Cargando…
The Zn(II)2Cys6-Type Transcription Factor ADA-6 Regulates Conidiation, Sexual Development, and Oxidative Stress Response in Neurospora crassa
Conidiation and sexual development are critical for reproduction, dispersal and better-adapted survival in many filamentous fungi. The Neurospora crassa gene ada-6 encodes a Zn(II)2Cys6-type transcription factor, whose deletion resulted in reduced conidial production and female sterility. In this st...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468284/ https://www.ncbi.nlm.nih.gov/pubmed/31024511 http://dx.doi.org/10.3389/fmicb.2019.00750 |
_version_ | 1783411400380514304 |
---|---|
author | Sun, Xianyun Wang, Fei Lan, Nan Liu, Bo Hu, Chengcheng Xue, Wei Zhang, Zhenying Li, Shaojie |
author_facet | Sun, Xianyun Wang, Fei Lan, Nan Liu, Bo Hu, Chengcheng Xue, Wei Zhang, Zhenying Li, Shaojie |
author_sort | Sun, Xianyun |
collection | PubMed |
description | Conidiation and sexual development are critical for reproduction, dispersal and better-adapted survival in many filamentous fungi. The Neurospora crassa gene ada-6 encodes a Zn(II)2Cys6-type transcription factor, whose deletion resulted in reduced conidial production and female sterility. In this study, we confirmed the positive contribution of ada-6 to conidiation and sexual development by detailed phenotypic characterization of its deletion mutant and the complemented mutant. To understand the regulatory mechanisms of ADA-6 in conidiation and sexual development, transcriptomic profiles generated by RNA-seq from the Δada-6 mutant and wild type during conidiation and sexual development were compared. During conidial development, differential expressed genes (DEGs) between the Δada-6 mutant and wild type are mainly involved in oxidation-reduction process and single-organism metabolic process. Several conidiation related genes are positively regulated by ADA-6, including genes that positively regulate conidiation (fluffy and acon-3), and genes preferentially expressed during conidial development (eas, con-6, con-8, con-10, con-13, pcp-1, and NCU9357), as the expression of these genes were lower in the Δada-6 mutant compared to wild type during conidial development. Phenotypic observation of deletion mutants for other genes with unknown function down-regulated by ada-6 deletion revealed that deletion mutants for four genes (NCU00929, NCU05260, NCU00116, and NCU04813) produced less conidia than wild type. Deletion of ada-6 resulted in female sterility, which might be due to that ADA-6 affects oxidation-reduction process and transmembrane transport process, and positively regulates the transcription of pre-2, poi-2, and NCU05832, three key genes participating in sexual development. In both conidiation and the sexual development process, ADA-6 regulates the transcription of cat-3 and other genes participating in reactive oxygen species production according to RNA-seq data, indicating a role of ADA-6 in oxidative stress response. This was further confirmed by the results that deletion of ada-6 led to hypersensitivity to oxidants H(2)O(2) and menadione. Together, these results proved that ADA-6, as a global regulator, plays a crucial role in conidiation, sexual development, and oxidative stress response of N. crassa. |
format | Online Article Text |
id | pubmed-6468284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64682842019-04-25 The Zn(II)2Cys6-Type Transcription Factor ADA-6 Regulates Conidiation, Sexual Development, and Oxidative Stress Response in Neurospora crassa Sun, Xianyun Wang, Fei Lan, Nan Liu, Bo Hu, Chengcheng Xue, Wei Zhang, Zhenying Li, Shaojie Front Microbiol Microbiology Conidiation and sexual development are critical for reproduction, dispersal and better-adapted survival in many filamentous fungi. The Neurospora crassa gene ada-6 encodes a Zn(II)2Cys6-type transcription factor, whose deletion resulted in reduced conidial production and female sterility. In this study, we confirmed the positive contribution of ada-6 to conidiation and sexual development by detailed phenotypic characterization of its deletion mutant and the complemented mutant. To understand the regulatory mechanisms of ADA-6 in conidiation and sexual development, transcriptomic profiles generated by RNA-seq from the Δada-6 mutant and wild type during conidiation and sexual development were compared. During conidial