Cargando…

The Putative C(2)H(2) Transcription Factor VadH Governs Development, Osmotic Stress Response, and Sterigmatocystin Production in Aspergillus nidulans

The VosA-VelB hetero-dimeric complex plays a pivotal role in regulating development and secondary metabolism in Aspergillus nidulans. In this work, we characterize a new VosA/VelB-activated gene called vadH, which is predicted to encode a 457-amino acid length protein containing four adjacent C(2)H(...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Xiaoyu, Zhao, Yanxia, Moon, Heungyun, Lim, Jieyin, Park, Hee-Soo, Liu, Zhiqiang, Yu, Jae-Hyuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776899/
https://www.ncbi.nlm.nih.gov/pubmed/36552763
http://dx.doi.org/10.3390/cells11243998
_version_ 1784855972138713088
author Li, Xiaoyu
Zhao, Yanxia
Moon, Heungyun
Lim, Jieyin
Park, Hee-Soo
Liu, Zhiqiang
Yu, Jae-Hyuk
author_facet Li, Xiaoyu
Zhao, Yanxia
Moon, Heungyun
Lim, Jieyin
Park, Hee-Soo
Liu, Zhiqiang
Yu, Jae-Hyuk
author_sort Li, Xiaoyu
collection PubMed
description The VosA-VelB hetero-dimeric complex plays a pivotal role in regulating development and secondary metabolism in Aspergillus nidulans. In this work, we characterize a new VosA/VelB-activated gene called vadH, which is predicted to encode a 457-amino acid length protein containing four adjacent C(2)H(2) zinc-finger domains. Mutational inactivation of vosA or velB led to reduced mRNA levels of vadH throughout the lifecycle, suggesting that VosA and VelB have a positive regulatory effect on the expression of vadH. The deletion of vadH resulted in decreased asexual development (conidiation) but elevated production of sexual fruiting bodies (cleistothecia), indicating that VadH balances asexual and sexual development in A. nidulans. Moreover, the vadH deletion mutant exhibited elevated susceptibility to hyperosmotic stress compared to wild type and showed elevated production of the mycotoxin sterigmatocystin (ST). Genome-wide expression analyses employing RNA-Seq have revealed that VadH is likely involved in regulating more genes and biological pathways in the developmental stages than those in the vegetative growth stage. The brlA, abaA, and wetA genes of the central regulatory pathway for conidiation are downregulated significantly in the vadH null mutant during asexual development. VadH also participates in regulating the genes, mat2, ppgA and lsdA, etc., related to sexual development, and some of the genes in the ST biosynthetic gene cluster. In summary, VadH is a putative transcription factor with four C(2)H(2) finger domains and is involved in regulating asexual/sexual development, osmotic stress response, and ST production in A. nidulans.
format Online
Article
Text
id pubmed-9776899
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-97768992022-12-23 The Putative C(2)H(2) Transcription Factor VadH Governs Development, Osmotic Stress Response, and Sterigmatocystin Production in Aspergillus nidulans Li, Xiaoyu Zhao, Yanxia Moon, Heungyun Lim, Jieyin Park, Hee-Soo Liu, Zhiqiang Yu, Jae-Hyuk Cells Article The VosA-VelB hetero-dimeric complex plays a pivotal role in regulating development and secondary metabolism in Aspergillus nidulans. In this work, we characterize a new VosA/VelB-activated gene called vadH, which is predicted to encode a 457-amino acid length protein containing four adjacent C(2)H(2) zinc-finger domains. Mutational inactivation of vosA or velB led to reduced mRNA levels of vadH throughout the lifecycle, suggesting that VosA and VelB have a positive regulatory effect on the expression of vadH. The deletion of vadH resulted in decreased asexual development (conidiation) but elevated production of sexual fruiting bodies (cleistothecia), indicating that VadH balances asexual and sexual development in A. nidulans. Moreover, the vadH deletion mutant exhibited elevated susceptibility to hyperosmotic stress compared to wild type and showed elevated production of the mycotoxin sterigmatocystin (ST). Genome-wide expression analyses employing RNA-Seq have revealed that VadH is likely involved in regulating more genes and biological pathways in the developmental stages than those in the vegetative growth stage. The brlA, abaA, and wetA genes of the central regulatory pathway for conidiation are downregulated significantly in the vadH null mutant during asexual development. VadH also participates in regulating the genes, mat2, ppgA and lsdA, etc., related to sexual development, and some of the genes in the ST biosynthetic gene cluster. In summary, VadH is a putative transcription factor with four C(2)H(2) finger domains and is involved in regulating asexual/sexual development, osmotic stress response, and ST production in A. nidulans. MDPI 2022-12-10 /pmc/articles/PMC9776899/ /pubmed/36552763 http://dx.doi.org/10.3390/cells11243998 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Li, Xiaoyu
Zhao, Yanxia
Moon, Heungyun
Lim, Jieyin
Park, Hee-Soo
Liu, Zhiqiang
Yu, Jae-Hyuk
The Putative C(2)H(2) Transcription Factor VadH Governs Development, Osmotic Stress Response, and Sterigmatocystin Production in Aspergillus nidulans
title The Putative C(2)H(2) Transcription Factor VadH Governs Development, Osmotic Stress Response, and Sterigmatocystin Production in Aspergillus nidulans
title_full The Putative C(2)H(2) Transcription Factor VadH Governs Development, Osmotic Stress Response, and Sterigmatocystin Production in Aspergillus nidulans
title_fullStr The Putative C(2)H(2) Transcription Factor VadH Governs Development, Osmotic Stress Response, and Sterigmatocystin Production in Aspergillus nidulans
title_full_unstemmed The Putative C(2)H(2) Transcription Factor VadH Governs Development, Osmotic Stress Response, and Sterigmatocystin Production in Aspergillus nidulans
title_short The Putative C(2)H(2) Transcription Factor VadH Governs Development, Osmotic Stress Response, and Sterigmatocystin Production in Aspergillus nidulans
title_sort putative c(2)h(2) transcription factor vadh governs development, osmotic stress response, and sterigmatocystin production in aspergillus nidulans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776899/
https://www.ncbi.nlm.nih.gov/pubmed/36552763
http://dx.doi.org/10.3390/cells11243998
work_keys_str_mv AT lixiaoyu theputativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT zhaoyanxia theputativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT moonheungyun theputativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT limjieyin theputativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT parkheesoo theputativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT liuzhiqiang theputativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT yujaehyuk theputativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT lixiaoyu putativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT zhaoyanxia putativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT moonheungyun putativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT limjieyin putativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT parkheesoo putativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT liuzhiqiang putativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans
AT yujaehyuk putativec2h2transcriptionfactorvadhgovernsdevelopmentosmoticstressresponseandsterigmatocystinproductioninaspergillusnidulans