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Dynamics of Autophagosome Formation

https://doi.org/10.1104/pp.17.01236

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What this work says

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

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Boron toxicity is alleviated by hydrogen sulfide in cucumber (Cucumis sativus L.) seedlings

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Isolation and characterization of autophagy‐defective mutants of Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1016/0014-5793(94)00672-5openalex-snapshot

Isolation of autophagocytosis mutants of Saccharomyces cerevisiae

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.bbrc.2004.11.117openalex-snapshot

An Arabidopsis homolog of RAPTOR/KOG1 is essential for early embryo development

inferredcites →https://doi.org/10.1016/j.biochi.2007.08.014openalex-snapshot

Regulation of macroautophagy by mTOR and Beclin 1 complexes

inferredcites →https://doi.org/10.1016/j.ceb.2009.12.004openalex-snapshot

The role of the Atg1/ULK1 complex in autophagy regulation

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.cub.2014.09.014openalex-snapshot

A Unique Plant ESCRT Component, FREE1, Regulates Multivesicular Body Protein Sorting and Plant Growth

inferredcites →https://doi.org/10.1016/j.cub.2016.06.008openalex-snapshot

Arabidopsis NAP1 Regulates the Formation of Autophagosomes

inferredcites →https://doi.org/10.1016/j.cub.2017.02.061openalex-snapshot

The Cytoskeleton–Autophagy Connection

inferredcites →https://doi.org/10.1016/j.febslet.2004.04.088openalex-snapshot

Arabidopsis homologues of the autophagy protein Atg8 are a novel family of microtubule binding proteins

inferredcites →https://doi.org/10.1016/j.jgg.2015.03.012openalex-snapshot

Fast-Suppressor Screening for New Components in Protein Trafficking, Organelle Biogenesis and Silencing Pathway in Arabidopsis thaliana Using DEX-Inducible FREE1-RNAi Plants

inferredcites →https://doi.org/10.1016/j.molp.2016.01.011openalex-snapshot

Biogenesis of Plant Prevacuolar Multivesicular Bodies

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.2015.09.006openalex-snapshot

Novel links in the plant TOR kinase signaling network

inferredcites →https://doi.org/10.1016/j.semcdb.2017.07.018openalex-snapshot

New advances in autophagy in plants: Regulation, selectivity and function

inferredcites →https://doi.org/10.1016/j.tcb.2013.06.005openalex-snapshot

IRE1: ER stress sensor and cell fate executor

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

ATG8 Expansion: A Driver of Selective Autophagy Diversification?

inferredcites →https://doi.org/10.1016/s0092-8674(00)81360-4openalex-snapshot

A Novel Mechanism for Regulating Activity of a Transcription Factor That Controls the Unfolded Protein Response

inferredcites →https://doi.org/10.1016/s0092-8674(02)00833-4openalex-snapshot

Raptor, a Binding Partner of Target of Rapamycin (TOR), Mediates TOR Action

inferredcites →https://doi.org/10.1038/nature06069openalex-snapshot

A central integrator of transcription networks in plant stress and energy signalling

inferredcites →https://doi.org/10.1038/nature07661openalex-snapshot

The unfolded protein response signals through high-order assembly of Ire1

inferredcites →https://doi.org/10.1038/ncb2152openalex-snapshot

AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1

inferredcites →https://doi.org/10.1038/ncomms10338openalex-snapshot

The Atg1–kinase complex tethers Atg9-vesicles to initiate autophagy

inferredcites →https://doi.org/10.1038/ncomms12420openalex-snapshot

Autophagy initiation by ULK complex assembly on ER tubulovesicular regions marked by ATG9 vesicles

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/nrm2708openalex-snapshot

Dynamics and diversity in autophagy mechanisms: lessons from yeast

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

The autophagosome: origins unknown, biogenesis complex

inferredcites →https://doi.org/10.1038/sj.embor.7400917openalex-snapshot

ATG1, an autophagy regulator, inhibits cell growth by negatively regulating S6 kinase

inferredcites →https://doi.org/10.1038/sj.embor.7401043openalex-snapshot

The Arabidopsis TOR kinase links plant growth, yield, stress resistance and mRNA translation

inferredcites →https://doi.org/10.1038/srep00029openalex-snapshot

Arabidopsis IRE1 catalyses unconventional splicing of bZIP60 mRNA to produce the active transcription factor

inferredcites →https://doi.org/10.1038/srep31697openalex-snapshot

Quantitative phosphoproteomics reveals the role of the AMPK plant ortholog SnRK1 as a metabolic master regulator under energy deprivation

inferredcites →https://doi.org/10.1042/bcj20160780openalex-snapshot

The lysosome: a crucial hub for AMPK and mTORC1 signalling

inferredcites →https://doi.org/10.1046/j.1365-2443.1996.d01-274.xopenalex-snapshot

