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Autophagy as a mediator of life and death in plants

https://doi.org/10.1016/j.pbi.2017.08.011

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What this work says

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

inferredcites →https://doi.org/10.1016/0014-5793(93)80398-eopenalex-snapshot

Isolation and characterization of autophagy‐defective mutants of Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1016/bs.ctdb.2015.07.012openalex-snapshot

Autophagy in Cell Life and Cell Death

inferredcites →https://doi.org/10.1016/bs.ircmb.2015.07.005openalex-snapshot

New Insight into the Mechanism and Function of Autophagy in Plant Cells

inferredcites →https://doi.org/10.1016/j.cell.2005.03.007openalex-snapshot

Autophagy Regulates Programmed Cell Death during the Plant Innate Immune Response

inferredcites →https://doi.org/10.1016/j.cell.2009.02.036openalex-snapshot

Autophagic Components Contribute to Hypersensitive Cell Death in Arabidopsis

inferredcites →https://doi.org/10.1016/j.celrep.2016.07.015openalex-snapshot

Autophagic Turnover of Inactive 26S Proteasomes in Yeast Is Directed by the Ubiquitin Receptor Cue5 and the Hsp42 Chaperone

inferredcites →https://doi.org/10.1016/j.chom.2016.01.005openalex-snapshot

Plant TRAF Proteins Regulate NLR Immune Receptor Turnover

inferredcites →https://doi.org/10.1016/j.chom.2016.07.005openalex-snapshot

Plant TRAF Proteins Regulate NLR Immune Receptor Turnover

inferredcites →https://doi.org/10.1016/j.cub.2016.02.051openalex-snapshot

Pathogen Tactics to Manipulate Plant Cell Death

inferredcites →https://doi.org/10.1016/j.cub.2016.05.005openalex-snapshot

TOR Signaling Promotes Accumulation of BZR1 to Balance Growth with Carbon Availability in Arabidopsis

inferredcites →https://doi.org/10.1016/j.devcel.2017.03.013openalex-snapshot

Selective Autophagy of BES1 Mediated by DSK2 Balances Plant Growth and Survival

inferredcites →https://doi.org/10.1016/j.molcel.2015.04.023openalex-snapshot

Autophagic Degradation of the 26S Proteasome Is Mediated by the Dual ATG8/Ubiquitin Receptor RPN10 in Arabidopsis

inferredcites →https://doi.org/10.1016/j.pbi.2015.08.010openalex-snapshot

Endocytic and autophagic pathways crosstalk in plants

inferredcites →https://doi.org/10.1016/j.pbi.2016.11.005openalex-snapshot

Dying two deaths — programmed cell death regulation in development and disease

inferredcites →https://doi.org/10.1016/j.semcancer.2006.12.001openalex-snapshot

Inducible cell death in plant immunity

inferredcites →https://doi.org/10.1016/j.tplants.2012.05.006openalex-snapshot

Autophagy: a multifaceted intracellular system for bulk and selective recycling

inferredcites →https://doi.org/10.1016/j.tplants.2014.07.007openalex-snapshot

Autophagy as initiator or executioner of cell death

inferredcites →https://doi.org/10.1016/j.tplants.2014.10.003openalex-snapshot

Only in dying, life: programmed cell death during plant development

inferredcites →https://doi.org/10.1016/j.tplants.2015.10.008openalex-snapshot

Autophagy in Plants – What's New on the Menu?

inferredcites →https://doi.org/10.1016/j.tplants.2016.11.015openalex-snapshot

ATG8 Expansion: A Driver of Selective Autophagy Diversification?

inferredcites →https://doi.org/10.1038/cdd.2011.36openalex-snapshot

Morphological classification of plant cell deaths

inferredcites →https://doi.org/10.1038/cdd.2014.50openalex-snapshot

The plant metacaspase AtMC1 in pathogen-triggered programmed cell death and aging: functional linkage with autophagy

inferredcites →https://doi.org/10.1038/cdd.2017.18openalex-snapshot

Metacaspases versus caspases in development and cell fate regulation

inferredcites →https://doi.org/10.1038/nature05286openalex-snapshot

The plant immune system

inferredcites →https://doi.org/10.1038/nature11162openalex-snapshot

NPR3 and NPR4 are receptors for the immune signal salicylic acid in plants

inferredcites →https://doi.org/10.1038/ncb2788openalex-snapshot

Emerging regulation and functions of autophagy

inferredcites →https://doi.org/10.1038/ncb2815openalex-snapshot

Erratum: Emerging regulation and functions of autophagy

inferredcites →https://doi.org/10.1038/ncomms5121openalex-snapshot

ATG5 defines a phagophore domain connected to the endoplasmic reticulum during autophagosome formation in plants