development, differential expressed genes (DEGs) between the Δada-6 mutant and wild type are mainly involved in oxidation-reduction process and single-organism metabolic process. Several conidiation related genes are positively regulated by ADA-6, including genes that positively regulate conidiation (fluffy and acon-3), and genes preferentially expressed during conidial development (eas, con-6, con-8, con-10, con-13, pcp-1, and NCU9357), as the expression of these genes were lower in the Δada-6 mutant compared to wild type during conidial development. Phenotypic observation of deletion mutants for other genes with unknown function down-regulated by ada-6 deletion revealed that deletion mutants for four genes (NCU00929, NCU05260, NCU00116, and NCU04813) produced less conidia than wild type. Deletion of ada-6 resulted in female sterility, which might be due to that ADA-6 affects oxidation-reduction process and transmembrane transport process, and positively regulates the transcription of pre-2, poi-2, and NCU05832, three key genes participating in sexual development. In both conidiation and the sexual development process, ADA-6 regulates the transcription of cat-3 and other genes participating in reactive oxygen species production according to RNA-seq data, indicating a role of ADA-6 in oxidative stress response. This was further confirmed by the results that deletion of ada-6 led to hypersensitivity to oxidants H(2)O(2) and menadione. Together, these results proved that ADA-6, as a global regulator, plays a crucial role in conidiation, sexual development, and oxidative stress response of N. crassa. Frontiers Media S.A. 2019-04-10 /pmc/articles/PMC6468284/ /pubmed/31024511 http://dx.doi.org/10.3389/fmicb.2019.00750 Text en Copyright © 2019 Sun, Wang, Lan, Liu, Hu, Xue, Zhang and Li. http://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 Sun, Xianyun Wang, Fei Lan, Nan Liu, Bo Hu, Chengcheng Xue, Wei Zhang, Zhenying Li, Shaojie The Zn(II)2Cys6-Type Transcription Factor ADA-6 Regulates Conidiation, Sexual Development, and Oxidative Stress Response in Neurospora crassa |
title | The Zn(II)2Cys6-Type Transcription Factor ADA-6 Regulates Conidiation, Sexual Development, and Oxidative Stress Response in Neurospora crassa |
title_full | The Zn(II)2Cys6-Type Transcription Factor ADA-6 Regulates Conidiation, Sexual Development, and Oxidative Stress Response in Neurospora crassa |
title_fullStr | The Zn(II)2Cys6-Type Transcription Factor ADA-6 Regulates Conidiation, Sexual Development, and Oxidative Stress Response in Neurospora crassa |
title_full_unstemmed | The Zn(II)2Cys6-Type Transcription Factor ADA-6 Regulates Conidiation, Sexual Development, and Oxidative Stress Response in Neurospora crassa |
title_short | The Zn(II)2Cys6-Type Transcription Factor ADA-6 Regulates Conidiation, Sexual Development, and Oxidative Stress Response in Neurospora crassa |
title_sort | zn(ii)2cys6-type transcription factor ada-6 regulates conidiation, sexual development, and oxidative stress response in neurospora crassa |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468284/ https://www.ncbi.nlm.nih.gov/pubmed/31024511 http://dx.doi.org/10.3389/fmicb.2019.00750 |
work_keys_str_mv | AT sunxianyun theznii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT wangfei theznii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT lannan theznii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT liubo theznii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT huchengcheng theznii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT xuewei theznii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT zhangzhenying theznii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT lishaojie theznii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT sunxianyun znii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT wangfei znii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT lannan znii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT liubo znii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT huchengcheng znii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT xuewei znii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT zhangzhenying znii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa AT lishaojie znii2cys6typetranscriptionfactorada6regulatesconidiationsexualdevelopmentandoxidativestressresponseinneurosporacrassa |