Signalling from endoplasmic reticulum to nucleus: transcription factor with a basic‐leucine zipper motif is required for the unfolded protein‐response pathway

inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00532.xopenalex-snapshot

Regulation of spinach SNF1‐related (SnRK1) kinases by protein kinases and phosphatases is associated with phosphorylation of the T loop and is regulated by 5′‐AMP

inferredcites →https://doi.org/10.1073/pnas.0408941102openalex-snapshot

An Arabidopsis transcription factor, AtbZIP60, regulates the endoplasmic reticulum stress response in a manner unique to plants

inferredcites →https://doi.org/10.1073/pnas.092141899openalex-snapshot

Expression and disruption of the Arabidopsis TOR (target of rapamycin) gene

inferredcites →https://doi.org/10.1073/pnas.1102117108openalex-snapshot

Heat induces the splicing by IRE1 of a mRNA encoding a transcription factor involved in the unfolded protein response in Arabidopsis

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.1616299114openalex-snapshot

ATG9 regulates autophagosome progression from the endoplasmic reticulum in Arabidopsis

inferredcites →https://doi.org/10.1074/jbc.273.7.3963openalex-snapshot

Tor, a Phosphatidylinositol Kinase Homologue, Controls Autophagy in Yeast

inferredcites →https://doi.org/10.1074/jbc.m112.411454openalex-snapshot

Atg9 Vesicles Recruit Vesicle-tethering Proteins Trs85 and Ypt1 to the Autophagosome Formation Site

inferredcites →https://doi.org/10.1074/jbc.m204630200openalex-snapshot

The APG8/12-activating Enzyme APG7 Is Required for Proper Nutrient Recycling and Senescence in Arabidopsis thaliana

inferredcites →https://doi.org/10.1080/15548627.2015.1098798openalex-snapshot

Tomato HsfA1a plays a critical role in plant drought tolerance by activating ATG genes and inducing autophagy

inferredcites →https://doi.org/10.1080/15548627.2015.1112483openalex-snapshot

Autophagy contributes to regulation of the hypoxia response during submergence in Arabidopsis thaliana

inferredcites →https://doi.org/10.1080/15548627.2015.1113365openalex-snapshot

Disruption of microtubules in plants suppresses macroautophagy and triggers starch excess-associated chloroplast autophagy

inferredcites →https://doi.org/10.1080/15548627.2017.1320633openalex-snapshot

Plant Bax Inhibitor-1 interacts with ATG6 to regulate autophagy and programmed cell death

inferredcites →https://doi.org/10.1083/jcb.131.3.591openalex-snapshot

Isolation and characterization of yeast mutants in the cytoplasm to vacuole protein targeting pathway.

inferredcites →https://doi.org/10.1083/jcb.150.6.1507openalex-snapshot

Tor-Mediated Induction of Autophagy via an Apg1 Protein Kinase Complex

inferredcites →https://doi.org/10.1083/jcb.200803137openalex-snapshot

Autophagosome formation from membrane compartments enriched in phosphatidylinositol 3-phosphate and dynamically connected to the endoplasmic reticulum

inferredcites →https://doi.org/10.1083/jcb.201202061openalex-snapshot

Atg9 vesicles are an important membrane source during early steps of autophagosome formation

inferredcites →https://doi.org/10.1091/mbc.e07-12-1257openalex-snapshot

The Atg16L Complex Specifies the Site of LC3 Lipidation for Membrane Biogenesis in Autophagy

inferredcites →https://doi.org/10.1091/mbc.e11-09-0746openalex-snapshot

Dynamic and transient interactions of Atg9 with autophagosomes, but not membrane integration, are required for autophagy

inferredcites →https://doi.org/10.1093/jxb/err145openalex-snapshot

Hydrogen sulphide enhances photosynthesis through promoting chloroplast biogenesis, photosynthetic enzyme expression, and thiol redox modification in Spinacia oleracea seedlings

inferredcites →https://doi.org/10.1093/jxb/eru438openalex-snapshot

Overexpression of the PP2A regulatory subunit Tap46 leads to enhanced plant growth through stimulation of the TOR signalling pathway

inferredcites →https://doi.org/10.1101/cshperspect.a018358openalex-snapshot

Endocytosis and Autophagy: Exploitation or Cooperation?