inferredcites →https://doi.org/10.1038/nrm3696openalex-snapshot

The autophagosome: origins unknown, biogenesis complex

inferredcites →https://doi.org/10.1038/nrm3999openalex-snapshot

Live to die another way: modes of programmed cell death and the signals emanating from dying cells

inferredcites →https://doi.org/10.1073/pnas.1421271112openalex-snapshot

Dual roles of an Arabidopsis ESCRT component FREE1 in regulating vacuolar protein transport and autophagic degradation

inferredcites →https://doi.org/10.1073/pnas.1610687114openalex-snapshot

Selective autophagy limits cauliflower mosaic virus infection by NBR1-mediated targeting of viral capsid protein and particles

inferredcites →https://doi.org/10.1073/pnas.1615455113openalex-snapshot

p62- and ubiquitin-dependent stress-induced autophagy of the mammalian 26S proteasome

inferredcites →https://doi.org/10.1073/pnas.1616299114openalex-snapshot

ATG9 regulates autophagosome progression from the endoplasmic reticulum in Arabidopsis

inferredcites →https://doi.org/10.1074/mcp.m111.014035openalex-snapshot

Identification of Autophagosome-associated Proteins and Regulators by Quantitative Proteomic Analysis and Genetic Screens

inferredcites →https://doi.org/10.1083/jcb.201307082openalex-snapshot

Autophagy and metacaspase determine the mode of cell death in plants

inferredcites →https://doi.org/10.1104/pp.011024openalex-snapshot

Leaf Senescence and Starvation-Induced Chlorosis Are Accelerated by the Disruption of an Arabidopsis Autophagy Gene

inferredcites →https://doi.org/10.1104/pp.114.253377openalex-snapshot

FYVE1 Is Essential for Vacuole Biogenesis and Intracellular Trafficking in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.114.254078openalex-snapshot

Establishment of Monitoring Methods for Autophagy in Rice Reveals Autophagic Recycling of Chloroplasts and Root Plastids during Energy Limitation

inferredcites →https://doi.org/10.1104/pp.16.01582openalex-snapshot

Control of Autophagy in Chlamydomonas Is Mediated through Redox-Dependent Inactivation of the ATG4 Protease

inferredcites →https://doi.org/10.1105/tpc.104.025395openalex-snapshot

Processing of ATG8s, Ubiquitin-Like Proteins, and Their Deconjugation by ATG4s Are Essential for Plant Autophagy

inferredcites →https://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

inferredcites →https://doi.org/10.1105/tpc.111.093112openalex-snapshot

A New Type of Compartment, Defined by Plant-Specific Atg8-Interacting Proteins, Is Induced upon Exposure of Arabidopsis Plants to Carbon Starvation

inferredcites →https://doi.org/10.1105/tpc.112.101535openalex-snapshot

Degradation of the Endoplasmic Reticulum by Autophagy during Endoplasmic Reticulum Stress in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.113.113399openalex-snapshot

The Deubiquitinating Enzyme AMSH1 and the ESCRT-III Subunit VPS2.1 Are Required for Autophagic Degradation inArabidopsis

inferredcites →https://doi.org/10.1105/tpc.113.116947openalex-snapshot

Highly Oxidized Peroxisomes Are Selectively Degraded via Autophagy in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.113.117192openalex-snapshot

Catalase andNO CATALASE ACTIVITY1Promote Autophagy-Dependent Cell Death inArabidopsis

inferredcites →https://doi.org/10.1105/tpc.113.118307openalex-snapshot

A BAR-Domain Protein SH3P2, Which Binds to Phosphatidylinositol 3-Phosphate and ATG8, Regulates Autophagosome Formation in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.113.120014openalex-snapshot

AUTOPHAGY-RELATED11 Plays a Critical Role in General Autophagy- and Senescence-Induced Mitophagy in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.114.132043openalex-snapshot

Retromer Contributes to Immunity-Associated Cell Death in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.114.134080openalex-snapshot

The Arabidopsis Abiotic Stress-Induced TSPO-Related Protein Reduces Cell-Surface Expression of the Aquaporin PIP2;7 through Protein-Protein Interactions and Autophagic Degradation

inferredcites →https://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

inferredcites →https://doi.org/10.1105/tpc.15.00158openalex-snapshot

Autophagic Recycling Plays a Central Role in Maize Nitrogen Remobilization

inferredcites →https://doi.org/10.1105/tpc.15.00626openalex-snapshot

Aspartyl Protease-Mediated Cleavage of BAG6 Is Necessary for Autophagy and Fungal Resistance in Plants

inferredcites →https://doi.org/10.1105/tpc.15.01012openalex-snapshot

An Autophagy-Related Kinase Is Essential for the Symbiotic Relationship between Phaseolus vulgaris and Both Rhizobia and Arbuscular Mycorrhizal Fungi

inferredcites →https://doi.org/10.1105/tpc.16.00637openalex-snapshot

Entire Photodamaged Chloroplasts Are Transported to the Central Vacuole by Autophagy

inferredcites →https://doi.org/10.1105/tpc.17.00056openalex-snapshot

TRAF Family Proteins Regulate Autophagy Dynamics by Modulating AUTOPHAGY PROTEIN6 Stability in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02416.xopenalex-snapshot

