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Profiling of deubiquitinases that control virulence in the pathogenic plant fungus Fusarium graminearum

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What this work says

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

inferredcites →https://doi.org/10.1002/advs.202002484openalex-snapshot
The Functional Deubiquitinating Enzymes in Control of Innate Antiviral Immunity
inferredcites →https://doi.org/10.1016/j.cell.2005.11.007openalex-snapshot
A Genomic and Functional Inventory of Deubiquitinating Enzymes
inferredcites →https://doi.org/10.1016/j.cell.2007.05.021openalex-snapshot
Atg8, a Ubiquitin-like Protein Required for Autophagosome Formation, Mediates Membrane Tethering and Hemifusion
inferredcites →https://doi.org/10.1016/j.cub.2021.01.074openalex-snapshot
A genome-scale phylogeny of the kingdom Fungi
inferredcites →https://doi.org/10.1016/j.mib.2012.09.004openalex-snapshot
Genetic control of infection-related development in Magnaporthe oryzae
inferredcites →https://doi.org/10.1016/j.molcel.2011.08.025openalex-snapshot
Systematic and Quantitative Assessment of the Ubiquitin-Modified Proteome
inferredcites →https://doi.org/10.1016/j.plaphy.2019.08.032openalex-snapshot
Protein partners of plant ubiquitin-specific proteases (UBPs)
inferredcites →https://doi.org/10.1016/j.tcb.2010.12.006openalex-snapshot
The Three Musketeers of Autophagy: phosphorylation, ubiquitylation and acetylation
inferredcites →https://doi.org/10.1038/35044114openalex-snapshot
A ubiquitin-like system mediates protein lipidation
inferredcites →https://doi.org/10.1038/cr.2016.39openalex-snapshot
Ubiquitin modifications
inferredcites →https://doi.org/10.1038/nbt.1654openalex-snapshot
Global analysis of lysine ubiquitination by ubiquitin remnant immunoaffinity profiling
inferredcites →https://doi.org/10.1038/nchembio.2326openalex-snapshot
Capzimin is a potent and specific inhibitor of proteasome isopeptidase Rpn11
inferredcites →https://doi.org/10.1038/nsmb.2771openalex-snapshot
Structure of the Rpn11–Rpn8 dimer reveals mechanisms of substrate deubiquitination during proteasomal degradation
inferredcites →https://doi.org/10.1038/s41467-018-05683-7openalex-snapshot
Wheat microbiome bacteria can reduce virulence of a plant pathogenic fungus by altering histone acetylation
inferredcites →https://doi.org/10.1038/s41579-019-0243-0openalex-snapshot
Protein post-translational modifications in bacteria
inferredcites →https://doi.org/10.1038/s41598-017-11640-zopenalex-snapshot
Genome-wide functional analysis reveals that autophagy is necessary for growth, sporulation, deoxynivalenol production and virulence in Fusarium graminearum
inferredcites →https://doi.org/10.1038/s43016-022-00655-zopenalex-snapshot
Emerging health threat and cost of Fusarium mycotoxins in European wheat
inferredcites →https://doi.org/10.1073/pnas.0901477106openalex-snapshot
Genome-wide functional analysis reveals that infection-associated fungal autophagy is necessary for rice blast disease
inferredcites →https://doi.org/10.1074/mcp.m110.003590openalex-snapshot
Mass Spectrometric Analysis of Lysine Ubiquitylation Reveals Promiscuity at Site Level
inferredcites →https://doi.org/10.1080/15548627.2019.1580104openalex-snapshot
Histone acetyltransferase MoHat1 acetylates autophagy-related proteins MoAtg3 and MoAtg9 to orchestrate functional appressorium formation and pathogenicity in Magnaporthe oryzae
inferredcites →https://doi.org/10.1080/15569540903092142openalex-snapshot
Genes, gene clusters, and biosynthesis of trichothecenes and fumonisins in Fusarium
inferredcites →https://doi.org/10.1093/molbev/mst022openalex-snapshot
The Repertoires of Ubiquitinating and Deubiquitinating Enzymes in Eukaryotic Genomes
inferredcites →https://doi.org/10.1093/nar/gkab844openalex-snapshot
Fusarium BP1 is a reader of H3K27 methylation
inferredcites →https://doi.org/10.1094/mpmi.2002.15.11.1119openalex-snapshot
A Mitogen-Activated Protein Kinase Gene ( MGV1 ) in Fusarium graminearum Is Required for Female Fertility, Heterokaryon Formation, and Plant Infection