inferredcites →https://doi.org/10.1101/gad.17420111openalex-snapshot

AMP-activated protein kinase—an energy sensor that regulates all aspects of cell function

inferredcites →https://doi.org/10.1104/pp.010636openalex-snapshot

Molecular Characterization of Two Arabidopsis Ire1 Homologs, Endoplasmic Reticulum-Located Transmembrane Protein Kinases

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.106.092106openalex-snapshot

Degradation of Oxidized Proteins by Autophagy during Oxidative Stress in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.106.093864openalex-snapshot

An Arabidopsis Homolog of YeastATG6/VPS30Is Essential for Pollen Germination

inferredcites →https://doi.org/10.1104/pp.108.122770openalex-snapshot

Mobilization of Rubisco and Stroma-Localized Fluorescent Proteins of Chloroplasts to the Vacuole by anATGGene-Dependent Autophagic Process

inferredcites →https://doi.org/10.1104/pp.109.147975openalex-snapshot

An O-Acetylserine(thiol)lyase Homolog with l -Cysteine Desulfhydrase Activity Regulates Cysteine Homeostasis in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.110.169045openalex-snapshot

Target of Rapamycin Regulates Development and Ribosomal RNA Expression through Kinase Domain in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.112.208108openalex-snapshot

The Rab GTPase RabG3b Positively Regulates Autophagy and Immunity-Associated Hypersensitive Cell Death in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.16.00110openalex-snapshot

Negative regulation of autophagy by sulfide in Arabidopsis thaliana is independent of reactive oxygen species

inferredcites →https://doi.org/10.1105/tpc.016121openalex-snapshot

The VTI Family of SNARE Proteins Is Necessary for Plant Viability and Mediates Different Protein Transport Pathways[W]

inferredcites →https://doi.org/10.1105/tpc.105.035931openalex-snapshot

Arabidopsis TARGET OF RAPAMYCIN Interacts with RAPTOR, Which Regulates the Activity of S6 Kinase in Response to Osmotic Stress Signals

inferredcites →https://doi.org/10.1105/tpc.11.3.459openalex-snapshot

Overexpression of BiP in Tobacco Alleviates Endoplasmic Reticulum Stress

inferredcites →https://doi.org/10.1105/tpc.110.074005openalex-snapshot

The PP2A Regulatory Subunit Tap46, a Component of the TOR Signaling Pathway, Modulates Growth and Metabolism in Plants

inferredcites →https://doi.org/10.1105/tpc.111.090993openalex-snapshot

The ATG1/ATG13 Protein Kinase Complex Is Both a Regulator and a Target of Autophagic Recycling in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.111.091306openalex-snapshot

Mutations in the Arabidopsis Homolog of LST8/GβL, a Partner of the Target of Rapamycin Kinase, Impair Plant Growth, Flowering, and Metabolic Adaptation to Long Days

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.112.105403openalex-snapshot

Cysteine-Generated Sulfide in the Cytosol Negatively Regulates Autophagy and Modulates the Transcriptional Profile in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.112.108993openalex-snapshot

Autophagy Contributes to Leaf Starch Degradation

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.113.118307openalex-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.114.129999openalex-snapshot

Arabidopsis ATG8-INTERACTING PROTEIN1 Is Involved in Autophagy-Dependent Vesicular Trafficking of Plastid Proteins to the Vacuole

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.114.135939openalex-snapshot

The Endosomal Protein CHARGED MULTIVESICULAR BODY PROTEIN1 Regulates the Autophagic Turnover of Plastids in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.16.00178openalex-snapshot

FYVE1/FREE1 Interacts with the PYL4 ABA Receptor and Mediates Its Delivery to the Vacuolar Degradation Pathway