Overexpression of constitutively active Arabidopsis RabG3b promotes xylem development in transgenic poplars

inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04315.xopenalex-snapshot

The Rab GTPase RabG3b functions in autophagy and contributes to tracheary element differentiation in Arabidopsis

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04546.xopenalex-snapshot

Autophagy differentially controls plant basal immunity to biotrophic and necrotrophic pathogens

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04553.xopenalex-snapshot

A critical role of autophagy in plant resistance to necrotrophic fungal pathogens

inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154005openalex-snapshot

The Role of Atg Proteins in Autophagosome Formation

inferredcites →https://doi.org/10.1146/annurev-phyto-081211-172955openalex-snapshot

Plant Immunity to Necrotrophs

inferredcites →https://doi.org/10.1155/2012/219625openalex-snapshot

Autophagy: More Than a Nonselective Pathway

inferredcites →https://doi.org/10.1159/000351979openalex-snapshot

The Mechanism and Physiological Function of Macroautophagy

inferredcites →https://doi.org/10.1186/s12870-015-0472-yopenalex-snapshot

Wheat homologs of yeast ATG6 function in autophagy and are implicated in powdery mildew immunity

inferredcites →https://doi.org/10.1242/bio.015529openalex-snapshot

METACASPASE9 modulates autophagy to confine cell death to the target cells during Arabidopsis vascular xylem differentiation

inferredcites →https://doi.org/10.1371/journal.pgen.1003196openalex-snapshot

NBR1-Mediated Selective Autophagy Targets Insoluble Ubiquitinated Protein Aggregates in Plant Stress Responses

inferredcites →https://doi.org/10.1371/journal.pgen.1005704openalex-snapshot

Retromer Is Essential for Autophagy-Dependent Plant Infection by the Rice Blast Fungus

inferredcites →https://doi.org/10.1371/journal.ppat.1003287openalex-snapshot

Cell Death Control: The Interplay of Apoptosis and Autophagy in the Pathogenicity of Sclerotinia sclerotiorum

inferredcites →https://doi.org/10.3389/fpls.2016.00260openalex-snapshot

Constitutive Negative Regulation of R Proteins in Arabidopsis also via Autophagy Related Pathway?

inferredcites →https://doi.org/10.4161/auto.28060openalex-snapshot

Autophagosome biogenesis in plants

inferredcites →https://doi.org/10.4161/auto.28236openalex-snapshot

Vacuolar cell death in plants

inferredcites →https://doi.org/10.4161/auto.28279openalex-snapshot

OsATG7 is required for autophagy-dependent lipid metabolism in rice postmeiotic anther development

inferredcites →https://doi.org/10.4161/auto.29320openalex-snapshot

ArabidopsisATG11, a scaffold that links the ATG1-ATG13 kinase complex to general autophagy and selective mitophagy

inferredcites →https://doi.org/10.4161/auto.29406openalex-snapshot

Autophagy deficiency leads to accumulation of ubiquitinated proteins, ER stress, and cell death inArabidopsis

inferredcites →https://doi.org/10.7554/elife.10856openalex-snapshot

An effector of the Irish potato famine pathogen antagonizes a host autophagy cargo receptor

inferredcites →https://doi.org/10.7554/elife.23897openalex-snapshot

Autophagy functions as an antiviral mechanism against geminiviruses in plants

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.4524446openalex-extracted

Autophagy Restricts Fungal Accommodation in the Roots of Arabidopsis Thaliana

inferred← citeshttps://doi.org/10.1002/1873-3468.14412openalex-snapshot

Cargo receptors and adaptors for selective autophagy in plant cells

inferred← citeshttps://doi.org/10.1002/1873-3468.14433openalex-snapshot

Hydrogen sulfide action in the regulation of plant autophagy

inferred← citeshttps://doi.org/10.1002/9781119312994.apr0665openalex-snapshot

Ubiquitin/Proteasome System in Plant Pathogen Responses

inferred← citeshttps://doi.org/10.1007/978-981-15-0606-2_3openalex-snapshot

Autophagy in Plant Immunity

inferred← citeshttps://doi.org/10.1007/s00018-022-04281-7openalex-snapshot

Interaction of ToLCNDV TrAP with SlATG8f marks it susceptible to degradation by autophagy

