Amanda Cristina Campos Antoniêto, David Batista Maués, Marcelo Candido, Iasmin Cartaxo Taveira, Roberto N Silva
{"title":"Rme1:揭示里氏木霉纤维素分解途径中的新抑制因子。","authors":"Amanda Cristina Campos Antoniêto, David Batista Maués, Marcelo Candido, Iasmin Cartaxo Taveira, Roberto N Silva","doi":"10.3390/jof11090658","DOIUrl":null,"url":null,"abstract":"<p><p>Thefilamentous fungus <i>Trichoderma reesei</i> is renowned for its exceptional ability to secrete cellulolytic enzymes, which play a crucial role in the hydrolysis of lignocellulose biomass. The expression of fungal cellulases is meticulously regulated at the transcriptional level, depending on the carbon source available in the medium. To obtain new insights into the transcriptional network controlling cellulase expression in <i>T. reesei</i>, we analyzed RNA-Seq data and identified and characterized a new transcription factor, Rme1, that regulates the expression of cellulolytic genes. Combining functional genomics and protein-DNA interaction assay, we showed that Rme1 acts as a repressor of cellulase production in <i>T. reesei</i> by directly regulating two critical genes involved in cellulose degradation: the cellobiohydrolase <i>cel7a</i> and the carbon catabolite repressor <i>cre1</i>. This is the first report of a transcription factor regulating Cre1. This study contributes to a better understanding of the complex regulation of the cellulolytic system of <i>T. reesei</i> and may be useful for the genetic modification of strains for the biorefinery industry.</p>","PeriodicalId":15878,"journal":{"name":"Journal of Fungi","volume":"11 9","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12470938/pdf/","citationCount":"0","resultStr":"{\"title\":\"Rme1: Unveiling a Novel Repressor in the Cellulolytic Pathway of <i>Trichoderma reesei</i>.\",\"authors\":\"Amanda Cristina Campos Antoniêto, David Batista Maués, Marcelo Candido, Iasmin Cartaxo Taveira, Roberto N Silva\",\"doi\":\"10.3390/jof11090658\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Thefilamentous fungus <i>Trichoderma reesei</i> is renowned for its exceptional ability to secrete cellulolytic enzymes, which play a crucial role in the hydrolysis of lignocellulose biomass. The expression of fungal cellulases is meticulously regulated at the transcriptional level, depending on the carbon source available in the medium. To obtain new insights into the transcriptional network controlling cellulase expression in <i>T. reesei</i>, we analyzed RNA-Seq data and identified and characterized a new transcription factor, Rme1, that regulates the expression of cellulolytic genes. Combining functional genomics and protein-DNA interaction assay, we showed that Rme1 acts as a repressor of cellulase production in <i>T. reesei</i> by directly regulating two critical genes involved in cellulose degradation: the cellobiohydrolase <i>cel7a</i> and the carbon catabolite repressor <i>cre1</i>. This is the first report of a transcription factor regulating Cre1. This study contributes to a better understanding of the complex regulation of the cellulolytic system of <i>T. reesei</i> and may be useful for the genetic modification of strains for the biorefinery industry.</p>\",\"PeriodicalId\":15878,\"journal\":{\"name\":\"Journal of Fungi\",\"volume\":\"11 9\",\"pages\":\"\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-09-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12470938/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Fungi\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3390/jof11090658\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fungi","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3390/jof11090658","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Rme1: Unveiling a Novel Repressor in the Cellulolytic Pathway of Trichoderma reesei.
Thefilamentous fungus Trichoderma reesei is renowned for its exceptional ability to secrete cellulolytic enzymes, which play a crucial role in the hydrolysis of lignocellulose biomass. The expression of fungal cellulases is meticulously regulated at the transcriptional level, depending on the carbon source available in the medium. To obtain new insights into the transcriptional network controlling cellulase expression in T. reesei, we analyzed RNA-Seq data and identified and characterized a new transcription factor, Rme1, that regulates the expression of cellulolytic genes. Combining functional genomics and protein-DNA interaction assay, we showed that Rme1 acts as a repressor of cellulase production in T. reesei by directly regulating two critical genes involved in cellulose degradation: the cellobiohydrolase cel7a and the carbon catabolite repressor cre1. This is the first report of a transcription factor regulating Cre1. This study contributes to a better understanding of the complex regulation of the cellulolytic system of T. reesei and may be useful for the genetic modification of strains for the biorefinery industry.
期刊介绍:
Journal of Fungi (ISSN 2309-608X) is an international, peer-reviewed scientific open access journal that provides an advanced forum for studies related to pathogenic fungi, fungal biology, and all other aspects of fungal research. The journal publishes reviews, regular research papers, and communications in quarterly issues. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on paper length. Full experimental details must be provided so that the results can be reproduced.