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Disruption of Autophagy Results in Constitutive Oxidative Stress inArabidopsis

https://doi.org/10.4161/auto.3847
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Redox Regulation of Autophagy in Arabidopsis: Reactive Oxygen Species Differential Effects
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How autophagy can restore proteostasis defects in multiple diseases?
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Mitochondrial Regulation of Plant Programmed Cell Death
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Role of Autophagy in Plant Nutrient Deficiency
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Physiological Functions of Autophagy
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Pollen Germination and Tube Growth
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Plant Mitochondrial Omics: State-of-the-Art Knowledge
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Autophagy in plants
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The autophagy-related protein OsCOST1 negatively regulates the salt tolerance in rice
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Autophagy-related gene, TdAtg8, in wild emmer wheat plays a role in drought and osmotic stress response
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Role of autophagy in plant growth and adaptation to salt stress
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From signal transduction to autophagy of plant cell organelles: lessons from yeast and mammals and plant-specific features
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Physcomitrium patens: an emerging model for autophagy study
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OsATG10b, an Autophagosome Component, Is Needed for Cell Survival against Oxidative Stresses in Rice
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The roles of autophagy in development and stress responses in Arabidopsis thaliana
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Influences of zinc oxide nanoparticles on Allium cepa root cells and the primary cause of phytotoxicity
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Role of plant autophagy in stress response
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The Botanical Dance of Death
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Function and regulation of macroautophagy in plants
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Oxidative distress in aging and age-related diseases: Spatiotemporal dysregulation of protein oxidation and degradation
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L’autophagie chez les plantes : mécanismes, régulations et fonctions
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Both silencing- and over-expression of pepper CaATG8c gene compromise plant tolerance to heat and salt stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105412openalex-snapshot
Autophagy accelerates cell death after desiccation and hydration stress in Physcomitrium
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105611openalex-snapshot
Autophagy confers aluminum tolerance by enhancing the antioxidant capacity and promoting oxidized protein degradation in wheat (Triticum aestivum.) roots
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2025.106122openalex-snapshot
Dimethyl sulfoxide synergistically mitigates cadmium-induced oxidative damage in pak choi by activating antioxidant and autophagy mechanisms
inferred← citeshttps://doi.org/10.1016/j.envpol.2021.117278openalex-snapshot
Multi-omics analyses on the response mechanisms of ‘Shine Muscat’ grapevine to low degree of excess copper stress (Low-ECS)
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Integrated transmission electron microscopy and proteomic analyses reveal the cytoarchitectural response to cucumber mosaic virus infection in tobacco
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121225openalex-snapshot
Molecular identification of sugarcane glyceraldehyde-3-phosphate dehydrogenases and their involvement in SCMV infection in sugarcane
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2022.129600openalex-snapshot
Autophagy alleviates indium-induced programmed cell death in wheat roots
inferred← citeshttps://doi.org/10.1016/j.jia.2025.05.002openalex-snapshot
The MdMYB306-MdERF114 module promotes tolerance to cadmium by regulating MdATG16 in apple
inferred← citeshttps://doi.org/10.1016/j.jplph.2025.154671openalex-snapshot
Autophagy, ROS, and their interplay in plant adaptive responses
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Plant autophagy—more than a starvation response
inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.12.003openalex-snapshot
Apple autophagy-related protein MdATG3s afford tolerance to multiple abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.03.026openalex-snapshot
Autophagy mediates hydrotropic response in Arabidopsis thaliana roots
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112371openalex-snapshot
Genome-wide identification and analysis of autophagy-related (ATG) genes in Lycium ruthenicum Murray reveals their crucial roles in salt stress tolerance
inferred← citeshttps://doi.org/10.1016/j.plaphy.2012.02.013openalex-snapshot
Oxidative stress-induced autophagy in plants: The role of mitochondria
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.11.049openalex-snapshot
Mutual regulation of ROS accumulation and cell autophagy in wheat roots under hypoxia stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2022.05.019openalex-snapshot
Characterization of 24-epibrassinolide-mediated modulation of the drought stress responses: Morphophysiology, antioxidant metabolism and hormones in grapevine (Vitis vinifera L.)
inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.109800openalex-snapshot
Redox regulation of autophagy in Arabidopsis: The different ROS effects
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2024.113204openalex-snapshot
SlATG5 is crucial for the accumulation of ROS in postharvest tomato fruit resistance to B.cinerea mediated by nitric oxide
inferred← citeshttps://doi.org/10.1016/j.scienta.2013.10.038openalex-snapshot
Isolation and characterization of MdATG18a, a WD40-repeat AuTophaGy-related gene responsive to leaf senescence and abiotic stress in Malus
inferred← citeshttps://doi.org/10.1016/j.semcdb.2009.04.012openalex-snapshot
Autophagy and plant innate immunity: Defense through degradation
inferred← citeshttps://doi.org/10.1016/j.stress.2026.101587openalex-snapshot
Autophagy-Related Genes (ATGs) Key Regulators of Abiotic and Biotic Stress Tolerance in Crop Plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2012.05.006openalex-snapshot
Autophagy: a multifaceted intracellular system for bulk and selective recycling
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.02.001openalex-snapshot
Linking Autophagy to Abiotic and Biotic Stress Responses
inferred← citeshttps://doi.org/10.1016/s0065-2296(10)54001-1openalex-snapshot
Pollen Germination and Tube Growth
inferred← citeshttps://doi.org/10.1016/s1874-6047(10)28012-5openalex-snapshot
Elucidating TOR Signaling in Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1021/acs.est.9b01648openalex-snapshot
Anatase TiO2 Nanoparticles Induce Autophagy and Chloroplast Degradation in Thale Cress (Arabidopsis thaliana)
inferred← citeshttps://doi.org/10.1038/s41438-018-0059-5openalex-snapshot
Overexpression of MdATG18a in apple improves resistance to Diplocarpon mali infection by enhancing antioxidant activity and salicylic acid levels
inferred← citeshttps://doi.org/10.1038/s41467-019-12782-6openalex-snapshot
Plant AtEH/Pan1 proteins drive autophagosome formation at ER-PM contact sites with actin and endocytic machinery
inferred← citeshttps://doi.org/10.1038/s41598-019-54361-1openalex-snapshot
Essential roles of autophagy in metabolic regulation in endosperm development during rice seed maturation
inferred← citeshttps://doi.org/10.1080/15548627.2017.1422856openalex-snapshot
Dicot-specific ATG8-interacting ATI3 proteins interact with conserved UBAC2 proteins and play critical roles in plant stress responses
inferred← citeshttps://doi.org/10.1080/15548627.2020.1847797openalex-snapshot
Hydrogen peroxide mediates spermidine-induced autophagy to alleviate salt stress in cucumber
inferred← citeshttps://doi.org/10.1080/15548627.2022.2046449openalex-snapshot
Phosphatidic acid suppresses autophagy through competitive inhibition by binding GAPC (glyceraldehyde-3-phosphate dehydrogenase) and PGK (phosphoglycerate kinase) proteins
inferred← citeshttps://doi.org/10.1093/jxb/eru039openalex-snapshot
Autophagy, plant senescence, and nutrient recycling
inferred← citeshttps://doi.org/10.1093/jxb/erw013openalex-snapshot
Interactions between 2-Cys peroxiredoxins and ascorbate in autophagosome formation during the heat stress response inSolanum lycopersicum
inferred← citeshttps://doi.org/10.1093/plcell/koac273openalex-snapshot
14-3-3 proteins contribute to autophagy by modulating SINAT-mediated degradation of ATG13
inferred← citeshttps://doi.org/10.1093/treephys/tpaa075openalex-snapshot
Overexpression of MdATG18a enhances alkaline tolerance and GABA shunt in apple through increased autophagy under alkaline conditions
inferred← citeshttps://doi.org/10.1101/2023.04.09.535952openalex-snapshot
Clathrin Light Chains are essential in negative regulation of cell death and immunity in Arabidopsis through interacting with autophagy pathway
inferred← citeshttps://doi.org/10.1101/gad.1599207openalex-snapshot
Autophagy: process and function
inferred← citeshttps://doi.org/10.1104/pp.108.122325openalex-snapshot
Unraveling the Tapestry of Networks Involving Reactive Oxygen Species in Plants
inferred← citeshttps://doi.org/10.1105/tpc.110.081570openalex-snapshot
TheArabidopsisMultistress Regulator TSPO Is a Heme Binding Membrane Protein and a Potential Scavenger of Porphyrins via an Autophagy-Dependent Degradation Mechanism
inferred← citeshttps://doi.org/10.1105/tpc.112.101535openalex-snapshot
Degradation of the Endoplasmic Reticulum by Autophagy during Endoplasmic Reticulum Stress in Arabidopsis
inferred← citeshttps://doi.org/10.1105/tpc.114.134692openalex-snapshot
Cytoplastic Glyceraldehyde-3-Phosphate Dehydrogenases Interact with ATG3 to Negatively Regulate Autophagy and Immunity in Nicotiana benthamiana
inferred← citeshttps://doi.org/10.1105/tpc.19.00413openalex-snapshot
Arabidopsis SINAT Proteins Control Autophagy by Mediating Ubiquitylation and Degradation of ATG13
inferred← citeshttps://doi.org/10.1111/febs.13712openalex-snapshot
To deliver or to degrade – an interplay of the ubiquitin–proteasome system, autophagy and vesicular transport in plants
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2010.02117.xopenalex-snapshot
Devil inside: does plant programmed cell death involve the endomembrane system?
