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Updated: Jun 20, 2025

Genome-wide Analysis of Histone Modifications Distribution using the Chromatin Immunoprecipitation Sequencing Method in Magnaporthe oryzae
Published on: June 2, 2021
A novel MAP kinase-interacting protein MoSmi1 regulates development and pathogenicity in Magnaporthe oryzae
Yu Wang1,2, Xinyue Cui1,2, Junlian Xiao1,2
1Department of Plant Pathology, College of Plant Protection, Anhui Agricultural University, Hefei, China.
Abstract:
The cell wall is the first barrier against external adversity and plays roles in maintaining normal physiological functions of fungi. Previously, we reported a nucleosome assembly protein, MoNap1, in Magnaporthe oryzae that plays a role in cell wall integrity (CWI), stress response, and pathogenicity. Moreover, MoNap1 negatively regulates the expression of MoSMI1 encoded by MGG_03970. Here, we demonstrated that deletion of MoSMI1 resulted in a significant defect in appressorium function, CWI, cell morphology, and pathogenicity. Further investigation revealed that MoSmi1 interacted with MoOsm1 and MoMps1 and affected the phosphorylation levels of MoOsm1, MoMps1, and MoPmk1, suggesting that MoSmi1 regulates biological functions by mediating mitogen-activated protein kinase (MAPK) signalling pathway in M. oryzae. In addition, transcriptome data revealed that MoSmi1 regulates many infection-related processes in M. oryzae, such as membrane-related pathway and oxidation reduction process. In conclusion, our study demonstrated that MoSmi1 regulates CWI by mediating the MAPK pathway to affect development and pathogenicity of M. oryzae.
Insights
The study reveals MoSmi1 is crucial for fungal cell wall integrity and pathogenicity in Magnaporthe oryzae. Deleting MoSmi1 impairs appressorium function and MAPK signaling, impacting fungal development.
Area of Science:
- Mycology
- Molecular Biology
- Plant Pathology
Background:
- The fungal cell wall is vital for maintaining physiological functions and resisting external stress.
- MoNap1, a nucleosome assembly protein in Magnaporthe oryzae, influences cell wall integrity (CWI), stress response, and pathogenicity.
- MoNap1 negatively regulates the expression of MoSMI1.
Purpose of the Study:
- To investigate the function of MoSMI1 in Magnaporthe oryzae.
- To elucidate the role of MoSmi1 in regulating cell wall integrity, development, and pathogenicity.
- To understand the molecular mechanisms underlying MoSmi1's function, particularly its interaction with signaling pathways.
Main Methods:
- Gene deletion of MoSMI1 in Magnaporthe oryzae.
- Analysis of appressorium function, cell morphology, and pathogenicity in MoSMI1 deletion mutants.
- Protein interaction studies (MoSmi1 with MoOsm1 and MoMps1).
- Phosphorylation level analysis of key MAPK pathway components (MoOsm1, MoMps1, MoPmk1).
- Transcriptome analysis to identify regulated processes.
Main Results:
- Deletion of MoSMI1 caused significant defects in appressorium function, CWI, cell morphology, and pathogenicity.
- MoSmi1 interacts with MoOsm1 and MoMps1, affecting the phosphorylation of MoOsm1, MoMps1, and MoPmk1.
- Transcriptome data indicated MoSmi1 regulates membrane-related pathways and oxidation-reduction processes.
- MoSmi1 plays a critical role in mediating the mitogen-activated protein kinase (MAPK) signaling pathway.
Conclusions:
- MoSmi1 is essential for maintaining cell wall integrity and pathogenicity in Magnaporthe oryzae.
- MoSmi1 regulates CWI and fungal development by mediating the MAPK signaling pathway.
- The findings highlight MoSmi1 as a key regulator of infection-related processes in M. oryzae.
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