Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Multi-proteomic profiling indicates potential regulatory signatures underlying rice resistance to Magnaporthe oryzae.

The Plant journal : for cell and molecular biology - 1 Apr 2026

Auler Priscila A, Montes-Serey Christian, Arge Luis W P, Song Gaoyuan, Walley Justin, Silva-Filho Marcio C

Abstract excerpt

Omics-driven approaches can capture systemic plant responses to pathogens. While transcriptomics is a mainstay, it alone cannot capture post-translational modifications or protein abundance. Because of this, we employed multi-proteomics to compare the proteome, phosphoproteome, and acetylome of two rice genotypes differing in resistance to Magnaporthe oryzae during early infection (12, 24, and 48 h...

Topics

Join the communities discussing this publication.

Ascomycota
Disease Resistance
Magnaporthe
Oryza
Plant Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Protein Processing, Post-Translational

Source

Open in PubMed Open full text

Identifiers

PMID: 42013299
DOI: 10.1111/tpj.70892
PMCID: PMC13099112

Genes

PTEN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multi-proteomic profiling indicates potential regulatory signatures underlying rice resistance to Magnaporthe oryzae.PMID 42013299Read ↗

Proteomic signatures uncover phenotypic plasticity of susceptible and resistant genotypes by wall remodelers in rice blast.Semantic proximity Read ↗

Genome-wide transcriptional profiling of appressorium development by the rice blast fungus Magnaporthe oryzae.Semantic proximity Read ↗

Understanding Rice-Magnaporthe Oryzae Interaction in Resistant and Susceptible Cultivars of Rice under Panicle Blast Infection Using a Time-Course Transcriptome Analysis.Semantic proximity Read ↗

iTRAQ proteomics reveals the regulatory response to Magnaporthe oryzae in durable resistant vs. susceptible rice genotypes.Semantic proximity Read ↗

High temperature effects on Pi54 conferred resistance to Magnaporthe oryzae in two genetic backgrounds of Oryza sativa.Semantic proximity Read ↗

Transcriptome analysis of protein kinase MoCK2 affect acetyl-CoA metabolism and import of CK2 interacting mitochondrial proteins into mitochondria in rice blast fungus <i>Magnaporthe oryzae</i>Semantic proximity Read ↗

Multi-omics analysis revealed that the protein kinase MoKin1 affected the cellular response to endoplasmic reticulum stress in the rice blast fungus, Magnaporthe oryzae.Semantic proximity Read ↗

MoPtc6, a Type 2C Protein Phosphatase Plays Critical Roles in the Development and Virulence of <i>Magnaporthe oryzae</i>Semantic proximity Read ↗

An array of signal-specific MoYpd1 isoforms determines full virulence in the pathogenic fungus <i>Magnaporthe oryzae</i>Semantic proximity Read ↗

OsCAMTA3 Negatively Regulates Disease Resistance to Magnaporthe oryzae by Associating with OsCAMTAPL in Rice.Semantic proximity Read ↗

Knockout of Pi21 by CRISPR/Cas9 and iTRAQ-Based Proteomic Analysis of Mutants Revealed New Insights into M. oryzae Resistance in Elite Rice Line.Semantic proximity Read ↗

Proteomic Responses to Drought Vary Widely Among Eight Diverse Genotypes of Rice (Oryza sativa).Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.