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The phosphatase Ptc6 is involved in virulence and MAPK signalling in Fusarium oxysporum

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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/yea.1109openalex-snapshot

Characterization of the transcriptional response to cell wall stress in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1002/yea.1739openalex-snapshot

Identification and characterization of the type 2C protein phosphatase Ptc4p in the human fungal pathogen Candida albicans

inferredcites →https://doi.org/10.1002/yea.1743openalex-snapshot

Candida albicans CaPTC6 is a functional homologue for Saccharomyces cerevisiae ScPTC6 and encodes a type 2C protein phosphatase

inferredcites →https://doi.org/10.1002/yea.1778openalex-snapshot

Functional characterization of the PP2C phosphatase CaPtc2p in the human fungal pathogen Candida albicans

inferredcites →https://doi.org/10.1002/yea.860openalex-snapshot

A series of double disruptants for protein phosphatase genes in Saccharomyces cerevisiae and their phenotypic analysis

inferredcites →https://doi.org/10.1006/abio.1987.9999openalex-snapshot

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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/10.1016/0003-2697(87)90021-2openalex-snapshot

Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction

inferredcites →https://doi.org/10.1016/0076-6879(92)16041-hopenalex-snapshot

[39] Transformation of filamentous fungi based on hygromycin b and phleomycin resistance markers

inferredcites →https://doi.org/10.1016/j.bbamcr.2007.05.003openalex-snapshot

Function and regulation in MAPK signaling pathways: Lessons learned from the yeast Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1016/j.celrep.2016.12.049openalex-snapshot

Ptc7p Dephosphorylates Select Mitochondrial Proteins to Enhance Metabolic Function

inferredcites →https://doi.org/10.1016/j.febslet.2006.04.002openalex-snapshot

YIL042c and YOR090c encode the kinase and phosphatase of the Saccharomyces cerevisiae pyruvate dehydrogenase complex

inferredcites →https://doi.org/10.1016/j.fgb.2010.12.004openalex-snapshot

The osmosensing signal transduction pathway from Botrytis cinerea regulates cell wall integrity and MAP kinase pathways control melanin biosynthesis with influence of light

inferredcites →https://doi.org/10.1016/j.fgb.2018.05.004openalex-snapshot

Role of the phosphatase Ptc1 in stress responses mediated by CWI and HOG pathways in Fusarium oxysporum

inferredcites →https://doi.org/10.1016/j.gene.2008.10.022openalex-snapshot

A serine/threonine protein phosphatase-like protein, CaPTC8, from Candida albicans defines a new PPM subfamily

inferredcites →https://doi.org/10.1016/j.jbiosc.2014.09.013openalex-snapshot

Type 2C protein phosphatase Ptc6 participates in activation of the Slt2-mediated cell wall integrity pathway in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1016/j.jmb.2007.09.025openalex-snapshot

Promiscuous Stimulation of ParF Protein Polymerization by Heterogeneous Centromere Binding Factors

inferredcites →https://doi.org/10.1016/s0014-5793(01)03125-8openalex-snapshot

A novel type 2C protein phosphatase from the human fungal pathogen Candida albicans

inferredcites →https://doi.org/10.1038/nature15516openalex-snapshot

Fungal pathogen uses sex pheromone receptor for chemotropic sensing of host plant signals

inferredcites →https://doi.org/10.1038/nmicrobiol.2016.43openalex-snapshot

A fungal pathogen secretes plant alkalinizing peptides to increase infection

inferredcites →https://doi.org/10.1038/s41564-019-0456-zopenalex-snapshot

Autocrine pheromone signalling regulates community behaviour in the fungal pathogen Fusarium oxysporum

inferredcites →https://doi.org/10.1046/j.1432-1327.2002.02814.xopenalex-snapshot

Involvement of GFA1, which encodes glutamine–fructose‐6‐phosphate amidotransferase, in the activation of the chitin synthesis pathway in response to cell‐wall defects in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1074/jbc.m117.787341openalex-snapshot