inferred← citeshttps://doi.org/10.1007/s00122-021-03783-5openalex-snapshot

Molecular characterization of SlATG18f in response to Tomato leaf curl New Delhi virus infection in tomato and development of a CAPS marker for leaf curl disease tolerance

inferred← citeshttps://doi.org/10.1007/s00425-021-03668-3openalex-snapshot

Autophagy—an underestimated coordinator of construction and destruction during plant root ontogeny

inferred← citeshttps://doi.org/10.1007/s00709-021-01610-8openalex-snapshot

Short-term waterlogging-induced autophagy in root cells of wheat can inhibit programmed cell death

inferred← citeshttps://doi.org/10.1007/s00709-025-02102-9openalex-snapshot

Plant programmed cell death in the context of diversity and evolution of PCD

inferred← citeshttps://doi.org/10.1007/s10571-020-00930-2openalex-snapshot

Valproic Acid Sensitizes Glioma Cells to Luteolin Through Induction of Apoptosis and Autophagy via Akt Signaling

inferred← citeshttps://doi.org/10.1007/s44281-023-00021-4openalex-snapshot

Transcription factors RhPIF4/8 and RhHY5 regulate autophagy-mediated petal senescence in rose (Rosa hybrida)

inferred← citeshttps://doi.org/10.1016/j.biori.2019.12.001openalex-snapshot

Abiotic stress and self-destruction: ZmATG8 and ZmATG12 gene transcription and osmotic stress responses in maize

inferred← citeshttps://doi.org/10.1016/j.cell.2019.05.026openalex-snapshot

Autophagy-Independent Functions of the Autophagy Machinery

inferred← citeshttps://doi.org/10.1016/j.cell.2020.07.016openalex-snapshot

Formation of NPR1 Condensates Promotes Cell Survival during the Plant Immune Response

inferred← citeshttps://doi.org/10.1016/j.cpb.2026.100595openalex-snapshot

Harnessing autophagy: Fine tuning plant programmed cell death for enhanced crop resilience and yield

inferred← citeshttps://doi.org/10.1016/j.cub.2022.03.053openalex-snapshot

Autophagy promotes programmed cell death and corpse clearance in specific cell types of the Arabidopsis root cap

inferred← citeshttps://doi.org/10.1016/j.devcel.2026.01.002openalex-snapshot

Mitogen-activated kinase 6 facilitates autophagy initiation to confer salt tolerance in maize

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.2022.129512openalex-snapshot

Perfluorinated alkyl substances affect the growth, physiology and root proteome of hydroponically grown maize plants

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.jhazmat.2026.141301openalex-snapshot

The critical role of autophagy in mitigating acid stress-induced hypersusceptibility response in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1016/j.jmb.2019.06.028openalex-snapshot

Plant Selective Autophagy—Still an Uncharted Territory With a Lot of Hidden Gems

inferred← citeshttps://doi.org/10.1016/j.micres.2021.126810openalex-snapshot

Bacterial effectors mimicking ubiquitin-proteasome pathway tweak plant immunity

inferred← citeshttps://doi.org/10.1016/j.mito.2018.04.008openalex-snapshot

Mitochondria-targeted quinones suppress the generation of reactive oxygen species, programmed cell death and senescence in plants

inferred← citeshttps://doi.org/10.1016/j.pbi.2025.102826openalex-snapshot

Every step you take: How pathogens hijack host proteostasis from transcription, through translation, to degradation

inferred← citeshttps://doi.org/10.1016/j.plantsci.2020.110713openalex-snapshot

Silencing ATG6 and PI3K accelerates petal senescence and reduces flower number and shoot biomass in petunia

inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111855openalex-snapshot

Involvement of plant signaling network and cell metabolic homeostasis in nitrogen deficiency-induced early leaf senescence

inferred← citeshttps://doi.org/10.1016/j.pmpp.2026.103526openalex-snapshot

Comparative transcriptomic responses of olive drupes pre-treated with Trichoderma atroviride culture filtrate or Candida oleophila cells during Phytophthora oleae infection in a postharvest scenario

inferred← citeshttps://doi.org/10.1016/j.sajb.2024.02.007openalex-snapshot

Genome-wide identification and expression analysis of autophagy-related genes (ATG) in Gossypium spp. reveals their crucial role in stress tolerance

inferred← citeshttps://doi.org/10.1016/j.tim.2020.02.010openalex-snapshot

Microbial Effector Proteins – A Journey through the Proteolytic Landscape

inferred← citeshttps://doi.org/10.1016/j.tplants.2019.03.005openalex-snapshot

Ferroptosis: Yet Another Way to Die

inferred← citeshttps://doi.org/10.1016/j.tplants.2019.05.002openalex-snapshot

Regulation of Ubiquitination Is Central to the Phosphate Starvation Response

inferred← citeshttps://doi.org/10.1016/j.tplants.2025.02.004openalex-snapshot

Hidden aging: the secret role of root senescence

inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100663openalex-snapshot

Liquid–liquid phase separation in plants: Advances and perspectives from model species to crops

