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Fungal effector Jsi1 hijacks plant JA/ET signaling through Topless

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What this work says

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

inferredcites →https://doi.org/10.1006/meth.2001.1262openalex-snapshot

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

inferredcites →https://doi.org/10.1007/978-1-61779-501-5_4openalex-snapshot

The Use of Agroinfiltration for Transient Expression of Plant Resistance and Fungal Effector Proteins in Nicotiana benthamiana Leaves

inferredcites →https://doi.org/10.1007/s00438-003-0926-zopenalex-snapshot

Identification of plant-regulated genes in Ustilago maydis by enhancer-trapping mutagenesis

inferredcites →https://doi.org/10.1007/s11103-019-00842-wopenalex-snapshot

The C-terminal WD40 repeats on the TOPLESS co-repressor function as a protein–protein interaction surface

inferredcites →https://doi.org/10.1007/s11103-019-00877-zopenalex-snapshot

Arabidopsis mlo3 mutant plants exhibit spontaneous callose deposition and signs of early leaf senescence

inferredcites →https://doi.org/10.1007/s11105-014-0782-5openalex-snapshot

Transcriptional Control of Glutaredoxin GRXC9 Expression by a Salicylic Acid-Dependent and NPR1-Independent Pathway in Arabidopsis

inferredcites →https://doi.org/10.1016/j.bdq.2015.01.005openalex-snapshot

How good is a PCR efficiency estimate: Recommendations for precise and robust qPCR efficiency assessments

inferredcites →https://doi.org/10.1016/j.cell.2016.04.038openalex-snapshot

Cistrome and Epicistrome Features Shape the Regulatory DNA Landscape

inferredcites →https://doi.org/10.1016/j.cell.2018.03.044openalex-snapshot

Opposite Roles of Salicylic Acid Receptors NPR1 and NPR3/NPR4 in Transcriptional Regulation of Plant Immunity

inferredcites →https://doi.org/10.1016/j.chom.2012.04.014openalex-snapshot

Coronatine Promotes Pseudomonas syringae Virulence in Plants by Activating a Signaling Cascade that Inhibits Salicylic Acid Accumulation

inferredcites →https://doi.org/10.1016/j.chom.2014.08.004openalex-snapshot

Convergent Targeting of a Common Host Protein-Network by Pathogen Effectors from Three Kingdoms of Life

inferredcites →https://doi.org/10.1016/j.chom.2017.01.003openalex-snapshot

Pseudomonas syringae Type III Effector HopBB1 Promotes Host Transcriptional Repressor Degradation to Regulate Phytohormone Responses and Virulence

inferredcites →https://doi.org/10.1016/j.ejcb.2015.06.007openalex-snapshot

Experimental approaches to investigate effector translocation into host cells in the Ustilago maydis/maize pathosystem

inferredcites →https://doi.org/10.1016/j.molp.2019.11.005openalex-snapshot

PBS3 and EPS1 Complete Salicylic Acid Biosynthesis from Isochorismate in Arabidopsis

inferredcites →https://doi.org/10.1016/j.plantsci.2013.08.008openalex-snapshot

The Arabidopsis transcriptional repressor ERF9 participates in resistance against necrotrophic fungi

inferredcites →https://doi.org/10.1038/nature05248openalex-snapshot

Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis

inferredcites →https://doi.org/10.1038/nature08854openalex-snapshot

NINJA connects the co-repressor TOPLESS to jasmonate signalling

inferredcites →https://doi.org/10.1038/nature10454openalex-snapshot

Metabolic priming by a secreted fungal effector

inferredcites →https://doi.org/10.1038/nrmicro.2017.33openalex-snapshot

Ustilago maydis effectors and their impact on virulence

inferredcites →https://doi.org/10.1038/s41467-018-04149-0openalex-snapshot

The Ustilago maydis repetitive effector Rsp3 blocks the antifungal activity of mannose-binding maize proteins

