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Updated: Nov 4, 2025

Genome-wide Analysis of Histone Modifications Distribution using the Chromatin Immunoprecipitation Sequencing Method in Magnaporthe oryzae
Published on: June 2, 2021
MoWhi2 regulates appressorium formation and pathogenicity via the MoTor signalling pathway in Magnaporthe oryzae
Huanbin Shi1, Shuai Meng1,2, Jiehua Qiu1
1State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China.
Abstract:
Magnaporthe oryzae causes rice blast disease, which seriously threatens the safety of food production. Understanding the mechanism of appressorium formation, which is one of the key steps for successful infection by M. oryzae, is helpful to formulate effective control strategies of rice blast. In this study, we identified MoWhi2, the homolog of Saccharomyces cerevisiae Whi2 (Whisky2), as an important regulator that controls appressorium formation in M. oryzae. When MoWHI2 was disrupted, multiple appressoria were formed by one conidium and pathogenicity was significantly reduced. A putative phosphatase, MoPsr1, was identified to interact with MoWhi2 using a yeast two-hybridization screening assay. The knockout mutant ΔMopsr1 displayed similar phenotypes to the ΔMowhi2 strain. Both the ΔMowhi2 and ΔMopsr1 mutants could form appressoria on a hydrophilic surface with cAMP levels increasing in comparison with the wild type (WT). The conidia of ΔMowhi2 and ΔMopsr1 formed a single appressorium per conidium, similar to WT, when the target of rapamycin (TOR) inhibitor rapamycin was present. In addition, compared with WT, the expression levels of MoTOR and the MoTor signalling activation marker gene MoRS3 were increased, suggesting that inappropriate activation of the MoTor signalling pathway is one of the important reasons for the defects in appressorium formation in the ΔMowhi2 and ΔMopsr1 strains. Our results provide insights into MoWhi2 and MoPsr1-mediated appressorium development and pathogenicity by regulating cAMP levels and the activation of MoTor signalling in M. oryzae.
Insights
Researchers identified MoWhi2 and MoPsr1 proteins that regulate rice blast fungus appressorium formation. Disrupting these proteins impairs pathogenicity by affecting cAMP levels and the MoTor signaling pathway.
Area of Science:
- Plant Pathology
- Molecular Mycology
- Fungal Pathogenesis
Background:
- Rice blast disease, caused by Magnaporthe oryzae, poses a significant threat to global food security.
- Appressorium formation is a critical stage in M. oryzae infection, making its regulatory mechanisms a key target for control strategies.
Purpose of the Study:
- To identify and characterize novel regulators of appressorium formation in Magnaporthe oryzae.
- To elucidate the roles of MoWhi2 and MoPsr1 in M. oryzae pathogenicity and infection processes.
Main Methods:
- Yeast two-hybridization screening to identify interacting proteins.
- Gene disruption (knockout) to analyze the function of MoWHI2 and MoPSR1.
- Phenotypic analysis of mutants, including appressoria formation assays and pathogenicity tests.
- Measurement of intracellular cAMP levels and analysis of MoTor signaling pathway activation.
Main Results:
- Disruption of MoWHI2 led to multiple appressoria formation and reduced pathogenicity.
- MoPsr1 was identified as an interacting protein of MoWhi2, and its knockout exhibited similar defects.
- Both mutants showed altered appressoria formation on hydrophilic surfaces, with increased cAMP levels.
- The target of rapamycin (TOR) inhibitor rapamycin restored single appressorium formation in mutants.
- Increased expression and activation of the MoTor signaling pathway were observed in the mutants, suggesting its dysregulation.
Conclusions:
- MoWhi2 and MoPsr1 are crucial regulators of appressorium development and pathogenicity in M. oryzae.
- These proteins likely mediate their effects by modulating intracellular cAMP levels and the activation of the MoTor signaling pathway.
- Understanding these regulatory mechanisms offers potential targets for developing novel rice blast control strategies.
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