inferred← citeshttps://doi.org/10.1038/s41467-018-03658-2openalex-snapshot

Beclin1 restricts RNA virus infection in plants through suppression and degradation of the viral polymerase

inferred← citeshttps://doi.org/10.1038/s41467-023-39426-0openalex-snapshot

A selective autophagy receptor VISP1 induces symptom recovery by targeting viral silencing suppressors

inferred← citeshttps://doi.org/10.1038/s41467-024-46902-8openalex-snapshot

Autophagy-mediated degradation of integumentary tapetum is critical for embryo pattern formation

inferred← citeshttps://doi.org/10.1038/s41467-024-54468-8openalex-snapshot

Autophagy modulates Arabidopsis male gametophyte fertility and controls actin organization

inferred← citeshttps://doi.org/10.1038/s41477-025-02077-8openalex-snapshot

Vacuolar sorting receptors coordinate lytic vacuolar and autophagic transport for plant effector-triggered immunity

inferred← citeshttps://doi.org/10.1038/s41477-026-02279-8openalex-snapshot

Root hair lifespan is antagonistically controlled by autophagy and programmed cell death

inferred← citeshttps://doi.org/10.1038/s41564-021-00896-xopenalex-snapshot

A cell surface-exposed protein complex with an essential virulence function in Ustilago maydis

inferred← citeshttps://doi.org/10.1071/bt17174openalex-snapshot

Autophagy is associated with male sterility in pistillate flowers of Maytenus obtusifolia (Celastraceae)

inferred← citeshttps://doi.org/10.1080/15548627.2018.1520547openalex-snapshot

Autophagy regulates glucose-mediated root meristem activity by modulating ROS production inArabidopsis

inferred← citeshttps://doi.org/10.1080/15548627.2020.1856492openalex-snapshot

Vacuolar processing enzyme translocates to the vacuole through the autophagy pathway to induce programmed cell death

inferred← citeshttps://doi.org/10.1080/15548627.2022.2153573openalex-snapshot

The Valsa Mali effector Vm1G-1794 protects the aggregated MdEF-Tu from autophagic degradation to promote infection in apple

inferred← citeshttps://doi.org/10.1080/15548627.2023.2247300openalex-snapshot

Interplay of energy metabolism and autophagy

inferred← citeshttps://doi.org/10.1080/15548627.2025.2569683openalex-snapshot

A secretory protein from “ candidatus Liberibacter asiaticus” targets SNARE protein CsVTI13 to suppress autophagosome-vacuole fusion and promote bacterial infection

inferred← citeshttps://doi.org/10.1080/15592324.2017.1393137openalex-snapshot

Partial or entire: Distinct responses of two types of chloroplast autophagy

inferred← citeshttps://doi.org/10.1093/aob/mcaf105openalex-snapshot

Revealing programmed cell death events during flower (petal) senescence

inferred← citeshttps://doi.org/10.1093/jxb/erab063openalex-snapshot

The ATG4 protease integrates redox and stress signals to regulate autophagy

inferred← citeshttps://doi.org/10.1093/jxb/erab094openalex-snapshot

Potential interaction between autophagy and auxin during maize leaf senescence

inferred← citeshttps://doi.org/10.1093/jxb/ery069openalex-snapshot

Autophagy-related approaches for improving nutrient use efficiency and crop yield protection

inferred← citeshttps://doi.org/10.1093/jxb/erz066openalex-snapshot

SnRK1 and TOR: modulating growth–defense trade-offs in plant stress responses

inferred← citeshttps://doi.org/10.1093/jxb/erz126openalex-snapshot

Plant proteases and programmed cell death

inferred← citeshttps://doi.org/10.1093/jxb/erz402openalex-snapshot

Arabidopsis GAAPs interacting with MAPR3 modulate the IRE1-dependent pathway upon endoplasmic reticulum stress

inferred← citeshttps://doi.org/10.1093/pcp/pcaa128openalex-snapshot

Suppression of Metacaspase- and Autophagy-Dependent Cell Death Improves Stress-Induced Microspore Embryogenesis in Brassica napus

inferred← citeshttps://doi.org/10.1093/plcell/koad325openalex-snapshot

The plant cell wall—dynamic, strong, and adaptable—is a natural shapeshifter

inferred← citeshttps://doi.org/10.1093/plcell/koae193openalex-snapshot

The lowdown on breakdown: Open questions in plant proteolysis

inferred← citeshttps://doi.org/10.1093/plcell/koaf186openalex-snapshot

Defense strategies for plant health: Disease resistance and tolerance

inferred← citeshttps://doi.org/10.1098/rsob.250446openalex-snapshot

Autophagy in the arms race: how pathogen effectors rewire immunity in plants

inferred← citeshttps://doi.org/10.1101/2022.08.07.503073openalex-snapshot

ATG5- and ATG7-mediated autophagy regulates pollen tube guidance and male fertility in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1101/2023.07.21.550010openalex-snapshot