Integrative proteomics and biochemical analyses define Ptc6p as the Saccharomyces cerevisiae pyruvate dehydrogenase phosphatase

inferredcites →https://doi.org/10.1074/jbc.m605940200openalex-snapshot

Aup1p, a Yeast Mitochondrial Protein Phosphatase Homolog, Is Required for Efficient Stationary Phase Mitophagy and Cell Survival

inferredcites →https://doi.org/10.1074/jbc.m607919200openalex-snapshot

Transcriptional Profiling of the Protein Phosphatase 2C Family in Yeast Provides Insights into the Unique Functional Roles of Ptc1

inferredcites →https://doi.org/10.1074/jbc.m708779200openalex-snapshot

Yeast Pyruvate Dehydrogenase Complex Is Regulated by a Concerted Activity of Two Kinases and Two Phosphatases

inferredcites →https://doi.org/10.1080/10409230701693342openalex-snapshot

Role of Type 2C Protein Phosphatases in Growth Regulation and in Cellular Stress Signaling

inferredcites →https://doi.org/10.1083/jcb.114.1.111openalex-snapshot

The function of chitin synthases 2 and 3 in the Saccharomyces cerevisiae cell cycle.

inferredcites →https://doi.org/10.1091/mbc.e08-09-0954openalex-snapshot

PTC1Is Required for Vacuole Inheritance and Promotes the Association of the Myosin-V Vacuole-specific Receptor Complex

inferredcites →https://doi.org/10.1093/genetics/60.3.461openalex-snapshot

COMPATIBILITY REACTIONS ON SOLID MEDIUM AND INTERSTRAIN INHIBITION IN USTILAGO MAYDIS

inferredcites →https://doi.org/10.1094/mpmi-22-7-0830openalex-snapshot

Fusarium oxysporum Ste12 Controls Invasive Growth and Virulence Downstream of the Fmk1 MAPK Cascade

inferredcites →https://doi.org/10.1094/mpmi.1998.11.2.91openalex-snapshot

Cloning, Expression, and Role in Pathogenicity of pg1 Encoding the Major Extracellular Endopolygalacturonase of the Vascular Wilt Pathogen Fusarium oxysporum

inferredcites →https://doi.org/10.1101/gad.10.21.2696openalex-snapshot

MAP kinase and cAMP signaling regulate infection structure formation and pathogenic growth in the rice blast fungus Magnaporthe grisea.

inferredcites →https://doi.org/10.1101/gad.13.22.2946openalex-snapshot

Dephosphorylation of cyclin-dependent kinases by type 2C protein phosphatases

inferredcites →https://doi.org/10.1105/tpc.110.075093openalex-snapshot

The Membrane Mucin Msb2 Regulates Invasive Growth and Plant Infection in Fusarium oxysporum

inferredcites →https://doi.org/10.1105/tpc.110.075937openalex-snapshot

A Nitrogen Response Pathway Regulates Virulence Functions in Fusarium oxysporum via the Protein Kinase TOR and the bZIP Protein MeaB

inferredcites →https://doi.org/10.1111/1462-2920.12126openalex-snapshot

Involvement of two type 2 C protein phosphatases B c P tc1 and B c P tc3 in the regulation of multiple stress tolerance and virulence of B otrytis cinerea

inferredcites →https://doi.org/10.1111/j.1364-3703.2009.00598.xopenalex-snapshot

The Type 2C protein phosphatase FgPtc1p of the plant fungal pathogen Fusarium graminearum is involved in lithium toxicity and virulence

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/j.1365-2958.2001.02307.xopenalex-snapshot

A MAP kinase of the vascular wilt fungus Fusarium oxysporum is essential for root penetration and pathogenesis

inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05370.xopenalex-snapshot

Role of protein phosphatases 2C on tolerance to lithium toxicity in the yeast Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1111/j.1472-765x.1985.tb01479.xopenalex-snapshot

Rapid preparation of DNA from filamentous fungi

inferredcites →https://doi.org/10.1111/j.1567-1364.2006.00160.xopenalex-snapshot

TheYCR079wgene confers a rapamycin-resistant function and encodes the sixth type 2C protein phosphatase inSaccharomyces cerevisiae

inferredcites →https://doi.org/10.1111/j.1567-1364.2012.00840.xopenalex-snapshot

Mithochondrial type 2C protein phosphatases CaPtc5p, CaPtc6p, and CaPtc7p play vital roles in cellular responses to antifungal drugs and cadmium inCandida albicans

inferredcites →https://doi.org/10.1111/mmi.12919openalex-snapshot

H igh osmolarity glycerol response PtcB phosphatase is important for A spergillus fumigatus virulence

inferredcites →https://doi.org/10.1111/mpp.12446openalex-snapshot

Three Fusarium oxysporum mitogen‐activated protein kinases (MAPKs) have distinct and complementary roles in stress adaptation and cross‐kingdom pathogenicity