inferredcites →https://doi.org/10.1098/rsob.190147openalex-snapshot
Cellular functions and molecular mechanisms of non-lysine ubiquitination
inferredcites →https://doi.org/10.1105/tpc.112.108613openalex-snapshot
Advanced Proteomic Analyses Yield a Deep Catalog of Ubiquitylation Targets in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.16.00007openalex-snapshot
UBIQUITIN-SPECIFIC PROTEASE 14 interacts with ULTRAVIOLET-B INSENSITIVE 4 to regulate endoreduplication and cell and organ growth in Arabidopsis
inferredcites →https://doi.org/10.1111/1462-2920.12334openalex-snapshot
The MAPKK FgMkk1 of F usarium graminearum regulates vegetative differentiation, multiple stress response, and virulence via the cell wall integrity and high‐osmolarity glycerol signaling pathways
inferredcites →https://doi.org/10.1111/1462-2920.15129openalex-snapshot
The RasGEF FgCdc25 regulates fungal development and virulence in Fusarium graminearum via cAMP and MAPK signalling pathways
inferredcites →https://doi.org/10.1111/j.1364-3703.2011.00783.xopenalex-snapshot
The Top 10 fungal pathogens in molecular plant pathology
inferredcites →https://doi.org/10.1111/mpp.12155openalex-snapshot
A transcription factor FgSte12 is required for pathogenicity in F usarium graminearum
inferredcites →https://doi.org/10.1111/mpp.13196openalex-snapshot
Deubiquitinase Ubp3 regulates ribophagy and deubiquitinates Smo1 for appressorium‐mediated infection by Magnaporthe oryzae
inferredcites →https://doi.org/10.1111/nph.12776openalex-snapshot
The TOR signaling pathway regulates vegetative development and virulence inFusarium graminearum
inferredcites →https://doi.org/10.1111/nph.13158openalex-snapshot
The transmembrane protein F g S ho1 regulates fungal development and pathogenicity via the MAPK module S te50‐ S te11‐ S te7 in F usarium graminearum
inferredcites →https://doi.org/10.1111/nph.13374openalex-snapshot
Functional analysis of the Fusarium graminearum phosphatome
inferredcites →https://doi.org/10.1111/pbi.12352openalex-snapshot
Host‐induced gene silencing of an essential chitin synthase gene confers durable resistance to F usarium head blight and seedling blight in wheat
inferredcites →https://doi.org/10.1111/pbi.13401openalex-snapshot
Host‐induced gene silencing of multiple genes of Fusarium graminearum enhances resistance to Fusarium head blight in wheat
inferredcites →https://doi.org/10.1126/science.1075898openalex-snapshot
Role of Rpn11 Metalloprotease in Deubiquitination and Degradation by the 26 S Proteasome
inferredcites →https://doi.org/10.1126/science.290.5497.1717openalex-snapshot
Autophagy as a Regulated Pathway of Cellular Degradation
inferredcites →https://doi.org/10.1128/aem.70.4.2044-2051.2004openalex-snapshot
Tri1 in Fusarium graminearum Encodes a P450 Oxygenase
inferredcites →https://doi.org/10.1128/cmr.16.3.497-516.2003openalex-snapshot
Mycotoxins
inferredcites →https://doi.org/10.1146/annurev-phyto-021320-010948openalex-snapshot
Emerging Roles of Posttranslational Modifications in Plant-Pathogenic Fungi and Bacteria
inferredcites →https://doi.org/10.1146/annurev-phyto-082718-100318openalex-snapshot
Fusarium graminearum Trichothecene Mycotoxins: Biosynthesis, Regulation, and Management
inferredcites →https://doi.org/10.1146/annurev.biochem.78.082307.091526openalex-snapshot
Regulation and Cellular Roles of Ubiquitin-Specific Deubiquitinating Enzymes
inferredcites →https://doi.org/10.1152/physrev.00002.2013openalex-snapshot
Deubiquitylases From Genes to Organism
inferredcites →https://doi.org/10.1158/0008-5472.can-10-1530openalex-snapshot
Deubiquitinase Inhibition by Small-Molecule WP1130 Triggers Aggresome Formation and Tumor Cell Apoptosis
inferredcites →https://doi.org/10.1186/s40168-021-01077-yopenalex-snapshot
Post-translational regulation of autophagy is involved in intra-microbiome suppression of fungal pathogens
inferredcites →https://doi.org/10.1261/rna.042838.113openalex-snapshot
The crystal structure of S. cerevisiae Sad1, a catalytically inactive deubiquitinase that is broadly required for pre-mRNA splicing
inferredcites →https://doi.org/10.1371/journal.pone.0063077openalex-snapshot
