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GPCR-mediated glucose sensing system regulates light-dependent fungal development and mycotoxin production
Microorganisms sense environmental fluctuations in nutrients and light, coordinating their growth and development accordingly. Despite their critical roles in fungi, only a few G-protein coupled receptors (GPCRs) have been characterized. The Aspergillus nidulans genome encodes 86 putative GPCRs. Her...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812930/ https://www.ncbi.nlm.nih.gov/pubmed/31609971 http://dx.doi.org/10.1371/journal.pgen.1008419 |
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author | dos Reis, Thaila Fernanda Mellado, Laura Lohmar, Jessica M. Silva, Lilian Pereira Zhou, Jing-Jiang Calvo, Ana M. Goldman, Gustavo H. Brown, Neil A. |
author_facet | dos Reis, Thaila Fernanda Mellado, Laura Lohmar, Jessica M. Silva, Lilian Pereira Zhou, Jing-Jiang Calvo, Ana M. Goldman, Gustavo H. Brown, Neil A. |
author_sort | dos Reis, Thaila Fernanda |
collection | PubMed |
description | Microorganisms sense environmental fluctuations in nutrients and light, coordinating their growth and development accordingly. Despite their critical roles in fungi, only a few G-protein coupled receptors (GPCRs) have been characterized. The Aspergillus nidulans genome encodes 86 putative GPCRs. Here, we characterise a carbon starvation-induced GPCR-mediated glucose sensing mechanism in A. nidulans. This includes two class V (gprH and gprI) and one class VII (gprM) GPCRs, which in response to glucose promote cAMP signalling, germination and hyphal growth, while negatively regulating sexual development in a light-dependent manner. We demonstrate that GprH regulates sexual development via influencing VeA activity, a key light-dependent regulator of fungal morphogenesis and secondary metabolism. We show that GprH and GprM are light-independent negative regulators of sterigmatocystin biosynthesis. Additionally, we reveal the epistatic interactions between the three GPCRs in regulating sexual development and sterigmatocystin production. In conclusion, GprH, GprM and GprI constitute a novel carbon starvation-induced glucose sensing mechanism that functions upstream of cAMP-PKA signalling to regulate fungal development and mycotoxin production. |
format | Online Article Text |
id | pubmed-6812930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-68129302019-11-02 GPCR-mediated glucose sensing system regulates light-dependent fungal development and mycotoxin production dos Reis, Thaila Fernanda Mellado, Laura Lohmar, Jessica M. Silva, Lilian Pereira Zhou, Jing-Jiang Calvo, Ana M. Goldman, Gustavo H. Brown, Neil A. PLoS Genet Research Article Microorganisms sense environmental fluctuations in nutrients and light, coordinating their growth and development accordingly. Despite their critical roles in fungi, only a few G-protein coupled receptors (GPCRs) have been characterized. The Aspergillus nidulans genome encodes 86 putative GPCRs. Here, we characterise a carbon starvation-induced GPCR-mediated glucose sensing mechanism in A. nidulans. This includes two class V (gprH and gprI) and one class VII (gprM) GPCRs, which in response to glucose promote cAMP signalling, germination and hyphal growth, while negatively regulating sexual development in a light-dependent manner. We demonstrate that GprH regulates sexual development via influencing VeA activity, a key light-dependent regulator of fungal morphogenesis and secondary metabolism. We show that GprH and GprM are light-independent negative regulators of sterigmatocystin biosynthesis. Additionally, we reveal the epistatic interactions between the three GPCRs in regulating sexual development and sterigmatocystin production. In conclusion, GprH, GprM and GprI constitute a novel carbon starvation-induced glucose sensing mechanism that functions upstream of cAMP-PKA signalling to regulate fungal development and mycotoxin production. Public Library of Science 2019-10-14 /pmc/articles/PMC6812930/ /pubmed/31609971 http://dx.doi.org/10.1371/journal.pgen.1008419 Text en © 2019 dos Reis et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article dos Reis, Thaila Fernanda Mellado, Laura Lohmar, Jessica M. Silva, Lilian Pereira Zhou, Jing-Jiang Calvo, Ana M. Goldman, Gustavo H. Brown, Neil A. GPCR-mediated glucose sensing system regulates light-dependent fungal development and mycotoxin production |
title | GPCR-mediated glucose sensing system regulates light-dependent fungal development and mycotoxin production |
title_full | GPCR-mediated glucose sensing system regulates light-dependent fungal development and mycotoxin production |
title_fullStr | GPCR-mediated glucose sensing system regulates light-dependent fungal development and mycotoxin production |
title_full_unstemmed | GPCR-mediated glucose sensing system regulates light-dependent fungal development and mycotoxin production |
title_short | GPCR-mediated glucose sensing system regulates light-dependent fungal development and mycotoxin production |
title_sort | gpcr-mediated glucose sensing system regulates light-dependent fungal development and mycotoxin production |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812930/ https://www.ncbi.nlm.nih.gov/pubmed/31609971 http://dx.doi.org/10.1371/journal.pgen.1008419 |
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