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The COP9 signalosome complex regulates fungal development and virulence in the wheat scab fungus Fusarium graminearum

The COP9 signalosome (Csn) complex is an evolutionarily conserved complex that regulates various important cellular processes. However, the function of the Csn complex in pathogenic fungi remains elusive. Here, the distribution of Csn subunits in the fungal kingdom was surveyed, and their biological...

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Autores principales: Chen, Ahai, Ren, Yiyi, Han, Xingmin, Liu, Chao, Zhou, Yifan, Xu, Chenghui, Qi, Hao, Ma, Zhonghua, Chen, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165099/
https://www.ncbi.nlm.nih.gov/pubmed/37168110
http://dx.doi.org/10.3389/fmicb.2023.1179676
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author Chen, Ahai
Ren, Yiyi
Han, Xingmin
Liu, Chao
Zhou, Yifan
Xu, Chenghui
Qi, Hao
Ma, Zhonghua
Chen, Yun
author_facet Chen, Ahai
Ren, Yiyi
Han, Xingmin
Liu, Chao
Zhou, Yifan
Xu, Chenghui
Qi, Hao
Ma, Zhonghua
Chen, Yun
author_sort Chen, Ahai
collection PubMed
description The COP9 signalosome (Csn) complex is an evolutionarily conserved complex that regulates various important cellular processes. However, the function of the Csn complex in pathogenic fungi remains elusive. Here, the distribution of Csn subunits in the fungal kingdom was surveyed, and their biological functions were systematically characterized in the fungal pathogen Fusarium graminearum, which is among the top 10 plant fungal pathogens. The results obtained from bioinformatic analyses suggested that the F. graminearum Csn complex consisted of seven subunits (Csn1–Csn7) and that Csn5 was the most conserved subunit across the fungi kingdom. Yeast two-hybrid assays demonstrated that the seven Csn subunits formed a complex in F. graminearum. The Csn complex was localized to both the nucleus and cytoplasm and necessary for hyphal growth, asexual and sexual development and stress response. Transcriptome profiling revealed that the Csn complex regulated the transcription abundance of TRI genes necessary for mycotoxin deoxynivalenol (DON) biosynthesis, subsequently regulating DON production to control fungal virulence. Collectively, the roles of the Csn complex in F. graminearum were comprehensively analyzed, providing new insights into the functions of the Csn complex in fungal virulence and suggesting that the complex may be a potential target for combating fungal diseases.
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spelling pubmed-101650992023-05-09 The COP9 signalosome complex regulates fungal development and virulence in the wheat scab fungus Fusarium graminearum Chen, Ahai Ren, Yiyi Han, Xingmin Liu, Chao Zhou, Yifan Xu, Chenghui Qi, Hao Ma, Zhonghua Chen, Yun Front Microbiol Microbiology The COP9 signalosome (Csn) complex is an evolutionarily conserved complex that regulates various important cellular processes. However, the function of the Csn complex in pathogenic fungi remains elusive. Here, the distribution of Csn subunits in the fungal kingdom was surveyed, and their biological functions were systematically characterized in the fungal pathogen Fusarium graminearum, which is among the top 10 plant fungal pathogens. The results obtained from bioinformatic analyses suggested that the F. graminearum Csn complex consisted of seven subunits (Csn1–Csn7) and that Csn5 was the most conserved subunit across the fungi kingdom. Yeast two-hybrid assays demonstrated that the seven Csn subunits formed a complex in F. graminearum. The Csn complex was localized to both the nucleus and cytoplasm and necessary for hyphal growth, asexual and sexual development and stress response. Transcriptome profiling revealed that the Csn complex regulated the transcription abundance of TRI genes necessary for mycotoxin deoxynivalenol (DON) biosynthesis, subsequently regulating DON production to control fungal virulence. Collectively, the roles of the Csn complex in F. graminearum were comprehensively analyzed, providing new insights into the functions of the Csn complex in fungal virulence and suggesting that the complex may be a potential target for combating fungal diseases. Frontiers Media S.A. 2023-04-24 /pmc/articles/PMC10165099/ /pubmed/37168110 http://dx.doi.org/10.3389/fmicb.2023.1179676 Text en Copyright © 2023 Chen, Ren, Han, Liu, Zhou, Xu, Qi, Ma and Chen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Chen, Ahai
Ren, Yiyi
Han, Xingmin
Liu, Chao
Zhou, Yifan
Xu, Chenghui
Qi, Hao
Ma, Zhonghua
Chen, Yun
The COP9 signalosome complex regulates fungal development and virulence in the wheat scab fungus Fusarium graminearum
title The COP9 signalosome complex regulates fungal development and virulence in the wheat scab fungus Fusarium graminearum
title_full The COP9 signalosome complex regulates fungal development and virulence in the wheat scab fungus Fusarium graminearum
title_fullStr The COP9 signalosome complex regulates fungal development and virulence in the wheat scab fungus Fusarium graminearum
title_full_unstemmed The COP9 signalosome complex regulates fungal development and virulence in the wheat scab fungus Fusarium graminearum
title_short The COP9 signalosome complex regulates fungal development and virulence in the wheat scab fungus Fusarium graminearum
title_sort cop9 signalosome complex regulates fungal development and virulence in the wheat scab fungus fusarium graminearum
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165099/
https://www.ncbi.nlm.nih.gov/pubmed/37168110
http://dx.doi.org/10.3389/fmicb.2023.1179676
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