Autophagy restricts fungal accommodation in the roots of Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1101/2024.09.02.610801openalex-snapshot

Raffinose induces autophagy to promote plant growth

inferred← citeshttps://doi.org/10.1101/2025.03.06.641815openalex-snapshot

The hollow truth: ethylene-triggered ROS, PCD, senescence, and autophagy drive hollow stem formation

inferred← citeshttps://doi.org/10.1105/tpc.17.00815openalex-snapshot

Bacteria Exploit Autophagy for Proteasome Degradation and Enhanced Virulence in Plants

inferred← citeshttps://doi.org/10.1105/tpc.19.00170openalex-snapshot

Dual Role for Autophagy in Lipid Metabolism in Arabidopsis

inferred← citeshttps://doi.org/10.1105/tpc.20.00766openalex-snapshot

Abscisic Acid-Triggered Persulfidation of the Cys Protease ATG4 Mediates Regulation of Autophagy by Sulfide

inferred← citeshttps://doi.org/10.1111/mpp.12852openalex-snapshot

Autophagy–virus interplay in plants: from antiviral recognition to proviral manipulation

inferred← citeshttps://doi.org/10.1111/nph.16268openalex-snapshot

Nuclear autophagy degrades a geminivirus nuclear protein to restrict viral infection in solanaceous plants

inferred← citeshttps://doi.org/10.1111/nph.16336openalex-snapshot

Disruption of Arabidopsis neutral ceramidases 1 and 2 results in specific sphingolipid imbalances triggering different phytohormone‐dependent plant cell death programmes

inferred← citeshttps://doi.org/10.1111/nph.16664openalex-snapshot

Plant proteostasis – shaping the proteome: a research community aiming to understand molecular mechanisms that control protein abundance

inferred← citeshttps://doi.org/10.1111/nph.20393openalex-snapshot

Blocking constitutive autophagy rescues the loss of acquired heat resistance in Arabidopsis fes1a

inferred← citeshttps://doi.org/10.1111/nph.70564openalex-snapshot

P3IPs activate autophagy by disrupting the GAPC2 – ATG3 interaction and target TuMV 6K2 for degradation

inferred← citeshttps://doi.org/10.1111/pce.14044openalex-snapshot

Arabidopsis FAR‐RED ELONGATED HYPOCOTYL3 negatively regulates carbon starvation responses

inferred← citeshttps://doi.org/10.1111/pce.15386openalex-snapshot

Ferritin From Striped Stem Borer (Chilo suppressalis) Oral Secretion Acts as an Effector Helping to Maintain Iron Homoeostasis and Impair Defenses in Rice

inferred← citeshttps://doi.org/10.1111/pce.15511openalex-snapshot

Sri Lankan cassava mosaic virus Silencing Suppressor AC4 Mediates Autophagic Degradation of SGS3/RDR6 Bodies in Plants

inferred← citeshttps://doi.org/10.1111/pce.70830openalex-snapshot

Selective Autophagy in Plant Immunity: Mechanisms, Regulation, and Emerging Concepts in Xenophagy

inferred← citeshttps://doi.org/10.1111/ppl.14409openalex-snapshot

Autophagy is suppressed by low temperatures and is dispensable for cold acclimation in Arabidopsis

inferred← citeshttps://doi.org/10.1111/ppl.70823openalex-snapshot

Over‐Expression of AtATG8h Enhances Resistance Against Biotrophic Pathogens but Compromises Resistance Against Necrotrophic Pathogen in Arabidopsis

inferred← citeshttps://doi.org/10.1111/tpj.14276openalex-snapshot

In situ transcriptomic and metabolomic study of the loss of photosynthesis in the leaves of mixotrophic plants exploiting fungi

inferred← citeshttps://doi.org/10.1111/tpj.14325openalex-snapshot

Arabidopsis seedlings display a remarkable resilience under severe mineral starvation using their metabolic plasticity to remain self‐sufficient for weeks

inferred← citeshttps://doi.org/10.1128/mbio.03665-24openalex-snapshot

A Ralstonia solanacearum effector regulates plant cell death by disrupting the homeostasis of the BPA1-ACD11 complex

inferred← citeshttps://doi.org/10.1134/s1021443722020212openalex-snapshot

Autophagy and the Energy Status of Plant Cells

inferred← citeshttps://doi.org/10.1134/s1062360420030029openalex-snapshot

Programmed Cell Death during Formation of the Embryo Sac and Seed

inferred← citeshttps://doi.org/10.1146/annurev-phyto-020620-114550openalex-snapshot