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02699.xopenalex-snapshot

Identification of genes in the bW/bE regulatory cascade in Ustilago maydis

inferredcites →https://doi.org/10.1073/pnas.0802332105openalex-snapshot

COI1 is a critical component of a receptor for jasmonate and the bacterial virulence factor coronatine

inferredcites →https://doi.org/10.1073/pnas.1002828107openalex-snapshot

Arabidopsis resistance protein SNC1 activates immune responses through association with a transcriptional corepressor

inferredcites →https://doi.org/10.1073/pnas.1703054114openalex-snapshot

Structure of the Arabidopsis TOPLESS corepressor provides insight into the evolution of transcriptional repression

inferredcites →https://doi.org/10.1074/jbc.m801392200openalex-snapshot

Activation of MAPK Kinase 9 Induces Ethylene and Camalexin Biosynthesis and Enhances Sensitivity to Salt Stress in Arabidopsis

inferredcites →https://doi.org/10.1093/bioinformatics/bts635openalex-snapshot

STAR: ultrafast universal RNA-seq aligner

inferredcites →https://doi.org/10.1093/bioinformatics/btu170openalex-snapshot

Trimmomatic: a flexible trimmer for Illumina sequence data

inferredcites →https://doi.org/10.1093/gbe/evv187openalex-snapshot

Deciphering Genome Content and Evolutionary Relationships of Isolates from the FungusMagnaporthe oryzaeAttacking Different Host Plants

inferredcites →https://doi.org/10.1093/mp/sss044openalex-snapshot

Transcriptional Activation and Production of Tryptophan-Derived Secondary Metabolites in Arabidopsis Roots Contributes to the Defense against the Fungal Vascular Pathogen Verticillium longisporum

inferredcites →https://doi.org/10.1093/nar/gku1200openalex-snapshot

Araport: the Arabidopsis Information Portal

inferredcites →https://doi.org/10.1093/pcp/pcp048openalex-snapshot

A Novel Group of Transcriptional Repressors in Arabidopsis

inferredcites →https://doi.org/10.1093/pcp/pcw187openalex-snapshot

Assessing the Role of ETHYLENE RESPONSE FACTOR Transcriptional Repressors in Salicylic Acid-Mediated Suppression of Jasmonic Acid-Responsive Genes

inferredcites →https://doi.org/10.1094/mpmi-06-14-0187-ropenalex-snapshot

ALD1 Regulates Basal Immune Components and Early Inducible Defense Responses in Arabidopsis

inferredcites →https://doi.org/10.1094/mpmi-23-5-0558openalex-snapshot

Wounding-Induced WRKY8 Is Involved in Basal Defense in Arabidopsis

inferredcites →https://doi.org/10.1101/sqb.2012.77.015933openalex-snapshot

Effector Biology of Plant-Associated Organisms: Concepts and Perspectives

inferredcites →https://doi.org/10.1104/pp.102.017814openalex-snapshot

A Role for the GCC-Box in Jasmonate-Mediated Activation of the PDF1.2 Gene of Arabidopsis

inferredcites →https://doi.org/10.1104/pp.105.063743openalex-snapshot

Genome-Wide Identification and Testing of Superior Reference Genes for Transcript Normalization in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.105.068544openalex-snapshot

Repressor- and Activator-Type Ethylene Response Factors Functioning in Jasmonate Signaling and Disease Resistance Identified via a Genome-Wide Screen of Arabidopsis Transcription Factor Gene Expression

inferredcites →https://doi.org/10.1104/pp.108.117523openalex-snapshot

The AP2/ERF Domain Transcription Factor ORA59 Integrates Jasmonic Acid and Ethylene Signals in Plant Defense

inferredcites →https://doi.org/10.1104/pp.109.151704openalex-snapshot

Genome-Wide Analysis of Ethylene-Responsive Element Binding Factor-Associated Amphiphilic Repression Motif-Containing Transcriptional Regulators in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.111.180661openalex-snapshot

Green Light Induces Shade Avoidance Symptoms

inferredcites →https://doi.org/10.1104/pp.111.186999openalex-snapshot

The TOPLESS Interactome: A Framework for Gene Repression in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.15.01246openalex-snapshot