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04546.xopenalex-snapshot
Autophagy differentially controls plant basal immunity to biotrophic and necrotrophic pathogens
inferred← citeshttps://doi.org/10.1111/j.1365-313x.2011.04553.xopenalex-snapshot
A critical role of autophagy in plant resistance to necrotrophic fungal pathogens
inferred← citeshttps://doi.org/10.1111/jipb.12941openalex-snapshot
Autophagy in plants: Physiological roles and post‐translational regulation
inferred← citeshttps://doi.org/10.1111/jpi.12091openalex-snapshot
Delay in leaf senescence of Malus hupehensis by long‐term melatonin application is associated with its regulation of metabolic status and protein degradation
inferred← citeshttps://doi.org/10.1111/jpi.12233openalex-snapshot
Melatonin enhances the occurrence of autophagy induced by oxidative stress in Arabidopsis seedlings
inferred← citeshttps://doi.org/10.1111/mpp.12118openalex-snapshot
The perplexing role of autophagy in plant innate immune responses
inferred← citeshttps://doi.org/10.1111/pbi.12794openalex-snapshot
Improvement of drought tolerance by overexpressing MdATG18a is mediated by modified antioxidant system and activated autophagy in transgenic apple
inferred← citeshttps://doi.org/10.1111/pce.12745openalex-snapshot
Microarray and genetic analysis reveals that csa‐miR159b plays a critical role in abscisic acid‐mediated heat tolerance in grafted cucumber plants
inferred← citeshttps://doi.org/10.1111/pce.13110openalex-snapshot
MdATG18a overexpression improves tolerance to nitrogen deficiency and regulates anthocyanin accumulation through increased autophagy in transgenic apple
inferred← citeshttps://doi.org/10.1128/ec.00081-15openalex-snapshot
Activation of Autophagy by Metals in Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1146/annurev-arplant-042811-105441openalex-snapshot
Autophagy: Pathways for Self-Eating in Plant Cells
inferred← citeshttps://doi.org/10.1146/annurev-arplant-060324-094912openalex-snapshot
Autophagy in Plant Health and Disease
inferred← citeshttps://doi.org/10.1155/2009/451357openalex-snapshot
Techniques to Study Autophagy in Plants
inferred← citeshttps://doi.org/10.1186/1471-2229-9-28openalex-snapshot
Differential patterns of reactive oxygen species and antioxidative mechanisms during atrazine injury and sucrose-induced tolerance in Arabidopsis thaliana plantlets
inferred← citeshttps://doi.org/10.1186/s12864-016-3113-4openalex-snapshot
Genome-wide analysis of autophagy-associated genes in foxtail millet (Setaria italica L.) and characterization of the function of SiATG8a in conferring tolerance to nitrogen starvation in rice
inferred← citeshttps://doi.org/10.1186/s12870-018-1439-6openalex-snapshot
Autophagy counteracts instantaneous cell death during seasonal senescence of the fine roots and leaves in Populus trichocarpa
inferred← citeshttps://doi.org/10.1186/s12870-019-1930-8openalex-snapshot
Proximity-dependent biotinylation screening identifies NbHYPK as a novel interacting partner of ATG8 in plants
inferred← citeshttps://doi.org/10.1186/s12870-021-03066-7openalex-snapshot
RNA-Seq analysis reveals potential regulators of programmed cell death and leaf remodelling in lace plant (Aponogeton madagascariensis)
inferred← citeshttps://doi.org/10.1186/s12915-025-02149-3openalex-snapshot
Proteomics revealed novel functions and drought tolerance of Arabidopsis thaliana protein kinase ATG1
inferred← citeshttps://doi.org/10.1199/tab.0116openalex-snapshot
The Secretory System of Arabidopsis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003196openalex-snapshot
NBR1-Mediated Selective Autophagy Targets Insoluble Ubiquitinated Protein Aggregates in Plant Stress Responses
inferred← citeshttps://doi.org/10.1371/journal.pone.0011883openalex-snapshot
TOR Is a Negative Regulator of Autophagy in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1371/journal.pone.0103364openalex-snapshot
Proteasome Inhibitors Activate Autophagy Involving Inhibition of PI3K-Akt-mTOR Pathway as an Anti-Oxidation Defense in Human RPE Cells
inferred← citeshttps://doi.org/10.1371/journal.ppat.1009963openalex-snapshot
eIF4A, a target of siRNA derived from rice stripe virus, negatively regulates antiviral autophagy by interacting with ATG5 in Nicotiana benthamiana
inferred← citeshttps://doi.org/10.31274/etd-180810-2589openalex-snapshot