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/10.1111/j.1365-313x.2006.02901.xopenalex-snapshot

Arabidopsis WRKY33 transcription factor is required for resistance to necrotrophic fungal pathogens

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03871.xopenalex-snapshot

SnRK1 (SNF1‐related kinase 1) has a central role in sugar and ABA signalling in Arabidopsis thaliana

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/10.1111/j.1469-8137.2010.03465.xopenalex-snapshot

Hydrogen sulphide, a novel gasotransmitter involved in guard cell signalling

inferredcites →https://doi.org/10.1111/j.1744-7909.2008.00769.xopenalex-snapshot

Hydrogen Sulfide Promotes Wheat Seed Germination and Alleviates Oxidative Damage against Copper Stress

inferredcites →https://doi.org/10.1111/j.1744-7909.2010.00946.xopenalex-snapshot

Hydrogen Sulfide Alleviates Aluminum Toxicity in Germinating Wheat Seedlings

inferredcites →https://doi.org/10.1111/j.1744-7909.2012.01178.xopenalex-snapshot

What to Eat: Evidence for Selective Autophagy in PlantsF

inferredcites →https://doi.org/10.1111/nph.13915openalex-snapshot

Managing the protein folding demands in the endoplasmic reticulum of plants

inferredcites →https://doi.org/10.1111/tpj.13091openalex-snapshot

Activation of autophagy by unfolded proteins during endoplasmic reticulum stress

inferredcites →https://doi.org/10.1111/tra.12101openalex-snapshot

Arabidopsis Exocyst Subcomplex Containing Subunit EXO70B1 Is Involved in Autophagy‐Related Transport to the Vacuole

inferredcites →https://doi.org/10.1126/science.1196371openalex-snapshot

Phosphorylation of ULK1 (hATG1) by AMP-Activated Protein Kinase Connects Energy Sensing to Mitophagy

inferredcites →https://doi.org/10.1128/mcb.01344-09openalex-snapshot

Tor Directly Controls the Atg1 Kinase Complex To Regulate Autophagy

inferredcites →https://doi.org/10.1128/mcb.21.17.5742-5752.2001openalex-snapshot

Antagonistic Controls of Autophagy and Glycogen Accumulation by Snf1p, the Yeast Homolog of AMP-Activated Protein Kinase, and the Cyclin-Dependent Kinase Pho85p

inferredcites →https://doi.org/10.1146/annurev-arplant-042811-105441openalex-snapshot

Autophagy: Pathways for Self-Eating in Plant Cells

inferredcites →https://doi.org/10.1159/000373980openalex-snapshot

Repertoires of Autophagy in the Pathogenesis of Ocular Diseases

inferredcites →https://doi.org/10.1186/1741-7007-3-12openalex-snapshot

The Arabidopsis AtRaptor genes are essential for post-embryonic plant growth

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.1005199openalex-snapshot

Beyond Glycolysis: GAPDHs Are Multi-functional Enzymes Involved in Regulation of ROS, Autophagy, and Plant Immune Responses

inferredcites →https://doi.org/10.1371/journal.pone.0011883openalex-snapshot

TOR Is a Negative Regulator of Autophagy in Arabidopsis thaliana

inferredcites →https://doi.org/10.1371/journal.pone.0015394openalex-snapshot

The Association of AMPK with ULK1 Regulates Autophagy

inferredcites →https://doi.org/10.1371/journal.pone.0031944openalex-snapshot

IRE1/bZIP60-Mediated Unfolded Protein Response Plays Distinct Roles in Plant Immunity and Abiotic Stress Responses

inferredcites →https://doi.org/10.1371/journal.pone.0182591openalex-snapshot

SnRK1 activates autophagy via the TOR signaling pathway in Arabidopsis thaliana

inferredcites →https://doi.org/10.15698/mic2016.12.546openalex-snapshot

Autophagy: machinery and regulation

inferredcites →https://doi.org/10.3389/fpls.2013.00450openalex-snapshot

Plant cytoplasmic GAPDH: redox post-translational modifications and moonlighting properties

inferredcites →https://doi.org/10.3389/fpls.2013.00543openalex-snapshot

The exocyst at the interface between cytoskeleton and membranes in eukaryotic cells