MultiSite Gateway-Compatible Cell Type-Specific Gene-Inducible System for Plants

inferredcites →https://doi.org/10.1105/tpc.007468openalex-snapshot

ETHYLENE RESPONSE FACTOR1 Integrates Signals from Ethylene and Jasmonate Pathways in Plant Defense[W]

inferredcites →https://doi.org/10.1105/tpc.010127openalex-snapshot

Repression Domains of Class II ERF Transcriptional Repressors Share an Essential Motif for Active Repression

inferredcites →https://doi.org/10.1105/tpc.016980openalex-snapshot

The WRKY70 Transcription Factor: A Node of Convergence for Jasmonate-Mediated and Salicylate-Mediated Signals in Plant Defense[W]

inferredcites →https://doi.org/10.1105/tpc.104.027441openalex-snapshot

Interaction of NIMIN1 with NPR1 Modulates PR Gene Expression in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.105.039107openalex-snapshot

Analysis of the Transcription Factor WUSCHEL and Its Functional Homologue in Antirrhinum Reveals a Potential Mechanism for Their Roles in Meristem Maintenance

inferredcites →https://doi.org/10.1105/tpc.106.048017openalex-snapshot

MYC2 Differentially Modulates Diverse Jasmonate-Dependent Functions in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.112.108548openalex-snapshot

Salicylic Acid Suppresses Jasmonic Acid Signaling Downstream of SCFCOI1-JAZ by Targeting GCC Promoter Motifs via Transcription Factor ORA59

inferredcites →https://doi.org/10.1105/tpc.114.131086openalex-snapshot

A Secreted Effector Protein of Ustilago maydis Guides Maize Leaf Cells to Form Tumors

inferredcites →https://doi.org/10.1105/tpc.13.8.1959openalex-snapshot

Repression Domains of Class II ERF Transcriptional Repressors Share an Essential Motif for Active Repression

inferredcites →https://doi.org/10.1105/tpc.17.00764openalex-snapshot

The Biotrophic Development of Ustilago maydis Studied by RNA-Seq Analysis

inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03590.xopenalex-snapshot

Reprogramming a maize plant: transcriptional and metabolic changes induced by the fungal biotroph Ustilago maydis

inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03831.xopenalex-snapshot

Fusarium oxysporum hijacks COI1‐mediated jasmonate signaling to promote disease development in Arabidopsis

inferredcites →https://doi.org/10.1111/mpp.12117openalex-snapshot

Host perception of jasmonates promotes infection by F usarium oxysporum formae speciales that produce isoleucine‐ and leucine‐conjugated jasmonates

inferredcites →https://doi.org/10.1111/mpp.12442openalex-snapshot

Characterization of ApB73, a virulence factor important for colonization of Zea mays by the smut Ustilago maydis

inferredcites →https://doi.org/10.1111/mpp.12869openalex-snapshot

RNA‐Seq of in planta ‐expressed Magnaporthe oryzae genes identifies MoSVP as a highly expressed gene required for pathogenicity at the initial stage of infection

inferredcites →https://doi.org/10.1126/science.1151461openalex-snapshot

TOPLESS Mediates Auxin-Dependent Transcriptional Repression During Arabidopsis Embryogenesis

inferredcites →https://doi.org/10.1126/science.1203659openalex-snapshot

Independently Evolved Virulence Effectors Converge onto Hubs in a Plant Immune System Network

inferredcites →https://doi.org/10.1146/annurev-arplant-042817-040047openalex-snapshot

Modularity in Jasmonate Signaling for Multistress Resilience

inferredcites →https://doi.org/10.1146/annurev-arplant-043014-114623openalex-snapshot

Fungal Effectors and Plant Susceptibility

inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154055openalex-snapshot

Hormonal Modulation of Plant Immunity

inferredcites →https://doi.org/10.1146/annurev.phyto.42.040803.140421openalex-snapshot