inferredcites →https://doi.org/10.1128/cmr.00014-07openalex-snapshot

Fusarium Infections in Immunocompromised Patients

inferredcites →https://doi.org/10.1128/ec.00129-08openalex-snapshot

Identification of the Putative Protein Phosphatase GenePTC1as a Virulence-Related Gene Using a Silkworm Model ofCandida albicansInfection

inferredcites →https://doi.org/10.1128/ec.00249-10openalex-snapshot

Type 2C Protein Phosphatases in Fungi

inferredcites →https://doi.org/10.1128/ec.00258-07openalex-snapshot

Vegetative Hyphal Fusion Is Not Essential for Plant Infection by Fusarium oxysporum

inferredcites →https://doi.org/10.1128/ec.1.6.1032-1040.2002openalex-snapshot

Role of Ptc2 Type 2C Ser/Thr Phosphatase in Yeast High-Osmolarity Glycerol Pathway Inactivation

inferredcites →https://doi.org/10.1128/mcb.01740-08openalex-snapshot

Normal Function of the Yeast TOR Pathway Requires the Type 2C Protein Phosphatase Ptc1

inferredcites →https://doi.org/10.1128/mcb.14.6.3634openalex-snapshot

TPD1 of Saccharomyces cerevisiae encodes a protein phosphatase 2C-like activity implicated in tRNA splicing and cell separation.

inferredcites →https://doi.org/10.1128/mcb.14.6.3742openalex-snapshot

Protein phosphatase 2C, encoded by ptc1+, is important in the heat shock response of Schizosaccharomyces pombe.

inferredcites →https://doi.org/10.1128/mmbr.69.2.262-291.2005openalex-snapshot

Cell Wall Integrity Signaling in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1139/w06-125openalex-snapshot

Expression ofCaPTC7is developmentally regulated during serum-induced morphogenesis in the human fungal pathogen Candida albicans

inferredcites →https://doi.org/10.1146/annurev-phyto-102313-050143openalex-snapshot

Protein Kinases in Plant-Pathogenic Fungi: Conserved Regulators of Infection

inferredcites →https://doi.org/10.1146/annurev.bi.58.070189.002321openalex-snapshot

THE STRUCTURE AND REGULATION OF PROTEIN PHOSPHATASES

inferredcites →https://doi.org/10.1152/physrev.1999.79.1.143openalex-snapshot

Mitogen-Activated Protein Kinase: Conservation of a Three-Kinase Module From Yeast to Human

inferredcites →https://doi.org/10.1371/journal.pone.0025311openalex-snapshot

A Type 2C Protein Phosphatase FgPtc3 Is Involved in Cell Wall Integrity, Lipid Metabolism, and Virulence in Fusarium graminearum

inferredcites →https://doi.org/10.1385/1-59745-227-0:1openalex-snapshot

Total Protein Extraction with TCA-Acetone

inferredcites →https://doi.org/10.1534/g3.113.008813openalex-snapshot

Global Analysis of Serine/Threonine and Tyrosine Protein Phosphatase Catalytic Subunit Genes inNeurospora crassaReveals Interplay Between Phosphatases and the p38 Mitogen-Activated Protein Kinase

inferredcites →https://doi.org/10.1534/g3.115.016766openalex-snapshot

Systematic Global Analysis of Genes Encoding Protein Phosphatases inAspergillus fumigatus

inferredcites →https://doi.org/10.3389/fmicb.2016.02014openalex-snapshot

Phenylpyrroles: 30 Years, Two Molecules and (Nearly) No Resistance

inferredcites →https://doi.org/10.3390/jof4010001openalex-snapshot

The CWI Pathway: Regulation of the Transcriptional Adaptive Response to Cell Wall Stress in Yeast

inferredcites →https://doi.org/10.4148/1941-4765.1150openalex-snapshot

Split-Marker Recombination for Efficient Targeted Deletion of Fungal Genes

inferredcites →https://doi.org/10.4148/1941-4765.1367openalex-snapshot

Improved Vectors for Selecting Resistance to Hygromycin

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.4869519openalex-extracted

Soil Microbes Determine Outcomes of Pathogenic Interactions Between Radopholus similis and Fusarium oxysporum V5w2 in Tissue Culture Banana Rhizospheres Starved of Nitrogen, Phosphorus, and Potassium

