Transcriptome Analysis Reveals That a Gti1/Pac2 Family Gene, CpSge1, Regulates Fungal Growth, Stress Response, and Virulence in Cryphonectria parasitica.
{"title":"Transcriptome Analysis Reveals That a Gti1/Pac2 Family Gene, <i>CpSge1</i>, Regulates Fungal Growth, Stress Response, and Virulence in <i>Cryphonectria parasitica</i>.","authors":"Xiaorong Lin, Yuchen Yang, Can Huang, Dianguang Xiong, Xiaolin Qiu, Chengming Tian","doi":"10.1094/PHYTO-11-24-0354-R","DOIUrl":null,"url":null,"abstract":"<p><p>The Gti1/Pac2 family comprises crucial transcription factors widely distributed in fungi with generally two members Gti1 (also known as Wor1, Ryp1 or Sge1) and Pac2, where the Gti1 homologues play significant roles in growth, spore production, and pathogenicity of various pathogenic fungi. Despite its recognized significance, the roles of this family in <i>Cryphonectria parasitica</i>, the pathogen responsible for chestnut blight (a globally significant forest disease) remain unexplored. In this study, <i>CpSge1</i> was identified in <i>C. parasitica</i> and then knocked out to explore its functions. The results showed that <i>CpSge1</i> significantly affected vegetative growth, conidiation, hydrophobicity, and stress tolerance of <i>C. parasitica</i>. Notably, the <i>CpSge1</i> deletion mutants were significantly less pathogenic compared to the wild type. Transcriptomic analysis of the wild type and the <i>CpSge1</i> deletion mutant during vegetative growth and infection stages revealed that CpSge1 regulated a number of pathogenicity-related genes in <i>C. parasitica</i>. Yeast one hybrid verified the direct binding of CpSge1 to the promoter regions of genes encoding pectin lyase <i>CpPL1</i> and major facilitator superfamily transporter <i>CpMF1</i>. In summary, these data suggest that <i>CpSge1</i> is the core regulator of fungal growth, stress tolerance, gene expression, and virulence in <i>C. parasitica</i>, which may improve our understanding on the molecular pathogenesis of <i>C. parasitica</i> and then help us to develop effective control strategies.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytopathology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1094/PHYTO-11-24-0354-R","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
The Gti1/Pac2 family comprises crucial transcription factors widely distributed in fungi with generally two members Gti1 (also known as Wor1, Ryp1 or Sge1) and Pac2, where the Gti1 homologues play significant roles in growth, spore production, and pathogenicity of various pathogenic fungi. Despite its recognized significance, the roles of this family in Cryphonectria parasitica, the pathogen responsible for chestnut blight (a globally significant forest disease) remain unexplored. In this study, CpSge1 was identified in C. parasitica and then knocked out to explore its functions. The results showed that CpSge1 significantly affected vegetative growth, conidiation, hydrophobicity, and stress tolerance of C. parasitica. Notably, the CpSge1 deletion mutants were significantly less pathogenic compared to the wild type. Transcriptomic analysis of the wild type and the CpSge1 deletion mutant during vegetative growth and infection stages revealed that CpSge1 regulated a number of pathogenicity-related genes in C. parasitica. Yeast one hybrid verified the direct binding of CpSge1 to the promoter regions of genes encoding pectin lyase CpPL1 and major facilitator superfamily transporter CpMF1. In summary, these data suggest that CpSge1 is the core regulator of fungal growth, stress tolerance, gene expression, and virulence in C. parasitica, which may improve our understanding on the molecular pathogenesis of C. parasitica and then help us to develop effective control strategies.
期刊介绍:
Phytopathology publishes articles on fundamental research that advances understanding of the nature of plant diseases, the agents that cause them, their spread, the losses they cause, and measures that can be used to control them. Phytopathology considers manuscripts covering all aspects of plant diseases including bacteriology, host-parasite biochemistry and cell biology, biological control, disease control and pest management, description of new pathogen species description of new pathogen species, ecology and population biology, epidemiology, disease etiology, host genetics and resistance, mycology, nematology, plant stress and abiotic disorders, postharvest pathology and mycotoxins, and virology. Papers dealing mainly with taxonomy, such as descriptions of new plant pathogen taxa are acceptable if they include plant disease research results such as pathogenicity, host range, etc. Taxonomic papers that focus on classification, identification, and nomenclature below the subspecies level may also be submitted to Phytopathology.