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YPR2 is a regulator of light modulated carbon and secondary metabolism in Trichoderma reesei
BACKGROUND: Filamentous fungi have evolved to succeed in nature by efficient growth and degradation of substrates, but also due to the production of secondary metabolites including mycotoxins. For Trichoderma reesei, as a biotechnological workhorse for homologous and heterologous protein production,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417087/ https://www.ncbi.nlm.nih.gov/pubmed/30866811 http://dx.doi.org/10.1186/s12864-019-5574-8 |
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author | Hitzenhammer, Eva Büschl, Christoph Sulyok, Michael Schuhmacher, Rainer Kluger, Bernhard Wischnitzki, Elisabeth Schmoll, Monika |
author_facet | Hitzenhammer, Eva Büschl, Christoph Sulyok, Michael Schuhmacher, Rainer Kluger, Bernhard Wischnitzki, Elisabeth Schmoll, Monika |
author_sort | Hitzenhammer, Eva |
collection | PubMed |
description | BACKGROUND: Filamentous fungi have evolved to succeed in nature by efficient growth and degradation of substrates, but also due to the production of secondary metabolites including mycotoxins. For Trichoderma reesei, as a biotechnological workhorse for homologous and heterologous protein production, secondary metabolite secretion is of particular importance for industrial application. Recent studies revealed an interconnected regulation of enzyme gene expression and carbon metabolism with secondary metabolism. RESULTS: Here, we investigated gene regulation by YPR2, one out of two transcription factors located within the SOR cluster of T. reesei, which is involved in biosynthesis of sorbicillinoids. Transcriptome analysis showed that YPR2 exerts its major function in constant darkness upon growth on cellulose. Targets (direct and indirect) of YPR2 overlap with induction specific genes as well as with targets of the carbon catabolite repressor CRE1 and a considerable proportion is regulated by photoreceptors as well. Functional category analysis revealed both effects on carbon metabolism and secondary metabolism. Further, we found indications for an involvement of YPR2 in regulation of siderophores. In agreement with transcriptome data, mass spectrometric analyses revealed a broad alteration in metabolite patterns in ∆ypr2. Additionally, YPR2 positively influenced alamethicin levels along with transcript levels of the alamethicin synthase tex1 and is essential for production of orsellinic acid in darkness. CONCLUSIONS: YPR2 is an important regulator balancing secondary metabolism with carbon metabolism in darkness and depending on the carbon source. The function of YPR2 reaches beyond the SOR cluster in which ypr2 is located and happens downstream of carbon catabolite repression mediated by CRE1. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5574-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6417087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64170872019-03-25 YPR2 is a regulator of light modulated carbon and secondary metabolism in Trichoderma reesei Hitzenhammer, Eva Büschl, Christoph Sulyok, Michael Schuhmacher, Rainer Kluger, Bernhard Wischnitzki, Elisabeth Schmoll, Monika BMC Genomics Research Article BACKGROUND: Filamentous fungi have evolved to succeed in nature by efficient growth and degradation of substrates, but also due to the production of secondary metabolites including mycotoxins. For Trichoderma reesei, as a biotechnological workhorse for homologous and heterologous protein production, secondary metabolite secretion is of particular importance for industrial application. Recent studies revealed an interconnected regulation of enzyme gene expression and carbon metabolism with secondary metabolism. RESULTS: Here, we investigated gene regulation by YPR2, one out of two transcription factors located within the SOR cluster of T. reesei, which is involved in biosynthesis of sorbicillinoids. Transcriptome analysis showed that YPR2 exerts its major function in constant darkness upon growth on cellulose. Targets (direct and indirect) of YPR2 overlap with induction specific genes as well as with targets of the carbon catabolite repressor CRE1 and a considerable proportion is regulated by photoreceptors as well. Functional category analysis revealed both effects on carbon metabolism and secondary metabolism. Further, we found indications for an involvement of YPR2 in regulation of siderophores. In agreement with transcriptome data, mass spectrometric analyses revealed a broad alteration in metabolite patterns in ∆ypr2. Additionally, YPR2 positively influenced alamethicin levels along with transcript levels of the alamethicin synthase tex1 and is essential for production of orsellinic acid in darkness. CONCLUSIONS: YPR2 is an important regulator balancing secondary metabolism with carbon metabolism in darkness and depending on the carbon source. The function of YPR2 reaches beyond the SOR cluster in which ypr2 is located and happens downstream of carbon catabolite repression mediated by CRE1. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5574-8) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-13 /pmc/articles/PMC6417087/ /pubmed/30866811 http://dx.doi.org/10.1186/s12864-019-5574-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Hitzenhammer, Eva Büschl, Christoph Sulyok, Michael Schuhmacher, Rainer Kluger, Bernhard Wischnitzki, Elisabeth Schmoll, Monika YPR2 is a regulator of light modulated carbon and secondary metabolism in Trichoderma reesei |
title | YPR2 is a regulator of light modulated carbon and secondary metabolism in Trichoderma reesei |
title_full | YPR2 is a regulator of light modulated carbon and secondary metabolism in Trichoderma reesei |
title_fullStr | YPR2 is a regulator of light modulated carbon and secondary metabolism in Trichoderma reesei |
title_full_unstemmed | YPR2 is a regulator of light modulated carbon and secondary metabolism in Trichoderma reesei |
title_short | YPR2 is a regulator of light modulated carbon and secondary metabolism in Trichoderma reesei |
title_sort | ypr2 is a regulator of light modulated carbon and secondary metabolism in trichoderma reesei |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417087/ https://www.ncbi.nlm.nih.gov/pubmed/30866811 http://dx.doi.org/10.1186/s12864-019-5574-8 |
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