inferredcites →https://doi.org/10.3389/fpls.2014.00174openalex-snapshot

Role and regulation of autophagy in heat stress responses of tomato plants

inferredcites →https://doi.org/10.3389/fpls.2014.00190openalex-snapshot

Mechanisms of regulation of SNF1/AMPK/SnRK1 protein kinases

inferredcites →https://doi.org/10.3389/fpls.2017.01201openalex-snapshot

The AMP-Activated Protein Kinase KIN10 Is Involved in the Regulation of Autophagy in Arabidopsis

inferredcites →https://doi.org/10.3389/fpls.2017.01204openalex-snapshot

TOR-Dependent and -Independent Pathways Regulate Autophagy in Arabidopsis thaliana

inferredcites →https://doi.org/10.3390/ijms15057624openalex-snapshot

Degradation of Organelles or Specific Organelle Components via Selective Autophagy in Plant Cells

inferredcites →https://doi.org/10.4161/auto.1.2.1840openalex-snapshot

Atg9 Cycles Between Mitochondria and the Pre-Autophagosomal Structure in Yeasts

inferredcites →https://doi.org/10.4161/auto.26275openalex-snapshot

Ultrastructure of autophagy in plant cells

inferredcites →https://doi.org/10.4161/auto.5.7.9290openalex-snapshot

Autophagy is required for tolerance of drought and salt stress in plants

inferredcites →https://doi.org/10.4161/auto.6555openalex-snapshot

The role of TOR in autophagy regulation from yeast to plants and mammals

inferredcites →https://doi.org/10.4161/psb.28523openalex-snapshot

Selective autophagy receptor Joka2 co-localizes with cytoskeleton in plant cells

What points at this work

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

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Hydrogen sulfide action in the regulation of plant autophagy

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Balancing Growth and Defense

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Autophagy in Cancer Therapy: Advances and Prospects

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Pepino mosaic virus antagonizes plant m6A modification by promoting the autophagic degradation of the m6A writer HAKAI

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An asymptomatic geminivirus activates autophagy and enhances plant defenses against diverse pathogens

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Barley yellow dwarf Virus-GAV movement protein activating wheat TaATG6-Mediated antiviral autophagy pathway

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Geminivirus βV1 protein activates bZIP17/28-mediated UPR signaling to facilitate viral pathogenicity but its activity is attenuated by autophagic degradation in plants

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Neuronal autosis is Na+/K+-ATPase alpha 3-dependent and involved in hypoxic-ischemic neuronal death

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Phosphatidylinositol-4-phosphate controls autophagosome formation in Arabidopsis thaliana

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Autophagy is induced during plant grafting to promote wound healing

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Small heat shock and J-domain proteins direct defense against areca palm velarivirus 1 by degrading coat protein via autophagy

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Noncanonical ATG8–ABS3 interaction controls senescence in plants

inferred← citeshttps://doi.org/10.1038/s41598-021-83067-6openalex-snapshot

Salicylic acid is a key player of Arabidopsis autophagy mutant susceptibility to the necrotrophic bacterium Dickeya dadantii

inferred← citeshttps://doi.org/10.1080/11263504.2024.2375333openalex-snapshot

Transition dynamics in plastid interconversion in land plants

inferred← citeshttps://doi.org/10.1080/15548627.2021.1976965openalex-snapshot

Mechanistic insights into an atypical interaction between ATG8 and SH3P2 in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1080/15548627.2021.1987674openalex-snapshot

Salicylic acid and the viral virulence factor 2b regulate the divergent roles of autophagy during cucumber mosaic virus infection

inferred← citeshttps://doi.org/10.1080/15548627.2022.2095838openalex-snapshot

Autophagy and its mediated mitochondrial quality control maintain pollen tube growth and male fertility in Arabidopsis

inferred← citeshttps://doi.org/10.1080/15548627.2023.2252273openalex-snapshot

Rhabdovirus encoded glycoprotein induces and harnesses host antiviral autophagy for maintaining its compatible infection

inferred← citeshttps://doi.org/10.1080/15548627.2025.2509330openalex-snapshot

Autophagy plays a dual role in chromoplast transition and degradation and is essential for fruit coloration and ripening