Research Advances in Potyviruses: From the Laboratory Bench to the Field

inferred← citeshttps://doi.org/10.1155/2024/9908323openalex-snapshot

Autophagy: A New Avenue and Biochemical Mechanisms to Mitigate the Climate Change

inferred← citeshttps://doi.org/10.1186/s12870-020-02651-6openalex-snapshot

Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.1186/s12870-020-02711-xopenalex-snapshot

Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.1186/s12870-025-07954-0openalex-snapshot

Raffinose induces autophagy to promote the growth of Arabidopsis Thaliana

inferred← citeshttps://doi.org/10.1242/dev.205087openalex-snapshot

Programmed cell death during plant development

inferred← citeshttps://doi.org/10.12677/br.2022.113039openalex-snapshot

Role of Autophagy in Plant Resistance to Virus Infection

inferred← citeshttps://doi.org/10.1360/tb-2024-0341openalex-snapshot

Role of plant autophagy in biotic stress response

inferred← citeshttps://doi.org/10.1371/journal.pbio.3000373openalex-snapshot

N-terminal β-strand underpins biochemical specialization of an ATG8 isoform

inferred← citeshttps://doi.org/10.1371/journal.pone.0281668openalex-snapshot

The role of Atg16 in autophagy, anthocyanin biosynthesis, and programmed cell death in leaves of the lace plant (Aponogeton madagascariensis)

inferred← citeshttps://doi.org/10.15252/embj.2021110352openalex-snapshot

A bacterial effector counteracts host autophagy by promoting degradation of an autophagy component

inferred← citeshttps://doi.org/10.15407/frg2023.05.371openalex-snapshot

What is missing to create new herbicides and solving the problem of resistance?

inferred← citeshttps://doi.org/10.2478/prolas-2019-0007openalex-snapshot

Ultrastructural Changes of Organelles in Root Cap Cells of Tobacco Under Salinity

inferred← citeshttps://doi.org/10.31489/2026feb3/17-29openalex-snapshot

Organelle Dynamics during Salinity-Induced Programmed Cell Death in Plants

inferred← citeshttps://doi.org/10.3389/fgene.2021.784545openalex-snapshot

Programmed Degradation of Pericarp Cells in Wheat Grains Depends on Autophagy

inferred← citeshttps://doi.org/10.3389/fpls.2018.01575openalex-snapshot

Exploring the Diversity of Mechanisms Associated With Plant Tolerance to Virus Infection

inferred← citeshttps://doi.org/10.3389/fpls.2020.579875openalex-snapshot

Knowing When to Self-Eat – Fine-Tuning Autophagy Through ATG8 Iso-forms in Plants

inferred← citeshttps://doi.org/10.3389/fpls.2022.840218openalex-snapshot

CRISPR/Cas9-Mediated Editing of Autophagy Gene 6 in Petunia Decreases Flower Longevity, Seed Yield, and Phosphorus Remobilization by Accelerating Ethylene Production and Senescence-Related Gene Expression

inferred← citeshttps://doi.org/10.3389/fpls.2022.904933openalex-snapshot

The Metacaspase TaMCA-Id Negatively Regulates Salt-Induced Programmed Cell Death and Functionally Links With Autophagy in Wheat

inferred← citeshttps://doi.org/10.3390/agronomy12081909openalex-snapshot

Salt-Induced Autophagy and Programmed Cell Death in Wheat

inferred← citeshttps://doi.org/10.3390/antiox10121884openalex-snapshot

Autophagy Is Involved in the Viability of Overexpressing Thioredoxin o1 Tobacco BY-2 Cells under Oxidative Conditions

inferred← citeshttps://doi.org/10.3390/antiox11020327openalex-snapshot

Hydrogen Sulfide: A Key Role in Autophagy Regulation from Plants to Mammalians

inferred← citeshttps://doi.org/10.3390/genes10040267openalex-snapshot

The Role and Regulation of Autophagy and the Proteasome During Aging and Senescence in Plants

inferred← citeshttps://doi.org/10.3390/ijms19061666openalex-snapshot

Wheat Gene TaATG8j Contributes to Stripe Rust Resistance

inferred← citeshttps://doi.org/10.3390/ijms20194754openalex-snapshot

Autophagic Machinery of Plant Peroxisomes

inferred← citeshttps://doi.org/10.3390/ijms21020562openalex-snapshot

Genomic Characterization and Expressional Profiles of Autophagy-Related Genes (ATGs) in Oilseed Crop Castor Bean (Ricinus communis L.)

