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Identifying Genes Devoted to the Cell Death Process in the Gene Regulatory Network of Ustilago maydis

Cell death is a process that can be divided into three morphological patterns: apoptosis, autophagy and necrosis. In fungi, cell death is induced in response to intracellular and extracellular perturbations, such as plant defense molecules, toxins and fungicides, among others. Ustilago maydis is a d...

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Autores principales: Soberanes-Gutiérrez, Cinthia V., Pérez-Rueda, Ernesto, Ruíz-Herrera, José, Galán-Vásquez, Edgardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175908/
https://www.ncbi.nlm.nih.gov/pubmed/34093501
http://dx.doi.org/10.3389/fmicb.2021.680290
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author Soberanes-Gutiérrez, Cinthia V.
Pérez-Rueda, Ernesto
Ruíz-Herrera, José
Galán-Vásquez, Edgardo
author_facet Soberanes-Gutiérrez, Cinthia V.
Pérez-Rueda, Ernesto
Ruíz-Herrera, José
Galán-Vásquez, Edgardo
author_sort Soberanes-Gutiérrez, Cinthia V.
collection PubMed
description Cell death is a process that can be divided into three morphological patterns: apoptosis, autophagy and necrosis. In fungi, cell death is induced in response to intracellular and extracellular perturbations, such as plant defense molecules, toxins and fungicides, among others. Ustilago maydis is a dimorphic fungus used as a model for pathogenic fungi of animals, including humans, and plants. Here, we reconstructed the transcriptional regulatory network of U. maydis, through homology inferences by using as templates the well-known gene regulatory networks (GRNs) of Saccharomyces cerevisiae, Aspergillus nidulans and Neurospora crassa. Based on this GRN, we identified transcription factors (TFs) as hubs and functional modules and calculated diverse topological metrics. In addition, we analyzed exhaustively the module related to cell death, with 60 TFs and 108 genes, where diverse cell proliferation, mating-type switching and meiosis, among other functions, were identified. To determine the role of some of these genes, we selected a set of 11 genes for expression analysis by qRT-PCR (sin3, rlm1, aif1, tdh3 [isoform A], tdh3 [isoform B], ald4, mca1, nuc1, tor1, ras1, and atg8) whose homologues in other fungi have been described as central in cell death. These genes were identified as downregulated at 72 h, in agreement with the beginning of the cell death process. Our results can serve as the basis for the study of transcriptional regulation, not only of the cell death process but also of all the cellular processes of U. maydis.
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spelling pubmed-81759082021-06-05 Identifying Genes Devoted to the Cell Death Process in the Gene Regulatory Network of Ustilago maydis Soberanes-Gutiérrez, Cinthia V. Pérez-Rueda, Ernesto Ruíz-Herrera, José Galán-Vásquez, Edgardo Front Microbiol Microbiology Cell death is a process that can be divided into three morphological patterns: apoptosis, autophagy and necrosis. In fungi, cell death is induced in response to intracellular and extracellular perturbations, such as plant defense molecules, toxins and fungicides, among others. Ustilago maydis is a dimorphic fungus used as a model for pathogenic fungi of animals, including humans, and plants. Here, we reconstructed the transcriptional regulatory network of U. maydis, through homology inferences by using as templates the well-known gene regulatory networks (GRNs) of Saccharomyces cerevisiae, Aspergillus nidulans and Neurospora crassa. Based on this GRN, we identified transcription factors (TFs) as hubs and functional modules and calculated diverse topological metrics. In addition, we analyzed exhaustively the module related to cell death, with 60 TFs and 108 genes, where diverse cell proliferation, mating-type switching and meiosis, among other functions, were identified. To determine the role of some of these genes, we selected a set of 11 genes for expression analysis by qRT-PCR (sin3, rlm1, aif1, tdh3 [isoform A], tdh3 [isoform B], ald4, mca1, nuc1, tor1, ras1, and atg8) whose homologues in other fungi have been described as central in cell death. These genes were identified as downregulated at 72 h, in agreement with the beginning of the cell death process. Our results can serve as the basis for the study of transcriptional regulation, not only of the cell death process but also of all the cellular processes of U. maydis. Frontiers Media S.A. 2021-05-21 /pmc/articles/PMC8175908/ /pubmed/34093501 http://dx.doi.org/10.3389/fmicb.2021.680290 Text en Copyright © 2021 Soberanes-Gutiérrez, Pérez-Rueda, Ruíz-Herrera and Galán-Vásquez. 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
Soberanes-Gutiérrez, Cinthia V.
Pérez-Rueda, Ernesto
Ruíz-Herrera, José
Galán-Vásquez, Edgardo
Identifying Genes Devoted to the Cell Death Process in the Gene Regulatory Network of Ustilago maydis
title Identifying Genes Devoted to the Cell Death Process in the Gene Regulatory Network of Ustilago maydis
title_full Identifying Genes Devoted to the Cell Death Process in the Gene Regulatory Network of Ustilago maydis
title_fullStr Identifying Genes Devoted to the Cell Death Process in the Gene Regulatory Network of Ustilago maydis
title_full_unstemmed Identifying Genes Devoted to the Cell Death Process in the Gene Regulatory Network of Ustilago maydis
title_short Identifying Genes Devoted to the Cell Death Process in the Gene Regulatory Network of Ustilago maydis
title_sort identifying genes devoted to the cell death process in the gene regulatory network of ustilago maydis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175908/
https://www.ncbi.nlm.nih.gov/pubmed/34093501
http://dx.doi.org/10.3389/fmicb.2021.680290
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