Analysis of the function and the regulation of autophagy in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.32615/bp.2019.127openalex-snapshot
Reactive oxygen species derived from NADPH oxidase regulate autophagy
inferred← citeshttps://doi.org/10.3389/fgene.2021.770742openalex-snapshot
Transcriptome Profiling of the Salt Stress Response in the Leaves and Roots of Halophytic Eutrema salsugineum
inferred← citeshttps://doi.org/10.3389/fpls.2014.00174openalex-snapshot
Role and regulation of autophagy in heat stress responses of tomato plants
inferred← citeshttps://doi.org/10.3389/fpls.2014.00629openalex-snapshot
Plant peroxisomes are degraded by starvation-induced and constitutive autophagy in tobacco BY-2 suspension-cultured cells
inferred← citeshttps://doi.org/10.3389/fpls.2017.01201openalex-snapshot
The AMP-Activated Protein Kinase KIN10 Is Involved in the Regulation of Autophagy in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2017.01204openalex-snapshot
TOR-Dependent and -Independent Pathways Regulate Autophagy in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3389/fpls.2020.00172openalex-snapshot
Impact of Autophagy on Gene Expression and Tapetal Programmed Cell Death During Pollen Development in Rice
inferred← citeshttps://doi.org/10.3389/fpls.2022.864215openalex-snapshot
Function of Protein Kinases in Leaf Senescence of Plants
inferred← citeshttps://doi.org/10.3389/fpls.2022.899054openalex-snapshot
Whole-Transcriptome Analysis Reveals Autophagy Is Involved in Early Senescence of zj-es Mutant Rice
inferred← citeshttps://doi.org/10.3389/fpls.2026.1861141openalex-snapshot
Autophagy in plants: molecular mechanisms and roles in abiotic stress responses
inferred← citeshttps://doi.org/10.3390/agronomy6010015openalex-snapshot
Identification of Barley (Hordeum vulgare L.) Autophagy Genes and Their Expression Levels during Leaf Senescence, Chronic Nitrogen Limitation and in Response to Dark Exposure
inferred← citeshttps://doi.org/10.3390/cells10061272openalex-snapshot
How Lipids Contribute to Autophagosome Biogenesis, a Critical Process in Plant Responses to Stresses
inferred← citeshttps://doi.org/10.3390/cells1030449openalex-snapshot
Role of Macroautophagy in Nutrient Homeostasis During Fungal Development and Pathogenesis
inferred← citeshttps://doi.org/10.3390/genes16111343openalex-snapshot
From Model to Crop: Roles of Macroautophagy in Arabidopsis and Legumes
inferred← citeshttps://doi.org/10.3390/ijms21010194openalex-snapshot
Autophagy-Like Cell Death Regulates Hydrogen Peroxide and Calcium Ion Distribution in Xa3/Xa26-Mediated Resistance to Xanthomonas oryzae pv. oryzae
inferred← citeshttps://doi.org/10.3390/ijms21124515openalex-snapshot
Autophagy-Related 2 Regulates Chlorophyll Degradation under Abiotic Stress Conditions in Arabidopsis
inferred← citeshttps://doi.org/10.3390/ijms23116236openalex-snapshot
Autophagy-Mediated Regulation of Different Meristems in Plants
inferred← citeshttps://doi.org/10.3390/ijms232113134openalex-snapshot
The Arabidopsis J-Protein AtDjC5 Facilitates Thermotolerance Likely by Aiding in the ER Stress Response
inferred← citeshttps://doi.org/10.3390/ijms24119732openalex-snapshot
Iron Availability Influences Protein Carbonylation in Arabidopsis thaliana Plants
inferred← citeshttps://doi.org/10.3390/ijms241512431openalex-snapshot
Multi-Omics Analysis Reveals Mechanisms of Strong Phosphorus Adaptation in Tea Plant Roots
inferred← citeshttps://doi.org/10.3390/plants10071451openalex-snapshot
Protein Carbonylation: Emerging Roles in Plant Redox Biology and Future Prospects
inferred← citeshttps://doi.org/10.4161/psb.24297openalex-snapshot
Links between ER stress and autophagy in plants
inferred← citeshttps://doi.org/10.70675/734b2109z0776z4d01za887zfbdb87abb532openalex-snapshot
Unravelling the contribution of lipids in plant autophagy : Identification and functional characterization of lipids implicated in the autophagic process in Arabidopsis
inferred← citeshttps://doi.org/10.70675/8dec47a6zbc9dz468dzaee2z3166c12ff27eopenalex-snapshot
Autophagy, senescence and nitrogen remobilization in barley
inferred← citeshttps://doi.org/10.70675/fbac1ecbzfdbbz4203z8130z3457fb28f495openalex-snapshot
Autophagie et ressources azotées : contrôle nutritionnel et recyclage métabolique
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