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.09.211openalex-snapshot

Insights into intracellular signaling network in Fusarium species

inferred← citeshttps://doi.org/10.1016/j.micres.2024.127975openalex-snapshot

Foisc1 regulates growth, conidiation, sensitivity to salicylic acid, and pathogenicity of Fusarium oxysporum f. sp. cubense tropical race 4

inferred← citeshttps://doi.org/10.1016/j.micres.2026.128589openalex-snapshot

The SET domain group protein FonSDG1 regulates virulence through modulating the expression of ammonium permeases in Fusarium oxysporum f. sp. niveum

inferred← citeshttps://doi.org/10.1021/acs.jafc.2c07539openalex-snapshot

Metabolomic and Transcriptome Analysis of the Inhibitory Effects of Bacillus subtilis Strain Z-14 against Fusarium oxysporum Causing Vascular Wilt Diseases in Cucumber

inferred← citeshttps://doi.org/10.1038/s42003-024-05942-yopenalex-snapshot

GlPRMT5 inhibits GlPP2C1 via symmetric dimethylation and regulates the biosynthesis of secondary metabolites in Ganoderma lucidum

inferred← citeshttps://doi.org/10.1094/phyto-09-22-0320-ropenalex-snapshot

The Phosphatase VdPtc3 Regulates Virulence inVerticillium dahliaeby Interacting with VdAtg1

inferred← citeshttps://doi.org/10.1101/2022.08.08.503127openalex-snapshot

Constitutive activation of TORC1 signaling attenuates virulence in the cross-kingdom fungal pathogen Fusarium oxysporum

inferred← citeshttps://doi.org/10.1101/2025.09.09.675095openalex-snapshot

Multilayered Transcriptomic Reprogramming and Spliceosomal Divergence Shape Bipolaris sorokiniana Pathogenicity

inferred← citeshttps://doi.org/10.1111/mpp.13292openalex-snapshot

Constitutive activation of TORC1 signalling attenuates virulence in the cross‐kingdom fungal pathogen Fusarium oxysporum

inferred← citeshttps://doi.org/10.1111/mpp.13427openalex-snapshot

Plant–pathogen interaction with root rot of Panax notoginseng as a model: Insight into pathogen pathogenesis, plant defence response and biological control

inferred← citeshttps://doi.org/10.1128/mbio.00157-23openalex-snapshot

Fusarium oxysporum f. sp. niveum Pumilio 1 Regulates Virulence on Watermelon through Interacting with the ARP2/3 Complex and Binding to an A-Rich Motif in the 3′ UTR of Diverse Transcripts

inferred← citeshttps://doi.org/10.1128/mbio.00977-23openalex-snapshot

PP2C phosphatases Ptc1 and Ptc2 dephosphorylate PGK1 to regulate autophagy and aflatoxin synthesis in the pathogenic fungus Aspergillus flavus

inferred← citeshttps://doi.org/10.1186/s12864-022-08856-3openalex-snapshot

Transcriptome-wide identification of walnut PP2C family genes in response to external stimulus

inferred← citeshttps://doi.org/10.1186/s12870-025-07764-4openalex-snapshot

Genome-wide identification and functional characterization of PP2C genes in the wild relative of sweet potato Ipomoea trifida

inferred← citeshttps://doi.org/10.3389/fpls.2022.969343openalex-snapshot

Mechanisms of plant cell wall surveillance in response to pathogens, cell wall-derived ligands and the effect of expansins to infection resistance or susceptibility

inferred← citeshttps://doi.org/10.3389/fsufs.2022.706072openalex-snapshot

Soil Microbes Determine Outcomes of Pathogenic Interactions Between Radopholus similis and Fusarium oxysporum V5w2 in Tissue Culture Banana Rhizospheres Starved of Nitrogen, Phosphorus, and Potassium

inferred← citeshttps://doi.org/10.3390/jof11050335openalex-snapshot

Type 2C Protein Phosphatase MoPtc6 Plays Critical Roles in the Development and Virulence of Magnaporthe oryzae

inferred← citeshttps://doi.org/10.3390/pathogens13100823openalex-snapshot

The Ubiquitous Wilt-Inducing Pathogen Fusarium oxysporum—A Review of Genes Studied with Mutant Analysis

inferred← citeshttps://doi.org/10.6084/m9.figshare.21069686openalex-snapshot

Additional file 1 of Transcriptome-wide identification of walnut PP2C family genes in response to external stimulus

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