inferred← citeshttps://doi.org/10.3390/ijms21176321openalex-snapshot

Emerging Roles of the Selective Autophagy in Plant Immunity and Stress Tolerance

inferred← citeshttps://doi.org/10.3390/ijms22084075openalex-snapshot

Autophagy in Plant Abiotic Stress Management

inferred← citeshttps://doi.org/10.3390/ijms222111749openalex-snapshot

Silencing Autophagy-Related Gene 2 (ATG2) Results in Accelerated Senescence and Enhanced Immunity in Soybean

inferred← citeshttps://doi.org/10.3390/ijms222312942openalex-snapshot

Initiation and Execution of Programmed Cell Death and Regulation of Reactive Oxygen Species in Plants

inferred← citeshttps://doi.org/10.3390/ijms242216508openalex-snapshot

Silencing GmATG7 Leads to Accelerated Senescence and Enhanced Disease Resistance in Soybean

inferred← citeshttps://doi.org/10.3390/ijms27188353openalex-snapshot

A Regulatory Network of Transcription and Hormones Controls PCD and Autophagy in Grape Seed Abortion

inferred← citeshttps://doi.org/10.3390/plants14162530openalex-snapshot

Functional Analysis of the Autophagy-Related Gene OsATG4b in Rice Grain Chalkiness Regulation

inferred← citeshttps://doi.org/10.3390/plants15091350openalex-snapshot

NBR1-Mediated Selective Autophagy in Plant Development and Stress Responses

inferred← citeshttps://doi.org/10.3390/plants8100361openalex-snapshot

Dynamics of Short-Term Metabolic Profiling in Radish Sprouts (Raphanus sativus L.) in Response to Nitrogen Deficiency

inferred← citeshttps://doi.org/10.3410/f.732790805.793544931openalex-snapshot

Faculty Opinions recommendation of Bacteria exploit autophagy for proteasome degradation and enhanced virulence in plants.

inferred← citeshttps://doi.org/10.37247/paagron2ed.2.22.5openalex-snapshot

Salt-Induced Autophagy and Programmed Cell Death in Wheat

inferred← citeshttps://doi.org/10.52547/pps.11.1.133openalex-snapshot

12- The role of autophagy in plants protection against pathogens

inferred← citeshttps://doi.org/10.5902/2179460x66067openalex-snapshot

Plant cytogenetics tests can predict toxic effects on human cells: genotoxic and mutagenic effects of Tityus serrulatus scorpion venom on vegetal and human cells

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997205openalex-snapshot

Additional file 10 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997208openalex-snapshot

Additional file 11 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997211openalex-snapshot

Additional file 12 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997214openalex-snapshot

Additional file 1 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997217openalex-snapshot

Additional file 2 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997220openalex-snapshot

Additional file 3 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997223openalex-snapshot

Additional file 4 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997226openalex-snapshot

Additional file 5 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997229openalex-snapshot

Additional file 6 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997232openalex-snapshot

Additional file 7 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997235openalex-snapshot

Additional file 8 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.12997238openalex-snapshot

Additional file 9 of Comprehensive analysis of the Ppatg3 mutant reveals that autophagy plays important roles in gametophore senescence in Physcomitrella patens

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167210openalex-snapshot

Additional file 10 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167213openalex-snapshot

Additional file 11 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167219openalex-snapshot

Additional file 1 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167222openalex-snapshot

Additional file 2 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167225openalex-snapshot

Additional file 3 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167228openalex-snapshot

Additional file 4 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167231openalex-snapshot

Additional file 5 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167234openalex-snapshot

Additional file 6 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167237openalex-snapshot

Additional file 7 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167240openalex-snapshot

Additional file 8 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.6084/m9.figshare.13167243openalex-snapshot

Additional file 9 of Transcriptomic and functional analyses reveal an antiviral role of autophagy during pepper mild mottle virus infection

inferred← citeshttps://doi.org/10.64898/2025.12.28.696759openalex-snapshot

Autophagy as a regulatory node integrating the carbon/nitrogen ratio with the auxin-driven chloronema-to-caulonema transition in Physcomitrium patens

inferred← citeshttps://doi.org/10.64898/2026.04.06.716646openalex-snapshot

Autophagy acts as a spatial organizer of cell-type-specific plant immunity

inferred← citeshttps://doi.org/10.70675/8a7bf4d1z207ez43dbza1a2z8ed747cc61e3openalex-snapshot

The Phytophthora parasitica effector Avh195 : an antagonist of host autophagy and promoter of the infection cycle

inferred← citeshttps://doi.org/10.70675/a464237azb310z49edz8c8dz7c504d1cc77fopenalex-snapshot

Evolution des interactions mycorhiziennes et de la mycohétérotrophie chez les orchidées

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