inferred← citeshttps://doi.org/10.1080/15548627.2026.2668859openalex-snapshot

SINAT proteins modulate autophagic vesicle degradation by regulating V-ATPase subunit proteolysis in Arabidopsis

inferred← citeshttps://doi.org/10.1080/15592324.2020.1839226openalex-snapshot

New insights into AtNBR1 as a selective autophagy cargo receptor in Arabidopsis

inferred← citeshttps://doi.org/10.1080/15592324.2021.1977527openalex-snapshot

An Overview of the Molecular Mechanisms and Functions of Autophagic Pathways in Plants

inferred← citeshttps://doi.org/10.1093/aob/mcae015openalex-snapshot

Conserved autophagy and diverse cell wall composition: unifying features of vascular tissues in evolutionarily distinct plants

inferred← citeshttps://doi.org/10.1093/jisesa/iead042openalex-snapshot

Comparison of toxic effects of 5 macrofungi against Drosophila melanogaster

inferred← citeshttps://doi.org/10.1093/jxb/erad211openalex-snapshot

Transcriptional and post-translational regulation of plant autophagy

inferred← citeshttps://doi.org/10.1093/jxb/ery070openalex-snapshot

Plant autophagy: mechanisms and functions

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/pcp/pcaa162openalex-snapshot

Autophagy Contributes to the Quality Control of Leaf Mitochondria

inferred← citeshttps://doi.org/10.1093/pcp/pcab029openalex-snapshot

Chloroplast proteotoxic stress-induced autophagy is involved in the degradation of chloroplast proteins in Chlamydomonas reinhardtii

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/plcell/koad168openalex-snapshot

SNF1-RELATED KINASE 1 and TARGET OF RAPAMYCIN control light-responsive splicing events and developmental characteristics in etiolated Arabidopsis seedlings

inferred← citeshttps://doi.org/10.1093/plcell/koae141openalex-snapshot

Protein degrons and degradation: Exploring substrate recognition and pathway selection in plants

inferred← citeshttps://doi.org/10.1093/plphys/kiaa120openalex-snapshot

Autophagy is required for lipid homeostasis during dark-induced senescence

inferred← citeshttps://doi.org/10.1093/plphys/kiad287openalex-snapshot

Arabidopsis AUTOPHAGY-RELATED2 is essential for ATG18a and ATG9 trafficking during autophagosome closure

inferred← citeshttps://doi.org/10.1093/plphys/kiad369openalex-snapshot

Closing the loop: Three musketeers of autophagy-ATG2, ATG18a, and ATG9

inferred← citeshttps://doi.org/10.1098/rsob.180162openalex-snapshot

Autophagy in crop plants: what's new beyond Arabidopsis ?

inferred← citeshttps://doi.org/10.1101/2020.02.14.949453openalex-snapshot

Autophagy is induced during plant grafting for wound healing

inferred← citeshttps://doi.org/10.1101/2025.08.25.671700openalex-snapshot

A singular lipid composition supports the progression of plant autophagy

inferred← citeshttps://doi.org/10.1104/pp.17.01777openalex-snapshot

Cellular Dynamics: Cellular Systems in the Time Domain

inferred← citeshttps://doi.org/10.1104/pp.18.01379openalex-snapshot

The Local Phosphate Deficiency Response Activates Endoplasmic Reticulum Stress-Dependent Autophagy

inferred← citeshttps://doi.org/10.1104/pp.20.00237openalex-snapshot

Chloroplast Autophagy and Ubiquitination Combine to Manage Oxidative Damage and Starvation Responses

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.19.00413openalex-snapshot

Arabidopsis SINAT Proteins Control Autophagy by Mediating Ubiquitylation and Degradation of ATG13

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/jipb.12941openalex-snapshot

Autophagy in plants: Physiological roles and post‐translational regulation

inferred← citeshttps://doi.org/10.1111/jipb.13233openalex-snapshot

Specialized endoplasmic reticulum‐derived vesicles in plants: Functional diversity, evolution, and biotechnological exploitation

inferred← citeshttps://doi.org/10.1111/jipb.13313openalex-snapshot

Coat protein of Chinese wheat mosaic virus upregulates and interacts with cytosolic glyceraldehyde‐3‐phosphate dehydrogenase, a negative regulator of plant autophagy, to promote virus infection

