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Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds

Birds (Aves) display high metabolic rates and oxygen consumption relative to mammals, increasing reactive oxygen species (ROS) formation. Although excess ROS reduces lifespan by causing extensive cellular dysfunction and damage, birds are remarkably long-lived. We address this paradox by identifying...

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Autores principales: Castiglione, Gianni M., Xu, Zhenhua, Zhou, Lingli, Duh, Elia J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234996/
https://www.ncbi.nlm.nih.gov/pubmed/32424161
http://dx.doi.org/10.1038/s41467-020-16129-4
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author Castiglione, Gianni M.
Xu, Zhenhua
Zhou, Lingli
Duh, Elia J.
author_facet Castiglione, Gianni M.
Xu, Zhenhua
Zhou, Lingli
Duh, Elia J.
author_sort Castiglione, Gianni M.
collection PubMed
description Birds (Aves) display high metabolic rates and oxygen consumption relative to mammals, increasing reactive oxygen species (ROS) formation. Although excess ROS reduces lifespan by causing extensive cellular dysfunction and damage, birds are remarkably long-lived. We address this paradox by identifying the constitutive activation of the NRF2 master antioxidant response in Neoaves (~95% of bird species), providing an adaptive mechanism capable of counterbalancing high ROS levels. We demonstrate that a KEAP1 mutation in the Neoavian ancestor disrupted the repression of NRF2 by KEAP1, leading to constitutive NRF2 activity and decreased oxidative stress in wild Neoaves tissues and cells. Our evidence suggests this ancient mutation induced a compensatory program in NRF2-target genes with functions beyond redox regulation—including feather development—while enabling significant metabolic rate increases that avoid trade-offs with lifespan. The strategy of NRF2 activation sought by intense clinical investigation therefore appears to have also unlocked a massively successful evolutionary trajectory.
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spelling pubmed-72349962020-05-20 Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds Castiglione, Gianni M. Xu, Zhenhua Zhou, Lingli Duh, Elia J. Nat Commun Article Birds (Aves) display high metabolic rates and oxygen consumption relative to mammals, increasing reactive oxygen species (ROS) formation. Although excess ROS reduces lifespan by causing extensive cellular dysfunction and damage, birds are remarkably long-lived. We address this paradox by identifying the constitutive activation of the NRF2 master antioxidant response in Neoaves (~95% of bird species), providing an adaptive mechanism capable of counterbalancing high ROS levels. We demonstrate that a KEAP1 mutation in the Neoavian ancestor disrupted the repression of NRF2 by KEAP1, leading to constitutive NRF2 activity and decreased oxidative stress in wild Neoaves tissues and cells. Our evidence suggests this ancient mutation induced a compensatory program in NRF2-target genes with functions beyond redox regulation—including feather development—while enabling significant metabolic rate increases that avoid trade-offs with lifespan. The strategy of NRF2 activation sought by intense clinical investigation therefore appears to have also unlocked a massively successful evolutionary trajectory. Nature Publishing Group UK 2020-05-18 /pmc/articles/PMC7234996/ /pubmed/32424161 http://dx.doi.org/10.1038/s41467-020-16129-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Castiglione, Gianni M.
Xu, Zhenhua
Zhou, Lingli
Duh, Elia J.
Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds
title Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds
title_full Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds
title_fullStr Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds
title_full_unstemmed Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds
title_short Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds
title_sort adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234996/
https://www.ncbi.nlm.nih.gov/pubmed/32424161
http://dx.doi.org/10.1038/s41467-020-16129-4
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