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Co-option of an extracellular protease for transcriptional control of nutrient degradation in the fungus Aspergillus nidulans
Nutrient acquisition is essential for all organisms. Fungi regulate their metabolism according to environmental nutrient availability through elaborate transcription regulatory programs. In filamentous fungi, a highly conserved GATA transcription factor AreA and its co-repressor NmrA govern expressi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683493/ https://www.ncbi.nlm.nih.gov/pubmed/34921231 http://dx.doi.org/10.1038/s42003-021-02925-1 |
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author | Li, Ang Parsania, Chirag Tan, Kaeling Todd, Richard B. Wong, Koon Ho |
author_facet | Li, Ang Parsania, Chirag Tan, Kaeling Todd, Richard B. Wong, Koon Ho |
author_sort | Li, Ang |
collection | PubMed |
description | Nutrient acquisition is essential for all organisms. Fungi regulate their metabolism according to environmental nutrient availability through elaborate transcription regulatory programs. In filamentous fungi, a highly conserved GATA transcription factor AreA and its co-repressor NmrA govern expression of genes involved in extracellular breakdown, uptake, and metabolism of nitrogen nutrients. Here, we show that the Aspergillus nidulans PnmB protease is a moonlighting protein with extracellular and intracellular functions for nitrogen acquisition and metabolism. PnmB serves not only as a secreted protease to degrade extracellular nutrients, but also as an intracellular protease to control the turnover of the co-repressor NmrA, accelerating AreA transcriptional activation upon nitrogen starvation. PnmB expression is controlled by AreA, which activates a positive feedback regulatory loop. Hence, we uncover a regulatory mechanism in the well-established controls determining the response to nitrogen starvation, revealing functional evolution of a protease gene for transcriptional regulation and extracellular nutrient breakdown. |
format | Online Article Text |
id | pubmed-8683493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86834932022-01-04 Co-option of an extracellular protease for transcriptional control of nutrient degradation in the fungus Aspergillus nidulans Li, Ang Parsania, Chirag Tan, Kaeling Todd, Richard B. Wong, Koon Ho Commun Biol Article Nutrient acquisition is essential for all organisms. Fungi regulate their metabolism according to environmental nutrient availability through elaborate transcription regulatory programs. In filamentous fungi, a highly conserved GATA transcription factor AreA and its co-repressor NmrA govern expression of genes involved in extracellular breakdown, uptake, and metabolism of nitrogen nutrients. Here, we show that the Aspergillus nidulans PnmB protease is a moonlighting protein with extracellular and intracellular functions for nitrogen acquisition and metabolism. PnmB serves not only as a secreted protease to degrade extracellular nutrients, but also as an intracellular protease to control the turnover of the co-repressor NmrA, accelerating AreA transcriptional activation upon nitrogen starvation. PnmB expression is controlled by AreA, which activates a positive feedback regulatory loop. Hence, we uncover a regulatory mechanism in the well-established controls determining the response to nitrogen starvation, revealing functional evolution of a protease gene for transcriptional regulation and extracellular nutrient breakdown. Nature Publishing Group UK 2021-12-17 /pmc/articles/PMC8683493/ /pubmed/34921231 http://dx.doi.org/10.1038/s42003-021-02925-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Li, Ang Parsania, Chirag Tan, Kaeling Todd, Richard B. Wong, Koon Ho Co-option of an extracellular protease for transcriptional control of nutrient degradation in the fungus Aspergillus nidulans |
title | Co-option of an extracellular protease for transcriptional control of nutrient degradation in the fungus Aspergillus nidulans |
title_full | Co-option of an extracellular protease for transcriptional control of nutrient degradation in the fungus Aspergillus nidulans |
title_fullStr | Co-option of an extracellular protease for transcriptional control of nutrient degradation in the fungus Aspergillus nidulans |
title_full_unstemmed | Co-option of an extracellular protease for transcriptional control of nutrient degradation in the fungus Aspergillus nidulans |
title_short | Co-option of an extracellular protease for transcriptional control of nutrient degradation in the fungus Aspergillus nidulans |
title_sort | co-option of an extracellular protease for transcriptional control of nutrient degradation in the fungus aspergillus nidulans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683493/ https://www.ncbi.nlm.nih.gov/pubmed/34921231 http://dx.doi.org/10.1038/s42003-021-02925-1 |
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