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.19134openalex-snapshot

Recent advances in plant endomembrane research and new microscopical techniques

inferred← citeshttps://doi.org/10.1111/nph.19811openalex-snapshot

Lipid turnover through lipophagy in the newly identified extremophilic green microalga Chlamydomonas urium

inferred← citeshttps://doi.org/10.1111/pce.70012openalex-snapshot

HIPP33 Contributes to Selective Autophagy‐Mediated Vacuolar Sequestration of Cadmium in Arabidopsis

inferred← citeshttps://doi.org/10.1111/tpj.15065openalex-snapshot

Systematic prediction of autophagy‐related proteins using Arabidopsis thaliana interactome data

inferred← citeshttps://doi.org/10.1111/tpj.15891openalex-snapshot

The ubiquitin–26S proteasome system and autophagy relay proteome homeostasis regulation during silique development

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

Autophagy and the Energy Status of Plant Cells

inferred← citeshttps://doi.org/10.1146/annurev-cellbio-010521-015047openalex-snapshot

Dynamic Nutrient Signaling Networks in Plants

inferred← citeshttps://doi.org/10.1146/annurev-virology-010220-054709openalex-snapshot

Autophagy in Plant-Virus Interactions

inferred← citeshttps://doi.org/10.1177/2058738420961304openalex-snapshot

The probiotic Bifidobacterium in the management of Coronavirus: A theoretical basis

inferred← citeshttps://doi.org/10.1186/s12870-025-07736-8openalex-snapshot

Interplay between autophagy, the unfolded protein response and the cytoplasmic heat stress response during heat stress in maize

inferred← citeshttps://doi.org/10.1186/s40538-023-00410-xopenalex-snapshot

Effects of combinational mycelia obtained via in vitro culture on ageing and reproduction in Drosophila melanogaster and their mechanisms

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.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/10.14201/gredos.145795openalex-snapshot

Estudio de genes de autofagia y la susceptibilidad a tuberculosis en españoles

inferred← citeshttps://doi.org/10.15421/0226013openalex-snapshot

Jasmonate-ethylene (JA/ET) signaling – metabolic defense system in the integrative model of plant immunity against phytophagous insects

inferred← citeshttps://doi.org/10.21037/tcr.2019.05.22openalex-snapshot

The molecular basis for p53 inhibition of autophagy in porcine fibroblast cells

inferred← citeshttps://doi.org/10.22201/fesz.23958723e.2024.641openalex-snapshot

El papel del ion calcio y la autofagia en la regulación del hidrotropismo en raíces: el caso de Arabidopsis thaliana

inferred← citeshttps://doi.org/10.31080/asmi.2022.05.1178openalex-snapshot

Autophagy Inducing Capacities of a Commercial Preparation Based on of Bacillus thuringiensis Cry1A-Cr2A Autophagy-Inducing Properties Toxins in Human Macrophages: Implication Against Mycobacterial Infections

inferred← citeshttps://doi.org/10.3389/fcimb.2021.786348openalex-snapshot

Clearance or Hijack: Universal Interplay Mechanisms Between Viruses and Host Autophagy From Plants to Animals

inferred← citeshttps://doi.org/10.3389/fpls.2018.01837openalex-snapshot

The Multivesicular Body and Autophagosome Pathways in Plants

inferred← citeshttps://doi.org/10.3389/fpls.2019.00280openalex-snapshot

Autophagic Turnover of Chloroplasts: Its Roles and Regulatory Mechanisms in Response to Sugar Starvation

inferred← citeshttps://doi.org/10.3389/fpls.2019.00359openalex-snapshot

Chloroplast Degradation: Multiple Routes Into the Vacuole

inferred← citeshttps://doi.org/10.3389/fpls.2020.00036openalex-snapshot

Algal Autophagy Is Necessary for the Regulation of Carbon Metabolism Under Nutrient Deficiency

inferred← citeshttps://doi.org/10.3389/fpls.2020.00565openalex-snapshot

Recent Advances in Membrane Shaping for Plant Autophagosome Biogenesis

inferred← citeshttps://doi.org/10.3389/fpls.2020.01109openalex-snapshot

Genome-Wide Identification of Apple Ubiquitin SINA E3 Ligase and Functional Characterization of MdSINA2

inferred← citeshttps://doi.org/10.3389/fpls.2020.579019openalex-snapshot

Degradation of Lipid Droplets in Plants and Algae—Right Time, Many Paths, One Goal

inferred← citeshttps://doi.org/10.3389/fpls.2022.1052358openalex-snapshot

Autophagy modulates growth and development in the moss Physcomitrium patens

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.2022.961096openalex-snapshot