SYSTEMIC ACQUIRED RESISTANCE

inferredcites →https://doi.org/10.1186/s12870-014-0214-6openalex-snapshot

Cadmium-induced ethylene production and responses in Arabidopsis thaliana rely on ACS2 and ACS6 gene expression

inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

inferredcites →https://doi.org/10.1371/journal.pbio.1001792openalex-snapshot

The Bacterial Effector HopX1 Targets JAZ Transcriptional Repressors to Activate Jasmonate Signaling and Promote Infection in Arabidopsis

inferredcites →https://doi.org/10.1371/journal.pbio.2005129openalex-snapshot

In vivo insertion pool sequencing identifies virulence factors in a complex fungal–host interaction

inferredcites →https://doi.org/10.1371/journal.pone.0035995openalex-snapshot

ERF5 and ERF6 Play Redundant Roles as Positive Regulators of JA/Et-Mediated Defense against Botrytis cinerea in Arabidopsis

inferredcites →https://doi.org/10.1371/journal.pone.0083043openalex-snapshot

GreenGate - A Novel, Versatile, and Efficient Cloning System for Plant Transgenesis

inferredcites →https://doi.org/10.1371/journal.ppat.1002684openalex-snapshot

The Ustilago maydis Effector Pep1 Suppresses Plant Immunity by Inhibition of Host Peroxidase Activity

inferredcites →https://doi.org/10.1371/journal.ppat.1002711openalex-snapshot

Large-Scale Gene Disruption in Magnaporthe oryzae Identifies MC69, a Secreted Protein Required for Infection by Monocot and Dicot Fungal Pathogens

inferredcites →https://doi.org/10.1371/journal.ppat.1003177openalex-snapshot

Compatibility in the Ustilago maydis–Maize Interaction Requires Inhibition of Host Cysteine Proteases by the Fungal Effector Pit2

inferredcites →https://doi.org/10.1371/journal.ppat.1005228openalex-snapshot

Structure Analysis Uncovers a Highly Diverse but Structurally Conserved Effector Family in Phytopathogenic Fungi

inferredcites →https://doi.org/10.1534/genetics.109.107102openalex-snapshot

A Combinatorial Interplay Among the 1-Aminocyclopropane-1-Carboxylate Isoforms Regulates Ethylene Biosynthesis in Arabidopsis thaliana

inferredcites →https://doi.org/10.3389/fpls.2015.00170openalex-snapshot

How salicylic acid takes transcriptional control over jasmonic acid signaling

inferredcites →https://doi.org/10.3389/fpls.2017.01210openalex-snapshot

DEWAX Transcription Factor Is Involved in Resistance to Botrytis cinerea in Arabidopsis thaliana and Camelina sativa

inferredcites →https://doi.org/10.3791/53364openalex-snapshot

Bacterial Leaf Infiltration Assay for Fine Characterization of Plant Defense Responses using the Arabidopsis thaliana-Pseudomonas syringae Pathosystem

inferredcites →https://doi.org/10.4161/psb.19283openalex-snapshot

TOPLESS co-repressor interactions and their evolutionary conservation in plants

inferredcites →https://doi.org/10.4161/psb.23891openalex-snapshot

The DELLA protein RGL3 positively contributes to jasmonate/ethylene defense responses

inferredcites →https://doi.org/10.7554/elife.01355openalex-snapshot

A secreted Ustilago maydis effector promotes virulence by targeting anthocyanin biosynthesis in maize

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.xplc.2020.100050openalex-snapshot

All Roads Lead to Susceptibility: The Many Modes of Action of Fungal and Oomycete Intracellular Effectors

inferred← citeshttps://doi.org/10.1016/j.xplc.2021.100269openalex-snapshot

TOPLESS promotes plant immunity by repressing auxin signaling and is targeted by the fungal effector Naked1

inferred← citeshttps://doi.org/10.3389/fmicb.2023.1178258openalex-snapshot

Susceptibility and plant immune control—a case of mycorrhizal strategy for plant colonization, symbiosis, and plant immune suppression

inferred← citeshttps://doi.org/10.3389/fpls.2020.543895openalex-snapshot

Engineering Smut Resistance in Maize by Site-Directed Mutagenesis of LIPOXYGENASE 3

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