled UV-B responses in plants
inferred← citeshttps://doi.org/10.1101/2025.10.11.681831openalex-snapshot
Arabidopsis YEATS domain proteins facilitate DNA double strand break repair via homologous recombination pathways
inferred← citeshttps://doi.org/10.1111/pce.14680openalex-snapshot
UV‐B responses in the spotlight: Dynamic photoreceptor interplay and cell‐type specificity
inferred← citeshttps://doi.org/10.1186/s13071-021-05085-7openalex-snapshot
Acaricidal efficacy of ultraviolet-C irradiation of Tetranychus urticae adults and eggs using a pulsed krypton fluoride excimer laser
inferred← citeshttps://doi.org/10.17660/actahortic.2020.1271.53openalex-snapshot
Preliminary evaluation of the impact of preharvest UV-C on lettuce: potential for the control of Xanthomonas campestris
inferred← citeshttps://doi.org/10.3103/s0095452717010029openalex-snapshot
Time-course of pathogen induced accumulation of callose as mechanical protective barrier in wheat seedlings
inferred← citeshttps://doi.org/10.3103/s0095452725020021openalex-snapshot
Callose Accumulation in Winter Wheat Seedlings under UV Irradiation
inferred← citeshttps://doi.org/10.3389/fmicb.2026.1789302openalex-snapshot
Enhancing UV-C and perchlorate resistance in Arabidopsis thaliana through the introduction of microbial genes from hypersaline environment
inferred← citeshttps://doi.org/10.3389/fpls.2020.00583openalex-snapshot
Plant Defense Stimulator Mediated Defense Activation Is Affected by Nitrate Fertilization and Developmental Stage in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2020.597642openalex-snapshot
Ultraviolet Radiation From a Plant Perspective: The Plant-Microorganism Context
inferred← citeshttps://doi.org/10.3390/horticulturae10090944openalex-snapshot
Ultraviolet-C Light Effects in Actinidia spp. Infected by Pseudomonas syringae pv. actinidiae
inferred← citeshttps://doi.org/10.3390/ijms241411323openalex-snapshot
Comparative Transcriptomics of Multi-Stress Responses in Pachycladon cheesemanii and Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/plants10112476openalex-snapshot
Seaweed Extract-Stimulated Priming in Arabidopsis thaliana and Solanum lycopersicum
inferred← citeshttps://doi.org/10.4018/979-8-2600-0036-6.ch014openalex-snapshot
Shielding Against Radiation
inferred← citeshttps://doi.org/10.70675/694e0288z837az400dzac17za146af0fbbcbopenalex-snapshot
Caractérisation de l’effet de stimulateurs de défense des plantes (SDP) en fonction du stade de développement et de l’apport en azote
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UV-induced accumulation of callosоe in winter wheat plants
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