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Evolutionary origin and function of NOX4-art, an arthropod specific NADPH oxidase

BACKGROUND: NADPH oxidases (NOX) are ROS producing enzymes that perform essential roles in cell physiology, including cell signaling and antimicrobial defense. This gene family is present in most eukaryotes, suggesting a common ancestor. To date, only a limited number of phylogenetic studies of meta...

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Autores principales: Gandara, Ana Caroline Paiva, Torres, André, Bahia, Ana Cristina, Oliveira, Pedro L., Schama, Renata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372347/
https://www.ncbi.nlm.nih.gov/pubmed/28356077
http://dx.doi.org/10.1186/s12862-017-0940-0
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author Gandara, Ana Caroline Paiva
Torres, André
Bahia, Ana Cristina
Oliveira, Pedro L.
Schama, Renata
author_facet Gandara, Ana Caroline Paiva
Torres, André
Bahia, Ana Cristina
Oliveira, Pedro L.
Schama, Renata
author_sort Gandara, Ana Caroline Paiva
collection PubMed
description BACKGROUND: NADPH oxidases (NOX) are ROS producing enzymes that perform essential roles in cell physiology, including cell signaling and antimicrobial defense. This gene family is present in most eukaryotes, suggesting a common ancestor. To date, only a limited number of phylogenetic studies of metazoan NOXes have been performed, with few arthropod genes. In arthropods, only NOX5 and DUOX genes have been found and a gene called NOXm was found in mosquitoes but its origin and function has not been examined. In this study, we analyzed the evolution of this gene family in arthropods. A thorough search of genomes and transcriptomes was performed enabling us to browse most branches of arthropod phylogeny. RESULTS: We have found that the subfamilies NOX5 and DUOX are present in all arthropod groups. We also show that a NOX gene, closely related to NOX4 and previously found only in mosquitoes (NOXm), can also be found in other taxonomic groups, leading us to rename it as NOX4-art. Although the accessory protein p22-phox, essential for NOX1-4 activation, was not found in any of the arthropods studied, NOX4-art of Aedes aegypti encodes an active protein that produces H(2)O(2). Although NOX4-art has been lost in a number of arthropod lineages, it has all the domains and many signature residues and motifs necessary for ROS production and, when silenced, H(2)O(2) production is considerably diminished in A. aegypti cells. CONCLUSIONS: Combining all bioinformatic analyses and laboratory work we have reached interesting conclusions regarding arthropod NOX gene family evolution. NOX5 and DUOX are present in all arthropod lineages but it seems that a NOX2-like gene was lost in the ancestral lineage leading to Ecdysozoa. The NOX4-art gene originated from a NOX4-like ancestor and is functional. Although no p22-phox was observed in arthropods, there was no evidence of neo-functionalization and this gene probably produces H(2)O(2) as in other metazoan NOX4 genes. Although functional and present in the genomes of many species, NOX4-art was lost in a number of arthropod lineages. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-0940-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-53723472017-03-31 Evolutionary origin and function of NOX4-art, an arthropod specific NADPH oxidase Gandara, Ana Caroline Paiva Torres, André Bahia, Ana Cristina Oliveira, Pedro L. Schama, Renata BMC Evol Biol Research Article BACKGROUND: NADPH oxidases (NOX) are ROS producing enzymes that perform essential roles in cell physiology, including cell signaling and antimicrobial defense. This gene family is present in most eukaryotes, suggesting a common ancestor. To date, only a limited number of phylogenetic studies of metazoan NOXes have been performed, with few arthropod genes. In arthropods, only NOX5 and DUOX genes have been found and a gene called NOXm was found in mosquitoes but its origin and function has not been examined. In this study, we analyzed the evolution of this gene family in arthropods. A thorough search of genomes and transcriptomes was performed enabling us to browse most branches of arthropod phylogeny. RESULTS: We have found that the subfamilies NOX5 and DUOX are present in all arthropod groups. We also show that a NOX gene, closely related to NOX4 and previously found only in mosquitoes (NOXm), can also be found in other taxonomic groups, leading us to rename it as NOX4-art. Although the accessory protein p22-phox, essential for NOX1-4 activation, was not found in any of the arthropods studied, NOX4-art of Aedes aegypti encodes an active protein that produces H(2)O(2). Although NOX4-art has been lost in a number of arthropod lineages, it has all the domains and many signature residues and motifs necessary for ROS production and, when silenced, H(2)O(2) production is considerably diminished in A. aegypti cells. CONCLUSIONS: Combining all bioinformatic analyses and laboratory work we have reached interesting conclusions regarding arthropod NOX gene family evolution. NOX5 and DUOX are present in all arthropod lineages but it seems that a NOX2-like gene was lost in the ancestral lineage leading to Ecdysozoa. The NOX4-art gene originated from a NOX4-like ancestor and is functional. Although no p22-phox was observed in arthropods, there was no evidence of neo-functionalization and this gene probably produces H(2)O(2) as in other metazoan NOX4 genes. Although functional and present in the genomes of many species, NOX4-art was lost in a number of arthropod lineages. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-017-0940-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-29 /pmc/articles/PMC5372347/ /pubmed/28356077 http://dx.doi.org/10.1186/s12862-017-0940-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Gandara, Ana Caroline Paiva
Torres, André
Bahia, Ana Cristina
Oliveira, Pedro L.
Schama, Renata
Evolutionary origin and function of NOX4-art, an arthropod specific NADPH oxidase
title Evolutionary origin and function of NOX4-art, an arthropod specific NADPH oxidase
title_full Evolutionary origin and function of NOX4-art, an arthropod specific NADPH oxidase
title_fullStr Evolutionary origin and function of NOX4-art, an arthropod specific NADPH oxidase
title_full_unstemmed Evolutionary origin and function of NOX4-art, an arthropod specific NADPH oxidase
title_short Evolutionary origin and function of NOX4-art, an arthropod specific NADPH oxidase
title_sort evolutionary origin and function of nox4-art, an arthropod specific nadph oxidase
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372347/
https://www.ncbi.nlm.nih.gov/pubmed/28356077
http://dx.doi.org/10.1186/s12862-017-0940-0
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