Cellular Development Associated with Induced Mycotoxin Synthesis in the Filamentous Fungus Fusarium graminearum
inferredcites →https://doi.org/10.1371/journal.ppat.1002460openalex-snapshot
Functional Analysis of the Kinome of the Wheat Scab Fungus Fusarium graminearum
inferredcites →https://doi.org/10.1371/journal.ppat.1006827openalex-snapshot
The fungal myosin I is essential for Fusarium toxisome formation
inferredcites →https://doi.org/10.3389/fmicb.2018.00769openalex-snapshot
A Deubiquitinating Enzyme Ubp14 Is Required for Development, Stress Response, Nutrient Utilization, and Pathogenesis of Magnaporthe oryzae
inferredcites →https://doi.org/10.3390/biom12101424openalex-snapshot
Recent Progress of Deubiquitinating Enzymes in Human and Plant Pathogenic Fungi
inferredcites →https://doi.org/10.3390/pathogens9030223openalex-snapshot
Molecular Diagnostics and Pathogenesis of Fungal Pathogens on Bast Fiber Crops
inferredcites →https://doi.org/10.4161/auto.1.2.1697openalex-snapshot
Lysosomal Turnover, but Not a Cellular Level, of Endogenous LC3 is a Marker for Autophagy
inferredcites →https://doi.org/10.4161/auto.21274openalex-snapshot
Autophagy vitalizes the pathogenicity of pathogenic fungi
inferredcites →https://doi.org/10.4161/auto.7075openalex-snapshot
The diverse roles of autophagy in medically important fungi

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.4827338openalex-extracted
Streptomyces Pratensis S10 Promotes Wheat Plant Growth and Induces Resistance in Wheat Seedlings Against Fusarium Graminearum
inferred← citeshttps://doi.org/10.1007/s44154-026-00285-6openalex-snapshot
A conserved Lsm8–exosome module maintains RNA splicing fidelity to control fungal stress adaptation and virulence
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2025.108841openalex-snapshot
Bioinformatic assessment of allergenicity, virulence, and secondary metabolites in Aspergillus species for industrial applications
inferred← citeshttps://doi.org/10.1016/j.funbio.2025.101640openalex-snapshot
Cyanidin 3-O-glucoside and other anthocyanins affect enniatins production in Fusarium avenaceum
inferred← citeshttps://doi.org/10.1016/j.isci.2025.114527openalex-snapshot
Otubain deubiquitinases: Multi-layered regulators of cell fate, development, and stress responses across kingdoms
inferred← citeshttps://doi.org/10.1016/j.micres.2025.128432openalex-snapshot
RNA granule-associated regulation of antiviral RNA interference by the RNA-binding E3 ubiquitin ligase in Fusarium graminearum
inferred← citeshttps://doi.org/10.1038/s41467-025-62932-2openalex-snapshot
Normal meiosis in the fungus Sclerotinia sclerotiorum despite the irregular distribution of haploid chromosomes between two nuclei
inferred← citeshttps://doi.org/10.1093/plcell/koae129openalex-snapshot
Erasing marks: Functions of plant deubiquitylating enzymes in modulating the ubiquitin code
inferred← citeshttps://doi.org/10.1128/aem.01187-25openalex-snapshot
Mechanisms of volatile organic compounds from bat cave environments against Pseudogymnoascus destructans in vitro
inferred← citeshttps://doi.org/10.1128/aem.01468-25openalex-snapshot
Comparative ubiquitinome analysis reveals the roles of protein ubiquitination in the heat stress response from Metarhizium robertsii
inferred← citeshttps://doi.org/10.1186/s12964-025-02487-3openalex-snapshot
Deubiquitinase MoAMSH inhibits autophagy by targeting MoAtg6 in Magnaporthe oryzae
inferred← citeshttps://doi.org/10.3390/jof10080578openalex-snapshot
Streptomyces pratensis S10 Promotes Wheat Plant Growth and Induces Resistance in Wheat Seedlings against Fusarium graminearum
inferred← citeshttps://doi.org/10.3390/jof11070495openalex-snapshot
Functional Characterization of Deubiquitinase UBP Family and Proteomic Analysis of Aaubp14-Mediated Pathogenicity Mechanism in Alternaria alternata
inferred← citeshttps://doi.org/10.3390/jof12050361openalex-snapshot
Functional Characterization of OTU Domain-Containing Deubiquitinases from Plant Pathogenic Fungi Reveals Distinct Immune Modulatory Mechanisms
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