FERONIA functions through Target of Rapamycin (TOR) to negatively regulate autophagy

inferred← citeshttps://doi.org/10.3389/fpls.2023.1093358openalex-snapshot

Biological insights from multi-omics analysis strategies: Complex pleotropic effects associated with autophagy

inferred← citeshttps://doi.org/10.3389/fpls.2023.1226498openalex-snapshot

A sword or a buffet: plant endomembrane system in viral infections

inferred← citeshttps://doi.org/10.3389/fpls.2024.1354561openalex-snapshot

Sugar signals pedal the cell cycle!

inferred← citeshttps://doi.org/10.3390/antiox10040508openalex-snapshot

Label-Free Quantitative Proteomic Analysis of Nitrogen Starvation in Arabidopsis Root Reveals New Aspects of H2S Signaling by Protein Persulfidation

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/cells7010005openalex-snapshot

Multiscale and Multimodal Approaches to Study Autophagy in Model Plants

inferred← citeshttps://doi.org/10.3390/cells8121627openalex-snapshot

Structural Biology and Electron Microscopy of the Autophagy Molecular Machinery

inferred← citeshttps://doi.org/10.3390/cells9010119openalex-snapshot

Coordination and Crosstalk between Autophagosome and Multivesicular Body Pathways in Plant Stress Responses

inferred← citeshttps://doi.org/10.3390/diseases9010008openalex-snapshot

The Biological Roles of lncRNAs and Future Prospects in Clinical Application

inferred← citeshttps://doi.org/10.3390/fermentation9030212openalex-snapshot

Effect and Mechanism of Lepista nuda Mycelia Obtained via In Vitro Culture on the Lifespan of Drosophila melanogaster

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

Autophagic Machinery of Plant Peroxisomes

inferred← citeshttps://doi.org/10.3390/ijms22031236openalex-snapshot

Plant Mitophagy in Comparison to Mammals: What Is Still Missing?

inferred← citeshttps://doi.org/10.3390/ijms22115429openalex-snapshot

Contribution of Massive Mitochondrial Fusion and Subsequent Fission in the Plant Life Cycle to the Integrity of the Mitochondrion and Its Genome

inferred← citeshttps://doi.org/10.3390/ijms23020891openalex-snapshot

The Landscape of Autophagy-Related (ATG) Genes and Functional Characterization of TaVAMP727 to Autophagy in Wheat

inferred← citeshttps://doi.org/10.3390/ijms24032221openalex-snapshot

To Kill or to Be Killed: How Does the Battle between the UPS and Autophagy Maintain the Intracellular Homeostasis in Eukaryotes?

inferred← citeshttps://doi.org/10.4103/1673-5374.382259openalex-snapshot

The autophagy protein Atg9 functions in glia and contributes to parkinsonian symptoms in a Drosophila model of Parkinson’s disease

inferred← citeshttps://doi.org/10.5336/intermed.2020-75706openalex-snapshot

Coronavirus Treatment with Bifidobacteria Species Through Autophagy: A Hypothetical Approach

inferred← citeshttps://doi.org/10.64898/2026.08.17.745281openalex-snapshot

Common excluder barley has more than one mechanism to remove Cd from chloroplasts

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/10.70675/8e9d0801z0e88z4631zac50z2d6e1bbbc9c5openalex-snapshot

Role of autophagy in nitrogen remobilization and adaptation to environment in plants

inferred← citeshttps://doi.org/10.70675/c349f8ecz721ez40f7z8ff6zd0754e9a03ebopenalex-snapshot

Entre silence, naissance et dégradation : vers la caractérisation de nouveaux mécanismes relatifs à la biologie des ARN de transfert et assurant l'homéostasie de la cellule végétale.

inferred← citeshttps://doi.org/10.7717/peerj.11513openalex-snapshot

Promoting effect of rapamycin on osteogenic differentiation of maxillary sinus membrane stem cells

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